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You searched for subject:(RGD). Showing records 1 – 30 of 92 total matches.

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1. Engrand, Philippe. Calix[4]arènes fonctionnels pour ancrage sur polymère naturel et antennisation par le tripeptide RGD préparé par synthèse convergente : Functional calix[4]arenes designed for attachment on natural polymer and labeling by convergent-made RGD tripeptide.

Degree: Docteur es, Chimie et Physico-Chimie Moléculaires, 2008, Université Henri Poincaré – Nancy I

Ce travail porte sur la valorisation du calix[4]arène comme complexant de métaux de transition, immobilisé sur un matériau, et comme vecteur de principe actifs, aptes… (more)

Subjects/Keywords: RGD

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APA (6th Edition):

Engrand, P. (2008). Calix[4]arènes fonctionnels pour ancrage sur polymère naturel et antennisation par le tripeptide RGD préparé par synthèse convergente : Functional calix[4]arenes designed for attachment on natural polymer and labeling by convergent-made RGD tripeptide. (Doctoral Dissertation). Université Henri Poincaré – Nancy I. Retrieved from http://www.theses.fr/2008NAN10143

Chicago Manual of Style (16th Edition):

Engrand, Philippe. “Calix[4]arènes fonctionnels pour ancrage sur polymère naturel et antennisation par le tripeptide RGD préparé par synthèse convergente : Functional calix[4]arenes designed for attachment on natural polymer and labeling by convergent-made RGD tripeptide.” 2008. Doctoral Dissertation, Université Henri Poincaré – Nancy I. Accessed October 29, 2020. http://www.theses.fr/2008NAN10143.

MLA Handbook (7th Edition):

Engrand, Philippe. “Calix[4]arènes fonctionnels pour ancrage sur polymère naturel et antennisation par le tripeptide RGD préparé par synthèse convergente : Functional calix[4]arenes designed for attachment on natural polymer and labeling by convergent-made RGD tripeptide.” 2008. Web. 29 Oct 2020.

Vancouver:

Engrand P. Calix[4]arènes fonctionnels pour ancrage sur polymère naturel et antennisation par le tripeptide RGD préparé par synthèse convergente : Functional calix[4]arenes designed for attachment on natural polymer and labeling by convergent-made RGD tripeptide. [Internet] [Doctoral dissertation]. Université Henri Poincaré – Nancy I; 2008. [cited 2020 Oct 29]. Available from: http://www.theses.fr/2008NAN10143.

Council of Science Editors:

Engrand P. Calix[4]arènes fonctionnels pour ancrage sur polymère naturel et antennisation par le tripeptide RGD préparé par synthèse convergente : Functional calix[4]arenes designed for attachment on natural polymer and labeling by convergent-made RGD tripeptide. [Doctoral Dissertation]. Université Henri Poincaré – Nancy I; 2008. Available from: http://www.theses.fr/2008NAN10143


University of New South Wales

2. Wang, Zhiyong. RGD peptide derivatives as tools for tumour imaging and therapy.

Degree: Chemical Sciences & Engineering, 2013, University of New South Wales

 The first project is a tumour imaging method based on iodinated micelle which can be applied as contrast agent for CT. the obtained micelle solution… (more)

Subjects/Keywords: Peptide; RGD; Fluorine

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APA (6th Edition):

Wang, Z. (2013). RGD peptide derivatives as tools for tumour imaging and therapy. (Masters Thesis). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/52850 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11523/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Wang, Zhiyong. “RGD peptide derivatives as tools for tumour imaging and therapy.” 2013. Masters Thesis, University of New South Wales. Accessed October 29, 2020. http://handle.unsw.edu.au/1959.4/52850 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11523/SOURCE01?view=true.

MLA Handbook (7th Edition):

Wang, Zhiyong. “RGD peptide derivatives as tools for tumour imaging and therapy.” 2013. Web. 29 Oct 2020.

Vancouver:

Wang Z. RGD peptide derivatives as tools for tumour imaging and therapy. [Internet] [Masters thesis]. University of New South Wales; 2013. [cited 2020 Oct 29]. Available from: http://handle.unsw.edu.au/1959.4/52850 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11523/SOURCE01?view=true.

Council of Science Editors:

Wang Z. RGD peptide derivatives as tools for tumour imaging and therapy. [Masters Thesis]. University of New South Wales; 2013. Available from: http://handle.unsw.edu.au/1959.4/52850 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11523/SOURCE01?view=true


University of Debrecen

3. Kis, Adrienn. Szingenikus tumorok és metasztázisok in vivo vizsgálata PET radiotracerekkel .

Degree: DE – Általános Orvostudományi Kar, 2014, University of Debrecen

Kutatómunkánk során a tumorokon belüli endothel sejtek felszínén fokozott mennyiségben expresszálódó αvβ3 integrin receptorok jelenlétét kívántuk in vivo képalkotó eljárásokkal kimutatni kémiailag indukált szingenikus patkány eredetű tumorokon 68Ga- NODAGA-RGD segítségével. Advisors/Committee Members: Trencsényi, György (advisor), Debreceni Egyetem::Általános Orvostudományi Kar::Nukleáris Medicina Intézet (advisor).

Subjects/Keywords: szingenikus; NODAGA-RGD; PET; 68Ga

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APA (6th Edition):

Kis, A. (2014). Szingenikus tumorok és metasztázisok in vivo vizsgálata PET radiotracerekkel . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/194860

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kis, Adrienn. “Szingenikus tumorok és metasztázisok in vivo vizsgálata PET radiotracerekkel .” 2014. Thesis, University of Debrecen. Accessed October 29, 2020. http://hdl.handle.net/2437/194860.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kis, Adrienn. “Szingenikus tumorok és metasztázisok in vivo vizsgálata PET radiotracerekkel .” 2014. Web. 29 Oct 2020.

Vancouver:

Kis A. Szingenikus tumorok és metasztázisok in vivo vizsgálata PET radiotracerekkel . [Internet] [Thesis]. University of Debrecen; 2014. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2437/194860.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kis A. Szingenikus tumorok és metasztázisok in vivo vizsgálata PET radiotracerekkel . [Thesis]. University of Debrecen; 2014. Available from: http://hdl.handle.net/2437/194860

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

4. Moncelet, Damien. Propriétés d'agent de ciblage et de molécules cytotoxiques pour l'IRM et la thérapie de gliomes : Properties of targeting agent and cytotoxic molecules for MRI and therapy of glioma.

Degree: Docteur es, Biochimie, 2014, Bordeaux

L'objectif de cette thèse concerne la possibilité d'améliorer le diagnostic et la thérapie des gliomes par le ciblage des intégrines à l’aide du RGD et… (more)

Subjects/Keywords: Gliomes; Thérapie; IRM; RGD; Alcoxyamines; Glioma; Therapy; MRI; RGD; Alkoxyamines

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APA (6th Edition):

Moncelet, D. (2014). Propriétés d'agent de ciblage et de molécules cytotoxiques pour l'IRM et la thérapie de gliomes : Properties of targeting agent and cytotoxic molecules for MRI and therapy of glioma. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2014BORD0166

Chicago Manual of Style (16th Edition):

Moncelet, Damien. “Propriétés d'agent de ciblage et de molécules cytotoxiques pour l'IRM et la thérapie de gliomes : Properties of targeting agent and cytotoxic molecules for MRI and therapy of glioma.” 2014. Doctoral Dissertation, Bordeaux. Accessed October 29, 2020. http://www.theses.fr/2014BORD0166.

MLA Handbook (7th Edition):

Moncelet, Damien. “Propriétés d'agent de ciblage et de molécules cytotoxiques pour l'IRM et la thérapie de gliomes : Properties of targeting agent and cytotoxic molecules for MRI and therapy of glioma.” 2014. Web. 29 Oct 2020.

Vancouver:

Moncelet D. Propriétés d'agent de ciblage et de molécules cytotoxiques pour l'IRM et la thérapie de gliomes : Properties of targeting agent and cytotoxic molecules for MRI and therapy of glioma. [Internet] [Doctoral dissertation]. Bordeaux; 2014. [cited 2020 Oct 29]. Available from: http://www.theses.fr/2014BORD0166.

Council of Science Editors:

Moncelet D. Propriétés d'agent de ciblage et de molécules cytotoxiques pour l'IRM et la thérapie de gliomes : Properties of targeting agent and cytotoxic molecules for MRI and therapy of glioma. [Doctoral Dissertation]. Bordeaux; 2014. Available from: http://www.theses.fr/2014BORD0166


Universidade do Rio Grande do Sul

5. Antonow, Michelli Barcelos. Desenvolvimento e caracterização físico-química de nanocápsulas multiparedes complexadas com zinco e funcionalizadas com RGD para reconhecimento por integrinas ανβ3 presentes em células tumorais.

Degree: 2016, Universidade do Rio Grande do Sul

A funcionalização de superfície nas nanocápsulas contendo doxorrubicina com o peptídeo RGD é uma estratégia promissora devido a ligação preferencial na integrina αvβ3 expressa em… (more)

Subjects/Keywords: RGD; Farmácia; Nanocapsules; Doxorubicin; αvβ3 integrin

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APA (6th Edition):

Antonow, M. B. (2016). Desenvolvimento e caracterização físico-química de nanocápsulas multiparedes complexadas com zinco e funcionalizadas com RGD para reconhecimento por integrinas ανβ3 presentes em células tumorais. (Thesis). Universidade do Rio Grande do Sul. Retrieved from http://hdl.handle.net/10183/149502

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Antonow, Michelli Barcelos. “Desenvolvimento e caracterização físico-química de nanocápsulas multiparedes complexadas com zinco e funcionalizadas com RGD para reconhecimento por integrinas ανβ3 presentes em células tumorais.” 2016. Thesis, Universidade do Rio Grande do Sul. Accessed October 29, 2020. http://hdl.handle.net/10183/149502.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Antonow, Michelli Barcelos. “Desenvolvimento e caracterização físico-química de nanocápsulas multiparedes complexadas com zinco e funcionalizadas com RGD para reconhecimento por integrinas ανβ3 presentes em células tumorais.” 2016. Web. 29 Oct 2020.

Vancouver:

Antonow MB. Desenvolvimento e caracterização físico-química de nanocápsulas multiparedes complexadas com zinco e funcionalizadas com RGD para reconhecimento por integrinas ανβ3 presentes em células tumorais. [Internet] [Thesis]. Universidade do Rio Grande do Sul; 2016. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/10183/149502.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Antonow MB. Desenvolvimento e caracterização físico-química de nanocápsulas multiparedes complexadas com zinco e funcionalizadas com RGD para reconhecimento por integrinas ανβ3 presentes em células tumorais. [Thesis]. Universidade do Rio Grande do Sul; 2016. Available from: http://hdl.handle.net/10183/149502

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Toronto

6. Shan, Dan. RGD-conjugated Nanoparticles for Targeted Inhibition of Metastasis of Integrin αvβ3-overexpressing Breast Cancer Cells.

Degree: 2013, University of Toronto

The use of actively targeted nanoparticles as a delivery system for both the diagnosis and treatment of cancer has been explored extensively. However, selective tumor… (more)

Subjects/Keywords: nanoparticle; RGD; metastasis; αvβ3 integrin receptor; 0491

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APA (6th Edition):

Shan, D. (2013). RGD-conjugated Nanoparticles for Targeted Inhibition of Metastasis of Integrin αvβ3-overexpressing Breast Cancer Cells. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/70026

Chicago Manual of Style (16th Edition):

Shan, Dan. “RGD-conjugated Nanoparticles for Targeted Inhibition of Metastasis of Integrin αvβ3-overexpressing Breast Cancer Cells.” 2013. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/70026.

MLA Handbook (7th Edition):

Shan, Dan. “RGD-conjugated Nanoparticles for Targeted Inhibition of Metastasis of Integrin αvβ3-overexpressing Breast Cancer Cells.” 2013. Web. 29 Oct 2020.

Vancouver:

Shan D. RGD-conjugated Nanoparticles for Targeted Inhibition of Metastasis of Integrin αvβ3-overexpressing Breast Cancer Cells. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/70026.

Council of Science Editors:

Shan D. RGD-conjugated Nanoparticles for Targeted Inhibition of Metastasis of Integrin αvβ3-overexpressing Breast Cancer Cells. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/70026

7. Hansson, Annasara. Développement et évaluation in vitro d’un dérivé de chitosan fonctionnalisé avec des peptides RGD pour la cicatrisation : Development and In vitro Evaluation of an RGD-Functionalized Chitosan Derivative for Wound Healing.

Degree: Docteur es, Sciences pharmaceutiques, 2012, Université Claude Bernard – Lyon I

L’objectif du travail présenté dans cette thèse était de développer des nanoparticulesfonctionnelles ayant la capacité d’induire l’adhésion et la migration de kératinocyteshumains normaux. L’utilisation de… (more)

Subjects/Keywords: RGD; Chitosan; Nanoparticules; Adhésion cellulaire; Cicatrisation; RGD; Chitosan; Nanoparticles; Cell adhesion; Wound healing; 615

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APA (6th Edition):

Hansson, A. (2012). Développement et évaluation in vitro d’un dérivé de chitosan fonctionnalisé avec des peptides RGD pour la cicatrisation : Development and In vitro Evaluation of an RGD-Functionalized Chitosan Derivative for Wound Healing. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2012LYO10182

Chicago Manual of Style (16th Edition):

Hansson, Annasara. “Développement et évaluation in vitro d’un dérivé de chitosan fonctionnalisé avec des peptides RGD pour la cicatrisation : Development and In vitro Evaluation of an RGD-Functionalized Chitosan Derivative for Wound Healing.” 2012. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed October 29, 2020. http://www.theses.fr/2012LYO10182.

MLA Handbook (7th Edition):

Hansson, Annasara. “Développement et évaluation in vitro d’un dérivé de chitosan fonctionnalisé avec des peptides RGD pour la cicatrisation : Development and In vitro Evaluation of an RGD-Functionalized Chitosan Derivative for Wound Healing.” 2012. Web. 29 Oct 2020.

Vancouver:

Hansson A. Développement et évaluation in vitro d’un dérivé de chitosan fonctionnalisé avec des peptides RGD pour la cicatrisation : Development and In vitro Evaluation of an RGD-Functionalized Chitosan Derivative for Wound Healing. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2012. [cited 2020 Oct 29]. Available from: http://www.theses.fr/2012LYO10182.

Council of Science Editors:

Hansson A. Développement et évaluation in vitro d’un dérivé de chitosan fonctionnalisé avec des peptides RGD pour la cicatrisation : Development and In vitro Evaluation of an RGD-Functionalized Chitosan Derivative for Wound Healing. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2012. Available from: http://www.theses.fr/2012LYO10182


Brno University of Technology

8. Jatzová, Katarína. Bioaktivní peptidy - nadějná složka kosmetických produktů.: Bioactive peptides as a component of anti-aging cosmetics.

Degree: 2018, Brno University of Technology

 Ageing is a natural part of every human life cycle. During ageing there are lots of changes in the organism. One of the main pillars… (more)

Subjects/Keywords: kozmetika; peptidy; koža; integrita; RGD; stárnutie; cosmetic; peptides; skin; integrity; RGD; ageing

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APA (6th Edition):

Jatzová, K. (2018). Bioaktivní peptidy - nadějná složka kosmetických produktů.: Bioactive peptides as a component of anti-aging cosmetics. (Thesis). Brno University of Technology. Retrieved from http://hdl.handle.net/11012/5969

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Jatzová, Katarína. “Bioaktivní peptidy - nadějná složka kosmetických produktů.: Bioactive peptides as a component of anti-aging cosmetics.” 2018. Thesis, Brno University of Technology. Accessed October 29, 2020. http://hdl.handle.net/11012/5969.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Jatzová, Katarína. “Bioaktivní peptidy - nadějná složka kosmetických produktů.: Bioactive peptides as a component of anti-aging cosmetics.” 2018. Web. 29 Oct 2020.

Vancouver:

Jatzová K. Bioaktivní peptidy - nadějná složka kosmetických produktů.: Bioactive peptides as a component of anti-aging cosmetics. [Internet] [Thesis]. Brno University of Technology; 2018. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/11012/5969.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Jatzová K. Bioaktivní peptidy - nadějná složka kosmetických produktů.: Bioactive peptides as a component of anti-aging cosmetics. [Thesis]. Brno University of Technology; 2018. Available from: http://hdl.handle.net/11012/5969

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Brno University of Technology

9. Malečková, Romana. Studium možností zvýšení biokompatibility povrchů organických polovodičů: Study of possibilities of increasing the biocompatibility of organic semiconductor surfaces.

Degree: 2018, Brno University of Technology

 This bachelor thesis deals with the possibility of biocompatibilization of organic semiconducting polymer PEDOT:PSS using RGD peptide for the construction of biosensors. Samples were prepared… (more)

Subjects/Keywords: Biosenzory; biokompatibilita; RGD peptid; PEDOT:PSS; kontaktní úhel; Biosensors; biocompatibility; RGD peptide; PDEOT:PSS; contact angle

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APA (6th Edition):

Malečková, R. (2018). Studium možností zvýšení biokompatibility povrchů organických polovodičů: Study of possibilities of increasing the biocompatibility of organic semiconductor surfaces. (Thesis). Brno University of Technology. Retrieved from http://hdl.handle.net/11012/81790

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Malečková, Romana. “Studium možností zvýšení biokompatibility povrchů organických polovodičů: Study of possibilities of increasing the biocompatibility of organic semiconductor surfaces.” 2018. Thesis, Brno University of Technology. Accessed October 29, 2020. http://hdl.handle.net/11012/81790.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Malečková, Romana. “Studium možností zvýšení biokompatibility povrchů organických polovodičů: Study of possibilities of increasing the biocompatibility of organic semiconductor surfaces.” 2018. Web. 29 Oct 2020.

Vancouver:

Malečková R. Studium možností zvýšení biokompatibility povrchů organických polovodičů: Study of possibilities of increasing the biocompatibility of organic semiconductor surfaces. [Internet] [Thesis]. Brno University of Technology; 2018. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/11012/81790.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Malečková R. Studium možností zvýšení biokompatibility povrchů organických polovodičů: Study of possibilities of increasing the biocompatibility of organic semiconductor surfaces. [Thesis]. Brno University of Technology; 2018. Available from: http://hdl.handle.net/11012/81790

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Johannes Gutenberg Universität Mainz

10. Heller, Martin. Design of cell adhesive and angiogenic titanium surfaces for cellular stimulation.

Degree: 2013, Johannes Gutenberg Universität Mainz

 Die Förderung der Zelladhäsion durch sogenannte biomimetische Oberflächen wird in der Medizin als vielversprechender Ansatz gesehen, um Komplikationen wie z. B. Fremdkörperreaktionen nach der Implantation… (more)

Subjects/Keywords: Titan; Biomimetische Oberflächenmodifizierung; Plasmapolymerisation; RGD-Peptid; VEGF; Taitanium, Biomimetic Surface Modification; Plasma Polymerisation; RGD-Peptide; VEGF; Generalities, Science

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APA (6th Edition):

Heller, M. (2013). Design of cell adhesive and angiogenic titanium surfaces for cellular stimulation. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2013/3413/

Chicago Manual of Style (16th Edition):

Heller, Martin. “Design of cell adhesive and angiogenic titanium surfaces for cellular stimulation.” 2013. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed October 29, 2020. http://ubm.opus.hbz-nrw.de/volltexte/2013/3413/.

MLA Handbook (7th Edition):

Heller, Martin. “Design of cell adhesive and angiogenic titanium surfaces for cellular stimulation.” 2013. Web. 29 Oct 2020.

Vancouver:

Heller M. Design of cell adhesive and angiogenic titanium surfaces for cellular stimulation. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2013. [cited 2020 Oct 29]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3413/.

Council of Science Editors:

Heller M. Design of cell adhesive and angiogenic titanium surfaces for cellular stimulation. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2013. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3413/

11. Oliveira, Érica Aparecida de. Estudo comparativo de radiofármacos para angiogênese na detecção de melanoma.

Degree: Mestrado, Tecnologia Nuclear - Aplicações, 2011, University of São Paulo

Diagnóstico precoce e tratamento de melanoma, um tumor cutâneo com o pior prognóstico, é extremamente importante para um resultado clínico favorável. A biblioteca de peptídeos… (more)

Subjects/Keywords: angiogênese; angiogenesis; melanoma; melanoma; NGR peptide; peptídeo NGR; peptídeo RGD; RGD peptide; technetium-99m; tecnécio-99m

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APA (6th Edition):

Oliveira, . A. d. (2011). Estudo comparativo de radiofármacos para angiogênese na detecção de melanoma. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/85/85131/tde-31102011-092818/ ;

Chicago Manual of Style (16th Edition):

Oliveira, Érica Aparecida de. “Estudo comparativo de radiofármacos para angiogênese na detecção de melanoma.” 2011. Masters Thesis, University of São Paulo. Accessed October 29, 2020. http://www.teses.usp.br/teses/disponiveis/85/85131/tde-31102011-092818/ ;.

MLA Handbook (7th Edition):

Oliveira, Érica Aparecida de. “Estudo comparativo de radiofármacos para angiogênese na detecção de melanoma.” 2011. Web. 29 Oct 2020.

Vancouver:

Oliveira Ad. Estudo comparativo de radiofármacos para angiogênese na detecção de melanoma. [Internet] [Masters thesis]. University of São Paulo; 2011. [cited 2020 Oct 29]. Available from: http://www.teses.usp.br/teses/disponiveis/85/85131/tde-31102011-092818/ ;.

Council of Science Editors:

Oliveira Ad. Estudo comparativo de radiofármacos para angiogênese na detecção de melanoma. [Masters Thesis]. University of São Paulo; 2011. Available from: http://www.teses.usp.br/teses/disponiveis/85/85131/tde-31102011-092818/ ;

12. Oliveira, Érica Aparecida de. Desenvolvimento de radiotraçadores angiogênicos para diagnóstico de glioma: estudo em modelo animal.

Degree: PhD, Tecnologia Nuclear - Aplicações, 2014, University of São Paulo

A imagem molecular oferece a perspectiva de detectar doenças bem antes de os sintomas surgirem. A vasculatura tumoral é vital no crescimento do tumor e… (more)

Subjects/Keywords: angiogênese; angiogenesis; glioma; glioma; GX1 peptide; peptídeo GX1; peptídeo RGD-GX1; RGD-GX1 peptide; technetium 99m; tecnécio 99m

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Oliveira, . A. d. (2014). Desenvolvimento de radiotraçadores angiogênicos para diagnóstico de glioma: estudo em modelo animal. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/85/85131/tde-02122014-143353/ ;

Chicago Manual of Style (16th Edition):

Oliveira, Érica Aparecida de. “Desenvolvimento de radiotraçadores angiogênicos para diagnóstico de glioma: estudo em modelo animal.” 2014. Doctoral Dissertation, University of São Paulo. Accessed October 29, 2020. http://www.teses.usp.br/teses/disponiveis/85/85131/tde-02122014-143353/ ;.

MLA Handbook (7th Edition):

Oliveira, Érica Aparecida de. “Desenvolvimento de radiotraçadores angiogênicos para diagnóstico de glioma: estudo em modelo animal.” 2014. Web. 29 Oct 2020.

Vancouver:

Oliveira Ad. Desenvolvimento de radiotraçadores angiogênicos para diagnóstico de glioma: estudo em modelo animal. [Internet] [Doctoral dissertation]. University of São Paulo; 2014. [cited 2020 Oct 29]. Available from: http://www.teses.usp.br/teses/disponiveis/85/85131/tde-02122014-143353/ ;.

Council of Science Editors:

Oliveira Ad. Desenvolvimento de radiotraçadores angiogênicos para diagnóstico de glioma: estudo em modelo animal. [Doctoral Dissertation]. University of São Paulo; 2014. Available from: http://www.teses.usp.br/teses/disponiveis/85/85131/tde-02122014-143353/ ;

13. Provost, Claire. Comparaison de radiotraceurs marqués au gallium-68 et au fluor-18 pour l’imagerie TEP de modèles précliniques de neuroblastome, de glioblastome ou de cancer bronchopulmonaire. : Comparison of gallium-68 and fluor-18 labelled radiotracers for PET imaging of preclinical models of neuroblastoma, glioblastoma or bronchopulmonary cancer.

Degree: Docteur es, Sciences de la vie et de la santé, 2018, Université Paris-Saclay (ComUE)

La Tomographie par Emission de Positons (TEP) est une modalité d’imagerie médicale en pleine expansion depuis une quinzaine d’années. En oncologie, la TEP au 18F-fluorodésoxyglucose… (more)

Subjects/Keywords: Fluor-18; Gallium-68; Tep; Édotréotide; Peptides RGD; Oncologie; Fluorine; Gallium-68; Tep; Edotreotide; RGD peptides; Oncology

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APA (6th Edition):

Provost, C. (2018). Comparaison de radiotraceurs marqués au gallium-68 et au fluor-18 pour l’imagerie TEP de modèles précliniques de neuroblastome, de glioblastome ou de cancer bronchopulmonaire. : Comparison of gallium-68 and fluor-18 labelled radiotracers for PET imaging of preclinical models of neuroblastoma, glioblastoma or bronchopulmonary cancer. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2018SACLS052

Chicago Manual of Style (16th Edition):

Provost, Claire. “Comparaison de radiotraceurs marqués au gallium-68 et au fluor-18 pour l’imagerie TEP de modèles précliniques de neuroblastome, de glioblastome ou de cancer bronchopulmonaire. : Comparison of gallium-68 and fluor-18 labelled radiotracers for PET imaging of preclinical models of neuroblastoma, glioblastoma or bronchopulmonary cancer.” 2018. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed October 29, 2020. http://www.theses.fr/2018SACLS052.

MLA Handbook (7th Edition):

Provost, Claire. “Comparaison de radiotraceurs marqués au gallium-68 et au fluor-18 pour l’imagerie TEP de modèles précliniques de neuroblastome, de glioblastome ou de cancer bronchopulmonaire. : Comparison of gallium-68 and fluor-18 labelled radiotracers for PET imaging of preclinical models of neuroblastoma, glioblastoma or bronchopulmonary cancer.” 2018. Web. 29 Oct 2020.

Vancouver:

Provost C. Comparaison de radiotraceurs marqués au gallium-68 et au fluor-18 pour l’imagerie TEP de modèles précliniques de neuroblastome, de glioblastome ou de cancer bronchopulmonaire. : Comparison of gallium-68 and fluor-18 labelled radiotracers for PET imaging of preclinical models of neuroblastoma, glioblastoma or bronchopulmonary cancer. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2018. [cited 2020 Oct 29]. Available from: http://www.theses.fr/2018SACLS052.

Council of Science Editors:

Provost C. Comparaison de radiotraceurs marqués au gallium-68 et au fluor-18 pour l’imagerie TEP de modèles précliniques de neuroblastome, de glioblastome ou de cancer bronchopulmonaire. : Comparison of gallium-68 and fluor-18 labelled radiotracers for PET imaging of preclinical models of neuroblastoma, glioblastoma or bronchopulmonary cancer. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2018. Available from: http://www.theses.fr/2018SACLS052


Université de Grenoble

14. Petitprin, Aurélie. Le RAFT-RGD radiomarqué avec un émetteur °- comme nouvel agent de radiothérapie interne vectorisée : Development of a new anti-cancer agent for targeted radionuclide therapy : ß- radiolabeled RAFT-RGD.

Degree: Docteur es, Biotechnologie, instrumentation, signal et imagerie pour la biologie, la médecine et l'environnement, 2013, Université de Grenoble

Le RAFT-RGD radiomarqué avec un émetteur β- comme nouvel agent de radiothérapie interne vectorisée. L'intégrine αvβ3 est fortement impliquée en oncogenèse à travers son rôle… (more)

Subjects/Keywords: RAFT-RGD; Cancer; Radiothérapie interne vectorisée; Alpha v beta 3; RAFT-RGD; Cancer; Targeted radionuclide therapy; Alpha v beta 3

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APA (6th Edition):

Petitprin, A. (2013). Le RAFT-RGD radiomarqué avec un émetteur °- comme nouvel agent de radiothérapie interne vectorisée : Development of a new anti-cancer agent for targeted radionuclide therapy : ß- radiolabeled RAFT-RGD. (Doctoral Dissertation). Université de Grenoble. Retrieved from http://www.theses.fr/2013GRENS002

Chicago Manual of Style (16th Edition):

Petitprin, Aurélie. “Le RAFT-RGD radiomarqué avec un émetteur °- comme nouvel agent de radiothérapie interne vectorisée : Development of a new anti-cancer agent for targeted radionuclide therapy : ß- radiolabeled RAFT-RGD.” 2013. Doctoral Dissertation, Université de Grenoble. Accessed October 29, 2020. http://www.theses.fr/2013GRENS002.

MLA Handbook (7th Edition):

Petitprin, Aurélie. “Le RAFT-RGD radiomarqué avec un émetteur °- comme nouvel agent de radiothérapie interne vectorisée : Development of a new anti-cancer agent for targeted radionuclide therapy : ß- radiolabeled RAFT-RGD.” 2013. Web. 29 Oct 2020.

Vancouver:

Petitprin A. Le RAFT-RGD radiomarqué avec un émetteur °- comme nouvel agent de radiothérapie interne vectorisée : Development of a new anti-cancer agent for targeted radionuclide therapy : ß- radiolabeled RAFT-RGD. [Internet] [Doctoral dissertation]. Université de Grenoble; 2013. [cited 2020 Oct 29]. Available from: http://www.theses.fr/2013GRENS002.

Council of Science Editors:

Petitprin A. Le RAFT-RGD radiomarqué avec un émetteur °- comme nouvel agent de radiothérapie interne vectorisée : Development of a new anti-cancer agent for targeted radionuclide therapy : ß- radiolabeled RAFT-RGD. [Doctoral Dissertation]. Université de Grenoble; 2013. Available from: http://www.theses.fr/2013GRENS002

15. 최, 민호. Three-dimensional cell culture on polyvinyl alcohol (PVA) nanofiber containing Arg-Gly-Asp (RGD) peptide.

Degree: 2019, Ajou University

Recently, the importance of nanofibers as a three-dimensional cell culture scaffold has been revealed. Research and development on nanofiber production using electrospinning has been actively… (more)

Subjects/Keywords: 전기방사 (electrospinning); 폴리비닐알코올 (polyvinyl alcohol; PVA); 나노섬유 (nanofiber); RGD 펩타이드 (RGD peptide); 3차원 세포 배양 (3D cell culture)

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APA (6th Edition):

최, . (2019). Three-dimensional cell culture on polyvinyl alcohol (PVA) nanofiber containing Arg-Gly-Asp (RGD) peptide. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/17902 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000028321

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

최, 민호. “Three-dimensional cell culture on polyvinyl alcohol (PVA) nanofiber containing Arg-Gly-Asp (RGD) peptide.” 2019. Thesis, Ajou University. Accessed October 29, 2020. http://repository.ajou.ac.kr/handle/201003/17902 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000028321.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

최, 민호. “Three-dimensional cell culture on polyvinyl alcohol (PVA) nanofiber containing Arg-Gly-Asp (RGD) peptide.” 2019. Web. 29 Oct 2020.

Vancouver:

최 . Three-dimensional cell culture on polyvinyl alcohol (PVA) nanofiber containing Arg-Gly-Asp (RGD) peptide. [Internet] [Thesis]. Ajou University; 2019. [cited 2020 Oct 29]. Available from: http://repository.ajou.ac.kr/handle/201003/17902 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000028321.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

최 . Three-dimensional cell culture on polyvinyl alcohol (PVA) nanofiber containing Arg-Gly-Asp (RGD) peptide. [Thesis]. Ajou University; 2019. Available from: http://repository.ajou.ac.kr/handle/201003/17902 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000028321

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

16. Thoreau, Fabien. Conception, synthèse et activité biologique de vecteurs peptidiques pour le ciblage et/ou la thérapie du cancer : Design, synthesis and biological activity of peptidic vectors for the diagnostic and/or therapy of tumours.

Degree: Docteur es, Chimie organique, 2017, Université Grenoble Alpes (ComUE)

Ces travaux de thèse portent sur la conception, la synthèse et l'étude biologique de vecteurs peptidiques pour des applications en diagnostic et/ou thérapie du cancer.Nous… (more)

Subjects/Keywords: Vectorisation; Ligation chimique; Rgd; Atwlppr; Intégrine avB3; Neuropiline-1; Vectorisation; Chemical ligation; Rgd; Atwlppr; Integrin avB3; Neuropilin-1

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Thoreau, F. (2017). Conception, synthèse et activité biologique de vecteurs peptidiques pour le ciblage et/ou la thérapie du cancer : Design, synthesis and biological activity of peptidic vectors for the diagnostic and/or therapy of tumours. (Doctoral Dissertation). Université Grenoble Alpes (ComUE). Retrieved from http://www.theses.fr/2017GREAV006

Chicago Manual of Style (16th Edition):

Thoreau, Fabien. “Conception, synthèse et activité biologique de vecteurs peptidiques pour le ciblage et/ou la thérapie du cancer : Design, synthesis and biological activity of peptidic vectors for the diagnostic and/or therapy of tumours.” 2017. Doctoral Dissertation, Université Grenoble Alpes (ComUE). Accessed October 29, 2020. http://www.theses.fr/2017GREAV006.

MLA Handbook (7th Edition):

Thoreau, Fabien. “Conception, synthèse et activité biologique de vecteurs peptidiques pour le ciblage et/ou la thérapie du cancer : Design, synthesis and biological activity of peptidic vectors for the diagnostic and/or therapy of tumours.” 2017. Web. 29 Oct 2020.

Vancouver:

Thoreau F. Conception, synthèse et activité biologique de vecteurs peptidiques pour le ciblage et/ou la thérapie du cancer : Design, synthesis and biological activity of peptidic vectors for the diagnostic and/or therapy of tumours. [Internet] [Doctoral dissertation]. Université Grenoble Alpes (ComUE); 2017. [cited 2020 Oct 29]. Available from: http://www.theses.fr/2017GREAV006.

Council of Science Editors:

Thoreau F. Conception, synthèse et activité biologique de vecteurs peptidiques pour le ciblage et/ou la thérapie du cancer : Design, synthesis and biological activity of peptidic vectors for the diagnostic and/or therapy of tumours. [Doctoral Dissertation]. Université Grenoble Alpes (ComUE); 2017. Available from: http://www.theses.fr/2017GREAV006

17. Tsiapa, Irene. Μεθοδολογίες μοριακής απεικόνισης με επισημασμένα νανοσωματίδια για τον ποσοτικό προσδιορισμό της χωροχρονικής κατανομής της αγγειογένεσης σε καρκινικούς όγκους.

Degree: 2013, University of Patras; Πανεπιστήμιο Πατρών

The aim of the present project is the in vivo evaluation of quantitative monitoring of angiogenesis making use of the molecular imaging methodology. A new… (more)

Subjects/Keywords: Μοριακή απεικόνιση; Αγγειογένεση; Νανοσωματίδια; RGD πεπτίδια; Ιντεγκρίνες ανβ3; Τεχνήτιο (99mTc); Molecular imaging; Angiogenesis; Nanoparticles; RGD peptides; Integrins ανβ3; Technetium (99mTc)

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APA (6th Edition):

Tsiapa, I. (2013). Μεθοδολογίες μοριακής απεικόνισης με επισημασμένα νανοσωματίδια για τον ποσοτικό προσδιορισμό της χωροχρονικής κατανομής της αγγειογένεσης σε καρκινικούς όγκους. (Thesis). University of Patras; Πανεπιστήμιο Πατρών. Retrieved from http://hdl.handle.net/10442/hedi/33119

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Tsiapa, Irene. “Μεθοδολογίες μοριακής απεικόνισης με επισημασμένα νανοσωματίδια για τον ποσοτικό προσδιορισμό της χωροχρονικής κατανομής της αγγειογένεσης σε καρκινικούς όγκους.” 2013. Thesis, University of Patras; Πανεπιστήμιο Πατρών. Accessed October 29, 2020. http://hdl.handle.net/10442/hedi/33119.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Tsiapa, Irene. “Μεθοδολογίες μοριακής απεικόνισης με επισημασμένα νανοσωματίδια για τον ποσοτικό προσδιορισμό της χωροχρονικής κατανομής της αγγειογένεσης σε καρκινικούς όγκους.” 2013. Web. 29 Oct 2020.

Vancouver:

Tsiapa I. Μεθοδολογίες μοριακής απεικόνισης με επισημασμένα νανοσωματίδια για τον ποσοτικό προσδιορισμό της χωροχρονικής κατανομής της αγγειογένεσης σε καρκινικούς όγκους. [Internet] [Thesis]. University of Patras; Πανεπιστήμιο Πατρών; 2013. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/10442/hedi/33119.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Tsiapa I. Μεθοδολογίες μοριακής απεικόνισης με επισημασμένα νανοσωματίδια για τον ποσοτικό προσδιορισμό της χωροχρονικής κατανομής της αγγειογένεσης σε καρκινικούς όγκους. [Thesis]. University of Patras; Πανεπιστήμιο Πατρών; 2013. Available from: http://hdl.handle.net/10442/hedi/33119

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Michigan Technological University

18. Salehi, Nasrin. ENGINEERING ANTIPHAGOCYTIC AND TARGETING THERAPEUTIC CARRIERS FOR CANCER TREATMENT.

Degree: PhD, Department of Chemical Engineering, 2016, Michigan Technological University

  Localizing the drug at the site of action is one of the most important goals of drug delivery systems. This requires developing a vehicle… (more)

Subjects/Keywords: CD47; Antiphagocytosis; Cancer; Targeting; Lentivirus; RGD; Molecular Biology

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APA (6th Edition):

Salehi, N. (2016). ENGINEERING ANTIPHAGOCYTIC AND TARGETING THERAPEUTIC CARRIERS FOR CANCER TREATMENT. (Doctoral Dissertation). Michigan Technological University. Retrieved from http://digitalcommons.mtu.edu/etdr/245

Chicago Manual of Style (16th Edition):

Salehi, Nasrin. “ENGINEERING ANTIPHAGOCYTIC AND TARGETING THERAPEUTIC CARRIERS FOR CANCER TREATMENT.” 2016. Doctoral Dissertation, Michigan Technological University. Accessed October 29, 2020. http://digitalcommons.mtu.edu/etdr/245.

MLA Handbook (7th Edition):

Salehi, Nasrin. “ENGINEERING ANTIPHAGOCYTIC AND TARGETING THERAPEUTIC CARRIERS FOR CANCER TREATMENT.” 2016. Web. 29 Oct 2020.

Vancouver:

Salehi N. ENGINEERING ANTIPHAGOCYTIC AND TARGETING THERAPEUTIC CARRIERS FOR CANCER TREATMENT. [Internet] [Doctoral dissertation]. Michigan Technological University; 2016. [cited 2020 Oct 29]. Available from: http://digitalcommons.mtu.edu/etdr/245.

Council of Science Editors:

Salehi N. ENGINEERING ANTIPHAGOCYTIC AND TARGETING THERAPEUTIC CARRIERS FOR CANCER TREATMENT. [Doctoral Dissertation]. Michigan Technological University; 2016. Available from: http://digitalcommons.mtu.edu/etdr/245


Universidade de Brasília

19. Otilie Eichler Vercillo. Reações Ugi na construção de ciclopeptóides : provável inibidor do complexo Tat/TAR do vírus HIV-1.

Degree: 2007, Universidade de Brasília

Peptóides são oligômeros de glicinas N-substituídas que mimetizam as propriedades e a estrutura natural dos peptídeos. Diferem dos peptídeos, por suas cadeias laterais estarem conectadas… (more)

Subjects/Keywords: complexo TAT/TAR; QUIMICA; Peptóides; HIV-1; peptídios RGD; Reações Ugi

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APA (6th Edition):

Vercillo, O. E. (2007). Reações Ugi na construção de ciclopeptóides : provável inibidor do complexo Tat/TAR do vírus HIV-1. (Thesis). Universidade de Brasília. Retrieved from http://bdtd.bce.unb.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=6115

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Vercillo, Otilie Eichler. “Reações Ugi na construção de ciclopeptóides : provável inibidor do complexo Tat/TAR do vírus HIV-1.” 2007. Thesis, Universidade de Brasília. Accessed October 29, 2020. http://bdtd.bce.unb.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=6115.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Vercillo, Otilie Eichler. “Reações Ugi na construção de ciclopeptóides : provável inibidor do complexo Tat/TAR do vírus HIV-1.” 2007. Web. 29 Oct 2020.

Vancouver:

Vercillo OE. Reações Ugi na construção de ciclopeptóides : provável inibidor do complexo Tat/TAR do vírus HIV-1. [Internet] [Thesis]. Universidade de Brasília; 2007. [cited 2020 Oct 29]. Available from: http://bdtd.bce.unb.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=6115.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Vercillo OE. Reações Ugi na construção de ciclopeptóides : provável inibidor do complexo Tat/TAR do vírus HIV-1. [Thesis]. Universidade de Brasília; 2007. Available from: http://bdtd.bce.unb.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=6115

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

20. Davila Ramos, Johanna. Syntheses and uses of modified polyelectrolytes for therapeutic hydrogels and films with controlled and selective protein adsorption : Synthèse et mise en oeuvre de polyélectrolytes modifiés pour des hydrogels thérapeutiques et des films à adsorption sélective et contrôlée de protéines.

Degree: Docteur es, Chimie physique, 2012, Université de Strasbourg

La première partie de cette thèse est dédiée à la modification de polyélectrolytes pour former des films de multicouche de polyélectrolytes (PEM) ayant des propriétés… (more)

Subjects/Keywords: Cyto-mechanoresponsive; RGD; Biotin; PEM; PEM; Polyelectrolyte; 547.8

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APA (6th Edition):

Davila Ramos, J. (2012). Syntheses and uses of modified polyelectrolytes for therapeutic hydrogels and films with controlled and selective protein adsorption : Synthèse et mise en oeuvre de polyélectrolytes modifiés pour des hydrogels thérapeutiques et des films à adsorption sélective et contrôlée de protéines. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2012STRAF005

Chicago Manual of Style (16th Edition):

Davila Ramos, Johanna. “Syntheses and uses of modified polyelectrolytes for therapeutic hydrogels and films with controlled and selective protein adsorption : Synthèse et mise en oeuvre de polyélectrolytes modifiés pour des hydrogels thérapeutiques et des films à adsorption sélective et contrôlée de protéines.” 2012. Doctoral Dissertation, Université de Strasbourg. Accessed October 29, 2020. http://www.theses.fr/2012STRAF005.

MLA Handbook (7th Edition):

Davila Ramos, Johanna. “Syntheses and uses of modified polyelectrolytes for therapeutic hydrogels and films with controlled and selective protein adsorption : Synthèse et mise en oeuvre de polyélectrolytes modifiés pour des hydrogels thérapeutiques et des films à adsorption sélective et contrôlée de protéines.” 2012. Web. 29 Oct 2020.

Vancouver:

Davila Ramos J. Syntheses and uses of modified polyelectrolytes for therapeutic hydrogels and films with controlled and selective protein adsorption : Synthèse et mise en oeuvre de polyélectrolytes modifiés pour des hydrogels thérapeutiques et des films à adsorption sélective et contrôlée de protéines. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2012. [cited 2020 Oct 29]. Available from: http://www.theses.fr/2012STRAF005.

Council of Science Editors:

Davila Ramos J. Syntheses and uses of modified polyelectrolytes for therapeutic hydrogels and films with controlled and selective protein adsorption : Synthèse et mise en oeuvre de polyélectrolytes modifiés pour des hydrogels thérapeutiques et des films à adsorption sélective et contrôlée de protéines. [Doctoral Dissertation]. Université de Strasbourg; 2012. Available from: http://www.theses.fr/2012STRAF005

21. E.M.V. Araldi. INTEGRIN ALPHAVBETA3 AS THERAPEUTIC TARGET AND IMAGING BIOMARKER FOR VASCULAR ENDOTHELIAL CELLS AND CANCER EPITHELIAL CELLS.

Degree: 2010, Università degli Studi di Milano

 Integrins are heterodimeric transmembrane proteins belonging to a family of cell adhesion receptors evolutionary old and that play pivotal roles in physiological and pathological processes,… (more)

Subjects/Keywords: integrins; angiogenesis; cancer; peptidomimetics; RGD; Settore BIO/10 - Biochimica

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APA (6th Edition):

Araldi, E. (2010). INTEGRIN ALPHAVBETA3 AS THERAPEUTIC TARGET AND IMAGING BIOMARKER FOR VASCULAR ENDOTHELIAL CELLS AND CANCER EPITHELIAL CELLS. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/150215

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Araldi, E.M.V.. “INTEGRIN ALPHAVBETA3 AS THERAPEUTIC TARGET AND IMAGING BIOMARKER FOR VASCULAR ENDOTHELIAL CELLS AND CANCER EPITHELIAL CELLS.” 2010. Thesis, Università degli Studi di Milano. Accessed October 29, 2020. http://hdl.handle.net/2434/150215.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Araldi, E.M.V.. “INTEGRIN ALPHAVBETA3 AS THERAPEUTIC TARGET AND IMAGING BIOMARKER FOR VASCULAR ENDOTHELIAL CELLS AND CANCER EPITHELIAL CELLS.” 2010. Web. 29 Oct 2020.

Vancouver:

Araldi E. INTEGRIN ALPHAVBETA3 AS THERAPEUTIC TARGET AND IMAGING BIOMARKER FOR VASCULAR ENDOTHELIAL CELLS AND CANCER EPITHELIAL CELLS. [Internet] [Thesis]. Università degli Studi di Milano; 2010. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2434/150215.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Araldi E. INTEGRIN ALPHAVBETA3 AS THERAPEUTIC TARGET AND IMAGING BIOMARKER FOR VASCULAR ENDOTHELIAL CELLS AND CANCER EPITHELIAL CELLS. [Thesis]. Università degli Studi di Milano; 2010. Available from: http://hdl.handle.net/2434/150215

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

22. Elsharif, Amal A. M. Functional investigation of dual αvβ3 and αllbβ3 integrin inhibition in haematological and solid tumour models.

Degree: PhD, 2018, University of Bradford

 Invasion and metastasis of cancer is the leading cause of increased mortality. In addition, haematological malignancies (leukaemia and lymphoma) are a significant cause of morbidity… (more)

Subjects/Keywords: RGD binding integrins; K562; Adhesion; Metastasis; Integrin antagonists; Cancer cells

Page 1 Page 2

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APA (6th Edition):

Elsharif, A. A. M. (2018). Functional investigation of dual αvβ3 and αllbβ3 integrin inhibition in haematological and solid tumour models. (Doctoral Dissertation). University of Bradford. Retrieved from http://hdl.handle.net/10454/16883

Chicago Manual of Style (16th Edition):

Elsharif, Amal A M. “Functional investigation of dual αvβ3 and αllbβ3 integrin inhibition in haematological and solid tumour models.” 2018. Doctoral Dissertation, University of Bradford. Accessed October 29, 2020. http://hdl.handle.net/10454/16883.

MLA Handbook (7th Edition):

Elsharif, Amal A M. “Functional investigation of dual αvβ3 and αllbβ3 integrin inhibition in haematological and solid tumour models.” 2018. Web. 29 Oct 2020.

Vancouver:

Elsharif AAM. Functional investigation of dual αvβ3 and αllbβ3 integrin inhibition in haematological and solid tumour models. [Internet] [Doctoral dissertation]. University of Bradford; 2018. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/10454/16883.

Council of Science Editors:

Elsharif AAM. Functional investigation of dual αvβ3 and αllbβ3 integrin inhibition in haematological and solid tumour models. [Doctoral Dissertation]. University of Bradford; 2018. Available from: http://hdl.handle.net/10454/16883

23. Marliete Maria Soares da Silva. Peçonhas de serpentes : proteômica, genômica e ação durante o desenvolvimento embrionário de codornas japonesas (Coturnix japonica) expostas ao campo magnético de baixa frequência.

Degree: 2012, Universidade Federal Rural de Pernambuco

O objetivo deste trabalho foi obter uma desintegrina RGD da peçonha de serpentes e avaliar sua ação junto ao campo magnético de baixa frequência no… (more)

Subjects/Keywords: Ciências Agrárias; Desintegrina RGD; Embrião de codorna; Peçonhas de serpentes; Proteômica; Biociência animal; Embryos quail; Low frequency magnetic field; RGD disintegrin; Snake venom; Campo magnétido de baixa frequência

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APA (6th Edition):

Silva, M. M. S. d. (2012). Peçonhas de serpentes : proteômica, genômica e ação durante o desenvolvimento embrionário de codornas japonesas (Coturnix japonica) expostas ao campo magnético de baixa frequência. (Thesis). Universidade Federal Rural de Pernambuco. Retrieved from http://200.17.137.108/tde_busca/arquivo.php?codArquivo=1704

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Silva, Marliete Maria Soares da. “Peçonhas de serpentes : proteômica, genômica e ação durante o desenvolvimento embrionário de codornas japonesas (Coturnix japonica) expostas ao campo magnético de baixa frequência.” 2012. Thesis, Universidade Federal Rural de Pernambuco. Accessed October 29, 2020. http://200.17.137.108/tde_busca/arquivo.php?codArquivo=1704.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Silva, Marliete Maria Soares da. “Peçonhas de serpentes : proteômica, genômica e ação durante o desenvolvimento embrionário de codornas japonesas (Coturnix japonica) expostas ao campo magnético de baixa frequência.” 2012. Web. 29 Oct 2020.

Vancouver:

Silva MMSd. Peçonhas de serpentes : proteômica, genômica e ação durante o desenvolvimento embrionário de codornas japonesas (Coturnix japonica) expostas ao campo magnético de baixa frequência. [Internet] [Thesis]. Universidade Federal Rural de Pernambuco; 2012. [cited 2020 Oct 29]. Available from: http://200.17.137.108/tde_busca/arquivo.php?codArquivo=1704.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Silva MMSd. Peçonhas de serpentes : proteômica, genômica e ação durante o desenvolvimento embrionário de codornas japonesas (Coturnix japonica) expostas ao campo magnético de baixa frequência. [Thesis]. Universidade Federal Rural de Pernambuco; 2012. Available from: http://200.17.137.108/tde_busca/arquivo.php?codArquivo=1704

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

24. R. Colombo. SYNTHESIS AND BIOLOGICAL EVALUATION OF POTENT INTEGRIN LIGANDS CONTAINING A DIKETOPIPERAZINE SCAFFOLD, AND OF THEIR CONJUGATES WITH CYTOTOXIC AGENTS.

Degree: 2013, Università degli Studi di Milano

 A library of eight bifunctional 2,5-diketopiperazine (DKP) scaffolds, which are formally derived from 2,3-diaminopropionic acid and aspartic acid (DKP1 - DKP7) or glutamic acid (DKP8)… (more)

Subjects/Keywords: angiogenesis; integrins; RGD; diketopiperazines; peptidomimetics; paclitaxel; tumor homing; targeted drug; paclitaxel conjugates; RGD conjugates; Settore CHIM/06 - Chimica Organica; Settore CHIM/08 - Chimica Farmaceutica; Settore BIO/14 - Farmacologia

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APA (6th Edition):

Colombo, R. (2013). SYNTHESIS AND BIOLOGICAL EVALUATION OF POTENT INTEGRIN LIGANDS CONTAINING A DIKETOPIPERAZINE SCAFFOLD, AND OF THEIR CONJUGATES WITH CYTOTOXIC AGENTS. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/214953

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Colombo, R.. “SYNTHESIS AND BIOLOGICAL EVALUATION OF POTENT INTEGRIN LIGANDS CONTAINING A DIKETOPIPERAZINE SCAFFOLD, AND OF THEIR CONJUGATES WITH CYTOTOXIC AGENTS.” 2013. Thesis, Università degli Studi di Milano. Accessed October 29, 2020. http://hdl.handle.net/2434/214953.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Colombo, R.. “SYNTHESIS AND BIOLOGICAL EVALUATION OF POTENT INTEGRIN LIGANDS CONTAINING A DIKETOPIPERAZINE SCAFFOLD, AND OF THEIR CONJUGATES WITH CYTOTOXIC AGENTS.” 2013. Web. 29 Oct 2020.

Vancouver:

Colombo R. SYNTHESIS AND BIOLOGICAL EVALUATION OF POTENT INTEGRIN LIGANDS CONTAINING A DIKETOPIPERAZINE SCAFFOLD, AND OF THEIR CONJUGATES WITH CYTOTOXIC AGENTS. [Internet] [Thesis]. Università degli Studi di Milano; 2013. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/2434/214953.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Colombo R. SYNTHESIS AND BIOLOGICAL EVALUATION OF POTENT INTEGRIN LIGANDS CONTAINING A DIKETOPIPERAZINE SCAFFOLD, AND OF THEIR CONJUGATES WITH CYTOTOXIC AGENTS. [Thesis]. Università degli Studi di Milano; 2013. Available from: http://hdl.handle.net/2434/214953

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

25. Akasov, Roman. Novel 3D in vitro models based on multicellular tumor spheroids to test anticancer drugs and drug delivery vehicles : Nouveaux modèles 3D in vitro à base de sphéroïdes multicellulaires tumoraux pour tester des substances anticancéreuses et des vecteurs de délivrance de médicaments.

Degree: Docteur es, Biotechnologies, 2017, Strasbourg; M.M. Shemyakin-Yu. A. Ovchinnikova Institute of bioorganic chemistry (Moscow)

Les sphéroïdes multicellulaires tumoraux (SMT) constituent un outil prometteur dans le domaine de l’étude biologique des tumeurs. Le but de la thèse était de développer… (more)

Subjects/Keywords: Sphéroïdes; Tumeurs; Peptides RGD cycliques; Principes actifs anticancéreux; Doxorubicine; Curcumine; Microréservoirs; Nano-émulsions; Micelles; Spheroids; Tumors; Cyclic RGD-peptides; Anticancer drugs; Doxorubicin; Curcumin; Microcontainers; Nano-emulsions; Micelles; 660.6

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APA (6th Edition):

Akasov, R. (2017). Novel 3D in vitro models based on multicellular tumor spheroids to test anticancer drugs and drug delivery vehicles : Nouveaux modèles 3D in vitro à base de sphéroïdes multicellulaires tumoraux pour tester des substances anticancéreuses et des vecteurs de délivrance de médicaments. (Doctoral Dissertation). Strasbourg; M.M. Shemyakin-Yu. A. Ovchinnikova Institute of bioorganic chemistry (Moscow). Retrieved from http://www.theses.fr/2017STRAF013

Chicago Manual of Style (16th Edition):

Akasov, Roman. “Novel 3D in vitro models based on multicellular tumor spheroids to test anticancer drugs and drug delivery vehicles : Nouveaux modèles 3D in vitro à base de sphéroïdes multicellulaires tumoraux pour tester des substances anticancéreuses et des vecteurs de délivrance de médicaments.” 2017. Doctoral Dissertation, Strasbourg; M.M. Shemyakin-Yu. A. Ovchinnikova Institute of bioorganic chemistry (Moscow). Accessed October 29, 2020. http://www.theses.fr/2017STRAF013.

MLA Handbook (7th Edition):

Akasov, Roman. “Novel 3D in vitro models based on multicellular tumor spheroids to test anticancer drugs and drug delivery vehicles : Nouveaux modèles 3D in vitro à base de sphéroïdes multicellulaires tumoraux pour tester des substances anticancéreuses et des vecteurs de délivrance de médicaments.” 2017. Web. 29 Oct 2020.

Vancouver:

Akasov R. Novel 3D in vitro models based on multicellular tumor spheroids to test anticancer drugs and drug delivery vehicles : Nouveaux modèles 3D in vitro à base de sphéroïdes multicellulaires tumoraux pour tester des substances anticancéreuses et des vecteurs de délivrance de médicaments. [Internet] [Doctoral dissertation]. Strasbourg; M.M. Shemyakin-Yu. A. Ovchinnikova Institute of bioorganic chemistry (Moscow); 2017. [cited 2020 Oct 29]. Available from: http://www.theses.fr/2017STRAF013.

Council of Science Editors:

Akasov R. Novel 3D in vitro models based on multicellular tumor spheroids to test anticancer drugs and drug delivery vehicles : Nouveaux modèles 3D in vitro à base de sphéroïdes multicellulaires tumoraux pour tester des substances anticancéreuses et des vecteurs de délivrance de médicaments. [Doctoral Dissertation]. Strasbourg; M.M. Shemyakin-Yu. A. Ovchinnikova Institute of bioorganic chemistry (Moscow); 2017. Available from: http://www.theses.fr/2017STRAF013

26. Τσιάπα, Ειρήνη. Μεθοδολογίες μοριακής απεικόνισης με επισημασμένα νανοσωματίδια για τον ποσοτικό προσδιορισμό της χωροχρονικής κατανομής της αγγειογένεσης σε καρκινικούς όγκους.

Degree: 2013, University of Patras

Αντικείμενο της παρούσας διατριβής αποτελεί η μελέτη της απεικόνισης και ποσοτικοποίησής της με χρήση τεχνικών μοριακής απεικόνισης. Ένα νέο κυκλικό πεπτιδικό παράγωγο RGDfK (Arg-Gly-Asp-D‐Phe–Lys), το… (more)

Subjects/Keywords: Μοριακή απεικόνιση; Αγγειογένεση; Νανοσωματίδια; RGD πεπτίδια; Ιντεγκρίνες ανβ3; Τεχνήτιο (99mTc); 616.994 064 2; Molecular imaging; Angiogenesis; Nanoparticles; RGD peptides; Integrins ανβ3; Technetium (99mTc)

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APA (6th Edition):

Τσιάπα, . (2013). Μεθοδολογίες μοριακής απεικόνισης με επισημασμένα νανοσωματίδια για τον ποσοτικό προσδιορισμό της χωροχρονικής κατανομής της αγγειογένεσης σε καρκινικούς όγκους. (Doctoral Dissertation). University of Patras. Retrieved from http://hdl.handle.net/10889/7222

Chicago Manual of Style (16th Edition):

Τσιάπα, Ειρήνη. “Μεθοδολογίες μοριακής απεικόνισης με επισημασμένα νανοσωματίδια για τον ποσοτικό προσδιορισμό της χωροχρονικής κατανομής της αγγειογένεσης σε καρκινικούς όγκους.” 2013. Doctoral Dissertation, University of Patras. Accessed October 29, 2020. http://hdl.handle.net/10889/7222.

MLA Handbook (7th Edition):

Τσιάπα, Ειρήνη. “Μεθοδολογίες μοριακής απεικόνισης με επισημασμένα νανοσωματίδια για τον ποσοτικό προσδιορισμό της χωροχρονικής κατανομής της αγγειογένεσης σε καρκινικούς όγκους.” 2013. Web. 29 Oct 2020.

Vancouver:

Τσιάπα . Μεθοδολογίες μοριακής απεικόνισης με επισημασμένα νανοσωματίδια για τον ποσοτικό προσδιορισμό της χωροχρονικής κατανομής της αγγειογένεσης σε καρκινικούς όγκους. [Internet] [Doctoral dissertation]. University of Patras; 2013. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/10889/7222.

Council of Science Editors:

Τσιάπα . Μεθοδολογίες μοριακής απεικόνισης με επισημασμένα νανοσωματίδια για τον ποσοτικό προσδιορισμό της χωροχρονικής κατανομής της αγγειογένεσης σε καρκινικούς όγκους. [Doctoral Dissertation]. University of Patras; 2013. Available from: http://hdl.handle.net/10889/7222


Université Paris-Sud – Paris XI

27. Flament, Julien. Développement de l'imagerie RMN par agents CEST : application à un modèle rongeur de tumeur cérébrale : Developpment of NMR imaging using CEST agents : application to brain tumor in a rodent model.

Degree: Docteur es, Imagerie médicale, 2012, Université Paris-Sud – Paris XI

L’objectif de cette thèse est de développer l’imagerie de transfert de saturation des agents de contraste lipoCEST pour la détection de l’angiogenèse dans un modèle… (more)

Subjects/Keywords: IRM; CEST; LipoCEST; Tumeur U87; Angiogenèse tumorale; Peptide RGD; Intégrine ανβ3; Modélisation; Quantification; MRI; CEST; LipoCEST; Tumor U87; Tumor angiogenesis; RGD peptide; - ανβ3 integrin; Modeling; Quantification

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APA (6th Edition):

Flament, J. (2012). Développement de l'imagerie RMN par agents CEST : application à un modèle rongeur de tumeur cérébrale : Developpment of NMR imaging using CEST agents : application to brain tumor in a rodent model. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2012PA112094

Chicago Manual of Style (16th Edition):

Flament, Julien. “Développement de l'imagerie RMN par agents CEST : application à un modèle rongeur de tumeur cérébrale : Developpment of NMR imaging using CEST agents : application to brain tumor in a rodent model.” 2012. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed October 29, 2020. http://www.theses.fr/2012PA112094.

MLA Handbook (7th Edition):

Flament, Julien. “Développement de l'imagerie RMN par agents CEST : application à un modèle rongeur de tumeur cérébrale : Developpment of NMR imaging using CEST agents : application to brain tumor in a rodent model.” 2012. Web. 29 Oct 2020.

Vancouver:

Flament J. Développement de l'imagerie RMN par agents CEST : application à un modèle rongeur de tumeur cérébrale : Developpment of NMR imaging using CEST agents : application to brain tumor in a rodent model. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2012. [cited 2020 Oct 29]. Available from: http://www.theses.fr/2012PA112094.

Council of Science Editors:

Flament J. Développement de l'imagerie RMN par agents CEST : application à un modèle rongeur de tumeur cérébrale : Developpment of NMR imaging using CEST agents : application to brain tumor in a rodent model. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2012. Available from: http://www.theses.fr/2012PA112094

28. Georgoulis, Anastasios. Μελέτη καρκινικών κυττάρων μαστού in vitro με βιοχημικές και ανοσοϊστοχημικές μεθόδους: in vitro μελέτη του ρόλου της ιντεργκρίνης ανβ3 στην παθογένεια του καρκίνου του μαστού.

Degree: 2011, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

 Breast cancer is the most common cancer in women around the world. The major cause of death among breast cancer patients is the development of… (more)

Subjects/Keywords: Διηθητικό πορογενές καρκίνωμα μαστού; Πρωτογενείς κυτταρικές καλλιέργειες; Ιντεγκρίνη αν β3; RGD πεπτίδια; Κυτταρική προσκόλληση; Υπερμικροσκοπική δομή; Infiltrating ductal breast carcinoma; Primary cell cultures; Integrin alphavbeta3; RGD peptides; Cell adhesion; Ultrastructure

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APA (6th Edition):

Georgoulis, A. (2011). Μελέτη καρκινικών κυττάρων μαστού in vitro με βιοχημικές και ανοσοϊστοχημικές μεθόδους: in vitro μελέτη του ρόλου της ιντεργκρίνης ανβ3 στην παθογένεια του καρκίνου του μαστού. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/31705

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Georgoulis, Anastasios. “Μελέτη καρκινικών κυττάρων μαστού in vitro με βιοχημικές και ανοσοϊστοχημικές μεθόδους: in vitro μελέτη του ρόλου της ιντεργκρίνης ανβ3 στην παθογένεια του καρκίνου του μαστού.” 2011. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed October 29, 2020. http://hdl.handle.net/10442/hedi/31705.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Georgoulis, Anastasios. “Μελέτη καρκινικών κυττάρων μαστού in vitro με βιοχημικές και ανοσοϊστοχημικές μεθόδους: in vitro μελέτη του ρόλου της ιντεργκρίνης ανβ3 στην παθογένεια του καρκίνου του μαστού.” 2011. Web. 29 Oct 2020.

Vancouver:

Georgoulis A. Μελέτη καρκινικών κυττάρων μαστού in vitro με βιοχημικές και ανοσοϊστοχημικές μεθόδους: in vitro μελέτη του ρόλου της ιντεργκρίνης ανβ3 στην παθογένεια του καρκίνου του μαστού. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2011. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/10442/hedi/31705.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Georgoulis A. Μελέτη καρκινικών κυττάρων μαστού in vitro με βιοχημικές και ανοσοϊστοχημικές μεθόδους: in vitro μελέτη του ρόλου της ιντεργκρίνης ανβ3 στην παθογένεια του καρκίνου του μαστού. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2011. Available from: http://hdl.handle.net/10442/hedi/31705

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Universidade do Rio Grande do Sul

29. Theisen, Maíra. Estudo computacional via dinâmica molecular de poli(vinil álcool) funcionalizado com tripetídeo RGD.

Degree: 2017, Universidade do Rio Grande do Sul

Hidrogéis são redes poliméricas tridimensionais ligadas entre si por reticulações químicas ou físicas, e podem absorver água ou fluidos biológicos. A estrutura permite que estes… (more)

Subjects/Keywords: Hydrogel; Hidrogéis; Poli(álcool vinílico); pH; Molecular dynamics; Dinâmica molecular; RGD; Poli(vinyl alcohol)

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APA (6th Edition):

Theisen, M. (2017). Estudo computacional via dinâmica molecular de poli(vinil álcool) funcionalizado com tripetídeo RGD. (Thesis). Universidade do Rio Grande do Sul. Retrieved from http://hdl.handle.net/10183/171735

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Theisen, Maíra. “Estudo computacional via dinâmica molecular de poli(vinil álcool) funcionalizado com tripetídeo RGD.” 2017. Thesis, Universidade do Rio Grande do Sul. Accessed October 29, 2020. http://hdl.handle.net/10183/171735.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Theisen, Maíra. “Estudo computacional via dinâmica molecular de poli(vinil álcool) funcionalizado com tripetídeo RGD.” 2017. Web. 29 Oct 2020.

Vancouver:

Theisen M. Estudo computacional via dinâmica molecular de poli(vinil álcool) funcionalizado com tripetídeo RGD. [Internet] [Thesis]. Universidade do Rio Grande do Sul; 2017. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/10183/171735.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Theisen M. Estudo computacional via dinâmica molecular de poli(vinil álcool) funcionalizado com tripetídeo RGD. [Thesis]. Universidade do Rio Grande do Sul; 2017. Available from: http://hdl.handle.net/10183/171735

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Saskatchewan

30. House, Nicole 1987-. RGDSK-FUNCTIONALIZED HELICAL ROSETTE NANOTUBE INTERACTIONS WITH INTEGRIN αvβ3-EXPRESSING BIOLOGICAL MILIEUS.

Degree: 2016, University of Saskatchewan

 The development of nanomaterials (NMs) for drug delivery vehicles is a rapidly growing field. One NM of interest are helical rosette nanotubes (RNT). Soluble, metal-free,… (more)

Subjects/Keywords: nanotechnology; rosette nanotube; RGD peptide; self-assembly; drug delivery; melanoma; isolated perfused lung; dendritic cell

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APA (6th Edition):

House, N. 1. (2016). RGDSK-FUNCTIONALIZED HELICAL ROSETTE NANOTUBE INTERACTIONS WITH INTEGRIN αvβ3-EXPRESSING BIOLOGICAL MILIEUS. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/7375

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

House, Nicole 1987-. “RGDSK-FUNCTIONALIZED HELICAL ROSETTE NANOTUBE INTERACTIONS WITH INTEGRIN αvβ3-EXPRESSING BIOLOGICAL MILIEUS.” 2016. Thesis, University of Saskatchewan. Accessed October 29, 2020. http://hdl.handle.net/10388/7375.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

House, Nicole 1987-. “RGDSK-FUNCTIONALIZED HELICAL ROSETTE NANOTUBE INTERACTIONS WITH INTEGRIN αvβ3-EXPRESSING BIOLOGICAL MILIEUS.” 2016. Web. 29 Oct 2020.

Vancouver:

House N1. RGDSK-FUNCTIONALIZED HELICAL ROSETTE NANOTUBE INTERACTIONS WITH INTEGRIN αvβ3-EXPRESSING BIOLOGICAL MILIEUS. [Internet] [Thesis]. University of Saskatchewan; 2016. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/10388/7375.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

House N1. RGDSK-FUNCTIONALIZED HELICAL ROSETTE NANOTUBE INTERACTIONS WITH INTEGRIN αvβ3-EXPRESSING BIOLOGICAL MILIEUS. [Thesis]. University of Saskatchewan; 2016. Available from: http://hdl.handle.net/10388/7375

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

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