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You searched for subject:(RET). Showing records 1 – 30 of 86 total matches.

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Queens University

1. Zhu, Shu Jun. RET receptor activation targets expression of the pleiotropic cytokine interleukin-11 .

Degree: Pathology and Molecular Medicine, 2015, Queens University

 The RET receptor has diverse roles in development and disease, modulating proliferation, survival, and migration of cells. Ligand-independent constitutively active forms of RET can lead… (more)

Subjects/Keywords: RET; IL-11

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APA (6th Edition):

Zhu, S. J. (2015). RET receptor activation targets expression of the pleiotropic cytokine interleukin-11 . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/12701

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):

Zhu, Shu Jun. “RET receptor activation targets expression of the pleiotropic cytokine interleukin-11 .” 2015. Thesis, Queens University. Accessed August 22, 2019. http://hdl.handle.net/1974/12701.

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

MLA Handbook (7th Edition):

Zhu, Shu Jun. “RET receptor activation targets expression of the pleiotropic cytokine interleukin-11 .” 2015. Web. 22 Aug 2019.

Vancouver:

Zhu SJ. RET receptor activation targets expression of the pleiotropic cytokine interleukin-11 . [Internet] [Thesis]. Queens University; 2015. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1974/12701.

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

Council of Science Editors:

Zhu SJ. RET receptor activation targets expression of the pleiotropic cytokine interleukin-11 . [Thesis]. Queens University; 2015. Available from: http://hdl.handle.net/1974/12701

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


University of New South Wales

2. Kaplinovsky, Tamila. The glial cell line-derived neurotrophic factor family in the olfactory system and brain.

Degree: Clinical School - St Vincent's Hospital, 2015, University of New South Wales

 Glial cell line-derived neurotrophic factor (GDNF) family signaling hasbeen implicated in development, survival and function of many different celltypes, including neurons in the central nervous… (more)

Subjects/Keywords: Parkinson's Disease; GDNF; RET

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APA (6th Edition):

Kaplinovsky, T. (2015). The glial cell line-derived neurotrophic factor family in the olfactory system and brain. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/55676 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:38452/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Kaplinovsky, Tamila. “The glial cell line-derived neurotrophic factor family in the olfactory system and brain.” 2015. Doctoral Dissertation, University of New South Wales. Accessed August 22, 2019. http://handle.unsw.edu.au/1959.4/55676 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:38452/SOURCE02?view=true.

MLA Handbook (7th Edition):

Kaplinovsky, Tamila. “The glial cell line-derived neurotrophic factor family in the olfactory system and brain.” 2015. Web. 22 Aug 2019.

Vancouver:

Kaplinovsky T. The glial cell line-derived neurotrophic factor family in the olfactory system and brain. [Internet] [Doctoral dissertation]. University of New South Wales; 2015. [cited 2019 Aug 22]. Available from: http://handle.unsw.edu.au/1959.4/55676 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:38452/SOURCE02?view=true.

Council of Science Editors:

Kaplinovsky T. The glial cell line-derived neurotrophic factor family in the olfactory system and brain. [Doctoral Dissertation]. University of New South Wales; 2015. Available from: http://handle.unsw.edu.au/1959.4/55676 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:38452/SOURCE02?view=true


Queens University

3. Yoganathan, Piriya. Elucidation of the Roles and Functional Implications of the RET Receptor Tyrosine Kinase in Cancer .

Degree: Pathology and Molecular Medicine, Queens University

RET is a receptor tyrosine kinase that plays important roles in normal development of the kidney, spermatogonia, and neuroendocrine tissues. RET is also implicated in… (more)

Subjects/Keywords: RET; cancer

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APA (6th Edition):

Yoganathan, P. (n.d.). Elucidation of the Roles and Functional Implications of the RET Receptor Tyrosine Kinase in Cancer . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/23929

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Yoganathan, Piriya. “Elucidation of the Roles and Functional Implications of the RET Receptor Tyrosine Kinase in Cancer .” Thesis, Queens University. Accessed August 22, 2019. http://hdl.handle.net/1974/23929.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Yoganathan, Piriya. “Elucidation of the Roles and Functional Implications of the RET Receptor Tyrosine Kinase in Cancer .” Web. 22 Aug 2019.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Yoganathan P. Elucidation of the Roles and Functional Implications of the RET Receptor Tyrosine Kinase in Cancer . [Internet] [Thesis]. Queens University; [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1974/23929.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Yoganathan P. Elucidation of the Roles and Functional Implications of the RET Receptor Tyrosine Kinase in Cancer . [Thesis]. Queens University; Available from: http://hdl.handle.net/1974/23929

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


Queens University

4. Kellar, Amelia. The Role of BetaPIX in RET-mediated Cell Migration .

Degree: Pathology and Molecular Medicine, 2009, Queens University

RET is a transmembrane receptor that is implicated in a variety of processes such as cell proliferation, differentiation, migration, survival, and death. One of the… (more)

Subjects/Keywords: Pathology; RET

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APA (6th Edition):

Kellar, A. (2009). The Role of BetaPIX in RET-mediated Cell Migration . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/5180

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):

Kellar, Amelia. “The Role of BetaPIX in RET-mediated Cell Migration .” 2009. Thesis, Queens University. Accessed August 22, 2019. http://hdl.handle.net/1974/5180.

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

MLA Handbook (7th Edition):

Kellar, Amelia. “The Role of BetaPIX in RET-mediated Cell Migration .” 2009. Web. 22 Aug 2019.

Vancouver:

Kellar A. The Role of BetaPIX in RET-mediated Cell Migration . [Internet] [Thesis]. Queens University; 2009. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1974/5180.

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

Council of Science Editors:

Kellar A. The Role of BetaPIX in RET-mediated Cell Migration . [Thesis]. Queens University; 2009. Available from: http://hdl.handle.net/1974/5180

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


Queens University

5. Richardson, Douglas. Subcellular Localization and Trafficking of the RET Receptor Tyrosine Kinase: Implications for Signalling and Disease .

Degree: Pathology and Molecular Medicine, 2012, Queens University

 The RET proto-oncogene encodes a receptor tyrosine kinase (RTK) that is widely expressed in neuroendocrine tissues and is essential for embryonic development of the kidney… (more)

Subjects/Keywords: RET; Intracellular Trafficking; Thyroid Carcinoma

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APA (6th Edition):

Richardson, D. (2012). Subcellular Localization and Trafficking of the RET Receptor Tyrosine Kinase: Implications for Signalling and Disease . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/7478

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):

Richardson, Douglas. “Subcellular Localization and Trafficking of the RET Receptor Tyrosine Kinase: Implications for Signalling and Disease .” 2012. Thesis, Queens University. Accessed August 22, 2019. http://hdl.handle.net/1974/7478.

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

MLA Handbook (7th Edition):

Richardson, Douglas. “Subcellular Localization and Trafficking of the RET Receptor Tyrosine Kinase: Implications for Signalling and Disease .” 2012. Web. 22 Aug 2019.

Vancouver:

Richardson D. Subcellular Localization and Trafficking of the RET Receptor Tyrosine Kinase: Implications for Signalling and Disease . [Internet] [Thesis]. Queens University; 2012. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1974/7478.

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

Council of Science Editors:

Richardson D. Subcellular Localization and Trafficking of the RET Receptor Tyrosine Kinase: Implications for Signalling and Disease . [Thesis]. Queens University; 2012. Available from: http://hdl.handle.net/1974/7478

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


Queens University

6. Lian, Eric. Characterization of isoform specific RET knockdown in cancer cell lines .

Degree: Pathology and Molecular Medicine, 2013, Queens University

 The REarranged in Transfection (RET) tyrosine kinase is an important signalling protein for the development of neural crest-derived tissues such as the enteric and sympathetic… (more)

Subjects/Keywords: Migration; RET; Cancer; Isoforms; shRNA; Invasion

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APA (6th Edition):

Lian, E. (2013). Characterization of isoform specific RET knockdown in cancer cell lines . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/8237

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):

Lian, Eric. “Characterization of isoform specific RET knockdown in cancer cell lines .” 2013. Thesis, Queens University. Accessed August 22, 2019. http://hdl.handle.net/1974/8237.

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

MLA Handbook (7th Edition):

Lian, Eric. “Characterization of isoform specific RET knockdown in cancer cell lines .” 2013. Web. 22 Aug 2019.

Vancouver:

Lian E. Characterization of isoform specific RET knockdown in cancer cell lines . [Internet] [Thesis]. Queens University; 2013. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1974/8237.

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

Council of Science Editors:

Lian E. Characterization of isoform specific RET knockdown in cancer cell lines . [Thesis]. Queens University; 2013. Available from: http://hdl.handle.net/1974/8237

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


Queens University

7. Cockburn, Jessica Grace. RET Mediated Gene Expression and Cell-Migration .

Degree: Pathology and Molecular Medicine, 2011, Queens University

 The RET receptor tyrosine kinase is important during development of neural crest-derived tissues, particularly the enteric and sympathetic nervous systems, and in kidney morphogenesis. Activation… (more)

Subjects/Keywords: Cell-Migration; RET; Gene Expression; Cancer

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APA (6th Edition):

Cockburn, J. G. (2011). RET Mediated Gene Expression and Cell-Migration . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/6859

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):

Cockburn, Jessica Grace. “RET Mediated Gene Expression and Cell-Migration .” 2011. Thesis, Queens University. Accessed August 22, 2019. http://hdl.handle.net/1974/6859.

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

MLA Handbook (7th Edition):

Cockburn, Jessica Grace. “RET Mediated Gene Expression and Cell-Migration .” 2011. Web. 22 Aug 2019.

Vancouver:

Cockburn JG. RET Mediated Gene Expression and Cell-Migration . [Internet] [Thesis]. Queens University; 2011. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1974/6859.

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

Council of Science Editors:

Cockburn JG. RET Mediated Gene Expression and Cell-Migration . [Thesis]. Queens University; 2011. Available from: http://hdl.handle.net/1974/6859

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


Université Paris-Sud – Paris XI

8. Delisle, Lucille. Role of the mutated ALK oncogene in neuroblastoma oncogenesis and in development : Rôle de l’oncogène ALK muté dans l’oncogenèse du neuroblastome et le développement.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2015, Université Paris-Sud – Paris XI

 Le neuroblastome (NB) est une tumeur pédiatrique du système nerveux sympathique. Des mutations activatrices du gène ALK (Anaplastic Lymphoma Kinase) ont été identifiées dans 8… (more)

Subjects/Keywords: Neuroblastome; ALK; Développement; RET; Modèle murin; Neuroblastoma; ALK; Developement; RET; Mouse model

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APA (6th Edition):

Delisle, L. (2015). Role of the mutated ALK oncogene in neuroblastoma oncogenesis and in development : Rôle de l’oncogène ALK muté dans l’oncogenèse du neuroblastome et le développement. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2015PA11T036

Chicago Manual of Style (16th Edition):

Delisle, Lucille. “Role of the mutated ALK oncogene in neuroblastoma oncogenesis and in development : Rôle de l’oncogène ALK muté dans l’oncogenèse du neuroblastome et le développement.” 2015. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed August 22, 2019. http://www.theses.fr/2015PA11T036.

MLA Handbook (7th Edition):

Delisle, Lucille. “Role of the mutated ALK oncogene in neuroblastoma oncogenesis and in development : Rôle de l’oncogène ALK muté dans l’oncogenèse du neuroblastome et le développement.” 2015. Web. 22 Aug 2019.

Vancouver:

Delisle L. Role of the mutated ALK oncogene in neuroblastoma oncogenesis and in development : Rôle de l’oncogène ALK muté dans l’oncogenèse du neuroblastome et le développement. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2015. [cited 2019 Aug 22]. Available from: http://www.theses.fr/2015PA11T036.

Council of Science Editors:

Delisle L. Role of the mutated ALK oncogene in neuroblastoma oncogenesis and in development : Rôle de l’oncogène ALK muté dans l’oncogenèse du neuroblastome et le développement. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2015. Available from: http://www.theses.fr/2015PA11T036


University of Helsinki

9. Vähämurto, Pauli. VEGF-C – RET -signaalitien vaikutus ihon, enterisen hermoston ja lymfaattisen kudoksen kehitykseen sekä sikiöiden elinkykyyn.

Degree: Institute of Biomedicine; Helsingfors universitet, Medicinska fakulteten, Biomedicinska institutionen, 2009, University of Helsinki

 Selvitin tutkimuksessani VEGF-C:n ja RET:n vaikutusta hiiren enterisen hermoston ja imusuoniston kehitykseen. Yhden ja kahden VEGF-C-alleelin puutos johti neuronien määrän vähenemiseen jejunumissa ja koolonissa. RET-alleelien… (more)

Subjects/Keywords: GFL; GDNF; Hirschsprung; lymphedema; VEGF-C; RET; Developmental Biology; Kehitysbiologia; Utvecklingsbiologi; GFL; GDNF; Hirschsprung; lymphedema; VEGF-C; RET

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APA (6th Edition):

Vähämurto, P. (2009). VEGF-C – RET -signaalitien vaikutus ihon, enterisen hermoston ja lymfaattisen kudoksen kehitykseen sekä sikiöiden elinkykyyn. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10250/8237

Chicago Manual of Style (16th Edition):

Vähämurto, Pauli. “VEGF-C – RET -signaalitien vaikutus ihon, enterisen hermoston ja lymfaattisen kudoksen kehitykseen sekä sikiöiden elinkykyyn.” 2009. Masters Thesis, University of Helsinki. Accessed August 22, 2019. http://hdl.handle.net/10250/8237.

MLA Handbook (7th Edition):

Vähämurto, Pauli. “VEGF-C – RET -signaalitien vaikutus ihon, enterisen hermoston ja lymfaattisen kudoksen kehitykseen sekä sikiöiden elinkykyyn.” 2009. Web. 22 Aug 2019.

Vancouver:

Vähämurto P. VEGF-C – RET -signaalitien vaikutus ihon, enterisen hermoston ja lymfaattisen kudoksen kehitykseen sekä sikiöiden elinkykyyn. [Internet] [Masters thesis]. University of Helsinki; 2009. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/10250/8237.

Council of Science Editors:

Vähämurto P. VEGF-C – RET -signaalitien vaikutus ihon, enterisen hermoston ja lymfaattisen kudoksen kehitykseen sekä sikiöiden elinkykyyn. [Masters Thesis]. University of Helsinki; 2009. Available from: http://hdl.handle.net/10250/8237


University of Helsinki

10. Huynh, Thi Le Hang. Lisääntyneen/vähentyneen GDNF-RET-signaalinvälitysketjun vaikutukset nigrostriataalisen radan dopamiinihermosoluihin.

Degree: Farmaceutiska fakulteten, 2010, University of Helsinki

In the written part of my master -thesis I discuss about GDNF signalling and more specifically how the changes in the GDNF/GFRα1/Ret signaling affect the… (more)

Subjects/Keywords: GDNF; GFRα1; RET; 6-OHDA; TH; dopamine; dopamiini; Farmakologi; Pharmacology; Farmakologia; GDNF; GFRα1; RET; 6-OHDA; TH; dopamine; dopamiini

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APA (6th Edition):

Huynh, T. L. H. (2010). Lisääntyneen/vähentyneen GDNF-RET-signaalinvälitysketjun vaikutukset nigrostriataalisen radan dopamiinihermosoluihin. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/17391

Chicago Manual of Style (16th Edition):

Huynh, Thi Le Hang. “Lisääntyneen/vähentyneen GDNF-RET-signaalinvälitysketjun vaikutukset nigrostriataalisen radan dopamiinihermosoluihin.” 2010. Masters Thesis, University of Helsinki. Accessed August 22, 2019. http://hdl.handle.net/10138/17391.

MLA Handbook (7th Edition):

Huynh, Thi Le Hang. “Lisääntyneen/vähentyneen GDNF-RET-signaalinvälitysketjun vaikutukset nigrostriataalisen radan dopamiinihermosoluihin.” 2010. Web. 22 Aug 2019.

Vancouver:

Huynh TLH. Lisääntyneen/vähentyneen GDNF-RET-signaalinvälitysketjun vaikutukset nigrostriataalisen radan dopamiinihermosoluihin. [Internet] [Masters thesis]. University of Helsinki; 2010. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/10138/17391.

Council of Science Editors:

Huynh TLH. Lisääntyneen/vähentyneen GDNF-RET-signaalinvälitysketjun vaikutukset nigrostriataalisen radan dopamiinihermosoluihin. [Masters Thesis]. University of Helsinki; 2010. Available from: http://hdl.handle.net/10138/17391

11. Dabbeche-Bouricha, Emna. Rôle du système immunitaire et de la synthase du monoxyde d’azote de type 2 (NOS2) dans un nouveau modèle murin de mélanome rapidement évolutif : implication pour les cancers humains : The role of the immune system and the Nitric-Oxide Synthase type 2 in a new mouse model of rapidly evolving melanoma : implications for human cancers.

Degree: Docteur es, Immunologie, 2015, Sorbonne Paris Cité; Université de Sfax (Tunisie)

 Le système immunitaire joue un rôle complexe, tantôt protecteur, tantôt facilitateur dans la relation hôte-tumeur. La souris transgénique pour le proto-oncogène humain RET développe un… (more)

Subjects/Keywords: RET; Souris NOD; Cellules myéloïdes; Dectin-1; NOS2; Cancers humains; RET; NOD mouse; Myeloid cells; Dectin-1; NOS2; Human cancers; 616.079

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APA (6th Edition):

Dabbeche-Bouricha, E. (2015). Rôle du système immunitaire et de la synthase du monoxyde d’azote de type 2 (NOS2) dans un nouveau modèle murin de mélanome rapidement évolutif : implication pour les cancers humains : The role of the immune system and the Nitric-Oxide Synthase type 2 in a new mouse model of rapidly evolving melanoma : implications for human cancers. (Doctoral Dissertation). Sorbonne Paris Cité; Université de Sfax (Tunisie). Retrieved from http://www.theses.fr/2015USPCB088

Chicago Manual of Style (16th Edition):

Dabbeche-Bouricha, Emna. “Rôle du système immunitaire et de la synthase du monoxyde d’azote de type 2 (NOS2) dans un nouveau modèle murin de mélanome rapidement évolutif : implication pour les cancers humains : The role of the immune system and the Nitric-Oxide Synthase type 2 in a new mouse model of rapidly evolving melanoma : implications for human cancers.” 2015. Doctoral Dissertation, Sorbonne Paris Cité; Université de Sfax (Tunisie). Accessed August 22, 2019. http://www.theses.fr/2015USPCB088.

MLA Handbook (7th Edition):

Dabbeche-Bouricha, Emna. “Rôle du système immunitaire et de la synthase du monoxyde d’azote de type 2 (NOS2) dans un nouveau modèle murin de mélanome rapidement évolutif : implication pour les cancers humains : The role of the immune system and the Nitric-Oxide Synthase type 2 in a new mouse model of rapidly evolving melanoma : implications for human cancers.” 2015. Web. 22 Aug 2019.

Vancouver:

Dabbeche-Bouricha E. Rôle du système immunitaire et de la synthase du monoxyde d’azote de type 2 (NOS2) dans un nouveau modèle murin de mélanome rapidement évolutif : implication pour les cancers humains : The role of the immune system and the Nitric-Oxide Synthase type 2 in a new mouse model of rapidly evolving melanoma : implications for human cancers. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; Université de Sfax (Tunisie); 2015. [cited 2019 Aug 22]. Available from: http://www.theses.fr/2015USPCB088.

Council of Science Editors:

Dabbeche-Bouricha E. Rôle du système immunitaire et de la synthase du monoxyde d’azote de type 2 (NOS2) dans un nouveau modèle murin de mélanome rapidement évolutif : implication pour les cancers humains : The role of the immune system and the Nitric-Oxide Synthase type 2 in a new mouse model of rapidly evolving melanoma : implications for human cancers. [Doctoral Dissertation]. Sorbonne Paris Cité; Université de Sfax (Tunisie); 2015. Available from: http://www.theses.fr/2015USPCB088

12. Hecht castro medeiros, Fabio. The role of reactive oxygen species in thyroid radio-carcinogenesis : Rôle des espèces réactives de l'oxygène dans la radio-carcinogenèse thyroïdienne.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2018, Paris Saclay; Universidade federal do Rio de Janeiro

Les cancers papillaires de la thyroïde (PTC) sont les tumeurs endocrines les plus courantes et représentent 2-3% de tous les cancers humains. Les altérations génétiques… (more)

Subjects/Keywords: Thyroïde; Duox1; Radio-Carcinogenèse; Ret/ptc; Stress oxidatif; Stress replicatif; Thyroid; Duox1; Radio-Carcinogenesis; Ret/ptc; Oxidative stress; Replicative stress

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APA (6th Edition):

Hecht castro medeiros, F. (2018). The role of reactive oxygen species in thyroid radio-carcinogenesis : Rôle des espèces réactives de l'oxygène dans la radio-carcinogenèse thyroïdienne. (Doctoral Dissertation). Paris Saclay; Universidade federal do Rio de Janeiro. Retrieved from http://www.theses.fr/2018SACLS085

Chicago Manual of Style (16th Edition):

Hecht castro medeiros, Fabio. “The role of reactive oxygen species in thyroid radio-carcinogenesis : Rôle des espèces réactives de l'oxygène dans la radio-carcinogenèse thyroïdienne.” 2018. Doctoral Dissertation, Paris Saclay; Universidade federal do Rio de Janeiro. Accessed August 22, 2019. http://www.theses.fr/2018SACLS085.

MLA Handbook (7th Edition):

Hecht castro medeiros, Fabio. “The role of reactive oxygen species in thyroid radio-carcinogenesis : Rôle des espèces réactives de l'oxygène dans la radio-carcinogenèse thyroïdienne.” 2018. Web. 22 Aug 2019.

Vancouver:

Hecht castro medeiros F. The role of reactive oxygen species in thyroid radio-carcinogenesis : Rôle des espèces réactives de l'oxygène dans la radio-carcinogenèse thyroïdienne. [Internet] [Doctoral dissertation]. Paris Saclay; Universidade federal do Rio de Janeiro; 2018. [cited 2019 Aug 22]. Available from: http://www.theses.fr/2018SACLS085.

Council of Science Editors:

Hecht castro medeiros F. The role of reactive oxygen species in thyroid radio-carcinogenesis : Rôle des espèces réactives de l'oxygène dans la radio-carcinogenèse thyroïdienne. [Doctoral Dissertation]. Paris Saclay; Universidade federal do Rio de Janeiro; 2018. Available from: http://www.theses.fr/2018SACLS085

13. 井山, 慶大. Identification of Three Novel Fusion Oncogenes, SQSTM1/NTRK3, AFAP1L2/RET, and PPFIBP2/RET, in Thyroid Cancers of Young Patients in Fukushima : 福島の若年甲状腺乳頭癌における3つの新規融合癌遺伝子(SQSTM1/NTRK3, AFAP1L2/RET, PPFIBP2/RET)の同定.

Degree: 博士(医学), 2017, Nagasaki University / 長崎大学

 Background: The BRAFV600E mutation is the most frequent genetic abnormality in adult papillary thyroid carcinomas (PTCs). On the other hand, various chromosomal rearrangements are more… (more)

Subjects/Keywords: fusion gene; rearrangement; oncogene; NTRK3; RET; papillary thyroid carcinoma

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APA (6th Edition):

井山, . (2017). Identification of Three Novel Fusion Oncogenes, SQSTM1/NTRK3, AFAP1L2/RET, and PPFIBP2/RET, in Thyroid Cancers of Young Patients in Fukushima : 福島の若年甲状腺乳頭癌における3つの新規融合癌遺伝子(SQSTM1/NTRK3, AFAP1L2/RET, PPFIBP2/RET)の同定. (Thesis). Nagasaki University / 長崎大学. Retrieved from http://hdl.handle.net/10069/38111

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):

井山, 慶大. “Identification of Three Novel Fusion Oncogenes, SQSTM1/NTRK3, AFAP1L2/RET, and PPFIBP2/RET, in Thyroid Cancers of Young Patients in Fukushima : 福島の若年甲状腺乳頭癌における3つの新規融合癌遺伝子(SQSTM1/NTRK3, AFAP1L2/RET, PPFIBP2/RET)の同定.” 2017. Thesis, Nagasaki University / 長崎大学. Accessed August 22, 2019. http://hdl.handle.net/10069/38111.

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

MLA Handbook (7th Edition):

井山, 慶大. “Identification of Three Novel Fusion Oncogenes, SQSTM1/NTRK3, AFAP1L2/RET, and PPFIBP2/RET, in Thyroid Cancers of Young Patients in Fukushima : 福島の若年甲状腺乳頭癌における3つの新規融合癌遺伝子(SQSTM1/NTRK3, AFAP1L2/RET, PPFIBP2/RET)の同定.” 2017. Web. 22 Aug 2019.

Vancouver:

井山 . Identification of Three Novel Fusion Oncogenes, SQSTM1/NTRK3, AFAP1L2/RET, and PPFIBP2/RET, in Thyroid Cancers of Young Patients in Fukushima : 福島の若年甲状腺乳頭癌における3つの新規融合癌遺伝子(SQSTM1/NTRK3, AFAP1L2/RET, PPFIBP2/RET)の同定. [Internet] [Thesis]. Nagasaki University / 長崎大学; 2017. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/10069/38111.

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

Council of Science Editors:

井山 . Identification of Three Novel Fusion Oncogenes, SQSTM1/NTRK3, AFAP1L2/RET, and PPFIBP2/RET, in Thyroid Cancers of Young Patients in Fukushima : 福島の若年甲状腺乳頭癌における3つの新規融合癌遺伝子(SQSTM1/NTRK3, AFAP1L2/RET, PPFIBP2/RET)の同定. [Thesis]. Nagasaki University / 長崎大学; 2017. Available from: http://hdl.handle.net/10069/38111

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


University of Helsinki

14. Roininen (os. Mertanen), Saara. Munuaisten kehitystä säätelevien pleksiini B2 – ja Ret-reseptoreiden välinen vuorovaikutus.

Degree: Medicinska fakulteten, 2016, University of Helsinki

 Munuaisen kehitystä on tutkittu laajasti. Yksi tunnetuimmista munuaisen kehitykseen liittyvistä tekijöistä on gliasoluperäisen neutrotrofisen kasvutekijän (Gdnf) aktivoima Ret-reseptorityrosinikinaasi (Ret). Ret:n aktivaatio aloittaa hiirimalleilla tehdyissä tutkimuksissa… (more)

Subjects/Keywords: Western blot; Pleksiini B2 – reseptori (pleksiini B2); Ret-reseptorityrosiinikinaasi (Ret); Ko-immunopresipitaatio (Co-IP); Biochemistry and Developmental Biology; Biokemia ja kehitysbiologia; Biokemi och utvecklingsbiologi; Western blot; Pleksiini B2 – reseptori (pleksiini B2); Ret-reseptorityrosiinikinaasi (Ret); Ko-immunopresipitaatio (Co-IP)

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APA (6th Edition):

Roininen (os. Mertanen), S. (2016). Munuaisten kehitystä säätelevien pleksiini B2 – ja Ret-reseptoreiden välinen vuorovaikutus. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/162941

Chicago Manual of Style (16th Edition):

Roininen (os. Mertanen), Saara. “Munuaisten kehitystä säätelevien pleksiini B2 – ja Ret-reseptoreiden välinen vuorovaikutus.” 2016. Masters Thesis, University of Helsinki. Accessed August 22, 2019. http://hdl.handle.net/10138/162941.

MLA Handbook (7th Edition):

Roininen (os. Mertanen), Saara. “Munuaisten kehitystä säätelevien pleksiini B2 – ja Ret-reseptoreiden välinen vuorovaikutus.” 2016. Web. 22 Aug 2019.

Vancouver:

Roininen (os. Mertanen) S. Munuaisten kehitystä säätelevien pleksiini B2 – ja Ret-reseptoreiden välinen vuorovaikutus. [Internet] [Masters thesis]. University of Helsinki; 2016. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/10138/162941.

Council of Science Editors:

Roininen (os. Mertanen) S. Munuaisten kehitystä säätelevien pleksiini B2 – ja Ret-reseptoreiden välinen vuorovaikutus. [Masters Thesis]. University of Helsinki; 2016. Available from: http://hdl.handle.net/10138/162941


The Ohio State University

15. Buckwalter, Tara Lynne Furminger. Phosphotyrosine-mediated signal transduction pathways essential for RET/PTC1-induced tumor formation.

Degree: PhD, Biochemistry, 2000, The Ohio State University

 The PTC1 oncogene is a rearranged form of the RET proto-oncogene detected in human papillary thyroid carcinomas (PCs). The tumorigenicity of PTC1 in thyroid tumors… (more)

Subjects/Keywords: thyroid tumor; phosphotyrosine; RET/PTC1

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APA (6th Edition):

Buckwalter, T. L. F. (2000). Phosphotyrosine-mediated signal transduction pathways essential for RET/PTC1-induced tumor formation. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu970163275

Chicago Manual of Style (16th Edition):

Buckwalter, Tara Lynne Furminger. “Phosphotyrosine-mediated signal transduction pathways essential for RET/PTC1-induced tumor formation.” 2000. Doctoral Dissertation, The Ohio State University. Accessed August 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu970163275.

MLA Handbook (7th Edition):

Buckwalter, Tara Lynne Furminger. “Phosphotyrosine-mediated signal transduction pathways essential for RET/PTC1-induced tumor formation.” 2000. Web. 22 Aug 2019.

Vancouver:

Buckwalter TLF. Phosphotyrosine-mediated signal transduction pathways essential for RET/PTC1-induced tumor formation. [Internet] [Doctoral dissertation]. The Ohio State University; 2000. [cited 2019 Aug 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu970163275.

Council of Science Editors:

Buckwalter TLF. Phosphotyrosine-mediated signal transduction pathways essential for RET/PTC1-induced tumor formation. [Doctoral Dissertation]. The Ohio State University; 2000. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu970163275


The Ohio State University

16. Knostman, Katherine A.B. Sodium/iodide symporter regulation by oncogenes in the mammary gland and thyroid gland using mouse models.

Degree: PhD, Veterinary Biosciences, 2007, The Ohio State University

 The objectives of this study are (1) to develop targeted sodium/iodide symporter (NIS)-mediated radionuclide imaging and therapy of breast cancer by elucidating NIS regulatory mechanisms;… (more)

Subjects/Keywords: breast cancer; thyroid cancer; bioluminescent imaging; RET/PTC; sodium/iodide symporter

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APA (6th Edition):

Knostman, K. A. B. (2007). Sodium/iodide symporter regulation by oncogenes in the mammary gland and thyroid gland using mouse models. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1181659993

Chicago Manual of Style (16th Edition):

Knostman, Katherine A B. “Sodium/iodide symporter regulation by oncogenes in the mammary gland and thyroid gland using mouse models.” 2007. Doctoral Dissertation, The Ohio State University. Accessed August 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1181659993.

MLA Handbook (7th Edition):

Knostman, Katherine A B. “Sodium/iodide symporter regulation by oncogenes in the mammary gland and thyroid gland using mouse models.” 2007. Web. 22 Aug 2019.

Vancouver:

Knostman KAB. Sodium/iodide symporter regulation by oncogenes in the mammary gland and thyroid gland using mouse models. [Internet] [Doctoral dissertation]. The Ohio State University; 2007. [cited 2019 Aug 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1181659993.

Council of Science Editors:

Knostman KAB. Sodium/iodide symporter regulation by oncogenes in the mammary gland and thyroid gland using mouse models. [Doctoral Dissertation]. The Ohio State University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1181659993

17. Castro, Lisandra Marisa Flores. Study of the role of RAF-1 in MAPK signaling in thyroid cancer cells.

Degree: 2014, RCAAP

Dissertação de Mestrado em Biotecnologia para as Ciências da Saúde

O cancro da tireóide é o tumor maligno mais comum do sistema endócrino, correspondendo a… (more)

Subjects/Keywords: Mutações; PTC; MAPK; BRAF; RET/PTC1; RAF-1; PI3K-AKT

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APA (6th Edition):

Castro, L. M. F. (2014). Study of the role of RAF-1 in MAPK signaling in thyroid cancer cells. (Thesis). RCAAP. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:http://repositorio.utad.pt/:10348/3371

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):

Castro, Lisandra Marisa Flores. “Study of the role of RAF-1 in MAPK signaling in thyroid cancer cells.” 2014. Thesis, RCAAP. Accessed August 22, 2019. http://www.rcaap.pt/detail.jsp?id=oai:http://repositorio.utad.pt/:10348/3371.

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

MLA Handbook (7th Edition):

Castro, Lisandra Marisa Flores. “Study of the role of RAF-1 in MAPK signaling in thyroid cancer cells.” 2014. Web. 22 Aug 2019.

Vancouver:

Castro LMF. Study of the role of RAF-1 in MAPK signaling in thyroid cancer cells. [Internet] [Thesis]. RCAAP; 2014. [cited 2019 Aug 22]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:http://repositorio.utad.pt/:10348/3371.

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

Council of Science Editors:

Castro LMF. Study of the role of RAF-1 in MAPK signaling in thyroid cancer cells. [Thesis]. RCAAP; 2014. Available from: http://www.rcaap.pt/detail.jsp?id=oai:http://repositorio.utad.pt/:10348/3371

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


NSYSU

18. Chao, Fang-Ping. The expression of TSG101 and RET gene in thyroid carcinoma specimens.

Degree: Master, Biological Sciences, 2001, NSYSU

 The aim of this thesis is to evaluate the expression of both TSG101 tumor susceptibility gene and ret oncogene in human thyroid carcinoma specimens. Functional… (more)

Subjects/Keywords: TSG101; immunohistochemistry; RET; RT-PCR

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APA (6th Edition):

Chao, F. (2001). The expression of TSG101 and RET gene in thyroid carcinoma specimens. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0828101-111807

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):

Chao, Fang-Ping. “The expression of TSG101 and RET gene in thyroid carcinoma specimens.” 2001. Thesis, NSYSU. Accessed August 22, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0828101-111807.

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

MLA Handbook (7th Edition):

Chao, Fang-Ping. “The expression of TSG101 and RET gene in thyroid carcinoma specimens.” 2001. Web. 22 Aug 2019.

Vancouver:

Chao F. The expression of TSG101 and RET gene in thyroid carcinoma specimens. [Internet] [Thesis]. NSYSU; 2001. [cited 2019 Aug 22]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0828101-111807.

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

Council of Science Editors:

Chao F. The expression of TSG101 and RET gene in thyroid carcinoma specimens. [Thesis]. NSYSU; 2001. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0828101-111807

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


University of Edinburgh

19. Myers, Samuel Harry. Development of novel receptor tyrosine kinase inhibitors by a chemocentric approach.

Degree: PhD, 2017, University of Edinburgh

 In recent years, there has been a major movement in the pharmaceutical industry towards the development of molecules that selectivity inhibit a previously-validated specific target.… (more)

Subjects/Keywords: phenotypic drug discovery; AXL kinase; drug library; FLT3; RET

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APA (6th Edition):

Myers, S. H. (2017). Development of novel receptor tyrosine kinase inhibitors by a chemocentric approach. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/28769

Chicago Manual of Style (16th Edition):

Myers, Samuel Harry. “Development of novel receptor tyrosine kinase inhibitors by a chemocentric approach.” 2017. Doctoral Dissertation, University of Edinburgh. Accessed August 22, 2019. http://hdl.handle.net/1842/28769.

MLA Handbook (7th Edition):

Myers, Samuel Harry. “Development of novel receptor tyrosine kinase inhibitors by a chemocentric approach.” 2017. Web. 22 Aug 2019.

Vancouver:

Myers SH. Development of novel receptor tyrosine kinase inhibitors by a chemocentric approach. [Internet] [Doctoral dissertation]. University of Edinburgh; 2017. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1842/28769.

Council of Science Editors:

Myers SH. Development of novel receptor tyrosine kinase inhibitors by a chemocentric approach. [Doctoral Dissertation]. University of Edinburgh; 2017. Available from: http://hdl.handle.net/1842/28769

20. K.K. Stantcheva. A SUBPOPULATION OF ITCH RECEPTORS MARKED BY RET EXPRESSION.

Degree: 2014, Università degli Studi di Milano

 Sensory neurons are a heterogeneous group of cells that are specialized to detect stimuli acting on the skin such as touch, temperature, pain and itch.… (more)

Subjects/Keywords: sensory neurons; ret; itch; Settore BIO/11 - Biologia Molecolare

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APA (6th Edition):

Stantcheva, K. (2014). A SUBPOPULATION OF ITCH RECEPTORS MARKED BY RET EXPRESSION. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/241111

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):

Stantcheva, K.K.. “A SUBPOPULATION OF ITCH RECEPTORS MARKED BY RET EXPRESSION.” 2014. Thesis, Università degli Studi di Milano. Accessed August 22, 2019. http://hdl.handle.net/2434/241111.

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

MLA Handbook (7th Edition):

Stantcheva, K.K.. “A SUBPOPULATION OF ITCH RECEPTORS MARKED BY RET EXPRESSION.” 2014. Web. 22 Aug 2019.

Vancouver:

Stantcheva K. A SUBPOPULATION OF ITCH RECEPTORS MARKED BY RET EXPRESSION. [Internet] [Thesis]. Università degli Studi di Milano; 2014. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2434/241111.

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

Council of Science Editors:

Stantcheva K. A SUBPOPULATION OF ITCH RECEPTORS MARKED BY RET EXPRESSION. [Thesis]. Università degli Studi di Milano; 2014. Available from: http://hdl.handle.net/2434/241111

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

21. Musser, Melissa Anne. Enteric nervous system deficits in the ganglionated bowel of Hirschsprung mouse models and patients.

Degree: PhD, Human Genetics, 2014, Vanderbilt University

 Hirschsprung disease, or congenital absence of ganglia in the distal intestine, occurs in approximately every 1 in 5000 live births. Although HSCR patients have the… (more)

Subjects/Keywords: Hirschsprung; enteric nervous system; neural crest; Sox10; Ret; Ednrb

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APA (6th Edition):

Musser, M. A. (2014). Enteric nervous system deficits in the ganglionated bowel of Hirschsprung mouse models and patients. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-11232014-234212/ ;

Chicago Manual of Style (16th Edition):

Musser, Melissa Anne. “Enteric nervous system deficits in the ganglionated bowel of Hirschsprung mouse models and patients.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed August 22, 2019. http://etd.library.vanderbilt.edu//available/etd-11232014-234212/ ;.

MLA Handbook (7th Edition):

Musser, Melissa Anne. “Enteric nervous system deficits in the ganglionated bowel of Hirschsprung mouse models and patients.” 2014. Web. 22 Aug 2019.

Vancouver:

Musser MA. Enteric nervous system deficits in the ganglionated bowel of Hirschsprung mouse models and patients. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2019 Aug 22]. Available from: http://etd.library.vanderbilt.edu//available/etd-11232014-234212/ ;.

Council of Science Editors:

Musser MA. Enteric nervous system deficits in the ganglionated bowel of Hirschsprung mouse models and patients. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://etd.library.vanderbilt.edu//available/etd-11232014-234212/ ;


Boston University

22. Li, Simin. Quantitative studies of RET activation, deactivation and trafficking kinetics upon stimulation by its natural ligand Artemin.

Degree: PhD, Chemistry, 2016, Boston University

 Receptor tyrosine kinases (RTKs) are key regulators of critical cellular processes, such as cell cycle, differentiation, proliferation, apoptosis and survival. Mutations, hyperactivity and loss of… (more)

Subjects/Keywords: Biochemistry; Artemin; RET; Cell signaling; Endocytosis; Receptor tyrosine kinase; Systems biology

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APA (6th Edition):

Li, S. (2016). Quantitative studies of RET activation, deactivation and trafficking kinetics upon stimulation by its natural ligand Artemin. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/17712

Chicago Manual of Style (16th Edition):

Li, Simin. “Quantitative studies of RET activation, deactivation and trafficking kinetics upon stimulation by its natural ligand Artemin.” 2016. Doctoral Dissertation, Boston University. Accessed August 22, 2019. http://hdl.handle.net/2144/17712.

MLA Handbook (7th Edition):

Li, Simin. “Quantitative studies of RET activation, deactivation and trafficking kinetics upon stimulation by its natural ligand Artemin.” 2016. Web. 22 Aug 2019.

Vancouver:

Li S. Quantitative studies of RET activation, deactivation and trafficking kinetics upon stimulation by its natural ligand Artemin. [Internet] [Doctoral dissertation]. Boston University; 2016. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2144/17712.

Council of Science Editors:

Li S. Quantitative studies of RET activation, deactivation and trafficking kinetics upon stimulation by its natural ligand Artemin. [Doctoral Dissertation]. Boston University; 2016. Available from: http://hdl.handle.net/2144/17712


University of Lund

23. Styring, Emelie. Clinical and Biological Patterns in Soft Tissue Sarcoma.

Degree: 2013, University of Lund

 Soft tissue sarcomas (STSs) are rare malignant tumors, of which 3/4 are high-grade and 1/3 metastasize. For optimal management, STSs should be treated at multidisciplinary… (more)

Subjects/Keywords: Ortopedi; angiosarcoma; radiation-associated sarcoma; irradiated; RET; KIT; MYC.

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APA (6th Edition):

Styring, E. (2013). Clinical and Biological Patterns in Soft Tissue Sarcoma. (Doctoral Dissertation). University of Lund. Retrieved from http://lup.lub.lu.se/record/3710251 ; http://portal.research.lu.se/ws/files/3767630/3710288.pdf

Chicago Manual of Style (16th Edition):

Styring, Emelie. “Clinical and Biological Patterns in Soft Tissue Sarcoma.” 2013. Doctoral Dissertation, University of Lund. Accessed August 22, 2019. http://lup.lub.lu.se/record/3710251 ; http://portal.research.lu.se/ws/files/3767630/3710288.pdf.

MLA Handbook (7th Edition):

Styring, Emelie. “Clinical and Biological Patterns in Soft Tissue Sarcoma.” 2013. Web. 22 Aug 2019.

Vancouver:

Styring E. Clinical and Biological Patterns in Soft Tissue Sarcoma. [Internet] [Doctoral dissertation]. University of Lund; 2013. [cited 2019 Aug 22]. Available from: http://lup.lub.lu.se/record/3710251 ; http://portal.research.lu.se/ws/files/3767630/3710288.pdf.

Council of Science Editors:

Styring E. Clinical and Biological Patterns in Soft Tissue Sarcoma. [Doctoral Dissertation]. University of Lund; 2013. Available from: http://lup.lub.lu.se/record/3710251 ; http://portal.research.lu.se/ws/files/3767630/3710288.pdf


Queens University

24. Rekab, Aisha. Evaluating the relationship between the RET receptor tyrosine kinase and TMEM127 .

Degree: Pathology and Molecular Medicine, Queens University

 Pheochromocytomas (PCC) are highly heritable neoplasms of the adrenal gland, carrying germline mutations in approximately 40% of cases. PCC susceptibility genes have been subdivided into… (more)

Subjects/Keywords: RET; TMEM127; Pheochromocytoma; Intracellular trafficking

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APA (6th Edition):

Rekab, A. (n.d.). Evaluating the relationship between the RET receptor tyrosine kinase and TMEM127 . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/26439

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Rekab, Aisha. “Evaluating the relationship between the RET receptor tyrosine kinase and TMEM127 .” Thesis, Queens University. Accessed August 22, 2019. http://hdl.handle.net/1974/26439.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Rekab, Aisha. “Evaluating the relationship between the RET receptor tyrosine kinase and TMEM127 .” Web. 22 Aug 2019.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Rekab A. Evaluating the relationship between the RET receptor tyrosine kinase and TMEM127 . [Internet] [Thesis]. Queens University; [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1974/26439.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Rekab A. Evaluating the relationship between the RET receptor tyrosine kinase and TMEM127 . [Thesis]. Queens University; Available from: http://hdl.handle.net/1974/26439

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


University of Sydney

25. Joo, Lauren Jin Suk. RET-regulated microRNAs as Recurrence Biomarkers and Therapeutic Targets in Medullary Thyroid Carcinoma .

Degree: 2018, University of Sydney

 Medullary thyroid carcinoma (MTC) is an aggressive malignancy which accounts for 3 – 5 % of all thyroid cancers. MTC originates from calcitonin-producing parafollicular C-cells… (more)

Subjects/Keywords: medullary thyroid carcinome; RET; microRNA; miR-153-3p; TKI; Cabozantinib

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APA (6th Edition):

Joo, L. J. S. (2018). RET-regulated microRNAs as Recurrence Biomarkers and Therapeutic Targets in Medullary Thyroid Carcinoma . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/19945

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):

Joo, Lauren Jin Suk. “RET-regulated microRNAs as Recurrence Biomarkers and Therapeutic Targets in Medullary Thyroid Carcinoma .” 2018. Thesis, University of Sydney. Accessed August 22, 2019. http://hdl.handle.net/2123/19945.

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

MLA Handbook (7th Edition):

Joo, Lauren Jin Suk. “RET-regulated microRNAs as Recurrence Biomarkers and Therapeutic Targets in Medullary Thyroid Carcinoma .” 2018. Web. 22 Aug 2019.

Vancouver:

Joo LJS. RET-regulated microRNAs as Recurrence Biomarkers and Therapeutic Targets in Medullary Thyroid Carcinoma . [Internet] [Thesis]. University of Sydney; 2018. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2123/19945.

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

Council of Science Editors:

Joo LJS. RET-regulated microRNAs as Recurrence Biomarkers and Therapeutic Targets in Medullary Thyroid Carcinoma . [Thesis]. University of Sydney; 2018. Available from: http://hdl.handle.net/2123/19945

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


Queens University

26. Kaur, Harvinder. Investigating the relationship between the RET receptor, Cbl and ARHGEF7 in downregulation of RET .

Degree: Pathology and Molecular Medicine, 2008, Queens University

 The RET proto-oncogene encodes a receptor tyrosine kinase (RTK), with two major isoforms, RET9 and RET51, which differ in their C-termini, and therefore recruit different… (more)

Subjects/Keywords: RET; Dpwnregulation; Cbl; ARHGEF7; Interactions

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APA (6th Edition):

Kaur, H. (2008). Investigating the relationship between the RET receptor, Cbl and ARHGEF7 in downregulation of RET . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/1313

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):

Kaur, Harvinder. “Investigating the relationship between the RET receptor, Cbl and ARHGEF7 in downregulation of RET .” 2008. Thesis, Queens University. Accessed August 22, 2019. http://hdl.handle.net/1974/1313.

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

MLA Handbook (7th Edition):

Kaur, Harvinder. “Investigating the relationship between the RET receptor, Cbl and ARHGEF7 in downregulation of RET .” 2008. Web. 22 Aug 2019.

Vancouver:

Kaur H. Investigating the relationship between the RET receptor, Cbl and ARHGEF7 in downregulation of RET . [Internet] [Thesis]. Queens University; 2008. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1974/1313.

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

Council of Science Editors:

Kaur H. Investigating the relationship between the RET receptor, Cbl and ARHGEF7 in downregulation of RET . [Thesis]. Queens University; 2008. Available from: http://hdl.handle.net/1974/1313

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

27. Negrão, Douglas Polcaro. Estudo de asfaltos modificados por polímeros do tipo RET para aplicações em pavimentos.

Degree: Mestrado, Engenharia de Transportes, 2006, University of São Paulo

O presente trabalho avalia as alterações de propriedades dos asfaltos pela modificação por polímero do tipo RET (Reactive Elastomeric Terpolymer) e de comportamento de misturas… (more)

Subjects/Keywords: Asfalto; Asfalto modificado por polímeros; Asphalt; Polímero RET; Polymer modified asphalt; RET

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APA (6th Edition):

Negrão, D. P. (2006). Estudo de asfaltos modificados por polímeros do tipo RET para aplicações em pavimentos. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/3/3138/tde-09032007-170249/ ;

Chicago Manual of Style (16th Edition):

Negrão, Douglas Polcaro. “Estudo de asfaltos modificados por polímeros do tipo RET para aplicações em pavimentos.” 2006. Masters Thesis, University of São Paulo. Accessed August 22, 2019. http://www.teses.usp.br/teses/disponiveis/3/3138/tde-09032007-170249/ ;.

MLA Handbook (7th Edition):

Negrão, Douglas Polcaro. “Estudo de asfaltos modificados por polímeros do tipo RET para aplicações em pavimentos.” 2006. Web. 22 Aug 2019.

Vancouver:

Negrão DP. Estudo de asfaltos modificados por polímeros do tipo RET para aplicações em pavimentos. [Internet] [Masters thesis]. University of São Paulo; 2006. [cited 2019 Aug 22]. Available from: http://www.teses.usp.br/teses/disponiveis/3/3138/tde-09032007-170249/ ;.

Council of Science Editors:

Negrão DP. Estudo de asfaltos modificados por polímeros do tipo RET para aplicações em pavimentos. [Masters Thesis]. University of São Paulo; 2006. Available from: http://www.teses.usp.br/teses/disponiveis/3/3138/tde-09032007-170249/ ;

28. Ricarte Filho, Júlio Cezar Marques. Envolvimento dos oncogenes BRAF, PIK3CA e AKT1 e do microRNA supressor de tumor let-7 na transformação maligna e progressão tumoral tiroidiana.

Degree: PhD, Biologia Celular e Tecidual, 2009, University of São Paulo

Neste estudo, geramos ensaios de espectrometria de massa para detecção de 111 mutações nos genes RET, BRAF, NRAS, HRAS, KRAS, PIK3CA e AKT1 e avaliamos… (more)

Subjects/Keywords: AKT1; AKT1; BRAF; BRAF; Câncer tiróide; Genotipagem por espectrometria de massa; Histologia; Histology; Let-7 microRNA; Mass spectrometry genotyping; MicroRNA let-7; Neoplasias; Neoplasms; RET/PTC; RET/PTC; Thyroid cancer

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APA (6th Edition):

Ricarte Filho, J. C. M. (2009). Envolvimento dos oncogenes BRAF, PIK3CA e AKT1 e do microRNA supressor de tumor let-7 na transformação maligna e progressão tumoral tiroidiana. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/42/42134/tde-06102009-094118/ ;

Chicago Manual of Style (16th Edition):

Ricarte Filho, Júlio Cezar Marques. “Envolvimento dos oncogenes BRAF, PIK3CA e AKT1 e do microRNA supressor de tumor let-7 na transformação maligna e progressão tumoral tiroidiana.” 2009. Doctoral Dissertation, University of São Paulo. Accessed August 22, 2019. http://www.teses.usp.br/teses/disponiveis/42/42134/tde-06102009-094118/ ;.

MLA Handbook (7th Edition):

Ricarte Filho, Júlio Cezar Marques. “Envolvimento dos oncogenes BRAF, PIK3CA e AKT1 e do microRNA supressor de tumor let-7 na transformação maligna e progressão tumoral tiroidiana.” 2009. Web. 22 Aug 2019.

Vancouver:

Ricarte Filho JCM. Envolvimento dos oncogenes BRAF, PIK3CA e AKT1 e do microRNA supressor de tumor let-7 na transformação maligna e progressão tumoral tiroidiana. [Internet] [Doctoral dissertation]. University of São Paulo; 2009. [cited 2019 Aug 22]. Available from: http://www.teses.usp.br/teses/disponiveis/42/42134/tde-06102009-094118/ ;.

Council of Science Editors:

Ricarte Filho JCM. Envolvimento dos oncogenes BRAF, PIK3CA e AKT1 e do microRNA supressor de tumor let-7 na transformação maligna e progressão tumoral tiroidiana. [Doctoral Dissertation]. University of São Paulo; 2009. Available from: http://www.teses.usp.br/teses/disponiveis/42/42134/tde-06102009-094118/ ;

29. Quedas, Elisangela Pereira de Souza. Análise do proto-oncogene RET em pacientes com carcinoma medular de tireóide e megacólon congênito de uma família com mutação germinativa p.C620R.

Degree: Mestrado, Endocrinologia, 2011, University of São Paulo

As Neoplasias endócrinas múltiplas (NEMs) são síndromes herdadas de modo dominante e causadas por mutações germinativas em genes específicos. Caracterizam-se pela presença de tumores em… (more)

Subjects/Keywords: Aganglionosis; Carcinoma medular de tireóide; CMT PHEO HPT; Congenital megacólon; Doença de Hirschsprung; Feocromocitoma; Hiperparatireoidismo primário; Hirschsprung; Multiple endocrine neoplasia type 2 (MEN2); Neoplasia endócrina múltipla tipo 2a; RET; RET

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

APA (6th Edition):

Quedas, E. P. d. S. (2011). Análise do proto-oncogene RET em pacientes com carcinoma medular de tireóide e megacólon congênito de uma família com mutação germinativa p.C620R. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5135/tde-11012012-152825/ ;

Chicago Manual of Style (16th Edition):

Quedas, Elisangela Pereira de Souza. “Análise do proto-oncogene RET em pacientes com carcinoma medular de tireóide e megacólon congênito de uma família com mutação germinativa p.C620R.” 2011. Masters Thesis, University of São Paulo. Accessed August 22, 2019. http://www.teses.usp.br/teses/disponiveis/5/5135/tde-11012012-152825/ ;.

MLA Handbook (7th Edition):

Quedas, Elisangela Pereira de Souza. “Análise do proto-oncogene RET em pacientes com carcinoma medular de tireóide e megacólon congênito de uma família com mutação germinativa p.C620R.” 2011. Web. 22 Aug 2019.

Vancouver:

Quedas EPdS. Análise do proto-oncogene RET em pacientes com carcinoma medular de tireóide e megacólon congênito de uma família com mutação germinativa p.C620R. [Internet] [Masters thesis]. University of São Paulo; 2011. [cited 2019 Aug 22]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5135/tde-11012012-152825/ ;.

Council of Science Editors:

Quedas EPdS. Análise do proto-oncogene RET em pacientes com carcinoma medular de tireóide e megacólon congênito de uma família com mutação germinativa p.C620R. [Masters Thesis]. University of São Paulo; 2011. Available from: http://www.teses.usp.br/teses/disponiveis/5/5135/tde-11012012-152825/ ;

30. Fuziwara, Cesar Seigi. Influência do MicroRNA let-7 e miR-17-92 como oncomiRs no câncer.

Degree: Mestrado, Biologia Celular e Tecidual, 2010, University of São Paulo

No câncer, alterações em microRNAs (miRNAs), pequenos RNAs que regulam a tradução protéica, exerce efeito oncogênico (oncomiR). Os oncomiRs regulam genes chave para a proliferação… (more)

Subjects/Keywords: Glândula tireóide; Let-7; Let-7; MicroRNA; MicroRNA; miR-17-92; miR-17-92; Neoplasias da tireóide; Proliferação RET/PTC; Proliferation; RET-PTC; Thyroid gland; Thyroid neoplasms

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

APA (6th Edition):

Fuziwara, C. S. (2010). Influência do MicroRNA let-7 e miR-17-92 como oncomiRs no câncer. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/42/42134/tde-27092010-152352/ ;

Chicago Manual of Style (16th Edition):

Fuziwara, Cesar Seigi. “Influência do MicroRNA let-7 e miR-17-92 como oncomiRs no câncer.” 2010. Masters Thesis, University of São Paulo. Accessed August 22, 2019. http://www.teses.usp.br/teses/disponiveis/42/42134/tde-27092010-152352/ ;.

MLA Handbook (7th Edition):

Fuziwara, Cesar Seigi. “Influência do MicroRNA let-7 e miR-17-92 como oncomiRs no câncer.” 2010. Web. 22 Aug 2019.

Vancouver:

Fuziwara CS. Influência do MicroRNA let-7 e miR-17-92 como oncomiRs no câncer. [Internet] [Masters thesis]. University of São Paulo; 2010. [cited 2019 Aug 22]. Available from: http://www.teses.usp.br/teses/disponiveis/42/42134/tde-27092010-152352/ ;.

Council of Science Editors:

Fuziwara CS. Influência do MicroRNA let-7 e miR-17-92 como oncomiRs no câncer. [Masters Thesis]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/42/42134/tde-27092010-152352/ ;

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