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You searched for subject:(Cell therapy). Showing records 1 – 30 of 723 total matches.

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California State University – Sacramento

1. Cicchetto, Andrew C. Genetically modified multipotent stromal cells for the treatment of osteoarthritis.

Degree: MA, Biological Sciences (Stem Cell, 2016, California State University – Sacramento

 Osteoarthritis (OA) is a degenerative joint disease estimated to affect 630 million people worldwide. OA is characterized by the progressive loss of articular cartilage, damage… (more)

Subjects/Keywords: Interleukin-10; Gene Therapy; Cell Therapy; Lentivirus

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

APA (6th Edition):

Cicchetto, A. C. (2016). Genetically modified multipotent stromal cells for the treatment of osteoarthritis. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/171158

Chicago Manual of Style (16th Edition):

Cicchetto, Andrew C. “Genetically modified multipotent stromal cells for the treatment of osteoarthritis.” 2016. Masters Thesis, California State University – Sacramento. Accessed October 22, 2019. http://hdl.handle.net/10211.3/171158.

MLA Handbook (7th Edition):

Cicchetto, Andrew C. “Genetically modified multipotent stromal cells for the treatment of osteoarthritis.” 2016. Web. 22 Oct 2019.

Vancouver:

Cicchetto AC. Genetically modified multipotent stromal cells for the treatment of osteoarthritis. [Internet] [Masters thesis]. California State University – Sacramento; 2016. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/10211.3/171158.

Council of Science Editors:

Cicchetto AC. Genetically modified multipotent stromal cells for the treatment of osteoarthritis. [Masters Thesis]. California State University – Sacramento; 2016. Available from: http://hdl.handle.net/10211.3/171158


University of New South Wales

2. Venugopal. Pathogenesis of blistering disorders.

Degree: Clinical School - St George Hospital, 2016, University of New South Wales

 Epidermolysis bullosa (EB) is a rare group of inherited blistering skin disordersmarked by skin fragility. Despite significant advances in research, there is no cureyet. My… (more)

Subjects/Keywords: Epidermolysis bullosa; Cell therapy

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APA (6th Edition):

Venugopal. (2016). Pathogenesis of blistering disorders. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/60291 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51706/SOURCE02?view=true

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

Venugopal. “Pathogenesis of blistering disorders.” 2016. Doctoral Dissertation, University of New South Wales. Accessed October 22, 2019. http://handle.unsw.edu.au/1959.4/60291 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51706/SOURCE02?view=true.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

Venugopal. “Pathogenesis of blistering disorders.” 2016. Web. 22 Oct 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

Venugopal. Pathogenesis of blistering disorders. [Internet] [Doctoral dissertation]. University of New South Wales; 2016. [cited 2019 Oct 22]. Available from: http://handle.unsw.edu.au/1959.4/60291 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51706/SOURCE02?view=true.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

Venugopal. Pathogenesis of blistering disorders. [Doctoral Dissertation]. University of New South Wales; 2016. Available from: http://handle.unsw.edu.au/1959.4/60291 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51706/SOURCE02?view=true

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete


Tampere University

3. Rajala, Kristiina. Development of human stem cell culture conditions for clinical cell therapy .

Degree: Solu- ja kudosteknologiakeskus Regea - Institute of Regenerative Medicine, 2010, Tampere University

 Erilaistumattomien kantasolujen erityispiirteitä ovat lähes rajaton jakautumiskyky sekä kyky erilaistua moniksi erilaistuneiksi solutyypeiksi. Näiden erityispiirteiden ansiosta kantasoluja voidaan hyödyntää sekä tutkimuksessa että regeneratiivisessa lääketieteessä. Pluripotentit… (more)

Subjects/Keywords: kantasolu; soluterapia; GMP; Stem cell; cell therapy

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APA (6th Edition):

Rajala, K. (2010). Development of human stem cell culture conditions for clinical cell therapy . (Doctoral Dissertation). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/66602

Chicago Manual of Style (16th Edition):

Rajala, Kristiina. “Development of human stem cell culture conditions for clinical cell therapy .” 2010. Doctoral Dissertation, Tampere University. Accessed October 22, 2019. https://trepo.tuni.fi/handle/10024/66602.

MLA Handbook (7th Edition):

Rajala, Kristiina. “Development of human stem cell culture conditions for clinical cell therapy .” 2010. Web. 22 Oct 2019.

Vancouver:

Rajala K. Development of human stem cell culture conditions for clinical cell therapy . [Internet] [Doctoral dissertation]. Tampere University; 2010. [cited 2019 Oct 22]. Available from: https://trepo.tuni.fi/handle/10024/66602.

Council of Science Editors:

Rajala K. Development of human stem cell culture conditions for clinical cell therapy . [Doctoral Dissertation]. Tampere University; 2010. Available from: https://trepo.tuni.fi/handle/10024/66602


University of Illinois – Chicago

4. Rady, Brian. Transcription Factors E2F Have a Role in Proliferation of Beta-Cells and Development of Type-2 Diabetes.

Degree: 2013, University of Illinois – Chicago

 This work pertains to the search for genetic targets to induce beta-cell proliferation. This proliferation was intended to support the advancement of islet cell transplant… (more)

Subjects/Keywords: Diabetes; cell therapy; beta-cell proliferation; cell-cycle

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APA (6th Edition):

Rady, B. (2013). Transcription Factors E2F Have a Role in Proliferation of Beta-Cells and Development of Type-2 Diabetes. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/10071

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):

Rady, Brian. “Transcription Factors E2F Have a Role in Proliferation of Beta-Cells and Development of Type-2 Diabetes.” 2013. Thesis, University of Illinois – Chicago. Accessed October 22, 2019. http://hdl.handle.net/10027/10071.

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

MLA Handbook (7th Edition):

Rady, Brian. “Transcription Factors E2F Have a Role in Proliferation of Beta-Cells and Development of Type-2 Diabetes.” 2013. Web. 22 Oct 2019.

Vancouver:

Rady B. Transcription Factors E2F Have a Role in Proliferation of Beta-Cells and Development of Type-2 Diabetes. [Internet] [Thesis]. University of Illinois – Chicago; 2013. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/10027/10071.

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

Council of Science Editors:

Rady B. Transcription Factors E2F Have a Role in Proliferation of Beta-Cells and Development of Type-2 Diabetes. [Thesis]. University of Illinois – Chicago; 2013. Available from: http://hdl.handle.net/10027/10071

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

5. Swami, Archana. Polymeric and metallic nanoparticles as carriers in biomedical applications.

Degree: 2003, University of Pune

Nanoparticle mediated delivery of biomolecules has attracted interest of the researchers working in the area of gene therapy. Nanoparticles being small and compact are well… (more)

Subjects/Keywords: Gene Therapy; Blood Components; Cell Culture; Nanoparticles

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APA (6th Edition):

Swami, A. (2003). Polymeric and metallic nanoparticles as carriers in biomedical applications. (Thesis). University of Pune. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/2686

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):

Swami, Archana. “Polymeric and metallic nanoparticles as carriers in biomedical applications.” 2003. Thesis, University of Pune. Accessed October 22, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/2686.

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

MLA Handbook (7th Edition):

Swami, Archana. “Polymeric and metallic nanoparticles as carriers in biomedical applications.” 2003. Web. 22 Oct 2019.

Vancouver:

Swami A. Polymeric and metallic nanoparticles as carriers in biomedical applications. [Internet] [Thesis]. University of Pune; 2003. [cited 2019 Oct 22]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/2686.

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

Council of Science Editors:

Swami A. Polymeric and metallic nanoparticles as carriers in biomedical applications. [Thesis]. University of Pune; 2003. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/2686

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

6. Bodas, Manish. Inhibition of IL-2 induced IL-10 production as a principle of phase specific immuno-therapy for visceral leishmaniasis.

Degree: 2006, University of Pune

Visceral leishmaniasis is a fatal disease caused by the protozoan parasite Leishmania donovani. T cells are known to mediate resistance or susceptibility against this ‘neglected… (more)

Subjects/Keywords: Biotechnology; Cell Science; Immuno therapy; Visceral Leishmaniasis

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APA (6th Edition):

Bodas, M. (2006). Inhibition of IL-2 induced IL-10 production as a principle of phase specific immuno-therapy for visceral leishmaniasis. (Thesis). University of Pune. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/2227

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):

Bodas, Manish. “Inhibition of IL-2 induced IL-10 production as a principle of phase specific immuno-therapy for visceral leishmaniasis.” 2006. Thesis, University of Pune. Accessed October 22, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/2227.

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

MLA Handbook (7th Edition):

Bodas, Manish. “Inhibition of IL-2 induced IL-10 production as a principle of phase specific immuno-therapy for visceral leishmaniasis.” 2006. Web. 22 Oct 2019.

Vancouver:

Bodas M. Inhibition of IL-2 induced IL-10 production as a principle of phase specific immuno-therapy for visceral leishmaniasis. [Internet] [Thesis]. University of Pune; 2006. [cited 2019 Oct 22]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/2227.

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

Council of Science Editors:

Bodas M. Inhibition of IL-2 induced IL-10 production as a principle of phase specific immuno-therapy for visceral leishmaniasis. [Thesis]. University of Pune; 2006. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/2227

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


National University of Ireland – Galway

7. O'Loughlin, Aonghus. Novel Cell-Based Therapies for the Treatment of Diabetic Ulceration .

Degree: 2012, National University of Ireland – Galway

 The focus of this research is on developing novel cell based therapies for the treatment of non-healing diabetic foot ulceration. The thesis begins with a… (more)

Subjects/Keywords: Diabetes; Ulceration; Wounds; Cell Therapy; Biomaterials

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APA (6th Edition):

O'Loughlin, A. (2012). Novel Cell-Based Therapies for the Treatment of Diabetic Ulceration . (Thesis). National University of Ireland – Galway. Retrieved from http://hdl.handle.net/10379/2731

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):

O'Loughlin, Aonghus. “Novel Cell-Based Therapies for the Treatment of Diabetic Ulceration .” 2012. Thesis, National University of Ireland – Galway. Accessed October 22, 2019. http://hdl.handle.net/10379/2731.

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

MLA Handbook (7th Edition):

O'Loughlin, Aonghus. “Novel Cell-Based Therapies for the Treatment of Diabetic Ulceration .” 2012. Web. 22 Oct 2019.

Vancouver:

O'Loughlin A. Novel Cell-Based Therapies for the Treatment of Diabetic Ulceration . [Internet] [Thesis]. National University of Ireland – Galway; 2012. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/10379/2731.

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

Council of Science Editors:

O'Loughlin A. Novel Cell-Based Therapies for the Treatment of Diabetic Ulceration . [Thesis]. National University of Ireland – Galway; 2012. Available from: http://hdl.handle.net/10379/2731

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


Loughborough University

8. Worrallo, Matthew J. Immobilised growth factors for scalable cell therapy manufacturing platforms.

Degree: PhD, 2018, Loughborough University

 Regenerative medicine has the potential to establish or restore normal function in defective tissues and organs. The realisation of such therapies is restricted due to… (more)

Subjects/Keywords: Growth factors; Cell therapy; Scalable; Immobilised

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APA (6th Edition):

Worrallo, M. J. (2018). Immobilised growth factors for scalable cell therapy manufacturing platforms. (Doctoral Dissertation). Loughborough University. Retrieved from https://dspace.lboro.ac.uk/2134/27912 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.734163

Chicago Manual of Style (16th Edition):

Worrallo, Matthew J. “Immobilised growth factors for scalable cell therapy manufacturing platforms.” 2018. Doctoral Dissertation, Loughborough University. Accessed October 22, 2019. https://dspace.lboro.ac.uk/2134/27912 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.734163.

MLA Handbook (7th Edition):

Worrallo, Matthew J. “Immobilised growth factors for scalable cell therapy manufacturing platforms.” 2018. Web. 22 Oct 2019.

Vancouver:

Worrallo MJ. Immobilised growth factors for scalable cell therapy manufacturing platforms. [Internet] [Doctoral dissertation]. Loughborough University; 2018. [cited 2019 Oct 22]. Available from: https://dspace.lboro.ac.uk/2134/27912 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.734163.

Council of Science Editors:

Worrallo MJ. Immobilised growth factors for scalable cell therapy manufacturing platforms. [Doctoral Dissertation]. Loughborough University; 2018. Available from: https://dspace.lboro.ac.uk/2134/27912 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.734163


University of Debrecen

9. Dumont, Therese. Stem cell transplantation in peripheral arterial diseases .

Degree: DE – Általános Orvostudományi Kar, University of Debrecen

 There is an increase number of patients suffering from peripheral arterial disease (PAD) and unfortunately, once in the late stage of critical limb ischemia, it… (more)

Subjects/Keywords: Stem cell therapy

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APA (6th Edition):

Dumont, T. (n.d.). Stem cell transplantation in peripheral arterial diseases . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/229987

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):

Dumont, Therese. “Stem cell transplantation in peripheral arterial diseases .” Thesis, University of Debrecen. Accessed October 22, 2019. http://hdl.handle.net/2437/229987.

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):

Dumont, Therese. “Stem cell transplantation in peripheral arterial diseases .” Web. 22 Oct 2019.

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

Vancouver:

Dumont T. Stem cell transplantation in peripheral arterial diseases . [Internet] [Thesis]. University of Debrecen; [cited 2019 Oct 22]. Available from: http://hdl.handle.net/2437/229987.

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:

Dumont T. Stem cell transplantation in peripheral arterial diseases . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/229987

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 Adelaide

10. Leong, Wai Khay. Stem cell and molecular investigations following focal cerebral ischemia.

Degree: 2012, University of Adelaide

 This thesis revolves around a general theme – cerebral ischemia. Stroke is the second leading cause of mortality after cardiovascular disease and the single primary… (more)

Subjects/Keywords: cell-based therapy; Npas4; ischemic stroke

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APA (6th Edition):

Leong, W. K. (2012). Stem cell and molecular investigations following focal cerebral ischemia. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/87114

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):

Leong, Wai Khay. “Stem cell and molecular investigations following focal cerebral ischemia.” 2012. Thesis, University of Adelaide. Accessed October 22, 2019. http://hdl.handle.net/2440/87114.

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

MLA Handbook (7th Edition):

Leong, Wai Khay. “Stem cell and molecular investigations following focal cerebral ischemia.” 2012. Web. 22 Oct 2019.

Vancouver:

Leong WK. Stem cell and molecular investigations following focal cerebral ischemia. [Internet] [Thesis]. University of Adelaide; 2012. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/2440/87114.

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

Council of Science Editors:

Leong WK. Stem cell and molecular investigations following focal cerebral ischemia. [Thesis]. University of Adelaide; 2012. Available from: http://hdl.handle.net/2440/87114

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


University of Toronto

11. Gortler, Hilary. The Effect of Bone Marrow-Derived Progenitor Cell Therapy to Improve Fracture Healing in a Diabetic Rat Critical Size Defect Model.

Degree: 2018, University of Toronto

Our study aimed to explore the efficacy of locally implanted endothelial progenitor cells (EPCs) from healthy and diabetic animals on bone defect healing in healthy… (more)

Subjects/Keywords: Cell Therapy; Diabetes; EPC; Regenerative Medicine; 0564

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APA (6th Edition):

Gortler, H. (2018). The Effect of Bone Marrow-Derived Progenitor Cell Therapy to Improve Fracture Healing in a Diabetic Rat Critical Size Defect Model. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/91425

Chicago Manual of Style (16th Edition):

Gortler, Hilary. “The Effect of Bone Marrow-Derived Progenitor Cell Therapy to Improve Fracture Healing in a Diabetic Rat Critical Size Defect Model.” 2018. Masters Thesis, University of Toronto. Accessed October 22, 2019. http://hdl.handle.net/1807/91425.

MLA Handbook (7th Edition):

Gortler, Hilary. “The Effect of Bone Marrow-Derived Progenitor Cell Therapy to Improve Fracture Healing in a Diabetic Rat Critical Size Defect Model.” 2018. Web. 22 Oct 2019.

Vancouver:

Gortler H. The Effect of Bone Marrow-Derived Progenitor Cell Therapy to Improve Fracture Healing in a Diabetic Rat Critical Size Defect Model. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1807/91425.

Council of Science Editors:

Gortler H. The Effect of Bone Marrow-Derived Progenitor Cell Therapy to Improve Fracture Healing in a Diabetic Rat Critical Size Defect Model. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/91425


University of Rochester

12. Xu, Yuexin. Optogenetically Engineered Chemokine Receptors in T cell Migration and Cancer Immunotherapy.

Degree: PhD, 2015, University of Rochester

 Chemokine receptors are promising therapeutic targets because chemokine mediated cell migrations play key roles in mediating leukocyte differentiation, survival, and tissuespecific homing. However, chemokine sensing… (more)

Subjects/Keywords: Optogenetics; Chemokine; T cell; Cancer therapy

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APA (6th Edition):

Xu, Y. (2015). Optogenetically Engineered Chemokine Receptors in T cell Migration and Cancer Immunotherapy. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/29774

Chicago Manual of Style (16th Edition):

Xu, Yuexin. “Optogenetically Engineered Chemokine Receptors in T cell Migration and Cancer Immunotherapy.” 2015. Doctoral Dissertation, University of Rochester. Accessed October 22, 2019. http://hdl.handle.net/1802/29774.

MLA Handbook (7th Edition):

Xu, Yuexin. “Optogenetically Engineered Chemokine Receptors in T cell Migration and Cancer Immunotherapy.” 2015. Web. 22 Oct 2019.

Vancouver:

Xu Y. Optogenetically Engineered Chemokine Receptors in T cell Migration and Cancer Immunotherapy. [Internet] [Doctoral dissertation]. University of Rochester; 2015. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1802/29774.

Council of Science Editors:

Xu Y. Optogenetically Engineered Chemokine Receptors in T cell Migration and Cancer Immunotherapy. [Doctoral Dissertation]. University of Rochester; 2015. Available from: http://hdl.handle.net/1802/29774


University of Victoria

13. Rieck, Kristy. Gold nanoparticle uptake in synchronized cell populations and the effect on radiation sensitization.

Degree: Department of Physics and Astronomy, 2019, University of Victoria

 To overcome the challenge in radiation therapy of delivering the prescribed dose to cancer cells while sparing normal tissue, preferential introduction of high Z material… (more)

Subjects/Keywords: Cell cycle; Radiation therapy; Gold nanoparticles

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APA (6th Edition):

Rieck, K. (2019). Gold nanoparticle uptake in synchronized cell populations and the effect on radiation sensitization. (Masters Thesis). University of Victoria. Retrieved from http://hdl.handle.net/1828/10714

Chicago Manual of Style (16th Edition):

Rieck, Kristy. “Gold nanoparticle uptake in synchronized cell populations and the effect on radiation sensitization.” 2019. Masters Thesis, University of Victoria. Accessed October 22, 2019. http://hdl.handle.net/1828/10714.

MLA Handbook (7th Edition):

Rieck, Kristy. “Gold nanoparticle uptake in synchronized cell populations and the effect on radiation sensitization.” 2019. Web. 22 Oct 2019.

Vancouver:

Rieck K. Gold nanoparticle uptake in synchronized cell populations and the effect on radiation sensitization. [Internet] [Masters thesis]. University of Victoria; 2019. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1828/10714.

Council of Science Editors:

Rieck K. Gold nanoparticle uptake in synchronized cell populations and the effect on radiation sensitization. [Masters Thesis]. University of Victoria; 2019. Available from: http://hdl.handle.net/1828/10714


Rice University

14. Mitra, Kinshuk. Barcoding tools to track development and function of stem cell constructs for biomedicine.

Degree: PhD, Bioengineering, 2019, Rice University

 Biological regeneration has long been explored as a breakthrough modality for human therapy. Degenerative diseases, a majority of which are a related to ageing, manifest… (more)

Subjects/Keywords: Regenerative medicine; bioengineering; cell therapy; synthetic biology

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APA (6th Edition):

Mitra, K. (2019). Barcoding tools to track development and function of stem cell constructs for biomedicine. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/105412

Chicago Manual of Style (16th Edition):

Mitra, Kinshuk. “Barcoding tools to track development and function of stem cell constructs for biomedicine.” 2019. Doctoral Dissertation, Rice University. Accessed October 22, 2019. http://hdl.handle.net/1911/105412.

MLA Handbook (7th Edition):

Mitra, Kinshuk. “Barcoding tools to track development and function of stem cell constructs for biomedicine.” 2019. Web. 22 Oct 2019.

Vancouver:

Mitra K. Barcoding tools to track development and function of stem cell constructs for biomedicine. [Internet] [Doctoral dissertation]. Rice University; 2019. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1911/105412.

Council of Science Editors:

Mitra K. Barcoding tools to track development and function of stem cell constructs for biomedicine. [Doctoral Dissertation]. Rice University; 2019. Available from: http://hdl.handle.net/1911/105412


Rice University

15. Mitra, Kinshuk. Barcoding tools to track development and function of stem cell constructs for biomedicine.

Degree: PhD, Bioengineering, 2019, Rice University

 Biological regeneration has long been explored as a breakthrough modality for human therapy. Degenerative diseases, a majority of which are a related to ageing, manifest… (more)

Subjects/Keywords: Regenerative medicine; bioengineering; cell therapy; synthetic biology

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APA (6th Edition):

Mitra, K. (2019). Barcoding tools to track development and function of stem cell constructs for biomedicine. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/105418

Chicago Manual of Style (16th Edition):

Mitra, Kinshuk. “Barcoding tools to track development and function of stem cell constructs for biomedicine.” 2019. Doctoral Dissertation, Rice University. Accessed October 22, 2019. http://hdl.handle.net/1911/105418.

MLA Handbook (7th Edition):

Mitra, Kinshuk. “Barcoding tools to track development and function of stem cell constructs for biomedicine.” 2019. Web. 22 Oct 2019.

Vancouver:

Mitra K. Barcoding tools to track development and function of stem cell constructs for biomedicine. [Internet] [Doctoral dissertation]. Rice University; 2019. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1911/105418.

Council of Science Editors:

Mitra K. Barcoding tools to track development and function of stem cell constructs for biomedicine. [Doctoral Dissertation]. Rice University; 2019. Available from: http://hdl.handle.net/1911/105418


Rice University

16. Mitra, Kinshuk. Barcoding tools to track development and function of stem cell constructs for biomedicine.

Degree: PhD, Bioengineering, 2019, Rice University

 Biological regeneration has long been explored as a breakthrough modality for human therapy. Degenerative diseases, a majority of which are a related to ageing, manifest… (more)

Subjects/Keywords: Regenerative medicine; bioengineering; cell therapy; synthetic biology

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APA (6th Edition):

Mitra, K. (2019). Barcoding tools to track development and function of stem cell constructs for biomedicine. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/105413

Chicago Manual of Style (16th Edition):

Mitra, Kinshuk. “Barcoding tools to track development and function of stem cell constructs for biomedicine.” 2019. Doctoral Dissertation, Rice University. Accessed October 22, 2019. http://hdl.handle.net/1911/105413.

MLA Handbook (7th Edition):

Mitra, Kinshuk. “Barcoding tools to track development and function of stem cell constructs for biomedicine.” 2019. Web. 22 Oct 2019.

Vancouver:

Mitra K. Barcoding tools to track development and function of stem cell constructs for biomedicine. [Internet] [Doctoral dissertation]. Rice University; 2019. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1911/105413.

Council of Science Editors:

Mitra K. Barcoding tools to track development and function of stem cell constructs for biomedicine. [Doctoral Dissertation]. Rice University; 2019. Available from: http://hdl.handle.net/1911/105413


University of New South Wales

17. Yan, Wenfei. Gene expression studies in Epidermolysis Bullosa –diagnostic and therapeutic applications.

Degree: Clinical School - St George Hospital, 2010, University of New South Wales

 Epidermolysis Bullosa (EB) is a group of inherited blistering disorders in response to mechanical trauma due to gene mutations. Despite great strides in research on… (more)

Subjects/Keywords: Genotype phenotype; Epidermolysis Bullosa; Cell therapy

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APA (6th Edition):

Yan, W. (2010). Gene expression studies in Epidermolysis Bullosa –diagnostic and therapeutic applications. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/50841 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9735/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Yan, Wenfei. “Gene expression studies in Epidermolysis Bullosa –diagnostic and therapeutic applications.” 2010. Doctoral Dissertation, University of New South Wales. Accessed October 22, 2019. http://handle.unsw.edu.au/1959.4/50841 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9735/SOURCE02?view=true.

MLA Handbook (7th Edition):

Yan, Wenfei. “Gene expression studies in Epidermolysis Bullosa –diagnostic and therapeutic applications.” 2010. Web. 22 Oct 2019.

Vancouver:

Yan W. Gene expression studies in Epidermolysis Bullosa –diagnostic and therapeutic applications. [Internet] [Doctoral dissertation]. University of New South Wales; 2010. [cited 2019 Oct 22]. Available from: http://handle.unsw.edu.au/1959.4/50841 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9735/SOURCE02?view=true.

Council of Science Editors:

Yan W. Gene expression studies in Epidermolysis Bullosa –diagnostic and therapeutic applications. [Doctoral Dissertation]. University of New South Wales; 2010. Available from: http://handle.unsw.edu.au/1959.4/50841 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9735/SOURCE02?view=true


University of Toronto

18. Glick, Michael. Characterization of Adult Progenitor Cells and their Fate in a Rat Femur Fracture Model.

Degree: 2015, University of Toronto

This study was carried out to characterize two progenitor cell populations in the context of orthopaedics and to examining their fate in a rat bone… (more)

Subjects/Keywords: Fracture Healing; Stem Cell Therapy; 0564

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

APA (6th Edition):

Glick, M. (2015). Characterization of Adult Progenitor Cells and their Fate in a Rat Femur Fracture Model. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/79821

Chicago Manual of Style (16th Edition):

Glick, Michael. “Characterization of Adult Progenitor Cells and their Fate in a Rat Femur Fracture Model.” 2015. Masters Thesis, University of Toronto. Accessed October 22, 2019. http://hdl.handle.net/1807/79821.

MLA Handbook (7th Edition):

Glick, Michael. “Characterization of Adult Progenitor Cells and their Fate in a Rat Femur Fracture Model.” 2015. Web. 22 Oct 2019.

Vancouver:

Glick M. Characterization of Adult Progenitor Cells and their Fate in a Rat Femur Fracture Model. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1807/79821.

Council of Science Editors:

Glick M. Characterization of Adult Progenitor Cells and their Fate in a Rat Femur Fracture Model. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/79821


University of Toronto

19. Nauth, Aaron. Endothelial Progenitor Cells (EPCs) for Fracture Healing and Angiogenesis: A Comparison with Mesenchymal Stem Cells (MSCs).

Degree: 2012, University of Toronto

The purpose of this study was to compare the effects of two types of stem/progenitor cells on the healing of critical sized bone defects in… (more)

Subjects/Keywords: Fracture Healing; Stem Cell Therapy; 0564

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APA (6th Edition):

Nauth, A. (2012). Endothelial Progenitor Cells (EPCs) for Fracture Healing and Angiogenesis: A Comparison with Mesenchymal Stem Cells (MSCs). (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/32271

Chicago Manual of Style (16th Edition):

Nauth, Aaron. “Endothelial Progenitor Cells (EPCs) for Fracture Healing and Angiogenesis: A Comparison with Mesenchymal Stem Cells (MSCs).” 2012. Masters Thesis, University of Toronto. Accessed October 22, 2019. http://hdl.handle.net/1807/32271.

MLA Handbook (7th Edition):

Nauth, Aaron. “Endothelial Progenitor Cells (EPCs) for Fracture Healing and Angiogenesis: A Comparison with Mesenchymal Stem Cells (MSCs).” 2012. Web. 22 Oct 2019.

Vancouver:

Nauth A. Endothelial Progenitor Cells (EPCs) for Fracture Healing and Angiogenesis: A Comparison with Mesenchymal Stem Cells (MSCs). [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1807/32271.

Council of Science Editors:

Nauth A. Endothelial Progenitor Cells (EPCs) for Fracture Healing and Angiogenesis: A Comparison with Mesenchymal Stem Cells (MSCs). [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/32271


Queen Mary, University of London

20. Choudhury, Tawfiq R. The therapeutic use of adult autologous bone marrow derived cells in ischaemic cardiomyopathy.

Degree: Thesis (M.D.), 2016, Queen Mary, University of London

 The effect of combined cytokine and cell therapy in ischaemic cardiomyopathy is unclear. Meta-analyses suggest improved cardiac function with cell therapy. The optimal cell delivery… (more)

Subjects/Keywords: ischaemic cardiomyopathy; cytokine and cell therapy

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APA (6th Edition):

Choudhury, T. R. (2016). The therapeutic use of adult autologous bone marrow derived cells in ischaemic cardiomyopathy. (Doctoral Dissertation). Queen Mary, University of London. Retrieved from http://qmro.qmul.ac.uk/xmlui/handle/123456789/12679 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.775194

Chicago Manual of Style (16th Edition):

Choudhury, Tawfiq R. “The therapeutic use of adult autologous bone marrow derived cells in ischaemic cardiomyopathy.” 2016. Doctoral Dissertation, Queen Mary, University of London. Accessed October 22, 2019. http://qmro.qmul.ac.uk/xmlui/handle/123456789/12679 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.775194.

MLA Handbook (7th Edition):

Choudhury, Tawfiq R. “The therapeutic use of adult autologous bone marrow derived cells in ischaemic cardiomyopathy.” 2016. Web. 22 Oct 2019.

Vancouver:

Choudhury TR. The therapeutic use of adult autologous bone marrow derived cells in ischaemic cardiomyopathy. [Internet] [Doctoral dissertation]. Queen Mary, University of London; 2016. [cited 2019 Oct 22]. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/12679 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.775194.

Council of Science Editors:

Choudhury TR. The therapeutic use of adult autologous bone marrow derived cells in ischaemic cardiomyopathy. [Doctoral Dissertation]. Queen Mary, University of London; 2016. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/12679 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.775194


Loughborough University

21. Worrallo, Matthew J. Immobilised growth factors for scalable cell therapy manufacturing platforms.

Degree: PhD, 2018, Loughborough University

 Regenerative medicine has the potential to establish or restore normal function in defective tissues and organs. The realisation of such therapies is restricted due to… (more)

Subjects/Keywords: Growth factors; Cell therapy; Scalable; Immobilised

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APA (6th Edition):

Worrallo, M. J. (2018). Immobilised growth factors for scalable cell therapy manufacturing platforms. (Doctoral Dissertation). Loughborough University. Retrieved from http://hdl.handle.net/2134/27912

Chicago Manual of Style (16th Edition):

Worrallo, Matthew J. “Immobilised growth factors for scalable cell therapy manufacturing platforms.” 2018. Doctoral Dissertation, Loughborough University. Accessed October 22, 2019. http://hdl.handle.net/2134/27912.

MLA Handbook (7th Edition):

Worrallo, Matthew J. “Immobilised growth factors for scalable cell therapy manufacturing platforms.” 2018. Web. 22 Oct 2019.

Vancouver:

Worrallo MJ. Immobilised growth factors for scalable cell therapy manufacturing platforms. [Internet] [Doctoral dissertation]. Loughborough University; 2018. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/2134/27912.

Council of Science Editors:

Worrallo MJ. Immobilised growth factors for scalable cell therapy manufacturing platforms. [Doctoral Dissertation]. Loughborough University; 2018. Available from: http://hdl.handle.net/2134/27912


Rice University

22. Mitra, Kinshuk. Barcoding tools to track development and function of stem cell constructs for biomedicine.

Degree: PhD, Engineering, 2019, Rice University

 Biological regeneration has long been explored as a breakthrough modality for human therapy. Degenerative diseases, a majority of which are a related to ageing, manifest… (more)

Subjects/Keywords: Regenerative medicine; bioengineering; cell therapy; synthetic biology

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APA (6th Edition):

Mitra, K. (2019). Barcoding tools to track development and function of stem cell constructs for biomedicine. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/105411

Chicago Manual of Style (16th Edition):

Mitra, Kinshuk. “Barcoding tools to track development and function of stem cell constructs for biomedicine.” 2019. Doctoral Dissertation, Rice University. Accessed October 22, 2019. http://hdl.handle.net/1911/105411.

MLA Handbook (7th Edition):

Mitra, Kinshuk. “Barcoding tools to track development and function of stem cell constructs for biomedicine.” 2019. Web. 22 Oct 2019.

Vancouver:

Mitra K. Barcoding tools to track development and function of stem cell constructs for biomedicine. [Internet] [Doctoral dissertation]. Rice University; 2019. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1911/105411.

Council of Science Editors:

Mitra K. Barcoding tools to track development and function of stem cell constructs for biomedicine. [Doctoral Dissertation]. Rice University; 2019. Available from: http://hdl.handle.net/1911/105411


Boston College

23. Arthur, Julian. Novel Therapies and Biochemical Insights for the GM1 and GM2 Gangliosidoses.

Degree: PhD, Biology, 2011, Boston College

 Gangliosides are glycosphingolipids (GSLs) containing sialic acids that play numerous roles in neuronal maturation, apoptotic signaling, angiogenesis, and cell surface receptor activity. The GM1 and… (more)

Subjects/Keywords: Ganglioside; Gene Therapy; Lysosome; Neurodegeneration; Stem Cell; Substrate Reduction Therapy

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APA (6th Edition):

Arthur, J. (2011). Novel Therapies and Biochemical Insights for the GM1 and GM2 Gangliosidoses. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101655

Chicago Manual of Style (16th Edition):

Arthur, Julian. “Novel Therapies and Biochemical Insights for the GM1 and GM2 Gangliosidoses.” 2011. Doctoral Dissertation, Boston College. Accessed October 22, 2019. http://dlib.bc.edu/islandora/object/bc-ir:101655.

MLA Handbook (7th Edition):

Arthur, Julian. “Novel Therapies and Biochemical Insights for the GM1 and GM2 Gangliosidoses.” 2011. Web. 22 Oct 2019.

Vancouver:

Arthur J. Novel Therapies and Biochemical Insights for the GM1 and GM2 Gangliosidoses. [Internet] [Doctoral dissertation]. Boston College; 2011. [cited 2019 Oct 22]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101655.

Council of Science Editors:

Arthur J. Novel Therapies and Biochemical Insights for the GM1 and GM2 Gangliosidoses. [Doctoral Dissertation]. Boston College; 2011. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101655


University of Manitoba

24. Malhi, Sarandeep. Development of polymeric micelles of combination anticancer compounds for targeting cancer stem cells and bulk tumor cells in breast cancer.

Degree: Pharmacy, 2019, University of Manitoba

 The conventional chemotherapies have minimal or spared effect on cancer stem cells, which are now considered to be a reason for chemotherapy resistance, relapse and… (more)

Subjects/Keywords: Polymeric micelles; Anti- cancer stem cell therapy; Combination therapy; Pharmacokinetics

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APA (6th Edition):

Malhi, S. (2019). Development of polymeric micelles of combination anticancer compounds for targeting cancer stem cells and bulk tumor cells in breast cancer. (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/33795

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):

Malhi, Sarandeep. “Development of polymeric micelles of combination anticancer compounds for targeting cancer stem cells and bulk tumor cells in breast cancer.” 2019. Thesis, University of Manitoba. Accessed October 22, 2019. http://hdl.handle.net/1993/33795.

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

MLA Handbook (7th Edition):

Malhi, Sarandeep. “Development of polymeric micelles of combination anticancer compounds for targeting cancer stem cells and bulk tumor cells in breast cancer.” 2019. Web. 22 Oct 2019.

Vancouver:

Malhi S. Development of polymeric micelles of combination anticancer compounds for targeting cancer stem cells and bulk tumor cells in breast cancer. [Internet] [Thesis]. University of Manitoba; 2019. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1993/33795.

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

Council of Science Editors:

Malhi S. Development of polymeric micelles of combination anticancer compounds for targeting cancer stem cells and bulk tumor cells in breast cancer. [Thesis]. University of Manitoba; 2019. Available from: http://hdl.handle.net/1993/33795

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


Universiteit Utrecht

25. Penders, A.F. Potential new sources for beta-cell replacement therapy in diabetes type 1 patients.

Degree: 2010, Universiteit Utrecht

 Long term complications in diabetes patients are a consequence of the constantly high blood glucose levels, hyperglycemia. In patients with type 1 diabetes hyperglycemia is… (more)

Subjects/Keywords: Geneeskunde; diabetes; hyperglycemia; insulin; beta-cell replacement therapy; stem cell transplantation

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APA (6th Edition):

Penders, A. F. (2010). Potential new sources for beta-cell replacement therapy in diabetes type 1 patients. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/40071

Chicago Manual of Style (16th Edition):

Penders, A F. “Potential new sources for beta-cell replacement therapy in diabetes type 1 patients.” 2010. Masters Thesis, Universiteit Utrecht. Accessed October 22, 2019. http://dspace.library.uu.nl:8080/handle/1874/40071.

MLA Handbook (7th Edition):

Penders, A F. “Potential new sources for beta-cell replacement therapy in diabetes type 1 patients.” 2010. Web. 22 Oct 2019.

Vancouver:

Penders AF. Potential new sources for beta-cell replacement therapy in diabetes type 1 patients. [Internet] [Masters thesis]. Universiteit Utrecht; 2010. [cited 2019 Oct 22]. Available from: http://dspace.library.uu.nl:8080/handle/1874/40071.

Council of Science Editors:

Penders AF. Potential new sources for beta-cell replacement therapy in diabetes type 1 patients. [Masters Thesis]. Universiteit Utrecht; 2010. Available from: http://dspace.library.uu.nl:8080/handle/1874/40071


Penn State University

26. Stamer, Mindy Marie. PRIMARY IN VITRO T CELL RESPONSES TO CYTOMEGALOVIRUS.

Degree: MS, Microbiology and Immunology, 2009, Penn State University

 Adoptive T cell therapy is commonly used for prophylactic and therapeutic treatment of cytomegalovirus (CMV) disease following HSC transplantation of CMV-seropositive recipients of CMV-seropositive donors.… (more)

Subjects/Keywords: T cells; adoptive T cell therapy; cytomegalovirus; T cell priming

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APA (6th Edition):

Stamer, M. M. (2009). PRIMARY IN VITRO T CELL RESPONSES TO CYTOMEGALOVIRUS. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/10539

Chicago Manual of Style (16th Edition):

Stamer, Mindy Marie. “PRIMARY IN VITRO T CELL RESPONSES TO CYTOMEGALOVIRUS.” 2009. Masters Thesis, Penn State University. Accessed October 22, 2019. https://etda.libraries.psu.edu/catalog/10539.

MLA Handbook (7th Edition):

Stamer, Mindy Marie. “PRIMARY IN VITRO T CELL RESPONSES TO CYTOMEGALOVIRUS.” 2009. Web. 22 Oct 2019.

Vancouver:

Stamer MM. PRIMARY IN VITRO T CELL RESPONSES TO CYTOMEGALOVIRUS. [Internet] [Masters thesis]. Penn State University; 2009. [cited 2019 Oct 22]. Available from: https://etda.libraries.psu.edu/catalog/10539.

Council of Science Editors:

Stamer MM. PRIMARY IN VITRO T CELL RESPONSES TO CYTOMEGALOVIRUS. [Masters Thesis]. Penn State University; 2009. Available from: https://etda.libraries.psu.edu/catalog/10539

27. 大坪, 嗣輝. Identification of Novel Targets for Antiangiogenic Therapy : 血管新生阻害療法のための新規標的分子の同定.

Degree: 博士(歯学), 2014, Hokkaido University / 北海道大学

Targeting tumor angiogenesis is an established strategy for cancer therapy. Molecular markers that can distinguish between physiological and pathological angiogenesis are required to develop more… (more)

Subjects/Keywords: tumor endothelial cell; tumor endothelial cell marker; tumor angiogenesis; antiangiogenic therapy

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APA (6th Edition):

大坪, . (2014). Identification of Novel Targets for Antiangiogenic Therapy : 血管新生阻害療法のための新規標的分子の同定. (Thesis). Hokkaido University / 北海道大学. Retrieved from http://hdl.handle.net/2115/56321 ; http://dx.doi.org/10.14943/doctoral.r6905

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):

大坪, 嗣輝. “Identification of Novel Targets for Antiangiogenic Therapy : 血管新生阻害療法のための新規標的分子の同定.” 2014. Thesis, Hokkaido University / 北海道大学. Accessed October 22, 2019. http://hdl.handle.net/2115/56321 ; http://dx.doi.org/10.14943/doctoral.r6905.

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

MLA Handbook (7th Edition):

大坪, 嗣輝. “Identification of Novel Targets for Antiangiogenic Therapy : 血管新生阻害療法のための新規標的分子の同定.” 2014. Web. 22 Oct 2019.

Vancouver:

大坪 . Identification of Novel Targets for Antiangiogenic Therapy : 血管新生阻害療法のための新規標的分子の同定. [Internet] [Thesis]. Hokkaido University / 北海道大学; 2014. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/2115/56321 ; http://dx.doi.org/10.14943/doctoral.r6905.

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

Council of Science Editors:

大坪 . Identification of Novel Targets for Antiangiogenic Therapy : 血管新生阻害療法のための新規標的分子の同定. [Thesis]. Hokkaido University / 北海道大学; 2014. Available from: http://hdl.handle.net/2115/56321 ; http://dx.doi.org/10.14943/doctoral.r6905

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


University of Illinois – Chicago

28. Xing, Yuan. Microfluidic Platform for In Vitro Study on the Development of Cell Therapy.

Degree: 2017, University of Illinois – Chicago

Cell therapy has emerged as a treatment of many endocrine disorders. Microfluidics has been developed for a myriad of biological applications and the intrinsic capability… (more)

Subjects/Keywords: Microfluidic; Cell-baed Therapy; Pancreatic Islet; Hypoparathyroidism; Microencapsulation; Cell Perfusion

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APA (6th Edition):

Xing, Y. (2017). Microfluidic Platform for In Vitro Study on the Development of Cell Therapy. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/22123

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):

Xing, Yuan. “Microfluidic Platform for In Vitro Study on the Development of Cell Therapy.” 2017. Thesis, University of Illinois – Chicago. Accessed October 22, 2019. http://hdl.handle.net/10027/22123.

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

MLA Handbook (7th Edition):

Xing, Yuan. “Microfluidic Platform for In Vitro Study on the Development of Cell Therapy.” 2017. Web. 22 Oct 2019.

Vancouver:

Xing Y. Microfluidic Platform for In Vitro Study on the Development of Cell Therapy. [Internet] [Thesis]. University of Illinois – Chicago; 2017. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/10027/22123.

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

Council of Science Editors:

Xing Y. Microfluidic Platform for In Vitro Study on the Development of Cell Therapy. [Thesis]. University of Illinois – Chicago; 2017. Available from: http://hdl.handle.net/10027/22123

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


University of Illinois – Chicago

29. Chatchavalvanich, Santipongse. Effects of A Gap Junction Inhibitor on Stem Cell Retention and Efficacy During Early Myocardial Ischemia.

Degree: 2013, University of Illinois – Chicago

 Bone marrow-derived mesenchymal stem cell (BM-MSC) replacement therapy is beneficial to the heart following ischemia but a significant loss of these cells within hours of… (more)

Subjects/Keywords: Stem Cell; Cell Therapy; Myocardial Infarction; Ischemia Reperfusion; Gap Junction; Hemodynamics

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APA (6th Edition):

Chatchavalvanich, S. (2013). Effects of A Gap Junction Inhibitor on Stem Cell Retention and Efficacy During Early Myocardial Ischemia. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/9772

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):

Chatchavalvanich, Santipongse. “Effects of A Gap Junction Inhibitor on Stem Cell Retention and Efficacy During Early Myocardial Ischemia.” 2013. Thesis, University of Illinois – Chicago. Accessed October 22, 2019. http://hdl.handle.net/10027/9772.

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

MLA Handbook (7th Edition):

Chatchavalvanich, Santipongse. “Effects of A Gap Junction Inhibitor on Stem Cell Retention and Efficacy During Early Myocardial Ischemia.” 2013. Web. 22 Oct 2019.

Vancouver:

Chatchavalvanich S. Effects of A Gap Junction Inhibitor on Stem Cell Retention and Efficacy During Early Myocardial Ischemia. [Internet] [Thesis]. University of Illinois – Chicago; 2013. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/10027/9772.

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

Council of Science Editors:

Chatchavalvanich S. Effects of A Gap Junction Inhibitor on Stem Cell Retention and Efficacy During Early Myocardial Ischemia. [Thesis]. University of Illinois – Chicago; 2013. Available from: http://hdl.handle.net/10027/9772

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


Queen Mary, University of London

30. Dodhy, Asad. Population based evaluation of actin cytoskeletal morphometric descriptors as characterisation of stem cell differentiation.

Degree: PhD, 2018, Queen Mary, University of London

 Stem cells have yet to contribute to their full potential in the field of regenerative medicine and further understanding of the underlying kinetics of cell(more)

Subjects/Keywords: Engineering and Materials Science; cell lineage; Stem cell therapy

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

APA (6th Edition):

Dodhy, A. (2018). Population based evaluation of actin cytoskeletal morphometric descriptors as characterisation of stem cell differentiation. (Doctoral Dissertation). Queen Mary, University of London. Retrieved from http://qmro.qmul.ac.uk/xmlui/handle/123456789/46030 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.766234

Chicago Manual of Style (16th Edition):

Dodhy, Asad. “Population based evaluation of actin cytoskeletal morphometric descriptors as characterisation of stem cell differentiation.” 2018. Doctoral Dissertation, Queen Mary, University of London. Accessed October 22, 2019. http://qmro.qmul.ac.uk/xmlui/handle/123456789/46030 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.766234.

MLA Handbook (7th Edition):

Dodhy, Asad. “Population based evaluation of actin cytoskeletal morphometric descriptors as characterisation of stem cell differentiation.” 2018. Web. 22 Oct 2019.

Vancouver:

Dodhy A. Population based evaluation of actin cytoskeletal morphometric descriptors as characterisation of stem cell differentiation. [Internet] [Doctoral dissertation]. Queen Mary, University of London; 2018. [cited 2019 Oct 22]. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/46030 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.766234.

Council of Science Editors:

Dodhy A. Population based evaluation of actin cytoskeletal morphometric descriptors as characterisation of stem cell differentiation. [Doctoral Dissertation]. Queen Mary, University of London; 2018. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/46030 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.766234

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