Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(Angiogenesis). Showing records 121 – 150 of 1405 total matches.

[1] [2] [3] [4] [5] [6] [7] … [47]

Search Limiters

Last 2 Years | English Only

Degrees

Levels

Languages

Country

▼ Search Limiters


University of Melbourne

121. Lee, Hye Suk Sophie. The role of Dlk1 in haematopoiesis, leukaemia and angiogenesis.

Degree: 2017, University of Melbourne

 Delta-Like Homologue 1 (DLK1), also known as Preadipocyte Factor 1 (PREF-1), is a non-canonical EGF-like NOTCH ligand. It is maternally imprinted at the Dlk1-Dio3 imprinted… (more)

Subjects/Keywords: Dlk1; haematopoietic stem cells; leukaemia; angiogenesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lee, H. S. S. (2017). The role of Dlk1 in haematopoiesis, leukaemia and angiogenesis. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/165200

Chicago Manual of Style (16th Edition):

Lee, Hye Suk Sophie. “The role of Dlk1 in haematopoiesis, leukaemia and angiogenesis.” 2017. Doctoral Dissertation, University of Melbourne. Accessed July 19, 2019. http://hdl.handle.net/11343/165200.

MLA Handbook (7th Edition):

Lee, Hye Suk Sophie. “The role of Dlk1 in haematopoiesis, leukaemia and angiogenesis.” 2017. Web. 19 Jul 2019.

Vancouver:

Lee HSS. The role of Dlk1 in haematopoiesis, leukaemia and angiogenesis. [Internet] [Doctoral dissertation]. University of Melbourne; 2017. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/11343/165200.

Council of Science Editors:

Lee HSS. The role of Dlk1 in haematopoiesis, leukaemia and angiogenesis. [Doctoral Dissertation]. University of Melbourne; 2017. Available from: http://hdl.handle.net/11343/165200


University of Ottawa

122. Behbahani, John. The Role of MicroRNAs in Endothelial Progenitor Cell Function .

Degree: 2016, University of Ottawa

 Cultures of peripheral blood mononuclear cells (MNCs) give rise to at least two different variants of endothelial progenitor cells (EPCs), early and late outgrowth EPCs.… (more)

Subjects/Keywords: Endothelial Progenitor Cells; MicroRNA; Angiogenesis; Stem Cell

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Behbahani, J. (2016). The Role of MicroRNAs in Endothelial Progenitor Cell Function . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/35080

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):

Behbahani, John. “The Role of MicroRNAs in Endothelial Progenitor Cell Function .” 2016. Thesis, University of Ottawa. Accessed July 19, 2019. http://hdl.handle.net/10393/35080.

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

MLA Handbook (7th Edition):

Behbahani, John. “The Role of MicroRNAs in Endothelial Progenitor Cell Function .” 2016. Web. 19 Jul 2019.

Vancouver:

Behbahani J. The Role of MicroRNAs in Endothelial Progenitor Cell Function . [Internet] [Thesis]. University of Ottawa; 2016. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/10393/35080.

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

Council of Science Editors:

Behbahani J. The Role of MicroRNAs in Endothelial Progenitor Cell Function . [Thesis]. University of Ottawa; 2016. Available from: http://hdl.handle.net/10393/35080

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


University of Edinburgh

123. Ogley, Robert James. Role of WT1 in Ischaemic Angiogenesis.

Degree: PhD, 2018, University of Edinburgh

 Ischaemia causes irreversible tissue damage in cardiovascular disease. Since regenerative angiogenesis fails to consistently induce sufficient reperfusion to facilitate repair, targeted manipulation of angiogenesis is… (more)

Subjects/Keywords: angiogenesis; Wilms' tumour suppressor; WT1; transcription factors

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ogley, R. J. (2018). Role of WT1 in Ischaemic Angiogenesis. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/31555

Chicago Manual of Style (16th Edition):

Ogley, Robert James. “Role of WT1 in Ischaemic Angiogenesis.” 2018. Doctoral Dissertation, University of Edinburgh. Accessed July 19, 2019. http://hdl.handle.net/1842/31555.

MLA Handbook (7th Edition):

Ogley, Robert James. “Role of WT1 in Ischaemic Angiogenesis.” 2018. Web. 19 Jul 2019.

Vancouver:

Ogley RJ. Role of WT1 in Ischaemic Angiogenesis. [Internet] [Doctoral dissertation]. University of Edinburgh; 2018. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1842/31555.

Council of Science Editors:

Ogley RJ. Role of WT1 in Ischaemic Angiogenesis. [Doctoral Dissertation]. University of Edinburgh; 2018. Available from: http://hdl.handle.net/1842/31555


Vanderbilt University

124. Boelte, Kimberly Covington. The role of Rgs2 in hematopoiesis and myeloid derived suppressor cells in cancer.

Degree: PhD, Cancer Biology, 2011, Vanderbilt University

 Myeloid derived suppressor cells (MDSCs) play an important role in cancer progression, and elucidating the mechanisms involved in the accumulation and function of these cells… (more)

Subjects/Keywords: tumor microenvironment; MCP-1; Rgs2; angiogenesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Boelte, K. C. (2011). The role of Rgs2 in hematopoiesis and myeloid derived suppressor cells in cancer. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-03292011-102758/ ;

Chicago Manual of Style (16th Edition):

Boelte, Kimberly Covington. “The role of Rgs2 in hematopoiesis and myeloid derived suppressor cells in cancer.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed July 19, 2019. http://etd.library.vanderbilt.edu/available/etd-03292011-102758/ ;.

MLA Handbook (7th Edition):

Boelte, Kimberly Covington. “The role of Rgs2 in hematopoiesis and myeloid derived suppressor cells in cancer.” 2011. Web. 19 Jul 2019.

Vancouver:

Boelte KC. The role of Rgs2 in hematopoiesis and myeloid derived suppressor cells in cancer. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2019 Jul 19]. Available from: http://etd.library.vanderbilt.edu/available/etd-03292011-102758/ ;.

Council of Science Editors:

Boelte KC. The role of Rgs2 in hematopoiesis and myeloid derived suppressor cells in cancer. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://etd.library.vanderbilt.edu/available/etd-03292011-102758/ ;


Vanderbilt University

125. Savage, Sara Renee. The role of PPARβ/δ in diabetic retinopathy.

Degree: PhD, Pharmacology, 2015, Vanderbilt University

 Diabetic retinopathy (DR) is disease of microvascular complications and is a leading cause of blindness in working age adults. DR consists of two main stages:… (more)

Subjects/Keywords: diabetic retinopathy; inflammation; transcription factor; angiogenesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Savage, S. R. (2015). The role of PPARβ/δ in diabetic retinopathy. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-08282015-120707/ ;

Chicago Manual of Style (16th Edition):

Savage, Sara Renee. “The role of PPARβ/δ in diabetic retinopathy.” 2015. Doctoral Dissertation, Vanderbilt University. Accessed July 19, 2019. http://etd.library.vanderbilt.edu/available/etd-08282015-120707/ ;.

MLA Handbook (7th Edition):

Savage, Sara Renee. “The role of PPARβ/δ in diabetic retinopathy.” 2015. Web. 19 Jul 2019.

Vancouver:

Savage SR. The role of PPARβ/δ in diabetic retinopathy. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2019 Jul 19]. Available from: http://etd.library.vanderbilt.edu/available/etd-08282015-120707/ ;.

Council of Science Editors:

Savage SR. The role of PPARβ/δ in diabetic retinopathy. [Doctoral Dissertation]. Vanderbilt University; 2015. Available from: http://etd.library.vanderbilt.edu/available/etd-08282015-120707/ ;


University of Arizona

126. Block, Katherine M. Design of Novel Cancer Therapeutics Through The Validation of PARG as a Therapeutic Target and the Evaluation of Small Molecule Inhibitors of Hypoxia-Induced Transcription .

Degree: 2010, University of Arizona

 Because of the severe toxicity and limiting side effects of traditional chemotherapy, there exists a critical need to develop better-tolerated, safer drugs to treat cancer.… (more)

Subjects/Keywords: Angiogenesis; Cancer; ETP; HIF; PARG; PARP

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Block, K. M. (2010). Design of Novel Cancer Therapeutics Through The Validation of PARG as a Therapeutic Target and the Evaluation of Small Molecule Inhibitors of Hypoxia-Induced Transcription . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/194826

Chicago Manual of Style (16th Edition):

Block, Katherine M. “Design of Novel Cancer Therapeutics Through The Validation of PARG as a Therapeutic Target and the Evaluation of Small Molecule Inhibitors of Hypoxia-Induced Transcription .” 2010. Doctoral Dissertation, University of Arizona. Accessed July 19, 2019. http://hdl.handle.net/10150/194826.

MLA Handbook (7th Edition):

Block, Katherine M. “Design of Novel Cancer Therapeutics Through The Validation of PARG as a Therapeutic Target and the Evaluation of Small Molecule Inhibitors of Hypoxia-Induced Transcription .” 2010. Web. 19 Jul 2019.

Vancouver:

Block KM. Design of Novel Cancer Therapeutics Through The Validation of PARG as a Therapeutic Target and the Evaluation of Small Molecule Inhibitors of Hypoxia-Induced Transcription . [Internet] [Doctoral dissertation]. University of Arizona; 2010. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/10150/194826.

Council of Science Editors:

Block KM. Design of Novel Cancer Therapeutics Through The Validation of PARG as a Therapeutic Target and the Evaluation of Small Molecule Inhibitors of Hypoxia-Induced Transcription . [Doctoral Dissertation]. University of Arizona; 2010. Available from: http://hdl.handle.net/10150/194826


Rice University

127. Clements, Thomas P. A Rice CRISPy Treat: Improving CRISPR-Cas9 gene editing in the zebrafish to facilitate analysis of genes implicated in neural angiogenesis in an F0 screen.

Degree: PhD, Natural Sciences, 2018, Rice University

 Scientists are eager for novel mutants to study gene function, evolutionary relationships, and even perform drug screens. Zebrafish are a well-established model for scientific research… (more)

Subjects/Keywords: zebrafish; crispr; exocas9; f0; angiogenesis; hemorrhage

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Clements, T. P. (2018). A Rice CRISPy Treat: Improving CRISPR-Cas9 gene editing in the zebrafish to facilitate analysis of genes implicated in neural angiogenesis in an F0 screen. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/105724

Chicago Manual of Style (16th Edition):

Clements, Thomas P. “A Rice CRISPy Treat: Improving CRISPR-Cas9 gene editing in the zebrafish to facilitate analysis of genes implicated in neural angiogenesis in an F0 screen.” 2018. Doctoral Dissertation, Rice University. Accessed July 19, 2019. http://hdl.handle.net/1911/105724.

MLA Handbook (7th Edition):

Clements, Thomas P. “A Rice CRISPy Treat: Improving CRISPR-Cas9 gene editing in the zebrafish to facilitate analysis of genes implicated in neural angiogenesis in an F0 screen.” 2018. Web. 19 Jul 2019.

Vancouver:

Clements TP. A Rice CRISPy Treat: Improving CRISPR-Cas9 gene editing in the zebrafish to facilitate analysis of genes implicated in neural angiogenesis in an F0 screen. [Internet] [Doctoral dissertation]. Rice University; 2018. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1911/105724.

Council of Science Editors:

Clements TP. A Rice CRISPy Treat: Improving CRISPR-Cas9 gene editing in the zebrafish to facilitate analysis of genes implicated in neural angiogenesis in an F0 screen. [Doctoral Dissertation]. Rice University; 2018. Available from: http://hdl.handle.net/1911/105724


University of Toronto

128. Madu, Tobechukwu Chukwuemeka. Advanced Microfluidic Platform for Epithelial and Endothelial Cell Dimorphic Coculture.

Degree: 2015, University of Toronto

Biological cells cultured in a 3D microenvironment are more realistic and exhibit characteristics found in vivo when compared to 2D cell cultures. However, culturing 3D… (more)

Subjects/Keywords: Angiogenesis; Microfabrication; Microfluidics; Tumor Spheroids; 0537

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Madu, T. C. (2015). Advanced Microfluidic Platform for Epithelial and Endothelial Cell Dimorphic Coculture. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/70470

Chicago Manual of Style (16th Edition):

Madu, Tobechukwu Chukwuemeka. “Advanced Microfluidic Platform for Epithelial and Endothelial Cell Dimorphic Coculture.” 2015. Masters Thesis, University of Toronto. Accessed July 19, 2019. http://hdl.handle.net/1807/70470.

MLA Handbook (7th Edition):

Madu, Tobechukwu Chukwuemeka. “Advanced Microfluidic Platform for Epithelial and Endothelial Cell Dimorphic Coculture.” 2015. Web. 19 Jul 2019.

Vancouver:

Madu TC. Advanced Microfluidic Platform for Epithelial and Endothelial Cell Dimorphic Coculture. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1807/70470.

Council of Science Editors:

Madu TC. Advanced Microfluidic Platform for Epithelial and Endothelial Cell Dimorphic Coculture. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/70470


University of Toronto

129. Kuzmic, Nikola. Modelling of Endothelial Cell Migration and Angiogenesis in Microfluidic Cell Culture Systems.

Degree: 2018, University of Toronto

Tumour-induced angiogenesis involves growth of new blood vessels from existing vasculature in response to signals induced by the undernourished part of tumour tissue. Due to… (more)

Subjects/Keywords: angiogenesis; computational modelling; endothelium; vasculature; 0541

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kuzmic, N. (2018). Modelling of Endothelial Cell Migration and Angiogenesis in Microfluidic Cell Culture Systems. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/91580

Chicago Manual of Style (16th Edition):

Kuzmic, Nikola. “Modelling of Endothelial Cell Migration and Angiogenesis in Microfluidic Cell Culture Systems.” 2018. Masters Thesis, University of Toronto. Accessed July 19, 2019. http://hdl.handle.net/1807/91580.

MLA Handbook (7th Edition):

Kuzmic, Nikola. “Modelling of Endothelial Cell Migration and Angiogenesis in Microfluidic Cell Culture Systems.” 2018. Web. 19 Jul 2019.

Vancouver:

Kuzmic N. Modelling of Endothelial Cell Migration and Angiogenesis in Microfluidic Cell Culture Systems. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1807/91580.

Council of Science Editors:

Kuzmic N. Modelling of Endothelial Cell Migration and Angiogenesis in Microfluidic Cell Culture Systems. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/91580


Boston University

130. Mucka, Patrick. The role of neuropilin 2 in physiological and pathological angiogenesis and lymphangiogenesis.

Degree: 2014, Boston University

 The generation of new lymphatic vessels through lymphangiogenesis has been implicated in many disease states. This process has some overlap with the better studied angiogenesis(more)

Subjects/Keywords: Biology; Angiogenesis; Lymphangiogenesis; Neuropilin; Cancer; Semaphorin

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Mucka, P. (2014). The role of neuropilin 2 in physiological and pathological angiogenesis and lymphangiogenesis. (Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/14693

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):

Mucka, Patrick. “The role of neuropilin 2 in physiological and pathological angiogenesis and lymphangiogenesis.” 2014. Thesis, Boston University. Accessed July 19, 2019. http://hdl.handle.net/2144/14693.

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

MLA Handbook (7th Edition):

Mucka, Patrick. “The role of neuropilin 2 in physiological and pathological angiogenesis and lymphangiogenesis.” 2014. Web. 19 Jul 2019.

Vancouver:

Mucka P. The role of neuropilin 2 in physiological and pathological angiogenesis and lymphangiogenesis. [Internet] [Thesis]. Boston University; 2014. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/2144/14693.

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

Council of Science Editors:

Mucka P. The role of neuropilin 2 in physiological and pathological angiogenesis and lymphangiogenesis. [Thesis]. Boston University; 2014. Available from: http://hdl.handle.net/2144/14693

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


University of Illinois – Urbana-Champaign

131. Weddell, Jared Colin. Quantitative methods to regulate angiogenesis: applications to cancer and cardiovascular disease.

Degree: MS, Bioengineering, 2015, University of Illinois – Urbana-Champaign

Angiogenesis, the growth of new microvasculature from pre-existing blood vessels, is essential for tumor growth and metastasis in several cancers, including breast cancer. The vascular… (more)

Subjects/Keywords: Angiogenesis; heterogeneity; breast cancer; cardiovascular disease

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Weddell, J. C. (2015). Quantitative methods to regulate angiogenesis: applications to cancer and cardiovascular disease. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/88030

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):

Weddell, Jared Colin. “Quantitative methods to regulate angiogenesis: applications to cancer and cardiovascular disease.” 2015. Thesis, University of Illinois – Urbana-Champaign. Accessed July 19, 2019. http://hdl.handle.net/2142/88030.

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

MLA Handbook (7th Edition):

Weddell, Jared Colin. “Quantitative methods to regulate angiogenesis: applications to cancer and cardiovascular disease.” 2015. Web. 19 Jul 2019.

Vancouver:

Weddell JC. Quantitative methods to regulate angiogenesis: applications to cancer and cardiovascular disease. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/2142/88030.

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

Council of Science Editors:

Weddell JC. Quantitative methods to regulate angiogenesis: applications to cancer and cardiovascular disease. [Thesis]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/88030

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


University of Illinois – Urbana-Champaign

132. Davila, Juanmahel. The role of Ras-related C3 botulinum toxin substrate 1 (RAC1)-dependent pathway in the regulation of uterine function during early pregnancy.

Degree: PhD, 5274, 2013, University of Illinois – Urbana-Champaign

 During implantation, uterine stromal cells differentiate into specialized decidual cells, which become secretory and support the growth of the embryo before placentation. At the same… (more)

Subjects/Keywords: Rac1; Pregnancy; Uterus; Decidua; Angiogenesis; Implantation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Davila, J. (2013). The role of Ras-related C3 botulinum toxin substrate 1 (RAC1)-dependent pathway in the regulation of uterine function during early pregnancy. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/45652

Chicago Manual of Style (16th Edition):

Davila, Juanmahel. “The role of Ras-related C3 botulinum toxin substrate 1 (RAC1)-dependent pathway in the regulation of uterine function during early pregnancy.” 2013. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 19, 2019. http://hdl.handle.net/2142/45652.

MLA Handbook (7th Edition):

Davila, Juanmahel. “The role of Ras-related C3 botulinum toxin substrate 1 (RAC1)-dependent pathway in the regulation of uterine function during early pregnancy.” 2013. Web. 19 Jul 2019.

Vancouver:

Davila J. The role of Ras-related C3 botulinum toxin substrate 1 (RAC1)-dependent pathway in the regulation of uterine function during early pregnancy. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/2142/45652.

Council of Science Editors:

Davila J. The role of Ras-related C3 botulinum toxin substrate 1 (RAC1)-dependent pathway in the regulation of uterine function during early pregnancy. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/45652

133. Cho, Eunhan. Angiogenesis and fibrosis in a volumetric skeletal muscle loss injury using mesenchymal stem cells in a PEGylated fibrin gel on an extracellular matrix.

Degree: Kinesiology and Health Education, 2015, University of Texas – Austin

 Volumetric Muscle Loss (VML) injury can result from trauma and in military personnel with wound in combat. VML lead to the loss of substantial mass… (more)

Subjects/Keywords: Angiogenesis; Fibrosis

…signaling, MSCs indirectly participating in increase cellular material, increase angiogenesis, and… …model, improved ventricular function, accelerated angiogenesis, reduced scarring was detected… …as a result of increased level of HGF and VEGF, showing that MSCs elicit a angiogenesis and… …together, MSCs have enormous beneficial potential on angiogenesis and nerve growth via growth… …vascularization and angiogenesis is poorly understood. The Role of PEGylated Fibrin Gel as Delivery… 

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Cho, E. (2015). Angiogenesis and fibrosis in a volumetric skeletal muscle loss injury using mesenchymal stem cells in a PEGylated fibrin gel on an extracellular matrix. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/33826

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):

Cho, Eunhan. “Angiogenesis and fibrosis in a volumetric skeletal muscle loss injury using mesenchymal stem cells in a PEGylated fibrin gel on an extracellular matrix.” 2015. Thesis, University of Texas – Austin. Accessed July 19, 2019. http://hdl.handle.net/2152/33826.

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

MLA Handbook (7th Edition):

Cho, Eunhan. “Angiogenesis and fibrosis in a volumetric skeletal muscle loss injury using mesenchymal stem cells in a PEGylated fibrin gel on an extracellular matrix.” 2015. Web. 19 Jul 2019.

Vancouver:

Cho E. Angiogenesis and fibrosis in a volumetric skeletal muscle loss injury using mesenchymal stem cells in a PEGylated fibrin gel on an extracellular matrix. [Internet] [Thesis]. University of Texas – Austin; 2015. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/2152/33826.

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

Council of Science Editors:

Cho E. Angiogenesis and fibrosis in a volumetric skeletal muscle loss injury using mesenchymal stem cells in a PEGylated fibrin gel on an extracellular matrix. [Thesis]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/33826

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


Australian National University

134. Jennings, Scott. Surgical trial of novel pro-angiogenic compounds that may accelerate wound healing .

Degree: 2015, Australian National University

 Chronic wounds and wounds that are difficult to heal are a major concern for Australian healthcare expenditure and a source of misery for those who… (more)

Subjects/Keywords: Wound Healing; Angiogenesis; Flavonoid; Lignan; T1; Naringenin

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Jennings, S. (2015). Surgical trial of novel pro-angiogenic compounds that may accelerate wound healing . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/105507

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):

Jennings, Scott. “Surgical trial of novel pro-angiogenic compounds that may accelerate wound healing .” 2015. Thesis, Australian National University. Accessed July 19, 2019. http://hdl.handle.net/1885/105507.

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

MLA Handbook (7th Edition):

Jennings, Scott. “Surgical trial of novel pro-angiogenic compounds that may accelerate wound healing .” 2015. Web. 19 Jul 2019.

Vancouver:

Jennings S. Surgical trial of novel pro-angiogenic compounds that may accelerate wound healing . [Internet] [Thesis]. Australian National University; 2015. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1885/105507.

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

Council of Science Editors:

Jennings S. Surgical trial of novel pro-angiogenic compounds that may accelerate wound healing . [Thesis]. Australian National University; 2015. Available from: http://hdl.handle.net/1885/105507

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


University of Vermont

135. Wo, Peibin. Assessment Of A Function For Threonyl-Trna Synthetase In Angiogenesis In A Mouse Ovarian Cancer Model.

Degree: MS, Cellular, Molecular and Biomedical Sciences, 2017, University of Vermont

  Despite the high mortality rate of ovarian cancer, there are few selective biomarkers that detect its progression and none have become successful targets for… (more)

Subjects/Keywords: angiogenesis; ovarian cancer; THREONYL-tRNA SYNTHETASE; Pharmacology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wo, P. (2017). Assessment Of A Function For Threonyl-Trna Synthetase In Angiogenesis In A Mouse Ovarian Cancer Model. (Thesis). University of Vermont. Retrieved from https://scholarworks.uvm.edu/graddis/839

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):

Wo, Peibin. “Assessment Of A Function For Threonyl-Trna Synthetase In Angiogenesis In A Mouse Ovarian Cancer Model.” 2017. Thesis, University of Vermont. Accessed July 19, 2019. https://scholarworks.uvm.edu/graddis/839.

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

MLA Handbook (7th Edition):

Wo, Peibin. “Assessment Of A Function For Threonyl-Trna Synthetase In Angiogenesis In A Mouse Ovarian Cancer Model.” 2017. Web. 19 Jul 2019.

Vancouver:

Wo P. Assessment Of A Function For Threonyl-Trna Synthetase In Angiogenesis In A Mouse Ovarian Cancer Model. [Internet] [Thesis]. University of Vermont; 2017. [cited 2019 Jul 19]. Available from: https://scholarworks.uvm.edu/graddis/839.

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

Council of Science Editors:

Wo P. Assessment Of A Function For Threonyl-Trna Synthetase In Angiogenesis In A Mouse Ovarian Cancer Model. [Thesis]. University of Vermont; 2017. Available from: https://scholarworks.uvm.edu/graddis/839

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


Texas Tech University

136. -0519-8840. Studying the anticancer properties of Parthenolide (PTL) in MCF-7 breast cancer cells.

Degree: MS, Nutritional Sciences, 2018, Texas Tech University

 Background: Breast cancer is considered as the most prevalent cancer in women world-wide. The average risk for a woman developing breast cancer in her life… (more)

Subjects/Keywords: Breast cancer; Parthenolide; Apoptosis; EMT; Angiogenesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

-0519-8840. (2018). Studying the anticancer properties of Parthenolide (PTL) in MCF-7 breast cancer cells. (Masters Thesis). Texas Tech University. Retrieved from http://hdl.handle.net/2346/74400

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

Chicago Manual of Style (16th Edition):

-0519-8840. “Studying the anticancer properties of Parthenolide (PTL) in MCF-7 breast cancer cells.” 2018. Masters Thesis, Texas Tech University. Accessed July 19, 2019. http://hdl.handle.net/2346/74400.

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

MLA Handbook (7th Edition):

-0519-8840. “Studying the anticancer properties of Parthenolide (PTL) in MCF-7 breast cancer cells.” 2018. Web. 19 Jul 2019.

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

Vancouver:

-0519-8840. Studying the anticancer properties of Parthenolide (PTL) in MCF-7 breast cancer cells. [Internet] [Masters thesis]. Texas Tech University; 2018. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/2346/74400.

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

Council of Science Editors:

-0519-8840. Studying the anticancer properties of Parthenolide (PTL) in MCF-7 breast cancer cells. [Masters Thesis]. Texas Tech University; 2018. Available from: http://hdl.handle.net/2346/74400

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


University of Rochester

137. Wang, Jing. G-protein Coupled Receptor Kinase-Interacting Protein 1 (GIT1) Regulates Endothelial Cell Function: Role in Podosome Formation, Extracellular Matrix Degradation and Migration.

Degree: PhD, 2009, University of Rochester

 We have previously shown that the G-protein coupled receptor (GPCR) kinase-interacting protein 1 (GIT1) is a scaffold that organizes signaling modules spatially and temporally. GIT1… (more)

Subjects/Keywords: GIT1; Endothelial Cell; Angiogenesis; VEGT; Cell Migration

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wang, J. (2009). G-protein Coupled Receptor Kinase-Interacting Protein 1 (GIT1) Regulates Endothelial Cell Function: Role in Podosome Formation, Extracellular Matrix Degradation and Migration. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/8298

Chicago Manual of Style (16th Edition):

Wang, Jing. “G-protein Coupled Receptor Kinase-Interacting Protein 1 (GIT1) Regulates Endothelial Cell Function: Role in Podosome Formation, Extracellular Matrix Degradation and Migration.” 2009. Doctoral Dissertation, University of Rochester. Accessed July 19, 2019. http://hdl.handle.net/1802/8298.

MLA Handbook (7th Edition):

Wang, Jing. “G-protein Coupled Receptor Kinase-Interacting Protein 1 (GIT1) Regulates Endothelial Cell Function: Role in Podosome Formation, Extracellular Matrix Degradation and Migration.” 2009. Web. 19 Jul 2019.

Vancouver:

Wang J. G-protein Coupled Receptor Kinase-Interacting Protein 1 (GIT1) Regulates Endothelial Cell Function: Role in Podosome Formation, Extracellular Matrix Degradation and Migration. [Internet] [Doctoral dissertation]. University of Rochester; 2009. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1802/8298.

Council of Science Editors:

Wang J. G-protein Coupled Receptor Kinase-Interacting Protein 1 (GIT1) Regulates Endothelial Cell Function: Role in Podosome Formation, Extracellular Matrix Degradation and Migration. [Doctoral Dissertation]. University of Rochester; 2009. Available from: http://hdl.handle.net/1802/8298


University of Rochester

138. Chen, Zhuoxun. Identification of Molecular Determinants of Testosterone-associated Angiogenesis and Neuronal Survival in Adult Songbird Forebrain.

Degree: PhD, 2012, University of Rochester

 The HVC of the adult songbird forebrain undergoes gonadal steroid-mediated survival of new neurons throughout life. Angiogenesis and neuronal recruitment are serially and causally linked… (more)

Subjects/Keywords: Neurogenesis; Angiogenesis; Songbird; Testosterone; Neuronal Survival

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Chen, Z. (2012). Identification of Molecular Determinants of Testosterone-associated Angiogenesis and Neuronal Survival in Adult Songbird Forebrain. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/21371

Chicago Manual of Style (16th Edition):

Chen, Zhuoxun. “Identification of Molecular Determinants of Testosterone-associated Angiogenesis and Neuronal Survival in Adult Songbird Forebrain.” 2012. Doctoral Dissertation, University of Rochester. Accessed July 19, 2019. http://hdl.handle.net/1802/21371.

MLA Handbook (7th Edition):

Chen, Zhuoxun. “Identification of Molecular Determinants of Testosterone-associated Angiogenesis and Neuronal Survival in Adult Songbird Forebrain.” 2012. Web. 19 Jul 2019.

Vancouver:

Chen Z. Identification of Molecular Determinants of Testosterone-associated Angiogenesis and Neuronal Survival in Adult Songbird Forebrain. [Internet] [Doctoral dissertation]. University of Rochester; 2012. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1802/21371.

Council of Science Editors:

Chen Z. Identification of Molecular Determinants of Testosterone-associated Angiogenesis and Neuronal Survival in Adult Songbird Forebrain. [Doctoral Dissertation]. University of Rochester; 2012. Available from: http://hdl.handle.net/1802/21371


University of Rochester

139. Szpunar, Mercedes J.; Brown, Edward B. Evidence for Sympathetic Nervous System Regulation of Breast Cancer Progression.

Degree: PhD, 2012, University of Rochester

 Breast cancer patients experience chronic emotional stress. A major pathway underlying the stress response is sympathetic nervous system release of norepinephrine (NE) and stimulation of… (more)

Subjects/Keywords: Norepinephrine; Angiogenesis; VEGF; IL-6; Desipramine; Dexmedetomidine

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Szpunar, Mercedes J.; Brown, E. B. (2012). Evidence for Sympathetic Nervous System Regulation of Breast Cancer Progression. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/25535

Chicago Manual of Style (16th Edition):

Szpunar, Mercedes J.; Brown, Edward B. “Evidence for Sympathetic Nervous System Regulation of Breast Cancer Progression.” 2012. Doctoral Dissertation, University of Rochester. Accessed July 19, 2019. http://hdl.handle.net/1802/25535.

MLA Handbook (7th Edition):

Szpunar, Mercedes J.; Brown, Edward B. “Evidence for Sympathetic Nervous System Regulation of Breast Cancer Progression.” 2012. Web. 19 Jul 2019.

Vancouver:

Szpunar, Mercedes J.; Brown EB. Evidence for Sympathetic Nervous System Regulation of Breast Cancer Progression. [Internet] [Doctoral dissertation]. University of Rochester; 2012. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1802/25535.

Council of Science Editors:

Szpunar, Mercedes J.; Brown EB. Evidence for Sympathetic Nervous System Regulation of Breast Cancer Progression. [Doctoral Dissertation]. University of Rochester; 2012. Available from: http://hdl.handle.net/1802/25535


University of Rochester

140. Bushway, Meghan. Analysis of Cellular Signaling Within the Human Placenta: Implications for Vascular Development and Trophoblast Cell Function.

Degree: PhD, 2014, University of Rochester

 The human placenta performs multiple essential functions during pregnancy, including gas and nutrient exchange, hormone production and protecting the genetically distinct fetus from maternal immune-mediated… (more)

Subjects/Keywords: Pregnancy; Angiogenesis; Interferon-Gamma; pSTAT3; pSTAT1

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bushway, M. (2014). Analysis of Cellular Signaling Within the Human Placenta: Implications for Vascular Development and Trophoblast Cell Function. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/28954

Chicago Manual of Style (16th Edition):

Bushway, Meghan. “Analysis of Cellular Signaling Within the Human Placenta: Implications for Vascular Development and Trophoblast Cell Function.” 2014. Doctoral Dissertation, University of Rochester. Accessed July 19, 2019. http://hdl.handle.net/1802/28954.

MLA Handbook (7th Edition):

Bushway, Meghan. “Analysis of Cellular Signaling Within the Human Placenta: Implications for Vascular Development and Trophoblast Cell Function.” 2014. Web. 19 Jul 2019.

Vancouver:

Bushway M. Analysis of Cellular Signaling Within the Human Placenta: Implications for Vascular Development and Trophoblast Cell Function. [Internet] [Doctoral dissertation]. University of Rochester; 2014. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1802/28954.

Council of Science Editors:

Bushway M. Analysis of Cellular Signaling Within the Human Placenta: Implications for Vascular Development and Trophoblast Cell Function. [Doctoral Dissertation]. University of Rochester; 2014. Available from: http://hdl.handle.net/1802/28954


University of Southern California

141. Dubey, Ramin. Modulation of transcription and receptor function with synthetic small molecules and multi-finctional integrin ligands.

Degree: PhD, Pharmaceutical Sciences, 2013, University of Southern California

Angiogenesis, the process of formation of new blood vessels, is a characteristic of most solid malignancies and is involved in promoting rapid growth of neoplastic… (more)

Subjects/Keywords: hypoxia; angiogenesis; transcription; drug discovery; integrin; inhibitor

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Dubey, R. (2013). Modulation of transcription and receptor function with synthetic small molecules and multi-finctional integrin ligands. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/124862/rec/4167

Chicago Manual of Style (16th Edition):

Dubey, Ramin. “Modulation of transcription and receptor function with synthetic small molecules and multi-finctional integrin ligands.” 2013. Doctoral Dissertation, University of Southern California. Accessed July 19, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/124862/rec/4167.

MLA Handbook (7th Edition):

Dubey, Ramin. “Modulation of transcription and receptor function with synthetic small molecules and multi-finctional integrin ligands.” 2013. Web. 19 Jul 2019.

Vancouver:

Dubey R. Modulation of transcription and receptor function with synthetic small molecules and multi-finctional integrin ligands. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2019 Jul 19]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/124862/rec/4167.

Council of Science Editors:

Dubey R. Modulation of transcription and receptor function with synthetic small molecules and multi-finctional integrin ligands. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/124862/rec/4167


University of Southern California

142. Li, Xiuqing. Tetraspanin18 regulates angiogenesis through VEGFR2 and notch pathways.

Degree: PhD, Pathobiology, 2012, University of Southern California

 This work is to identify one of Tetraspanin family members, designated Tetraspanin18 (Tspan18), for expression in the developing blood vessels. Tspan18 knock down in zebrafish… (more)

Subjects/Keywords: Tetraspanin; VEGF; VEGF receptor; angiogenesis; Notch; Dll4

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Li, X. (2012). Tetraspanin18 regulates angiogenesis through VEGFR2 and notch pathways. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/623623/rec/6396

Chicago Manual of Style (16th Edition):

Li, Xiuqing. “Tetraspanin18 regulates angiogenesis through VEGFR2 and notch pathways.” 2012. Doctoral Dissertation, University of Southern California. Accessed July 19, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/623623/rec/6396.

MLA Handbook (7th Edition):

Li, Xiuqing. “Tetraspanin18 regulates angiogenesis through VEGFR2 and notch pathways.” 2012. Web. 19 Jul 2019.

Vancouver:

Li X. Tetraspanin18 regulates angiogenesis through VEGFR2 and notch pathways. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2019 Jul 19]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/623623/rec/6396.

Council of Science Editors:

Li X. Tetraspanin18 regulates angiogenesis through VEGFR2 and notch pathways. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/623623/rec/6396


Université Paris-Sud – Paris XI

143. Nakhlé, Jessica. Rôle de la thrombospondine-1 dans la migration, l’invasion et la dissémination métastatique dans les carcinomes prostatiques et mammaires : Role of the Thrombospondin 1 in Tumor Migration, Invasion and Metastatic Dissemination in Prostate Cancer and Breast Cancer.

Degree: Docteur es, Biologie cellulaire, biologie moléculaire et biochimie, 2012, Université Paris-Sud – Paris XI

Les métastases représentent l’étape ultime de la progression tumorale. Les traitements inhibiteurs de l’angiogenèse offrent de nouvelles perspectives thérapeutiques, notamment pour les stades invasifs, mais… (more)

Subjects/Keywords: Angiogenèse; Hypoxie; Métastases; Angiogenesis; Hypoxia; Metastasis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Nakhlé, J. (2012). Rôle de la thrombospondine-1 dans la migration, l’invasion et la dissémination métastatique dans les carcinomes prostatiques et mammaires : Role of the Thrombospondin 1 in Tumor Migration, Invasion and Metastatic Dissemination in Prostate Cancer and Breast Cancer. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2012PA11T088

Chicago Manual of Style (16th Edition):

Nakhlé, Jessica. “Rôle de la thrombospondine-1 dans la migration, l’invasion et la dissémination métastatique dans les carcinomes prostatiques et mammaires : Role of the Thrombospondin 1 in Tumor Migration, Invasion and Metastatic Dissemination in Prostate Cancer and Breast Cancer.” 2012. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed July 19, 2019. http://www.theses.fr/2012PA11T088.

MLA Handbook (7th Edition):

Nakhlé, Jessica. “Rôle de la thrombospondine-1 dans la migration, l’invasion et la dissémination métastatique dans les carcinomes prostatiques et mammaires : Role of the Thrombospondin 1 in Tumor Migration, Invasion and Metastatic Dissemination in Prostate Cancer and Breast Cancer.” 2012. Web. 19 Jul 2019.

Vancouver:

Nakhlé J. Rôle de la thrombospondine-1 dans la migration, l’invasion et la dissémination métastatique dans les carcinomes prostatiques et mammaires : Role of the Thrombospondin 1 in Tumor Migration, Invasion and Metastatic Dissemination in Prostate Cancer and Breast Cancer. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2012. [cited 2019 Jul 19]. Available from: http://www.theses.fr/2012PA11T088.

Council of Science Editors:

Nakhlé J. Rôle de la thrombospondine-1 dans la migration, l’invasion et la dissémination métastatique dans les carcinomes prostatiques et mammaires : Role of the Thrombospondin 1 in Tumor Migration, Invasion and Metastatic Dissemination in Prostate Cancer and Breast Cancer. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2012. Available from: http://www.theses.fr/2012PA11T088


Universitat Politècnica de València

144. Baiget Orts, María Amparo. HYALURONAN BASED BIOMATERIALS FOR CENTRAL NERVOUS TISSUE REGENERATION .

Degree: 2012, Universitat Politècnica de València

 The aim of this Thesis is to investigate the use of hyaluronic acid as a material for the design of scaffolds aimed at CNS regeneration.… (more)

Subjects/Keywords: Angiogenesis; Biomaterials; Hyaluronic acid; Central nervous system

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Baiget Orts, M. A. (2012). HYALURONAN BASED BIOMATERIALS FOR CENTRAL NERVOUS TISSUE REGENERATION . (Doctoral Dissertation). Universitat Politècnica de València. Retrieved from http://hdl.handle.net/10251/14576

Chicago Manual of Style (16th Edition):

Baiget Orts, María Amparo. “HYALURONAN BASED BIOMATERIALS FOR CENTRAL NERVOUS TISSUE REGENERATION .” 2012. Doctoral Dissertation, Universitat Politècnica de València. Accessed July 19, 2019. http://hdl.handle.net/10251/14576.

MLA Handbook (7th Edition):

Baiget Orts, María Amparo. “HYALURONAN BASED BIOMATERIALS FOR CENTRAL NERVOUS TISSUE REGENERATION .” 2012. Web. 19 Jul 2019.

Vancouver:

Baiget Orts MA. HYALURONAN BASED BIOMATERIALS FOR CENTRAL NERVOUS TISSUE REGENERATION . [Internet] [Doctoral dissertation]. Universitat Politècnica de València; 2012. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/10251/14576.

Council of Science Editors:

Baiget Orts MA. HYALURONAN BASED BIOMATERIALS FOR CENTRAL NERVOUS TISSUE REGENERATION . [Doctoral Dissertation]. Universitat Politècnica de València; 2012. Available from: http://hdl.handle.net/10251/14576


University of New South Wales

145. Kuljaca, Selena. Mechanisms and treatment strategies to overcome resistance to non-cytotoxic therapy in cancer.

Degree: Women's & Children's Health, 2010, University of New South Wales

 As anti-cancer agents, retinoid induce cell growth arrest and differentiation, while HDACIs cause cell differentiation, growth inhibition, death and inhibit angiogenesis in many cancer types.… (more)

Subjects/Keywords: Resistance; Cancer; Non-cytotoxic treatment; Angiogenesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kuljaca, S. (2010). Mechanisms and treatment strategies to overcome resistance to non-cytotoxic therapy in cancer. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/44699 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:7999/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Kuljaca, Selena. “Mechanisms and treatment strategies to overcome resistance to non-cytotoxic therapy in cancer.” 2010. Doctoral Dissertation, University of New South Wales. Accessed July 19, 2019. http://handle.unsw.edu.au/1959.4/44699 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:7999/SOURCE02?view=true.

MLA Handbook (7th Edition):

Kuljaca, Selena. “Mechanisms and treatment strategies to overcome resistance to non-cytotoxic therapy in cancer.” 2010. Web. 19 Jul 2019.

Vancouver:

Kuljaca S. Mechanisms and treatment strategies to overcome resistance to non-cytotoxic therapy in cancer. [Internet] [Doctoral dissertation]. University of New South Wales; 2010. [cited 2019 Jul 19]. Available from: http://handle.unsw.edu.au/1959.4/44699 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:7999/SOURCE02?view=true.

Council of Science Editors:

Kuljaca S. Mechanisms and treatment strategies to overcome resistance to non-cytotoxic therapy in cancer. [Doctoral Dissertation]. University of New South Wales; 2010. Available from: http://handle.unsw.edu.au/1959.4/44699 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:7999/SOURCE02?view=true


University of Toronto

146. Smith, Alexandra Helen. Multigene Therapy by Ultrasound-mediated Plasmid Delivery: Temporally Separated Delivery of Vascular Endothelial Growth Factor and Angiopoietin-1 Promotes Sustained Angiogenesis in Chronically Ischemic Skeletal Muscle.

Degree: 2010, University of Toronto

Endogenously, VEGF initiates angiogenesis, then later Angiopoietin (Ang)-1 matures vessels. We hypothesized that multigene therapy of VEGF before Ang1 to ischemic hindlimb tissue would result… (more)

Subjects/Keywords: cardiovascular disease; angiogenesis; gene therapy; ultrasound; 0564

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Smith, A. H. (2010). Multigene Therapy by Ultrasound-mediated Plasmid Delivery: Temporally Separated Delivery of Vascular Endothelial Growth Factor and Angiopoietin-1 Promotes Sustained Angiogenesis in Chronically Ischemic Skeletal Muscle. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/25804

Chicago Manual of Style (16th Edition):

Smith, Alexandra Helen. “Multigene Therapy by Ultrasound-mediated Plasmid Delivery: Temporally Separated Delivery of Vascular Endothelial Growth Factor and Angiopoietin-1 Promotes Sustained Angiogenesis in Chronically Ischemic Skeletal Muscle.” 2010. Masters Thesis, University of Toronto. Accessed July 19, 2019. http://hdl.handle.net/1807/25804.

MLA Handbook (7th Edition):

Smith, Alexandra Helen. “Multigene Therapy by Ultrasound-mediated Plasmid Delivery: Temporally Separated Delivery of Vascular Endothelial Growth Factor and Angiopoietin-1 Promotes Sustained Angiogenesis in Chronically Ischemic Skeletal Muscle.” 2010. Web. 19 Jul 2019.

Vancouver:

Smith AH. Multigene Therapy by Ultrasound-mediated Plasmid Delivery: Temporally Separated Delivery of Vascular Endothelial Growth Factor and Angiopoietin-1 Promotes Sustained Angiogenesis in Chronically Ischemic Skeletal Muscle. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1807/25804.

Council of Science Editors:

Smith AH. Multigene Therapy by Ultrasound-mediated Plasmid Delivery: Temporally Separated Delivery of Vascular Endothelial Growth Factor and Angiopoietin-1 Promotes Sustained Angiogenesis in Chronically Ischemic Skeletal Muscle. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/25804

147. Lytras, Dimitrios. Μελέτη της αγγειογένεσης και της λεμφαγγειογένεσης στο αδενοκαρκίνωμα του παγκρέατος με ανοσοϊστοχημικές τεχνικές.

Degree: 2014, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

Tumor angiogenesis and lymphangiogenesis, based on microvessel density(MVD) assessment have been associated with poor prognosis, in several studies ofsolid tumors. Expression of endoglin (CD105), a… (more)

Subjects/Keywords: Πάγκρεας; Αδενοκαρκίνωμα; Αγγειογένεση; Λεμφαγγειογένεση; Pancreas; Angiogenesis; lymhangiogenesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lytras, D. (2014). Μελέτη της αγγειογένεσης και της λεμφαγγειογένεσης στο αδενοκαρκίνωμα του παγκρέατος με ανοσοϊστοχημικές τεχνικές. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/42464

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):

Lytras, Dimitrios. “Μελέτη της αγγειογένεσης και της λεμφαγγειογένεσης στο αδενοκαρκίνωμα του παγκρέατος με ανοσοϊστοχημικές τεχνικές.” 2014. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed July 19, 2019. http://hdl.handle.net/10442/hedi/42464.

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

MLA Handbook (7th Edition):

Lytras, Dimitrios. “Μελέτη της αγγειογένεσης και της λεμφαγγειογένεσης στο αδενοκαρκίνωμα του παγκρέατος με ανοσοϊστοχημικές τεχνικές.” 2014. Web. 19 Jul 2019.

Vancouver:

Lytras D. Μελέτη της αγγειογένεσης και της λεμφαγγειογένεσης στο αδενοκαρκίνωμα του παγκρέατος με ανοσοϊστοχημικές τεχνικές. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2014. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/10442/hedi/42464.

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

Council of Science Editors:

Lytras D. Μελέτη της αγγειογένεσης και της λεμφαγγειογένεσης στο αδενοκαρκίνωμα του παγκρέατος με ανοσοϊστοχημικές τεχνικές. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2014. Available from: http://hdl.handle.net/10442/hedi/42464

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


Queensland University of Technology

148. Addison-Smith, Elizabeth Anne. Mathematical modelling of tumour-induced angiogenesis.

Degree: 2010, Queensland University of Technology

 The growth of solid tumours beyond a critical size is dependent upon angiogenesis, the formation of new blood vessels from an existing vasculature. Tumours may… (more)

Subjects/Keywords: angiogenesis; mathematical modelling; chemotaxis; blood vessels; VEGF; capillaries; stochastic; tumour angiogenesis; mathematical biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Addison-Smith, E. A. (2010). Mathematical modelling of tumour-induced angiogenesis. (Thesis). Queensland University of Technology. Retrieved from https://eprints.qut.edu.au/48804/

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):

Addison-Smith, Elizabeth Anne. “Mathematical modelling of tumour-induced angiogenesis.” 2010. Thesis, Queensland University of Technology. Accessed July 19, 2019. https://eprints.qut.edu.au/48804/.

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

MLA Handbook (7th Edition):

Addison-Smith, Elizabeth Anne. “Mathematical modelling of tumour-induced angiogenesis.” 2010. Web. 19 Jul 2019.

Vancouver:

Addison-Smith EA. Mathematical modelling of tumour-induced angiogenesis. [Internet] [Thesis]. Queensland University of Technology; 2010. [cited 2019 Jul 19]. Available from: https://eprints.qut.edu.au/48804/.

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

Council of Science Editors:

Addison-Smith EA. Mathematical modelling of tumour-induced angiogenesis. [Thesis]. Queensland University of Technology; 2010. Available from: https://eprints.qut.edu.au/48804/

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


University of Helsinki

149. Lahtinen, Ida. Tumorigenesis in celiac disease.

Degree: Farmaceutiska fakulteten, 2011, University of Helsinki

Celiac disease is life-long autoimmune disorder of the small intestine, which is caused by a reaction to gliadin found in wheat, rye and barley in… (more)

Subjects/Keywords: Celiac disease; tumorigenesis; transglutaminase 2; angiogenesis; Farmakologi; Pharmacology; Farmakologia; Celiac disease; tumorigenesis; transglutaminase 2; angiogenesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lahtinen, I. (2011). Tumorigenesis in celiac disease. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/27796

Chicago Manual of Style (16th Edition):

Lahtinen, Ida. “Tumorigenesis in celiac disease.” 2011. Masters Thesis, University of Helsinki. Accessed July 19, 2019. http://hdl.handle.net/10138/27796.

MLA Handbook (7th Edition):

Lahtinen, Ida. “Tumorigenesis in celiac disease.” 2011. Web. 19 Jul 2019.

Vancouver:

Lahtinen I. Tumorigenesis in celiac disease. [Internet] [Masters thesis]. University of Helsinki; 2011. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/10138/27796.

Council of Science Editors:

Lahtinen I. Tumorigenesis in celiac disease. [Masters Thesis]. University of Helsinki; 2011. Available from: http://hdl.handle.net/10138/27796


University of Vienna

150. Abdeen, Dana. Identification of novel regulators of sprouting angiogenesis using haploid ES cells.

Degree: 2017, University of Vienna

Die Expansion, Remodellierung und Reifung von Blutgefäßen ist ein wichtiges physiologisches Ereignis, das die embryonalen Entwicklungsstadien erfüllt und an der Pathophysiologie der Erwachsenen wie Augenerkrankungen… (more)

Subjects/Keywords: 42.13 Molekularbiologie; Angiogenesis / Haploid ES cells / Hyposprouters / Hypersprouters; Angiogenesis / Haploid ES cells / Hyposprouters / Hypersprouters

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Abdeen, D. (2017). Identification of novel regulators of sprouting angiogenesis using haploid ES cells. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/50257/

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):

Abdeen, Dana. “Identification of novel regulators of sprouting angiogenesis using haploid ES cells.” 2017. Thesis, University of Vienna. Accessed July 19, 2019. http://othes.univie.ac.at/50257/.

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

MLA Handbook (7th Edition):

Abdeen, Dana. “Identification of novel regulators of sprouting angiogenesis using haploid ES cells.” 2017. Web. 19 Jul 2019.

Vancouver:

Abdeen D. Identification of novel regulators of sprouting angiogenesis using haploid ES cells. [Internet] [Thesis]. University of Vienna; 2017. [cited 2019 Jul 19]. Available from: http://othes.univie.ac.at/50257/.

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

Council of Science Editors:

Abdeen D. Identification of novel regulators of sprouting angiogenesis using haploid ES cells. [Thesis]. University of Vienna; 2017. Available from: http://othes.univie.ac.at/50257/

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

[1] [2] [3] [4] [5] [6] [7] … [47]

.