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You searched for subject:(Integrins). Showing records 1 – 30 of 260 total matches.

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Rutgers University

1. Sikora, Jacqueline, 1989-. Towards determining the mechanism of recognition and binding to collagen by alpha 1 beta 1 and alpha 2 beta 1 integrins.

Degree: MS, Chemistry and Chemical Biology, 2014, Rutgers University

 Collagen is the most abundant protein in the human body. There are several collagen‐binding integrins, which exist as transmembrane proteins and serve to transmit cellular… (more)

Subjects/Keywords: Integrins; Collagen

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APA (6th Edition):

Sikora, Jacqueline, 1. (2014). Towards determining the mechanism of recognition and binding to collagen by alpha 1 beta 1 and alpha 2 beta 1 integrins. (Masters Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/45457/

Chicago Manual of Style (16th Edition):

Sikora, Jacqueline, 1989-. “Towards determining the mechanism of recognition and binding to collagen by alpha 1 beta 1 and alpha 2 beta 1 integrins.” 2014. Masters Thesis, Rutgers University. Accessed September 16, 2019. https://rucore.libraries.rutgers.edu/rutgers-lib/45457/.

MLA Handbook (7th Edition):

Sikora, Jacqueline, 1989-. “Towards determining the mechanism of recognition and binding to collagen by alpha 1 beta 1 and alpha 2 beta 1 integrins.” 2014. Web. 16 Sep 2019.

Vancouver:

Sikora, Jacqueline 1. Towards determining the mechanism of recognition and binding to collagen by alpha 1 beta 1 and alpha 2 beta 1 integrins. [Internet] [Masters thesis]. Rutgers University; 2014. [cited 2019 Sep 16]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/45457/.

Council of Science Editors:

Sikora, Jacqueline 1. Towards determining the mechanism of recognition and binding to collagen by alpha 1 beta 1 and alpha 2 beta 1 integrins. [Masters Thesis]. Rutgers University; 2014. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/45457/


University of Louisville

2. Massey, Veronica L. Integrin inhibitor cycloRGDfV blunts enhanced LPS-induced liver injury caused by ethanol in mice.

Degree: MS, 2012, University of Louisville

 Background. Progression of alcoholic liver disease (ALD) is associated with an increase in fibrin extracellular matrix (ECM) and inflammation. Previous studies have shown that this… (more)

Subjects/Keywords: Liver; alcohol; integrins

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APA (6th Edition):

Massey, V. L. (2012). Integrin inhibitor cycloRGDfV blunts enhanced LPS-induced liver injury caused by ethanol in mice. (Masters Thesis). University of Louisville. Retrieved from 10.18297/etd/912 ; https://ir.library.louisville.edu/etd/912

Chicago Manual of Style (16th Edition):

Massey, Veronica L. “Integrin inhibitor cycloRGDfV blunts enhanced LPS-induced liver injury caused by ethanol in mice.” 2012. Masters Thesis, University of Louisville. Accessed September 16, 2019. 10.18297/etd/912 ; https://ir.library.louisville.edu/etd/912.

MLA Handbook (7th Edition):

Massey, Veronica L. “Integrin inhibitor cycloRGDfV blunts enhanced LPS-induced liver injury caused by ethanol in mice.” 2012. Web. 16 Sep 2019.

Vancouver:

Massey VL. Integrin inhibitor cycloRGDfV blunts enhanced LPS-induced liver injury caused by ethanol in mice. [Internet] [Masters thesis]. University of Louisville; 2012. [cited 2019 Sep 16]. Available from: 10.18297/etd/912 ; https://ir.library.louisville.edu/etd/912.

Council of Science Editors:

Massey VL. Integrin inhibitor cycloRGDfV blunts enhanced LPS-induced liver injury caused by ethanol in mice. [Masters Thesis]. University of Louisville; 2012. Available from: 10.18297/etd/912 ; https://ir.library.louisville.edu/etd/912


University of Aberdeen

3. Andriu, Alexandra. Evaluating the utility of αvβ3 integrin antagonists to detect and treat angiogenic tumour cells.

Degree: PhD, 2018, University of Aberdeen

 Tumour angiogenesis, the formation of new blood vessels within a tumour, is a hallmark of cancers, that allows them to grow beyond a critical size… (more)

Subjects/Keywords: Tumors; Integrins; Neovascularization

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APA (6th Edition):

Andriu, A. (2018). Evaluating the utility of αvβ3 integrin antagonists to detect and treat angiogenic tumour cells. (Doctoral Dissertation). University of Aberdeen. Retrieved from http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=240026 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767334

Chicago Manual of Style (16th Edition):

Andriu, Alexandra. “Evaluating the utility of αvβ3 integrin antagonists to detect and treat angiogenic tumour cells.” 2018. Doctoral Dissertation, University of Aberdeen. Accessed September 16, 2019. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=240026 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767334.

MLA Handbook (7th Edition):

Andriu, Alexandra. “Evaluating the utility of αvβ3 integrin antagonists to detect and treat angiogenic tumour cells.” 2018. Web. 16 Sep 2019.

Vancouver:

Andriu A. Evaluating the utility of αvβ3 integrin antagonists to detect and treat angiogenic tumour cells. [Internet] [Doctoral dissertation]. University of Aberdeen; 2018. [cited 2019 Sep 16]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=240026 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767334.

Council of Science Editors:

Andriu A. Evaluating the utility of αvβ3 integrin antagonists to detect and treat angiogenic tumour cells. [Doctoral Dissertation]. University of Aberdeen; 2018. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=240026 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767334


University of Tasmania

4. Phillips, JL. Regulation of ITGA6 and ITGB4 integrin genes by RUNX1 and epigenetic mechanisms.

Degree: 2017, University of Tasmania

 Disruption to regulatory mechanisms controlling gene expression is a hallmark of leukaemia, with disruption to transcription factors being one of the most prevalent. By identifying… (more)

Subjects/Keywords: gene regulation; integrins; epigenetics RUNX1

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APA (6th Edition):

Phillips, J. (2017). Regulation of ITGA6 and ITGB4 integrin genes by RUNX1 and epigenetic mechanisms. (Thesis). University of Tasmania. Retrieved from https://eprints.utas.edu.au/23900/1/Phillips_whole_thesis.pdf ; Phillips, JL ORCID: 0000-0002-5559-3072 <https://orcid.org/0000-0002-5559-3072> 2017 , 'Regulation of ITGA6 and ITGB4 integrin genes by RUNX1 and epigenetic mechanisms', PhD thesis, University of Tasmania.

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):

Phillips, JL. “Regulation of ITGA6 and ITGB4 integrin genes by RUNX1 and epigenetic mechanisms.” 2017. Thesis, University of Tasmania. Accessed September 16, 2019. https://eprints.utas.edu.au/23900/1/Phillips_whole_thesis.pdf ; Phillips, JL ORCID: 0000-0002-5559-3072 <https://orcid.org/0000-0002-5559-3072> 2017 , 'Regulation of ITGA6 and ITGB4 integrin genes by RUNX1 and epigenetic mechanisms', PhD thesis, University of Tasmania..

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

MLA Handbook (7th Edition):

Phillips, JL. “Regulation of ITGA6 and ITGB4 integrin genes by RUNX1 and epigenetic mechanisms.” 2017. Web. 16 Sep 2019.

Vancouver:

Phillips J. Regulation of ITGA6 and ITGB4 integrin genes by RUNX1 and epigenetic mechanisms. [Internet] [Thesis]. University of Tasmania; 2017. [cited 2019 Sep 16]. Available from: https://eprints.utas.edu.au/23900/1/Phillips_whole_thesis.pdf ; Phillips, JL ORCID: 0000-0002-5559-3072 <https://orcid.org/0000-0002-5559-3072> 2017 , 'Regulation of ITGA6 and ITGB4 integrin genes by RUNX1 and epigenetic mechanisms', PhD thesis, University of Tasmania..

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

Council of Science Editors:

Phillips J. Regulation of ITGA6 and ITGB4 integrin genes by RUNX1 and epigenetic mechanisms. [Thesis]. University of Tasmania; 2017. Available from: https://eprints.utas.edu.au/23900/1/Phillips_whole_thesis.pdf ; Phillips, JL ORCID: 0000-0002-5559-3072 <https://orcid.org/0000-0002-5559-3072> 2017 , 'Regulation of ITGA6 and ITGB4 integrin genes by RUNX1 and epigenetic mechanisms', PhD thesis, University of Tasmania.

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


University of Manchester

5. Olabi, Safiah. The Role of β1-integrin in Mammary Stem and Progenitor Fate.

Degree: 2016, University of Manchester

 The mammary gland contains a subset of cells with regenerative capacity that is able to generate both luminal and myoepithelial mammary epithelial lineages. Those cells… (more)

Subjects/Keywords: Mammary stem cells; Integrins; Rac1

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APA (6th Edition):

Olabi, S. (2016). The Role of β1-integrin in Mammary Stem and Progenitor Fate. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:303007

Chicago Manual of Style (16th Edition):

Olabi, Safiah. “The Role of β1-integrin in Mammary Stem and Progenitor Fate.” 2016. Doctoral Dissertation, University of Manchester. Accessed September 16, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:303007.

MLA Handbook (7th Edition):

Olabi, Safiah. “The Role of β1-integrin in Mammary Stem and Progenitor Fate.” 2016. Web. 16 Sep 2019.

Vancouver:

Olabi S. The Role of β1-integrin in Mammary Stem and Progenitor Fate. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Sep 16]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:303007.

Council of Science Editors:

Olabi S. The Role of β1-integrin in Mammary Stem and Progenitor Fate. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:303007


University of Texas Southwestern Medical Center

6. Cupka, Dorothy Lynn. Development of an αᵥβ₆-Binding Peptide for In Vivo Applications: Modulation of Serum Stability and Biodistribution.

Degree: 2015, University of Texas Southwestern Medical Center

 Targeted delivery of imaging and therapeutic agents to tumors improves detection, characterization, and treatment of many types of cancers. Peptides are capable of efficient and… (more)

Subjects/Keywords: Antigens, Neoplasm; Integrins; Neoplasms; Peptides

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APA (6th Edition):

Cupka, D. L. (2015). Development of an αᵥβ₆-Binding Peptide for In Vivo Applications: Modulation of Serum Stability and Biodistribution. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4208

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):

Cupka, Dorothy Lynn. “Development of an αᵥβ₆-Binding Peptide for In Vivo Applications: Modulation of Serum Stability and Biodistribution.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed September 16, 2019. http://hdl.handle.net/2152.5/4208.

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

MLA Handbook (7th Edition):

Cupka, Dorothy Lynn. “Development of an αᵥβ₆-Binding Peptide for In Vivo Applications: Modulation of Serum Stability and Biodistribution.” 2015. Web. 16 Sep 2019.

Vancouver:

Cupka DL. Development of an αᵥβ₆-Binding Peptide for In Vivo Applications: Modulation of Serum Stability and Biodistribution. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2152.5/4208.

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

Council of Science Editors:

Cupka DL. Development of an αᵥβ₆-Binding Peptide for In Vivo Applications: Modulation of Serum Stability and Biodistribution. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4208

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


University of Oxford

7. Douglass, Wendy A. The structure and function of integrins.

Degree: PhD, 1997, University of Oxford

Integrins are a family of αβ heterodimeric cell surface glycoproteins formed by the noncovalent association of a specific integrin α and β subunit. At present… (more)

Subjects/Keywords: 572; Integrins; Structure

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APA (6th Edition):

Douglass, W. A. (1997). The structure and function of integrins. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:cfdfd40c-b350-4500-83e4-2650f9fe455d ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618371

Chicago Manual of Style (16th Edition):

Douglass, Wendy A. “The structure and function of integrins.” 1997. Doctoral Dissertation, University of Oxford. Accessed September 16, 2019. http://ora.ox.ac.uk/objects/uuid:cfdfd40c-b350-4500-83e4-2650f9fe455d ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618371.

MLA Handbook (7th Edition):

Douglass, Wendy A. “The structure and function of integrins.” 1997. Web. 16 Sep 2019.

Vancouver:

Douglass WA. The structure and function of integrins. [Internet] [Doctoral dissertation]. University of Oxford; 1997. [cited 2019 Sep 16]. Available from: http://ora.ox.ac.uk/objects/uuid:cfdfd40c-b350-4500-83e4-2650f9fe455d ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618371.

Council of Science Editors:

Douglass WA. The structure and function of integrins. [Doctoral Dissertation]. University of Oxford; 1997. Available from: http://ora.ox.ac.uk/objects/uuid:cfdfd40c-b350-4500-83e4-2650f9fe455d ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618371


University of Edinburgh

8. Fonseca, Ana Cristina Nunes Lopes da. Role of integrins and neuregulins in axoglial interaction in central nervous system myelination.

Degree: PhD, 2015, University of Edinburgh

 Oligodendrocytes in the central nervous system (CNS) are responsible for wrapping axons with myelin in order to insulate them and allow for a faster conduction… (more)

Subjects/Keywords: 616.8; myelination; multiple sclerosis; schizophrenia; neuregulins; integrins

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APA (6th Edition):

Fonseca, A. C. N. L. d. (2015). Role of integrins and neuregulins in axoglial interaction in central nervous system myelination. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/10028

Chicago Manual of Style (16th Edition):

Fonseca, Ana Cristina Nunes Lopes da. “Role of integrins and neuregulins in axoglial interaction in central nervous system myelination.” 2015. Doctoral Dissertation, University of Edinburgh. Accessed September 16, 2019. http://hdl.handle.net/1842/10028.

MLA Handbook (7th Edition):

Fonseca, Ana Cristina Nunes Lopes da. “Role of integrins and neuregulins in axoglial interaction in central nervous system myelination.” 2015. Web. 16 Sep 2019.

Vancouver:

Fonseca ACNLd. Role of integrins and neuregulins in axoglial interaction in central nervous system myelination. [Internet] [Doctoral dissertation]. University of Edinburgh; 2015. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1842/10028.

Council of Science Editors:

Fonseca ACNLd. Role of integrins and neuregulins in axoglial interaction in central nervous system myelination. [Doctoral Dissertation]. University of Edinburgh; 2015. Available from: http://hdl.handle.net/1842/10028


Universiteit Utrecht

9. Heus, C. de. GTPase Rap1 contribution to tumor development.

Degree: 2012, Universiteit Utrecht

 The currently available anti-cancer treatments are most effective when a patient is diagnosed with cancer before metastatic formation. To prevent metastatic formation it is important… (more)

Subjects/Keywords: GTPase; Rap1; Tuomr metastasis; Integrins; Cadherins

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APA (6th Edition):

Heus, C. d. (2012). GTPase Rap1 contribution to tumor development. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/257057

Chicago Manual of Style (16th Edition):

Heus, C de. “GTPase Rap1 contribution to tumor development.” 2012. Masters Thesis, Universiteit Utrecht. Accessed September 16, 2019. http://dspace.library.uu.nl:8080/handle/1874/257057.

MLA Handbook (7th Edition):

Heus, C de. “GTPase Rap1 contribution to tumor development.” 2012. Web. 16 Sep 2019.

Vancouver:

Heus Cd. GTPase Rap1 contribution to tumor development. [Internet] [Masters thesis]. Universiteit Utrecht; 2012. [cited 2019 Sep 16]. Available from: http://dspace.library.uu.nl:8080/handle/1874/257057.

Council of Science Editors:

Heus Cd. GTPase Rap1 contribution to tumor development. [Masters Thesis]. Universiteit Utrecht; 2012. Available from: http://dspace.library.uu.nl:8080/handle/1874/257057

10. Rooney, Nicholas. Investigating the role of Integrin Linked Kinase in mammary epithelial cell differentiation.

Degree: PhD, 2014, University of Manchester

 Epithelial cell adhesion to the surrounding extracellular matrix (ECM) is necessary for their proper behaviour and function. During pregnancy and lactation mammary epithelial cells (MECs)… (more)

Subjects/Keywords: 611; ILK; MEC; differentiation; Prolactin; integrins; Pix

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APA (6th Edition):

Rooney, N. (2014). Investigating the role of Integrin Linked Kinase in mammary epithelial cell differentiation. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/investigating-the-role-of-integrin-linked-kinase-in-mammary-epithelial-cell-differentiation(7ea57786-1b8a-4391-bfbf-2cda9977877e).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.603219

Chicago Manual of Style (16th Edition):

Rooney, Nicholas. “Investigating the role of Integrin Linked Kinase in mammary epithelial cell differentiation.” 2014. Doctoral Dissertation, University of Manchester. Accessed September 16, 2019. https://www.research.manchester.ac.uk/portal/en/theses/investigating-the-role-of-integrin-linked-kinase-in-mammary-epithelial-cell-differentiation(7ea57786-1b8a-4391-bfbf-2cda9977877e).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.603219.

MLA Handbook (7th Edition):

Rooney, Nicholas. “Investigating the role of Integrin Linked Kinase in mammary epithelial cell differentiation.” 2014. Web. 16 Sep 2019.

Vancouver:

Rooney N. Investigating the role of Integrin Linked Kinase in mammary epithelial cell differentiation. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2019 Sep 16]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/investigating-the-role-of-integrin-linked-kinase-in-mammary-epithelial-cell-differentiation(7ea57786-1b8a-4391-bfbf-2cda9977877e).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.603219.

Council of Science Editors:

Rooney N. Investigating the role of Integrin Linked Kinase in mammary epithelial cell differentiation. [Doctoral Dissertation]. University of Manchester; 2014. Available from: https://www.research.manchester.ac.uk/portal/en/theses/investigating-the-role-of-integrin-linked-kinase-in-mammary-epithelial-cell-differentiation(7ea57786-1b8a-4391-bfbf-2cda9977877e).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.603219

11. Moreno Layseca, Paulina. The role of β1-integrin in normal and oncogene-mediated proliferation in breast epithelia.

Degree: PhD, 2015, University of Manchester

 Luminal epithelial cells in the mammary gland require two types of signals to proliferate: soluble signals (growth factor signals) and signals from the extracellular matrix… (more)

Subjects/Keywords: 611; Integrins; Proliferation; Mammary epithelial cells

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APA (6th Edition):

Moreno Layseca, P. (2015). The role of β1-integrin in normal and oncogene-mediated proliferation in breast epithelia. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/the-role-of-1integrin-in-normal-and-oncogenemediated-proliferation-in-breast-epithelia(635388a7-5382-4cb5-82d1-d098b2092e2e).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.634970

Chicago Manual of Style (16th Edition):

Moreno Layseca, Paulina. “The role of β1-integrin in normal and oncogene-mediated proliferation in breast epithelia.” 2015. Doctoral Dissertation, University of Manchester. Accessed September 16, 2019. https://www.research.manchester.ac.uk/portal/en/theses/the-role-of-1integrin-in-normal-and-oncogenemediated-proliferation-in-breast-epithelia(635388a7-5382-4cb5-82d1-d098b2092e2e).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.634970.

MLA Handbook (7th Edition):

Moreno Layseca, Paulina. “The role of β1-integrin in normal and oncogene-mediated proliferation in breast epithelia.” 2015. Web. 16 Sep 2019.

Vancouver:

Moreno Layseca P. The role of β1-integrin in normal and oncogene-mediated proliferation in breast epithelia. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2019 Sep 16]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-role-of-1integrin-in-normal-and-oncogenemediated-proliferation-in-breast-epithelia(635388a7-5382-4cb5-82d1-d098b2092e2e).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.634970.

Council of Science Editors:

Moreno Layseca P. The role of β1-integrin in normal and oncogene-mediated proliferation in breast epithelia. [Doctoral Dissertation]. University of Manchester; 2015. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-role-of-1integrin-in-normal-and-oncogenemediated-proliferation-in-breast-epithelia(635388a7-5382-4cb5-82d1-d098b2092e2e).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.634970


University of Edinburgh

12. Greenhalgh, Stephen Nicholas. Cellular and molecular mechanisms of liver regeneration.

Degree: PhD, 2017, University of Edinburgh

 Improved understanding of how the liver regenerates would be of great value, particularly given the dearth of therapies for end-stage liver disease. Currently, the only… (more)

Subjects/Keywords: av integrins; liver regeneration; animal model

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APA (6th Edition):

Greenhalgh, S. N. (2017). Cellular and molecular mechanisms of liver regeneration. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/28846

Chicago Manual of Style (16th Edition):

Greenhalgh, Stephen Nicholas. “Cellular and molecular mechanisms of liver regeneration.” 2017. Doctoral Dissertation, University of Edinburgh. Accessed September 16, 2019. http://hdl.handle.net/1842/28846.

MLA Handbook (7th Edition):

Greenhalgh, Stephen Nicholas. “Cellular and molecular mechanisms of liver regeneration.” 2017. Web. 16 Sep 2019.

Vancouver:

Greenhalgh SN. Cellular and molecular mechanisms of liver regeneration. [Internet] [Doctoral dissertation]. University of Edinburgh; 2017. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1842/28846.

Council of Science Editors:

Greenhalgh SN. Cellular and molecular mechanisms of liver regeneration. [Doctoral Dissertation]. University of Edinburgh; 2017. Available from: http://hdl.handle.net/1842/28846


University of Ottawa

13. Bugiel, Steven. β1 Integrin Regulates PC3 Prostate Cancer Cell Phenotypes in part via Regulation of Matricellular SPARC .

Degree: 2016, University of Ottawa

 We have shown herein that β1 integrin stably depleted PC3 sub-clonal cells confer a trend towards increased survival of mice compared to β1 integrin expressing… (more)

Subjects/Keywords: Prostate Cancer; Metastasis; Integrins; Extracellular Matrix; SPARC

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APA (6th Edition):

Bugiel, S. (2016). β1 Integrin Regulates PC3 Prostate Cancer Cell Phenotypes in part via Regulation of Matricellular SPARC . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/34785

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):

Bugiel, Steven. “β1 Integrin Regulates PC3 Prostate Cancer Cell Phenotypes in part via Regulation of Matricellular SPARC .” 2016. Thesis, University of Ottawa. Accessed September 16, 2019. http://hdl.handle.net/10393/34785.

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

MLA Handbook (7th Edition):

Bugiel, Steven. “β1 Integrin Regulates PC3 Prostate Cancer Cell Phenotypes in part via Regulation of Matricellular SPARC .” 2016. Web. 16 Sep 2019.

Vancouver:

Bugiel S. β1 Integrin Regulates PC3 Prostate Cancer Cell Phenotypes in part via Regulation of Matricellular SPARC . [Internet] [Thesis]. University of Ottawa; 2016. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/10393/34785.

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

Council of Science Editors:

Bugiel S. β1 Integrin Regulates PC3 Prostate Cancer Cell Phenotypes in part via Regulation of Matricellular SPARC . [Thesis]. University of Ottawa; 2016. Available from: http://hdl.handle.net/10393/34785

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


Cornell University

14. Kang, Sungkwon. Engineering Leukocyte Integrins For Therapeutic Development Against Inflammatory Diseases .

Degree: 2012, Cornell University

 Inflammation is considered as a hallmark of host defense against infections and injuries. On the flipside, prolonged and non-resolving chronic inflammation is also associated with… (more)

Subjects/Keywords: protein engineering; leukocyte integrins; targeted delivery

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APA (6th Edition):

Kang, S. (2012). Engineering Leukocyte Integrins For Therapeutic Development Against Inflammatory Diseases . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/29487

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):

Kang, Sungkwon. “Engineering Leukocyte Integrins For Therapeutic Development Against Inflammatory Diseases .” 2012. Thesis, Cornell University. Accessed September 16, 2019. http://hdl.handle.net/1813/29487.

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

MLA Handbook (7th Edition):

Kang, Sungkwon. “Engineering Leukocyte Integrins For Therapeutic Development Against Inflammatory Diseases .” 2012. Web. 16 Sep 2019.

Vancouver:

Kang S. Engineering Leukocyte Integrins For Therapeutic Development Against Inflammatory Diseases . [Internet] [Thesis]. Cornell University; 2012. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1813/29487.

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

Council of Science Editors:

Kang S. Engineering Leukocyte Integrins For Therapeutic Development Against Inflammatory Diseases . [Thesis]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/29487

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


University of Oxford

15. Iqbal, Sarah. Molecular studies of stiff skin-causing mutations in fibrillin-1.

Degree: PhD, 2011, University of Oxford

 Fibrillin-1 is the main component of the 10-12 nm microfibrils, which are found in several elastic and non-elastic tissues. Human fibrillin-1 contains multiple calcium-binding epidermal… (more)

Subjects/Keywords: 616.042; Biochemistry; Biology; Fibrillin; Extracellular matrix; integrins

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APA (6th Edition):

Iqbal, S. (2011). Molecular studies of stiff skin-causing mutations in fibrillin-1. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:c23ac97b-dbf3-44b3-9e56-7a860038519e ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.543727

Chicago Manual of Style (16th Edition):

Iqbal, Sarah. “Molecular studies of stiff skin-causing mutations in fibrillin-1.” 2011. Doctoral Dissertation, University of Oxford. Accessed September 16, 2019. http://ora.ox.ac.uk/objects/uuid:c23ac97b-dbf3-44b3-9e56-7a860038519e ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.543727.

MLA Handbook (7th Edition):

Iqbal, Sarah. “Molecular studies of stiff skin-causing mutations in fibrillin-1.” 2011. Web. 16 Sep 2019.

Vancouver:

Iqbal S. Molecular studies of stiff skin-causing mutations in fibrillin-1. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2019 Sep 16]. Available from: http://ora.ox.ac.uk/objects/uuid:c23ac97b-dbf3-44b3-9e56-7a860038519e ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.543727.

Council of Science Editors:

Iqbal S. Molecular studies of stiff skin-causing mutations in fibrillin-1. [Doctoral Dissertation]. University of Oxford; 2011. Available from: http://ora.ox.ac.uk/objects/uuid:c23ac97b-dbf3-44b3-9e56-7a860038519e ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.543727


University of Aberdeen

16. Andriu, Alexandra.; Fleming, I. N.; Zanda, Matteo.; University of Aberdeen.School of Medicine, Medical Sciences and Nutrition.; University of Aberdeen.Development Trust. Evaluating the utility of αvβ3 integrin antagonists to detect and treat angiogenic tumour cells.

Degree: School of Medicine, Medical Sciences and Nutrition., 2018, University of Aberdeen

Subjects/Keywords: Tumors; Integrins.; Neovascularization.

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APA (6th Edition):

Andriu, Alexandra.; Fleming, I. N.; Zanda, Matteo.; University of Aberdeen.School of Medicine, M. S. a. N. ;. U. o. A. D. T. (2018). Evaluating the utility of αvβ3 integrin antagonists to detect and treat angiogenic tumour cells. (Doctoral Dissertation). University of Aberdeen. Retrieved from http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=240026 ; http://digitool.abdn.ac.uk:1801/webclient/DeliveryManager?pid=240026&custom_att_2=simple_viewer

Chicago Manual of Style (16th Edition):

Andriu, Alexandra.; Fleming, I. N.; Zanda, Matteo.; University of Aberdeen.School of Medicine, Medical Sciences and Nutrition ; University of Aberdeen Development Trust. “Evaluating the utility of αvβ3 integrin antagonists to detect and treat angiogenic tumour cells.” 2018. Doctoral Dissertation, University of Aberdeen. Accessed September 16, 2019. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=240026 ; http://digitool.abdn.ac.uk:1801/webclient/DeliveryManager?pid=240026&custom_att_2=simple_viewer.

MLA Handbook (7th Edition):

Andriu, Alexandra.; Fleming, I. N.; Zanda, Matteo.; University of Aberdeen.School of Medicine, Medical Sciences and Nutrition ; University of Aberdeen Development Trust. “Evaluating the utility of αvβ3 integrin antagonists to detect and treat angiogenic tumour cells.” 2018. Web. 16 Sep 2019.

Vancouver:

Andriu, Alexandra.; Fleming, I. N.; Zanda, Matteo.; University of Aberdeen.School of Medicine MSaN;UoADT. Evaluating the utility of αvβ3 integrin antagonists to detect and treat angiogenic tumour cells. [Internet] [Doctoral dissertation]. University of Aberdeen; 2018. [cited 2019 Sep 16]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=240026 ; http://digitool.abdn.ac.uk:1801/webclient/DeliveryManager?pid=240026&custom_att_2=simple_viewer.

Council of Science Editors:

Andriu, Alexandra.; Fleming, I. N.; Zanda, Matteo.; University of Aberdeen.School of Medicine MSaN;UoADT. Evaluating the utility of αvβ3 integrin antagonists to detect and treat angiogenic tumour cells. [Doctoral Dissertation]. University of Aberdeen; 2018. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=240026 ; http://digitool.abdn.ac.uk:1801/webclient/DeliveryManager?pid=240026&custom_att_2=simple_viewer


McMaster University

17. Ahmadzai, Mohammad Mustafa. Integrins are Mechanosensors that Modulate Human Eosinophil Activation.

Degree: MSMS, 2014, McMaster University

Eosinophils are end-point effectors of inflammation that contribute to the clinical severity of asthma. Eosinophil homing to the asthmatic lung is primarily guided by eotaxin-1,… (more)

Subjects/Keywords: Eosinophils; Intracellular Calcium; Integrins; Mechanosensitive; Inflammation; Asthma

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APA (6th Edition):

Ahmadzai, M. M. (2014). Integrins are Mechanosensors that Modulate Human Eosinophil Activation. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/16394

Chicago Manual of Style (16th Edition):

Ahmadzai, Mohammad Mustafa. “Integrins are Mechanosensors that Modulate Human Eosinophil Activation.” 2014. Masters Thesis, McMaster University. Accessed September 16, 2019. http://hdl.handle.net/11375/16394.

MLA Handbook (7th Edition):

Ahmadzai, Mohammad Mustafa. “Integrins are Mechanosensors that Modulate Human Eosinophil Activation.” 2014. Web. 16 Sep 2019.

Vancouver:

Ahmadzai MM. Integrins are Mechanosensors that Modulate Human Eosinophil Activation. [Internet] [Masters thesis]. McMaster University; 2014. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/11375/16394.

Council of Science Editors:

Ahmadzai MM. Integrins are Mechanosensors that Modulate Human Eosinophil Activation. [Masters Thesis]. McMaster University; 2014. Available from: http://hdl.handle.net/11375/16394


University of Texas Southwestern Medical Center

18. Gray, Bethany Powell. Peptide Targeted Drug Delivery to Non-Small Cell Lung Cancer.

Degree: 2012, University of Texas Southwestern Medical Center

 Non-small cell lung cancer (NSCLC) is a notoriously deadly disease. The integrin αᵥβ₆ is emerging as a viable target for NSCLC; it is expressed in… (more)

Subjects/Keywords: Carcinoma, Non-Small-Cell Lung; Integrins; Peptides

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APA (6th Edition):

Gray, B. P. (2012). Peptide Targeted Drug Delivery to Non-Small Cell Lung Cancer. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1248

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):

Gray, Bethany Powell. “Peptide Targeted Drug Delivery to Non-Small Cell Lung Cancer.” 2012. Thesis, University of Texas Southwestern Medical Center. Accessed September 16, 2019. http://hdl.handle.net/2152.5/1248.

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

MLA Handbook (7th Edition):

Gray, Bethany Powell. “Peptide Targeted Drug Delivery to Non-Small Cell Lung Cancer.” 2012. Web. 16 Sep 2019.

Vancouver:

Gray BP. Peptide Targeted Drug Delivery to Non-Small Cell Lung Cancer. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2012. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2152.5/1248.

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

Council of Science Editors:

Gray BP. Peptide Targeted Drug Delivery to Non-Small Cell Lung Cancer. [Thesis]. University of Texas Southwestern Medical Center; 2012. Available from: http://hdl.handle.net/2152.5/1248

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


University of Texas Southwestern Medical Center

19. Lin, Mai. Molecular Imaging of αvβ6–Positive Tumors and Pancreatic β-Cell Mass by Radiolabeled Peptides.

Degree: 2011, University of Texas Southwestern Medical Center

 Conventional diagnostic methodologies of lung cancer and diabetes are limited by sensitivity and specificity. In consequence, patients usually get diagnosed when the symptoms appear and… (more)

Subjects/Keywords: Diabetes Mellitus; Lung Neoplasms; Integrins; Molecular Imaging

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APA (6th Edition):

Lin, M. (2011). Molecular Imaging of αvβ6–Positive Tumors and Pancreatic β-Cell Mass by Radiolabeled Peptides. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/856

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):

Lin, Mai. “Molecular Imaging of αvβ6–Positive Tumors and Pancreatic β-Cell Mass by Radiolabeled Peptides.” 2011. Thesis, University of Texas Southwestern Medical Center. Accessed September 16, 2019. http://hdl.handle.net/2152.5/856.

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

MLA Handbook (7th Edition):

Lin, Mai. “Molecular Imaging of αvβ6–Positive Tumors and Pancreatic β-Cell Mass by Radiolabeled Peptides.” 2011. Web. 16 Sep 2019.

Vancouver:

Lin M. Molecular Imaging of αvβ6–Positive Tumors and Pancreatic β-Cell Mass by Radiolabeled Peptides. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2011. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2152.5/856.

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

Council of Science Editors:

Lin M. Molecular Imaging of αvβ6–Positive Tumors and Pancreatic β-Cell Mass by Radiolabeled Peptides. [Thesis]. University of Texas Southwestern Medical Center; 2011. Available from: http://hdl.handle.net/2152.5/856

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


University of Toronto

20. Gallant, Reid Carey. Alpha-Dystroglycan Plays Functional Roles in Platelet Aggregation and Thrombus Growth.

Degree: 2017, University of Toronto

Fibrinogen (Fg) and von Willebrand factor (VWF) have been considered essential for platelet adhesion and aggregation. However, platelet aggregation still occurs in mice lacking Fg… (more)

Subjects/Keywords: Blood; Hemostasis; Integrins; Platelets; Thrombosis; 0571

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APA (6th Edition):

Gallant, R. C. (2017). Alpha-Dystroglycan Plays Functional Roles in Platelet Aggregation and Thrombus Growth. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/79252

Chicago Manual of Style (16th Edition):

Gallant, Reid Carey. “Alpha-Dystroglycan Plays Functional Roles in Platelet Aggregation and Thrombus Growth.” 2017. Masters Thesis, University of Toronto. Accessed September 16, 2019. http://hdl.handle.net/1807/79252.

MLA Handbook (7th Edition):

Gallant, Reid Carey. “Alpha-Dystroglycan Plays Functional Roles in Platelet Aggregation and Thrombus Growth.” 2017. Web. 16 Sep 2019.

Vancouver:

Gallant RC. Alpha-Dystroglycan Plays Functional Roles in Platelet Aggregation and Thrombus Growth. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1807/79252.

Council of Science Editors:

Gallant RC. Alpha-Dystroglycan Plays Functional Roles in Platelet Aggregation and Thrombus Growth. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/79252


University of Sydney

21. Lee, Pearl. Fibroblast Attachment Sites on Tropoelastin .

Degree: 2018, University of Sydney

 Tropoelastin is the dominant monomer that assembles to form elastin, which confers elasticity to vertebrate elastic tissues including skin, arteries and lungs. This thesis explores… (more)

Subjects/Keywords: elastin; integrins; cell adhesion; cellular interactions

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APA (6th Edition):

Lee, P. (2018). Fibroblast Attachment Sites on Tropoelastin . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/18382

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):

Lee, Pearl. “Fibroblast Attachment Sites on Tropoelastin .” 2018. Thesis, University of Sydney. Accessed September 16, 2019. http://hdl.handle.net/2123/18382.

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

MLA Handbook (7th Edition):

Lee, Pearl. “Fibroblast Attachment Sites on Tropoelastin .” 2018. Web. 16 Sep 2019.

Vancouver:

Lee P. Fibroblast Attachment Sites on Tropoelastin . [Internet] [Thesis]. University of Sydney; 2018. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2123/18382.

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

Council of Science Editors:

Lee P. Fibroblast Attachment Sites on Tropoelastin . [Thesis]. University of Sydney; 2018. Available from: http://hdl.handle.net/2123/18382

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


University of Florida

22. Plattner, Alexander. Using the pQE-TriSystem Vector for αVβ5 Integrin Protein Expression in Mammalian and Insect Cell Systems.

Degree: 2013, University of Florida

 The pQE-TriSystem vector by QIAGEN is a versatile vector that can be used for protein expression in both mammalian cell systems and baculovirus-infected insect cell… (more)

Subjects/Keywords: DNA; Gels; Infections; Insects; Integrins; Nickel; Plasmids; Purification; Receptors; Transfection; Cells; Genetic vectors; Integrins; Proteins

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APA (6th Edition):

Plattner, A. (2013). Using the pQE-TriSystem Vector for αVβ5 Integrin Protein Expression in Mammalian and Insect Cell Systems. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00058336

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):

Plattner, Alexander. “Using the pQE-TriSystem Vector for αVβ5 Integrin Protein Expression in Mammalian and Insect Cell Systems.” 2013. Thesis, University of Florida. Accessed September 16, 2019. http://ufdc.ufl.edu/AA00058336.

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

MLA Handbook (7th Edition):

Plattner, Alexander. “Using the pQE-TriSystem Vector for αVβ5 Integrin Protein Expression in Mammalian and Insect Cell Systems.” 2013. Web. 16 Sep 2019.

Vancouver:

Plattner A. Using the pQE-TriSystem Vector for αVβ5 Integrin Protein Expression in Mammalian and Insect Cell Systems. [Internet] [Thesis]. University of Florida; 2013. [cited 2019 Sep 16]. Available from: http://ufdc.ufl.edu/AA00058336.

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

Council of Science Editors:

Plattner A. Using the pQE-TriSystem Vector for αVβ5 Integrin Protein Expression in Mammalian and Insect Cell Systems. [Thesis]. University of Florida; 2013. Available from: http://ufdc.ufl.edu/AA00058336

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


University of Florida

23. Woodhouse, Andrew. Integrin Expression for Use in Complexing Studies with Adeno-Associated Virus Serotype 2.

Degree: 2010, University of Florida

 The focus of my research has been to determine role the human integrins co-receptors αVβ5 and α5β1 play in the cell surface binding and internalization… (more)

Subjects/Keywords: Bacteria; Bromides; Dependovirus; Digestion; DNA; Electrophoresis; Enzymes; Gels; Insects; Integrins; Adenoviruses; Integrins

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APA (6th Edition):

Woodhouse, A. (2010). Integrin Expression for Use in Complexing Studies with Adeno-Associated Virus Serotype 2. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00057438

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):

Woodhouse, Andrew. “Integrin Expression for Use in Complexing Studies with Adeno-Associated Virus Serotype 2.” 2010. Thesis, University of Florida. Accessed September 16, 2019. http://ufdc.ufl.edu/AA00057438.

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

MLA Handbook (7th Edition):

Woodhouse, Andrew. “Integrin Expression for Use in Complexing Studies with Adeno-Associated Virus Serotype 2.” 2010. Web. 16 Sep 2019.

Vancouver:

Woodhouse A. Integrin Expression for Use in Complexing Studies with Adeno-Associated Virus Serotype 2. [Internet] [Thesis]. University of Florida; 2010. [cited 2019 Sep 16]. Available from: http://ufdc.ufl.edu/AA00057438.

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

Council of Science Editors:

Woodhouse A. Integrin Expression for Use in Complexing Studies with Adeno-Associated Virus Serotype 2. [Thesis]. University of Florida; 2010. Available from: http://ufdc.ufl.edu/AA00057438

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


University of Florida

24. Tartaglia, Lawrence J. Biophysical Characterization of the Cellular Interactions of Adeno-Associated Virus Serotype 2.

Degree: PhD, Medical Sciences - Biochemistry and Molecular Biology (IDP), 2013, University of Florida

 Adeno-Associated Viruses (AAVs) are currently among the mostfrequently used gene delivery vectors for gene therapy. Due to theirnon-pathogenicity, long term transgene expression, and ability to… (more)

Subjects/Keywords: Antibodies; Capsid; Dependovirus; Elution; Infections; Integrins; Kinetics; Purification; Receptors; Viruses; aav2  – defensins  – expression  – integrins  – pfastbac1  – pqetrisystem  – recombinant

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APA (6th Edition):

Tartaglia, L. J. (2013). Biophysical Characterization of the Cellular Interactions of Adeno-Associated Virus Serotype 2. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0045756

Chicago Manual of Style (16th Edition):

Tartaglia, Lawrence J. “Biophysical Characterization of the Cellular Interactions of Adeno-Associated Virus Serotype 2.” 2013. Doctoral Dissertation, University of Florida. Accessed September 16, 2019. http://ufdc.ufl.edu/UFE0045756.

MLA Handbook (7th Edition):

Tartaglia, Lawrence J. “Biophysical Characterization of the Cellular Interactions of Adeno-Associated Virus Serotype 2.” 2013. Web. 16 Sep 2019.

Vancouver:

Tartaglia LJ. Biophysical Characterization of the Cellular Interactions of Adeno-Associated Virus Serotype 2. [Internet] [Doctoral dissertation]. University of Florida; 2013. [cited 2019 Sep 16]. Available from: http://ufdc.ufl.edu/UFE0045756.

Council of Science Editors:

Tartaglia LJ. Biophysical Characterization of the Cellular Interactions of Adeno-Associated Virus Serotype 2. [Doctoral Dissertation]. University of Florida; 2013. Available from: http://ufdc.ufl.edu/UFE0045756

25. Möller, Laura Artoni. Interação celular na placenta de gestações de bovinos clonados com especial ênfase às integrinas.

Degree: PhD, Anatomia dos Animais Domésticos e Silvestres, 2009, University of São Paulo

 Integrinas são glicoproteínas transmembrânicas envolvidas na adesão célula-célula e célula-proteina da matriz extracellular (ECM) que participam da migração e fusão de células trofoblásticas gigantes (TGC)… (more)

Subjects/Keywords: ECM; ECM; Integrinas; Integrins; Placenta; Placenta; SCNT; SCNT; TIMPs; TIMPs

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APA (6th Edition):

Möller, L. A. (2009). Interação celular na placenta de gestações de bovinos clonados com especial ênfase às integrinas. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/10/10132/tde-02122009-091433/ ;

Chicago Manual of Style (16th Edition):

Möller, Laura Artoni. “Interação celular na placenta de gestações de bovinos clonados com especial ênfase às integrinas.” 2009. Doctoral Dissertation, University of São Paulo. Accessed September 16, 2019. http://www.teses.usp.br/teses/disponiveis/10/10132/tde-02122009-091433/ ;.

MLA Handbook (7th Edition):

Möller, Laura Artoni. “Interação celular na placenta de gestações de bovinos clonados com especial ênfase às integrinas.” 2009. Web. 16 Sep 2019.

Vancouver:

Möller LA. Interação celular na placenta de gestações de bovinos clonados com especial ênfase às integrinas. [Internet] [Doctoral dissertation]. University of São Paulo; 2009. [cited 2019 Sep 16]. Available from: http://www.teses.usp.br/teses/disponiveis/10/10132/tde-02122009-091433/ ;.

Council of Science Editors:

Möller LA. Interação celular na placenta de gestações de bovinos clonados com especial ênfase às integrinas. [Doctoral Dissertation]. University of São Paulo; 2009. Available from: http://www.teses.usp.br/teses/disponiveis/10/10132/tde-02122009-091433/ ;


University of Alberta

26. Searles, Gordon Edward. Adhesion of human melanocytes to extracellular matrices by integrins: effect of cell differentiation and growth on cell-substate adhesion.

Degree: MS, Department of Medicine, 1995, University of Alberta

Subjects/Keywords: Melanoma – Cytopathology.; Melanocytes.; Integrins.

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APA (6th Edition):

Searles, G. E. (1995). Adhesion of human melanocytes to extracellular matrices by integrins: effect of cell differentiation and growth on cell-substate adhesion. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/3484zj73d

Chicago Manual of Style (16th Edition):

Searles, Gordon Edward. “Adhesion of human melanocytes to extracellular matrices by integrins: effect of cell differentiation and growth on cell-substate adhesion.” 1995. Masters Thesis, University of Alberta. Accessed September 16, 2019. https://era.library.ualberta.ca/files/3484zj73d.

MLA Handbook (7th Edition):

Searles, Gordon Edward. “Adhesion of human melanocytes to extracellular matrices by integrins: effect of cell differentiation and growth on cell-substate adhesion.” 1995. Web. 16 Sep 2019.

Vancouver:

Searles GE. Adhesion of human melanocytes to extracellular matrices by integrins: effect of cell differentiation and growth on cell-substate adhesion. [Internet] [Masters thesis]. University of Alberta; 1995. [cited 2019 Sep 16]. Available from: https://era.library.ualberta.ca/files/3484zj73d.

Council of Science Editors:

Searles GE. Adhesion of human melanocytes to extracellular matrices by integrins: effect of cell differentiation and growth on cell-substate adhesion. [Masters Thesis]. University of Alberta; 1995. Available from: https://era.library.ualberta.ca/files/3484zj73d


Texas A&M University

27. Duran, Camille L. Noncanonical NF-KB Signaling Drives Glioma Invasion by Promoting MT1-MMP Activation, Pseudopodia Formation, and ITGA11 Expression.

Degree: 2017, Texas A&M University

 A hallmark of high grade glioma is highly aggressive, diffuse invasion into normal brain tissue, contributing to a 100% recurrence rate and resistance to current… (more)

Subjects/Keywords: glioma; cell invasion; noncanonical NF-kappaB; integrins; MT1-MMP

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APA (6th Edition):

Duran, C. L. (2017). Noncanonical NF-KB Signaling Drives Glioma Invasion by Promoting MT1-MMP Activation, Pseudopodia Formation, and ITGA11 Expression. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/161332

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):

Duran, Camille L. “Noncanonical NF-KB Signaling Drives Glioma Invasion by Promoting MT1-MMP Activation, Pseudopodia Formation, and ITGA11 Expression.” 2017. Thesis, Texas A&M University. Accessed September 16, 2019. http://hdl.handle.net/1969.1/161332.

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

MLA Handbook (7th Edition):

Duran, Camille L. “Noncanonical NF-KB Signaling Drives Glioma Invasion by Promoting MT1-MMP Activation, Pseudopodia Formation, and ITGA11 Expression.” 2017. Web. 16 Sep 2019.

Vancouver:

Duran CL. Noncanonical NF-KB Signaling Drives Glioma Invasion by Promoting MT1-MMP Activation, Pseudopodia Formation, and ITGA11 Expression. [Internet] [Thesis]. Texas A&M University; 2017. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1969.1/161332.

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

Council of Science Editors:

Duran CL. Noncanonical NF-KB Signaling Drives Glioma Invasion by Promoting MT1-MMP Activation, Pseudopodia Formation, and ITGA11 Expression. [Thesis]. Texas A&M University; 2017. Available from: http://hdl.handle.net/1969.1/161332

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


The Ohio State University

28. Stevens, Rachel L. Characterization of Novel Extracellular and Intracellular Modifiers of Apurinic/Apyrimidinic Endonuclease 1.

Degree: PhD, Molecular, Cellular and Developmental Biology, 2010, The Ohio State University

  Maintaining genomic integrity is essential for cellular viability. Alteration of bases can occur via exposure to reactive oxygen species. There exist cellular repair mechanisms… (more)

Subjects/Keywords: Cellular Biology; Molecular Biology; Base Excision Repair; APE1, Integrins, PIN1

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APA (6th Edition):

Stevens, R. L. (2010). Characterization of Novel Extracellular and Intracellular Modifiers of Apurinic/Apyrimidinic Endonuclease 1. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1275417842

Chicago Manual of Style (16th Edition):

Stevens, Rachel L. “Characterization of Novel Extracellular and Intracellular Modifiers of Apurinic/Apyrimidinic Endonuclease 1.” 2010. Doctoral Dissertation, The Ohio State University. Accessed September 16, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1275417842.

MLA Handbook (7th Edition):

Stevens, Rachel L. “Characterization of Novel Extracellular and Intracellular Modifiers of Apurinic/Apyrimidinic Endonuclease 1.” 2010. Web. 16 Sep 2019.

Vancouver:

Stevens RL. Characterization of Novel Extracellular and Intracellular Modifiers of Apurinic/Apyrimidinic Endonuclease 1. [Internet] [Doctoral dissertation]. The Ohio State University; 2010. [cited 2019 Sep 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1275417842.

Council of Science Editors:

Stevens RL. Characterization of Novel Extracellular and Intracellular Modifiers of Apurinic/Apyrimidinic Endonuclease 1. [Doctoral Dissertation]. The Ohio State University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1275417842


Universiteit Utrecht

29. Gaarenstroom, T.Y. Mechanotransduction via Integrins.

Degree: 2009, Universiteit Utrecht

 During life and development, tissues and individual cells within an organism are under several types of mechanical stress. Forces are being exerted upon cell-matrix adhesions… (more)

Subjects/Keywords: Geneeskunde; integrins, cytoskeleton, cancer, development, signal transduction, Rho GTPases

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APA (6th Edition):

Gaarenstroom, T. Y. (2009). Mechanotransduction via Integrins. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/37293

Chicago Manual of Style (16th Edition):

Gaarenstroom, T Y. “Mechanotransduction via Integrins.” 2009. Masters Thesis, Universiteit Utrecht. Accessed September 16, 2019. http://dspace.library.uu.nl:8080/handle/1874/37293.

MLA Handbook (7th Edition):

Gaarenstroom, T Y. “Mechanotransduction via Integrins.” 2009. Web. 16 Sep 2019.

Vancouver:

Gaarenstroom TY. Mechanotransduction via Integrins. [Internet] [Masters thesis]. Universiteit Utrecht; 2009. [cited 2019 Sep 16]. Available from: http://dspace.library.uu.nl:8080/handle/1874/37293.

Council of Science Editors:

Gaarenstroom TY. Mechanotransduction via Integrins. [Masters Thesis]. Universiteit Utrecht; 2009. Available from: http://dspace.library.uu.nl:8080/handle/1874/37293

30. Δαλέτος, Γεώργιος. Ανάπτυξη νέων συνθετικών ολιγοπεπτιδίων της κυστεΐνης και μελέτη της δράσης αυτών έναντι της α4β1 ιντεγκρίνης.

Degree: 2010, University of Patras

Oι ιντεγκρίνες είναι κυτταρικοί υποδοχείς, οι οποίοι αλληλεπιδρούν με την εξωκυττάρια ύλη. Μέχρι σήμερα έχουν ανακαλυφθεί 18α και 8β υπομονάδες συνδυασμός των οποίων δημιουργεί 24… (more)

Subjects/Keywords: Ολιγοπεπτίδια; Κυστεΐνη; α4β1; Ιντεγκρίνες; 616.106; Oligopeptides; Cysteine; Integrins

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APA (6th Edition):

Δαλέτος, . (2010). Ανάπτυξη νέων συνθετικών ολιγοπεπτιδίων της κυστεΐνης και μελέτη της δράσης αυτών έναντι της α4β1 ιντεγκρίνης. (Masters Thesis). University of Patras. Retrieved from http://nemertes.lis.upatras.gr/jspui/handle/10889/4627

Chicago Manual of Style (16th Edition):

Δαλέτος, Γεώργιος. “Ανάπτυξη νέων συνθετικών ολιγοπεπτιδίων της κυστεΐνης και μελέτη της δράσης αυτών έναντι της α4β1 ιντεγκρίνης.” 2010. Masters Thesis, University of Patras. Accessed September 16, 2019. http://nemertes.lis.upatras.gr/jspui/handle/10889/4627.

MLA Handbook (7th Edition):

Δαλέτος, Γεώργιος. “Ανάπτυξη νέων συνθετικών ολιγοπεπτιδίων της κυστεΐνης και μελέτη της δράσης αυτών έναντι της α4β1 ιντεγκρίνης.” 2010. Web. 16 Sep 2019.

Vancouver:

Δαλέτος . Ανάπτυξη νέων συνθετικών ολιγοπεπτιδίων της κυστεΐνης και μελέτη της δράσης αυτών έναντι της α4β1 ιντεγκρίνης. [Internet] [Masters thesis]. University of Patras; 2010. [cited 2019 Sep 16]. Available from: http://nemertes.lis.upatras.gr/jspui/handle/10889/4627.

Council of Science Editors:

Δαλέτος . Ανάπτυξη νέων συνθετικών ολιγοπεπτιδίων της κυστεΐνης και μελέτη της δράσης αυτών έναντι της α4β1 ιντεγκρίνης. [Masters Thesis]. University of Patras; 2010. Available from: http://nemertes.lis.upatras.gr/jspui/handle/10889/4627

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