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You searched for subject:(vascular smooth muscle). Showing records 1 – 30 of 274 total matches.

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University of Cambridge

1. Nakagaki Silva, Erick Eidy. Identification of RBPMS as a smooth muscle master splicing regulator via association of its gene with super-enhancers .

Degree: 2020, University of Cambridge

 Alternative splicing (AS) is primarily regulated by regulatory RNA-binding proteins (RBPs). It has been suggested that a small number of master splicing regulators might control… (more)

Subjects/Keywords: RBPMS; Vascular smooth muscle cells; Alternative splicing; PAC1 cells

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APA (6th Edition):

Nakagaki Silva, E. E. (2020). Identification of RBPMS as a smooth muscle master splicing regulator via association of its gene with super-enhancers . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/297676

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):

Nakagaki Silva, Erick Eidy. “Identification of RBPMS as a smooth muscle master splicing regulator via association of its gene with super-enhancers .” 2020. Thesis, University of Cambridge. Accessed October 23, 2019. https://www.repository.cam.ac.uk/handle/1810/297676.

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

MLA Handbook (7th Edition):

Nakagaki Silva, Erick Eidy. “Identification of RBPMS as a smooth muscle master splicing regulator via association of its gene with super-enhancers .” 2020. Web. 23 Oct 2019.

Vancouver:

Nakagaki Silva EE. Identification of RBPMS as a smooth muscle master splicing regulator via association of its gene with super-enhancers . [Internet] [Thesis]. University of Cambridge; 2020. [cited 2019 Oct 23]. Available from: https://www.repository.cam.ac.uk/handle/1810/297676.

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

Council of Science Editors:

Nakagaki Silva EE. Identification of RBPMS as a smooth muscle master splicing regulator via association of its gene with super-enhancers . [Thesis]. University of Cambridge; 2020. Available from: https://www.repository.cam.ac.uk/handle/1810/297676

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


Université de Montréal

2. Arts, Monique. Systemic sclerosis immunoglobulin induces growth and a pro-fibrotic state in vascular smooth muscle cells through the epidermal growth factor receptor .

Degree: 2019, Université de Montréal

Subjects/Keywords: Sclérose systémique; Sclérodermie; Autoanticorps; Cellules musculaires lisses vasculaires; Inhibiteurs des protéines kinases; Transactivation des récepteurs; RPDGF; REGF; Systemic sclerosis; Scleroderma; Vascular smooth muscle cells; Autoantibodies; Protein kinase inhibitors; Receptor transactivation; Platelet-derived growth factor receptor; Epidermal growth factor receptor; PDGFR; EGFR

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APA (6th Edition):

Arts, M. (2019). Systemic sclerosis immunoglobulin induces growth and a pro-fibrotic state in vascular smooth muscle cells through the epidermal growth factor receptor . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/22094

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):

Arts, Monique. “Systemic sclerosis immunoglobulin induces growth and a pro-fibrotic state in vascular smooth muscle cells through the epidermal growth factor receptor .” 2019. Thesis, Université de Montréal. Accessed October 23, 2019. http://hdl.handle.net/1866/22094.

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

MLA Handbook (7th Edition):

Arts, Monique. “Systemic sclerosis immunoglobulin induces growth and a pro-fibrotic state in vascular smooth muscle cells through the epidermal growth factor receptor .” 2019. Web. 23 Oct 2019.

Vancouver:

Arts M. Systemic sclerosis immunoglobulin induces growth and a pro-fibrotic state in vascular smooth muscle cells through the epidermal growth factor receptor . [Internet] [Thesis]. Université de Montréal; 2019. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/1866/22094.

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

Council of Science Editors:

Arts M. Systemic sclerosis immunoglobulin induces growth and a pro-fibrotic state in vascular smooth muscle cells through the epidermal growth factor receptor . [Thesis]. Université de Montréal; 2019. Available from: http://hdl.handle.net/1866/22094

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


University of Cambridge

3. Harman, Jennifer. Investigating the role of histone H3 lysine 9 dimethylation in regulating disease-associated vascular smooth muscle cell gene expression .

Degree: 2019, University of Cambridge

 Widespread changes in gene expression accompany vascular smooth muscle cell (VSMC) phenotypic switching, a hallmark of vascular disease. Upon insult, VSMCs downregulate contractile proteins and… (more)

Subjects/Keywords: Vascular smooth muscle cell; H3K9me2; Vascular smooth muscle cell phenotypic switch

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APA (6th Edition):

Harman, J. (2019). Investigating the role of histone H3 lysine 9 dimethylation in regulating disease-associated vascular smooth muscle cell gene expression . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/289975

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):

Harman, Jennifer. “Investigating the role of histone H3 lysine 9 dimethylation in regulating disease-associated vascular smooth muscle cell gene expression .” 2019. Thesis, University of Cambridge. Accessed October 23, 2019. https://www.repository.cam.ac.uk/handle/1810/289975.

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

MLA Handbook (7th Edition):

Harman, Jennifer. “Investigating the role of histone H3 lysine 9 dimethylation in regulating disease-associated vascular smooth muscle cell gene expression .” 2019. Web. 23 Oct 2019.

Vancouver:

Harman J. Investigating the role of histone H3 lysine 9 dimethylation in regulating disease-associated vascular smooth muscle cell gene expression . [Internet] [Thesis]. University of Cambridge; 2019. [cited 2019 Oct 23]. Available from: https://www.repository.cam.ac.uk/handle/1810/289975.

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

Council of Science Editors:

Harman J. Investigating the role of histone H3 lysine 9 dimethylation in regulating disease-associated vascular smooth muscle cell gene expression . [Thesis]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/289975

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


University of Sydney

4. Manuneedhi Cholan, Pradeep. TRAIL: A novel atheroprotective mechanism in the vasculature .

Degree: 2019, University of Sydney

 The vasculature is critical for the maintenance of cardiovascular homeostasis. Cardiovascular disease (CVD) is characterised by endothelial cell (EC) and vascular smooth muscle cell (VSMC)… (more)

Subjects/Keywords: TRAIL; CVD; endothelium; vascular smooth muscle cells; Angiotensin II

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APA (6th Edition):

Manuneedhi Cholan, P. (2019). TRAIL: A novel atheroprotective mechanism in the vasculature . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/20949

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):

Manuneedhi Cholan, Pradeep. “TRAIL: A novel atheroprotective mechanism in the vasculature .” 2019. Thesis, University of Sydney. Accessed October 23, 2019. http://hdl.handle.net/2123/20949.

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

MLA Handbook (7th Edition):

Manuneedhi Cholan, Pradeep. “TRAIL: A novel atheroprotective mechanism in the vasculature .” 2019. Web. 23 Oct 2019.

Vancouver:

Manuneedhi Cholan P. TRAIL: A novel atheroprotective mechanism in the vasculature . [Internet] [Thesis]. University of Sydney; 2019. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/2123/20949.

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

Council of Science Editors:

Manuneedhi Cholan P. TRAIL: A novel atheroprotective mechanism in the vasculature . [Thesis]. University of Sydney; 2019. Available from: http://hdl.handle.net/2123/20949

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


University of Cambridge

5. Harman, Jennifer. Investigating the role of histone H3 lysine 9 dimethylation in regulating disease-associated vascular smooth muscle cell gene expression.

Degree: PhD, 2019, University of Cambridge

 Widespread changes in gene expression accompany vascular smooth muscle cell (VSMC) phenotypic switching, a hallmark of vascular disease. Upon insult, VSMCs downregulate contractile proteins and… (more)

Subjects/Keywords: Vascular smooth muscle cell; H3K9me2; Vascular smooth muscle cell phenotypic switch

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APA (6th Edition):

Harman, J. (2019). Investigating the role of histone H3 lysine 9 dimethylation in regulating disease-associated vascular smooth muscle cell gene expression. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/289975 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767866

Chicago Manual of Style (16th Edition):

Harman, Jennifer. “Investigating the role of histone H3 lysine 9 dimethylation in regulating disease-associated vascular smooth muscle cell gene expression.” 2019. Doctoral Dissertation, University of Cambridge. Accessed October 23, 2019. https://www.repository.cam.ac.uk/handle/1810/289975 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767866.

MLA Handbook (7th Edition):

Harman, Jennifer. “Investigating the role of histone H3 lysine 9 dimethylation in regulating disease-associated vascular smooth muscle cell gene expression.” 2019. Web. 23 Oct 2019.

Vancouver:

Harman J. Investigating the role of histone H3 lysine 9 dimethylation in regulating disease-associated vascular smooth muscle cell gene expression. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2019 Oct 23]. Available from: https://www.repository.cam.ac.uk/handle/1810/289975 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767866.

Council of Science Editors:

Harman J. Investigating the role of histone H3 lysine 9 dimethylation in regulating disease-associated vascular smooth muscle cell gene expression. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/289975 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.767866


University of Cambridge

6. Reinhold, Johannes. Mitochondrial function in atherosclerosis and vascular smooth muscle cells.

Degree: PhD, 2019, University of Cambridge

 Atherosclerosis is the leading cause of death in the Western world. Although mitochondrial DNA (mtDNA) damage has been implicated in atherosclerosis, it is unclear whether… (more)

Subjects/Keywords: Atherosclerosis; Mitochondria; vascular smooth muscle cells

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APA (6th Edition):

Reinhold, J. (2019). Mitochondrial function in atherosclerosis and vascular smooth muscle cells. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/288352 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763838

Chicago Manual of Style (16th Edition):

Reinhold, Johannes. “Mitochondrial function in atherosclerosis and vascular smooth muscle cells.” 2019. Doctoral Dissertation, University of Cambridge. Accessed October 23, 2019. https://www.repository.cam.ac.uk/handle/1810/288352 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763838.

MLA Handbook (7th Edition):

Reinhold, Johannes. “Mitochondrial function in atherosclerosis and vascular smooth muscle cells.” 2019. Web. 23 Oct 2019.

Vancouver:

Reinhold J. Mitochondrial function in atherosclerosis and vascular smooth muscle cells. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2019 Oct 23]. Available from: https://www.repository.cam.ac.uk/handle/1810/288352 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763838.

Council of Science Editors:

Reinhold J. Mitochondrial function in atherosclerosis and vascular smooth muscle cells. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/288352 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763838


Queen Mary, University of London

7. Afzal, T. A. Functional roles of microRNA-214 in modulating smooth muscle cell functions and neointima formation.

Degree: PhD, 2019, Queen Mary, University of London

Vascular Smooth Muscle cells (VSMCs) have very important role in pathogenesis of atherosclerosis and neointima formation. VSMCs phenotype switching and resultant increase in migration and… (more)

Subjects/Keywords: Vascular Smooth Muscle cells; neointima formation; microRNA; vascular disease.

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APA (6th Edition):

Afzal, T. A. (2019). Functional roles of microRNA-214 in modulating smooth muscle cell functions and neointima formation. (Doctoral Dissertation). Queen Mary, University of London. Retrieved from http://qmro.qmul.ac.uk/xmlui/handle/123456789/56650 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.775323

Chicago Manual of Style (16th Edition):

Afzal, T A. “Functional roles of microRNA-214 in modulating smooth muscle cell functions and neointima formation.” 2019. Doctoral Dissertation, Queen Mary, University of London. Accessed October 23, 2019. http://qmro.qmul.ac.uk/xmlui/handle/123456789/56650 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.775323.

MLA Handbook (7th Edition):

Afzal, T A. “Functional roles of microRNA-214 in modulating smooth muscle cell functions and neointima formation.” 2019. Web. 23 Oct 2019.

Vancouver:

Afzal TA. Functional roles of microRNA-214 in modulating smooth muscle cell functions and neointima formation. [Internet] [Doctoral dissertation]. Queen Mary, University of London; 2019. [cited 2019 Oct 23]. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/56650 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.775323.

Council of Science Editors:

Afzal TA. Functional roles of microRNA-214 in modulating smooth muscle cell functions and neointima formation. [Doctoral Dissertation]. Queen Mary, University of London; 2019. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/56650 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.775323


Freie Universität Berlin

8. Braun, Diana. Hypoxie und Nierengefäßfunktion.

Degree: 2019, Freie Universität Berlin

 The ischemia reperfusion injury (IRI) is an important pathophysiological factor in the development of acute kidney injury (AKI). IRI goes along with hypoxia and re-oxygenation… (more)

Subjects/Keywords: hypoxia; ischemia/ reperfusion injury; nitric oxide; cGMP; sGC; relaxation; vascular smooth muscle; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit

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APA (6th Edition):

Braun, D. (2019). Hypoxie und Nierengefäßfunktion. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-1791

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):

Braun, Diana. “Hypoxie und Nierengefäßfunktion.” 2019. Thesis, Freie Universität Berlin. Accessed October 23, 2019. http://dx.doi.org/10.17169/refubium-1791.

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

MLA Handbook (7th Edition):

Braun, Diana. “Hypoxie und Nierengefäßfunktion.” 2019. Web. 23 Oct 2019.

Vancouver:

Braun D. Hypoxie und Nierengefäßfunktion. [Internet] [Thesis]. Freie Universität Berlin; 2019. [cited 2019 Oct 23]. Available from: http://dx.doi.org/10.17169/refubium-1791.

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

Council of Science Editors:

Braun D. Hypoxie und Nierengefäßfunktion. [Thesis]. Freie Universität Berlin; 2019. Available from: http://dx.doi.org/10.17169/refubium-1791

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

9. El Dirani, Zeinab. Effet de l’hypoxie intermittente et de l’entraînement physique intensif sur la structure et la fonction du tissu musculaire chez le rat. : The effects of intermittent hypoxia and intensive physical training on the structure and the function of muscle tissue in rat.

Degree: Docteur es, Physiologie physiopathologies pharmacologie, 2018, Grenoble Alpes; Université libanaise

 Le syndrome d'apnée obstructive du sommeil (SAOS), est une maladie chronique qui se caractérise par des interruptions répétées de la respiration durant le sommeil en… (more)

Subjects/Keywords: Hypoxie intermittente chronique; Apnée du sommeil; Cellules musculaires lisses et squelettiques; Élasticité; Contractilité vasculaire; Vieillissement; Chronic intermittent hypoxia; Sleep apnea; Smooth and skeletal muscle cells; Elasticity; Vascular contractility; Aging; 610

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APA (6th Edition):

El Dirani, Z. (2018). Effet de l’hypoxie intermittente et de l’entraînement physique intensif sur la structure et la fonction du tissu musculaire chez le rat. : The effects of intermittent hypoxia and intensive physical training on the structure and the function of muscle tissue in rat. (Doctoral Dissertation). Grenoble Alpes; Université libanaise. Retrieved from http://www.theses.fr/2018GREAV067

Chicago Manual of Style (16th Edition):

El Dirani, Zeinab. “Effet de l’hypoxie intermittente et de l’entraînement physique intensif sur la structure et la fonction du tissu musculaire chez le rat. : The effects of intermittent hypoxia and intensive physical training on the structure and the function of muscle tissue in rat.” 2018. Doctoral Dissertation, Grenoble Alpes; Université libanaise. Accessed October 23, 2019. http://www.theses.fr/2018GREAV067.

MLA Handbook (7th Edition):

El Dirani, Zeinab. “Effet de l’hypoxie intermittente et de l’entraînement physique intensif sur la structure et la fonction du tissu musculaire chez le rat. : The effects of intermittent hypoxia and intensive physical training on the structure and the function of muscle tissue in rat.” 2018. Web. 23 Oct 2019.

Vancouver:

El Dirani Z. Effet de l’hypoxie intermittente et de l’entraînement physique intensif sur la structure et la fonction du tissu musculaire chez le rat. : The effects of intermittent hypoxia and intensive physical training on the structure and the function of muscle tissue in rat. [Internet] [Doctoral dissertation]. Grenoble Alpes; Université libanaise; 2018. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2018GREAV067.

Council of Science Editors:

El Dirani Z. Effet de l’hypoxie intermittente et de l’entraînement physique intensif sur la structure et la fonction du tissu musculaire chez le rat. : The effects of intermittent hypoxia and intensive physical training on the structure and the function of muscle tissue in rat. [Doctoral Dissertation]. Grenoble Alpes; Université libanaise; 2018. Available from: http://www.theses.fr/2018GREAV067


Clemson University

10. Bradley, Suzanne Nicole. Stretching Vascular Smooth Muscle Cells on Micropatterned Surfaces.

Degree: MS, Bioengineering, 2018, Clemson University

Vascular smooth muscle cells regulate blood flow by contracting and relaxing blood vessels. Vascular smooth muscle cells display one of two distinct phenotypes: contractile or… (more)

Subjects/Keywords: Cell Stretching; Micropatterning; Microstamping; Vascular Smooth Muscle Cells

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APA (6th Edition):

Bradley, S. N. (2018). Stretching Vascular Smooth Muscle Cells on Micropatterned Surfaces. (Masters Thesis). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_theses/2957

Chicago Manual of Style (16th Edition):

Bradley, Suzanne Nicole. “Stretching Vascular Smooth Muscle Cells on Micropatterned Surfaces.” 2018. Masters Thesis, Clemson University. Accessed October 23, 2019. https://tigerprints.clemson.edu/all_theses/2957.

MLA Handbook (7th Edition):

Bradley, Suzanne Nicole. “Stretching Vascular Smooth Muscle Cells on Micropatterned Surfaces.” 2018. Web. 23 Oct 2019.

Vancouver:

Bradley SN. Stretching Vascular Smooth Muscle Cells on Micropatterned Surfaces. [Internet] [Masters thesis]. Clemson University; 2018. [cited 2019 Oct 23]. Available from: https://tigerprints.clemson.edu/all_theses/2957.

Council of Science Editors:

Bradley SN. Stretching Vascular Smooth Muscle Cells on Micropatterned Surfaces. [Masters Thesis]. Clemson University; 2018. Available from: https://tigerprints.clemson.edu/all_theses/2957


University of Cambridge

11. Chappell, Joel. Vascular smooth muscle cell heterogeneity and plasticity in models of cardiovascular disease .

Degree: 2018, University of Cambridge

Vascular smooth muscle cell (VSMC) accumulation is a hallmark of atherosclerosis and vascular injury. However, fundamental aspects of proliferation and the phenotypic changes within individual… (more)

Subjects/Keywords: vascular smooth muscle cells; single cell RNA sequencing; cellular heterogeneity; heart disease; atherosclerosis; carotid ligation; clonal expansion; brainbow; multi-colour lineage tracing; confetti

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APA (6th Edition):

Chappell, J. (2018). Vascular smooth muscle cell heterogeneity and plasticity in models of cardiovascular disease . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/274543

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):

Chappell, Joel. “Vascular smooth muscle cell heterogeneity and plasticity in models of cardiovascular disease .” 2018. Thesis, University of Cambridge. Accessed October 23, 2019. https://www.repository.cam.ac.uk/handle/1810/274543.

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

MLA Handbook (7th Edition):

Chappell, Joel. “Vascular smooth muscle cell heterogeneity and plasticity in models of cardiovascular disease .” 2018. Web. 23 Oct 2019.

Vancouver:

Chappell J. Vascular smooth muscle cell heterogeneity and plasticity in models of cardiovascular disease . [Internet] [Thesis]. University of Cambridge; 2018. [cited 2019 Oct 23]. Available from: https://www.repository.cam.ac.uk/handle/1810/274543.

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

Council of Science Editors:

Chappell J. Vascular smooth muscle cell heterogeneity and plasticity in models of cardiovascular disease . [Thesis]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/274543

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

12. Benito, Manuel. Potential role of insulin receptor isoforms and IGF receptors in plaque instability of human and experimental atherosclerosis.

Degree: 2018, BioMed Central

Subjects/Keywords: Apoptosis; Atherosclerosis; Insulin receptor isoforms; Insulin-like growth factor receptor; Vascular smooth muscle cells; Medicina

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APA (6th Edition):

Benito, M. (2018). Potential role of insulin receptor isoforms and IGF receptors in plaque instability of human and experimental atherosclerosis. (Thesis). BioMed Central. Retrieved from http://hdl.handle.net/10486/682524

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):

Benito, Manuel. “Potential role of insulin receptor isoforms and IGF receptors in plaque instability of human and experimental atherosclerosis.” 2018. Thesis, BioMed Central. Accessed October 23, 2019. http://hdl.handle.net/10486/682524.

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

MLA Handbook (7th Edition):

Benito, Manuel. “Potential role of insulin receptor isoforms and IGF receptors in plaque instability of human and experimental atherosclerosis.” 2018. Web. 23 Oct 2019.

Vancouver:

Benito M. Potential role of insulin receptor isoforms and IGF receptors in plaque instability of human and experimental atherosclerosis. [Internet] [Thesis]. BioMed Central; 2018. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10486/682524.

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

Council of Science Editors:

Benito M. Potential role of insulin receptor isoforms and IGF receptors in plaque instability of human and experimental atherosclerosis. [Thesis]. BioMed Central; 2018. Available from: http://hdl.handle.net/10486/682524

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

13. Salaices, M. HuR mediates the synergistic effects of angiotensin II and IL-1β on vascular COX-2 expression and cell migration.

Degree: 2018, The British Pharmacological Society

Subjects/Keywords: Cell migration; Cytokines; Inflammatory mediators; Smooth muscle cells; Vascular remodeling; Farmacia

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APA (6th Edition):

Salaices, M. (2018). HuR mediates the synergistic effects of angiotensin II and IL-1β on vascular COX-2 expression and cell migration. (Thesis). The British Pharmacological Society. Retrieved from http://hdl.handle.net/10486/671177

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):

Salaices, M. “HuR mediates the synergistic effects of angiotensin II and IL-1β on vascular COX-2 expression and cell migration.” 2018. Thesis, The British Pharmacological Society. Accessed October 23, 2019. http://hdl.handle.net/10486/671177.

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

MLA Handbook (7th Edition):

Salaices, M. “HuR mediates the synergistic effects of angiotensin II and IL-1β on vascular COX-2 expression and cell migration.” 2018. Web. 23 Oct 2019.

Vancouver:

Salaices M. HuR mediates the synergistic effects of angiotensin II and IL-1β on vascular COX-2 expression and cell migration. [Internet] [Thesis]. The British Pharmacological Society; 2018. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10486/671177.

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

Council of Science Editors:

Salaices M. HuR mediates the synergistic effects of angiotensin II and IL-1β on vascular COX-2 expression and cell migration. [Thesis]. The British Pharmacological Society; 2018. Available from: http://hdl.handle.net/10486/671177

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

14. Roszkowska, Monika. Mécanismes moléculaires de la transdifférenciation des cellules musculaires lisses et calcification dans l'athérosclérose : Molecular mechanisms of vascular smooth muscle cell trans-differentiation and calcification in atherosclerosis.

Degree: Docteur es, Biochimie, 2018, Lyon; Instytut biologii doświadczalnej im. M. Nenckiego (Pologne)

Chez les patients atteints d'athérosclérose, les calcifications vasculaires sont une caracteristique des plaques d'athérome. Elles résultent de la trans-différenciation des cellules musculaires lisses (CMLs) en… (more)

Subjects/Keywords: Cellule musculaire lisse; Phosphatase alcaline; Calcification vasculaire; Chondrocyte; Vascular smooth muscle cell; Tissue-nonspecific alkaline phosphatase; Vascular calcification; Chondrocyte; 572

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APA (6th Edition):

Roszkowska, M. (2018). Mécanismes moléculaires de la transdifférenciation des cellules musculaires lisses et calcification dans l'athérosclérose : Molecular mechanisms of vascular smooth muscle cell trans-differentiation and calcification in atherosclerosis. (Doctoral Dissertation). Lyon; Instytut biologii doświadczalnej im. M. Nenckiego (Pologne). Retrieved from http://www.theses.fr/2018LYSE1059

Chicago Manual of Style (16th Edition):

Roszkowska, Monika. “Mécanismes moléculaires de la transdifférenciation des cellules musculaires lisses et calcification dans l'athérosclérose : Molecular mechanisms of vascular smooth muscle cell trans-differentiation and calcification in atherosclerosis.” 2018. Doctoral Dissertation, Lyon; Instytut biologii doświadczalnej im. M. Nenckiego (Pologne). Accessed October 23, 2019. http://www.theses.fr/2018LYSE1059.

MLA Handbook (7th Edition):

Roszkowska, Monika. “Mécanismes moléculaires de la transdifférenciation des cellules musculaires lisses et calcification dans l'athérosclérose : Molecular mechanisms of vascular smooth muscle cell trans-differentiation and calcification in atherosclerosis.” 2018. Web. 23 Oct 2019.

Vancouver:

Roszkowska M. Mécanismes moléculaires de la transdifférenciation des cellules musculaires lisses et calcification dans l'athérosclérose : Molecular mechanisms of vascular smooth muscle cell trans-differentiation and calcification in atherosclerosis. [Internet] [Doctoral dissertation]. Lyon; Instytut biologii doświadczalnej im. M. Nenckiego (Pologne); 2018. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2018LYSE1059.

Council of Science Editors:

Roszkowska M. Mécanismes moléculaires de la transdifférenciation des cellules musculaires lisses et calcification dans l'athérosclérose : Molecular mechanisms of vascular smooth muscle cell trans-differentiation and calcification in atherosclerosis. [Doctoral Dissertation]. Lyon; Instytut biologii doświadczalnej im. M. Nenckiego (Pologne); 2018. Available from: http://www.theses.fr/2018LYSE1059


Kyoto University

15. Isehaq, Saif Said Al-Huseini. Deletion of IκB-Kinase β in Smooth Muscle Cells Induces Vascular Calcification Through β-Catenin-Runt-Related Transcription Factor 2 Signaling .

Degree: 2018, Kyoto University

Subjects/Keywords: Vascular calcification; Inflammation; NF-kappaB; β-catenin; Smooth muscle cells

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APA (6th Edition):

Isehaq, S. S. A. (2018). Deletion of IκB-Kinase β in Smooth Muscle Cells Induces Vascular Calcification Through β-Catenin-Runt-Related Transcription Factor 2 Signaling . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/232306

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):

Isehaq, Saif Said Al-Huseini. “Deletion of IκB-Kinase β in Smooth Muscle Cells Induces Vascular Calcification Through β-Catenin-Runt-Related Transcription Factor 2 Signaling .” 2018. Thesis, Kyoto University. Accessed October 23, 2019. http://hdl.handle.net/2433/232306.

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

MLA Handbook (7th Edition):

Isehaq, Saif Said Al-Huseini. “Deletion of IκB-Kinase β in Smooth Muscle Cells Induces Vascular Calcification Through β-Catenin-Runt-Related Transcription Factor 2 Signaling .” 2018. Web. 23 Oct 2019.

Vancouver:

Isehaq SSA. Deletion of IκB-Kinase β in Smooth Muscle Cells Induces Vascular Calcification Through β-Catenin-Runt-Related Transcription Factor 2 Signaling . [Internet] [Thesis]. Kyoto University; 2018. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/2433/232306.

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

Council of Science Editors:

Isehaq SSA. Deletion of IκB-Kinase β in Smooth Muscle Cells Induces Vascular Calcification Through β-Catenin-Runt-Related Transcription Factor 2 Signaling . [Thesis]. Kyoto University; 2018. Available from: http://hdl.handle.net/2433/232306

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


Virginia Tech

16. Ledford, Benjamin. Keratose Hydrogels Promote Vascular Smooth Muscle Differentiation from c-kit+ Human Cardiac Stem Cells: Underlying Mechanism and Therapeutic Potential.

Degree: PhD, Biomedical and Veterinary Sciences, 2018, Virginia Tech

 Cardiovascular disease is the leading cause of death in the United States, and coronary artery disease (CAD) kills over 370,000 people annually. There are available… (more)

Subjects/Keywords: Keratin/Keratose; Biomaterials; Human c-kit+ cardiac stem cells; Differentiation; Vascular smooth muscle cells; Hind limb ischemic mouse model; Laser Doppler Imaging; Blood flow; Cardiovascular diseases

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APA (6th Edition):

Ledford, B. (2018). Keratose Hydrogels Promote Vascular Smooth Muscle Differentiation from c-kit+ Human Cardiac Stem Cells: Underlying Mechanism and Therapeutic Potential. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/93593

Chicago Manual of Style (16th Edition):

Ledford, Benjamin. “Keratose Hydrogels Promote Vascular Smooth Muscle Differentiation from c-kit+ Human Cardiac Stem Cells: Underlying Mechanism and Therapeutic Potential.” 2018. Doctoral Dissertation, Virginia Tech. Accessed October 23, 2019. http://hdl.handle.net/10919/93593.

MLA Handbook (7th Edition):

Ledford, Benjamin. “Keratose Hydrogels Promote Vascular Smooth Muscle Differentiation from c-kit+ Human Cardiac Stem Cells: Underlying Mechanism and Therapeutic Potential.” 2018. Web. 23 Oct 2019.

Vancouver:

Ledford B. Keratose Hydrogels Promote Vascular Smooth Muscle Differentiation from c-kit+ Human Cardiac Stem Cells: Underlying Mechanism and Therapeutic Potential. [Internet] [Doctoral dissertation]. Virginia Tech; 2018. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10919/93593.

Council of Science Editors:

Ledford B. Keratose Hydrogels Promote Vascular Smooth Muscle Differentiation from c-kit+ Human Cardiac Stem Cells: Underlying Mechanism and Therapeutic Potential. [Doctoral Dissertation]. Virginia Tech; 2018. Available from: http://hdl.handle.net/10919/93593


Université de Montréal

17. Charles, Ricardo. Rôle des ARFs dans la migration et la régulation phénotypique des cellules du muscle lisse vasculaire .

Degree: 2018, Université de Montréal

Subjects/Keywords: Muscle lisse vasculaire; ARF6; ARF1; Athérosclérose; Angiotensine II; Bêta-arrestine; Clathrine; ERK; Akt; Vascular smooth muscle; Atherosclerosis; Angiotensin II; Beta-arrestin; Clathrin

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APA (6th Edition):

Charles, R. (2018). Rôle des ARFs dans la migration et la régulation phénotypique des cellules du muscle lisse vasculaire . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/20267

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):

Charles, Ricardo. “Rôle des ARFs dans la migration et la régulation phénotypique des cellules du muscle lisse vasculaire .” 2018. Thesis, Université de Montréal. Accessed October 23, 2019. http://hdl.handle.net/1866/20267.

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

MLA Handbook (7th Edition):

Charles, Ricardo. “Rôle des ARFs dans la migration et la régulation phénotypique des cellules du muscle lisse vasculaire .” 2018. Web. 23 Oct 2019.

Vancouver:

Charles R. Rôle des ARFs dans la migration et la régulation phénotypique des cellules du muscle lisse vasculaire . [Internet] [Thesis]. Université de Montréal; 2018. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/1866/20267.

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

Council of Science Editors:

Charles R. Rôle des ARFs dans la migration et la régulation phénotypique des cellules du muscle lisse vasculaire . [Thesis]. Université de Montréal; 2018. Available from: http://hdl.handle.net/1866/20267

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


University of California – Irvine

18. Albay, Ricardo. Characterization of a pathogenic conformation of amyloid immunoreactivity in Alzheimer’s Disease and Cerebral Amyloid Angiopathy.

Degree: Biological Sciences, 2018, University of California – Irvine

 ABSTRACT OF THE DISSERTATIONCharacterization of a pathogenic conformation of amyloid immunoreactivity in Alzheimer’s Disease and Cerebral Amyloid AngiopathyByRicardo Albay IIIDoctor of Philosophy in Biological SciencesUniversity… (more)

Subjects/Keywords: Molecular biology; Biochemistry; Alzheimer's Disease; amyloid; antibody; ; Cerebral Vascular Angiopathy; smooth muscle

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APA (6th Edition):

Albay, R. (2018). Characterization of a pathogenic conformation of amyloid immunoreactivity in Alzheimer’s Disease and Cerebral Amyloid Angiopathy. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/1xp4f2kt

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):

Albay, Ricardo. “Characterization of a pathogenic conformation of amyloid immunoreactivity in Alzheimer’s Disease and Cerebral Amyloid Angiopathy.” 2018. Thesis, University of California – Irvine. Accessed October 23, 2019. http://www.escholarship.org/uc/item/1xp4f2kt.

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

MLA Handbook (7th Edition):

Albay, Ricardo. “Characterization of a pathogenic conformation of amyloid immunoreactivity in Alzheimer’s Disease and Cerebral Amyloid Angiopathy.” 2018. Web. 23 Oct 2019.

Vancouver:

Albay R. Characterization of a pathogenic conformation of amyloid immunoreactivity in Alzheimer’s Disease and Cerebral Amyloid Angiopathy. [Internet] [Thesis]. University of California – Irvine; 2018. [cited 2019 Oct 23]. Available from: http://www.escholarship.org/uc/item/1xp4f2kt.

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

Council of Science Editors:

Albay R. Characterization of a pathogenic conformation of amyloid immunoreactivity in Alzheimer’s Disease and Cerebral Amyloid Angiopathy. [Thesis]. University of California – Irvine; 2018. Available from: http://www.escholarship.org/uc/item/1xp4f2kt

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


Boston University

19. Rim, Nae Gyune. Micropatterned cell sheets as structural building blocks for biomimetic vascular patch application.

Degree: PhD, Biomedical Engineering, 2018, Boston University

 To successfully develop a functional tissue-engineered vascular patch, recapitulating the hierarchical structure of vessel is critical to mimic mechanical properties. Here, we use a cell… (more)

Subjects/Keywords: Biomedical engineering; Finite element modeling; Hydrogel; Tensile testing; Vascular smooth muscle cell

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APA (6th Edition):

Rim, N. G. (2018). Micropatterned cell sheets as structural building blocks for biomimetic vascular patch application. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/30707

Chicago Manual of Style (16th Edition):

Rim, Nae Gyune. “Micropatterned cell sheets as structural building blocks for biomimetic vascular patch application.” 2018. Doctoral Dissertation, Boston University. Accessed October 23, 2019. http://hdl.handle.net/2144/30707.

MLA Handbook (7th Edition):

Rim, Nae Gyune. “Micropatterned cell sheets as structural building blocks for biomimetic vascular patch application.” 2018. Web. 23 Oct 2019.

Vancouver:

Rim NG. Micropatterned cell sheets as structural building blocks for biomimetic vascular patch application. [Internet] [Doctoral dissertation]. Boston University; 2018. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/2144/30707.

Council of Science Editors:

Rim NG. Micropatterned cell sheets as structural building blocks for biomimetic vascular patch application. [Doctoral Dissertation]. Boston University; 2018. Available from: http://hdl.handle.net/2144/30707

20. Mallis, Panagioits. Δημιουργία αγγείων από ανθρώπινο ομφάλιο λώρο και μελέτη της λειτουργικότητας τους πριν και μετά την κρυοκατάψυξη τους.

Degree: 2018, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

One of the biggest challenges in modern medicine is the development of functional small diameter vascular grafts (<2 mm). These grafts can be applied widely… (more)

Subjects/Keywords: Αγγειακά μοσχεύματα; ομφαλικές αρτηρίες; καρδιαγγιαγειακή νόσος; Μεσεγχυματικά στελεχιαία κύτταρα; Στεφανιαία αρτηρία; Λεία Μυϊκά Κύτταρα των Αγγείων; vascular grafts; umbilical arteries; Cardiovascular disease; Mesenchymal stem cells; Coronary artery; Vascular smooth muscle cells

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APA (6th Edition):

Mallis, P. (2018). Δημιουργία αγγείων από ανθρώπινο ομφάλιο λώρο και μελέτη της λειτουργικότητας τους πριν και μετά την κρυοκατάψυξη τους. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/44482

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):

Mallis, Panagioits. “Δημιουργία αγγείων από ανθρώπινο ομφάλιο λώρο και μελέτη της λειτουργικότητας τους πριν και μετά την κρυοκατάψυξη τους.” 2018. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed October 23, 2019. http://hdl.handle.net/10442/hedi/44482.

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

MLA Handbook (7th Edition):

Mallis, Panagioits. “Δημιουργία αγγείων από ανθρώπινο ομφάλιο λώρο και μελέτη της λειτουργικότητας τους πριν και μετά την κρυοκατάψυξη τους.” 2018. Web. 23 Oct 2019.

Vancouver:

Mallis P. Δημιουργία αγγείων από ανθρώπινο ομφάλιο λώρο και μελέτη της λειτουργικότητας τους πριν και μετά την κρυοκατάψυξη τους. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2018. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10442/hedi/44482.

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

Council of Science Editors:

Mallis P. Δημιουργία αγγείων από ανθρώπινο ομφάλιο λώρο και μελέτη της λειτουργικότητας τους πριν και μετά την κρυοκατάψυξη τους. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2018. Available from: http://hdl.handle.net/10442/hedi/44482

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

21. Skafi, Najwa. Role of Phospholipase D in Vascular Calcification : Le rôle de la phospholipase D dans la calcification vasculaire.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2017, Lyon; Université libanaise

 La calcification vasculaire est l’accumulation de cristaux de calcium dans les vaisseaux sanguins à travers un processus pathologique qui ressemble à la formation de l’os… (more)

Subjects/Keywords: Phospholipase D; Calcification vasculaire; Phosphatase alcaline; Cellules musculaires lisses; Insuffisance rénale chronique; Aorte; Phospholipase D; Vascular calcification; Alkaline phosphatase; Smooth muscle cells; Chronic kidney disease; Aorta; 571.6

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APA (6th Edition):

Skafi, N. (2017). Role of Phospholipase D in Vascular Calcification : Le rôle de la phospholipase D dans la calcification vasculaire. (Doctoral Dissertation). Lyon; Université libanaise. Retrieved from http://www.theses.fr/2017LYSE1339

Chicago Manual of Style (16th Edition):

Skafi, Najwa. “Role of Phospholipase D in Vascular Calcification : Le rôle de la phospholipase D dans la calcification vasculaire.” 2017. Doctoral Dissertation, Lyon; Université libanaise. Accessed October 23, 2019. http://www.theses.fr/2017LYSE1339.

MLA Handbook (7th Edition):

Skafi, Najwa. “Role of Phospholipase D in Vascular Calcification : Le rôle de la phospholipase D dans la calcification vasculaire.” 2017. Web. 23 Oct 2019.

Vancouver:

Skafi N. Role of Phospholipase D in Vascular Calcification : Le rôle de la phospholipase D dans la calcification vasculaire. [Internet] [Doctoral dissertation]. Lyon; Université libanaise; 2017. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2017LYSE1339.

Council of Science Editors:

Skafi N. Role of Phospholipase D in Vascular Calcification : Le rôle de la phospholipase D dans la calcification vasculaire. [Doctoral Dissertation]. Lyon; Université libanaise; 2017. Available from: http://www.theses.fr/2017LYSE1339

22. Ribeiro mesquita, Thássio Ricardo. Specific activation of the alternative cardiac promoter of Cacna1c by the mineralocorticoid receptor : Activation spécifique du promoteur cardiaque alternatif du Cacna1c par le récepteur aux minéralocorticoïdes.

Degree: Docteur es, Physiologie, physiopathologie, 2017, Paris Saclay; Universidade Federal de Sergipe

Les antagonistes des récepteurs aux minéralocorticoïdes (MR) appartiennent à l'arsenal thérapeutique pour le traitement de diverses maladies cardiovasculaires, mais les mécanismes conférant leurs effets bénéfiques… (more)

Subjects/Keywords: Canaux Ca2+ de type L; Aldostérone; Récepteur aux minéralocorticoïde; Cœur; Muscle lisse vasculaire; L-Type Ca2+ channel; Aldosterone; Mineralocorticoid receptor; Heart; Vascular smooth muscle cells

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APA (6th Edition):

Ribeiro mesquita, T. R. (2017). Specific activation of the alternative cardiac promoter of Cacna1c by the mineralocorticoid receptor : Activation spécifique du promoteur cardiaque alternatif du Cacna1c par le récepteur aux minéralocorticoïdes. (Doctoral Dissertation). Paris Saclay; Universidade Federal de Sergipe. Retrieved from http://www.theses.fr/2017SACLS530

Chicago Manual of Style (16th Edition):

Ribeiro mesquita, Thássio Ricardo. “Specific activation of the alternative cardiac promoter of Cacna1c by the mineralocorticoid receptor : Activation spécifique du promoteur cardiaque alternatif du Cacna1c par le récepteur aux minéralocorticoïdes.” 2017. Doctoral Dissertation, Paris Saclay; Universidade Federal de Sergipe. Accessed October 23, 2019. http://www.theses.fr/2017SACLS530.

MLA Handbook (7th Edition):

Ribeiro mesquita, Thássio Ricardo. “Specific activation of the alternative cardiac promoter of Cacna1c by the mineralocorticoid receptor : Activation spécifique du promoteur cardiaque alternatif du Cacna1c par le récepteur aux minéralocorticoïdes.” 2017. Web. 23 Oct 2019.

Vancouver:

Ribeiro mesquita TR. Specific activation of the alternative cardiac promoter of Cacna1c by the mineralocorticoid receptor : Activation spécifique du promoteur cardiaque alternatif du Cacna1c par le récepteur aux minéralocorticoïdes. [Internet] [Doctoral dissertation]. Paris Saclay; Universidade Federal de Sergipe; 2017. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2017SACLS530.

Council of Science Editors:

Ribeiro mesquita TR. Specific activation of the alternative cardiac promoter of Cacna1c by the mineralocorticoid receptor : Activation spécifique du promoteur cardiaque alternatif du Cacna1c par le récepteur aux minéralocorticoïdes. [Doctoral Dissertation]. Paris Saclay; Universidade Federal de Sergipe; 2017. Available from: http://www.theses.fr/2017SACLS530


University of Western Ontario

23. Watson, Alanna R. Nicotinamide Phosphoribosyltransferase In Smooth Muscle Cells And Aortic Integrity.

Degree: 2017, University of Western Ontario

 The thoracic aortic wall can degenerate over time with catastrophic consequences. Vascular smooth muscle cells (SMCs) can resist and repair artery damage but their capacities… (more)

Subjects/Keywords: Vascular smooth muscle cells; Aortic disease; Nampt; DNA damage; Cell senescence; Extracellular matrix; Nicotinamide riboside; Biochemical Phenomena, Metabolism, and Nutrition

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APA (6th Edition):

Watson, A. R. (2017). Nicotinamide Phosphoribosyltransferase In Smooth Muscle Cells And Aortic Integrity. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/5060

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):

Watson, Alanna R. “Nicotinamide Phosphoribosyltransferase In Smooth Muscle Cells And Aortic Integrity.” 2017. Thesis, University of Western Ontario. Accessed October 23, 2019. https://ir.lib.uwo.ca/etd/5060.

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

MLA Handbook (7th Edition):

Watson, Alanna R. “Nicotinamide Phosphoribosyltransferase In Smooth Muscle Cells And Aortic Integrity.” 2017. Web. 23 Oct 2019.

Vancouver:

Watson AR. Nicotinamide Phosphoribosyltransferase In Smooth Muscle Cells And Aortic Integrity. [Internet] [Thesis]. University of Western Ontario; 2017. [cited 2019 Oct 23]. Available from: https://ir.lib.uwo.ca/etd/5060.

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

Council of Science Editors:

Watson AR. Nicotinamide Phosphoribosyltransferase In Smooth Muscle Cells And Aortic Integrity. [Thesis]. University of Western Ontario; 2017. Available from: https://ir.lib.uwo.ca/etd/5060

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

24. Zhang, Liang. Évaluation du rôle de nouvelles isoformes de PDE dans la compartimentation des nucléotides cycliques dans les cellules musculaires lisses vasculaires et les cardiomyocytes : Evaluation of the role of new PDE isoforms in cyclic nucleotide compartmentation in vascular smooth muscle cells and cardiomyocytes.

Degree: Docteur es, Physiologie, physiopathologie, 2017, Paris Saclay

 Les deux nucléotides cycliques, AMPc et GMPc, sont des seconds messagers importants qui régulent une grande variété de fonctions cellulaires, en particulier la fonction contractile… (more)

Subjects/Keywords: AMPc; GMPc; Phosphodiestérase; Cellule musculaire lisse vasculaire; Myocyte cardiaque; Camp; Cgmp; Phosphodiesterase; Vascular smooth muscle cell; Cardiac myocyte

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APA (6th Edition):

Zhang, L. (2017). Évaluation du rôle de nouvelles isoformes de PDE dans la compartimentation des nucléotides cycliques dans les cellules musculaires lisses vasculaires et les cardiomyocytes : Evaluation of the role of new PDE isoforms in cyclic nucleotide compartmentation in vascular smooth muscle cells and cardiomyocytes. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2017SACLS290

Chicago Manual of Style (16th Edition):

Zhang, Liang. “Évaluation du rôle de nouvelles isoformes de PDE dans la compartimentation des nucléotides cycliques dans les cellules musculaires lisses vasculaires et les cardiomyocytes : Evaluation of the role of new PDE isoforms in cyclic nucleotide compartmentation in vascular smooth muscle cells and cardiomyocytes.” 2017. Doctoral Dissertation, Paris Saclay. Accessed October 23, 2019. http://www.theses.fr/2017SACLS290.

MLA Handbook (7th Edition):

Zhang, Liang. “Évaluation du rôle de nouvelles isoformes de PDE dans la compartimentation des nucléotides cycliques dans les cellules musculaires lisses vasculaires et les cardiomyocytes : Evaluation of the role of new PDE isoforms in cyclic nucleotide compartmentation in vascular smooth muscle cells and cardiomyocytes.” 2017. Web. 23 Oct 2019.

Vancouver:

Zhang L. Évaluation du rôle de nouvelles isoformes de PDE dans la compartimentation des nucléotides cycliques dans les cellules musculaires lisses vasculaires et les cardiomyocytes : Evaluation of the role of new PDE isoforms in cyclic nucleotide compartmentation in vascular smooth muscle cells and cardiomyocytes. [Internet] [Doctoral dissertation]. Paris Saclay; 2017. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2017SACLS290.

Council of Science Editors:

Zhang L. Évaluation du rôle de nouvelles isoformes de PDE dans la compartimentation des nucléotides cycliques dans les cellules musculaires lisses vasculaires et les cardiomyocytes : Evaluation of the role of new PDE isoforms in cyclic nucleotide compartmentation in vascular smooth muscle cells and cardiomyocytes. [Doctoral Dissertation]. Paris Saclay; 2017. Available from: http://www.theses.fr/2017SACLS290


Loma Linda University

25. Hubbell, Margaret C. The Role of VEGF and Smooth Muscle Phenotype in Hypoxic Remodeling of Ovine Carotid and Cerebral Arteries.

Degree: PhD, Basic Sciences, 2017, Loma Linda University

  Arteries are a dynamic tissue with multiple cell types that incorporate systemic and local factors to maintain homeostasis. Hypoxia stimulates capillary angiogenesis to effectively… (more)

Subjects/Keywords: Medical Biochemistry; Medical Sciences; Medicine and Health Sciences; Hypoxia-Ischemia, Brain - Physiopathology; Endothelium, Vascular; Muscle, Smooth, Vascular; Cardiovascular System - Physiopathology; Fetal Hypoxia - Physiopathology;

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

APA (6th Edition):

Hubbell, M. C. (2017). The Role of VEGF and Smooth Muscle Phenotype in Hypoxic Remodeling of Ovine Carotid and Cerebral Arteries. (Doctoral Dissertation). Loma Linda University. Retrieved from https://scholarsrepository.llu.edu/etd/464

Chicago Manual of Style (16th Edition):

Hubbell, Margaret C. “The Role of VEGF and Smooth Muscle Phenotype in Hypoxic Remodeling of Ovine Carotid and Cerebral Arteries.” 2017. Doctoral Dissertation, Loma Linda University. Accessed October 23, 2019. https://scholarsrepository.llu.edu/etd/464.

MLA Handbook (7th Edition):

Hubbell, Margaret C. “The Role of VEGF and Smooth Muscle Phenotype in Hypoxic Remodeling of Ovine Carotid and Cerebral Arteries.” 2017. Web. 23 Oct 2019.

Vancouver:

Hubbell MC. The Role of VEGF and Smooth Muscle Phenotype in Hypoxic Remodeling of Ovine Carotid and Cerebral Arteries. [Internet] [Doctoral dissertation]. Loma Linda University; 2017. [cited 2019 Oct 23]. Available from: https://scholarsrepository.llu.edu/etd/464.

Council of Science Editors:

Hubbell MC. The Role of VEGF and Smooth Muscle Phenotype in Hypoxic Remodeling of Ovine Carotid and Cerebral Arteries. [Doctoral Dissertation]. Loma Linda University; 2017. Available from: https://scholarsrepository.llu.edu/etd/464


University of Minnesota

26. Steucke, Kerianne. Empirical Determination of Vascular Smooth Muscle Cell Mechano-Adaptation.

Degree: PhD, Biomedical Engineering, 2017, University of Minnesota

 Patient-specific vascular modeling seeks to provide physicians with predictive data that will enable them to make better treatment decisions and improve patient outcomes. To achieve… (more)

Subjects/Keywords: Biomechanics; Cardiovascular Disease; Mechano-Adaptation; Vascular Smooth Muscle Cells

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APA (6th Edition):

Steucke, K. (2017). Empirical Determination of Vascular Smooth Muscle Cell Mechano-Adaptation. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/201104

Chicago Manual of Style (16th Edition):

Steucke, Kerianne. “Empirical Determination of Vascular Smooth Muscle Cell Mechano-Adaptation.” 2017. Doctoral Dissertation, University of Minnesota. Accessed October 23, 2019. http://hdl.handle.net/11299/201104.

MLA Handbook (7th Edition):

Steucke, Kerianne. “Empirical Determination of Vascular Smooth Muscle Cell Mechano-Adaptation.” 2017. Web. 23 Oct 2019.

Vancouver:

Steucke K. Empirical Determination of Vascular Smooth Muscle Cell Mechano-Adaptation. [Internet] [Doctoral dissertation]. University of Minnesota; 2017. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/11299/201104.

Council of Science Editors:

Steucke K. Empirical Determination of Vascular Smooth Muscle Cell Mechano-Adaptation. [Doctoral Dissertation]. University of Minnesota; 2017. Available from: http://hdl.handle.net/11299/201104


University of Western Ontario

27. Ghoreishi, Sina A. Nicotinamide Riboside and the Aortic Response to Angiotensin II Infusion in Mice.

Degree: 2017, University of Western Ontario

 Damage to vascular cells of the aorta drives vascular dysfunction and disease. Nicotinamide adenine dinucleotide (NAD+) is a cellular metabolite critical to cellular health, but… (more)

Subjects/Keywords: NAD+; nicotinamide riboside; angiotensin II; aorta; endothelial cells; vascular smooth muscle cells; Circulatory and Respiratory Physiology

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APA (6th Edition):

Ghoreishi, S. A. (2017). Nicotinamide Riboside and the Aortic Response to Angiotensin II Infusion in Mice. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/4788

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):

Ghoreishi, Sina A. “Nicotinamide Riboside and the Aortic Response to Angiotensin II Infusion in Mice.” 2017. Thesis, University of Western Ontario. Accessed October 23, 2019. https://ir.lib.uwo.ca/etd/4788.

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

MLA Handbook (7th Edition):

Ghoreishi, Sina A. “Nicotinamide Riboside and the Aortic Response to Angiotensin II Infusion in Mice.” 2017. Web. 23 Oct 2019.

Vancouver:

Ghoreishi SA. Nicotinamide Riboside and the Aortic Response to Angiotensin II Infusion in Mice. [Internet] [Thesis]. University of Western Ontario; 2017. [cited 2019 Oct 23]. Available from: https://ir.lib.uwo.ca/etd/4788.

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

Council of Science Editors:

Ghoreishi SA. Nicotinamide Riboside and the Aortic Response to Angiotensin II Infusion in Mice. [Thesis]. University of Western Ontario; 2017. Available from: https://ir.lib.uwo.ca/etd/4788

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

28. Padget, Rachel Lee. The Effect of Hemodynamic Force on the Maturation of Blood Vessels during Embryogenesis.

Degree: MSin Biology, Biology, 2017, Missouri State University

  Throughout embryonic development, blood vessels are derived from endothelial cells by way of vasculogenesis. During angiogenesis, vessels remodel to form a hierarchy of large-diameter… (more)

Subjects/Keywords: Vascular smooth muscle cells; vessel maturation; vascular development; angiogenesis; hemodynamic force; Biophysics; Developmental Biology; Laboratory and Basic Science Research

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APA (6th Edition):

Padget, R. L. (2017). The Effect of Hemodynamic Force on the Maturation of Blood Vessels during Embryogenesis. (Masters Thesis). Missouri State University. Retrieved from https://bearworks.missouristate.edu/theses/3116

Chicago Manual of Style (16th Edition):

Padget, Rachel Lee. “The Effect of Hemodynamic Force on the Maturation of Blood Vessels during Embryogenesis.” 2017. Masters Thesis, Missouri State University. Accessed October 23, 2019. https://bearworks.missouristate.edu/theses/3116.

MLA Handbook (7th Edition):

Padget, Rachel Lee. “The Effect of Hemodynamic Force on the Maturation of Blood Vessels during Embryogenesis.” 2017. Web. 23 Oct 2019.

Vancouver:

Padget RL. The Effect of Hemodynamic Force on the Maturation of Blood Vessels during Embryogenesis. [Internet] [Masters thesis]. Missouri State University; 2017. [cited 2019 Oct 23]. Available from: https://bearworks.missouristate.edu/theses/3116.

Council of Science Editors:

Padget RL. The Effect of Hemodynamic Force on the Maturation of Blood Vessels during Embryogenesis. [Masters Thesis]. Missouri State University; 2017. Available from: https://bearworks.missouristate.edu/theses/3116

29. Vallin, Benjamin. Caractérisation fonctionnelle de nouvelles isoformes d'adénylyl cyclase 8 identifiées dans les cellules musculaires lisses vasculaires trans-différenciées : Functional characterization of new adenylyl cyclase 8 isoforms identified in trans-differentiated vascular smooth muscle cells.

Degree: Docteur es, Physiologie, Physiopathologie et Thérapeutique, 2017, Université Pierre et Marie Curie – Paris VI

La trans-différenciation des cellules musculaires lisses vasculaires (CMLV) vers un phénotype migratoire, prolifératif et sécrétoire joue un rôle clé dans la progression des lésions athéromateuses… (more)

Subjects/Keywords: Cellule musculaire lisse vasculaire; Trans-différenciation; AMP cyclique; Adénylyl cyclase 8; Hétéro-dimérisation; Dominant-négatif; Vascular smooth muscle cell; Adenylyl cyclase 8; Cyclic AMP; 612.74

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APA (6th Edition):

Vallin, B. (2017). Caractérisation fonctionnelle de nouvelles isoformes d'adénylyl cyclase 8 identifiées dans les cellules musculaires lisses vasculaires trans-différenciées : Functional characterization of new adenylyl cyclase 8 isoforms identified in trans-differentiated vascular smooth muscle cells. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2017PA066117

Chicago Manual of Style (16th Edition):

Vallin, Benjamin. “Caractérisation fonctionnelle de nouvelles isoformes d'adénylyl cyclase 8 identifiées dans les cellules musculaires lisses vasculaires trans-différenciées : Functional characterization of new adenylyl cyclase 8 isoforms identified in trans-differentiated vascular smooth muscle cells.” 2017. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed October 23, 2019. http://www.theses.fr/2017PA066117.

MLA Handbook (7th Edition):

Vallin, Benjamin. “Caractérisation fonctionnelle de nouvelles isoformes d'adénylyl cyclase 8 identifiées dans les cellules musculaires lisses vasculaires trans-différenciées : Functional characterization of new adenylyl cyclase 8 isoforms identified in trans-differentiated vascular smooth muscle cells.” 2017. Web. 23 Oct 2019.

Vancouver:

Vallin B. Caractérisation fonctionnelle de nouvelles isoformes d'adénylyl cyclase 8 identifiées dans les cellules musculaires lisses vasculaires trans-différenciées : Functional characterization of new adenylyl cyclase 8 isoforms identified in trans-differentiated vascular smooth muscle cells. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2017PA066117.

Council of Science Editors:

Vallin B. Caractérisation fonctionnelle de nouvelles isoformes d'adénylyl cyclase 8 identifiées dans les cellules musculaires lisses vasculaires trans-différenciées : Functional characterization of new adenylyl cyclase 8 isoforms identified in trans-differentiated vascular smooth muscle cells. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. Available from: http://www.theses.fr/2017PA066117


University of Western Ontario

30. Xu, Yiwen. Automated Vascular Smooth Muscle Segmentation, Reconstruction, Classification and Simulation on Whole-Slide Histology.

Degree: 2017, University of Western Ontario

 Histology of the microvasculature depicts detailed characteristics relevant to tissue perfusion. One important histologic feature is the smooth muscle component of the microvessel wall, which… (more)

Subjects/Keywords: Microvasculature; Regeneration; Vascular Smooth Muscle; Whole-slide Imaging; Histology; Immunohistochemistry; Reconstruction; Simulation; Segmentation; Machine Learning; Circulatory and Respiratory Physiology; Medical Biophysics

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

APA (6th Edition):

Xu, Y. (2017). Automated Vascular Smooth Muscle Segmentation, Reconstruction, Classification and Simulation on Whole-Slide Histology. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/4566

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):

Xu, Yiwen. “Automated Vascular Smooth Muscle Segmentation, Reconstruction, Classification and Simulation on Whole-Slide Histology.” 2017. Thesis, University of Western Ontario. Accessed October 23, 2019. https://ir.lib.uwo.ca/etd/4566.

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

MLA Handbook (7th Edition):

Xu, Yiwen. “Automated Vascular Smooth Muscle Segmentation, Reconstruction, Classification and Simulation on Whole-Slide Histology.” 2017. Web. 23 Oct 2019.

Vancouver:

Xu Y. Automated Vascular Smooth Muscle Segmentation, Reconstruction, Classification and Simulation on Whole-Slide Histology. [Internet] [Thesis]. University of Western Ontario; 2017. [cited 2019 Oct 23]. Available from: https://ir.lib.uwo.ca/etd/4566.

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

Council of Science Editors:

Xu Y. Automated Vascular Smooth Muscle Segmentation, Reconstruction, Classification and Simulation on Whole-Slide Histology. [Thesis]. University of Western Ontario; 2017. Available from: https://ir.lib.uwo.ca/etd/4566

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

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