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You searched for subject:(GTPases Rho). Showing records 1 – 30 of 95 total matches.

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University of Hong Kong

1. Tirrell, Lee Sean. The role of RhoA GTPase activating protein DLC2 in painful diabetic neuropathy.

Degree: M. Phil., 2013, University of Hong Kong

 Neuropathy is a major complication that affects nearly half of all patients with diabetes, greatly decreasing their quality of life. Patients experience a wide range… (more)

Subjects/Keywords: Diabetic neuropathies; Rho GTPases

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APA (6th Edition):

Tirrell, L. S. (2013). The role of RhoA GTPase activating protein DLC2 in painful diabetic neuropathy. (Masters Thesis). University of Hong Kong. Retrieved from Tirrell, L. S.. (2013). The role of RhoA GTPase activating protein DLC2 in painful diabetic neuropathy. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5153739 ; http://dx.doi.org/10.5353/th_b5153739 ; http://hdl.handle.net/10722/195956

Chicago Manual of Style (16th Edition):

Tirrell, Lee Sean. “The role of RhoA GTPase activating protein DLC2 in painful diabetic neuropathy.” 2013. Masters Thesis, University of Hong Kong. Accessed July 23, 2019. Tirrell, L. S.. (2013). The role of RhoA GTPase activating protein DLC2 in painful diabetic neuropathy. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5153739 ; http://dx.doi.org/10.5353/th_b5153739 ; http://hdl.handle.net/10722/195956.

MLA Handbook (7th Edition):

Tirrell, Lee Sean. “The role of RhoA GTPase activating protein DLC2 in painful diabetic neuropathy.” 2013. Web. 23 Jul 2019.

Vancouver:

Tirrell LS. The role of RhoA GTPase activating protein DLC2 in painful diabetic neuropathy. [Internet] [Masters thesis]. University of Hong Kong; 2013. [cited 2019 Jul 23]. Available from: Tirrell, L. S.. (2013). The role of RhoA GTPase activating protein DLC2 in painful diabetic neuropathy. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5153739 ; http://dx.doi.org/10.5353/th_b5153739 ; http://hdl.handle.net/10722/195956.

Council of Science Editors:

Tirrell LS. The role of RhoA GTPase activating protein DLC2 in painful diabetic neuropathy. [Masters Thesis]. University of Hong Kong; 2013. Available from: Tirrell, L. S.. (2013). The role of RhoA GTPase activating protein DLC2 in painful diabetic neuropathy. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5153739 ; http://dx.doi.org/10.5353/th_b5153739 ; http://hdl.handle.net/10722/195956


Oregon State University

2. Christensen, Todd M. Identification and characterization of seven ROP GTPases in Zea mays.

Degree: MS, Botany and Plant Pathology, 2004, Oregon State University

 Regulation of cell division and expansion are critical for plant development. The mechanisms that control these processes are not clearly understood in higher plants. In… (more)

Subjects/Keywords: Rho GTPases

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APA (6th Edition):

Christensen, T. M. (2004). Identification and characterization of seven ROP GTPases in Zea mays. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/22949

Chicago Manual of Style (16th Edition):

Christensen, Todd M. “Identification and characterization of seven ROP GTPases in Zea mays.” 2004. Masters Thesis, Oregon State University. Accessed July 23, 2019. http://hdl.handle.net/1957/22949.

MLA Handbook (7th Edition):

Christensen, Todd M. “Identification and characterization of seven ROP GTPases in Zea mays.” 2004. Web. 23 Jul 2019.

Vancouver:

Christensen TM. Identification and characterization of seven ROP GTPases in Zea mays. [Internet] [Masters thesis]. Oregon State University; 2004. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/1957/22949.

Council of Science Editors:

Christensen TM. Identification and characterization of seven ROP GTPases in Zea mays. [Masters Thesis]. Oregon State University; 2004. Available from: http://hdl.handle.net/1957/22949


Columbia University

3. Zhuravlev, Yelena. A study on the role of polarity, Rho family GTPases, and cell fate in cytokinesis.

Degree: 2017, Columbia University

 Cytokinesis is the physical partition of one cell into two. In Chapter 1, I provide a brief introduction to cytokinesis and some of the proteins… (more)

Subjects/Keywords: Cytology; Cytokinesis; Rho GTPases

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APA (6th Edition):

Zhuravlev, Y. (2017). A study on the role of polarity, Rho family GTPases, and cell fate in cytokinesis. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8QR58MD

Chicago Manual of Style (16th Edition):

Zhuravlev, Yelena. “A study on the role of polarity, Rho family GTPases, and cell fate in cytokinesis.” 2017. Doctoral Dissertation, Columbia University. Accessed July 23, 2019. https://doi.org/10.7916/D8QR58MD.

MLA Handbook (7th Edition):

Zhuravlev, Yelena. “A study on the role of polarity, Rho family GTPases, and cell fate in cytokinesis.” 2017. Web. 23 Jul 2019.

Vancouver:

Zhuravlev Y. A study on the role of polarity, Rho family GTPases, and cell fate in cytokinesis. [Internet] [Doctoral dissertation]. Columbia University; 2017. [cited 2019 Jul 23]. Available from: https://doi.org/10.7916/D8QR58MD.

Council of Science Editors:

Zhuravlev Y. A study on the role of polarity, Rho family GTPases, and cell fate in cytokinesis. [Doctoral Dissertation]. Columbia University; 2017. Available from: https://doi.org/10.7916/D8QR58MD


University of Notre Dame

4. David Johnson. Effects of P190b Over-Expression on Mammary Epithelial Cell Morphology and Behavior</h1>.

Degree: MS, Biological Sciences, 2009, University of Notre Dame

  p190B RhoGAP is a negative regulator of the RHO GTPase signaling pathway. Rho signaling is involved in proliferation, migration, polarity and cytoskeletal rearrangement. It… (more)

Subjects/Keywords: Breast cancer; Rho GTPases; p190B

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APA (6th Edition):

Johnson, D. (2009). Effects of P190b Over-Expression on Mammary Epithelial Cell Morphology and Behavior</h1>. (Masters Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/9880vq3005s

Chicago Manual of Style (16th Edition):

Johnson, David. “Effects of P190b Over-Expression on Mammary Epithelial Cell Morphology and Behavior</h1>.” 2009. Masters Thesis, University of Notre Dame. Accessed July 23, 2019. https://curate.nd.edu/show/9880vq3005s.

MLA Handbook (7th Edition):

Johnson, David. “Effects of P190b Over-Expression on Mammary Epithelial Cell Morphology and Behavior</h1>.” 2009. Web. 23 Jul 2019.

Vancouver:

Johnson D. Effects of P190b Over-Expression on Mammary Epithelial Cell Morphology and Behavior</h1>. [Internet] [Masters thesis]. University of Notre Dame; 2009. [cited 2019 Jul 23]. Available from: https://curate.nd.edu/show/9880vq3005s.

Council of Science Editors:

Johnson D. Effects of P190b Over-Expression on Mammary Epithelial Cell Morphology and Behavior</h1>. [Masters Thesis]. University of Notre Dame; 2009. Available from: https://curate.nd.edu/show/9880vq3005s


Université Montpellier II

5. Cannet, Aude. Rôle du Rho-GEF Trio dans la division cellulaire : Role of Rho-GEF Trio in the cell division.

Degree: Docteur es, Biologie Santé, 2014, Université Montpellier II

 Durant la division cellulaire, la cellule subit des changements importants dans sa forme et son adhésion qui dépendent de l'efficacité du remodelage du cytosquelette d'actine.… (more)

Subjects/Keywords: Trio; Rho GTPases; Mitose; Trio; Rho GTPases; Mitosis

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APA (6th Edition):

Cannet, A. (2014). Rôle du Rho-GEF Trio dans la division cellulaire : Role of Rho-GEF Trio in the cell division. (Doctoral Dissertation). Université Montpellier II. Retrieved from http://www.theses.fr/2014MON20124

Chicago Manual of Style (16th Edition):

Cannet, Aude. “Rôle du Rho-GEF Trio dans la division cellulaire : Role of Rho-GEF Trio in the cell division.” 2014. Doctoral Dissertation, Université Montpellier II. Accessed July 23, 2019. http://www.theses.fr/2014MON20124.

MLA Handbook (7th Edition):

Cannet, Aude. “Rôle du Rho-GEF Trio dans la division cellulaire : Role of Rho-GEF Trio in the cell division.” 2014. Web. 23 Jul 2019.

Vancouver:

Cannet A. Rôle du Rho-GEF Trio dans la division cellulaire : Role of Rho-GEF Trio in the cell division. [Internet] [Doctoral dissertation]. Université Montpellier II; 2014. [cited 2019 Jul 23]. Available from: http://www.theses.fr/2014MON20124.

Council of Science Editors:

Cannet A. Rôle du Rho-GEF Trio dans la division cellulaire : Role of Rho-GEF Trio in the cell division. [Doctoral Dissertation]. Université Montpellier II; 2014. Available from: http://www.theses.fr/2014MON20124

6. Piquet, Leo. Régulation de l’expression de Rnd3 dans les cellules tumorales : Regulation of Rnd3 expression in tumor cells.

Degree: Docteur es, Biologie cellulaire et physiopathologie, 2016, Bordeaux

La protéine Rnd3 est un membre atypique de la famille des Rho GTPases. Dénuée d’activité GTPasique, elle est ainsi constitutivement sous forme active et liée… (more)

Subjects/Keywords: Rho GTPases; Mécanotransduction; Cancer; Rho GTPases; Mechanotranduction; Cancer

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APA (6th Edition):

Piquet, L. (2016). Régulation de l’expression de Rnd3 dans les cellules tumorales : Regulation of Rnd3 expression in tumor cells. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2016BORD0272

Chicago Manual of Style (16th Edition):

Piquet, Leo. “Régulation de l’expression de Rnd3 dans les cellules tumorales : Regulation of Rnd3 expression in tumor cells.” 2016. Doctoral Dissertation, Bordeaux. Accessed July 23, 2019. http://www.theses.fr/2016BORD0272.

MLA Handbook (7th Edition):

Piquet, Leo. “Régulation de l’expression de Rnd3 dans les cellules tumorales : Regulation of Rnd3 expression in tumor cells.” 2016. Web. 23 Jul 2019.

Vancouver:

Piquet L. Régulation de l’expression de Rnd3 dans les cellules tumorales : Regulation of Rnd3 expression in tumor cells. [Internet] [Doctoral dissertation]. Bordeaux; 2016. [cited 2019 Jul 23]. Available from: http://www.theses.fr/2016BORD0272.

Council of Science Editors:

Piquet L. Régulation de l’expression de Rnd3 dans les cellules tumorales : Regulation of Rnd3 expression in tumor cells. [Doctoral Dissertation]. Bordeaux; 2016. Available from: http://www.theses.fr/2016BORD0272

7. Petit, Dominique. Caractérisation de ARHGAP19, une nouvelle GAP de Rho impliquée dans la mitose des Lymphocytes T : Characterization of ARHGAP19, a Novel Rho GAP Involved in T-Cell Mitosis.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2016, Paris Saclay

Dans le but de déterminer le rôle des Rho GTPases et de leurs régulateurs dans les cellules hématopoïétiques, une analyse des niveaux d’expressions de 300… (more)

Subjects/Keywords: Rho GTPases; Rho GAP; Mitose; Cytokinese; Changements de formes; Rho GTPases; Rho GAP; Mitosis; Cytokinesis; Cell shape changes

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APA (6th Edition):

Petit, D. (2016). Caractérisation de ARHGAP19, une nouvelle GAP de Rho impliquée dans la mitose des Lymphocytes T : Characterization of ARHGAP19, a Novel Rho GAP Involved in T-Cell Mitosis. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2016SACLS018

Chicago Manual of Style (16th Edition):

Petit, Dominique. “Caractérisation de ARHGAP19, une nouvelle GAP de Rho impliquée dans la mitose des Lymphocytes T : Characterization of ARHGAP19, a Novel Rho GAP Involved in T-Cell Mitosis.” 2016. Doctoral Dissertation, Paris Saclay. Accessed July 23, 2019. http://www.theses.fr/2016SACLS018.

MLA Handbook (7th Edition):

Petit, Dominique. “Caractérisation de ARHGAP19, une nouvelle GAP de Rho impliquée dans la mitose des Lymphocytes T : Characterization of ARHGAP19, a Novel Rho GAP Involved in T-Cell Mitosis.” 2016. Web. 23 Jul 2019.

Vancouver:

Petit D. Caractérisation de ARHGAP19, une nouvelle GAP de Rho impliquée dans la mitose des Lymphocytes T : Characterization of ARHGAP19, a Novel Rho GAP Involved in T-Cell Mitosis. [Internet] [Doctoral dissertation]. Paris Saclay; 2016. [cited 2019 Jul 23]. Available from: http://www.theses.fr/2016SACLS018.

Council of Science Editors:

Petit D. Caractérisation de ARHGAP19, une nouvelle GAP de Rho impliquée dans la mitose des Lymphocytes T : Characterization of ARHGAP19, a Novel Rho GAP Involved in T-Cell Mitosis. [Doctoral Dissertation]. Paris Saclay; 2016. Available from: http://www.theses.fr/2016SACLS018


Columbia University

8. Jordan, Shawn. The molecular regulation of cytokinesis in the Caenorhabditis elegans zygote.

Degree: 2015, Columbia University

 The division of one cell to form two cells, or cytokinesis, is fundamental to the development of all known multi-cellular organisms, as well as the… (more)

Subjects/Keywords: Caenorhabditis elegans; Rho GTPases; Cytokinesis; Cytology

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APA (6th Edition):

Jordan, S. (2015). The molecular regulation of cytokinesis in the Caenorhabditis elegans zygote. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8P849ZS

Chicago Manual of Style (16th Edition):

Jordan, Shawn. “The molecular regulation of cytokinesis in the Caenorhabditis elegans zygote.” 2015. Doctoral Dissertation, Columbia University. Accessed July 23, 2019. https://doi.org/10.7916/D8P849ZS.

MLA Handbook (7th Edition):

Jordan, Shawn. “The molecular regulation of cytokinesis in the Caenorhabditis elegans zygote.” 2015. Web. 23 Jul 2019.

Vancouver:

Jordan S. The molecular regulation of cytokinesis in the Caenorhabditis elegans zygote. [Internet] [Doctoral dissertation]. Columbia University; 2015. [cited 2019 Jul 23]. Available from: https://doi.org/10.7916/D8P849ZS.

Council of Science Editors:

Jordan S. The molecular regulation of cytokinesis in the Caenorhabditis elegans zygote. [Doctoral Dissertation]. Columbia University; 2015. Available from: https://doi.org/10.7916/D8P849ZS

9. Debbio, Carolina Beltrame Del. GTPases Rho e o potencial regenerativo da retina de mamíferos.

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

O Corpo Ciliar (CC) é uma fonte de células tronco da retina de animais adultos, mas sua ativação permanece desconhecida. GTPases Rho são proteínas que… (more)

Subjects/Keywords: Ciliary Body; Corpo Ciliar; GTPases Rho; Progenitores retinianos; Proliferação; Proliferation; Retinal progenitor cells; Rho GTPases

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APA (6th Edition):

Debbio, C. B. D. (2010). GTPases Rho e o potencial regenerativo da retina de mamíferos. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/42/42134/tde-25032010-150345/ ;

Chicago Manual of Style (16th Edition):

Debbio, Carolina Beltrame Del. “GTPases Rho e o potencial regenerativo da retina de mamíferos.” 2010. Doctoral Dissertation, University of São Paulo. Accessed July 23, 2019. http://www.teses.usp.br/teses/disponiveis/42/42134/tde-25032010-150345/ ;.

MLA Handbook (7th Edition):

Debbio, Carolina Beltrame Del. “GTPases Rho e o potencial regenerativo da retina de mamíferos.” 2010. Web. 23 Jul 2019.

Vancouver:

Debbio CBD. GTPases Rho e o potencial regenerativo da retina de mamíferos. [Internet] [Doctoral dissertation]. University of São Paulo; 2010. [cited 2019 Jul 23]. Available from: http://www.teses.usp.br/teses/disponiveis/42/42134/tde-25032010-150345/ ;.

Council of Science Editors:

Debbio CBD. GTPases Rho e o potencial regenerativo da retina de mamíferos. [Doctoral Dissertation]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/42/42134/tde-25032010-150345/ ;

10. Croise, Pauline. Sécrétion des phéochromocytomes : impact sur le développement tumoral et rôle des GTPases Rho : Secretion in pheochromocytomas : impact in tumor development and role of the Rho GTPases.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2015, Université de Strasbourg

La sécrétion d'hormones et de neuropeptides par les cellules neuroendocrines est assurée par un processus d'exocytose, contrôlé notamment par les GTPases Rho. La compréhension des… (more)

Subjects/Keywords: Phéochromocytomes; Sécrétion; GTPases Rho; Développement tumoral; Pheochromocytomas; Secretion; Rho GTPases; Tumoral development; 572.4; 616.99

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APA (6th Edition):

Croise, P. (2015). Sécrétion des phéochromocytomes : impact sur le développement tumoral et rôle des GTPases Rho : Secretion in pheochromocytomas : impact in tumor development and role of the Rho GTPases. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2015STRAJ001

Chicago Manual of Style (16th Edition):

Croise, Pauline. “Sécrétion des phéochromocytomes : impact sur le développement tumoral et rôle des GTPases Rho : Secretion in pheochromocytomas : impact in tumor development and role of the Rho GTPases.” 2015. Doctoral Dissertation, Université de Strasbourg. Accessed July 23, 2019. http://www.theses.fr/2015STRAJ001.

MLA Handbook (7th Edition):

Croise, Pauline. “Sécrétion des phéochromocytomes : impact sur le développement tumoral et rôle des GTPases Rho : Secretion in pheochromocytomas : impact in tumor development and role of the Rho GTPases.” 2015. Web. 23 Jul 2019.

Vancouver:

Croise P. Sécrétion des phéochromocytomes : impact sur le développement tumoral et rôle des GTPases Rho : Secretion in pheochromocytomas : impact in tumor development and role of the Rho GTPases. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2015. [cited 2019 Jul 23]. Available from: http://www.theses.fr/2015STRAJ001.

Council of Science Editors:

Croise P. Sécrétion des phéochromocytomes : impact sur le développement tumoral et rôle des GTPases Rho : Secretion in pheochromocytomas : impact in tumor development and role of the Rho GTPases. [Doctoral Dissertation]. Université de Strasbourg; 2015. Available from: http://www.theses.fr/2015STRAJ001

11. Socoro Yuste, Nuria. Dérégulations protéomiques et fonctionnelles des Syndromes Myéloproliferatifs Philadephia négatifs : Proteomic and functional deregulations in Philadelphia negative Myeloproliferative Neoplasms.

Degree: Docteur es, Biotechnologie, instrumentation, signal et imagerie pour la biologie, la médecine et l'environnement, 2015, Grenoble Alpes

En plus des anomalies génétiques, plusieurs études ont rapporté des altérations des protéines chez les patients atteintes de Syndromes Myéloprolifératifs (SMP) Ph- qui pourraient participer… (more)

Subjects/Keywords: Syndromes myéloproliferatifs; Protéomique; Rho GTPases; Erythrocytes; Myeloproliferatif Neoplasms; Proteomic; Rho GTPases; Erythrocytes; 610

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APA (6th Edition):

Socoro Yuste, N. (2015). Dérégulations protéomiques et fonctionnelles des Syndromes Myéloproliferatifs Philadephia négatifs : Proteomic and functional deregulations in Philadelphia negative Myeloproliferative Neoplasms. (Doctoral Dissertation). Grenoble Alpes. Retrieved from http://www.theses.fr/2015GREAS018

Chicago Manual of Style (16th Edition):

Socoro Yuste, Nuria. “Dérégulations protéomiques et fonctionnelles des Syndromes Myéloproliferatifs Philadephia négatifs : Proteomic and functional deregulations in Philadelphia negative Myeloproliferative Neoplasms.” 2015. Doctoral Dissertation, Grenoble Alpes. Accessed July 23, 2019. http://www.theses.fr/2015GREAS018.

MLA Handbook (7th Edition):

Socoro Yuste, Nuria. “Dérégulations protéomiques et fonctionnelles des Syndromes Myéloproliferatifs Philadephia négatifs : Proteomic and functional deregulations in Philadelphia negative Myeloproliferative Neoplasms.” 2015. Web. 23 Jul 2019.

Vancouver:

Socoro Yuste N. Dérégulations protéomiques et fonctionnelles des Syndromes Myéloproliferatifs Philadephia négatifs : Proteomic and functional deregulations in Philadelphia negative Myeloproliferative Neoplasms. [Internet] [Doctoral dissertation]. Grenoble Alpes; 2015. [cited 2019 Jul 23]. Available from: http://www.theses.fr/2015GREAS018.

Council of Science Editors:

Socoro Yuste N. Dérégulations protéomiques et fonctionnelles des Syndromes Myéloproliferatifs Philadephia négatifs : Proteomic and functional deregulations in Philadelphia negative Myeloproliferative Neoplasms. [Doctoral Dissertation]. Grenoble Alpes; 2015. Available from: http://www.theses.fr/2015GREAS018


Université Montpellier II

12. Plutoni, Cédric. Etude du rôle de la P-cadhérine dans la migration cellulaire collective : The rôle of P-cadherin in collective cell migration.

Degree: Docteur es, Biologie Santé, 2014, Université Montpellier II

 La migration cellulaire collective (MCC) est un processus fondamental qui intervient au cours du développement, de la réparation tissulaire, de l'invasion tumorale et de la… (more)

Subjects/Keywords: P-Cadhérine; Migration cellulaire collective; GTPases-Rho; P-Cadherin; Collective cell migration; Rho-GTPases

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APA (6th Edition):

Plutoni, C. (2014). Etude du rôle de la P-cadhérine dans la migration cellulaire collective : The rôle of P-cadherin in collective cell migration. (Doctoral Dissertation). Université Montpellier II. Retrieved from http://www.theses.fr/2014MON20123

Chicago Manual of Style (16th Edition):

Plutoni, Cédric. “Etude du rôle de la P-cadhérine dans la migration cellulaire collective : The rôle of P-cadherin in collective cell migration.” 2014. Doctoral Dissertation, Université Montpellier II. Accessed July 23, 2019. http://www.theses.fr/2014MON20123.

MLA Handbook (7th Edition):

Plutoni, Cédric. “Etude du rôle de la P-cadhérine dans la migration cellulaire collective : The rôle of P-cadherin in collective cell migration.” 2014. Web. 23 Jul 2019.

Vancouver:

Plutoni C. Etude du rôle de la P-cadhérine dans la migration cellulaire collective : The rôle of P-cadherin in collective cell migration. [Internet] [Doctoral dissertation]. Université Montpellier II; 2014. [cited 2019 Jul 23]. Available from: http://www.theses.fr/2014MON20123.

Council of Science Editors:

Plutoni C. Etude du rôle de la P-cadhérine dans la migration cellulaire collective : The rôle of P-cadherin in collective cell migration. [Doctoral Dissertation]. Université Montpellier II; 2014. Available from: http://www.theses.fr/2014MON20123

13. Libanje, Fotine. Etude de la contribution des voies de signalisation dépendantes des RhoGTPases à l'invasion collective des carcinomes colorectaux : Deciphering the Contribution of RhoGTPases Dependent Signaling Pathways to the Collective Invasion of Colorectal Carcinoma.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2017, Paris Saclay

La progression métastatique des cancers est responsable de 90% des décès liés à la maladie. Cette cascade est initiée par l’invasion des cellules cancéreuses du… (more)

Subjects/Keywords: Invasion collective; Rho-GTPases; Cancer colorectal; Collective invasion; Rho-GTPases; Colorectal carcinoma

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APA (6th Edition):

Libanje, F. (2017). Etude de la contribution des voies de signalisation dépendantes des RhoGTPases à l'invasion collective des carcinomes colorectaux : Deciphering the Contribution of RhoGTPases Dependent Signaling Pathways to the Collective Invasion of Colorectal Carcinoma. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2017SACLS503

Chicago Manual of Style (16th Edition):

Libanje, Fotine. “Etude de la contribution des voies de signalisation dépendantes des RhoGTPases à l'invasion collective des carcinomes colorectaux : Deciphering the Contribution of RhoGTPases Dependent Signaling Pathways to the Collective Invasion of Colorectal Carcinoma.” 2017. Doctoral Dissertation, Paris Saclay. Accessed July 23, 2019. http://www.theses.fr/2017SACLS503.

MLA Handbook (7th Edition):

Libanje, Fotine. “Etude de la contribution des voies de signalisation dépendantes des RhoGTPases à l'invasion collective des carcinomes colorectaux : Deciphering the Contribution of RhoGTPases Dependent Signaling Pathways to the Collective Invasion of Colorectal Carcinoma.” 2017. Web. 23 Jul 2019.

Vancouver:

Libanje F. Etude de la contribution des voies de signalisation dépendantes des RhoGTPases à l'invasion collective des carcinomes colorectaux : Deciphering the Contribution of RhoGTPases Dependent Signaling Pathways to the Collective Invasion of Colorectal Carcinoma. [Internet] [Doctoral dissertation]. Paris Saclay; 2017. [cited 2019 Jul 23]. Available from: http://www.theses.fr/2017SACLS503.

Council of Science Editors:

Libanje F. Etude de la contribution des voies de signalisation dépendantes des RhoGTPases à l'invasion collective des carcinomes colorectaux : Deciphering the Contribution of RhoGTPases Dependent Signaling Pathways to the Collective Invasion of Colorectal Carcinoma. [Doctoral Dissertation]. Paris Saclay; 2017. Available from: http://www.theses.fr/2017SACLS503


Case Western Reserve University

14. Xue, Feng. Specific ECM Engagement Differentially Modulates T Cell Cytoskeletal Reorganization By Rho GTPases.

Degree: MSs, Pathology, 2009, Case Western Reserve University

 When T cells adhere to the ECM, under certain circumstances they will polarize and exhibit the morphology of a migrating cell. We are investigating three… (more)

Subjects/Keywords: Integrins; ECM; fibronectin; CELL; PBT; RHO GTPASES; GTPASES

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

APA (6th Edition):

Xue, F. (2009). Specific ECM Engagement Differentially Modulates T Cell Cytoskeletal Reorganization By Rho GTPases. (Masters Thesis). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1221770198

Chicago Manual of Style (16th Edition):

Xue, Feng. “Specific ECM Engagement Differentially Modulates T Cell Cytoskeletal Reorganization By Rho GTPases.” 2009. Masters Thesis, Case Western Reserve University. Accessed July 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1221770198.

MLA Handbook (7th Edition):

Xue, Feng. “Specific ECM Engagement Differentially Modulates T Cell Cytoskeletal Reorganization By Rho GTPases.” 2009. Web. 23 Jul 2019.

Vancouver:

Xue F. Specific ECM Engagement Differentially Modulates T Cell Cytoskeletal Reorganization By Rho GTPases. [Internet] [Masters thesis]. Case Western Reserve University; 2009. [cited 2019 Jul 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1221770198.

Council of Science Editors:

Xue F. Specific ECM Engagement Differentially Modulates T Cell Cytoskeletal Reorganization By Rho GTPases. [Masters Thesis]. Case Western Reserve University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1221770198


Universiteit Utrecht

15. Prummel, K.D. Regulation of endothelial cell-cell junctions and vascular permeability by Rho GEFs and GAPs.

Degree: 2014, Universiteit Utrecht

 The endothelial monolayer covers the luminal side of blood and lymphatic vessels and functions as a physical barrier. The cell-cell junctions between the endothelial cells… (more)

Subjects/Keywords: endothelial permeability; Rho GTPases; Rho GEFs; Rho GEFs; cell-cell junction regulation

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APA (6th Edition):

Prummel, K. D. (2014). Regulation of endothelial cell-cell junctions and vascular permeability by Rho GEFs and GAPs. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/291004

Chicago Manual of Style (16th Edition):

Prummel, K D. “Regulation of endothelial cell-cell junctions and vascular permeability by Rho GEFs and GAPs.” 2014. Masters Thesis, Universiteit Utrecht. Accessed July 23, 2019. http://dspace.library.uu.nl:8080/handle/1874/291004.

MLA Handbook (7th Edition):

Prummel, K D. “Regulation of endothelial cell-cell junctions and vascular permeability by Rho GEFs and GAPs.” 2014. Web. 23 Jul 2019.

Vancouver:

Prummel KD. Regulation of endothelial cell-cell junctions and vascular permeability by Rho GEFs and GAPs. [Internet] [Masters thesis]. Universiteit Utrecht; 2014. [cited 2019 Jul 23]. Available from: http://dspace.library.uu.nl:8080/handle/1874/291004.

Council of Science Editors:

Prummel KD. Regulation of endothelial cell-cell junctions and vascular permeability by Rho GEFs and GAPs. [Masters Thesis]. Universiteit Utrecht; 2014. Available from: http://dspace.library.uu.nl:8080/handle/1874/291004

16. Garcia, Elsa. Détection de la virulence bactérienne : caractérisation de la réponse immunitaire anti-virulence déclenchée par la toxine CNF1 d’Escherichia coli : Detection of bacterial virulence : characterization of the anti-virulence immune response triggered by the Escherichia coli toxin CNF1.

Degree: Docteur es, Immunologie et microbiologie, 2017, Côte d'Azur

Notre système immunitaire détecte les microorganismes via des molécules absentes de l’hôte appelées MAMPs. Mais étant donné que les MAMPs sont exprimés par tous les… (more)

Subjects/Keywords: Immunité innée; Virulence; Rho GTPases; Toxines bactériennes; Inflammasome; Innate immunity; Virulence; Rho GTPases; Bacterial toxins; Inflammasome

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APA (6th Edition):

Garcia, E. (2017). Détection de la virulence bactérienne : caractérisation de la réponse immunitaire anti-virulence déclenchée par la toxine CNF1 d’Escherichia coli : Detection of bacterial virulence : characterization of the anti-virulence immune response triggered by the Escherichia coli toxin CNF1. (Doctoral Dissertation). Côte d'Azur. Retrieved from http://www.theses.fr/2017AZUR4071

Chicago Manual of Style (16th Edition):

Garcia, Elsa. “Détection de la virulence bactérienne : caractérisation de la réponse immunitaire anti-virulence déclenchée par la toxine CNF1 d’Escherichia coli : Detection of bacterial virulence : characterization of the anti-virulence immune response triggered by the Escherichia coli toxin CNF1.” 2017. Doctoral Dissertation, Côte d'Azur. Accessed July 23, 2019. http://www.theses.fr/2017AZUR4071.

MLA Handbook (7th Edition):

Garcia, Elsa. “Détection de la virulence bactérienne : caractérisation de la réponse immunitaire anti-virulence déclenchée par la toxine CNF1 d’Escherichia coli : Detection of bacterial virulence : characterization of the anti-virulence immune response triggered by the Escherichia coli toxin CNF1.” 2017. Web. 23 Jul 2019.

Vancouver:

Garcia E. Détection de la virulence bactérienne : caractérisation de la réponse immunitaire anti-virulence déclenchée par la toxine CNF1 d’Escherichia coli : Detection of bacterial virulence : characterization of the anti-virulence immune response triggered by the Escherichia coli toxin CNF1. [Internet] [Doctoral dissertation]. Côte d'Azur; 2017. [cited 2019 Jul 23]. Available from: http://www.theses.fr/2017AZUR4071.

Council of Science Editors:

Garcia E. Détection de la virulence bactérienne : caractérisation de la réponse immunitaire anti-virulence déclenchée par la toxine CNF1 d’Escherichia coli : Detection of bacterial virulence : characterization of the anti-virulence immune response triggered by the Escherichia coli toxin CNF1. [Doctoral Dissertation]. Côte d'Azur; 2017. Available from: http://www.theses.fr/2017AZUR4071


IUPUI

17. Zhang, Hao. Mechanisms of Cytoskeletal Dysregulation in the Kidney Proximal Tubule During ATP Depletion and Ischemia.

Degree: 2009, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Knowledge of the molecular and cellular mechanisms of ischemic injury is necessary for understanding acute kidney injury and devising optimal… (more)

Subjects/Keywords: Actin Cytoskeleton, Kidney Ischemia, Cortactin, Dynamin, AMPK, Rho GTPases; Kidneys; Ischemia; Hydrolases; Microfilament proteins; Rho GTPases

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APA (6th Edition):

Zhang, H. (2009). Mechanisms of Cytoskeletal Dysregulation in the Kidney Proximal Tubule During ATP Depletion and Ischemia. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/1957

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):

Zhang, Hao. “Mechanisms of Cytoskeletal Dysregulation in the Kidney Proximal Tubule During ATP Depletion and Ischemia.” 2009. Thesis, IUPUI. Accessed July 23, 2019. http://hdl.handle.net/1805/1957.

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

MLA Handbook (7th Edition):

Zhang, Hao. “Mechanisms of Cytoskeletal Dysregulation in the Kidney Proximal Tubule During ATP Depletion and Ischemia.” 2009. Web. 23 Jul 2019.

Vancouver:

Zhang H. Mechanisms of Cytoskeletal Dysregulation in the Kidney Proximal Tubule During ATP Depletion and Ischemia. [Internet] [Thesis]. IUPUI; 2009. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/1805/1957.

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

Council of Science Editors:

Zhang H. Mechanisms of Cytoskeletal Dysregulation in the Kidney Proximal Tubule During ATP Depletion and Ischemia. [Thesis]. IUPUI; 2009. Available from: http://hdl.handle.net/1805/1957

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


University of Cincinnati

18. Sipes, Nisha Schuler. Cdc42 signaling in extracellular matrix remodeling in three dimensions.

Degree: PhD, Medicine : Cell and Molecular Biology, 2009, University of Cincinnati

Rho family GTPases are intracellular signal transducers important in cell growth, morphogenesis, motility, cytoskeleton organization, endocytosis and exocytosis. These functions are critical for development,… (more)

Subjects/Keywords: Molecular Biology; Rho GTPases; Cdc42; extracellular matrix; signaling; 3D

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APA (6th Edition):

Sipes, N. S. (2009). Cdc42 signaling in extracellular matrix remodeling in three dimensions. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1253622562

Chicago Manual of Style (16th Edition):

Sipes, Nisha Schuler. “Cdc42 signaling in extracellular matrix remodeling in three dimensions.” 2009. Doctoral Dissertation, University of Cincinnati. Accessed July 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1253622562.

MLA Handbook (7th Edition):

Sipes, Nisha Schuler. “Cdc42 signaling in extracellular matrix remodeling in three dimensions.” 2009. Web. 23 Jul 2019.

Vancouver:

Sipes NS. Cdc42 signaling in extracellular matrix remodeling in three dimensions. [Internet] [Doctoral dissertation]. University of Cincinnati; 2009. [cited 2019 Jul 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1253622562.

Council of Science Editors:

Sipes NS. Cdc42 signaling in extracellular matrix remodeling in three dimensions. [Doctoral Dissertation]. University of Cincinnati; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1253622562


Universiteit Utrecht

19. 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 July 23, 2019. http://dspace.library.uu.nl:8080/handle/1874/37293.

MLA Handbook (7th Edition):

Gaarenstroom, T Y. “Mechanotransduction via Integrins.” 2009. Web. 23 Jul 2019.

Vancouver:

Gaarenstroom TY. Mechanotransduction via Integrins. [Internet] [Masters thesis]. Universiteit Utrecht; 2009. [cited 2019 Jul 23]. 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

20. Tsukada, Yuki. Quantitative Analyses for the Systems of Rho-family Small GTPases and Regulation of Cellular Morphodynamics : Rhoファミリー低分子量GTP結合タンパク質と細胞形態制御に関する定量的な研究; Rho ファミリー テイブンシリョウ GTP ケツゴウ タンパクシツ ト サイボウ ケイタイ セイギョ ニ カンスル テイリョウテキナ ケンキュウ.

Degree: Nara Institute of Science and Technology / 奈良先端科学技術大学院大学

Subjects/Keywords: Rho-family small GTPases

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APA (6th Edition):

Tsukada, Y. (n.d.). Quantitative Analyses for the Systems of Rho-family Small GTPases and Regulation of Cellular Morphodynamics : Rhoファミリー低分子量GTP結合タンパク質と細胞形態制御に関する定量的な研究; Rho ファミリー テイブンシリョウ GTP ケツゴウ タンパクシツ ト サイボウ ケイタイ セイギョ ニ カンスル テイリョウテキナ ケンキュウ. (Thesis). Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Retrieved from http://hdl.handle.net/10061/4964

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

Chicago Manual of Style (16th Edition):

Tsukada, Yuki. “Quantitative Analyses for the Systems of Rho-family Small GTPases and Regulation of Cellular Morphodynamics : Rhoファミリー低分子量GTP結合タンパク質と細胞形態制御に関する定量的な研究; Rho ファミリー テイブンシリョウ GTP ケツゴウ タンパクシツ ト サイボウ ケイタイ セイギョ ニ カンスル テイリョウテキナ ケンキュウ.” Thesis, Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Accessed July 23, 2019. http://hdl.handle.net/10061/4964.

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

MLA Handbook (7th Edition):

Tsukada, Yuki. “Quantitative Analyses for the Systems of Rho-family Small GTPases and Regulation of Cellular Morphodynamics : Rhoファミリー低分子量GTP結合タンパク質と細胞形態制御に関する定量的な研究; Rho ファミリー テイブンシリョウ GTP ケツゴウ タンパクシツ ト サイボウ ケイタイ セイギョ ニ カンスル テイリョウテキナ ケンキュウ.” Web. 23 Jul 2019.

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

Vancouver:

Tsukada Y. Quantitative Analyses for the Systems of Rho-family Small GTPases and Regulation of Cellular Morphodynamics : Rhoファミリー低分子量GTP結合タンパク質と細胞形態制御に関する定量的な研究; Rho ファミリー テイブンシリョウ GTP ケツゴウ タンパクシツ ト サイボウ ケイタイ セイギョ ニ カンスル テイリョウテキナ ケンキュウ. [Internet] [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; [cited 2019 Jul 23]. Available from: http://hdl.handle.net/10061/4964.

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

Council of Science Editors:

Tsukada Y. Quantitative Analyses for the Systems of Rho-family Small GTPases and Regulation of Cellular Morphodynamics : Rhoファミリー低分子量GTP結合タンパク質と細胞形態制御に関する定量的な研究; Rho ファミリー テイブンシリョウ GTP ケツゴウ タンパクシツ ト サイボウ ケイタイ セイギョ ニ カンスル テイリョウテキナ ケンキュウ. [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; Available from: http://hdl.handle.net/10061/4964

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


Queens University

21. Arulanandam, Rozanne. Novel mechanisms of Stat3 activation .

Degree: Pathology and Molecular Medicine, 2010, Queens University

 Stat3 (signal transducer and activator of transcription-3) is activated by a number of receptor and non-receptor tyrosine kinases, while a constitutively active form of Stat3… (more)

Subjects/Keywords: Stat3; Rho GTPases; Cadherins; Cell-cell adhesion; IL6; gp130

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APA (6th Edition):

Arulanandam, R. (2010). Novel mechanisms of Stat3 activation . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/5442

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):

Arulanandam, Rozanne. “Novel mechanisms of Stat3 activation .” 2010. Thesis, Queens University. Accessed July 23, 2019. http://hdl.handle.net/1974/5442.

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

MLA Handbook (7th Edition):

Arulanandam, Rozanne. “Novel mechanisms of Stat3 activation .” 2010. Web. 23 Jul 2019.

Vancouver:

Arulanandam R. Novel mechanisms of Stat3 activation . [Internet] [Thesis]. Queens University; 2010. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/1974/5442.

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

Council of Science Editors:

Arulanandam R. Novel mechanisms of Stat3 activation . [Thesis]. Queens University; 2010. Available from: http://hdl.handle.net/1974/5442

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


University of Hong Kong

22. Ma, Wei. Study of the roles of RhoE in human hepatocellular carcinoma.

Degree: PhD, 2013, University of Hong Kong

 Hepatocellular carcinoma (HCC) is the seventh most prevalent cancer and the third leading cause of cancer-related mortality globally. Metastasis is a major cause of mortality.… (more)

Subjects/Keywords: Liver - Cancer - Molecular aspects; Rho GTPases; Protein kinases

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APA (6th Edition):

Ma, W. (2013). Study of the roles of RhoE in human hepatocellular carcinoma. (Doctoral Dissertation). University of Hong Kong. Retrieved from Ma, W. [馬威]. (2013). Study of the roles of RhoE in human hepatocellular carcinoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5108667 ; http://dx.doi.org/10.5353/th_b5108667 ; http://hdl.handle.net/10722/205869

Chicago Manual of Style (16th Edition):

Ma, Wei. “Study of the roles of RhoE in human hepatocellular carcinoma.” 2013. Doctoral Dissertation, University of Hong Kong. Accessed July 23, 2019. Ma, W. [馬威]. (2013). Study of the roles of RhoE in human hepatocellular carcinoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5108667 ; http://dx.doi.org/10.5353/th_b5108667 ; http://hdl.handle.net/10722/205869.

MLA Handbook (7th Edition):

Ma, Wei. “Study of the roles of RhoE in human hepatocellular carcinoma.” 2013. Web. 23 Jul 2019.

Vancouver:

Ma W. Study of the roles of RhoE in human hepatocellular carcinoma. [Internet] [Doctoral dissertation]. University of Hong Kong; 2013. [cited 2019 Jul 23]. Available from: Ma, W. [馬威]. (2013). Study of the roles of RhoE in human hepatocellular carcinoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5108667 ; http://dx.doi.org/10.5353/th_b5108667 ; http://hdl.handle.net/10722/205869.

Council of Science Editors:

Ma W. Study of the roles of RhoE in human hepatocellular carcinoma. [Doctoral Dissertation]. University of Hong Kong; 2013. Available from: Ma, W. [馬威]. (2013). Study of the roles of RhoE in human hepatocellular carcinoma. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5108667 ; http://dx.doi.org/10.5353/th_b5108667 ; http://hdl.handle.net/10722/205869


University of Cincinnati

23. Zandvakili, Inuk. RhoA as a Potential Target in Lung Cancer.

Degree: PhD, Medicine: Molecular and Developmental Biology, 2015, University of Cincinnati

 Many cancers are driven by oncogenic K-Ras, yet K-Ras has remained largely undruggable. In this dissertation we explore inhibiting K-Ras signaling by targeting downstream signaling… (more)

Subjects/Keywords: Surgery; RhoA; KRas; Rho GTPases; Lung Cancer; RhoC; Lung Adenocarcinoma

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APA (6th Edition):

Zandvakili, I. (2015). RhoA as a Potential Target in Lung Cancer. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1445342196

Chicago Manual of Style (16th Edition):

Zandvakili, Inuk. “RhoA as a Potential Target in Lung Cancer.” 2015. Doctoral Dissertation, University of Cincinnati. Accessed July 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1445342196.

MLA Handbook (7th Edition):

Zandvakili, Inuk. “RhoA as a Potential Target in Lung Cancer.” 2015. Web. 23 Jul 2019.

Vancouver:

Zandvakili I. RhoA as a Potential Target in Lung Cancer. [Internet] [Doctoral dissertation]. University of Cincinnati; 2015. [cited 2019 Jul 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1445342196.

Council of Science Editors:

Zandvakili I. RhoA as a Potential Target in Lung Cancer. [Doctoral Dissertation]. University of Cincinnati; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1445342196


Columbia University

24. Du, Jing. Unbiased Expression Profiling Identifies a Novel Notch Signaling Target RND1 as Regulator of Angiogenesis.

Degree: 2019, Columbia University

 Notch signaling controls normal and pathological angiogenesis through transcriptional regulation of a wide network of target genes. Despite intensive studies of the endothelial Notch function,… (more)

Subjects/Keywords: Molecular biology; Neovascularization; Rho GTPases; Cellular signal transduction

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APA (6th Edition):

Du, J. (2019). Unbiased Expression Profiling Identifies a Novel Notch Signaling Target RND1 as Regulator of Angiogenesis. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/d8-pmrg-g821

Chicago Manual of Style (16th Edition):

Du, Jing. “Unbiased Expression Profiling Identifies a Novel Notch Signaling Target RND1 as Regulator of Angiogenesis.” 2019. Doctoral Dissertation, Columbia University. Accessed July 23, 2019. https://doi.org/10.7916/d8-pmrg-g821.

MLA Handbook (7th Edition):

Du, Jing. “Unbiased Expression Profiling Identifies a Novel Notch Signaling Target RND1 as Regulator of Angiogenesis.” 2019. Web. 23 Jul 2019.

Vancouver:

Du J. Unbiased Expression Profiling Identifies a Novel Notch Signaling Target RND1 as Regulator of Angiogenesis. [Internet] [Doctoral dissertation]. Columbia University; 2019. [cited 2019 Jul 23]. Available from: https://doi.org/10.7916/d8-pmrg-g821.

Council of Science Editors:

Du J. Unbiased Expression Profiling Identifies a Novel Notch Signaling Target RND1 as Regulator of Angiogenesis. [Doctoral Dissertation]. Columbia University; 2019. Available from: https://doi.org/10.7916/d8-pmrg-g821


Cornell University

25. Stalnecker, Clint. Targeting Altered Cancer Cell Metabolism: Mitochondrial Glutaminase Regulation And Inhibition By Small Molecules .

Degree: 2016, Cornell University

Subjects/Keywords: Cacner metabolism; glutaminase; Rho-GTPases

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APA (6th Edition):

Stalnecker, C. (2016). Targeting Altered Cancer Cell Metabolism: Mitochondrial Glutaminase Regulation And Inhibition By Small Molecules . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/45141

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):

Stalnecker, Clint. “Targeting Altered Cancer Cell Metabolism: Mitochondrial Glutaminase Regulation And Inhibition By Small Molecules .” 2016. Thesis, Cornell University. Accessed July 23, 2019. http://hdl.handle.net/1813/45141.

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

MLA Handbook (7th Edition):

Stalnecker, Clint. “Targeting Altered Cancer Cell Metabolism: Mitochondrial Glutaminase Regulation And Inhibition By Small Molecules .” 2016. Web. 23 Jul 2019.

Vancouver:

Stalnecker C. Targeting Altered Cancer Cell Metabolism: Mitochondrial Glutaminase Regulation And Inhibition By Small Molecules . [Internet] [Thesis]. Cornell University; 2016. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/1813/45141.

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

Council of Science Editors:

Stalnecker C. Targeting Altered Cancer Cell Metabolism: Mitochondrial Glutaminase Regulation And Inhibition By Small Molecules . [Thesis]. Cornell University; 2016. Available from: http://hdl.handle.net/1813/45141

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

26. Teiti, Lotefa. Régulation de l'expression de ligands de l'immunité par la voie Rho/ROCK sur les mélanomes : Regulation of immune ligands' expression by Rho/rock pathway on melanoma.

Degree: Docteur es, Cancérologie, 2015, Université Toulouse III – Paul Sabatier

 Ma thèse porte sur l'étude des rôles régulateurs des GTPases Rho et de leurs effecteurs ROCK sur l'expression de ligands du système immunitaire, sur des… (more)

Subjects/Keywords: Mélanome; Système immunitaire; GTPases Rho; ROCK; FasL; CD70; MICA; Métastases

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APA (6th Edition):

Teiti, L. (2015). Régulation de l'expression de ligands de l'immunité par la voie Rho/ROCK sur les mélanomes : Regulation of immune ligands' expression by Rho/rock pathway on melanoma. (Doctoral Dissertation). Université Toulouse III – Paul Sabatier. Retrieved from http://www.theses.fr/2015TOU30053

Chicago Manual of Style (16th Edition):

Teiti, Lotefa. “Régulation de l'expression de ligands de l'immunité par la voie Rho/ROCK sur les mélanomes : Regulation of immune ligands' expression by Rho/rock pathway on melanoma.” 2015. Doctoral Dissertation, Université Toulouse III – Paul Sabatier. Accessed July 23, 2019. http://www.theses.fr/2015TOU30053.

MLA Handbook (7th Edition):

Teiti, Lotefa. “Régulation de l'expression de ligands de l'immunité par la voie Rho/ROCK sur les mélanomes : Regulation of immune ligands' expression by Rho/rock pathway on melanoma.” 2015. Web. 23 Jul 2019.

Vancouver:

Teiti L. Régulation de l'expression de ligands de l'immunité par la voie Rho/ROCK sur les mélanomes : Regulation of immune ligands' expression by Rho/rock pathway on melanoma. [Internet] [Doctoral dissertation]. Université Toulouse III – Paul Sabatier; 2015. [cited 2019 Jul 23]. Available from: http://www.theses.fr/2015TOU30053.

Council of Science Editors:

Teiti L. Régulation de l'expression de ligands de l'immunité par la voie Rho/ROCK sur les mélanomes : Regulation of immune ligands' expression by Rho/rock pathway on melanoma. [Doctoral Dissertation]. Université Toulouse III – Paul Sabatier; 2015. Available from: http://www.theses.fr/2015TOU30053


Wright State University

27. Aljagthmi, Amjad Ahmed. DNp63a suppresses cell invasion by targeting rac1 through mir-320a.

Degree: MS, Biochemistry and Molecular Biology, 2017, Wright State University

 DNp63a, a member of the p53 family of transcription factors, is overexpressed in a number of cancers and known to play a role in proliferation,… (more)

Subjects/Keywords: Biogeochemistry; Molecular Biology; DNp63a; Rac1; PAK1; miR320a; microRNA; invasion; GTPases; Rho

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APA (6th Edition):

Aljagthmi, A. A. (2017). DNp63a suppresses cell invasion by targeting rac1 through mir-320a. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright150237950487141

Chicago Manual of Style (16th Edition):

Aljagthmi, Amjad Ahmed. “DNp63a suppresses cell invasion by targeting rac1 through mir-320a.” 2017. Masters Thesis, Wright State University. Accessed July 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=wright150237950487141.

MLA Handbook (7th Edition):

Aljagthmi, Amjad Ahmed. “DNp63a suppresses cell invasion by targeting rac1 through mir-320a.” 2017. Web. 23 Jul 2019.

Vancouver:

Aljagthmi AA. DNp63a suppresses cell invasion by targeting rac1 through mir-320a. [Internet] [Masters thesis]. Wright State University; 2017. [cited 2019 Jul 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright150237950487141.

Council of Science Editors:

Aljagthmi AA. DNp63a suppresses cell invasion by targeting rac1 through mir-320a. [Masters Thesis]. Wright State University; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright150237950487141

28. Evans, Joseph Corey. Regulation of Dendritic Spine Development and Cell Migration through Asef2-mediated Signaling.

Degree: PhD, Biological Sciences, 2014, Vanderbilt University

Rho GTPases are molecular switches that mediate the formation of dendritic spines â actin-enriched protrusions that make excitatory synapses with nearby neurons. Once activated by… (more)

Subjects/Keywords: dendritic spine; Guanine nucleotide exchange factor; neuron; Rho GTPases; cell migration

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APA (6th Edition):

Evans, J. C. (2014). Regulation of Dendritic Spine Development and Cell Migration through Asef2-mediated Signaling. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-07232014-132105/ ;

Chicago Manual of Style (16th Edition):

Evans, Joseph Corey. “Regulation of Dendritic Spine Development and Cell Migration through Asef2-mediated Signaling.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed July 23, 2019. http://etd.library.vanderbilt.edu/available/etd-07232014-132105/ ;.

MLA Handbook (7th Edition):

Evans, Joseph Corey. “Regulation of Dendritic Spine Development and Cell Migration through Asef2-mediated Signaling.” 2014. Web. 23 Jul 2019.

Vancouver:

Evans JC. Regulation of Dendritic Spine Development and Cell Migration through Asef2-mediated Signaling. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2019 Jul 23]. Available from: http://etd.library.vanderbilt.edu/available/etd-07232014-132105/ ;.

Council of Science Editors:

Evans JC. Regulation of Dendritic Spine Development and Cell Migration through Asef2-mediated Signaling. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://etd.library.vanderbilt.edu/available/etd-07232014-132105/ ;


Université du Québec à Montréal

29. Martin, Emmanuel. L'élongation embryonnaire précoce du Caenorhabditis elegans : caractérisation de la voie PIX-1/PAK-1.

Degree: 2016, Université du Québec à Montréal

 La morphogenèse des tissus est essentielle pour le développement des métazoaires. Elle requiert une coordination d'évènements cellulaires variés, tels que l'adhésion, la migration et le… (more)

Subjects/Keywords: Cænorhabditis elegans; Embryologie; Morphogenèse; Épithélium; GTPases rho; Transduction du signal cellulaire

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

APA (6th Edition):

Martin, E. (2016). L'élongation embryonnaire précoce du Caenorhabditis elegans : caractérisation de la voie PIX-1/PAK-1. (Thesis). Université du Québec à Montréal. Retrieved from http://archipel.uqam.ca/9082/1/D3144.pdf

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):

Martin, Emmanuel. “L'élongation embryonnaire précoce du Caenorhabditis elegans : caractérisation de la voie PIX-1/PAK-1.” 2016. Thesis, Université du Québec à Montréal. Accessed July 23, 2019. http://archipel.uqam.ca/9082/1/D3144.pdf.

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

MLA Handbook (7th Edition):

Martin, Emmanuel. “L'élongation embryonnaire précoce du Caenorhabditis elegans : caractérisation de la voie PIX-1/PAK-1.” 2016. Web. 23 Jul 2019.

Vancouver:

Martin E. L'élongation embryonnaire précoce du Caenorhabditis elegans : caractérisation de la voie PIX-1/PAK-1. [Internet] [Thesis]. Université du Québec à Montréal; 2016. [cited 2019 Jul 23]. Available from: http://archipel.uqam.ca/9082/1/D3144.pdf.

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

Council of Science Editors:

Martin E. L'élongation embryonnaire précoce du Caenorhabditis elegans : caractérisation de la voie PIX-1/PAK-1. [Thesis]. Université du Québec à Montréal; 2016. Available from: http://archipel.uqam.ca/9082/1/D3144.pdf

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


University of New Mexico

30. Kenney, Shelby. Characterization of R-ketorolac as a single enantiomer selective inhibitor of Cdc42 and Rac1 in ovarian cancer.

Degree: Biomedical Sciences Graduate Program, 2015, University of New Mexico

 Ovarian cancer is the 5th leading cause of cancer death for women in the United States and is frequently diagnosed at an advanced stage with… (more)

Subjects/Keywords: Cdc42; Rac1; ovarian cancer; ketorolac; migration; adhesion; Rho GTPases

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APA (6th Edition):

Kenney, S. (2015). Characterization of R-ketorolac as a single enantiomer selective inhibitor of Cdc42 and Rac1 in ovarian cancer. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/132

Chicago Manual of Style (16th Edition):

Kenney, Shelby. “Characterization of R-ketorolac as a single enantiomer selective inhibitor of Cdc42 and Rac1 in ovarian cancer.” 2015. Doctoral Dissertation, University of New Mexico. Accessed July 23, 2019. https://digitalrepository.unm.edu/biom_etds/132.

MLA Handbook (7th Edition):

Kenney, Shelby. “Characterization of R-ketorolac as a single enantiomer selective inhibitor of Cdc42 and Rac1 in ovarian cancer.” 2015. Web. 23 Jul 2019.

Vancouver:

Kenney S. Characterization of R-ketorolac as a single enantiomer selective inhibitor of Cdc42 and Rac1 in ovarian cancer. [Internet] [Doctoral dissertation]. University of New Mexico; 2015. [cited 2019 Jul 23]. Available from: https://digitalrepository.unm.edu/biom_etds/132.

Council of Science Editors:

Kenney S. Characterization of R-ketorolac as a single enantiomer selective inhibitor of Cdc42 and Rac1 in ovarian cancer. [Doctoral Dissertation]. University of New Mexico; 2015. Available from: https://digitalrepository.unm.edu/biom_etds/132

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