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You searched for subject:(Jun). Showing records 1 – 30 of 102 total matches.

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University of Southern California

1. Ramrakhiani, Ambika. Hepatic c-Jun overexpression metabolically reprograms cancer cells through mTORC2/AKT pathway.

Degree: MS, Molecular Microbiology and Immunology, 2014, University of Southern California

 The term metabolic syndrome describes the association between obesity, insulin resistance, and the risk of several prominent chronic diseases, including cancer. The link between many… (more)

Subjects/Keywords: c-Jun; diabetes; insulin pathway

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APA (6th Edition):

Ramrakhiani, A. (2014). Hepatic c-Jun overexpression metabolically reprograms cancer cells through mTORC2/AKT pathway. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/445587/rec/3147

Chicago Manual of Style (16th Edition):

Ramrakhiani, Ambika. “Hepatic c-Jun overexpression metabolically reprograms cancer cells through mTORC2/AKT pathway.” 2014. Masters Thesis, University of Southern California. Accessed April 19, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/445587/rec/3147.

MLA Handbook (7th Edition):

Ramrakhiani, Ambika. “Hepatic c-Jun overexpression metabolically reprograms cancer cells through mTORC2/AKT pathway.” 2014. Web. 19 Apr 2019.

Vancouver:

Ramrakhiani A. Hepatic c-Jun overexpression metabolically reprograms cancer cells through mTORC2/AKT pathway. [Internet] [Masters thesis]. University of Southern California; 2014. [cited 2019 Apr 19]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/445587/rec/3147.

Council of Science Editors:

Ramrakhiani A. Hepatic c-Jun overexpression metabolically reprograms cancer cells through mTORC2/AKT pathway. [Masters Thesis]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/445587/rec/3147


NSYSU

2. Wu, Chang-Ching. Studies on Zhong Jun Shuai in the middle stage of State of Jin.

Degree: Master, Chinese Literature, 2012, NSYSU

 For a period about two hundred and thirty years before 479 BC. Jing holds supreme power over all neighbouring hostile countries and protected emperor Zhou.… (more)

Subjects/Keywords: Zuo-Jhuan; Jing; Zhong Jun Shuai; Chih Di; Liou Jun

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APA (6th Edition):

Wu, C. (2012). Studies on Zhong Jun Shuai in the middle stage of State of Jin. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0911112-105315

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):

Wu, Chang-Ching. “Studies on Zhong Jun Shuai in the middle stage of State of Jin.” 2012. Thesis, NSYSU. Accessed April 19, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0911112-105315.

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

MLA Handbook (7th Edition):

Wu, Chang-Ching. “Studies on Zhong Jun Shuai in the middle stage of State of Jin.” 2012. Web. 19 Apr 2019.

Vancouver:

Wu C. Studies on Zhong Jun Shuai in the middle stage of State of Jin. [Internet] [Thesis]. NSYSU; 2012. [cited 2019 Apr 19]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0911112-105315.

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

Council of Science Editors:

Wu C. Studies on Zhong Jun Shuai in the middle stage of State of Jin. [Thesis]. NSYSU; 2012. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0911112-105315

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

3. Lima, Joelma Sousa de. Expressão imunohistoquímica das proteínas c-Jun não fosforilada/fosforilada e p27 em leucoplasias de pacientes fumantes e não fumantes.

Degree: Mestrado, Patologia Bucal, 2012, University of São Paulo

Em diversos casos, o câncer bucal é precedido por lesões pré-malignas, como por exemplo, a leucoplasia, sendo que o tabaco é um fator de risco.… (more)

Subjects/Keywords: c-Jun protein; Displasia epitelial; Epithelial dysplasia; Leucoplasia Oral; Oral leukoplakia; p27 protein; pc-Jun protein; Proteína c-Jun; Proteína p-c-Jun; Proteína p27; Tabagismo; Tobacco

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APA (6th Edition):

Lima, J. S. d. (2012). Expressão imunohistoquímica das proteínas c-Jun não fosforilada/fosforilada e p27 em leucoplasias de pacientes fumantes e não fumantes. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/23/23141/tde-13042013-113357/ ;

Chicago Manual of Style (16th Edition):

Lima, Joelma Sousa de. “Expressão imunohistoquímica das proteínas c-Jun não fosforilada/fosforilada e p27 em leucoplasias de pacientes fumantes e não fumantes.” 2012. Masters Thesis, University of São Paulo. Accessed April 19, 2019. http://www.teses.usp.br/teses/disponiveis/23/23141/tde-13042013-113357/ ;.

MLA Handbook (7th Edition):

Lima, Joelma Sousa de. “Expressão imunohistoquímica das proteínas c-Jun não fosforilada/fosforilada e p27 em leucoplasias de pacientes fumantes e não fumantes.” 2012. Web. 19 Apr 2019.

Vancouver:

Lima JSd. Expressão imunohistoquímica das proteínas c-Jun não fosforilada/fosforilada e p27 em leucoplasias de pacientes fumantes e não fumantes. [Internet] [Masters thesis]. University of São Paulo; 2012. [cited 2019 Apr 19]. Available from: http://www.teses.usp.br/teses/disponiveis/23/23141/tde-13042013-113357/ ;.

Council of Science Editors:

Lima JSd. Expressão imunohistoquímica das proteínas c-Jun não fosforilada/fosforilada e p27 em leucoplasias de pacientes fumantes e não fumantes. [Masters Thesis]. University of São Paulo; 2012. Available from: http://www.teses.usp.br/teses/disponiveis/23/23141/tde-13042013-113357/ ;


University of Toronto

4. Vaidya, Anup Shirish. Elucidating the Role of ARKL1 in Regulating Epstein-Barr Virus (EBV) Iinfection.

Degree: 2016, University of Toronto

ARKL1 and Arkadia were previously identified as proteins that bind to the CK2β KSSR motif. Since the Epstein-Barr virus (EBV) protein Epstein-Barr nuclear antigen 1… (more)

Subjects/Keywords: Arkadia; ARKL1; EBV; Jun; Polycomb; Reactivation; 0410

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APA (6th Edition):

Vaidya, A. S. (2016). Elucidating the Role of ARKL1 in Regulating Epstein-Barr Virus (EBV) Iinfection. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/76190

Chicago Manual of Style (16th Edition):

Vaidya, Anup Shirish. “Elucidating the Role of ARKL1 in Regulating Epstein-Barr Virus (EBV) Iinfection.” 2016. Masters Thesis, University of Toronto. Accessed April 19, 2019. http://hdl.handle.net/1807/76190.

MLA Handbook (7th Edition):

Vaidya, Anup Shirish. “Elucidating the Role of ARKL1 in Regulating Epstein-Barr Virus (EBV) Iinfection.” 2016. Web. 19 Apr 2019.

Vancouver:

Vaidya AS. Elucidating the Role of ARKL1 in Regulating Epstein-Barr Virus (EBV) Iinfection. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/1807/76190.

Council of Science Editors:

Vaidya AS. Elucidating the Role of ARKL1 in Regulating Epstein-Barr Virus (EBV) Iinfection. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/76190


Princeton University

5. Lei, Qinyuan. TOWARDS A MATERIALIST CONCEPTION OF SCIENCE—SCIENCE DEBATES IN INTERWAR & WARTIME JAPAN, 1920-1945 .

Degree: PhD, 2018, Princeton University

 In the wake of imperialist wars and cultural revolutions in the late 1910s and 1920s, intellectuals and activists in Japan and China faced the immediate… (more)

Subjects/Keywords: imperialism; Japan; Marxism; science; technology; Tosaka Jun

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APA (6th Edition):

Lei, Q. (2018). TOWARDS A MATERIALIST CONCEPTION OF SCIENCE—SCIENCE DEBATES IN INTERWAR & WARTIME JAPAN, 1920-1945 . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp017p88ck31r

Chicago Manual of Style (16th Edition):

Lei, Qinyuan. “TOWARDS A MATERIALIST CONCEPTION OF SCIENCE—SCIENCE DEBATES IN INTERWAR & WARTIME JAPAN, 1920-1945 .” 2018. Doctoral Dissertation, Princeton University. Accessed April 19, 2019. http://arks.princeton.edu/ark:/88435/dsp017p88ck31r.

MLA Handbook (7th Edition):

Lei, Qinyuan. “TOWARDS A MATERIALIST CONCEPTION OF SCIENCE—SCIENCE DEBATES IN INTERWAR & WARTIME JAPAN, 1920-1945 .” 2018. Web. 19 Apr 2019.

Vancouver:

Lei Q. TOWARDS A MATERIALIST CONCEPTION OF SCIENCE—SCIENCE DEBATES IN INTERWAR & WARTIME JAPAN, 1920-1945 . [Internet] [Doctoral dissertation]. Princeton University; 2018. [cited 2019 Apr 19]. Available from: http://arks.princeton.edu/ark:/88435/dsp017p88ck31r.

Council of Science Editors:

Lei Q. TOWARDS A MATERIALIST CONCEPTION OF SCIENCE—SCIENCE DEBATES IN INTERWAR & WARTIME JAPAN, 1920-1945 . [Doctoral Dissertation]. Princeton University; 2018. Available from: http://arks.princeton.edu/ark:/88435/dsp017p88ck31r

6. Silva, Flavio Sousa. Clonagem, expressão, purificação e caracterização estrutural da região AP-1 da oncoproteína Jun.

Degree: Mestrado, Tecnologia Nuclear - Aplicações, 2014, University of São Paulo

A proteína jun é um dos principais integrantes do complexo AP-1 e está envolvido nos processos inflamatórios, diferenciação, apoptose e migração celular. Esta proteína pode… (more)

Subjects/Keywords: AP-1; AP-1; cancer; câncer; Jun; Jun; oncogene; oncogene; oncoprotein; oncoproteína

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APA (6th Edition):

Silva, F. S. (2014). Clonagem, expressão, purificação e caracterização estrutural da região AP-1 da oncoproteína Jun. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/85/85131/tde-18092014-091537/ ;

Chicago Manual of Style (16th Edition):

Silva, Flavio Sousa. “Clonagem, expressão, purificação e caracterização estrutural da região AP-1 da oncoproteína Jun.” 2014. Masters Thesis, University of São Paulo. Accessed April 19, 2019. http://www.teses.usp.br/teses/disponiveis/85/85131/tde-18092014-091537/ ;.

MLA Handbook (7th Edition):

Silva, Flavio Sousa. “Clonagem, expressão, purificação e caracterização estrutural da região AP-1 da oncoproteína Jun.” 2014. Web. 19 Apr 2019.

Vancouver:

Silva FS. Clonagem, expressão, purificação e caracterização estrutural da região AP-1 da oncoproteína Jun. [Internet] [Masters thesis]. University of São Paulo; 2014. [cited 2019 Apr 19]. Available from: http://www.teses.usp.br/teses/disponiveis/85/85131/tde-18092014-091537/ ;.

Council of Science Editors:

Silva FS. Clonagem, expressão, purificação e caracterização estrutural da região AP-1 da oncoproteína Jun. [Masters Thesis]. University of São Paulo; 2014. Available from: http://www.teses.usp.br/teses/disponiveis/85/85131/tde-18092014-091537/ ;

7. Rabarimeriarijaona, Sitraka. Mécanismes physiopathologiques de la forme AR-CMT2A de la maladie de Charcot-Marie-Tooth : Physiopathological mecanisms study of the autosomal recessive form AR-CMT2A of Charcot-Marie-Tooth desease.

Degree: Docteur es, Pathologie humaine. Génétique humaine, 2014, Aix Marseille Université

La maladie de Charcot-Marie-Tooth (CMT) est une maladie neurologique héréditaire du système nerveux périphérique. A ce jour, près de 80 gènes sont décrits comme étant… (more)

Subjects/Keywords: Cmt; Lamine; C-Jun; Hes5; Lmna; Cmt; Lamin; C-Jun; Hes5; Lmna

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APA (6th Edition):

Rabarimeriarijaona, S. (2014). Mécanismes physiopathologiques de la forme AR-CMT2A de la maladie de Charcot-Marie-Tooth : Physiopathological mecanisms study of the autosomal recessive form AR-CMT2A of Charcot-Marie-Tooth desease. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2014AIXM5087

Chicago Manual of Style (16th Edition):

Rabarimeriarijaona, Sitraka. “Mécanismes physiopathologiques de la forme AR-CMT2A de la maladie de Charcot-Marie-Tooth : Physiopathological mecanisms study of the autosomal recessive form AR-CMT2A of Charcot-Marie-Tooth desease.” 2014. Doctoral Dissertation, Aix Marseille Université. Accessed April 19, 2019. http://www.theses.fr/2014AIXM5087.

MLA Handbook (7th Edition):

Rabarimeriarijaona, Sitraka. “Mécanismes physiopathologiques de la forme AR-CMT2A de la maladie de Charcot-Marie-Tooth : Physiopathological mecanisms study of the autosomal recessive form AR-CMT2A of Charcot-Marie-Tooth desease.” 2014. Web. 19 Apr 2019.

Vancouver:

Rabarimeriarijaona S. Mécanismes physiopathologiques de la forme AR-CMT2A de la maladie de Charcot-Marie-Tooth : Physiopathological mecanisms study of the autosomal recessive form AR-CMT2A of Charcot-Marie-Tooth desease. [Internet] [Doctoral dissertation]. Aix Marseille Université 2014. [cited 2019 Apr 19]. Available from: http://www.theses.fr/2014AIXM5087.

Council of Science Editors:

Rabarimeriarijaona S. Mécanismes physiopathologiques de la forme AR-CMT2A de la maladie de Charcot-Marie-Tooth : Physiopathological mecanisms study of the autosomal recessive form AR-CMT2A of Charcot-Marie-Tooth desease. [Doctoral Dissertation]. Aix Marseille Université 2014. Available from: http://www.theses.fr/2014AIXM5087

8. Côrtes, Arthur Rodriguez Gonzalez. Comparação imunoistoquímica das expressões das proteínas p27 e c-jun na carcinogênese intra-oral.

Degree: Mestrado, Patologia Bucal, 2009, University of São Paulo

A expressão de diversas proteínas do ciclo celular tem sido estudada em vários tipos de lesões malignas. Entre as principais está a p27, que é… (more)

Subjects/Keywords: Carcinoma epidermóide; Carcinoma epidermóide; Displasia epitelial; Displasia epitelial; Imunoistoquímica; Imunoistoquímica; p27 c-jun; p27 c-jun

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APA (6th Edition):

Côrtes, A. R. G. (2009). Comparação imunoistoquímica das expressões das proteínas p27 e c-jun na carcinogênese intra-oral. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/23/23141/tde-19122009-111607/ ;

Chicago Manual of Style (16th Edition):

Côrtes, Arthur Rodriguez Gonzalez. “Comparação imunoistoquímica das expressões das proteínas p27 e c-jun na carcinogênese intra-oral.” 2009. Masters Thesis, University of São Paulo. Accessed April 19, 2019. http://www.teses.usp.br/teses/disponiveis/23/23141/tde-19122009-111607/ ;.

MLA Handbook (7th Edition):

Côrtes, Arthur Rodriguez Gonzalez. “Comparação imunoistoquímica das expressões das proteínas p27 e c-jun na carcinogênese intra-oral.” 2009. Web. 19 Apr 2019.

Vancouver:

Côrtes ARG. Comparação imunoistoquímica das expressões das proteínas p27 e c-jun na carcinogênese intra-oral. [Internet] [Masters thesis]. University of São Paulo; 2009. [cited 2019 Apr 19]. Available from: http://www.teses.usp.br/teses/disponiveis/23/23141/tde-19122009-111607/ ;.

Council of Science Editors:

Côrtes ARG. Comparação imunoistoquímica das expressões das proteínas p27 e c-jun na carcinogênese intra-oral. [Masters Thesis]. University of São Paulo; 2009. Available from: http://www.teses.usp.br/teses/disponiveis/23/23141/tde-19122009-111607/ ;

9. Acien, Caroline. Rôle du facteur de transcription c-Jun dans l'ontogénie et l'homéostasie des macrophages : The role of c-Jun in macrophage ontogeny and homeostasie.

Degree: Docteur es, Immunologie, 2014, Aix Marseille Université

Pour étudier le rôle de c-Jun dans les macrophages, nous avons développé deux modèles murins présentant une délétion spécifique de Jun dans la lignée de… (more)

Subjects/Keywords: C-Jun; Macrophages; Homéostasie; Prolifération; Cycle cellulaire; Cellules souches; C-Jun; Macrophages; Homeostasis; Proliferation; Cell cycle; Stem cells; 571

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APA (6th Edition):

Acien, C. (2014). Rôle du facteur de transcription c-Jun dans l'ontogénie et l'homéostasie des macrophages : The role of c-Jun in macrophage ontogeny and homeostasie. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2014AIXM4010

Chicago Manual of Style (16th Edition):

Acien, Caroline. “Rôle du facteur de transcription c-Jun dans l'ontogénie et l'homéostasie des macrophages : The role of c-Jun in macrophage ontogeny and homeostasie.” 2014. Doctoral Dissertation, Aix Marseille Université. Accessed April 19, 2019. http://www.theses.fr/2014AIXM4010.

MLA Handbook (7th Edition):

Acien, Caroline. “Rôle du facteur de transcription c-Jun dans l'ontogénie et l'homéostasie des macrophages : The role of c-Jun in macrophage ontogeny and homeostasie.” 2014. Web. 19 Apr 2019.

Vancouver:

Acien C. Rôle du facteur de transcription c-Jun dans l'ontogénie et l'homéostasie des macrophages : The role of c-Jun in macrophage ontogeny and homeostasie. [Internet] [Doctoral dissertation]. Aix Marseille Université 2014. [cited 2019 Apr 19]. Available from: http://www.theses.fr/2014AIXM4010.

Council of Science Editors:

Acien C. Rôle du facteur de transcription c-Jun dans l'ontogénie et l'homéostasie des macrophages : The role of c-Jun in macrophage ontogeny and homeostasie. [Doctoral Dissertation]. Aix Marseille Université 2014. Available from: http://www.theses.fr/2014AIXM4010


University of Alberta

10. Zhang, Jing Xi. Investigating the functions of the c-Jun and JunB transcription factors in classical Hodgkin Lymphoma.

Degree: MS, Department of Medical Microbiology and Immunology, 2016, University of Alberta

 Classical Hodgkin lymphoma (cHL) is characterized by the presence of abnormal mononuclear Hodgkin and multinuclear Reed-Sternberg (HRS) cells, which are thought to be derived from… (more)

Subjects/Keywords: AP-1; JunB; c-Jun; classical Hodgkin lymphoma

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APA (6th Edition):

Zhang, J. X. (2016). Investigating the functions of the c-Jun and JunB transcription factors in classical Hodgkin Lymphoma. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/csj139218c

Chicago Manual of Style (16th Edition):

Zhang, Jing Xi. “Investigating the functions of the c-Jun and JunB transcription factors in classical Hodgkin Lymphoma.” 2016. Masters Thesis, University of Alberta. Accessed April 19, 2019. https://era.library.ualberta.ca/files/csj139218c.

MLA Handbook (7th Edition):

Zhang, Jing Xi. “Investigating the functions of the c-Jun and JunB transcription factors in classical Hodgkin Lymphoma.” 2016. Web. 19 Apr 2019.

Vancouver:

Zhang JX. Investigating the functions of the c-Jun and JunB transcription factors in classical Hodgkin Lymphoma. [Internet] [Masters thesis]. University of Alberta; 2016. [cited 2019 Apr 19]. Available from: https://era.library.ualberta.ca/files/csj139218c.

Council of Science Editors:

Zhang JX. Investigating the functions of the c-Jun and JunB transcription factors in classical Hodgkin Lymphoma. [Masters Thesis]. University of Alberta; 2016. Available from: https://era.library.ualberta.ca/files/csj139218c

11. Ito, Satoyasu; Ozawa, Kentaro; Zhao, Jing; Kyotani, Yoji; Nagayama, Kosuke. Olmesartan inhibits cultured rat aortic smooth muscle cell death induced by cyclic mechanical stretch through the inhibition of the c-Jun N-terminal kinase and p38 signaling pathways. : オルメサルタンは、JNK及びp38シグナル経路を抑制することで、周期的機械的伸展による培養大動脈平滑筋細胞死を抑制する.

Degree: 博士(医学), 2015, Nara Medical University / 奈良県立医科大学

Acute aortic dissection (AAD) is a life-threating disease; however, there is almost no effective pharmacotherapy for it. An increase in c-Jun N-terminal kinase (JNK) phosphorylation… (more)

Subjects/Keywords: Stretch; c-Jun N-terminal kinase; p38; Acute aortic dissection; Olmesartan

Page 1

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APA (6th Edition):

Ito, Satoyasu; Ozawa, Kentaro; Zhao, Jing; Kyotani, Yoji; Nagayama, K. (2015). Olmesartan inhibits cultured rat aortic smooth muscle cell death induced by cyclic mechanical stretch through the inhibition of the c-Jun N-terminal kinase and p38 signaling pathways. : オルメサルタンは、JNK及びp38シグナル経路を抑制することで、周期的機械的伸展による培養大動脈平滑筋細胞死を抑制する. (Thesis). Nara Medical University / 奈良県立医科大学. Retrieved from http://hdl.handle.net/10564/2939

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):

Ito, Satoyasu; Ozawa, Kentaro; Zhao, Jing; Kyotani, Yoji; Nagayama, Kosuke. “Olmesartan inhibits cultured rat aortic smooth muscle cell death induced by cyclic mechanical stretch through the inhibition of the c-Jun N-terminal kinase and p38 signaling pathways. : オルメサルタンは、JNK及びp38シグナル経路を抑制することで、周期的機械的伸展による培養大動脈平滑筋細胞死を抑制する.” 2015. Thesis, Nara Medical University / 奈良県立医科大学. Accessed April 19, 2019. http://hdl.handle.net/10564/2939.

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

MLA Handbook (7th Edition):

Ito, Satoyasu; Ozawa, Kentaro; Zhao, Jing; Kyotani, Yoji; Nagayama, Kosuke. “Olmesartan inhibits cultured rat aortic smooth muscle cell death induced by cyclic mechanical stretch through the inhibition of the c-Jun N-terminal kinase and p38 signaling pathways. : オルメサルタンは、JNK及びp38シグナル経路を抑制することで、周期的機械的伸展による培養大動脈平滑筋細胞死を抑制する.” 2015. Web. 19 Apr 2019.

Vancouver:

Ito, Satoyasu; Ozawa, Kentaro; Zhao, Jing; Kyotani, Yoji; Nagayama K. Olmesartan inhibits cultured rat aortic smooth muscle cell death induced by cyclic mechanical stretch through the inhibition of the c-Jun N-terminal kinase and p38 signaling pathways. : オルメサルタンは、JNK及びp38シグナル経路を抑制することで、周期的機械的伸展による培養大動脈平滑筋細胞死を抑制する. [Internet] [Thesis]. Nara Medical University / 奈良県立医科大学; 2015. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/10564/2939.

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

Council of Science Editors:

Ito, Satoyasu; Ozawa, Kentaro; Zhao, Jing; Kyotani, Yoji; Nagayama K. Olmesartan inhibits cultured rat aortic smooth muscle cell death induced by cyclic mechanical stretch through the inhibition of the c-Jun N-terminal kinase and p38 signaling pathways. : オルメサルタンは、JNK及びp38シグナル経路を抑制することで、周期的機械的伸展による培養大動脈平滑筋細胞死を抑制する. [Thesis]. Nara Medical University / 奈良県立医科大学; 2015. Available from: http://hdl.handle.net/10564/2939

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

12. ROLIM, Leonardo do Nascimento. Estudos fisiológicos, bioquímicos e moleculares de isolados de Ganoderma lucidum (Fr.) karst. cultivados pela técnica Jun-Cao .

Degree: 2009, Universidade Federal de Pernambuco

 Ganoderma lucidum é um basidiomiceto muito popular na medicina tradicional chinesa, sendo chamado de Lingzhi ou cogumelo da imortalidade . Estudos revelaram diversas propriedades farmacológicas… (more)

Subjects/Keywords: Cogumelos; Ganoderma lucidum; Jun-Cao; Análises bioquímicas; RAPD

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APA (6th Edition):

ROLIM, L. d. N. (2009). Estudos fisiológicos, bioquímicos e moleculares de isolados de Ganoderma lucidum (Fr.) karst. cultivados pela técnica Jun-Cao . (Thesis). Universidade Federal de Pernambuco. Retrieved from http://repositorio.ufpe.br/handle/123456789/399

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):

ROLIM, Leonardo do Nascimento. “Estudos fisiológicos, bioquímicos e moleculares de isolados de Ganoderma lucidum (Fr.) karst. cultivados pela técnica Jun-Cao .” 2009. Thesis, Universidade Federal de Pernambuco. Accessed April 19, 2019. http://repositorio.ufpe.br/handle/123456789/399.

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

MLA Handbook (7th Edition):

ROLIM, Leonardo do Nascimento. “Estudos fisiológicos, bioquímicos e moleculares de isolados de Ganoderma lucidum (Fr.) karst. cultivados pela técnica Jun-Cao .” 2009. Web. 19 Apr 2019.

Vancouver:

ROLIM LdN. Estudos fisiológicos, bioquímicos e moleculares de isolados de Ganoderma lucidum (Fr.) karst. cultivados pela técnica Jun-Cao . [Internet] [Thesis]. Universidade Federal de Pernambuco; 2009. [cited 2019 Apr 19]. Available from: http://repositorio.ufpe.br/handle/123456789/399.

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

Council of Science Editors:

ROLIM LdN. Estudos fisiológicos, bioquímicos e moleculares de isolados de Ganoderma lucidum (Fr.) karst. cultivados pela técnica Jun-Cao . [Thesis]. Universidade Federal de Pernambuco; 2009. Available from: http://repositorio.ufpe.br/handle/123456789/399

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


Case Western Reserve University

13. Wang, Wei-Ming. AP-1-MEDIATED REGULATION OF HPV CHROMATIN TRANSCRIPTION.

Degree: PhD, Biochemistry, 2008, Case Western Reserve University

 AP-1 complexes are a family of transcription factors ubiquitously expressed in different cell types. Transcriptional regulation mediated by AP-1 has been extensively studied; AP-1 mainly… (more)

Subjects/Keywords: AP-1; p300; HPV; chromatin; transcription; Jun; Fos

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APA (6th Edition):

Wang, W. (2008). AP-1-MEDIATED REGULATION OF HPV CHROMATIN TRANSCRIPTION. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1199480473

Chicago Manual of Style (16th Edition):

Wang, Wei-Ming. “AP-1-MEDIATED REGULATION OF HPV CHROMATIN TRANSCRIPTION.” 2008. Doctoral Dissertation, Case Western Reserve University. Accessed April 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1199480473.

MLA Handbook (7th Edition):

Wang, Wei-Ming. “AP-1-MEDIATED REGULATION OF HPV CHROMATIN TRANSCRIPTION.” 2008. Web. 19 Apr 2019.

Vancouver:

Wang W. AP-1-MEDIATED REGULATION OF HPV CHROMATIN TRANSCRIPTION. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2008. [cited 2019 Apr 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1199480473.

Council of Science Editors:

Wang W. AP-1-MEDIATED REGULATION OF HPV CHROMATIN TRANSCRIPTION. [Doctoral Dissertation]. Case Western Reserve University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1199480473


University of Arizona

14. Pomerantz, Michael Ward, 1944-. A critical study of "Chih-yeh," a short story by Hsiao Chün .

Degree: 1971, University of Arizona

Subjects/Keywords: Xiao; Jun; 1908-  – Chih-yeh.

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APA (6th Edition):

Pomerantz, Michael Ward, 1. (1971). A critical study of "Chih-yeh," a short story by Hsiao Chün . (Masters Thesis). University of Arizona. Retrieved from http://hdl.handle.net/10150/318584

Chicago Manual of Style (16th Edition):

Pomerantz, Michael Ward, 1944-. “A critical study of "Chih-yeh," a short story by Hsiao Chün .” 1971. Masters Thesis, University of Arizona. Accessed April 19, 2019. http://hdl.handle.net/10150/318584.

MLA Handbook (7th Edition):

Pomerantz, Michael Ward, 1944-. “A critical study of "Chih-yeh," a short story by Hsiao Chün .” 1971. Web. 19 Apr 2019.

Vancouver:

Pomerantz, Michael Ward 1. A critical study of "Chih-yeh," a short story by Hsiao Chün . [Internet] [Masters thesis]. University of Arizona; 1971. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/10150/318584.

Council of Science Editors:

Pomerantz, Michael Ward 1. A critical study of "Chih-yeh," a short story by Hsiao Chün . [Masters Thesis]. University of Arizona; 1971. Available from: http://hdl.handle.net/10150/318584


Delft University of Technology

15. Chang, H.J. In search for balance in contrasts: graduation project for a designcentre in Rotterdam:.

Degree: Architecture, 2008, Delft University of Technology

 There is no Rotterdam identity. Rotterdam has characterizations that everybody can sense namely the big contrasts in Rotterdam. Contrasts originated from top-down-planning of urban renewal… (more)

Subjects/Keywords: public realm; public building; rotterdam; hui jun chang; design

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APA (6th Edition):

Chang, H. J. (2008). In search for balance in contrasts: graduation project for a designcentre in Rotterdam:. (Masters Thesis). Delft University of Technology. Retrieved from http://resolver.tudelft.nl/uuid:c02cfae3-5070-4fa5-99de-039a016ec637

Chicago Manual of Style (16th Edition):

Chang, H J. “In search for balance in contrasts: graduation project for a designcentre in Rotterdam:.” 2008. Masters Thesis, Delft University of Technology. Accessed April 19, 2019. http://resolver.tudelft.nl/uuid:c02cfae3-5070-4fa5-99de-039a016ec637.

MLA Handbook (7th Edition):

Chang, H J. “In search for balance in contrasts: graduation project for a designcentre in Rotterdam:.” 2008. Web. 19 Apr 2019.

Vancouver:

Chang HJ. In search for balance in contrasts: graduation project for a designcentre in Rotterdam:. [Internet] [Masters thesis]. Delft University of Technology; 2008. [cited 2019 Apr 19]. Available from: http://resolver.tudelft.nl/uuid:c02cfae3-5070-4fa5-99de-039a016ec637.

Council of Science Editors:

Chang HJ. In search for balance in contrasts: graduation project for a designcentre in Rotterdam:. [Masters Thesis]. Delft University of Technology; 2008. Available from: http://resolver.tudelft.nl/uuid:c02cfae3-5070-4fa5-99de-039a016ec637


University of New South Wales

16. Sheahan, Anjali Viswa. Targeting stress-induced signaling pathways in pancreatic cancer and vascular disease.

Degree: Medical Sciences, 2013, University of New South Wales

 Cellular stress is a consequence of oncogenic transformation that ultimately results in a highly proliferative cell with malignant potential. Reduced vascular perfusion is a result… (more)

Subjects/Keywords: Vascular disease; Cellular stress; Pancreatic cancer; c-Jun; ATF-4; YrdC

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APA (6th Edition):

Sheahan, A. V. (2013). Targeting stress-induced signaling pathways in pancreatic cancer and vascular disease. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/53689 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12384/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Sheahan, Anjali Viswa. “Targeting stress-induced signaling pathways in pancreatic cancer and vascular disease.” 2013. Doctoral Dissertation, University of New South Wales. Accessed April 19, 2019. http://handle.unsw.edu.au/1959.4/53689 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12384/SOURCE02?view=true.

MLA Handbook (7th Edition):

Sheahan, Anjali Viswa. “Targeting stress-induced signaling pathways in pancreatic cancer and vascular disease.” 2013. Web. 19 Apr 2019.

Vancouver:

Sheahan AV. Targeting stress-induced signaling pathways in pancreatic cancer and vascular disease. [Internet] [Doctoral dissertation]. University of New South Wales; 2013. [cited 2019 Apr 19]. Available from: http://handle.unsw.edu.au/1959.4/53689 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12384/SOURCE02?view=true.

Council of Science Editors:

Sheahan AV. Targeting stress-induced signaling pathways in pancreatic cancer and vascular disease. [Doctoral Dissertation]. University of New South Wales; 2013. Available from: http://handle.unsw.edu.au/1959.4/53689 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12384/SOURCE02?view=true


University of Southern California

17. Tao, Litao. Investigation of the molecular mechanisms of ototoxicity.

Degree: PhD, Genetic, Molecular and Cellular Biology, 2014, University of Southern California

 Sensory hair cells are essential for transforming the mechanical vibrations of sound into electric signals that our nervous system can interpret. However, sensory hair cells… (more)

Subjects/Keywords: aminoglycoside antibiotics; ototoxicity; cyclin-dependent kinase 2; c-Jun; RNA sequencing

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APA (6th Edition):

Tao, L. (2014). Investigation of the molecular mechanisms of ototoxicity. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/426847/rec/3645

Chicago Manual of Style (16th Edition):

Tao, Litao. “Investigation of the molecular mechanisms of ototoxicity.” 2014. Doctoral Dissertation, University of Southern California. Accessed April 19, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/426847/rec/3645.

MLA Handbook (7th Edition):

Tao, Litao. “Investigation of the molecular mechanisms of ototoxicity.” 2014. Web. 19 Apr 2019.

Vancouver:

Tao L. Investigation of the molecular mechanisms of ototoxicity. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2019 Apr 19]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/426847/rec/3645.

Council of Science Editors:

Tao L. Investigation of the molecular mechanisms of ototoxicity. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/426847/rec/3645


University of Southern California

18. Lee, Jennifer Yeh. The discovery of a novel 105kDa complex comprised of BUB3, C-JUN and SUMO-1 and its relationship to ovarian cancer development.

Degree: PhD, Pathobiology, 2009, University of Southern California

 This work is based on the hypothesis that post-translational modifications catalyzed by ubiquitin and SUMO play an important role in tumor development and progression. Nuclear… (more)

Subjects/Keywords: BUB3; C-JUN; SUMO-1; mitotic checkpoint; aneuploidy; tetraploidy

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APA (6th Edition):

Lee, J. Y. (2009). The discovery of a novel 105kDa complex comprised of BUB3, C-JUN and SUMO-1 and its relationship to ovarian cancer development. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/271059/rec/6562

Chicago Manual of Style (16th Edition):

Lee, Jennifer Yeh. “The discovery of a novel 105kDa complex comprised of BUB3, C-JUN and SUMO-1 and its relationship to ovarian cancer development.” 2009. Doctoral Dissertation, University of Southern California. Accessed April 19, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/271059/rec/6562.

MLA Handbook (7th Edition):

Lee, Jennifer Yeh. “The discovery of a novel 105kDa complex comprised of BUB3, C-JUN and SUMO-1 and its relationship to ovarian cancer development.” 2009. Web. 19 Apr 2019.

Vancouver:

Lee JY. The discovery of a novel 105kDa complex comprised of BUB3, C-JUN and SUMO-1 and its relationship to ovarian cancer development. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2019 Apr 19]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/271059/rec/6562.

Council of Science Editors:

Lee JY. The discovery of a novel 105kDa complex comprised of BUB3, C-JUN and SUMO-1 and its relationship to ovarian cancer development. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/271059/rec/6562

19. Schlummer, Stefanie. Synthese und biologische Evaluierung von Lipo-, Glyco- und Phosphopeptiden.

Degree: 2005, Universität Dortmund

 Um Aussagen über komplexe molekularbiologische Vorgänge zu treffen, werden an diesen Prozessen beteiligte Proteine bzw. Partialstrukturen dieser Proteine als wichtige Hilfsmittel eingesetzt. Viele dieser Proteine… (more)

Subjects/Keywords: Glycopeptide; glycopeptides; Kernimport; Lipopeptide; lipopeptides; NLS; NLS; N-Ras; N-Ras; nuclear import; Phosphopeptide; phosphopeptides; semisynthetic Proteins; Semisynthetische Proteine; v-Jun-protein; v-Jun-Protein; 540

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APA (6th Edition):

Schlummer, S. (2005). Synthese und biologische Evaluierung von Lipo-, Glyco- und Phosphopeptiden. (Thesis). Universität Dortmund. Retrieved from http://hdl.handle.net/2003/21355

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):

Schlummer, Stefanie. “Synthese und biologische Evaluierung von Lipo-, Glyco- und Phosphopeptiden.” 2005. Thesis, Universität Dortmund. Accessed April 19, 2019. http://hdl.handle.net/2003/21355.

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

MLA Handbook (7th Edition):

Schlummer, Stefanie. “Synthese und biologische Evaluierung von Lipo-, Glyco- und Phosphopeptiden.” 2005. Web. 19 Apr 2019.

Vancouver:

Schlummer S. Synthese und biologische Evaluierung von Lipo-, Glyco- und Phosphopeptiden. [Internet] [Thesis]. Universität Dortmund; 2005. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/2003/21355.

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

Council of Science Editors:

Schlummer S. Synthese und biologische Evaluierung von Lipo-, Glyco- und Phosphopeptiden. [Thesis]. Universität Dortmund; 2005. Available from: http://hdl.handle.net/2003/21355

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

20. Rejas, Roberto Anaximandro Garcia. Estudo da imunoexpressão das proteínas C-JUN e JUNB em carcinoma adenóide cístico e adenocarcinoma polimorfo de baixo grau de malignidade de glândulas salivares.

Degree: Mestrado, Patologia Bucal, 2008, University of São Paulo

O carcinoma adenóide cístico e o adenocarcinoma polimorfo de baixo grau de malignidade são neoplasmas de glândulas salivares. O carcinoma adenóide cístico pode apresentar-se em… (more)

Subjects/Keywords: Adenocarcinoma polimorfo de baixo grau de malignidade; Adenoid cystic carcinoma; C-jun; C-jun; Carcinoma adenóide cístico; JunB; JunB; Polymorphous low-grade adenocarcinoma

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APA (6th Edition):

Rejas, R. A. G. (2008). Estudo da imunoexpressão das proteínas C-JUN e JUNB em carcinoma adenóide cístico e adenocarcinoma polimorfo de baixo grau de malignidade de glândulas salivares. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/23/23141/tde-20012009-151227/ ;

Chicago Manual of Style (16th Edition):

Rejas, Roberto Anaximandro Garcia. “Estudo da imunoexpressão das proteínas C-JUN e JUNB em carcinoma adenóide cístico e adenocarcinoma polimorfo de baixo grau de malignidade de glândulas salivares.” 2008. Masters Thesis, University of São Paulo. Accessed April 19, 2019. http://www.teses.usp.br/teses/disponiveis/23/23141/tde-20012009-151227/ ;.

MLA Handbook (7th Edition):

Rejas, Roberto Anaximandro Garcia. “Estudo da imunoexpressão das proteínas C-JUN e JUNB em carcinoma adenóide cístico e adenocarcinoma polimorfo de baixo grau de malignidade de glândulas salivares.” 2008. Web. 19 Apr 2019.

Vancouver:

Rejas RAG. Estudo da imunoexpressão das proteínas C-JUN e JUNB em carcinoma adenóide cístico e adenocarcinoma polimorfo de baixo grau de malignidade de glândulas salivares. [Internet] [Masters thesis]. University of São Paulo; 2008. [cited 2019 Apr 19]. Available from: http://www.teses.usp.br/teses/disponiveis/23/23141/tde-20012009-151227/ ;.

Council of Science Editors:

Rejas RAG. Estudo da imunoexpressão das proteínas C-JUN e JUNB em carcinoma adenóide cístico e adenocarcinoma polimorfo de baixo grau de malignidade de glândulas salivares. [Masters Thesis]. University of São Paulo; 2008. Available from: http://www.teses.usp.br/teses/disponiveis/23/23141/tde-20012009-151227/ ;


University of Helsinki

21. Kärpänen, Terhi. Das Onkogen jun und seine Zielgene: Klonierung und Sequenzierung der Hühner-BKJ-cDNA.

Degree: 1997, University of Helsinki

Subjects/Keywords: BKJ; jun; Onkogen; Zelltransformation; Zielgen; Biochemie; BKJ; jun; Onkogen; Zelltransformation; Zielgen

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APA (6th Edition):

Kärpänen, T. (1997). Das Onkogen jun und seine Zielgene: Klonierung und Sequenzierung der Hühner-BKJ-cDNA. (Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/157196

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):

Kärpänen, Terhi. “Das Onkogen jun und seine Zielgene: Klonierung und Sequenzierung der Hühner-BKJ-cDNA.” 1997. Thesis, University of Helsinki. Accessed April 19, 2019. http://hdl.handle.net/10138/157196.

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

MLA Handbook (7th Edition):

Kärpänen, Terhi. “Das Onkogen jun und seine Zielgene: Klonierung und Sequenzierung der Hühner-BKJ-cDNA.” 1997. Web. 19 Apr 2019.

Vancouver:

Kärpänen T. Das Onkogen jun und seine Zielgene: Klonierung und Sequenzierung der Hühner-BKJ-cDNA. [Internet] [Thesis]. University of Helsinki; 1997. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/10138/157196.

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

Council of Science Editors:

Kärpänen T. Das Onkogen jun und seine Zielgene: Klonierung und Sequenzierung der Hühner-BKJ-cDNA. [Thesis]. University of Helsinki; 1997. Available from: http://hdl.handle.net/10138/157196

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


University of Helsinki

22. Jänne, Marja. Onkoproteiinit Fos ja Jun transkription säätelijöinä.

Degree: 1994, University of Helsinki

Subjects/Keywords: Fos; Jun; transkriptiotekijä AP-1; leusiiniketju; Biokemia; Fos; Jun; transkriptiotekijä AP-1; leusiiniketju

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APA (6th Edition):

Jänne, M. (1994). Onkoproteiinit Fos ja Jun transkription säätelijöinä. (Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/157690

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):

Jänne, Marja. “Onkoproteiinit Fos ja Jun transkription säätelijöinä.” 1994. Thesis, University of Helsinki. Accessed April 19, 2019. http://hdl.handle.net/10138/157690.

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

MLA Handbook (7th Edition):

Jänne, Marja. “Onkoproteiinit Fos ja Jun transkription säätelijöinä.” 1994. Web. 19 Apr 2019.

Vancouver:

Jänne M. Onkoproteiinit Fos ja Jun transkription säätelijöinä. [Internet] [Thesis]. University of Helsinki; 1994. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/10138/157690.

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

Council of Science Editors:

Jänne M. Onkoproteiinit Fos ja Jun transkription säätelijöinä. [Thesis]. University of Helsinki; 1994. Available from: http://hdl.handle.net/10138/157690

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


University of Southern California

23. Barker, Lexie. The invisible cuisine: why Filipino food has gone unnoticed.

Degree: MA, Specialized Journalism, 2014, University of Southern California

 Filipinos are one of the largest immigrant groups in the United States, yet their food remains largely invisible in mainstream American cuisine. Embarking on a… (more)

Subjects/Keywords: Filipino food; Filipino cuisine; adobo; kare-kare; crab mentality; Filipino immigrants; Amy Besa; purple yam; Cendrillon; Jun Belen; jun-Blog; Nicole Ponseca; Maharlika; Jeepney

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APA (6th Edition):

Barker, L. (2014). The invisible cuisine: why Filipino food has gone unnoticed. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/436660/rec/6916

Chicago Manual of Style (16th Edition):

Barker, Lexie. “The invisible cuisine: why Filipino food has gone unnoticed.” 2014. Masters Thesis, University of Southern California. Accessed April 19, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/436660/rec/6916.

MLA Handbook (7th Edition):

Barker, Lexie. “The invisible cuisine: why Filipino food has gone unnoticed.” 2014. Web. 19 Apr 2019.

Vancouver:

Barker L. The invisible cuisine: why Filipino food has gone unnoticed. [Internet] [Masters thesis]. University of Southern California; 2014. [cited 2019 Apr 19]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/436660/rec/6916.

Council of Science Editors:

Barker L. The invisible cuisine: why Filipino food has gone unnoticed. [Masters Thesis]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/436660/rec/6916


Texas Medical Center

24. SHIN, JI-HYUN. THE NOVEL UPSTREAM REGULATOR OF FBXW7.

Degree: PhD, 2014, Texas Medical Center

  SCFFBXW7 is a tumor suppressor E3 ligase protein that targets numerous oncoproteins such as Cyclin E, c-Myc, c-Jun and MCL1. The deregulation of these… (more)

Subjects/Keywords: FBXW7; COP1; AKT; CSN6; Cyclin E; c-Jun; Medicine and Health Sciences

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APA (6th Edition):

SHIN, J. (2014). THE NOVEL UPSTREAM REGULATOR OF FBXW7. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/434

Chicago Manual of Style (16th Edition):

SHIN, JI-HYUN. “THE NOVEL UPSTREAM REGULATOR OF FBXW7.” 2014. Doctoral Dissertation, Texas Medical Center. Accessed April 19, 2019. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/434.

MLA Handbook (7th Edition):

SHIN, JI-HYUN. “THE NOVEL UPSTREAM REGULATOR OF FBXW7.” 2014. Web. 19 Apr 2019.

Vancouver:

SHIN J. THE NOVEL UPSTREAM REGULATOR OF FBXW7. [Internet] [Doctoral dissertation]. Texas Medical Center; 2014. [cited 2019 Apr 19]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/434.

Council of Science Editors:

SHIN J. THE NOVEL UPSTREAM REGULATOR OF FBXW7. [Doctoral Dissertation]. Texas Medical Center; 2014. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/434


University of Kansas

25. Saito, Chieko. PROTECTIVE STRATEGIES AGAINST ACETAMINOPHEN INDUCED HEPATOTOXICITY.

Degree: PhD, Pharmacology, Toxicology & Therapeutics, 2010, University of Kansas

 Acetaminophen (APAP) is a widely used analgesic, which is safe at therapeutic levels. APAP is mainly conjugated with glucuronic acid and sulfate to form water-soluble,… (more)

Subjects/Keywords: Health sciences; Toxicology; Acetaminophen; C-jun n-terminal kinase; Glutathione; Metallothionein; N-acetylcysteine

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

APA (6th Edition):

Saito, C. (2010). PROTECTIVE STRATEGIES AGAINST ACETAMINOPHEN INDUCED HEPATOTOXICITY. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/6369

Chicago Manual of Style (16th Edition):

Saito, Chieko. “PROTECTIVE STRATEGIES AGAINST ACETAMINOPHEN INDUCED HEPATOTOXICITY.” 2010. Doctoral Dissertation, University of Kansas. Accessed April 19, 2019. http://hdl.handle.net/1808/6369.

MLA Handbook (7th Edition):

Saito, Chieko. “PROTECTIVE STRATEGIES AGAINST ACETAMINOPHEN INDUCED HEPATOTOXICITY.” 2010. Web. 19 Apr 2019.

Vancouver:

Saito C. PROTECTIVE STRATEGIES AGAINST ACETAMINOPHEN INDUCED HEPATOTOXICITY. [Internet] [Doctoral dissertation]. University of Kansas; 2010. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/1808/6369.

Council of Science Editors:

Saito C. PROTECTIVE STRATEGIES AGAINST ACETAMINOPHEN INDUCED HEPATOTOXICITY. [Doctoral Dissertation]. University of Kansas; 2010. Available from: http://hdl.handle.net/1808/6369


University of Cincinnati

26. Meng, Qinghang. Role of MAP3K1 in Ocular Surface Development.

Degree: PhD, Medicine: Toxicology (Environmental Health), 2014, University of Cincinnati

 Mammalian eye development requires fusion of the upper and lower eyelids in embryogenesis. Many genetic mutations cause defective eyelid closure in mouse embryogenesis, resulting in… (more)

Subjects/Keywords: Developmental Biology; embryonic eyelid closure; MAP3K1; c-Jun; TCDD; tarsal muscles; extraocular muscles

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

APA (6th Edition):

Meng, Q. (2014). Role of MAP3K1 in Ocular Surface Development. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1406901599

Chicago Manual of Style (16th Edition):

Meng, Qinghang. “Role of MAP3K1 in Ocular Surface Development.” 2014. Doctoral Dissertation, University of Cincinnati. Accessed April 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1406901599.

MLA Handbook (7th Edition):

Meng, Qinghang. “Role of MAP3K1 in Ocular Surface Development.” 2014. Web. 19 Apr 2019.

Vancouver:

Meng Q. Role of MAP3K1 in Ocular Surface Development. [Internet] [Doctoral dissertation]. University of Cincinnati; 2014. [cited 2019 Apr 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1406901599.

Council of Science Editors:

Meng Q. Role of MAP3K1 in Ocular Surface Development. [Doctoral Dissertation]. University of Cincinnati; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1406901599


Université de Montréal

27. Larocque, Émilie. Caractérisation des transcrits antisens chez les rétrovirus HTLV et étude comparative des fonctions des protéines traduites à partir de ces transcrits antisens .

Degree: 2015, Université de Montréal

 Le premier membre de la famille des rétrovirus humains HTLV (Virus T-lymphotropique Humain), HTLV-1, a été découvert en 1980 et l’on estime aujourd’hui à plus… (more)

Subjects/Keywords: Rétrovirus; HTLV; APH; HBZ; Jun; Tax; B23; NoLS; Retrovirus; Antisense transcription; Nucleoli; Transcription antisens; Nucléole

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

APA (6th Edition):

Larocque, . (2015). Caractérisation des transcrits antisens chez les rétrovirus HTLV et étude comparative des fonctions des protéines traduites à partir de ces transcrits antisens . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/13038

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):

Larocque, Émilie. “Caractérisation des transcrits antisens chez les rétrovirus HTLV et étude comparative des fonctions des protéines traduites à partir de ces transcrits antisens .” 2015. Thesis, Université de Montréal. Accessed April 19, 2019. http://hdl.handle.net/1866/13038.

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

MLA Handbook (7th Edition):

Larocque, Émilie. “Caractérisation des transcrits antisens chez les rétrovirus HTLV et étude comparative des fonctions des protéines traduites à partir de ces transcrits antisens .” 2015. Web. 19 Apr 2019.

Vancouver:

Larocque . Caractérisation des transcrits antisens chez les rétrovirus HTLV et étude comparative des fonctions des protéines traduites à partir de ces transcrits antisens . [Internet] [Thesis]. Université de Montréal; 2015. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/1866/13038.

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

Council of Science Editors:

Larocque . Caractérisation des transcrits antisens chez les rétrovirus HTLV et étude comparative des fonctions des protéines traduites à partir de ces transcrits antisens . [Thesis]. Université de Montréal; 2015. Available from: http://hdl.handle.net/1866/13038

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


Kent State University

28. Chakrabarti, Arindam. PKR DEPENDENT UPREGULATION OF IMMEDIATE EARLY GENES AND ANTI-INFLAMMATORY CYTOKINE IL-10.

Degree: PhD, College of Biomedical Sciences, 2007, Kent State University

 Viral infection induces expression and activation of several genes involved directly or indirectly in antiviral defense. Protein kinase R (PKR), a Ser/Thr kinase induced by… (more)

Subjects/Keywords: Biology, Molecular; PKR; IL-10; c-jun; egr-1; immediate early genes

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

APA (6th Edition):

Chakrabarti, A. (2007). PKR DEPENDENT UPREGULATION OF IMMEDIATE EARLY GENES AND ANTI-INFLAMMATORY CYTOKINE IL-10. (Doctoral Dissertation). Kent State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=kent1176136341

Chicago Manual of Style (16th Edition):

Chakrabarti, Arindam. “PKR DEPENDENT UPREGULATION OF IMMEDIATE EARLY GENES AND ANTI-INFLAMMATORY CYTOKINE IL-10.” 2007. Doctoral Dissertation, Kent State University. Accessed April 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=kent1176136341.

MLA Handbook (7th Edition):

Chakrabarti, Arindam. “PKR DEPENDENT UPREGULATION OF IMMEDIATE EARLY GENES AND ANTI-INFLAMMATORY CYTOKINE IL-10.” 2007. Web. 19 Apr 2019.

Vancouver:

Chakrabarti A. PKR DEPENDENT UPREGULATION OF IMMEDIATE EARLY GENES AND ANTI-INFLAMMATORY CYTOKINE IL-10. [Internet] [Doctoral dissertation]. Kent State University; 2007. [cited 2019 Apr 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1176136341.

Council of Science Editors:

Chakrabarti A. PKR DEPENDENT UPREGULATION OF IMMEDIATE EARLY GENES AND ANTI-INFLAMMATORY CYTOKINE IL-10. [Doctoral Dissertation]. Kent State University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1176136341


University of Southern California

29. Ta, Trong Shawn. Becoming Teresa Teng, becoming-Taiwanese.

Degree: MA, East Asian Area Studies, 2009, University of Southern California

 Teresa Teng was loved by millions of Chinese across the world, and after her death, the People's Republic of China expropriated her music to symbolically… (more)

Subjects/Keywords: Asian studies; history; music; Taiwan; Taiwanese identity; China; Teresa Teng; Deng Li-jun

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

APA (6th Edition):

Ta, T. S. (2009). Becoming Teresa Teng, becoming-Taiwanese. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/279974/rec/1052

Chicago Manual of Style (16th Edition):

Ta, Trong Shawn. “Becoming Teresa Teng, becoming-Taiwanese.” 2009. Masters Thesis, University of Southern California. Accessed April 19, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/279974/rec/1052.

MLA Handbook (7th Edition):

Ta, Trong Shawn. “Becoming Teresa Teng, becoming-Taiwanese.” 2009. Web. 19 Apr 2019.

Vancouver:

Ta TS. Becoming Teresa Teng, becoming-Taiwanese. [Internet] [Masters thesis]. University of Southern California; 2009. [cited 2019 Apr 19]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/279974/rec/1052.

Council of Science Editors:

Ta TS. Becoming Teresa Teng, becoming-Taiwanese. [Masters Thesis]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/279974/rec/1052


University of Illinois – Chicago

30. Lowry, Jessica L. A Novel c-Jun-N-Terminal Kinase Pathway Stimulates High Output eNOS-derived NO in Inflamed Endothelium.

Degree: 2013, University of Illinois – Chicago

 High levels of nitric oxide (NO) generated in the vasculature under inflammatory conditions are usually attributed to inducible nitric oxide synthase (iNOS), but the role… (more)

Subjects/Keywords: Nitric Oxide; c-Jun-N-Terminal Kinase; endothelial nitric oxide synthase; inflammation; migration

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

APA (6th Edition):

Lowry, J. L. (2013). A Novel c-Jun-N-Terminal Kinase Pathway Stimulates High Output eNOS-derived NO in Inflamed Endothelium. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/10054

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):

Lowry, Jessica L. “A Novel c-Jun-N-Terminal Kinase Pathway Stimulates High Output eNOS-derived NO in Inflamed Endothelium.” 2013. Thesis, University of Illinois – Chicago. Accessed April 19, 2019. http://hdl.handle.net/10027/10054.

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

MLA Handbook (7th Edition):

Lowry, Jessica L. “A Novel c-Jun-N-Terminal Kinase Pathway Stimulates High Output eNOS-derived NO in Inflamed Endothelium.” 2013. Web. 19 Apr 2019.

Vancouver:

Lowry JL. A Novel c-Jun-N-Terminal Kinase Pathway Stimulates High Output eNOS-derived NO in Inflamed Endothelium. [Internet] [Thesis]. University of Illinois – Chicago; 2013. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/10027/10054.

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

Council of Science Editors:

Lowry JL. A Novel c-Jun-N-Terminal Kinase Pathway Stimulates High Output eNOS-derived NO in Inflamed Endothelium. [Thesis]. University of Illinois – Chicago; 2013. Available from: http://hdl.handle.net/10027/10054

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

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