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You searched for subject:(Cbl). Showing records 1 – 30 of 42 total matches.

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University of Rochester

1. Stripay, Jennifer L. Targeting a Network of Cancer Control Nodes through Rescue of c-Cbl; A Novel Therapeutic Approach for Glioblastoma Multiforme.

Degree: PhD, 2016, University of Rochester

 Glioblastoma multiforme is the most common primary brain tumor in adults, the most malignant of all intracranial tumors, and is associated with inevitable recurrence and… (more)

Subjects/Keywords: Cancer; cbl; Glioblastoma; Redox; Therapy

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

APA (6th Edition):

Stripay, J. L. (2016). Targeting a Network of Cancer Control Nodes through Rescue of c-Cbl; A Novel Therapeutic Approach for Glioblastoma Multiforme. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/31636

Chicago Manual of Style (16th Edition):

Stripay, Jennifer L. “Targeting a Network of Cancer Control Nodes through Rescue of c-Cbl; A Novel Therapeutic Approach for Glioblastoma Multiforme.” 2016. Doctoral Dissertation, University of Rochester. Accessed August 10, 2020. http://hdl.handle.net/1802/31636.

MLA Handbook (7th Edition):

Stripay, Jennifer L. “Targeting a Network of Cancer Control Nodes through Rescue of c-Cbl; A Novel Therapeutic Approach for Glioblastoma Multiforme.” 2016. Web. 10 Aug 2020.

Vancouver:

Stripay JL. Targeting a Network of Cancer Control Nodes through Rescue of c-Cbl; A Novel Therapeutic Approach for Glioblastoma Multiforme. [Internet] [Doctoral dissertation]. University of Rochester; 2016. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/1802/31636.

Council of Science Editors:

Stripay JL. Targeting a Network of Cancer Control Nodes through Rescue of c-Cbl; A Novel Therapeutic Approach for Glioblastoma Multiforme. [Doctoral Dissertation]. University of Rochester; 2016. Available from: http://hdl.handle.net/1802/31636


University of Melbourne

2. Sannang, Rowena Tenri. Suppressors of oncogenic Cbl in the Drosophila eye.

Degree: 2018, University of Melbourne

Cbl is an E3 ligase, and downregulates several cellular signalling pathways, in this role by targeting receptor tyrosine kinases for endocytosis. Mammalian Cbl was first… (more)

Subjects/Keywords: Drosophila; Cbl; Ras; Akap200; oncogene

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APA (6th Edition):

Sannang, R. T. (2018). Suppressors of oncogenic Cbl in the Drosophila eye. (Masters Thesis). University of Melbourne. Retrieved from http://hdl.handle.net/11343/218164

Chicago Manual of Style (16th Edition):

Sannang, Rowena Tenri. “Suppressors of oncogenic Cbl in the Drosophila eye.” 2018. Masters Thesis, University of Melbourne. Accessed August 10, 2020. http://hdl.handle.net/11343/218164.

MLA Handbook (7th Edition):

Sannang, Rowena Tenri. “Suppressors of oncogenic Cbl in the Drosophila eye.” 2018. Web. 10 Aug 2020.

Vancouver:

Sannang RT. Suppressors of oncogenic Cbl in the Drosophila eye. [Internet] [Masters thesis]. University of Melbourne; 2018. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/11343/218164.

Council of Science Editors:

Sannang RT. Suppressors of oncogenic Cbl in the Drosophila eye. [Masters Thesis]. University of Melbourne; 2018. Available from: http://hdl.handle.net/11343/218164


Temple University

3. Brennan, Tracy A. Abrogation of Cbl-PI3K Interaction Increases Bone Volume and Osteoblast Proliferation.

Degree: PhD, 2011, Temple University

Cell Biology

Cbl is a multivalent protein that interacts with a number of signaling molecules that affect cell proliferation, migration and apoptosis. Although it is… (more)

Subjects/Keywords: Cellular Biology; Biology; Bone; Cbl; Osteoblasts; PI3K

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APA (6th Edition):

Brennan, T. A. (2011). Abrogation of Cbl-PI3K Interaction Increases Bone Volume and Osteoblast Proliferation. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,107475

Chicago Manual of Style (16th Edition):

Brennan, Tracy A. “Abrogation of Cbl-PI3K Interaction Increases Bone Volume and Osteoblast Proliferation.” 2011. Doctoral Dissertation, Temple University. Accessed August 10, 2020. http://digital.library.temple.edu/u?/p245801coll10,107475.

MLA Handbook (7th Edition):

Brennan, Tracy A. “Abrogation of Cbl-PI3K Interaction Increases Bone Volume and Osteoblast Proliferation.” 2011. Web. 10 Aug 2020.

Vancouver:

Brennan TA. Abrogation of Cbl-PI3K Interaction Increases Bone Volume and Osteoblast Proliferation. [Internet] [Doctoral dissertation]. Temple University; 2011. [cited 2020 Aug 10]. Available from: http://digital.library.temple.edu/u?/p245801coll10,107475.

Council of Science Editors:

Brennan TA. Abrogation of Cbl-PI3K Interaction Increases Bone Volume and Osteoblast Proliferation. [Doctoral Dissertation]. Temple University; 2011. Available from: http://digital.library.temple.edu/u?/p245801coll10,107475


Boston University

4. Prince-Wright, Lawrence. C-CBL phosphorylation status influences colorectal cancer cell survival in a Wnt-dependent manner.

Degree: MS, Medical Sciences, 2015, Boston University

 Hyperactive Wnt signaling is the seminal event in colorectal cancer (CRC) pathogenesis, where β-catenin serves as a key Wnt mediator enhancing CRC cell proliferation and… (more)

Subjects/Keywords: Medicine; Cancer; c-Cbl; CRC; Colorectal carcinoma

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APA (6th Edition):

Prince-Wright, L. (2015). C-CBL phosphorylation status influences colorectal cancer cell survival in a Wnt-dependent manner. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/16145

Chicago Manual of Style (16th Edition):

Prince-Wright, Lawrence. “C-CBL phosphorylation status influences colorectal cancer cell survival in a Wnt-dependent manner.” 2015. Masters Thesis, Boston University. Accessed August 10, 2020. http://hdl.handle.net/2144/16145.

MLA Handbook (7th Edition):

Prince-Wright, Lawrence. “C-CBL phosphorylation status influences colorectal cancer cell survival in a Wnt-dependent manner.” 2015. Web. 10 Aug 2020.

Vancouver:

Prince-Wright L. C-CBL phosphorylation status influences colorectal cancer cell survival in a Wnt-dependent manner. [Internet] [Masters thesis]. Boston University; 2015. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/2144/16145.

Council of Science Editors:

Prince-Wright L. C-CBL phosphorylation status influences colorectal cancer cell survival in a Wnt-dependent manner. [Masters Thesis]. Boston University; 2015. Available from: http://hdl.handle.net/2144/16145


University of Southern California

5. Kotak, Kamal M. The role of cap gene in skeletal and cardiac muscle function.

Degree: MS, Clinical & Biomedical Investigations, 2009, University of Southern California

 Objective: The goal of this study was to evaluate the role of the CAP gene in skeletal and cardiac muscle contraction. Accumulating evidence suggests that… (more)

Subjects/Keywords: CAP; SoHo; cbl

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APA (6th Edition):

Kotak, K. M. (2009). The role of cap gene in skeletal and cardiac muscle function. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/205282/rec/7205

Chicago Manual of Style (16th Edition):

Kotak, Kamal M. “The role of cap gene in skeletal and cardiac muscle function.” 2009. Masters Thesis, University of Southern California. Accessed August 10, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/205282/rec/7205.

MLA Handbook (7th Edition):

Kotak, Kamal M. “The role of cap gene in skeletal and cardiac muscle function.” 2009. Web. 10 Aug 2020.

Vancouver:

Kotak KM. The role of cap gene in skeletal and cardiac muscle function. [Internet] [Masters thesis]. University of Southern California; 2009. [cited 2020 Aug 10]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/205282/rec/7205.

Council of Science Editors:

Kotak KM. The role of cap gene in skeletal and cardiac muscle function. [Masters Thesis]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/205282/rec/7205


RMIT University

6. Alzahrani, W. Role of c-Cbl in skeletal muscle energy metabolism in relation to obesity.

Degree: 2017, RMIT University

 The obesity epidemic has already reached alarming rates in both developed and developing countries. Positive energy balance due to high calorie intake with decreased energy… (more)

Subjects/Keywords: Fields of Research; Obesity; c-Cbl; Skeletal muscle; Energy metabolism; c-Cbl knockdown or overexpression

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APA (6th Edition):

Alzahrani, W. (2017). Role of c-Cbl in skeletal muscle energy metabolism in relation to obesity. (Thesis). RMIT University. Retrieved from http://researchbank.rmit.edu.au/view/rmit:162360

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):

Alzahrani, W. “Role of c-Cbl in skeletal muscle energy metabolism in relation to obesity.” 2017. Thesis, RMIT University. Accessed August 10, 2020. http://researchbank.rmit.edu.au/view/rmit:162360.

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

MLA Handbook (7th Edition):

Alzahrani, W. “Role of c-Cbl in skeletal muscle energy metabolism in relation to obesity.” 2017. Web. 10 Aug 2020.

Vancouver:

Alzahrani W. Role of c-Cbl in skeletal muscle energy metabolism in relation to obesity. [Internet] [Thesis]. RMIT University; 2017. [cited 2020 Aug 10]. Available from: http://researchbank.rmit.edu.au/view/rmit:162360.

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

Council of Science Editors:

Alzahrani W. Role of c-Cbl in skeletal muscle energy metabolism in relation to obesity. [Thesis]. RMIT University; 2017. Available from: http://researchbank.rmit.edu.au/view/rmit:162360

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

7. Yakoub, Sadok. Un rôle protecteur contre le stress oxydant pour l’E3-Ubiquitine ligase c-Cbl : utilité comme marqueur pronostic des carcinomes : A protective role against oxidative stress for the E3-ubiquitin ligase c-Cbl : usefulness as a prognostic marker for carcinomas.

Degree: Docteur es, Biologie cellulaire et moléculaire, 2009, Université Claude Bernard – Lyon I

Le travail présenté a porté sur l’analyse in vivo du proto-oncogène c-cbl, dont la forme connue est c-Cbl (p120cbl). Il s’agit d’une E3-Ubiquitine ligase et… (more)

Subjects/Keywords: C-Cbl; Androgéno-dépendance; Prostate; Testicule; Apoptose; Stress oxydant; Cancer; C-Cbl; Androgen-dependency; Prostate; Testis; Apoptosis; Oxidative stress; Cancer; 614.5999

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APA (6th Edition):

Yakoub, S. (2009). Un rôle protecteur contre le stress oxydant pour l’E3-Ubiquitine ligase c-Cbl : utilité comme marqueur pronostic des carcinomes : A protective role against oxidative stress for the E3-ubiquitin ligase c-Cbl : usefulness as a prognostic marker for carcinomas. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2009LYO10220

Chicago Manual of Style (16th Edition):

Yakoub, Sadok. “Un rôle protecteur contre le stress oxydant pour l’E3-Ubiquitine ligase c-Cbl : utilité comme marqueur pronostic des carcinomes : A protective role against oxidative stress for the E3-ubiquitin ligase c-Cbl : usefulness as a prognostic marker for carcinomas.” 2009. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed August 10, 2020. http://www.theses.fr/2009LYO10220.

MLA Handbook (7th Edition):

Yakoub, Sadok. “Un rôle protecteur contre le stress oxydant pour l’E3-Ubiquitine ligase c-Cbl : utilité comme marqueur pronostic des carcinomes : A protective role against oxidative stress for the E3-ubiquitin ligase c-Cbl : usefulness as a prognostic marker for carcinomas.” 2009. Web. 10 Aug 2020.

Vancouver:

Yakoub S. Un rôle protecteur contre le stress oxydant pour l’E3-Ubiquitine ligase c-Cbl : utilité comme marqueur pronostic des carcinomes : A protective role against oxidative stress for the E3-ubiquitin ligase c-Cbl : usefulness as a prognostic marker for carcinomas. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2009. [cited 2020 Aug 10]. Available from: http://www.theses.fr/2009LYO10220.

Council of Science Editors:

Yakoub S. Un rôle protecteur contre le stress oxydant pour l’E3-Ubiquitine ligase c-Cbl : utilité comme marqueur pronostic des carcinomes : A protective role against oxidative stress for the E3-ubiquitin ligase c-Cbl : usefulness as a prognostic marker for carcinomas. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2009. Available from: http://www.theses.fr/2009LYO10220


Temple University

8. Buitrago Murcia, Claudia Lorena. Cbl proteins in platelet functional responses.

Degree: PhD, 2012, Temple University

Physiology

c-Cbl protein functions as an E3 ligase and scaffolding protein, where three residues, Y700, Y731, and Y774, upon phosphorylation, have been shown to initiate… (more)

Subjects/Keywords: Physiology; Cellular biology; Cbl; hemostasis; kinases; platelets; signaling

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APA (6th Edition):

Buitrago Murcia, C. L. (2012). Cbl proteins in platelet functional responses. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,198139

Chicago Manual of Style (16th Edition):

Buitrago Murcia, Claudia Lorena. “Cbl proteins in platelet functional responses.” 2012. Doctoral Dissertation, Temple University. Accessed August 10, 2020. http://digital.library.temple.edu/u?/p245801coll10,198139.

MLA Handbook (7th Edition):

Buitrago Murcia, Claudia Lorena. “Cbl proteins in platelet functional responses.” 2012. Web. 10 Aug 2020.

Vancouver:

Buitrago Murcia CL. Cbl proteins in platelet functional responses. [Internet] [Doctoral dissertation]. Temple University; 2012. [cited 2020 Aug 10]. Available from: http://digital.library.temple.edu/u?/p245801coll10,198139.

Council of Science Editors:

Buitrago Murcia CL. Cbl proteins in platelet functional responses. [Doctoral Dissertation]. Temple University; 2012. Available from: http://digital.library.temple.edu/u?/p245801coll10,198139


Temple University

9. Lee, Hojin. S1_Scrambled_siRNA [Digital file].

Degree: 2008, Temple University

Microbiology and Immunology;

Ph.D.;

c-Cbl functions as a multifunctional adaptor and an E3 ubiquitin protein ligase. Several studies have shown that c-Cbl is involved in… (more)

Subjects/Keywords: Biology, Cell;

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APA (6th Edition):

Lee, H. (2008). S1_Scrambled_siRNA [Digital file]. (Thesis). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,254229

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

Chicago Manual of Style (16th Edition):

Lee, Hojin. “S1_Scrambled_siRNA [Digital file].” 2008. Thesis, Temple University. Accessed August 10, 2020. http://digital.library.temple.edu/u?/p245801coll10,254229.

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

MLA Handbook (7th Edition):

Lee, Hojin. “S1_Scrambled_siRNA [Digital file].” 2008. Web. 10 Aug 2020.

Vancouver:

Lee H. S1_Scrambled_siRNA [Digital file]. [Internet] [Thesis]. Temple University; 2008. [cited 2020 Aug 10]. Available from: http://digital.library.temple.edu/u?/p245801coll10,254229.

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

Council of Science Editors:

Lee H. S1_Scrambled_siRNA [Digital file]. [Thesis]. Temple University; 2008. Available from: http://digital.library.temple.edu/u?/p245801coll10,254229

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


Temple University

10. Lee, Hojin. S2_RhoA_siRNA [Digital file].

Degree: 2008, Temple University

Microbiology and Immunology;

Ph.D.;

c-Cbl functions as a multifunctional adaptor and an E3 ubiquitin protein ligase. Several studies have shown that c-Cbl is involved in… (more)

Subjects/Keywords: Biology, Cell;

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APA (6th Edition):

Lee, H. (2008). S2_RhoA_siRNA [Digital file]. (Thesis). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,254230

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

Chicago Manual of Style (16th Edition):

Lee, Hojin. “S2_RhoA_siRNA [Digital file].” 2008. Thesis, Temple University. Accessed August 10, 2020. http://digital.library.temple.edu/u?/p245801coll10,254230.

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

MLA Handbook (7th Edition):

Lee, Hojin. “S2_RhoA_siRNA [Digital file].” 2008. Web. 10 Aug 2020.

Vancouver:

Lee H. S2_RhoA_siRNA [Digital file]. [Internet] [Thesis]. Temple University; 2008. [cited 2020 Aug 10]. Available from: http://digital.library.temple.edu/u?/p245801coll10,254230.

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

Council of Science Editors:

Lee H. S2_RhoA_siRNA [Digital file]. [Thesis]. Temple University; 2008. Available from: http://digital.library.temple.edu/u?/p245801coll10,254230

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


Temple University

11. Lee, Hojin. S3_Rac1_siRNA [Digital file].

Degree: 2008, Temple University

Microbiology and Immunology;

Ph.D.;

c-Cbl functions as a multifunctional adaptor and an E3 ubiquitin protein ligase. Several studies have shown that c-Cbl is involved in… (more)

Subjects/Keywords: Biology, Cell;

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APA (6th Edition):

Lee, H. (2008). S3_Rac1_siRNA [Digital file]. (Thesis). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,254231

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

Chicago Manual of Style (16th Edition):

Lee, Hojin. “S3_Rac1_siRNA [Digital file].” 2008. Thesis, Temple University. Accessed August 10, 2020. http://digital.library.temple.edu/u?/p245801coll10,254231.

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

MLA Handbook (7th Edition):

Lee, Hojin. “S3_Rac1_siRNA [Digital file].” 2008. Web. 10 Aug 2020.

Vancouver:

Lee H. S3_Rac1_siRNA [Digital file]. [Internet] [Thesis]. Temple University; 2008. [cited 2020 Aug 10]. Available from: http://digital.library.temple.edu/u?/p245801coll10,254231.

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

Council of Science Editors:

Lee H. S3_Rac1_siRNA [Digital file]. [Thesis]. Temple University; 2008. Available from: http://digital.library.temple.edu/u?/p245801coll10,254231

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


Temple University

12. Lee, Hojin. THE MOLECULAR MECHANISMS OF THE EFFECTS OF C-CBL ON CYTOSKELETON-MEDIATED PHENOMENA.

Degree: PhD, 2008, Temple University

Microbiology and Immunology

c-Cbl functions as a multifunctional adaptor and an E3 ubiquitin protein ligase. Several studies have shown that c-Cbl is involved in cytoskeleton-mediated… (more)

Subjects/Keywords: Biology, Cell; c-Cbl; Cytoskeleton; small GTPases; Signaling; Glioma; Invasion

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APA (6th Edition):

Lee, H. (2008). THE MOLECULAR MECHANISMS OF THE EFFECTS OF C-CBL ON CYTOSKELETON-MEDIATED PHENOMENA. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,20447

Chicago Manual of Style (16th Edition):

Lee, Hojin. “THE MOLECULAR MECHANISMS OF THE EFFECTS OF C-CBL ON CYTOSKELETON-MEDIATED PHENOMENA.” 2008. Doctoral Dissertation, Temple University. Accessed August 10, 2020. http://digital.library.temple.edu/u?/p245801coll10,20447.

MLA Handbook (7th Edition):

Lee, Hojin. “THE MOLECULAR MECHANISMS OF THE EFFECTS OF C-CBL ON CYTOSKELETON-MEDIATED PHENOMENA.” 2008. Web. 10 Aug 2020.

Vancouver:

Lee H. THE MOLECULAR MECHANISMS OF THE EFFECTS OF C-CBL ON CYTOSKELETON-MEDIATED PHENOMENA. [Internet] [Doctoral dissertation]. Temple University; 2008. [cited 2020 Aug 10]. Available from: http://digital.library.temple.edu/u?/p245801coll10,20447.

Council of Science Editors:

Lee H. THE MOLECULAR MECHANISMS OF THE EFFECTS OF C-CBL ON CYTOSKELETON-MEDIATED PHENOMENA. [Doctoral Dissertation]. Temple University; 2008. Available from: http://digital.library.temple.edu/u?/p245801coll10,20447


NSYSU

13. Cheng, Hsueh-Tsen. Anti-lymphangiogenic action of SAHA on breast cancer.

Degree: PhD, Institute of Biomedical Sciences, 2013, NSYSU

 HDAC inhibitor suberoylanilide hydroxamic acid (SAHA) exhibits anti-tumor effects on various types of human cancers and is now approved by U.S FDA for clinical cancer… (more)

Subjects/Keywords: HDAC inhibitor SAHA; lymphangiogenesis; breast cancer; VEGF-C; c-Cbl

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APA (6th Edition):

Cheng, H. (2013). Anti-lymphangiogenic action of SAHA on breast cancer. (Doctoral Dissertation). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0403113-151923

Chicago Manual of Style (16th Edition):

Cheng, Hsueh-Tsen. “Anti-lymphangiogenic action of SAHA on breast cancer.” 2013. Doctoral Dissertation, NSYSU. Accessed August 10, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0403113-151923.

MLA Handbook (7th Edition):

Cheng, Hsueh-Tsen. “Anti-lymphangiogenic action of SAHA on breast cancer.” 2013. Web. 10 Aug 2020.

Vancouver:

Cheng H. Anti-lymphangiogenic action of SAHA on breast cancer. [Internet] [Doctoral dissertation]. NSYSU; 2013. [cited 2020 Aug 10]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0403113-151923.

Council of Science Editors:

Cheng H. Anti-lymphangiogenic action of SAHA on breast cancer. [Doctoral Dissertation]. NSYSU; 2013. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0403113-151923


University of Miami

14. Seales, Dawn. Development and Partial Characterization of Agonistic OX40 Aptamer anti-CBLB siRNA Conjugates.

Degree: MS, Cancer Biology (Medicine), 2012, University of Miami

 Tumors that develop in patients with fully functional immune systems evolve different mechanisms of immune suppression that must be counteracted for tumor immunotherapy to be… (more)

Subjects/Keywords: Aptamer; siRNA; OX40; Cbl-b; T-cell activation; Immunosuppression

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APA (6th Edition):

Seales, D. (2012). Development and Partial Characterization of Agonistic OX40 Aptamer anti-CBLB siRNA Conjugates. (Thesis). University of Miami. Retrieved from https://scholarlyrepository.miami.edu/oa_theses/376

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):

Seales, Dawn. “Development and Partial Characterization of Agonistic OX40 Aptamer anti-CBLB siRNA Conjugates.” 2012. Thesis, University of Miami. Accessed August 10, 2020. https://scholarlyrepository.miami.edu/oa_theses/376.

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

MLA Handbook (7th Edition):

Seales, Dawn. “Development and Partial Characterization of Agonistic OX40 Aptamer anti-CBLB siRNA Conjugates.” 2012. Web. 10 Aug 2020.

Vancouver:

Seales D. Development and Partial Characterization of Agonistic OX40 Aptamer anti-CBLB siRNA Conjugates. [Internet] [Thesis]. University of Miami; 2012. [cited 2020 Aug 10]. Available from: https://scholarlyrepository.miami.edu/oa_theses/376.

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

Council of Science Editors:

Seales D. Development and Partial Characterization of Agonistic OX40 Aptamer anti-CBLB siRNA Conjugates. [Thesis]. University of Miami; 2012. Available from: https://scholarlyrepository.miami.edu/oa_theses/376

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


University of California – San Francisco

15. Lemus-Hernandez, Armando Josue. Identification of Pseudomonas aeruginosa ExoT amino acid residues necessary for its proteasomal dependent degradation in the host cytoplasm.

Degree: Biomedical Sciences, 2011, University of California – San Francisco

 The opportunistic human pathogen Pseudomonas aeruginosa utilizes a type III secretion system to deliver virulence factors that disrupt host cell processes and host innate immunity.… (more)

Subjects/Keywords: Microbiology; Immunology; Cellular biology; Cbl-b; ExoT; Proteasome degradation; Pseudomonas aeruginosa

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APA (6th Edition):

Lemus-Hernandez, A. J. (2011). Identification of Pseudomonas aeruginosa ExoT amino acid residues necessary for its proteasomal dependent degradation in the host cytoplasm. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/6nd7x7z7

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):

Lemus-Hernandez, Armando Josue. “Identification of Pseudomonas aeruginosa ExoT amino acid residues necessary for its proteasomal dependent degradation in the host cytoplasm.” 2011. Thesis, University of California – San Francisco. Accessed August 10, 2020. http://www.escholarship.org/uc/item/6nd7x7z7.

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

MLA Handbook (7th Edition):

Lemus-Hernandez, Armando Josue. “Identification of Pseudomonas aeruginosa ExoT amino acid residues necessary for its proteasomal dependent degradation in the host cytoplasm.” 2011. Web. 10 Aug 2020.

Vancouver:

Lemus-Hernandez AJ. Identification of Pseudomonas aeruginosa ExoT amino acid residues necessary for its proteasomal dependent degradation in the host cytoplasm. [Internet] [Thesis]. University of California – San Francisco; 2011. [cited 2020 Aug 10]. Available from: http://www.escholarship.org/uc/item/6nd7x7z7.

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

Council of Science Editors:

Lemus-Hernandez AJ. Identification of Pseudomonas aeruginosa ExoT amino acid residues necessary for its proteasomal dependent degradation in the host cytoplasm. [Thesis]. University of California – San Francisco; 2011. Available from: http://www.escholarship.org/uc/item/6nd7x7z7

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


University of Toronto

16. Richmond, Terri. Negative Regulatory Mechanisms Underlying EPO Receptor Signaling and Erythropoiesis.

Degree: 2009, University of Toronto

Erythropoietin (EPO) is the primary cytokine regulator of erythropoiesis. Fundamental to this action is the ability of EPO to bind the EPO receptor (EPO-R), and… (more)

Subjects/Keywords: Erythropoietin; Cbl; 0379; 0307

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APA (6th Edition):

Richmond, T. (2009). Negative Regulatory Mechanisms Underlying EPO Receptor Signaling and Erythropoiesis. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/19214

Chicago Manual of Style (16th Edition):

Richmond, Terri. “Negative Regulatory Mechanisms Underlying EPO Receptor Signaling and Erythropoiesis.” 2009. Doctoral Dissertation, University of Toronto. Accessed August 10, 2020. http://hdl.handle.net/1807/19214.

MLA Handbook (7th Edition):

Richmond, Terri. “Negative Regulatory Mechanisms Underlying EPO Receptor Signaling and Erythropoiesis.” 2009. Web. 10 Aug 2020.

Vancouver:

Richmond T. Negative Regulatory Mechanisms Underlying EPO Receptor Signaling and Erythropoiesis. [Internet] [Doctoral dissertation]. University of Toronto; 2009. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/1807/19214.

Council of Science Editors:

Richmond T. Negative Regulatory Mechanisms Underlying EPO Receptor Signaling and Erythropoiesis. [Doctoral Dissertation]. University of Toronto; 2009. Available from: http://hdl.handle.net/1807/19214


University of Toronto

17. Tran, Charles Wan-Yuen. Investigating factors that govern T cell and dendritic cell function as therapeutic strategies for immune therapy.

Degree: PhD, 2017, University of Toronto

In 1909, Paul Ehrlich first suggested that the immune system protects against cancer. Over a century later, significant progress has been made towards understanding the… (more)

Subjects/Keywords: cancer; Cbl-b; dendritic cell; HIF-1a; immunotherapy; T cell; 0982

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APA (6th Edition):

Tran, C. W. (2017). Investigating factors that govern T cell and dendritic cell function as therapeutic strategies for immune therapy. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/91191

Chicago Manual of Style (16th Edition):

Tran, Charles Wan-Yuen. “Investigating factors that govern T cell and dendritic cell function as therapeutic strategies for immune therapy.” 2017. Doctoral Dissertation, University of Toronto. Accessed August 10, 2020. http://hdl.handle.net/1807/91191.

MLA Handbook (7th Edition):

Tran, Charles Wan-Yuen. “Investigating factors that govern T cell and dendritic cell function as therapeutic strategies for immune therapy.” 2017. Web. 10 Aug 2020.

Vancouver:

Tran CW. Investigating factors that govern T cell and dendritic cell function as therapeutic strategies for immune therapy. [Internet] [Doctoral dissertation]. University of Toronto; 2017. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/1807/91191.

Council of Science Editors:

Tran CW. Investigating factors that govern T cell and dendritic cell function as therapeutic strategies for immune therapy. [Doctoral Dissertation]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/91191


Universitat de Valencia

18. Ibáñez Company, María Amparo. Caracterización molecular de las leucemias mieloides agudas de novo .

Degree: 2013, Universitat de Valencia

 La secuenciación es la técnica de elección para identificar mutaciones. Sin embargo, tiene un coste elevado, es laboriosa y su sensibilidad es limitada. Recientemente, el… (more)

Subjects/Keywords: LMA de novo; DNMT3A; C-CBL; ASXL1; IDH

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APA (6th Edition):

Ibáñez Company, M. A. (2013). Caracterización molecular de las leucemias mieloides agudas de novo . (Doctoral Dissertation). Universitat de Valencia. Retrieved from http://hdl.handle.net/10550/29949

Chicago Manual of Style (16th Edition):

Ibáñez Company, María Amparo. “Caracterización molecular de las leucemias mieloides agudas de novo .” 2013. Doctoral Dissertation, Universitat de Valencia. Accessed August 10, 2020. http://hdl.handle.net/10550/29949.

MLA Handbook (7th Edition):

Ibáñez Company, María Amparo. “Caracterización molecular de las leucemias mieloides agudas de novo .” 2013. Web. 10 Aug 2020.

Vancouver:

Ibáñez Company MA. Caracterización molecular de las leucemias mieloides agudas de novo . [Internet] [Doctoral dissertation]. Universitat de Valencia; 2013. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/10550/29949.

Council of Science Editors:

Ibáñez Company MA. Caracterización molecular de las leucemias mieloides agudas de novo . [Doctoral Dissertation]. Universitat de Valencia; 2013. Available from: http://hdl.handle.net/10550/29949


Queens University

19. Kaur, Harvinder. Investigating the relationship between the RET receptor, Cbl and ARHGEF7 in downregulation of RET .

Degree: Pathology and Molecular Medicine, 2008, Queens University

 The RET proto-oncogene encodes a receptor tyrosine kinase (RTK), with two major isoforms, RET9 and RET51, which differ in their C-termini, and therefore recruit different… (more)

Subjects/Keywords: RET ; Dpwnregulation ; Cbl ; ARHGEF7 ; Interactions

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APA (6th Edition):

Kaur, H. (2008). Investigating the relationship between the RET receptor, Cbl and ARHGEF7 in downregulation of RET . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/1313

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):

Kaur, Harvinder. “Investigating the relationship between the RET receptor, Cbl and ARHGEF7 in downregulation of RET .” 2008. Thesis, Queens University. Accessed August 10, 2020. http://hdl.handle.net/1974/1313.

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

MLA Handbook (7th Edition):

Kaur, Harvinder. “Investigating the relationship between the RET receptor, Cbl and ARHGEF7 in downregulation of RET .” 2008. Web. 10 Aug 2020.

Vancouver:

Kaur H. Investigating the relationship between the RET receptor, Cbl and ARHGEF7 in downregulation of RET . [Internet] [Thesis]. Queens University; 2008. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/1974/1313.

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

Council of Science Editors:

Kaur H. Investigating the relationship between the RET receptor, Cbl and ARHGEF7 in downregulation of RET . [Thesis]. Queens University; 2008. Available from: http://hdl.handle.net/1974/1313

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


Jawaharlal Nehru University

20. Mahajan, Shilpi. Isolation and functional characterization of calcineurin B-like protein (CBL) and CBL-interacting protein kinase (CIPK) from pea; -.

Degree: International Centre for Genetic Engineering and Biotechnology, 2005, Jawaharlal Nehru University

none

Bibliography p.158-178,Published papers page no.is not given.

Advisors/Committee Members: Tuteja, Narendra.

Subjects/Keywords: Isolation; protein kinase (CIPK); calcineurin B; CBL-interacting protein; protein (CBL)

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APA (6th Edition):

Mahajan, S. (2005). Isolation and functional characterization of calcineurin B-like protein (CBL) and CBL-interacting protein kinase (CIPK) from pea; -. (Thesis). Jawaharlal Nehru University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/16759

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):

Mahajan, Shilpi. “Isolation and functional characterization of calcineurin B-like protein (CBL) and CBL-interacting protein kinase (CIPK) from pea; -.” 2005. Thesis, Jawaharlal Nehru University. Accessed August 10, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/16759.

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

MLA Handbook (7th Edition):

Mahajan, Shilpi. “Isolation and functional characterization of calcineurin B-like protein (CBL) and CBL-interacting protein kinase (CIPK) from pea; -.” 2005. Web. 10 Aug 2020.

Vancouver:

Mahajan S. Isolation and functional characterization of calcineurin B-like protein (CBL) and CBL-interacting protein kinase (CIPK) from pea; -. [Internet] [Thesis]. Jawaharlal Nehru University; 2005. [cited 2020 Aug 10]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/16759.

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

Council of Science Editors:

Mahajan S. Isolation and functional characterization of calcineurin B-like protein (CBL) and CBL-interacting protein kinase (CIPK) from pea; -. [Thesis]. Jawaharlal Nehru University; 2005. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/16759

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


Penn State University

21. Chen, Xu. demand response and generation capacity investment in the electricity market.

Degree: PhD, Energy and Mineral Engineering, 2013, Penn State University

 Demand Response (DR) plays an important role in electricity markets by reducing peak load, deferring costly infrastructure upgrades and enhancing system reliability. Most DR programs… (more)

Subjects/Keywords: Demand response; Customer baseline load (CBL); Market manipulation; Electricity markets; electricity restructuring

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APA (6th Edition):

Chen, X. (2013). demand response and generation capacity investment in the electricity market. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/19632

Chicago Manual of Style (16th Edition):

Chen, Xu. “demand response and generation capacity investment in the electricity market.” 2013. Doctoral Dissertation, Penn State University. Accessed August 10, 2020. https://etda.libraries.psu.edu/catalog/19632.

MLA Handbook (7th Edition):

Chen, Xu. “demand response and generation capacity investment in the electricity market.” 2013. Web. 10 Aug 2020.

Vancouver:

Chen X. demand response and generation capacity investment in the electricity market. [Internet] [Doctoral dissertation]. Penn State University; 2013. [cited 2020 Aug 10]. Available from: https://etda.libraries.psu.edu/catalog/19632.

Council of Science Editors:

Chen X. demand response and generation capacity investment in the electricity market. [Doctoral Dissertation]. Penn State University; 2013. Available from: https://etda.libraries.psu.edu/catalog/19632


University of Rochester

22. Cui, Wanchang. Combination of low level environmental toxicants with chemotherapeutics disturbs oligodendrocyte progenitor cell function through activation of the redox/Fyn/c-Cbl pathway.

Degree: PhD, 2009, University of Rochester

 In this study, we focused on studying the combined toxicity of environmental toxicants and chemotherapeutic agents on oligodendrocyte-type-2 astrocyte precursor cells, also referred as oligodendrocyte… (more)

Subjects/Keywords: Chemotherapeutics; Synergy; O-2A/OPC; Environmental toxicants; Redox/Fyn/c-Cbl pathway

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APA (6th Edition):

Cui, W. (2009). Combination of low level environmental toxicants with chemotherapeutics disturbs oligodendrocyte progenitor cell function through activation of the redox/Fyn/c-Cbl pathway. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/6629

Chicago Manual of Style (16th Edition):

Cui, Wanchang. “Combination of low level environmental toxicants with chemotherapeutics disturbs oligodendrocyte progenitor cell function through activation of the redox/Fyn/c-Cbl pathway.” 2009. Doctoral Dissertation, University of Rochester. Accessed August 10, 2020. http://hdl.handle.net/1802/6629.

MLA Handbook (7th Edition):

Cui, Wanchang. “Combination of low level environmental toxicants with chemotherapeutics disturbs oligodendrocyte progenitor cell function through activation of the redox/Fyn/c-Cbl pathway.” 2009. Web. 10 Aug 2020.

Vancouver:

Cui W. Combination of low level environmental toxicants with chemotherapeutics disturbs oligodendrocyte progenitor cell function through activation of the redox/Fyn/c-Cbl pathway. [Internet] [Doctoral dissertation]. University of Rochester; 2009. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/1802/6629.

Council of Science Editors:

Cui W. Combination of low level environmental toxicants with chemotherapeutics disturbs oligodendrocyte progenitor cell function through activation of the redox/Fyn/c-Cbl pathway. [Doctoral Dissertation]. University of Rochester; 2009. Available from: http://hdl.handle.net/1802/6629


University of Rochester

23. Chen, Hsing-Yu. Identification of the Mechanism of Tamoxifen Resistance in Basal-like Breast Cancers.

Degree: PhD, 2013, University of Rochester

 Two of the most substantial challenges in cancer research are to identify means of overcoming resistance of malignant cells to existing therapies and limiting the… (more)

Subjects/Keywords: Tamoxifen; Basal-Like Breast Cancer; c-Cbl; Oligodendrocyte Progenitor Cells; MEK1/2; Cdc42

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APA (6th Edition):

Chen, H. (2013). Identification of the Mechanism of Tamoxifen Resistance in Basal-like Breast Cancers. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/27253

Chicago Manual of Style (16th Edition):

Chen, Hsing-Yu. “Identification of the Mechanism of Tamoxifen Resistance in Basal-like Breast Cancers.” 2013. Doctoral Dissertation, University of Rochester. Accessed August 10, 2020. http://hdl.handle.net/1802/27253.

MLA Handbook (7th Edition):

Chen, Hsing-Yu. “Identification of the Mechanism of Tamoxifen Resistance in Basal-like Breast Cancers.” 2013. Web. 10 Aug 2020.

Vancouver:

Chen H. Identification of the Mechanism of Tamoxifen Resistance in Basal-like Breast Cancers. [Internet] [Doctoral dissertation]. University of Rochester; 2013. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/1802/27253.

Council of Science Editors:

Chen H. Identification of the Mechanism of Tamoxifen Resistance in Basal-like Breast Cancers. [Doctoral Dissertation]. University of Rochester; 2013. Available from: http://hdl.handle.net/1802/27253


Massey University

24. Mohanarajah, Selvarajah. Designing CBL systems for complex domains using problem transformation and fuzzy logic.

Degree: PhD, Computer Science, 2007, Massey University

 Some disciplines are inherently complex and challenging to learn. This research attempts to design an instructional strategy for CBL systems to simplify learning certain complex… (more)

Subjects/Keywords: CBL systems; Fuzzy logic; Problem transformation

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APA (6th Edition):

Mohanarajah, S. (2007). Designing CBL systems for complex domains using problem transformation and fuzzy logic. (Doctoral Dissertation). Massey University. Retrieved from http://hdl.handle.net/10179/743

Chicago Manual of Style (16th Edition):

Mohanarajah, Selvarajah. “Designing CBL systems for complex domains using problem transformation and fuzzy logic.” 2007. Doctoral Dissertation, Massey University. Accessed August 10, 2020. http://hdl.handle.net/10179/743.

MLA Handbook (7th Edition):

Mohanarajah, Selvarajah. “Designing CBL systems for complex domains using problem transformation and fuzzy logic.” 2007. Web. 10 Aug 2020.

Vancouver:

Mohanarajah S. Designing CBL systems for complex domains using problem transformation and fuzzy logic. [Internet] [Doctoral dissertation]. Massey University; 2007. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/10179/743.

Council of Science Editors:

Mohanarajah S. Designing CBL systems for complex domains using problem transformation and fuzzy logic. [Doctoral Dissertation]. Massey University; 2007. Available from: http://hdl.handle.net/10179/743


University of Texas Southwestern Medical Center

25. Bulut, Gamze Betul. Ubiquitination of EpoR and p85 in Ligand Induced EpoR Down-Regulation.

Degree: 2014, University of Texas Southwestern Medical Center

 Erythropoietin (Epo) is the primary cytokine that drives red blood cell production and signals through its receptor, the EpoR, on erythroid progenitor cells. Epo binding… (more)

Subjects/Keywords: Class Ia Phosphatidylinositol 3-Kinase; Endocytosis; Erythropoietin; Proto-Oncogene Proteins c-cbl; Receptors, Erythropoietin

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APA (6th Edition):

Bulut, G. B. (2014). Ubiquitination of EpoR and p85 in Ligand Induced EpoR Down-Regulation. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/3581

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):

Bulut, Gamze Betul. “Ubiquitination of EpoR and p85 in Ligand Induced EpoR Down-Regulation.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed August 10, 2020. http://hdl.handle.net/2152.5/3581.

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

MLA Handbook (7th Edition):

Bulut, Gamze Betul. “Ubiquitination of EpoR and p85 in Ligand Induced EpoR Down-Regulation.” 2014. Web. 10 Aug 2020.

Vancouver:

Bulut GB. Ubiquitination of EpoR and p85 in Ligand Induced EpoR Down-Regulation. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/2152.5/3581.

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

Council of Science Editors:

Bulut GB. Ubiquitination of EpoR and p85 in Ligand Induced EpoR Down-Regulation. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/3581

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

26. Lindberg, Angelica. Architecture and Learning - The role of physical space in educational settings .

Degree: Chalmers tekniska högskola / Institutionen för vetenskapens kommunikation och lärande (CLS), 2020, Chalmers University of Technology

 The engineering education is in the midst of transformation, and with that, a need for new learning environments arises. This study investigates the impact of… (more)

Subjects/Keywords: space; perceived learning; engineering; education; CBL; learning environment; pedagogy; instructor; architecture; design

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APA (6th Edition):

Lindberg, A. (2020). Architecture and Learning - The role of physical space in educational settings . (Thesis). Chalmers University of Technology. Retrieved from http://hdl.handle.net/20.500.12380/300990

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):

Lindberg, Angelica. “Architecture and Learning - The role of physical space in educational settings .” 2020. Thesis, Chalmers University of Technology. Accessed August 10, 2020. http://hdl.handle.net/20.500.12380/300990.

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

MLA Handbook (7th Edition):

Lindberg, Angelica. “Architecture and Learning - The role of physical space in educational settings .” 2020. Web. 10 Aug 2020.

Vancouver:

Lindberg A. Architecture and Learning - The role of physical space in educational settings . [Internet] [Thesis]. Chalmers University of Technology; 2020. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/20.500.12380/300990.

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

Council of Science Editors:

Lindberg A. Architecture and Learning - The role of physical space in educational settings . [Thesis]. Chalmers University of Technology; 2020. Available from: http://hdl.handle.net/20.500.12380/300990

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


Universidade Estadual de Campinas

27. Fonseca, Jose Pedro. Vias de sinalização de estresses em plantas = análise da região promotora do gene NIMIN-1 de Arabidopsis thaliana e da proteína ScCBL1 de cana-de-açúcar (Saccharum spp.).

Degree: 2010, Universidade Estadual de Campinas

 Resumo: Estresses bióticos e abióticos como a seca, salinidade e ataque por patógenos são responsáveis por perdas significantes em culturas de grãos ao redor do… (more)

Subjects/Keywords: Gene NIMIN-1; Arabidopsis; TGA; Cana-de-açucar - Melhoramento genético; Proteina CBL; Transdução de sinal celular

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APA (6th Edition):

Fonseca, J. P. (2010). Vias de sinalização de estresses em plantas = análise da região promotora do gene NIMIN-1 de Arabidopsis thaliana e da proteína ScCBL1 de cana-de-açúcar (Saccharum spp.). (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/317450

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):

Fonseca, Jose Pedro. “Vias de sinalização de estresses em plantas = análise da região promotora do gene NIMIN-1 de Arabidopsis thaliana e da proteína ScCBL1 de cana-de-açúcar (Saccharum spp.). ” 2010. Thesis, Universidade Estadual de Campinas. Accessed August 10, 2020. http://repositorio.unicamp.br/jspui/handle/REPOSIP/317450.

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

MLA Handbook (7th Edition):

Fonseca, Jose Pedro. “Vias de sinalização de estresses em plantas = análise da região promotora do gene NIMIN-1 de Arabidopsis thaliana e da proteína ScCBL1 de cana-de-açúcar (Saccharum spp.). ” 2010. Web. 10 Aug 2020.

Vancouver:

Fonseca JP. Vias de sinalização de estresses em plantas = análise da região promotora do gene NIMIN-1 de Arabidopsis thaliana e da proteína ScCBL1 de cana-de-açúcar (Saccharum spp.). [Internet] [Thesis]. Universidade Estadual de Campinas; 2010. [cited 2020 Aug 10]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/317450.

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

Council of Science Editors:

Fonseca JP. Vias de sinalização de estresses em plantas = análise da região promotora do gene NIMIN-1 de Arabidopsis thaliana e da proteína ScCBL1 de cana-de-açúcar (Saccharum spp.). [Thesis]. Universidade Estadual de Campinas; 2010. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/317450

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

28. SUN QINGXIANG. Structural Basis for the Inhibition Mechanism of HUman CSE and a study on c-CBL complexes.

Degree: 2010, National University of Singapore

Subjects/Keywords: CSE; c-Cbl; H2S; inhibitor; multiple phosphorylation; structural biology

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APA (6th Edition):

QINGXIANG, S. (2010). Structural Basis for the Inhibition Mechanism of HUman CSE and a study on c-CBL complexes. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/20681

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):

QINGXIANG, SUN. “Structural Basis for the Inhibition Mechanism of HUman CSE and a study on c-CBL complexes.” 2010. Thesis, National University of Singapore. Accessed August 10, 2020. http://scholarbank.nus.edu.sg/handle/10635/20681.

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

MLA Handbook (7th Edition):

QINGXIANG, SUN. “Structural Basis for the Inhibition Mechanism of HUman CSE and a study on c-CBL complexes.” 2010. Web. 10 Aug 2020.

Vancouver:

QINGXIANG S. Structural Basis for the Inhibition Mechanism of HUman CSE and a study on c-CBL complexes. [Internet] [Thesis]. National University of Singapore; 2010. [cited 2020 Aug 10]. Available from: http://scholarbank.nus.edu.sg/handle/10635/20681.

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

Council of Science Editors:

QINGXIANG S. Structural Basis for the Inhibition Mechanism of HUman CSE and a study on c-CBL complexes. [Thesis]. National University of Singapore; 2010. Available from: http://scholarbank.nus.edu.sg/handle/10635/20681

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


University of Pennsylvania

29. Chirino, Leilani Marie. Negative Regulation Of Nk Cell Activation By Cbl-B And Tam Receptors.

Degree: 2019, University of Pennsylvania

 Natural Killer (NK) cells are innate immune cells equipped with the ability to rapidly kill stressed cells that are neoplastic or virally-infected. NK cells are… (more)

Subjects/Keywords: Cbl-b; Natural Killer; NK cells; TAM receptors; TAMs; Allergy and Immunology; Biochemistry; Immunology and Infectious Disease; Medical Immunology; Molecular Biology

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

APA (6th Edition):

Chirino, L. M. (2019). Negative Regulation Of Nk Cell Activation By Cbl-B And Tam Receptors. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/3674

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):

Chirino, Leilani Marie. “Negative Regulation Of Nk Cell Activation By Cbl-B And Tam Receptors.” 2019. Thesis, University of Pennsylvania. Accessed August 10, 2020. https://repository.upenn.edu/edissertations/3674.

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

MLA Handbook (7th Edition):

Chirino, Leilani Marie. “Negative Regulation Of Nk Cell Activation By Cbl-B And Tam Receptors.” 2019. Web. 10 Aug 2020.

Vancouver:

Chirino LM. Negative Regulation Of Nk Cell Activation By Cbl-B And Tam Receptors. [Internet] [Thesis]. University of Pennsylvania; 2019. [cited 2020 Aug 10]. Available from: https://repository.upenn.edu/edissertations/3674.

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

Council of Science Editors:

Chirino LM. Negative Regulation Of Nk Cell Activation By Cbl-B And Tam Receptors. [Thesis]. University of Pennsylvania; 2019. Available from: https://repository.upenn.edu/edissertations/3674

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


University of Arizona

30. Epstein, Andrew Michael. Fragile X Protein Regulates Cellular Proliferation and Oocyte Polarity by Controlling cb1 Levels During Drosophila Oogenesis .

Degree: 2008, University of Arizona

 Fragile X Protein (FMRP) is an RNA binding protein linked to the most common form of inherited mental retardation, Fragile X syndrome (FraX). Despite its… (more)

Subjects/Keywords: cbl; Drosophila; Fragile X; oocyte polarity; Oogenesis

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

APA (6th Edition):

Epstein, A. M. (2008). Fragile X Protein Regulates Cellular Proliferation and Oocyte Polarity by Controlling cb1 Levels During Drosophila Oogenesis . (Masters Thesis). University of Arizona. Retrieved from http://hdl.handle.net/10150/193434

Chicago Manual of Style (16th Edition):

Epstein, Andrew Michael. “Fragile X Protein Regulates Cellular Proliferation and Oocyte Polarity by Controlling cb1 Levels During Drosophila Oogenesis .” 2008. Masters Thesis, University of Arizona. Accessed August 10, 2020. http://hdl.handle.net/10150/193434.

MLA Handbook (7th Edition):

Epstein, Andrew Michael. “Fragile X Protein Regulates Cellular Proliferation and Oocyte Polarity by Controlling cb1 Levels During Drosophila Oogenesis .” 2008. Web. 10 Aug 2020.

Vancouver:

Epstein AM. Fragile X Protein Regulates Cellular Proliferation and Oocyte Polarity by Controlling cb1 Levels During Drosophila Oogenesis . [Internet] [Masters thesis]. University of Arizona; 2008. [cited 2020 Aug 10]. Available from: http://hdl.handle.net/10150/193434.

Council of Science Editors:

Epstein AM. Fragile X Protein Regulates Cellular Proliferation and Oocyte Polarity by Controlling cb1 Levels During Drosophila Oogenesis . [Masters Thesis]. University of Arizona; 2008. Available from: http://hdl.handle.net/10150/193434

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