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You searched for subject:( Wnt Proteins metabolism). Showing records 31 – 60 of 18338 total matches.

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University of Aberdeen

31. Martin, Jennifer. Wnt regulated transcription factor networks mediate vertebrate cardiogenesis.

Degree: 2009, University of Aberdeen

 Induction of vertebrate heart development requires inhibition of canonical/<i>β</i>-catenin dependent Wnt signalling, activation of non-canonical/<i>β</i>-catenin independent Wnt signalling and transcription factor activation. Wnt/<i>β</i>-catenin signalling may… (more)

Subjects/Keywords: 571.861; Cardiovascular system : Wnt proteins : Transcription factors : Genetic transcription

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APA (6th Edition):

Martin, J. (2009). Wnt regulated transcription factor networks mediate vertebrate cardiogenesis. (Doctoral Dissertation). University of Aberdeen. Retrieved from http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=25801 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.499647

Chicago Manual of Style (16th Edition):

Martin, Jennifer. “Wnt regulated transcription factor networks mediate vertebrate cardiogenesis.” 2009. Doctoral Dissertation, University of Aberdeen. Accessed December 10, 2019. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=25801 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.499647.

MLA Handbook (7th Edition):

Martin, Jennifer. “Wnt regulated transcription factor networks mediate vertebrate cardiogenesis.” 2009. Web. 10 Dec 2019.

Vancouver:

Martin J. Wnt regulated transcription factor networks mediate vertebrate cardiogenesis. [Internet] [Doctoral dissertation]. University of Aberdeen; 2009. [cited 2019 Dec 10]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=25801 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.499647.

Council of Science Editors:

Martin J. Wnt regulated transcription factor networks mediate vertebrate cardiogenesis. [Doctoral Dissertation]. University of Aberdeen; 2009. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=25801 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.499647


University of Hong Kong

32. Wong, Wai-leong, Dickson. Biphasic and dual roles of renal tubular Wnt/β-catenin signaling in proteinuric nephropathy.

Degree: PhD, 2016, University of Hong Kong

abstract

Medicine

Doctoral

Doctor of Philosophy

Subjects/Keywords: Proteinuria; Wnt proteins; Kidneys - Diseases

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APA (6th Edition):

Wong, Wai-leong, D. (2016). Biphasic and dual roles of renal tubular Wnt/β-catenin signaling in proteinuric nephropathy. (Doctoral Dissertation). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/238361

Chicago Manual of Style (16th Edition):

Wong, Wai-leong, Dickson. “Biphasic and dual roles of renal tubular Wnt/β-catenin signaling in proteinuric nephropathy.” 2016. Doctoral Dissertation, University of Hong Kong. Accessed December 10, 2019. http://hdl.handle.net/10722/238361.

MLA Handbook (7th Edition):

Wong, Wai-leong, Dickson. “Biphasic and dual roles of renal tubular Wnt/β-catenin signaling in proteinuric nephropathy.” 2016. Web. 10 Dec 2019.

Vancouver:

Wong, Wai-leong D. Biphasic and dual roles of renal tubular Wnt/β-catenin signaling in proteinuric nephropathy. [Internet] [Doctoral dissertation]. University of Hong Kong; 2016. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/10722/238361.

Council of Science Editors:

Wong, Wai-leong D. Biphasic and dual roles of renal tubular Wnt/β-catenin signaling in proteinuric nephropathy. [Doctoral Dissertation]. University of Hong Kong; 2016. Available from: http://hdl.handle.net/10722/238361


University of Hong Kong

33. 黃偉亮; Wong, Wai-leong, Dickson. Biphasic and dual roles of renal tubular Wnt/β-catenin signaling in proteinuric nephropathy.

Degree: PhD, 2016, University of Hong Kong

published_or_final_version

Medicine

Doctoral

Doctor of Philosophy

Subjects/Keywords: Wnt proteins; Proteinuria; Kidneys - Diseases

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APA (6th Edition):

黃偉亮; Wong, Wai-leong, D. (2016). Biphasic and dual roles of renal tubular Wnt/β-catenin signaling in proteinuric nephropathy. (Doctoral Dissertation). University of Hong Kong. Retrieved from Wong, W. D. [黃偉亮]. (2016). Biphasic and dual roles of renal tubular Wnt/β-catenin signaling in proteinuric nephropathy. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5816248. ; http://dx.doi.org/10.5353/th_b5816248 ; http://hdl.handle.net/10722/248964

Chicago Manual of Style (16th Edition):

黃偉亮; Wong, Wai-leong, Dickson. “Biphasic and dual roles of renal tubular Wnt/β-catenin signaling in proteinuric nephropathy.” 2016. Doctoral Dissertation, University of Hong Kong. Accessed December 10, 2019. Wong, W. D. [黃偉亮]. (2016). Biphasic and dual roles of renal tubular Wnt/β-catenin signaling in proteinuric nephropathy. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5816248. ; http://dx.doi.org/10.5353/th_b5816248 ; http://hdl.handle.net/10722/248964.

MLA Handbook (7th Edition):

黃偉亮; Wong, Wai-leong, Dickson. “Biphasic and dual roles of renal tubular Wnt/β-catenin signaling in proteinuric nephropathy.” 2016. Web. 10 Dec 2019.

Vancouver:

黃偉亮; Wong, Wai-leong D. Biphasic and dual roles of renal tubular Wnt/β-catenin signaling in proteinuric nephropathy. [Internet] [Doctoral dissertation]. University of Hong Kong; 2016. [cited 2019 Dec 10]. Available from: Wong, W. D. [黃偉亮]. (2016). Biphasic and dual roles of renal tubular Wnt/β-catenin signaling in proteinuric nephropathy. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5816248. ; http://dx.doi.org/10.5353/th_b5816248 ; http://hdl.handle.net/10722/248964.

Council of Science Editors:

黃偉亮; Wong, Wai-leong D. Biphasic and dual roles of renal tubular Wnt/β-catenin signaling in proteinuric nephropathy. [Doctoral Dissertation]. University of Hong Kong; 2016. Available from: Wong, W. D. [黃偉亮]. (2016). Biphasic and dual roles of renal tubular Wnt/β-catenin signaling in proteinuric nephropathy. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5816248. ; http://dx.doi.org/10.5353/th_b5816248 ; http://hdl.handle.net/10722/248964


University of Aberdeen

34. Gibb, Natalie L.; University of Aberdeen.Cardiovascular Research Program. sfrp 1 promotes myocardial differentiation in Xenopus laevis by inhibiting canonical wnt6 signalling.

Degree: Cardiovascular Research Program., 2013, University of Aberdeen

Subjects/Keywords: Xenopus laevis.; Wnt proteins.

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APA (6th Edition):

Gibb, N. L. ;. U. o. A. C. R. P. (2013). sfrp 1 promotes myocardial differentiation in Xenopus laevis by inhibiting canonical wnt6 signalling. (Doctoral Dissertation). University of Aberdeen. Retrieved from http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=196016 ; http://digitool2.abdn.ac.uk:1801/webclient/DeliveryManager?pid=196016&custom_att_2=simple_viewer

Chicago Manual of Style (16th Edition):

Gibb, Natalie L ; University of Aberdeen Cardiovascular Research Program. “sfrp 1 promotes myocardial differentiation in Xenopus laevis by inhibiting canonical wnt6 signalling.” 2013. Doctoral Dissertation, University of Aberdeen. Accessed December 10, 2019. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=196016 ; http://digitool2.abdn.ac.uk:1801/webclient/DeliveryManager?pid=196016&custom_att_2=simple_viewer.

MLA Handbook (7th Edition):

Gibb, Natalie L ; University of Aberdeen Cardiovascular Research Program. “sfrp 1 promotes myocardial differentiation in Xenopus laevis by inhibiting canonical wnt6 signalling.” 2013. Web. 10 Dec 2019.

Vancouver:

Gibb NL;UoACRP. sfrp 1 promotes myocardial differentiation in Xenopus laevis by inhibiting canonical wnt6 signalling. [Internet] [Doctoral dissertation]. University of Aberdeen; 2013. [cited 2019 Dec 10]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=196016 ; http://digitool2.abdn.ac.uk:1801/webclient/DeliveryManager?pid=196016&custom_att_2=simple_viewer.

Council of Science Editors:

Gibb NL;UoACRP. sfrp 1 promotes myocardial differentiation in Xenopus laevis by inhibiting canonical wnt6 signalling. [Doctoral Dissertation]. University of Aberdeen; 2013. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=196016 ; http://digitool2.abdn.ac.uk:1801/webclient/DeliveryManager?pid=196016&custom_att_2=simple_viewer

35. Akindahunsi, Oluwole O. Evidence of functional distinction between WNT5A Isoform A and Isoform B in osteosarcoma cells.

Degree: 2014, University of North Carolina – Greensboro

 WNT5A is a secreted ligand involved in differentiation, proliferation, cell movement, and apoptosis. Various studies have shown WNT5A misregulation in cancer and that it can… (more)

Subjects/Keywords: Wnt proteins; Osteosarcoma

…functional distinctions between WNT5A isoforms A and B. WNT Proteins and Function The WNT proteins… …class of proteins that function as secreted ligands. There are a total of 19 WNT ligands, each… …endoplasmic reticulum (ER)Golgi system. WNT proteins undergo palmitoylation of cysteine… …accounts for the proteins hydrophobicity and poor solubility. This WNT modification is performed… …binding (Bhanot et al., 1996). A single WNT can bind multiple Fz proteins and vice… 

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APA (6th Edition):

Akindahunsi, O. O. (2014). Evidence of functional distinction between WNT5A Isoform A and Isoform B in osteosarcoma cells. (Masters Thesis). University of North Carolina – Greensboro. Retrieved from http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=17657

Chicago Manual of Style (16th Edition):

Akindahunsi, Oluwole O. “Evidence of functional distinction between WNT5A Isoform A and Isoform B in osteosarcoma cells.” 2014. Masters Thesis, University of North Carolina – Greensboro. Accessed December 10, 2019. http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=17657.

MLA Handbook (7th Edition):

Akindahunsi, Oluwole O. “Evidence of functional distinction between WNT5A Isoform A and Isoform B in osteosarcoma cells.” 2014. Web. 10 Dec 2019.

Vancouver:

Akindahunsi OO. Evidence of functional distinction between WNT5A Isoform A and Isoform B in osteosarcoma cells. [Internet] [Masters thesis]. University of North Carolina – Greensboro; 2014. [cited 2019 Dec 10]. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=17657.

Council of Science Editors:

Akindahunsi OO. Evidence of functional distinction between WNT5A Isoform A and Isoform B in osteosarcoma cells. [Masters Thesis]. University of North Carolina – Greensboro; 2014. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=17657


University of North Carolina – Greensboro

36. Manner, III Carl J. Functional distinctions between two isoforms of WNT5A.

Degree: 2016, University of North Carolina – Greensboro

 WNT5A is a secreted protein ligand with important roles in development, adult tissue homeostasis, and many basic cellular functions. In cancers, aberrant WNT5A signaling is… (more)

Subjects/Keywords: Wnt proteins; Cellular signal transduction; Colon (Anatomy) – Cancer; Rectum – Cancer; Embryology

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APA (6th Edition):

Manner, I. C. J. (2016). Functional distinctions between two isoforms of WNT5A. (Masters Thesis). University of North Carolina – Greensboro. Retrieved from http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=19729

Chicago Manual of Style (16th Edition):

Manner, III Carl J. “Functional distinctions between two isoforms of WNT5A.” 2016. Masters Thesis, University of North Carolina – Greensboro. Accessed December 10, 2019. http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=19729.

MLA Handbook (7th Edition):

Manner, III Carl J. “Functional distinctions between two isoforms of WNT5A.” 2016. Web. 10 Dec 2019.

Vancouver:

Manner ICJ. Functional distinctions between two isoforms of WNT5A. [Internet] [Masters thesis]. University of North Carolina – Greensboro; 2016. [cited 2019 Dec 10]. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=19729.

Council of Science Editors:

Manner ICJ. Functional distinctions between two isoforms of WNT5A. [Masters Thesis]. University of North Carolina – Greensboro; 2016. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=19729


University of New South Wales

37. Dawson, Amanda Caroline. Evaluation of novel molecular markers from the WNT pathway : a stepwise regression model for pancreatic cancer survival.

Degree: Clinical School - St Vincent's Hospital, 2007, University of New South Wales

 Optimisation of the conventional tripartite of pancreatic cancer (PC) treatment have led to significant improvements in mortality, however further knowledge of the underlying molecular processes… (more)

Subjects/Keywords: Pancreas  – Cancer; Pancreatitis; Wnt proteins

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APA (6th Edition):

Dawson, A. C. (2007). Evaluation of novel molecular markers from the WNT pathway : a stepwise regression model for pancreatic cancer survival. (Masters Thesis). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/31528 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:1621/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Dawson, Amanda Caroline. “Evaluation of novel molecular markers from the WNT pathway : a stepwise regression model for pancreatic cancer survival.” 2007. Masters Thesis, University of New South Wales. Accessed December 10, 2019. http://handle.unsw.edu.au/1959.4/31528 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:1621/SOURCE01?view=true.

MLA Handbook (7th Edition):

Dawson, Amanda Caroline. “Evaluation of novel molecular markers from the WNT pathway : a stepwise regression model for pancreatic cancer survival.” 2007. Web. 10 Dec 2019.

Vancouver:

Dawson AC. Evaluation of novel molecular markers from the WNT pathway : a stepwise regression model for pancreatic cancer survival. [Internet] [Masters thesis]. University of New South Wales; 2007. [cited 2019 Dec 10]. Available from: http://handle.unsw.edu.au/1959.4/31528 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:1621/SOURCE01?view=true.

Council of Science Editors:

Dawson AC. Evaluation of novel molecular markers from the WNT pathway : a stepwise regression model for pancreatic cancer survival. [Masters Thesis]. University of New South Wales; 2007. Available from: http://handle.unsw.edu.au/1959.4/31528 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:1621/SOURCE01?view=true


University of Texas Southwestern Medical Center

38. Jacob, Leni Susan. Functional Genomics Based Interrogation of Cell-Fate Determination Pathways.

Degree: 2011, University of Texas Southwestern Medical Center

 The Hedgehog (Hh) and Wnt signal transduction pathways are master regulators of embryogenesis and tissue renewal and represent anticancer therapeutic targets. Using genome-wide RNA interference… (more)

Subjects/Keywords: Signal Transduction; Protein-Serine-Threonine Kinases; Wnt Proteins

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APA (6th Edition):

Jacob, L. S. (2011). Functional Genomics Based Interrogation of Cell-Fate Determination Pathways. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/884

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):

Jacob, Leni Susan. “Functional Genomics Based Interrogation of Cell-Fate Determination Pathways.” 2011. Thesis, University of Texas Southwestern Medical Center. Accessed December 10, 2019. http://hdl.handle.net/2152.5/884.

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

MLA Handbook (7th Edition):

Jacob, Leni Susan. “Functional Genomics Based Interrogation of Cell-Fate Determination Pathways.” 2011. Web. 10 Dec 2019.

Vancouver:

Jacob LS. Functional Genomics Based Interrogation of Cell-Fate Determination Pathways. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2011. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/2152.5/884.

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

Council of Science Editors:

Jacob LS. Functional Genomics Based Interrogation of Cell-Fate Determination Pathways. [Thesis]. University of Texas Southwestern Medical Center; 2011. Available from: http://hdl.handle.net/2152.5/884

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


University of Texas Southwestern Medical Center

39. Merkel, Calli E. Beta-Catenin and Development of the Urogenital System.

Degree: 2009, University of Texas Southwestern Medical Center

 The urogenital system is composed of the kidneys, gonads, urinary and reproductive tracts. Components of the urogenital system play many important roles in the body;… (more)

Subjects/Keywords: Urogenital System; Kidney; Wnt Proteins

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APA (6th Edition):

Merkel, C. E. (2009). Beta-Catenin and Development of the Urogenital System. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/442

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):

Merkel, Calli E. “Beta-Catenin and Development of the Urogenital System.” 2009. Thesis, University of Texas Southwestern Medical Center. Accessed December 10, 2019. http://hdl.handle.net/2152.5/442.

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

MLA Handbook (7th Edition):

Merkel, Calli E. “Beta-Catenin and Development of the Urogenital System.” 2009. Web. 10 Dec 2019.

Vancouver:

Merkel CE. Beta-Catenin and Development of the Urogenital System. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2009. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/2152.5/442.

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

Council of Science Editors:

Merkel CE. Beta-Catenin and Development of the Urogenital System. [Thesis]. University of Texas Southwestern Medical Center; 2009. Available from: http://hdl.handle.net/2152.5/442

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


University of Washington

40. Fagnan, Erin. Mechanisms for Scaffold-Mediated Regulation of Kinase Activity in the Wnt Signaling Pathway.

Degree: PhD, 2019, University of Washington

 Cellular signaling is a complex process involving numerous pathways. Many of these pathways are connected through shared proteins, creating branch points that may result in… (more)

Subjects/Keywords: Axin; Cell Signaling; GSK3; Scaffold Proteins; Wnt pathway; Chemistry; Biochemistry; Chemistry

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APA (6th Edition):

Fagnan, E. (2019). Mechanisms for Scaffold-Mediated Regulation of Kinase Activity in the Wnt Signaling Pathway. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/44746

Chicago Manual of Style (16th Edition):

Fagnan, Erin. “Mechanisms for Scaffold-Mediated Regulation of Kinase Activity in the Wnt Signaling Pathway.” 2019. Doctoral Dissertation, University of Washington. Accessed December 10, 2019. http://hdl.handle.net/1773/44746.

MLA Handbook (7th Edition):

Fagnan, Erin. “Mechanisms for Scaffold-Mediated Regulation of Kinase Activity in the Wnt Signaling Pathway.” 2019. Web. 10 Dec 2019.

Vancouver:

Fagnan E. Mechanisms for Scaffold-Mediated Regulation of Kinase Activity in the Wnt Signaling Pathway. [Internet] [Doctoral dissertation]. University of Washington; 2019. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/1773/44746.

Council of Science Editors:

Fagnan E. Mechanisms for Scaffold-Mediated Regulation of Kinase Activity in the Wnt Signaling Pathway. [Doctoral Dissertation]. University of Washington; 2019. Available from: http://hdl.handle.net/1773/44746


University of Alberta

41. McCarthy, Amanda Marie. An investigation of endogenous ghrelin and growth hormone-releasing hormone following the consumption of two different relative doses of oral l-arginine.

Degree: MS, Physical Education and Recreation, 2011, University of Alberta

 Individuals consume the amino acid L-arginine (L-arg) to obtain an anabolic response. However, little is known concerning the mechanism for using an oral dose. The… (more)

Subjects/Keywords: Growth hormone releasing factor; Ghrelin  – Metabolism; Arginine  – Metabolism; Proteins  – Metabolism; Somatotropin

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APA (6th Edition):

McCarthy, A. M. (2011). An investigation of endogenous ghrelin and growth hormone-releasing hormone following the consumption of two different relative doses of oral l-arginine. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/05741s32t

Chicago Manual of Style (16th Edition):

McCarthy, Amanda Marie. “An investigation of endogenous ghrelin and growth hormone-releasing hormone following the consumption of two different relative doses of oral l-arginine.” 2011. Masters Thesis, University of Alberta. Accessed December 10, 2019. https://era.library.ualberta.ca/files/05741s32t.

MLA Handbook (7th Edition):

McCarthy, Amanda Marie. “An investigation of endogenous ghrelin and growth hormone-releasing hormone following the consumption of two different relative doses of oral l-arginine.” 2011. Web. 10 Dec 2019.

Vancouver:

McCarthy AM. An investigation of endogenous ghrelin and growth hormone-releasing hormone following the consumption of two different relative doses of oral l-arginine. [Internet] [Masters thesis]. University of Alberta; 2011. [cited 2019 Dec 10]. Available from: https://era.library.ualberta.ca/files/05741s32t.

Council of Science Editors:

McCarthy AM. An investigation of endogenous ghrelin and growth hormone-releasing hormone following the consumption of two different relative doses of oral l-arginine. [Masters Thesis]. University of Alberta; 2011. Available from: https://era.library.ualberta.ca/files/05741s32t

42. Tsedensodnom, Orkhontuya. Identification and Characterization of T Cell Factor-4 (TCF-4) Isoforms of Wnt Signaling in Hepatocellular Carcinoma (HCC).

Degree: PhD, Molecular Biology, Cell Biology, and Biochemistry, 2010, Brown University

 Background and Aims: The canonical Wnt signaling pathway is frequently activated in hepatocellular carcinoma (HCC). Although b-catenin is the principle effector protein of Wnt pathway,… (more)

Subjects/Keywords: Wnt

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APA (6th Edition):

Tsedensodnom, O. (2010). Identification and Characterization of T Cell Factor-4 (TCF-4) Isoforms of Wnt Signaling in Hepatocellular Carcinoma (HCC). (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:11109/

Chicago Manual of Style (16th Edition):

Tsedensodnom, Orkhontuya. “Identification and Characterization of T Cell Factor-4 (TCF-4) Isoforms of Wnt Signaling in Hepatocellular Carcinoma (HCC).” 2010. Doctoral Dissertation, Brown University. Accessed December 10, 2019. https://repository.library.brown.edu/studio/item/bdr:11109/.

MLA Handbook (7th Edition):

Tsedensodnom, Orkhontuya. “Identification and Characterization of T Cell Factor-4 (TCF-4) Isoforms of Wnt Signaling in Hepatocellular Carcinoma (HCC).” 2010. Web. 10 Dec 2019.

Vancouver:

Tsedensodnom O. Identification and Characterization of T Cell Factor-4 (TCF-4) Isoforms of Wnt Signaling in Hepatocellular Carcinoma (HCC). [Internet] [Doctoral dissertation]. Brown University; 2010. [cited 2019 Dec 10]. Available from: https://repository.library.brown.edu/studio/item/bdr:11109/.

Council of Science Editors:

Tsedensodnom O. Identification and Characterization of T Cell Factor-4 (TCF-4) Isoforms of Wnt Signaling in Hepatocellular Carcinoma (HCC). [Doctoral Dissertation]. Brown University; 2010. Available from: https://repository.library.brown.edu/studio/item/bdr:11109/


University of Southern California

43. Chiu, Cathleen Tsz Ka. Canonical and non-canonical Wnt signaling in the patterning of multipotent stem cells during feather development.

Degree: MS, Experimental & Molecular Pathology, 2010, University of Southern California

 The formation of complex ectodermal organs begins with multipotent stem cells that undergo many basic cellular events. During the formation of a complex organ, there… (more)

Subjects/Keywords: Wnt

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APA (6th Edition):

Chiu, C. T. K. (2010). Canonical and non-canonical Wnt signaling in the patterning of multipotent stem cells during feather development. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/89175/rec/1222

Chicago Manual of Style (16th Edition):

Chiu, Cathleen Tsz Ka. “Canonical and non-canonical Wnt signaling in the patterning of multipotent stem cells during feather development.” 2010. Masters Thesis, University of Southern California. Accessed December 10, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/89175/rec/1222.

MLA Handbook (7th Edition):

Chiu, Cathleen Tsz Ka. “Canonical and non-canonical Wnt signaling in the patterning of multipotent stem cells during feather development.” 2010. Web. 10 Dec 2019.

Vancouver:

Chiu CTK. Canonical and non-canonical Wnt signaling in the patterning of multipotent stem cells during feather development. [Internet] [Masters thesis]. University of Southern California; 2010. [cited 2019 Dec 10]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/89175/rec/1222.

Council of Science Editors:

Chiu CTK. Canonical and non-canonical Wnt signaling in the patterning of multipotent stem cells during feather development. [Masters Thesis]. University of Southern California; 2010. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/89175/rec/1222


University of Western Australia

44. Berry, Clare Alexandra. Cells from breastmilk and the mammary gland : characterisation of storage, apoptosis and Wnt signalling.

Degree: PhD, 2009, University of Western Australia

greater insight into mammary cell physiology without the need for invasive tissue biopsy. Optimisation of collection and storage of breastmilk enabled the investigation of changes… (more)

Subjects/Keywords: Breast milk; Mammary glands; Wnt proteins; Cells from breastmilk; Wnt signalling; Breast cancer; Mammary gland biology

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APA (6th Edition):

Berry, C. A. (2009). Cells from breastmilk and the mammary gland : characterisation of storage, apoptosis and Wnt signalling. (Doctoral Dissertation). University of Western Australia. Retrieved from http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=13138&local_base=GEN01-INS01

Chicago Manual of Style (16th Edition):

Berry, Clare Alexandra. “Cells from breastmilk and the mammary gland : characterisation of storage, apoptosis and Wnt signalling.” 2009. Doctoral Dissertation, University of Western Australia. Accessed December 10, 2019. http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=13138&local_base=GEN01-INS01.

MLA Handbook (7th Edition):

Berry, Clare Alexandra. “Cells from breastmilk and the mammary gland : characterisation of storage, apoptosis and Wnt signalling.” 2009. Web. 10 Dec 2019.

Vancouver:

Berry CA. Cells from breastmilk and the mammary gland : characterisation of storage, apoptosis and Wnt signalling. [Internet] [Doctoral dissertation]. University of Western Australia; 2009. [cited 2019 Dec 10]. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=13138&local_base=GEN01-INS01.

Council of Science Editors:

Berry CA. Cells from breastmilk and the mammary gland : characterisation of storage, apoptosis and Wnt signalling. [Doctoral Dissertation]. University of Western Australia; 2009. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=13138&local_base=GEN01-INS01

45. Kerdidani, Dimitra. Ο ρόλος των πρωτεϊνών WNT στη διαφυγή του μη-μικροκυτταρικού καρκίνου του πνεύμονα από μηχανισμούς ανοσοεπιτήρησης.

Degree: 2019, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

Lung adenocarcinoma (LUAD)-derived Wnts increase cancer cell proliferative/stemness potential, but whether they impact the immune microenvironment is unknown. Here we show that LUAD cells use… (more)

Subjects/Keywords: Δενδριτικά κύτταρα; πρωτεϊνες WNT; Ανοσοκαταστολή; Μη-μικροκυτταρικός καρκίνος πνεύμονα; Dendritic cells; WNT proteins; Immunosuppression; Non-small cell lung cancer

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APA (6th Edition):

Kerdidani, D. (2019). Ο ρόλος των πρωτεϊνών WNT στη διαφυγή του μη-μικροκυτταρικού καρκίνου του πνεύμονα από μηχανισμούς ανοσοεπιτήρησης. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/45869

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):

Kerdidani, Dimitra. “Ο ρόλος των πρωτεϊνών WNT στη διαφυγή του μη-μικροκυτταρικού καρκίνου του πνεύμονα από μηχανισμούς ανοσοεπιτήρησης.” 2019. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed December 10, 2019. http://hdl.handle.net/10442/hedi/45869.

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

MLA Handbook (7th Edition):

Kerdidani, Dimitra. “Ο ρόλος των πρωτεϊνών WNT στη διαφυγή του μη-μικροκυτταρικού καρκίνου του πνεύμονα από μηχανισμούς ανοσοεπιτήρησης.” 2019. Web. 10 Dec 2019.

Vancouver:

Kerdidani D. Ο ρόλος των πρωτεϊνών WNT στη διαφυγή του μη-μικροκυτταρικού καρκίνου του πνεύμονα από μηχανισμούς ανοσοεπιτήρησης. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2019. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/10442/hedi/45869.

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

Council of Science Editors:

Kerdidani D. Ο ρόλος των πρωτεϊνών WNT στη διαφυγή του μη-μικροκυτταρικού καρκίνου του πνεύμονα από μηχανισμούς ανοσοεπιτήρησης. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2019. Available from: http://hdl.handle.net/10442/hedi/45869

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


Hong Kong University of Science and Technology

46. Qiu, Yifei. Cell biological studies of C. elegans seipin in heterologous model systems.

Degree: 2016, Hong Kong University of Science and Technology

 Lipid droplets (LDs) are conserved organelles for energy storage in cells. It contains a core of neutral lipids, i.e. triacylglycerols and sterol esters, surrounded by… (more)

Subjects/Keywords: Lipids; Metabolism; Proteins; Caenorhabditis elegans; Genetics

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APA (6th Edition):

Qiu, Y. (2016). Cell biological studies of C. elegans seipin in heterologous model systems. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1626283 ; http://repository.ust.hk/ir/bitstream/1783.1-87400/1/th_redirect.html

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):

Qiu, Yifei. “Cell biological studies of C. elegans seipin in heterologous model systems.” 2016. Thesis, Hong Kong University of Science and Technology. Accessed December 10, 2019. https://doi.org/10.14711/thesis-b1626283 ; http://repository.ust.hk/ir/bitstream/1783.1-87400/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Qiu, Yifei. “Cell biological studies of C. elegans seipin in heterologous model systems.” 2016. Web. 10 Dec 2019.

Vancouver:

Qiu Y. Cell biological studies of C. elegans seipin in heterologous model systems. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2016. [cited 2019 Dec 10]. Available from: https://doi.org/10.14711/thesis-b1626283 ; http://repository.ust.hk/ir/bitstream/1783.1-87400/1/th_redirect.html.

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

Council of Science Editors:

Qiu Y. Cell biological studies of C. elegans seipin in heterologous model systems. [Thesis]. Hong Kong University of Science and Technology; 2016. Available from: https://doi.org/10.14711/thesis-b1626283 ; http://repository.ust.hk/ir/bitstream/1783.1-87400/1/th_redirect.html

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


Hong Kong University of Science and Technology

47. Hu, Wenbao. TRIP-Br1 mediates degradation of multiple adenylyl cyclase isoforms by XIAP E3 ligase.

Degree: 2015, Hong Kong University of Science and Technology

 Adenylyl cyclases (ACs) catalyze conversion of ATP to cAMP, a second messenger of utmost importance that regulates a vast array of biological processes in all… (more)

Subjects/Keywords: Adenylate cyclase; Proteins; Metabolism; Ubiquitin; Ligases

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APA (6th Edition):

Hu, W. (2015). TRIP-Br1 mediates degradation of multiple adenylyl cyclase isoforms by XIAP E3 ligase. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1514880 ; http://repository.ust.hk/ir/bitstream/1783.1-80226/1/th_redirect.html

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):

Hu, Wenbao. “TRIP-Br1 mediates degradation of multiple adenylyl cyclase isoforms by XIAP E3 ligase.” 2015. Thesis, Hong Kong University of Science and Technology. Accessed December 10, 2019. https://doi.org/10.14711/thesis-b1514880 ; http://repository.ust.hk/ir/bitstream/1783.1-80226/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Hu, Wenbao. “TRIP-Br1 mediates degradation of multiple adenylyl cyclase isoforms by XIAP E3 ligase.” 2015. Web. 10 Dec 2019.

Vancouver:

Hu W. TRIP-Br1 mediates degradation of multiple adenylyl cyclase isoforms by XIAP E3 ligase. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2015. [cited 2019 Dec 10]. Available from: https://doi.org/10.14711/thesis-b1514880 ; http://repository.ust.hk/ir/bitstream/1783.1-80226/1/th_redirect.html.

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

Council of Science Editors:

Hu W. TRIP-Br1 mediates degradation of multiple adenylyl cyclase isoforms by XIAP E3 ligase. [Thesis]. Hong Kong University of Science and Technology; 2015. Available from: https://doi.org/10.14711/thesis-b1514880 ; http://repository.ust.hk/ir/bitstream/1783.1-80226/1/th_redirect.html

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


University of Hong Kong

48. Chen, Meipian. Effects of iron overload on apoptosis and titin proteolysis in cardiomyocytes.

Degree: PhD, 2013, University of Hong Kong

 Iron is one of the essential elements involved in various fundamental biological activities. However, excess iron may bypass the negative feedback regulatory systems, leading to… (more)

Subjects/Keywords: Apoptosis; Proteins - Metabolism; Heart cells; Iron - Pathophysiology

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APA (6th Edition):

Chen, M. (2013). Effects of iron overload on apoptosis and titin proteolysis in cardiomyocytes. (Doctoral Dissertation). University of Hong Kong. Retrieved from Chen, M. [陈美翩]. (2013). Effects of iron overload on apoptosis and titin proteolysis in cardiomyocytes. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5106511 ; http://dx.doi.org/10.5353/th_b5106511 ; http://hdl.handle.net/10722/193425

Chicago Manual of Style (16th Edition):

Chen, Meipian. “Effects of iron overload on apoptosis and titin proteolysis in cardiomyocytes.” 2013. Doctoral Dissertation, University of Hong Kong. Accessed December 10, 2019. Chen, M. [陈美翩]. (2013). Effects of iron overload on apoptosis and titin proteolysis in cardiomyocytes. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5106511 ; http://dx.doi.org/10.5353/th_b5106511 ; http://hdl.handle.net/10722/193425.

MLA Handbook (7th Edition):

Chen, Meipian. “Effects of iron overload on apoptosis and titin proteolysis in cardiomyocytes.” 2013. Web. 10 Dec 2019.

Vancouver:

Chen M. Effects of iron overload on apoptosis and titin proteolysis in cardiomyocytes. [Internet] [Doctoral dissertation]. University of Hong Kong; 2013. [cited 2019 Dec 10]. Available from: Chen, M. [陈美翩]. (2013). Effects of iron overload on apoptosis and titin proteolysis in cardiomyocytes. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5106511 ; http://dx.doi.org/10.5353/th_b5106511 ; http://hdl.handle.net/10722/193425.

Council of Science Editors:

Chen M. Effects of iron overload on apoptosis and titin proteolysis in cardiomyocytes. [Doctoral Dissertation]. University of Hong Kong; 2013. Available from: Chen, M. [陈美翩]. (2013). Effects of iron overload on apoptosis and titin proteolysis in cardiomyocytes. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5106511 ; http://dx.doi.org/10.5353/th_b5106511 ; http://hdl.handle.net/10722/193425


Montana State University

49. Hamerly, Timothy Kyle. Development of a protein-based sensor assay for rapid classification of complex biological samples.

Degree: College of Letters & Science, 2016, Montana State University

 Metabolomics, one of the core 'omics' fields within the umbrella of systems biology, is the study of the small molecules which can be used to… (more)

Subjects/Keywords: Mass spectrometry.; Proteins.; Metabolism.; Classification.; Systems biology.

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APA (6th Edition):

Hamerly, T. K. (2016). Development of a protein-based sensor assay for rapid classification of complex biological samples. (Thesis). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/13787

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):

Hamerly, Timothy Kyle. “Development of a protein-based sensor assay for rapid classification of complex biological samples.” 2016. Thesis, Montana State University. Accessed December 10, 2019. https://scholarworks.montana.edu/xmlui/handle/1/13787.

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

MLA Handbook (7th Edition):

Hamerly, Timothy Kyle. “Development of a protein-based sensor assay for rapid classification of complex biological samples.” 2016. Web. 10 Dec 2019.

Vancouver:

Hamerly TK. Development of a protein-based sensor assay for rapid classification of complex biological samples. [Internet] [Thesis]. Montana State University; 2016. [cited 2019 Dec 10]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/13787.

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

Council of Science Editors:

Hamerly TK. Development of a protein-based sensor assay for rapid classification of complex biological samples. [Thesis]. Montana State University; 2016. Available from: https://scholarworks.montana.edu/xmlui/handle/1/13787

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


Oregon State University

50. Purintrapiban, Juntipa. Coordination of protease systems on muscle protein degradation and identification of calpain substrates using the yeast two-hybrid system.

Degree: PhD, Animal Science, 1999, Oregon State University

 The first goal of this study was to evaluate the roles of different intracellular proteolytic systems in accelerated skeletal muscle protein degradation. Total, myofibrillar and… (more)

Subjects/Keywords: Muscle proteins  – Metabolism

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APA (6th Edition):

Purintrapiban, J. (1999). Coordination of protease systems on muscle protein degradation and identification of calpain substrates using the yeast two-hybrid system. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/32967

Chicago Manual of Style (16th Edition):

Purintrapiban, Juntipa. “Coordination of protease systems on muscle protein degradation and identification of calpain substrates using the yeast two-hybrid system.” 1999. Doctoral Dissertation, Oregon State University. Accessed December 10, 2019. http://hdl.handle.net/1957/32967.

MLA Handbook (7th Edition):

Purintrapiban, Juntipa. “Coordination of protease systems on muscle protein degradation and identification of calpain substrates using the yeast two-hybrid system.” 1999. Web. 10 Dec 2019.

Vancouver:

Purintrapiban J. Coordination of protease systems on muscle protein degradation and identification of calpain substrates using the yeast two-hybrid system. [Internet] [Doctoral dissertation]. Oregon State University; 1999. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/1957/32967.

Council of Science Editors:

Purintrapiban J. Coordination of protease systems on muscle protein degradation and identification of calpain substrates using the yeast two-hybrid system. [Doctoral Dissertation]. Oregon State University; 1999. Available from: http://hdl.handle.net/1957/32967


Oregon State University

51. Wang, Mei-Chuan. Effects of ciliary neutrophic factor (CNTF) on protein turnover in cultured L8 rat muscle cells.

Degree: MS, Animal Science, 1997, Oregon State University

 Skeletal muscle proteins are the largest amino acid pool in animal body and are continuously degraded and resynthesized. Dozens of factors have been shown to… (more)

Subjects/Keywords: Muscle proteins  – Metabolism

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APA (6th Edition):

Wang, M. (1997). Effects of ciliary neutrophic factor (CNTF) on protein turnover in cultured L8 rat muscle cells. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/33711

Chicago Manual of Style (16th Edition):

Wang, Mei-Chuan. “Effects of ciliary neutrophic factor (CNTF) on protein turnover in cultured L8 rat muscle cells.” 1997. Masters Thesis, Oregon State University. Accessed December 10, 2019. http://hdl.handle.net/1957/33711.

MLA Handbook (7th Edition):

Wang, Mei-Chuan. “Effects of ciliary neutrophic factor (CNTF) on protein turnover in cultured L8 rat muscle cells.” 1997. Web. 10 Dec 2019.

Vancouver:

Wang M. Effects of ciliary neutrophic factor (CNTF) on protein turnover in cultured L8 rat muscle cells. [Internet] [Masters thesis]. Oregon State University; 1997. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/1957/33711.

Council of Science Editors:

Wang M. Effects of ciliary neutrophic factor (CNTF) on protein turnover in cultured L8 rat muscle cells. [Masters Thesis]. Oregon State University; 1997. Available from: http://hdl.handle.net/1957/33711


Oregon State University

52. Huang, Jing, 1961-. Control of muscle protein degradation and steady-state poly(ADP-ribose) polymerase concentration by calpain.

Degree: PhD, Genetics, 1998, Oregon State University

 The first goal of this study was to understand the role of calpains in skeletal muscle protein degradation in cultured cells. We have developed a… (more)

Subjects/Keywords: Muscle proteins  – Metabolism

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APA (6th Edition):

Huang, Jing, 1. (1998). Control of muscle protein degradation and steady-state poly(ADP-ribose) polymerase concentration by calpain. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/33998

Chicago Manual of Style (16th Edition):

Huang, Jing, 1961-. “Control of muscle protein degradation and steady-state poly(ADP-ribose) polymerase concentration by calpain.” 1998. Doctoral Dissertation, Oregon State University. Accessed December 10, 2019. http://hdl.handle.net/1957/33998.

MLA Handbook (7th Edition):

Huang, Jing, 1961-. “Control of muscle protein degradation and steady-state poly(ADP-ribose) polymerase concentration by calpain.” 1998. Web. 10 Dec 2019.

Vancouver:

Huang, Jing 1. Control of muscle protein degradation and steady-state poly(ADP-ribose) polymerase concentration by calpain. [Internet] [Doctoral dissertation]. Oregon State University; 1998. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/1957/33998.

Council of Science Editors:

Huang, Jing 1. Control of muscle protein degradation and steady-state poly(ADP-ribose) polymerase concentration by calpain. [Doctoral Dissertation]. Oregon State University; 1998. Available from: http://hdl.handle.net/1957/33998


University of British Columbia

53. Cheeke, Peter Robert. The changes of the serum protein-bound iodine during growth in the Holstein calf and the Wistar albino rat .

Degree: 1965, University of British Columbia

 The changes in the level of circulating thyroid hormone, or protein-bound iodine (PBI), in the male Holstein calf and the Wistar Albino rat during a… (more)

Subjects/Keywords: Proteins  – Metabolism; Iodine

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APA (6th Edition):

Cheeke, P. R. (1965). The changes of the serum protein-bound iodine during growth in the Holstein calf and the Wistar albino rat . (Thesis). University of British Columbia. Retrieved from http://hdl.handle.net/2429/37086

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):

Cheeke, Peter Robert. “The changes of the serum protein-bound iodine during growth in the Holstein calf and the Wistar albino rat .” 1965. Thesis, University of British Columbia. Accessed December 10, 2019. http://hdl.handle.net/2429/37086.

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

MLA Handbook (7th Edition):

Cheeke, Peter Robert. “The changes of the serum protein-bound iodine during growth in the Holstein calf and the Wistar albino rat .” 1965. Web. 10 Dec 2019.

Vancouver:

Cheeke PR. The changes of the serum protein-bound iodine during growth in the Holstein calf and the Wistar albino rat . [Internet] [Thesis]. University of British Columbia; 1965. [cited 2019 Dec 10]. Available from: http://hdl.handle.net/2429/37086.

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

Council of Science Editors:

Cheeke PR. The changes of the serum protein-bound iodine during growth in the Holstein calf and the Wistar albino rat . [Thesis]. University of British Columbia; 1965. Available from: http://hdl.handle.net/2429/37086

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

54. Desmons, Aurore. Étude du métabolisme des protéines carbamylées intracellulaires : Study of intracellular metabolism of carbamylated proteins.

Degree: Docteur es, Médecine - STS, 2018, Reims

La réaction de carbamylation, comme les réactions de glycation, d’oxydation ou de carbonylation, fait partie des modifications post-traductionnelles non enzymatiques des protéines. Elle correspond à… (more)

Subjects/Keywords: Carbamylation; Métabolisme; Protéines; Carbamylation; Metabolism; Proteins; 570

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APA (6th Edition):

Desmons, A. (2018). Étude du métabolisme des protéines carbamylées intracellulaires : Study of intracellular metabolism of carbamylated proteins. (Doctoral Dissertation). Reims. Retrieved from http://www.theses.fr/2018REIMM209

Chicago Manual of Style (16th Edition):

Desmons, Aurore. “Étude du métabolisme des protéines carbamylées intracellulaires : Study of intracellular metabolism of carbamylated proteins.” 2018. Doctoral Dissertation, Reims. Accessed December 10, 2019. http://www.theses.fr/2018REIMM209.

MLA Handbook (7th Edition):

Desmons, Aurore. “Étude du métabolisme des protéines carbamylées intracellulaires : Study of intracellular metabolism of carbamylated proteins.” 2018. Web. 10 Dec 2019.

Vancouver:

Desmons A. Étude du métabolisme des protéines carbamylées intracellulaires : Study of intracellular metabolism of carbamylated proteins. [Internet] [Doctoral dissertation]. Reims; 2018. [cited 2019 Dec 10]. Available from: http://www.theses.fr/2018REIMM209.

Council of Science Editors:

Desmons A. Étude du métabolisme des protéines carbamylées intracellulaires : Study of intracellular metabolism of carbamylated proteins. [Doctoral Dissertation]. Reims; 2018. Available from: http://www.theses.fr/2018REIMM209


University of Guelph

55. Delfosse, Kathleen. Investigations of the Effects of Subcellular Sugar Levels on Plastid Morphology .

Degree: 2018, University of Guelph

 Plastid extensions, known as stromules, are an enigmatic feature of all land plants observed to date but the mechanism by which they extend remains unknown.… (more)

Subjects/Keywords: Stromule; Plastids; Fluorescent proteins; Chloroplast metabolism; Microscopy

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APA (6th Edition):

Delfosse, K. (2018). Investigations of the Effects of Subcellular Sugar Levels on Plastid Morphology . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/12585

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):

Delfosse, Kathleen. “Investigations of the Effects of Subcellular Sugar Levels on Plastid Morphology .” 2018. Thesis, University of Guelph. Accessed December 10, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/12585.

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

MLA Handbook (7th Edition):

Delfosse, Kathleen. “Investigations of the Effects of Subcellular Sugar Levels on Plastid Morphology .” 2018. Web. 10 Dec 2019.

Vancouver:

Delfosse K. Investigations of the Effects of Subcellular Sugar Levels on Plastid Morphology . [Internet] [Thesis]. University of Guelph; 2018. [cited 2019 Dec 10]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/12585.

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

Council of Science Editors:

Delfosse K. Investigations of the Effects of Subcellular Sugar Levels on Plastid Morphology . [Thesis]. University of Guelph; 2018. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/12585

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


Michigan State University

56. Bolourchi-Vaghefi, Simin D. Wheat as the source of protein for human adults ; effect of wheat protein on nitrogen balance, urea, and amino acid metabolism.

Degree: PhD, Department of Foods and Nutrition, 1967, Michigan State University

Subjects/Keywords: Wheat; Proteins – Metabolism

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APA (6th Edition):

Bolourchi-Vaghefi, S. D. (1967). Wheat as the source of protein for human adults ; effect of wheat protein on nitrogen balance, urea, and amino acid metabolism. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:41256

Chicago Manual of Style (16th Edition):

Bolourchi-Vaghefi, Simin D. “Wheat as the source of protein for human adults ; effect of wheat protein on nitrogen balance, urea, and amino acid metabolism.” 1967. Doctoral Dissertation, Michigan State University. Accessed December 10, 2019. http://etd.lib.msu.edu/islandora/object/etd:41256.

MLA Handbook (7th Edition):

Bolourchi-Vaghefi, Simin D. “Wheat as the source of protein for human adults ; effect of wheat protein on nitrogen balance, urea, and amino acid metabolism.” 1967. Web. 10 Dec 2019.

Vancouver:

Bolourchi-Vaghefi SD. Wheat as the source of protein for human adults ; effect of wheat protein on nitrogen balance, urea, and amino acid metabolism. [Internet] [Doctoral dissertation]. Michigan State University; 1967. [cited 2019 Dec 10]. Available from: http://etd.lib.msu.edu/islandora/object/etd:41256.

Council of Science Editors:

Bolourchi-Vaghefi SD. Wheat as the source of protein for human adults ; effect of wheat protein on nitrogen balance, urea, and amino acid metabolism. [Doctoral Dissertation]. Michigan State University; 1967. Available from: http://etd.lib.msu.edu/islandora/object/etd:41256


Michigan State University

57. Barry, Mary M. Influence of medium and high protein diets on the chlorine metabolism of two preschool children.

Degree: MS, 1933, Michigan State University

Subjects/Keywords: Proteins; Chlorine; Metabolism

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APA (6th Edition):

Barry, M. M. (1933). Influence of medium and high protein diets on the chlorine metabolism of two preschool children. (Masters Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:43002

Chicago Manual of Style (16th Edition):

Barry, Mary M. “Influence of medium and high protein diets on the chlorine metabolism of two preschool children.” 1933. Masters Thesis, Michigan State University. Accessed December 10, 2019. http://etd.lib.msu.edu/islandora/object/etd:43002.

MLA Handbook (7th Edition):

Barry, Mary M. “Influence of medium and high protein diets on the chlorine metabolism of two preschool children.” 1933. Web. 10 Dec 2019.

Vancouver:

Barry MM. Influence of medium and high protein diets on the chlorine metabolism of two preschool children. [Internet] [Masters thesis]. Michigan State University; 1933. [cited 2019 Dec 10]. Available from: http://etd.lib.msu.edu/islandora/object/etd:43002.

Council of Science Editors:

Barry MM. Influence of medium and high protein diets on the chlorine metabolism of two preschool children. [Masters Thesis]. Michigan State University; 1933. Available from: http://etd.lib.msu.edu/islandora/object/etd:43002


University of California – Irvine

58. Chen, George Tsun-Te. Wnt Signaling Regulation of Colon Cancer Metabolism and Invasion.

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

 The Wnt signaling pathway is a highly conserved cell-to-cell communication network in animals, and it regulates many gene programs essential for organism growth and development.… (more)

Subjects/Keywords: Oncology; Biology; Genetics; Cell Migration; Colon Cancer; Metabolism; Tumor heterogeneity; Turing pattern; Wnt Signaling

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APA (6th Edition):

Chen, G. T. (2018). Wnt Signaling Regulation of Colon Cancer Metabolism and Invasion. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/95x9n1c4

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):

Chen, George Tsun-Te. “Wnt Signaling Regulation of Colon Cancer Metabolism and Invasion.” 2018. Thesis, University of California – Irvine. Accessed December 10, 2019. http://www.escholarship.org/uc/item/95x9n1c4.

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

MLA Handbook (7th Edition):

Chen, George Tsun-Te. “Wnt Signaling Regulation of Colon Cancer Metabolism and Invasion.” 2018. Web. 10 Dec 2019.

Vancouver:

Chen GT. Wnt Signaling Regulation of Colon Cancer Metabolism and Invasion. [Internet] [Thesis]. University of California – Irvine; 2018. [cited 2019 Dec 10]. Available from: http://www.escholarship.org/uc/item/95x9n1c4.

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

Council of Science Editors:

Chen GT. Wnt Signaling Regulation of Colon Cancer Metabolism and Invasion. [Thesis]. University of California – Irvine; 2018. Available from: http://www.escholarship.org/uc/item/95x9n1c4

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


University of Iowa

59. Kluz, Paige Nicole. The multifaceted roles of CD177 in mammary tissue development and breast cancer.

Degree: PhD, Free Radical and Radiation Biology, 2018, University of Iowa

  Aiming to identify immune molecules with a novel function in cancer pathogenesis, we found the cluster of differentiation 177 (CD177), a known neutrophil antigen,… (more)

Subjects/Keywords: beta-Catenin; Breast Cancer; CD177; E-Cadherin; Metabolism; Wnt; Other Biochemistry, Biophysics, and Structural Biology

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

APA (6th Edition):

Kluz, P. N. (2018). The multifaceted roles of CD177 in mammary tissue development and breast cancer. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/6600

Chicago Manual of Style (16th Edition):

Kluz, Paige Nicole. “The multifaceted roles of CD177 in mammary tissue development and breast cancer.” 2018. Doctoral Dissertation, University of Iowa. Accessed December 10, 2019. https://ir.uiowa.edu/etd/6600.

MLA Handbook (7th Edition):

Kluz, Paige Nicole. “The multifaceted roles of CD177 in mammary tissue development and breast cancer.” 2018. Web. 10 Dec 2019.

Vancouver:

Kluz PN. The multifaceted roles of CD177 in mammary tissue development and breast cancer. [Internet] [Doctoral dissertation]. University of Iowa; 2018. [cited 2019 Dec 10]. Available from: https://ir.uiowa.edu/etd/6600.

Council of Science Editors:

Kluz PN. The multifaceted roles of CD177 in mammary tissue development and breast cancer. [Doctoral Dissertation]. University of Iowa; 2018. Available from: https://ir.uiowa.edu/etd/6600

60. Dismuke, Adria Decker. Wnt signaling in the mouse small intestine.

Degree: PhD, 2009, Oregon Health Sciences University

Subjects/Keywords: Mice; Intestines; Wnt Proteins; Stem Cells

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

APA (6th Edition):

Dismuke, A. D. (2009). Wnt signaling in the mouse small intestine. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M47H1GJH ; http://digitalcommons.ohsu.edu/etd/625

Chicago Manual of Style (16th Edition):

Dismuke, Adria Decker. “Wnt signaling in the mouse small intestine.” 2009. Doctoral Dissertation, Oregon Health Sciences University. Accessed December 10, 2019. doi:10.6083/M47H1GJH ; http://digitalcommons.ohsu.edu/etd/625.

MLA Handbook (7th Edition):

Dismuke, Adria Decker. “Wnt signaling in the mouse small intestine.” 2009. Web. 10 Dec 2019.

Vancouver:

Dismuke AD. Wnt signaling in the mouse small intestine. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 2009. [cited 2019 Dec 10]. Available from: doi:10.6083/M47H1GJH ; http://digitalcommons.ohsu.edu/etd/625.

Council of Science Editors:

Dismuke AD. Wnt signaling in the mouse small intestine. [Doctoral Dissertation]. Oregon Health Sciences University; 2009. Available from: doi:10.6083/M47H1GJH ; http://digitalcommons.ohsu.edu/etd/625

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