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Dates: 2015 – 2019

You searched for subject:( Wnt Proteins metabolism). Showing records 1 – 30 of 4448 total matches.

[1] [2] [3] [4] [5] … [149]

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Rutgers University

1. Sun, Jiaxin, 1989-. Analysis of the structure of Wntless protein and its role in supporting Wnt secretion at the endoplasmic reticulum compartment.

Degree: PhD, Biology, 2017, Rutgers University

Wnts are secreted glycolipoproteins fundamental for embryonic development and adult tissue homeostasis. Abnormal Wnt signal transduction is associated with human diseases, most notably colon cancers.… (more)

Subjects/Keywords: Wnt proteins

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APA (6th Edition):

Sun, Jiaxin, 1. (2017). Analysis of the structure of Wntless protein and its role in supporting Wnt secretion at the endoplasmic reticulum compartment. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/55293/

Chicago Manual of Style (16th Edition):

Sun, Jiaxin, 1989-. “Analysis of the structure of Wntless protein and its role in supporting Wnt secretion at the endoplasmic reticulum compartment.” 2017. Doctoral Dissertation, Rutgers University. Accessed December 09, 2019. https://rucore.libraries.rutgers.edu/rutgers-lib/55293/.

MLA Handbook (7th Edition):

Sun, Jiaxin, 1989-. “Analysis of the structure of Wntless protein and its role in supporting Wnt secretion at the endoplasmic reticulum compartment.” 2017. Web. 09 Dec 2019.

Vancouver:

Sun, Jiaxin 1. Analysis of the structure of Wntless protein and its role in supporting Wnt secretion at the endoplasmic reticulum compartment. [Internet] [Doctoral dissertation]. Rutgers University; 2017. [cited 2019 Dec 09]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/55293/.

Council of Science Editors:

Sun, Jiaxin 1. Analysis of the structure of Wntless protein and its role in supporting Wnt secretion at the endoplasmic reticulum compartment. [Doctoral Dissertation]. Rutgers University; 2017. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/55293/


McMaster University

2. RANAWADE, AYUSH. PRY-1/AXIN REGULATE AGING, LIPID METABOLISM AND SEAM-CELL ASYMMETRIC CELL DIVISION IN CAENORHABDITIS ELEGANS.

Degree: PhD, 2017, McMaster University

The nematode, Caenorhabditis elegans is an ideal animal model to study conserved mechanisms of developmental and postdevelopmental processes. Here, I describe the role of an… (more)

Subjects/Keywords: C. ELEGANS; WNT SIGNALING; LIPID METABOLISM; AGING

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APA (6th Edition):

RANAWADE, A. (2017). PRY-1/AXIN REGULATE AGING, LIPID METABOLISM AND SEAM-CELL ASYMMETRIC CELL DIVISION IN CAENORHABDITIS ELEGANS. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/22095

Chicago Manual of Style (16th Edition):

RANAWADE, AYUSH. “PRY-1/AXIN REGULATE AGING, LIPID METABOLISM AND SEAM-CELL ASYMMETRIC CELL DIVISION IN CAENORHABDITIS ELEGANS.” 2017. Doctoral Dissertation, McMaster University. Accessed December 09, 2019. http://hdl.handle.net/11375/22095.

MLA Handbook (7th Edition):

RANAWADE, AYUSH. “PRY-1/AXIN REGULATE AGING, LIPID METABOLISM AND SEAM-CELL ASYMMETRIC CELL DIVISION IN CAENORHABDITIS ELEGANS.” 2017. Web. 09 Dec 2019.

Vancouver:

RANAWADE A. PRY-1/AXIN REGULATE AGING, LIPID METABOLISM AND SEAM-CELL ASYMMETRIC CELL DIVISION IN CAENORHABDITIS ELEGANS. [Internet] [Doctoral dissertation]. McMaster University; 2017. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/11375/22095.

Council of Science Editors:

RANAWADE A. PRY-1/AXIN REGULATE AGING, LIPID METABOLISM AND SEAM-CELL ASYMMETRIC CELL DIVISION IN CAENORHABDITIS ELEGANS. [Doctoral Dissertation]. McMaster University; 2017. Available from: http://hdl.handle.net/11375/22095


Hong Kong University of Science and Technology

3. Xu, Li. Wnt3a induces the transcription of acetylcholinesterase : an enzyme playing a role in osteoblastic differentiation.

Degree: 2017, Hong Kong University of Science and Technology

 Acetylcholinesterase (AChE) is known to be a key enzyme that needs for terminating cholinergic transmission in vertebrate. By alternative splicing, three variants of transcripts are… (more)

Subjects/Keywords: Wnt proteins; Acetylcholinesterase; Enzymes; Regulation; Osteoblasts

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APA (6th Edition):

Xu, L. (2017). Wnt3a induces the transcription of acetylcholinesterase : an enzyme playing a role in osteoblastic differentiation. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-991012564567103412 ; http://repository.ust.hk/ir/bitstream/1783.1-91186/1/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):

Xu, Li. “Wnt3a induces the transcription of acetylcholinesterase : an enzyme playing a role in osteoblastic differentiation.” 2017. Thesis, Hong Kong University of Science and Technology. Accessed December 09, 2019. https://doi.org/10.14711/thesis-991012564567103412 ; http://repository.ust.hk/ir/bitstream/1783.1-91186/1/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):

Xu, Li. “Wnt3a induces the transcription of acetylcholinesterase : an enzyme playing a role in osteoblastic differentiation.” 2017. Web. 09 Dec 2019.

Vancouver:

Xu L. Wnt3a induces the transcription of acetylcholinesterase : an enzyme playing a role in osteoblastic differentiation. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2017. [cited 2019 Dec 09]. Available from: https://doi.org/10.14711/thesis-991012564567103412 ; http://repository.ust.hk/ir/bitstream/1783.1-91186/1/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:

Xu L. Wnt3a induces the transcription of acetylcholinesterase : an enzyme playing a role in osteoblastic differentiation. [Thesis]. Hong Kong University of Science and Technology; 2017. Available from: https://doi.org/10.14711/thesis-991012564567103412 ; http://repository.ust.hk/ir/bitstream/1783.1-91186/1/th_redirect.html

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


Rutgers University

4. Das, Soumyashree, 1986-. Regulation of Wnt delivery at intestinal stem cell niche.

Degree: PhD, Biology, 2016, Rutgers University

Communication between stem cells and its niche-supporting cells maintains the homeostasis of adult tissues. Wnt signaling is a critical regulator of stem cell niche, but… (more)

Subjects/Keywords: Drug delivery systems; Stem cells; Wnt proteins

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APA (6th Edition):

Das, Soumyashree, 1. (2016). Regulation of Wnt delivery at intestinal stem cell niche. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/49357/

Chicago Manual of Style (16th Edition):

Das, Soumyashree, 1986-. “Regulation of Wnt delivery at intestinal stem cell niche.” 2016. Doctoral Dissertation, Rutgers University. Accessed December 09, 2019. https://rucore.libraries.rutgers.edu/rutgers-lib/49357/.

MLA Handbook (7th Edition):

Das, Soumyashree, 1986-. “Regulation of Wnt delivery at intestinal stem cell niche.” 2016. Web. 09 Dec 2019.

Vancouver:

Das, Soumyashree 1. Regulation of Wnt delivery at intestinal stem cell niche. [Internet] [Doctoral dissertation]. Rutgers University; 2016. [cited 2019 Dec 09]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/49357/.

Council of Science Editors:

Das, Soumyashree 1. Regulation of Wnt delivery at intestinal stem cell niche. [Doctoral Dissertation]. Rutgers University; 2016. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/49357/


University of Texas Southwestern Medical Center

5. Tuladhar, Rubina. Mechanisms of Genome Buffering and Cell Fate Coordination in Adult Tissue Homeostasis.

Degree: 2016, University of Texas Southwestern Medical Center

 Self-renewal competency of adult stem cells is essential for tissue homeostasis. The corruption of genes essential for genome preservation or for niche-stem cell interactions frequently… (more)

Subjects/Keywords: Acyltransferases; CRISPR-Cas Systems; Homeostasis; Membrane Proteins; Signal Transduction; Wnt Proteins

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APA (6th Edition):

Tuladhar, R. (2016). Mechanisms of Genome Buffering and Cell Fate Coordination in Adult Tissue Homeostasis. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5744

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):

Tuladhar, Rubina. “Mechanisms of Genome Buffering and Cell Fate Coordination in Adult Tissue Homeostasis.” 2016. Thesis, University of Texas Southwestern Medical Center. Accessed December 09, 2019. http://hdl.handle.net/2152.5/5744.

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

MLA Handbook (7th Edition):

Tuladhar, Rubina. “Mechanisms of Genome Buffering and Cell Fate Coordination in Adult Tissue Homeostasis.” 2016. Web. 09 Dec 2019.

Vancouver:

Tuladhar R. Mechanisms of Genome Buffering and Cell Fate Coordination in Adult Tissue Homeostasis. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2016. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/2152.5/5744.

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

Council of Science Editors:

Tuladhar R. Mechanisms of Genome Buffering and Cell Fate Coordination in Adult Tissue Homeostasis. [Thesis]. University of Texas Southwestern Medical Center; 2016. Available from: http://hdl.handle.net/2152.5/5744

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

6. KÃtia do Nascimento Gomes. Assessment of effect of doxycycline associated or not with dexamethasone on alveolar bone repair model in rats.

Degree: PhD, 2015, Universidade Federal do Ceará

The alveolar bone repair model, through dental excision in rats, allows the longitudinal study of local and systemic parameters. This allows learning the pathophysiology in… (more)

Subjects/Keywords: FARMACOLOGIA; AlvÃolo Dental; ReabsorÃÃo Ãssea; Doxiciclina; ProteÃnas Wnt; Tooth Socket; Bone Resorption; Doxycycline; Wnt Proteins

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APA (6th Edition):

Gomes, K. d. N. (2015). Assessment of effect of doxycycline associated or not with dexamethasone on alveolar bone repair model in rats. (Doctoral Dissertation). Universidade Federal do Ceará. Retrieved from http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=17591 ;

Chicago Manual of Style (16th Edition):

Gomes, KÃtia do Nascimento. “Assessment of effect of doxycycline associated or not with dexamethasone on alveolar bone repair model in rats.” 2015. Doctoral Dissertation, Universidade Federal do Ceará. Accessed December 09, 2019. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=17591 ;.

MLA Handbook (7th Edition):

Gomes, KÃtia do Nascimento. “Assessment of effect of doxycycline associated or not with dexamethasone on alveolar bone repair model in rats.” 2015. Web. 09 Dec 2019.

Vancouver:

Gomes KdN. Assessment of effect of doxycycline associated or not with dexamethasone on alveolar bone repair model in rats. [Internet] [Doctoral dissertation]. Universidade Federal do Ceará 2015. [cited 2019 Dec 09]. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=17591 ;.

Council of Science Editors:

Gomes KdN. Assessment of effect of doxycycline associated or not with dexamethasone on alveolar bone repair model in rats. [Doctoral Dissertation]. Universidade Federal do Ceará 2015. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=17591 ;


Hong Kong University of Science and Technology

7. Ji, Xianglin LIFS. Nutrient dependent turnover of lipid droplet associated proteins.

Degree: 2015, Hong Kong University of Science and Technology

 Lipid droplets (LDs) are conserved organelles for cellular fat storage. In C.elegans, numerous LDs can be found in intestinal cells, where fat is primarily stored.… (more)

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

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APA (6th Edition):

Ji, X. L. (2015). Nutrient dependent turnover of lipid droplet associated proteins. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1514897 ; http://repository.ust.hk/ir/bitstream/1783.1-94920/1/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):

Ji, Xianglin LIFS. “Nutrient dependent turnover of lipid droplet associated proteins.” 2015. Thesis, Hong Kong University of Science and Technology. Accessed December 09, 2019. https://doi.org/10.14711/thesis-b1514897 ; http://repository.ust.hk/ir/bitstream/1783.1-94920/1/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):

Ji, Xianglin LIFS. “Nutrient dependent turnover of lipid droplet associated proteins.” 2015. Web. 09 Dec 2019.

Vancouver:

Ji XL. Nutrient dependent turnover of lipid droplet associated proteins. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2015. [cited 2019 Dec 09]. Available from: https://doi.org/10.14711/thesis-b1514897 ; http://repository.ust.hk/ir/bitstream/1783.1-94920/1/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:

Ji XL. Nutrient dependent turnover of lipid droplet associated proteins. [Thesis]. Hong Kong University of Science and Technology; 2015. Available from: https://doi.org/10.14711/thesis-b1514897 ; http://repository.ust.hk/ir/bitstream/1783.1-94920/1/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

8. 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 09, 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. 09 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 09]. 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

9. 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 09, 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. 09 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 09]. 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 North Carolina – Greensboro

10. 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 09, 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. 09 Dec 2019.

Vancouver:

Manner ICJ. Functional distinctions between two isoforms of WNT5A. [Internet] [Masters thesis]. University of North Carolina – Greensboro; 2016. [cited 2019 Dec 09]. 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 Washington

11. 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 09, 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. 09 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 09]. 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

12. 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 09, 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. 09 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 09]. 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

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

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 09, 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. 09 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 09]. 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

14. 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 09, 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. 09 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 09]. 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


Montana State University

15. 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 09, 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. 09 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 09]. 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

16. 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 09, 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. 09 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 09]. 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

17. 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 09, 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. 09 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 09]. 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


University of California – Irvine

18. 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 09, 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. 09 Dec 2019.

Vancouver:

Chen GT. Wnt Signaling Regulation of Colon Cancer Metabolism and Invasion. [Internet] [Thesis]. University of California – Irvine; 2018. [cited 2019 Dec 09]. 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

19. 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 (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 09, 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. 09 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 09]. 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

20. Iyengar, Sharanya. Insights into Melanocyte Regeneration and Melanoma Initiation Using the Zebrafish Model System: A Dissertation.

Degree: Cancer Biology, Program in Molecular Medicine, 2015, U of Massachusetts : Med

  During regeneration, cells must coordinate proliferation and differentiation to rebuild tissues that are lost. Understanding how source cells execute the regeneration process has been… (more)

Subjects/Keywords: Melanocytes; Melanoma; Zebrafish; Cell Differentiation; Regeneration; Wnt Proteins; Cancer Biology; Cell Biology; Neoplasms

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APA (6th Edition):

Iyengar, S. (2015). Insights into Melanocyte Regeneration and Melanoma Initiation Using the Zebrafish Model System: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/796

Chicago Manual of Style (16th Edition):

Iyengar, Sharanya. “Insights into Melanocyte Regeneration and Melanoma Initiation Using the Zebrafish Model System: A Dissertation.” 2015. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 09, 2019. http://escholarship.umassmed.edu/gsbs_diss/796.

MLA Handbook (7th Edition):

Iyengar, Sharanya. “Insights into Melanocyte Regeneration and Melanoma Initiation Using the Zebrafish Model System: A Dissertation.” 2015. Web. 09 Dec 2019.

Vancouver:

Iyengar S. Insights into Melanocyte Regeneration and Melanoma Initiation Using the Zebrafish Model System: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2015. [cited 2019 Dec 09]. Available from: http://escholarship.umassmed.edu/gsbs_diss/796.

Council of Science Editors:

Iyengar S. Insights into Melanocyte Regeneration and Melanoma Initiation Using the Zebrafish Model System: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2015. Available from: http://escholarship.umassmed.edu/gsbs_diss/796

21. Santos, Carla Cristine Crude dos. Ação de agonistas da via Wnt/beta-catenina em células T CD4+ murinas.

Degree: Mestrado, Alergia e Imunopatologia, 2015, University of São Paulo

A via canônica Wnt/beta-catenina regula várias funções em vertebrados, incluindo diferenciação de células T, bem como a proliferação, sobrevivência, morfogênese e migração de vários tipos… (more)

Subjects/Keywords: beta catenin; beta catenina; Expressão gênica; Gene expression; Glycogen synthase kinase 3; Homeostase; Homeostasis; Linfócitos T; Lithium; Lítio; Proteínas Wnt; Quinase 3 da glicogênio sintase; T-lymphocytes; Via de sinalização Wnt; Wnt proteins; Wnt signaling pathway

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APA (6th Edition):

Santos, C. C. C. d. (2015). Ação de agonistas da via Wnt/beta-catenina em células T CD4+ murinas. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5146/tde-26082015-110639/ ;

Chicago Manual of Style (16th Edition):

Santos, Carla Cristine Crude dos. “Ação de agonistas da via Wnt/beta-catenina em células T CD4+ murinas.” 2015. Masters Thesis, University of São Paulo. Accessed December 09, 2019. http://www.teses.usp.br/teses/disponiveis/5/5146/tde-26082015-110639/ ;.

MLA Handbook (7th Edition):

Santos, Carla Cristine Crude dos. “Ação de agonistas da via Wnt/beta-catenina em células T CD4+ murinas.” 2015. Web. 09 Dec 2019.

Vancouver:

Santos CCCd. Ação de agonistas da via Wnt/beta-catenina em células T CD4+ murinas. [Internet] [Masters thesis]. University of São Paulo; 2015. [cited 2019 Dec 09]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5146/tde-26082015-110639/ ;.

Council of Science Editors:

Santos CCCd. Ação de agonistas da via Wnt/beta-catenina em células T CD4+ murinas. [Masters Thesis]. University of São Paulo; 2015. Available from: http://www.teses.usp.br/teses/disponiveis/5/5146/tde-26082015-110639/ ;

22. Désert, Romain. Effets phénotypiques de deux mécanismes d’activation de la voie Wnt/beta caténine dans le carcinome hépatocellulaire : Molecular phenotypes and clinical features associated with two types of Wnt/beta catenin activation in hepatocellular carcinoma.

Degree: Docteur es, Biologie et sciences de la santé, 2016, Rennes 1

Le carcinome hépatocellulaire (CHC) est une des principales causes de mortalité par cancer dans le monde. Dans environ 50% des tumeurs, on observe les signes… (more)

Subjects/Keywords: Carcinome hépatocellulaire; Voie Wnt/beta catenine; Métabolisme hépatique; Remodelage matriciel; Fibrose tumorale; Hepatocellular carcinoma; Wnt/beta catenin pathway; Liver metabolism; Extracellular matrix remodeling; Tumor fibrosis

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APA (6th Edition):

Désert, R. (2016). Effets phénotypiques de deux mécanismes d’activation de la voie Wnt/beta caténine dans le carcinome hépatocellulaire : Molecular phenotypes and clinical features associated with two types of Wnt/beta catenin activation in hepatocellular carcinoma. (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2016REN1B044

Chicago Manual of Style (16th Edition):

Désert, Romain. “Effets phénotypiques de deux mécanismes d’activation de la voie Wnt/beta caténine dans le carcinome hépatocellulaire : Molecular phenotypes and clinical features associated with two types of Wnt/beta catenin activation in hepatocellular carcinoma.” 2016. Doctoral Dissertation, Rennes 1. Accessed December 09, 2019. http://www.theses.fr/2016REN1B044.

MLA Handbook (7th Edition):

Désert, Romain. “Effets phénotypiques de deux mécanismes d’activation de la voie Wnt/beta caténine dans le carcinome hépatocellulaire : Molecular phenotypes and clinical features associated with two types of Wnt/beta catenin activation in hepatocellular carcinoma.” 2016. Web. 09 Dec 2019.

Vancouver:

Désert R. Effets phénotypiques de deux mécanismes d’activation de la voie Wnt/beta caténine dans le carcinome hépatocellulaire : Molecular phenotypes and clinical features associated with two types of Wnt/beta catenin activation in hepatocellular carcinoma. [Internet] [Doctoral dissertation]. Rennes 1; 2016. [cited 2019 Dec 09]. Available from: http://www.theses.fr/2016REN1B044.

Council of Science Editors:

Désert R. Effets phénotypiques de deux mécanismes d’activation de la voie Wnt/beta caténine dans le carcinome hépatocellulaire : Molecular phenotypes and clinical features associated with two types of Wnt/beta catenin activation in hepatocellular carcinoma. [Doctoral Dissertation]. Rennes 1; 2016. Available from: http://www.theses.fr/2016REN1B044


University of Hong Kong

23. Yuen, Ching-kiu. The involvement of Wnt/beta-catenin in maintenance of stem cell properties in the CD133⁺ subpopulation of cervical cancer cells.

Degree: M. Phil., 2016, University of Hong Kong

abstract

Obstetrics and Gynaecology

Master

Master of Philosophy

Subjects/Keywords: Cervix uteri - Cancer; Cancer cells; Wnt genes; Stem cells; Wnt proteins

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APA (6th Edition):

Yuen, C. (2016). The involvement of Wnt/beta-catenin in maintenance of stem cell properties in the CD133⁺ subpopulation of cervical cancer cells. (Masters Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/226724

Chicago Manual of Style (16th Edition):

Yuen, Ching-kiu. “The involvement of Wnt/beta-catenin in maintenance of stem cell properties in the CD133⁺ subpopulation of cervical cancer cells.” 2016. Masters Thesis, University of Hong Kong. Accessed December 09, 2019. http://hdl.handle.net/10722/226724.

MLA Handbook (7th Edition):

Yuen, Ching-kiu. “The involvement of Wnt/beta-catenin in maintenance of stem cell properties in the CD133⁺ subpopulation of cervical cancer cells.” 2016. Web. 09 Dec 2019.

Vancouver:

Yuen C. The involvement of Wnt/beta-catenin in maintenance of stem cell properties in the CD133⁺ subpopulation of cervical cancer cells. [Internet] [Masters thesis]. University of Hong Kong; 2016. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/10722/226724.

Council of Science Editors:

Yuen C. The involvement of Wnt/beta-catenin in maintenance of stem cell properties in the CD133⁺ subpopulation of cervical cancer cells. [Masters Thesis]. University of Hong Kong; 2016. Available from: http://hdl.handle.net/10722/226724


University of Hong Kong

24. Yuen, Ching-kiu. The involvement of Wnt/beta-catenin in maintenance of stem cell properties in the CD133⁺ subpopulation of cervical cancer cells.

Degree: M. Phil., 2016, University of Hong Kong

published_or_final_version

Obstetrics and Gynaecology

Master

Master of Philosophy

Subjects/Keywords: Wnt proteins; Cancer - Cervix uteri; Wnt genes; Cancer cells; Stem cells

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APA (6th Edition):

Yuen, C. (2016). The involvement of Wnt/beta-catenin in maintenance of stem cell properties in the CD133⁺ subpopulation of cervical cancer cells. (Masters Thesis). University of Hong Kong. Retrieved from Yuen, C. [阮政喬]. (2016). The involvement of Wnt/beta-catenin in maintenance of stem cell properties in the CD133⁺ subpopulation of cervical cancer cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5760910. ; http://dx.doi.org/10.5353/th_b5760910 ; http://hdl.handle.net/10722/239409

Chicago Manual of Style (16th Edition):

Yuen, Ching-kiu. “The involvement of Wnt/beta-catenin in maintenance of stem cell properties in the CD133⁺ subpopulation of cervical cancer cells.” 2016. Masters Thesis, University of Hong Kong. Accessed December 09, 2019. Yuen, C. [阮政喬]. (2016). The involvement of Wnt/beta-catenin in maintenance of stem cell properties in the CD133⁺ subpopulation of cervical cancer cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5760910. ; http://dx.doi.org/10.5353/th_b5760910 ; http://hdl.handle.net/10722/239409.

MLA Handbook (7th Edition):

Yuen, Ching-kiu. “The involvement of Wnt/beta-catenin in maintenance of stem cell properties in the CD133⁺ subpopulation of cervical cancer cells.” 2016. Web. 09 Dec 2019.

Vancouver:

Yuen C. The involvement of Wnt/beta-catenin in maintenance of stem cell properties in the CD133⁺ subpopulation of cervical cancer cells. [Internet] [Masters thesis]. University of Hong Kong; 2016. [cited 2019 Dec 09]. Available from: Yuen, C. [阮政喬]. (2016). The involvement of Wnt/beta-catenin in maintenance of stem cell properties in the CD133⁺ subpopulation of cervical cancer cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5760910. ; http://dx.doi.org/10.5353/th_b5760910 ; http://hdl.handle.net/10722/239409.

Council of Science Editors:

Yuen C. The involvement of Wnt/beta-catenin in maintenance of stem cell properties in the CD133⁺ subpopulation of cervical cancer cells. [Masters Thesis]. University of Hong Kong; 2016. Available from: Yuen, C. [阮政喬]. (2016). The involvement of Wnt/beta-catenin in maintenance of stem cell properties in the CD133⁺ subpopulation of cervical cancer cells. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5760910. ; http://dx.doi.org/10.5353/th_b5760910 ; http://hdl.handle.net/10722/239409

25. Racicot, Riccardo. One-Carbon Metabolism Related B-Vitamins Alter The Expression Of MicroRNAS And Target Genes Within The Wnt Signaling Pathway In Mouse Colonic Epithelium.

Degree: 2016, University of Massachusetts

  ABSTRACT It has been widely recognized that microRNAs are involved in nearly all cellular processes that have been investigated and contribute to a variety… (more)

Subjects/Keywords: One-carbon metabolism; microRNA; Wnt pathway; Colorectal cancer; Animal Diseases; Disorders of Environmental Origin; Neoplasms; Nutritional and Metabolic Diseases

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

APA (6th Edition):

Racicot, R. (2016). One-Carbon Metabolism Related B-Vitamins Alter The Expression Of MicroRNAS And Target Genes Within The Wnt Signaling Pathway In Mouse Colonic Epithelium. (Thesis). University of Massachusetts. Retrieved from https://scholarworks.umass.edu/masters_theses_2/372

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):

Racicot, Riccardo. “One-Carbon Metabolism Related B-Vitamins Alter The Expression Of MicroRNAS And Target Genes Within The Wnt Signaling Pathway In Mouse Colonic Epithelium.” 2016. Thesis, University of Massachusetts. Accessed December 09, 2019. https://scholarworks.umass.edu/masters_theses_2/372.

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

MLA Handbook (7th Edition):

Racicot, Riccardo. “One-Carbon Metabolism Related B-Vitamins Alter The Expression Of MicroRNAS And Target Genes Within The Wnt Signaling Pathway In Mouse Colonic Epithelium.” 2016. Web. 09 Dec 2019.

Vancouver:

Racicot R. One-Carbon Metabolism Related B-Vitamins Alter The Expression Of MicroRNAS And Target Genes Within The Wnt Signaling Pathway In Mouse Colonic Epithelium. [Internet] [Thesis]. University of Massachusetts; 2016. [cited 2019 Dec 09]. Available from: https://scholarworks.umass.edu/masters_theses_2/372.

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

Council of Science Editors:

Racicot R. One-Carbon Metabolism Related B-Vitamins Alter The Expression Of MicroRNAS And Target Genes Within The Wnt Signaling Pathway In Mouse Colonic Epithelium. [Thesis]. University of Massachusetts; 2016. Available from: https://scholarworks.umass.edu/masters_theses_2/372

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


East Carolina University

26. Hoggard, Jason Andrew. Proposed regulatory role of noncatalytic Adams in ectodomain shedding.

Degree: 2015, East Carolina University

 Members of the ADAM (A Disintegrin And Metalloprotease) protein family uniquely exhibit both proteolytic and adhesive properties. Specifically, ADAMs catalyze the conversion of cell-surface proteins(more)

Subjects/Keywords: Biochemistry; Molecular biology; ADAM; Disintegrin; Ectodomain; Metalloprotease; Shedding; MDC; Inflammation – metabolism; ADAM Proteins – metabolism

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

APA (6th Edition):

Hoggard, J. A. (2015). Proposed regulatory role of noncatalytic Adams in ectodomain shedding. (Thesis). East Carolina University. Retrieved from http://hdl.handle.net/10342/5014

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):

Hoggard, Jason Andrew. “Proposed regulatory role of noncatalytic Adams in ectodomain shedding.” 2015. Thesis, East Carolina University. Accessed December 09, 2019. http://hdl.handle.net/10342/5014.

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

MLA Handbook (7th Edition):

Hoggard, Jason Andrew. “Proposed regulatory role of noncatalytic Adams in ectodomain shedding.” 2015. Web. 09 Dec 2019.

Vancouver:

Hoggard JA. Proposed regulatory role of noncatalytic Adams in ectodomain shedding. [Internet] [Thesis]. East Carolina University; 2015. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/10342/5014.

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

Council of Science Editors:

Hoggard JA. Proposed regulatory role of noncatalytic Adams in ectodomain shedding. [Thesis]. East Carolina University; 2015. Available from: http://hdl.handle.net/10342/5014

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

27. A. Rossi. ROLE OF THE POLYCOMB GROUP PROTEINS IN THE ADULT INTESTINAL STEM CELLS HOMEOSTASIS.

Degree: 2015, Università degli Studi di Milano

 Polycomb group proteins (PcG) are among the most important gatekeepers that ensure the correct establishment and maintenance of cellular identity in metazoans. This occurs by… (more)

Subjects/Keywords: Polycomb; PRC1; H2AK119Ubq; intestine; ISCs; Ink4a-Arf; Zic proteins; Tcf4 complex; ß-Catenin; Wnt pathway; Settore BIO/11 - Biologia Molecolare

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APA (6th Edition):

Rossi, A. (2015). ROLE OF THE POLYCOMB GROUP PROTEINS IN THE ADULT INTESTINAL STEM CELLS HOMEOSTASIS. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/260390

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):

Rossi, A.. “ROLE OF THE POLYCOMB GROUP PROTEINS IN THE ADULT INTESTINAL STEM CELLS HOMEOSTASIS.” 2015. Thesis, Università degli Studi di Milano. Accessed December 09, 2019. http://hdl.handle.net/2434/260390.

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

MLA Handbook (7th Edition):

Rossi, A.. “ROLE OF THE POLYCOMB GROUP PROTEINS IN THE ADULT INTESTINAL STEM CELLS HOMEOSTASIS.” 2015. Web. 09 Dec 2019.

Vancouver:

Rossi A. ROLE OF THE POLYCOMB GROUP PROTEINS IN THE ADULT INTESTINAL STEM CELLS HOMEOSTASIS. [Internet] [Thesis]. Università degli Studi di Milano; 2015. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/2434/260390.

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

Council of Science Editors:

Rossi A. ROLE OF THE POLYCOMB GROUP PROTEINS IN THE ADULT INTESTINAL STEM CELLS HOMEOSTASIS. [Thesis]. Università degli Studi di Milano; 2015. Available from: http://hdl.handle.net/2434/260390

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


IUPUI

28. Martin, Kyle B. Identification of altered Ras signaling and intermediate filament hyperphosphorylation in giant axonal neuropathy.

Degree: 2015, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Giant axonal neuropathy (GAN) is a rare genetic disease that causes progressive damage to the nervous system. Neurons in GAN… (more)

Subjects/Keywords: Giant axonal neuropathy; Gigaxonin; Galectin-1; Intermediate filaments; Phosphorylation; Nerves, Peripheral  – Diseases; Neuropathy; Cykoskeletal proteins; Intermediate filament proteins; Cytoplasmic filaments; Proteins  – Metabolism  – Disorders; Proteins  – Pathophysiology; Proteins  – Synthesis

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

APA (6th Edition):

Martin, K. B. (2015). Identification of altered Ras signaling and intermediate filament hyperphosphorylation in giant axonal neuropathy. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/7935

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

Chicago Manual of Style (16th Edition):

Martin, Kyle B. “Identification of altered Ras signaling and intermediate filament hyperphosphorylation in giant axonal neuropathy.” 2015. Thesis, IUPUI. Accessed December 09, 2019. http://hdl.handle.net/1805/7935.

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

MLA Handbook (7th Edition):

Martin, Kyle B. “Identification of altered Ras signaling and intermediate filament hyperphosphorylation in giant axonal neuropathy.” 2015. Web. 09 Dec 2019.

Vancouver:

Martin KB. Identification of altered Ras signaling and intermediate filament hyperphosphorylation in giant axonal neuropathy. [Internet] [Thesis]. IUPUI; 2015. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/1805/7935.

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

Council of Science Editors:

Martin KB. Identification of altered Ras signaling and intermediate filament hyperphosphorylation in giant axonal neuropathy. [Thesis]. IUPUI; 2015. Available from: http://hdl.handle.net/1805/7935

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


University of Saskatchewan

29. Prusinkiewicz, Martin. The role of metal metabolism and heat shock protein genes on replicative lifespan of the budding yeast, Saccharomyces cerevisiae.

Degree: 2015, University of Saskatchewan

 A variety of genes that influence aging have been identified in a broad selection of organisms including Saccharomyces cerevisiae (yeast), Caenorhabditis elegans (worms), Drosophila (fruit… (more)

Subjects/Keywords: Yeast; Aging; Replicative Lifespan; Metal Metabolism; Heat Shock Proteins; FET; SSA

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

APA (6th Edition):

Prusinkiewicz, M. (2015). The role of metal metabolism and heat shock protein genes on replicative lifespan of the budding yeast, Saccharomyces cerevisiae. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2015-12-2367

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):

Prusinkiewicz, Martin. “The role of metal metabolism and heat shock protein genes on replicative lifespan of the budding yeast, Saccharomyces cerevisiae.” 2015. Thesis, University of Saskatchewan. Accessed December 09, 2019. http://hdl.handle.net/10388/ETD-2015-12-2367.

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

MLA Handbook (7th Edition):

Prusinkiewicz, Martin. “The role of metal metabolism and heat shock protein genes on replicative lifespan of the budding yeast, Saccharomyces cerevisiae.” 2015. Web. 09 Dec 2019.

Vancouver:

Prusinkiewicz M. The role of metal metabolism and heat shock protein genes on replicative lifespan of the budding yeast, Saccharomyces cerevisiae. [Internet] [Thesis]. University of Saskatchewan; 2015. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/10388/ETD-2015-12-2367.

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

Council of Science Editors:

Prusinkiewicz M. The role of metal metabolism and heat shock protein genes on replicative lifespan of the budding yeast, Saccharomyces cerevisiae. [Thesis]. University of Saskatchewan; 2015. Available from: http://hdl.handle.net/10388/ETD-2015-12-2367

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

30. Cannone, Giuseppe. Structural investigation of the archaeal replicative machinery by electron microscopy and digital image processing.

Degree: PhD, 2015, University of Edinburgh

 Previous studies suggest a degree of homology between eukaryotic replication, transcription and translation proteins and archaeal ones. Hence, Archaea are considered a simplified model for… (more)

Subjects/Keywords: 572.8; eukaryotic DNA metabolism; eukaryotic MCM proteins; PCNA; Okazaki fragment maturation

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

APA (6th Edition):

Cannone, G. (2015). Structural investigation of the archaeal replicative machinery by electron microscopy and digital image processing. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/17070

Chicago Manual of Style (16th Edition):

Cannone, Giuseppe. “Structural investigation of the archaeal replicative machinery by electron microscopy and digital image processing.” 2015. Doctoral Dissertation, University of Edinburgh. Accessed December 09, 2019. http://hdl.handle.net/1842/17070.

MLA Handbook (7th Edition):

Cannone, Giuseppe. “Structural investigation of the archaeal replicative machinery by electron microscopy and digital image processing.” 2015. Web. 09 Dec 2019.

Vancouver:

Cannone G. Structural investigation of the archaeal replicative machinery by electron microscopy and digital image processing. [Internet] [Doctoral dissertation]. University of Edinburgh; 2015. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/1842/17070.

Council of Science Editors:

Cannone G. Structural investigation of the archaeal replicative machinery by electron microscopy and digital image processing. [Doctoral Dissertation]. University of Edinburgh; 2015. Available from: http://hdl.handle.net/1842/17070

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