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Dates: 2005 – 2009

You searched for subject:( Wnt Proteins metabolism). Showing records 1 – 30 of 3221 total matches.

[1] [2] [3] [4] [5] … [108]

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1. Roarty, Kevin Patrick. The role of TGF-[beta] and Wnt5a in mammary gland development and tumorigenesis.

Degree: PhD, 2008, University of Alabama – Birmingham

Breast cancer is the second most common cancer worldwide behind lung cancer, affecting women of all ages, races, ethnicities, and socioeconomic strata. Concerted efforts have… (more)

Subjects/Keywords: Gene Expression Regulation, Developmental <; br>; Mammary Glands, Animal  – growth & development <; br>; Mammary Glands, Animal  – metabolism <; br>; Transforming Growth Factor beta1  – pharmacology <; br>; Wnt Proteins  – metabolism

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

APA (6th Edition):

Roarty, K. P. (2008). The role of TGF-[beta] and Wnt5a in mammary gland development and tumorigenesis. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,337

Chicago Manual of Style (16th Edition):

Roarty, Kevin Patrick. “The role of TGF-[beta] and Wnt5a in mammary gland development and tumorigenesis.” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,337.

MLA Handbook (7th Edition):

Roarty, Kevin Patrick. “The role of TGF-[beta] and Wnt5a in mammary gland development and tumorigenesis.” 2008. Web. 06 Dec 2019.

Vancouver:

Roarty KP. The role of TGF-[beta] and Wnt5a in mammary gland development and tumorigenesis. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,337.

Council of Science Editors:

Roarty KP. The role of TGF-[beta] and Wnt5a in mammary gland development and tumorigenesis. [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,337


University of Missouri – Columbia

2. Rahmatpanah, Farahnaz B. Large scale CpG island methylation profiling of small B cell lymphoma.

Degree: 2008, University of Missouri – Columbia

 DNA methylation plays a significant role in cellular differentiation and biologic activity through silencing of gene expression and also appears to be a factor in… (more)

Subjects/Keywords: DNA  – Methylation; Lymphomas  – Genetic aspects; Gene silencing; CD antigens  – Metabolism  – Genetic aspects; Wnt proteins  – Antagonists

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APA (6th Edition):

Rahmatpanah, F. B. (2008). Large scale CpG island methylation profiling of small B cell lymphoma. (Thesis). University of Missouri – Columbia. Retrieved from https://doi.org/10.32469/10355/6863

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):

Rahmatpanah, Farahnaz B. “Large scale CpG island methylation profiling of small B cell lymphoma.” 2008. Thesis, University of Missouri – Columbia. Accessed December 06, 2019. https://doi.org/10.32469/10355/6863.

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

MLA Handbook (7th Edition):

Rahmatpanah, Farahnaz B. “Large scale CpG island methylation profiling of small B cell lymphoma.” 2008. Web. 06 Dec 2019.

Vancouver:

Rahmatpanah FB. Large scale CpG island methylation profiling of small B cell lymphoma. [Internet] [Thesis]. University of Missouri – Columbia; 2008. [cited 2019 Dec 06]. Available from: https://doi.org/10.32469/10355/6863.

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

Council of Science Editors:

Rahmatpanah FB. Large scale CpG island methylation profiling of small B cell lymphoma. [Thesis]. University of Missouri – Columbia; 2008. Available from: https://doi.org/10.32469/10355/6863

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

3. Chan, Chih-Chiang. Feedback Regulation of Wnt Signaling by Naked Cuticle (Nkd) During Drosophila Embryogenesis.

Degree: 2008, University of Texas Southwestern Medical Center

Wnt/beta -catenin signals are essential for many developmental and physiological processes in animals. Deregulation of the Wnt signaling pathway in mammals can cause diseases such… (more)

Subjects/Keywords: Wnt Proteins; Drosophila melanogaster; Drosophila Proteins

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APA (6th Edition):

Chan, C. (2008). Feedback Regulation of Wnt Signaling by Naked Cuticle (Nkd) During Drosophila Embryogenesis. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/677

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):

Chan, Chih-Chiang. “Feedback Regulation of Wnt Signaling by Naked Cuticle (Nkd) During Drosophila Embryogenesis.” 2008. Thesis, University of Texas Southwestern Medical Center. Accessed December 06, 2019. http://hdl.handle.net/2152.5/677.

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

MLA Handbook (7th Edition):

Chan, Chih-Chiang. “Feedback Regulation of Wnt Signaling by Naked Cuticle (Nkd) During Drosophila Embryogenesis.” 2008. Web. 06 Dec 2019.

Vancouver:

Chan C. Feedback Regulation of Wnt Signaling by Naked Cuticle (Nkd) During Drosophila Embryogenesis. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2008. [cited 2019 Dec 06]. Available from: http://hdl.handle.net/2152.5/677.

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

Council of Science Editors:

Chan C. Feedback Regulation of Wnt Signaling by Naked Cuticle (Nkd) During Drosophila Embryogenesis. [Thesis]. University of Texas Southwestern Medical Center; 2008. Available from: http://hdl.handle.net/2152.5/677

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


University of Aberdeen

4. 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 06, 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. 06 Dec 2019.

Vancouver:

Martin J. Wnt regulated transcription factor networks mediate vertebrate cardiogenesis. [Internet] [Doctoral dissertation]. University of Aberdeen; 2009. [cited 2019 Dec 06]. 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 New South Wales

5. 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 06, 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. 06 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 06]. 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

6. 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 06, 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. 06 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 06]. 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 Western Australia

7. 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 06, 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. 06 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 06]. 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

8. 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 (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 06, 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. 06 Dec 2019.

Vancouver:

Dismuke AD. Wnt signaling in the mouse small intestine. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 2009. [cited 2019 Dec 06]. 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

9. Ramachandran, Preethi. Cytoskeletal Regulation and Morphogen Signaling During Synaptic Outgrowth at the Drosophila Larval Neuromuscular Junction : A Dissertation.

Degree: Neuroscience, Department of Neurobiology; Budnik Lab, 2009, U of Massachusetts : Med

  Synaptic plasticity, in its broadest sense, can be defined as the ability of synapses to be modified structurally and functionally in response to various… (more)

Subjects/Keywords: Synapses; Actins; Cytoskeleton; Protein Kinase; Wnt Proteins; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Enzymes and Coenzymes; Macromolecular Substances

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APA (6th Edition):

Ramachandran, P. (2009). Cytoskeletal Regulation and Morphogen Signaling During Synaptic Outgrowth at the Drosophila Larval Neuromuscular Junction : A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/442

Chicago Manual of Style (16th Edition):

Ramachandran, Preethi. “Cytoskeletal Regulation and Morphogen Signaling During Synaptic Outgrowth at the Drosophila Larval Neuromuscular Junction : A Dissertation.” 2009. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. https://escholarship.umassmed.edu/gsbs_diss/442.

MLA Handbook (7th Edition):

Ramachandran, Preethi. “Cytoskeletal Regulation and Morphogen Signaling During Synaptic Outgrowth at the Drosophila Larval Neuromuscular Junction : A Dissertation.” 2009. Web. 06 Dec 2019.

Vancouver:

Ramachandran P. Cytoskeletal Regulation and Morphogen Signaling During Synaptic Outgrowth at the Drosophila Larval Neuromuscular Junction : A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2009. [cited 2019 Dec 06]. Available from: https://escholarship.umassmed.edu/gsbs_diss/442.

Council of Science Editors:

Ramachandran P. Cytoskeletal Regulation and Morphogen Signaling During Synaptic Outgrowth at the Drosophila Larval Neuromuscular Junction : A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2009. Available from: https://escholarship.umassmed.edu/gsbs_diss/442

10. Silva, Roseli da. Envolvimento da Beta-catenina na via Wnt em meduloblastomas: estudo molecular e imunohistoquímico.

Degree: Mestrado, Neurologia, 2007, University of São Paulo

 Meduloblastoma é um tumor embrionário maligno e invasivo do cerebelo, com manifestação preferencial em crianças, sendo predominantemente de diferenciação neuronal e tendência natural a metastatização… (more)

Subjects/Keywords: Beta catenina; Beta-catenin 3 - medulloblastoma; Immunohistochemistry; Imunohistoquímica; Meduloblastoma; Mutação; Mutation; Polymerase chain reaction; Proteínas Wnt; Reação em cadeia da polimerase; WNT proteins

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APA (6th Edition):

Silva, R. d. (2007). Envolvimento da Beta-catenina na via Wnt em meduloblastomas: estudo molecular e imunohistoquímico. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5138/tde-08102007-095147/ ;

Chicago Manual of Style (16th Edition):

Silva, Roseli da. “Envolvimento da Beta-catenina na via Wnt em meduloblastomas: estudo molecular e imunohistoquímico.” 2007. Masters Thesis, University of São Paulo. Accessed December 06, 2019. http://www.teses.usp.br/teses/disponiveis/5/5138/tde-08102007-095147/ ;.

MLA Handbook (7th Edition):

Silva, Roseli da. “Envolvimento da Beta-catenina na via Wnt em meduloblastomas: estudo molecular e imunohistoquímico.” 2007. Web. 06 Dec 2019.

Vancouver:

Silva Rd. Envolvimento da Beta-catenina na via Wnt em meduloblastomas: estudo molecular e imunohistoquímico. [Internet] [Masters thesis]. University of São Paulo; 2007. [cited 2019 Dec 06]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5138/tde-08102007-095147/ ;.

Council of Science Editors:

Silva Rd. Envolvimento da Beta-catenina na via Wnt em meduloblastomas: estudo molecular e imunohistoquímico. [Masters Thesis]. University of São Paulo; 2007. Available from: http://www.teses.usp.br/teses/disponiveis/5/5138/tde-08102007-095147/ ;


University of Missouri – Columbia

11. Dhar, Srijita. Transcriptional regulation of ADAM-12 expression under normal and osteoarthritic conditions.

Degree: 2009, University of Missouri – Columbia

 [ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT AUTHOR'S REQUEST.] ADAM 12 overexpression is linked to the pathology of diseases including osteoarthritis, cancer, cardiac hypertrophy,… (more)

Subjects/Keywords: Membrane proteins  – Physiological transport; Osteoarthritis  – Pathogenesis; Articular cartilage  – Metabolism; NF-kappa B (DNA-binding protein)  – Metabolism; Transforming growth factors-beta  – Metabolism; Bone cells  – Metabolism; Synovial membranes  – Metabolism; Metalloproteinases  – Metabolism; ADAM Proteins  – metabolism; Cartilage, Articular  – metabolism; Osteoarthritis  – pathology; Transforming Growth Factor beta  – pharmacology; NF-kappa B  – metabolism; Sp1 Transcription Factor  – metabolism; Osteoblasts  – metabolism; Synovial Membrane  – metabolism

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APA (6th Edition):

Dhar, S. (2009). Transcriptional regulation of ADAM-12 expression under normal and osteoarthritic conditions. (Thesis). University of Missouri – Columbia. Retrieved from https://doi.org/10.32469/10355/10290

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):

Dhar, Srijita. “Transcriptional regulation of ADAM-12 expression under normal and osteoarthritic conditions.” 2009. Thesis, University of Missouri – Columbia. Accessed December 06, 2019. https://doi.org/10.32469/10355/10290.

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

MLA Handbook (7th Edition):

Dhar, Srijita. “Transcriptional regulation of ADAM-12 expression under normal and osteoarthritic conditions.” 2009. Web. 06 Dec 2019.

Vancouver:

Dhar S. Transcriptional regulation of ADAM-12 expression under normal and osteoarthritic conditions. [Internet] [Thesis]. University of Missouri – Columbia; 2009. [cited 2019 Dec 06]. Available from: https://doi.org/10.32469/10355/10290.

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

Council of Science Editors:

Dhar S. Transcriptional regulation of ADAM-12 expression under normal and osteoarthritic conditions. [Thesis]. University of Missouri – Columbia; 2009. Available from: https://doi.org/10.32469/10355/10290

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


McGill University

12. Charest-Marcotte, Alexis, 1984-. Functional interaction between PROX1, ERR[alpha] and PGC-1[alpha] in the control of energy metabolism.

Degree: MS, Department of Biochemistry., 2009, McGill University

 Nuclear receptors play crucial roles in the transcriptional regulation of many biological processes such as development and cellular differentiation. ERRalpha is known, along with coactivator… (more)

Subjects/Keywords: Liver  – metabolism.; Homeodomain Proteins  – metabolism.; Receptors, Estrogen  – metabolism.; Heat-Shock Proteins  – metabolism.

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APA (6th Edition):

Charest-Marcotte, Alexis, 1. (2009). Functional interaction between PROX1, ERR[alpha] and PGC-1[alpha] in the control of energy metabolism. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile111571.pdf

Chicago Manual of Style (16th Edition):

Charest-Marcotte, Alexis, 1984-. “Functional interaction between PROX1, ERR[alpha] and PGC-1[alpha] in the control of energy metabolism.” 2009. Masters Thesis, McGill University. Accessed December 06, 2019. http://digitool.library.mcgill.ca/thesisfile111571.pdf.

MLA Handbook (7th Edition):

Charest-Marcotte, Alexis, 1984-. “Functional interaction between PROX1, ERR[alpha] and PGC-1[alpha] in the control of energy metabolism.” 2009. Web. 06 Dec 2019.

Vancouver:

Charest-Marcotte, Alexis 1. Functional interaction between PROX1, ERR[alpha] and PGC-1[alpha] in the control of energy metabolism. [Internet] [Masters thesis]. McGill University; 2009. [cited 2019 Dec 06]. Available from: http://digitool.library.mcgill.ca/thesisfile111571.pdf.

Council of Science Editors:

Charest-Marcotte, Alexis 1. Functional interaction between PROX1, ERR[alpha] and PGC-1[alpha] in the control of energy metabolism. [Masters Thesis]. McGill University; 2009. Available from: http://digitool.library.mcgill.ca/thesisfile111571.pdf


University of Missouri – Columbia

13. Martin, Tara R. Exploring the cell surface: identification and characterization of lipoproteins in Mycoplasma mycoides subsp. mycoides large colony, Mycoplasma mycoides subsp. capri, and Mycoplasma capricolum subsp. capricolum.

Degree: 2009, University of Missouri – Columbia

 The Mycoplasma mycoides cluster is a group of genetically and antigenically related pathogenic bacteria that infect ruminants. The M. mycoides cluster members that are the… (more)

Subjects/Keywords: Mycoplasma mycoides  – physiology; Mycoplasma mycoides  – genetics; Bacterial Proteins  – metabolism; Bacterial Proteins  – genetics; Lipoproteins  – metabolism; Lipoproteins  – genetics

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APA (6th Edition):

Martin, T. R. (2009). Exploring the cell surface: identification and characterization of lipoproteins in Mycoplasma mycoides subsp. mycoides large colony, Mycoplasma mycoides subsp. capri, and Mycoplasma capricolum subsp. capricolum. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/9564

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, Tara R. “Exploring the cell surface: identification and characterization of lipoproteins in Mycoplasma mycoides subsp. mycoides large colony, Mycoplasma mycoides subsp. capri, and Mycoplasma capricolum subsp. capricolum.” 2009. Thesis, University of Missouri – Columbia. Accessed December 06, 2019. http://hdl.handle.net/10355/9564.

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

MLA Handbook (7th Edition):

Martin, Tara R. “Exploring the cell surface: identification and characterization of lipoproteins in Mycoplasma mycoides subsp. mycoides large colony, Mycoplasma mycoides subsp. capri, and Mycoplasma capricolum subsp. capricolum.” 2009. Web. 06 Dec 2019.

Vancouver:

Martin TR. Exploring the cell surface: identification and characterization of lipoproteins in Mycoplasma mycoides subsp. mycoides large colony, Mycoplasma mycoides subsp. capri, and Mycoplasma capricolum subsp. capricolum. [Internet] [Thesis]. University of Missouri – Columbia; 2009. [cited 2019 Dec 06]. Available from: http://hdl.handle.net/10355/9564.

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

Council of Science Editors:

Martin TR. Exploring the cell surface: identification and characterization of lipoproteins in Mycoplasma mycoides subsp. mycoides large colony, Mycoplasma mycoides subsp. capri, and Mycoplasma capricolum subsp. capricolum. [Thesis]. University of Missouri – Columbia; 2009. Available from: http://hdl.handle.net/10355/9564

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


University of Aberdeen

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

Degree: School of Medical Sciences., 2008, University of Aberdeen

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

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APA (6th Edition):

Martin, J. (2008). Wnt regulated transcription factor networks mediate vertebrate cardiogenesis. (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=25801 ; http://digitool2.abdn.ac.uk:1801/webclient/DeliveryManager?pid=25801&custom_att_2=simple_viewer

Chicago Manual of Style (16th Edition):

Martin, Jennifer. “Wnt regulated transcription factor networks mediate vertebrate cardiogenesis.” 2008. Doctoral Dissertation, University of Aberdeen. Accessed December 06, 2019. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=25801 ; http://digitool2.abdn.ac.uk:1801/webclient/DeliveryManager?pid=25801&custom_att_2=simple_viewer.

MLA Handbook (7th Edition):

Martin, Jennifer. “Wnt regulated transcription factor networks mediate vertebrate cardiogenesis.” 2008. Web. 06 Dec 2019.

Vancouver:

Martin J. Wnt regulated transcription factor networks mediate vertebrate cardiogenesis. [Internet] [Doctoral dissertation]. University of Aberdeen; 2008. [cited 2019 Dec 06]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=25801 ; http://digitool2.abdn.ac.uk:1801/webclient/DeliveryManager?pid=25801&custom_att_2=simple_viewer.

Council of Science Editors:

Martin J. Wnt regulated transcription factor networks mediate vertebrate cardiogenesis. [Doctoral Dissertation]. University of Aberdeen; 2008. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=25801 ; http://digitool2.abdn.ac.uk:1801/webclient/DeliveryManager?pid=25801&custom_att_2=simple_viewer


McGill University

15. Buscarlet, Manuel. The neural progenitor to neuron transition : role and regulation of GrouchoTLE proteins.

Degree: PhD, Division of Neuroscience., 2008, McGill University

Groucho/transducin-like Enhancer of split (Gro/TLE) family proteins are corepressors found as part of multiple transcriptional complexes that play significant roles during many developmental processes, including… (more)

Subjects/Keywords: Neurons  – metabolism.; Cerebral Cortex  – metabolism.; Repressor Proteins  – metabolism.

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APA (6th Edition):

Buscarlet, M. (2008). The neural progenitor to neuron transition : role and regulation of GrouchoTLE proteins. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile115670.pdf

Chicago Manual of Style (16th Edition):

Buscarlet, Manuel. “The neural progenitor to neuron transition : role and regulation of GrouchoTLE proteins.” 2008. Doctoral Dissertation, McGill University. Accessed December 06, 2019. http://digitool.library.mcgill.ca/thesisfile115670.pdf.

MLA Handbook (7th Edition):

Buscarlet, Manuel. “The neural progenitor to neuron transition : role and regulation of GrouchoTLE proteins.” 2008. Web. 06 Dec 2019.

Vancouver:

Buscarlet M. The neural progenitor to neuron transition : role and regulation of GrouchoTLE proteins. [Internet] [Doctoral dissertation]. McGill University; 2008. [cited 2019 Dec 06]. Available from: http://digitool.library.mcgill.ca/thesisfile115670.pdf.

Council of Science Editors:

Buscarlet M. The neural progenitor to neuron transition : role and regulation of GrouchoTLE proteins. [Doctoral Dissertation]. McGill University; 2008. Available from: http://digitool.library.mcgill.ca/thesisfile115670.pdf

16. Danilchanka, Olga V. Diffusion pathways through the outer membrane of mycobacteria.

Degree: PhD, 2009, University of Alabama – Birmingham

The extraordinary capacity of Mycobacterium tuberculosis (Mtb) to adapt to environmental changes during infection contributes to its success as a pathogen. While the unique outer… (more)

Subjects/Keywords: Anti-Bacterial Agents  – metabolism<; br>; Bacterial Proteins  – metabolism<; br>; Chloramphenicol  – metabolism<; br>; Fluoroquinolones  – metabolism<; br>; Membrane Transport Proteins  – metabolism<; br>; Mycobacterium smegmatis<; br>; Mycobacterium tuberculosis  – metabolism<; br>; Porins  – metabolism

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APA (6th Edition):

Danilchanka, O. V. (2009). Diffusion pathways through the outer membrane of mycobacteria. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1150

Chicago Manual of Style (16th Edition):

Danilchanka, Olga V. “Diffusion pathways through the outer membrane of mycobacteria.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1150.

MLA Handbook (7th Edition):

Danilchanka, Olga V. “Diffusion pathways through the outer membrane of mycobacteria.” 2009. Web. 06 Dec 2019.

Vancouver:

Danilchanka OV. Diffusion pathways through the outer membrane of mycobacteria. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1150.

Council of Science Editors:

Danilchanka OV. Diffusion pathways through the outer membrane of mycobacteria. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1150

17. Moore, Carlene Drucilla. The role of centaurin alpha-1 in the regulation of neuronal differentiation.

Degree: PhD, 2008, University of Alabama – Birmingham

In the nervous system, PI 3-kinase has been implicated in neuronal differentiation. My studies have focused on a candidate neuronal PI 3-kinase target centaurin alpha-1,… (more)

Subjects/Keywords: 1-Phosphatidylinositol 3-Kinase <; br>; Adaptor Proteins, Signal Transducing  – metabolism <; br>; Dendrites  – metabolism <; br>; Dendrites  – ultrastructure <; br>; GTPase-Activating Proteins  – metabolism <; br>; Hippocampus  – cytology <; br>; Nerve Tissue Proteins  – metabolism <; br>; Neurons  – metabolism

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APA (6th Edition):

Moore, C. D. (2008). The role of centaurin alpha-1 in the regulation of neuronal differentiation. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,208

Chicago Manual of Style (16th Edition):

Moore, Carlene Drucilla. “The role of centaurin alpha-1 in the regulation of neuronal differentiation.” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,208.

MLA Handbook (7th Edition):

Moore, Carlene Drucilla. “The role of centaurin alpha-1 in the regulation of neuronal differentiation.” 2008. Web. 06 Dec 2019.

Vancouver:

Moore CD. The role of centaurin alpha-1 in the regulation of neuronal differentiation. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,208.

Council of Science Editors:

Moore CD. The role of centaurin alpha-1 in the regulation of neuronal differentiation. [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,208

18. Silveira, Alexandra C. Characterization of SUDS3 as a BRMS1 family member in breast cancer.

Degree: PhD, 2008, University of Alabama – Birmingham

BRMS1 and SUDS3 belong to a protein family characterized by the Sds3-like domain. These proteins are core members of SIN3-HDAC chromatin remodeling complexes and thus,… (more)

Subjects/Keywords: Breast Neoplasms  – metabolism <; br>; Carrier Proteins  – metabolism <; br>; Chromatin Assembly and Disassembly <; br>; Histone Deacetylases  – metabolism <; br>; Neoplasm Proteins  – metabolism <; br>; Repressor Proteins/metabolism

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APA (6th Edition):

Silveira, A. C. (2008). Characterization of SUDS3 as a BRMS1 family member in breast cancer. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,339

Chicago Manual of Style (16th Edition):

Silveira, Alexandra C. “Characterization of SUDS3 as a BRMS1 family member in breast cancer.” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,339.

MLA Handbook (7th Edition):

Silveira, Alexandra C. “Characterization of SUDS3 as a BRMS1 family member in breast cancer.” 2008. Web. 06 Dec 2019.

Vancouver:

Silveira AC. Characterization of SUDS3 as a BRMS1 family member in breast cancer. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,339.

Council of Science Editors:

Silveira AC. Characterization of SUDS3 as a BRMS1 family member in breast cancer. [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,339

19. Grabski, Robert. Using RNA interference to study the function of the tethering protein p115 in ER-Golgi traffic.

Degree: PhD, 2008, University of Alabama – Birmingham

Metazoan cells are characterized with elaborate network of intracellular membranous compartments. These membranes allow the cell to spatially separate antagonistic processes and environments, and maintain… (more)

Subjects/Keywords: Carrier Proteins  – metabolism <; br>; Golgi Apparatus  – metabolism <; br>; Membrane Proteins  – metabolism <; br>; Protein Transport <; br>; RNA Interference

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APA (6th Edition):

Grabski, R. (2008). Using RNA interference to study the function of the tethering protein p115 in ER-Golgi traffic. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,328

Chicago Manual of Style (16th Edition):

Grabski, Robert. “Using RNA interference to study the function of the tethering protein p115 in ER-Golgi traffic.” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,328.

MLA Handbook (7th Edition):

Grabski, Robert. “Using RNA interference to study the function of the tethering protein p115 in ER-Golgi traffic.” 2008. Web. 06 Dec 2019.

Vancouver:

Grabski R. Using RNA interference to study the function of the tethering protein p115 in ER-Golgi traffic. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,328.

Council of Science Editors:

Grabski R. Using RNA interference to study the function of the tethering protein p115 in ER-Golgi traffic. [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,328


McGill University

20. Faubert, Amélie. Towards the identification of cellular and molecular regulators of hematopoietic stem cell self-renewal.

Degree: PhD, Division of Experimental Medicine., 2007, McGill University

Self-renewal is central to the expansion of normal and cancerous stem cells. Its understanding is therefore critical for future advances in transplantation-based therapies and cancer… (more)

Subjects/Keywords: Hematopoietic Stem Cells  – metabolism.; Homeodomain Proteins  – metabolism.; Proto-Oncogene Proteins  – metabolism.

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APA (6th Edition):

Faubert, A. (2007). Towards the identification of cellular and molecular regulators of hematopoietic stem cell self-renewal. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile103195.pdf

Chicago Manual of Style (16th Edition):

Faubert, Amélie. “Towards the identification of cellular and molecular regulators of hematopoietic stem cell self-renewal.” 2007. Doctoral Dissertation, McGill University. Accessed December 06, 2019. http://digitool.library.mcgill.ca/thesisfile103195.pdf.

MLA Handbook (7th Edition):

Faubert, Amélie. “Towards the identification of cellular and molecular regulators of hematopoietic stem cell self-renewal.” 2007. Web. 06 Dec 2019.

Vancouver:

Faubert A. Towards the identification of cellular and molecular regulators of hematopoietic stem cell self-renewal. [Internet] [Doctoral dissertation]. McGill University; 2007. [cited 2019 Dec 06]. Available from: http://digitool.library.mcgill.ca/thesisfile103195.pdf.

Council of Science Editors:

Faubert A. Towards the identification of cellular and molecular regulators of hematopoietic stem cell self-renewal. [Doctoral Dissertation]. McGill University; 2007. Available from: http://digitool.library.mcgill.ca/thesisfile103195.pdf


McGill University

21. Jani, Klodiana. The role of integrin-dependent cell matrix adhesion in muscle development.

Degree: PhD, Department of Biology., 2009, McGill University

Cell adhesion is essential to cell motility and tissue integrity and is regulated by the Integrin family of transmembrane receptors. Integrin binds to ligand extracellularly… (more)

Subjects/Keywords: Striated muscle  – Metabolism.; Integrins  – Metabolism.; Cell adhesion.; Muscle, Skeletal  – metabolism.; Integrins  – metabolism.; Drosophila Proteins  – metabolism.; Carrier Proteins  – metabolism.; Adaptor Proteins, Signal Transducing  – metabolism.; Cell Adhesion  – physiology.

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APA (6th Edition):

Jani, K. (2009). The role of integrin-dependent cell matrix adhesion in muscle development. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile115688.pdf

Chicago Manual of Style (16th Edition):

Jani, Klodiana. “The role of integrin-dependent cell matrix adhesion in muscle development.” 2009. Doctoral Dissertation, McGill University. Accessed December 06, 2019. http://digitool.library.mcgill.ca/thesisfile115688.pdf.

MLA Handbook (7th Edition):

Jani, Klodiana. “The role of integrin-dependent cell matrix adhesion in muscle development.” 2009. Web. 06 Dec 2019.

Vancouver:

Jani K. The role of integrin-dependent cell matrix adhesion in muscle development. [Internet] [Doctoral dissertation]. McGill University; 2009. [cited 2019 Dec 06]. Available from: http://digitool.library.mcgill.ca/thesisfile115688.pdf.

Council of Science Editors:

Jani K. The role of integrin-dependent cell matrix adhesion in muscle development. [Doctoral Dissertation]. McGill University; 2009. Available from: http://digitool.library.mcgill.ca/thesisfile115688.pdf

22. Joo, Heui Yun. Understanding the regulatory mechanisms of UBP-M and H2A deubiquitination in chromatin and cellular functions.

Degree: PhD, 2009, University of Alabama – Birmingham

Posttranslational modifications of histones regulate important chromatin and cellular functions. Among them, ubiquitination of histone H2A is correlated to transcriptional repression, such as HOX gene… (more)

Subjects/Keywords: Chromatin  – physiology<; br>; Endopeptidases  – metabolism<; br>; Histones  – metabolism<; br>; Ubiquitin Thiolesterase  – metabolism<; br>; Xenopus Proteins  – metabolism<; br>; Xenopus laevis  – embryology

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APA (6th Edition):

Joo, H. Y. (2009). Understanding the regulatory mechanisms of UBP-M and H2A deubiquitination in chromatin and cellular functions. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1101

Chicago Manual of Style (16th Edition):

Joo, Heui Yun. “Understanding the regulatory mechanisms of UBP-M and H2A deubiquitination in chromatin and cellular functions.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1101.

MLA Handbook (7th Edition):

Joo, Heui Yun. “Understanding the regulatory mechanisms of UBP-M and H2A deubiquitination in chromatin and cellular functions.” 2009. Web. 06 Dec 2019.

Vancouver:

Joo HY. Understanding the regulatory mechanisms of UBP-M and H2A deubiquitination in chromatin and cellular functions. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1101.

Council of Science Editors:

Joo HY. Understanding the regulatory mechanisms of UBP-M and H2A deubiquitination in chromatin and cellular functions. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1101


McGill University

23. Beauchamp, Pascal. The functional role of the RNA-binding protein HuR in the regulation of muscle cell differentiation.

Degree: MS, Department of Biochemistry., 2008, McGill University

 Muscle tissue development (myogenesis) involves the formation of specific fibers (myotubes) from muscle cells (myoblasts). For this to occur, the sequential expression of Myogenic Regulatory… (more)

Subjects/Keywords: Myoblasts  – cytology.; Myoblasts  – metabolism.; RNA-Binding Proteins  – metabolism.; Antigens, Surface  – metabolism.; Caspases  – metabolism.

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APA (6th Edition):

Beauchamp, P. (2008). The functional role of the RNA-binding protein HuR in the regulation of muscle cell differentiation. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile111586.pdf

Chicago Manual of Style (16th Edition):

Beauchamp, Pascal. “The functional role of the RNA-binding protein HuR in the regulation of muscle cell differentiation.” 2008. Masters Thesis, McGill University. Accessed December 06, 2019. http://digitool.library.mcgill.ca/thesisfile111586.pdf.

MLA Handbook (7th Edition):

Beauchamp, Pascal. “The functional role of the RNA-binding protein HuR in the regulation of muscle cell differentiation.” 2008. Web. 06 Dec 2019.

Vancouver:

Beauchamp P. The functional role of the RNA-binding protein HuR in the regulation of muscle cell differentiation. [Internet] [Masters thesis]. McGill University; 2008. [cited 2019 Dec 06]. Available from: http://digitool.library.mcgill.ca/thesisfile111586.pdf.

Council of Science Editors:

Beauchamp P. The functional role of the RNA-binding protein HuR in the regulation of muscle cell differentiation. [Masters Thesis]. McGill University; 2008. Available from: http://digitool.library.mcgill.ca/thesisfile111586.pdf


McGill University

24. Ainsworth, Julia. Comparison of p53 and MAGI-3 regulation mediated by the E6 protein from high-risk human papillomavirus types 18 and 33.

Degree: MS, Department of Microbiology and Immunology., 2007, McGill University

The HPV E6-p53 interaction is well-understood, but not for all high-risk HPV types. In addition, HPV E6 p53-independent functions are gaining recognition for their importance… (more)

Subjects/Keywords: Viral Envelope Proteins  – metabolism.; Oncogene Proteins, Viral  – metabolism.; Papillomaviridae  – physiology.; Tumor Suppressor Protein p53  – metabolism.; Membrane Proteins  – metabolism.

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APA (6th Edition):

Ainsworth, J. (2007). Comparison of p53 and MAGI-3 regulation mediated by the E6 protein from high-risk human papillomavirus types 18 and 33. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile112368.pdf

Chicago Manual of Style (16th Edition):

Ainsworth, Julia. “Comparison of p53 and MAGI-3 regulation mediated by the E6 protein from high-risk human papillomavirus types 18 and 33.” 2007. Masters Thesis, McGill University. Accessed December 06, 2019. http://digitool.library.mcgill.ca/thesisfile112368.pdf.

MLA Handbook (7th Edition):

Ainsworth, Julia. “Comparison of p53 and MAGI-3 regulation mediated by the E6 protein from high-risk human papillomavirus types 18 and 33.” 2007. Web. 06 Dec 2019.

Vancouver:

Ainsworth J. Comparison of p53 and MAGI-3 regulation mediated by the E6 protein from high-risk human papillomavirus types 18 and 33. [Internet] [Masters thesis]. McGill University; 2007. [cited 2019 Dec 06]. Available from: http://digitool.library.mcgill.ca/thesisfile112368.pdf.

Council of Science Editors:

Ainsworth J. Comparison of p53 and MAGI-3 regulation mediated by the E6 protein from high-risk human papillomavirus types 18 and 33. [Masters Thesis]. McGill University; 2007. Available from: http://digitool.library.mcgill.ca/thesisfile112368.pdf

25. Ding, Huiping. Regulation of tau functions by posttranslational modifications of tau and histone deacetylase 6.

Degree: PhD, 2008, University of Alabama – Birmingham

Alzheimer’s disease (AD), the most common neurodegenerative disease, is pathologically characterized by senile plaques composed of amyloid [beta] peptide and neurofibrillary tangles composed of hyperphosphorylated… (more)

Subjects/Keywords: Alzheimer Disease  – metabolism<; br>; Brain  – metabolism<; br>; Caspases  – metabolism<; br>; Histone Deacetylases  – metabolism<; br>; Microtubules  – metabolism<; br>; Neurons  – metabolism<; br>; tau Proteins  – metabolism

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APA (6th Edition):

Ding, H. (2008). Regulation of tau functions by posttranslational modifications of tau and histone deacetylase 6. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,439

Chicago Manual of Style (16th Edition):

Ding, Huiping. “Regulation of tau functions by posttranslational modifications of tau and histone deacetylase 6.” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,439.

MLA Handbook (7th Edition):

Ding, Huiping. “Regulation of tau functions by posttranslational modifications of tau and histone deacetylase 6.” 2008. Web. 06 Dec 2019.

Vancouver:

Ding H. Regulation of tau functions by posttranslational modifications of tau and histone deacetylase 6. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,439.

Council of Science Editors:

Ding H. Regulation of tau functions by posttranslational modifications of tau and histone deacetylase 6. [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,439

26. Yu, Jei-Hwa. MAPKs regulate nuclear import of human papillomavirus type 11 replicative helicase E1.

Degree: PhD, 2008, University of Alabama – Birmingham

Papillomaviruses (PV) are prevalent pathogens that infect human or animal squamous epithelia. Its genome is a double strand circular DNA of approximately 7.9 kb. It… (more)

Subjects/Keywords: DNA Helicases  – metabolism <; br>; DNA-Binding Proteins  – metabolism <; br>; Human papillomavirus 11  – physiology <; br>; Mitogen-Activated Protein Kinases  – metabolism <; br>; Nuclear Localization Signals  – metabolism <; br>; Replication Origin <; br>; Viral Proteins  – metabolism

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APA (6th Edition):

Yu, J. (2008). MAPKs regulate nuclear import of human papillomavirus type 11 replicative helicase E1. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,213

Chicago Manual of Style (16th Edition):

Yu, Jei-Hwa. “MAPKs regulate nuclear import of human papillomavirus type 11 replicative helicase E1.” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,213.

MLA Handbook (7th Edition):

Yu, Jei-Hwa. “MAPKs regulate nuclear import of human papillomavirus type 11 replicative helicase E1.” 2008. Web. 06 Dec 2019.

Vancouver:

Yu J. MAPKs regulate nuclear import of human papillomavirus type 11 replicative helicase E1. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,213.

Council of Science Editors:

Yu J. MAPKs regulate nuclear import of human papillomavirus type 11 replicative helicase E1. [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,213

27. Maitra, Sushmit. The AU-rich element mRNA decay-promoting activity of BRF1 is regulated by mitogen-activated protein kinase activated protein kinase.

Degree: PhD, 2008, University of Alabama – Birmingham

Regulated mRNA decay is a highly important process for the tight control of gene expression. Inherently unstable mRNAs contain AU-rich elements (AREs) in the 3’… (more)

Subjects/Keywords: Intracellular Signaling Peptides and Proteins  – metabolism <; br>; Protein-Serine-Threonine Kinases  – metabolism <; br>; RNA, Messenger  – metabolism <; br>; RNA Stability  – physiology <; br>; RNA-Binding Proteins  – metabolism <; br>; TATA-Binding Protein Associated Factors  – metabolism

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APA (6th Edition):

Maitra, S. (2008). The AU-rich element mRNA decay-promoting activity of BRF1 is regulated by mitogen-activated protein kinase activated protein kinase. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,379

Chicago Manual of Style (16th Edition):

Maitra, Sushmit. “The AU-rich element mRNA decay-promoting activity of BRF1 is regulated by mitogen-activated protein kinase activated protein kinase.” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,379.

MLA Handbook (7th Edition):

Maitra, Sushmit. “The AU-rich element mRNA decay-promoting activity of BRF1 is regulated by mitogen-activated protein kinase activated protein kinase.” 2008. Web. 06 Dec 2019.

Vancouver:

Maitra S. The AU-rich element mRNA decay-promoting activity of BRF1 is regulated by mitogen-activated protein kinase activated protein kinase. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,379.

Council of Science Editors:

Maitra S. The AU-rich element mRNA decay-promoting activity of BRF1 is regulated by mitogen-activated protein kinase activated protein kinase. [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,379


University of Missouri – Columbia

28. Furrer, Jason L., 1976-. Enterobactin export in escherichia coli via P43 (ents) and associated components.

Degree: PhD, 2006, University of Missouri – Columbia

 Ferric iron, critical for the metabolic functions of many microorganisms, is generally insoluble at neutral pH or quickly complexed by host iron storage proteins. To… (more)

Subjects/Keywords: Ions  – metabolism; Escherichia coli  – metabolism; Enterobactin  – metabolism; Escherichia coli Proteins  – metabolism; Bacterial Outer Membrane Proteins  – metabolism

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APA (6th Edition):

Furrer, Jason L., 1. (2006). Enterobactin export in escherichia coli via P43 (ents) and associated components. (Doctoral Dissertation). University of Missouri – Columbia. Retrieved from https://doi.org/10.32469/10355/4392

Chicago Manual of Style (16th Edition):

Furrer, Jason L., 1976-. “Enterobactin export in escherichia coli via P43 (ents) and associated components.” 2006. Doctoral Dissertation, University of Missouri – Columbia. Accessed December 06, 2019. https://doi.org/10.32469/10355/4392.

MLA Handbook (7th Edition):

Furrer, Jason L., 1976-. “Enterobactin export in escherichia coli via P43 (ents) and associated components.” 2006. Web. 06 Dec 2019.

Vancouver:

Furrer, Jason L. 1. Enterobactin export in escherichia coli via P43 (ents) and associated components. [Internet] [Doctoral dissertation]. University of Missouri – Columbia; 2006. [cited 2019 Dec 06]. Available from: https://doi.org/10.32469/10355/4392.

Council of Science Editors:

Furrer, Jason L. 1. Enterobactin export in escherichia coli via P43 (ents) and associated components. [Doctoral Dissertation]. University of Missouri – Columbia; 2006. Available from: https://doi.org/10.32469/10355/4392

29. Hock, Thomas D. Regulation of the human heme oxygenase-1 gene.

Degree: PhD, 2007, University of Alabama – Birmingham

The heme oxygenase-1 (HO-1) gene encodes a microsomal enzyme that catalyzes the conversion of heme to carbon monoxide, Iron, and biliverdin. HO-1 transcription is induced… (more)

Subjects/Keywords: Heme Oxygenase-1  – genetics <; br>; Proto-Oncogene Proteins c-jun  – metabolism <; br>; Transcription Factors  – metabolism

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

APA (6th Edition):

Hock, T. D. (2007). Regulation of the human heme oxygenase-1 gene. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,126

Chicago Manual of Style (16th Edition):

Hock, Thomas D. “Regulation of the human heme oxygenase-1 gene.” 2007. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,126.

MLA Handbook (7th Edition):

Hock, Thomas D. “Regulation of the human heme oxygenase-1 gene.” 2007. Web. 06 Dec 2019.

Vancouver:

Hock TD. Regulation of the human heme oxygenase-1 gene. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2007. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,126.

Council of Science Editors:

Hock TD. Regulation of the human heme oxygenase-1 gene. [Doctoral Dissertation]. University of Alabama – Birmingham; 2007. Available from: http://contentdm.mhsl.uab.edu/u?/etd,126

30. Matthews, Tori A. Pathological modifications of tau induce toxicity and facilitate cell death.

Degree: PhD, 2009, University of Alabama – Birmingham

lzheimer’s disease (AD) is a progressive neurodegenerative disorder characterized by two major pathophysiological hallmarks, beta-amyloid (A[Beta]) plaques and tau tangles. In AD and other tau… (more)

Subjects/Keywords: Caspases  – metabolism<; br>; Cell Death  – physiology<; br>; Microtubules  – metabolism<; br>; tau Proteins  – physiology

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

APA (6th Edition):

Matthews, T. A. (2009). Pathological modifications of tau induce toxicity and facilitate cell death. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,607

Chicago Manual of Style (16th Edition):

Matthews, Tori A. “Pathological modifications of tau induce toxicity and facilitate cell death.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,607.

MLA Handbook (7th Edition):

Matthews, Tori A. “Pathological modifications of tau induce toxicity and facilitate cell death.” 2009. Web. 06 Dec 2019.

Vancouver:

Matthews TA. Pathological modifications of tau induce toxicity and facilitate cell death. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,607.

Council of Science Editors:

Matthews TA. Pathological modifications of tau induce toxicity and facilitate cell death. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,607

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