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You searched for subject:(Nuclear Proteins). Showing records 1 – 30 of 239 total matches.

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Hong Kong University of Science and Technology

1. Diao, Yarui. Pax7BP, a novel Pax7-binding protein, bridges Pax7 and the H3K4 histone methyltransferase complex and mediates the expression of Pax7 target genes in myoblasts.

Degree: 2011, Hong Kong University of Science and Technology

 Muscle satellite cells (i.e., muscle stem cells) are mainly responsible for postnatal muscle growth and regeneration. Pax7, a transcription factor of the paired-domain-containing proteins, is… (more)

Subjects/Keywords: Muscles  – Growth ; Muscle proteins ; Nuclear proteins

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APA (6th Edition):

Diao, Y. (2011). Pax7BP, a novel Pax7-binding protein, bridges Pax7 and the H3K4 histone methyltransferase complex and mediates the expression of Pax7 target genes in myoblasts. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-7259 ; https://doi.org/10.14711/thesis-b1136417 ; http://repository.ust.hk/ir/bitstream/1783.1-7259/1/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):

Diao, Yarui. “Pax7BP, a novel Pax7-binding protein, bridges Pax7 and the H3K4 histone methyltransferase complex and mediates the expression of Pax7 target genes in myoblasts.” 2011. Thesis, Hong Kong University of Science and Technology. Accessed July 15, 2020. http://repository.ust.hk/ir/Record/1783.1-7259 ; https://doi.org/10.14711/thesis-b1136417 ; http://repository.ust.hk/ir/bitstream/1783.1-7259/1/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):

Diao, Yarui. “Pax7BP, a novel Pax7-binding protein, bridges Pax7 and the H3K4 histone methyltransferase complex and mediates the expression of Pax7 target genes in myoblasts.” 2011. Web. 15 Jul 2020.

Vancouver:

Diao Y. Pax7BP, a novel Pax7-binding protein, bridges Pax7 and the H3K4 histone methyltransferase complex and mediates the expression of Pax7 target genes in myoblasts. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2011. [cited 2020 Jul 15]. Available from: http://repository.ust.hk/ir/Record/1783.1-7259 ; https://doi.org/10.14711/thesis-b1136417 ; http://repository.ust.hk/ir/bitstream/1783.1-7259/1/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:

Diao Y. Pax7BP, a novel Pax7-binding protein, bridges Pax7 and the H3K4 histone methyltransferase complex and mediates the expression of Pax7 target genes in myoblasts. [Thesis]. Hong Kong University of Science and Technology; 2011. Available from: http://repository.ust.hk/ir/Record/1783.1-7259 ; https://doi.org/10.14711/thesis-b1136417 ; http://repository.ust.hk/ir/bitstream/1783.1-7259/1/th_redirect.html

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


University of Leicester

2. Shak, Caroline. Investigating the recruitment of centrosomal proteins to the nuclear envelope during myogenesis.

Degree: PhD, 2020, University of Leicester

 Several stages of nuclear movement and positioning occur during the differentiation of myoblasts into myotubes and myofibres, allowing nuclei to be spread along the cell… (more)

Subjects/Keywords: Centrosomal Proteins; nuclear envelope; myogenesis

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APA (6th Edition):

Shak, C. (2020). Investigating the recruitment of centrosomal proteins to the nuclear envelope during myogenesis. (Doctoral Dissertation). University of Leicester. Retrieved from https://doi.org/10.25392/leicester.data.11638017.v1 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.798213

Chicago Manual of Style (16th Edition):

Shak, Caroline. “Investigating the recruitment of centrosomal proteins to the nuclear envelope during myogenesis.” 2020. Doctoral Dissertation, University of Leicester. Accessed July 15, 2020. https://doi.org/10.25392/leicester.data.11638017.v1 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.798213.

MLA Handbook (7th Edition):

Shak, Caroline. “Investigating the recruitment of centrosomal proteins to the nuclear envelope during myogenesis.” 2020. Web. 15 Jul 2020.

Vancouver:

Shak C. Investigating the recruitment of centrosomal proteins to the nuclear envelope during myogenesis. [Internet] [Doctoral dissertation]. University of Leicester; 2020. [cited 2020 Jul 15]. Available from: https://doi.org/10.25392/leicester.data.11638017.v1 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.798213.

Council of Science Editors:

Shak C. Investigating the recruitment of centrosomal proteins to the nuclear envelope during myogenesis. [Doctoral Dissertation]. University of Leicester; 2020. Available from: https://doi.org/10.25392/leicester.data.11638017.v1 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.798213


Hong Kong University of Science and Technology

3. Cheung, Man Hei. The role of NOC3 in DNA replication in human cells.

Degree: 2015, Hong Kong University of Science and Technology

 Noc3 (Nucleolar complex associated protein) was originally identified by a genetic screen in budding yeast Saccharomyces cerevisiae. It was reported that it plays crucial roles… (more)

Subjects/Keywords: DNA replication ; Nuclear proteins

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APA (6th Edition):

Cheung, M. H. (2015). The role of NOC3 in DNA replication in human cells. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-80225 ; https://doi.org/10.14711/thesis-b1514893 ; http://repository.ust.hk/ir/bitstream/1783.1-80225/1/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):

Cheung, Man Hei. “The role of NOC3 in DNA replication in human cells.” 2015. Thesis, Hong Kong University of Science and Technology. Accessed July 15, 2020. http://repository.ust.hk/ir/Record/1783.1-80225 ; https://doi.org/10.14711/thesis-b1514893 ; http://repository.ust.hk/ir/bitstream/1783.1-80225/1/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):

Cheung, Man Hei. “The role of NOC3 in DNA replication in human cells.” 2015. Web. 15 Jul 2020.

Vancouver:

Cheung MH. The role of NOC3 in DNA replication in human cells. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2015. [cited 2020 Jul 15]. Available from: http://repository.ust.hk/ir/Record/1783.1-80225 ; https://doi.org/10.14711/thesis-b1514893 ; http://repository.ust.hk/ir/bitstream/1783.1-80225/1/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:

Cheung MH. The role of NOC3 in DNA replication in human cells. [Thesis]. Hong Kong University of Science and Technology; 2015. Available from: http://repository.ust.hk/ir/Record/1783.1-80225 ; https://doi.org/10.14711/thesis-b1514893 ; http://repository.ust.hk/ir/bitstream/1783.1-80225/1/th_redirect.html

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


Penn State University

4. Gao, Zhizhen. DEPLETION OF NUCLEAR ENVELOPE COMPONENTS CAUSES A NOVEL CENTROSOME ATTACHMENT DEFECT.

Degree: MS, Biochemistry, Microbiology, and Molecular Biology, 2008, Penn State University

 The attachment of the centrosome to the nucleus is essential for C. elegans development. Two genes, zyg-12 and sun-1, are essential for centrosome attachment; zyg-12… (more)

Subjects/Keywords: Lamin-binding proteins; Nuclear lamins; Nuclear size; Centrosome attachment; Nuclear Pores

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APA (6th Edition):

Gao, Z. (2008). DEPLETION OF NUCLEAR ENVELOPE COMPONENTS CAUSES A NOVEL CENTROSOME ATTACHMENT DEFECT. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/8654

Chicago Manual of Style (16th Edition):

Gao, Zhizhen. “DEPLETION OF NUCLEAR ENVELOPE COMPONENTS CAUSES A NOVEL CENTROSOME ATTACHMENT DEFECT.” 2008. Masters Thesis, Penn State University. Accessed July 15, 2020. https://etda.libraries.psu.edu/catalog/8654.

MLA Handbook (7th Edition):

Gao, Zhizhen. “DEPLETION OF NUCLEAR ENVELOPE COMPONENTS CAUSES A NOVEL CENTROSOME ATTACHMENT DEFECT.” 2008. Web. 15 Jul 2020.

Vancouver:

Gao Z. DEPLETION OF NUCLEAR ENVELOPE COMPONENTS CAUSES A NOVEL CENTROSOME ATTACHMENT DEFECT. [Internet] [Masters thesis]. Penn State University; 2008. [cited 2020 Jul 15]. Available from: https://etda.libraries.psu.edu/catalog/8654.

Council of Science Editors:

Gao Z. DEPLETION OF NUCLEAR ENVELOPE COMPONENTS CAUSES A NOVEL CENTROSOME ATTACHMENT DEFECT. [Masters Thesis]. Penn State University; 2008. Available from: https://etda.libraries.psu.edu/catalog/8654


University of Texas Southwestern Medical Center

5. McKean, William Bennion, Jr. Protein Composition and Subcellular Localization of the De Novo Lipogenic Metabolon.

Degree: 2016, University of Texas Southwestern Medical Center

Pages 11-34 are incorrectly numbered as pages 9-32, and pages 35-124 are incorrectly numbered as pages 34-123.

Fatty acids are the major components of triglycerides,… (more)

Subjects/Keywords: Fatty Acids; Microtubule-Associated Proteins; Models, Molecular; Nuclear Proteins; Transcription Factors

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APA (6th Edition):

McKean, William Bennion, J. (2016). Protein Composition and Subcellular Localization of the De Novo Lipogenic Metabolon. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5311

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):

McKean, William Bennion, Jr. “Protein Composition and Subcellular Localization of the De Novo Lipogenic Metabolon.” 2016. Thesis, University of Texas Southwestern Medical Center. Accessed July 15, 2020. http://hdl.handle.net/2152.5/5311.

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

MLA Handbook (7th Edition):

McKean, William Bennion, Jr. “Protein Composition and Subcellular Localization of the De Novo Lipogenic Metabolon.” 2016. Web. 15 Jul 2020.

Vancouver:

McKean, William Bennion J. Protein Composition and Subcellular Localization of the De Novo Lipogenic Metabolon. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2016. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/2152.5/5311.

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

Council of Science Editors:

McKean, William Bennion J. Protein Composition and Subcellular Localization of the De Novo Lipogenic Metabolon. [Thesis]. University of Texas Southwestern Medical Center; 2016. Available from: http://hdl.handle.net/2152.5/5311

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

6. Zhang, Zi Chao. Characterization of Nuclear Localization Signals of Karyopherin-Mediated Nuclear Import.

Degree: PhD, Cell Regulation, 2012, University of Texas Southwestern Medical Center

 Nucleocytoplasmic transport is mediated by Karyopherin beta (Kap beta) proteins in a Ran-dependent manner. Ten import Kap betas recognize their cargos through the nuclear localization… (more)

Subjects/Keywords: Nucleocytoplasmic Transport Proteins; RNA-Binding Proteins; Nuclear Localization Signals

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APA (6th Edition):

Zhang, Z. C. (2012). Characterization of Nuclear Localization Signals of Karyopherin-Mediated Nuclear Import. (Doctoral Dissertation). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1105

Chicago Manual of Style (16th Edition):

Zhang, Zi Chao. “Characterization of Nuclear Localization Signals of Karyopherin-Mediated Nuclear Import.” 2012. Doctoral Dissertation, University of Texas Southwestern Medical Center. Accessed July 15, 2020. http://hdl.handle.net/2152.5/1105.

MLA Handbook (7th Edition):

Zhang, Zi Chao. “Characterization of Nuclear Localization Signals of Karyopherin-Mediated Nuclear Import.” 2012. Web. 15 Jul 2020.

Vancouver:

Zhang ZC. Characterization of Nuclear Localization Signals of Karyopherin-Mediated Nuclear Import. [Internet] [Doctoral dissertation]. University of Texas Southwestern Medical Center; 2012. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/2152.5/1105.

Council of Science Editors:

Zhang ZC. Characterization of Nuclear Localization Signals of Karyopherin-Mediated Nuclear Import. [Doctoral Dissertation]. University of Texas Southwestern Medical Center; 2012. Available from: http://hdl.handle.net/2152.5/1105

7. Melanson, Suzanne Marie. Functional Interaction of BPV-1 E2 with the Papillomavirus Genome: A Dissertation.

Degree: Immunology and Microbiology, Department of Medicine, 2009, U of Massachusetts : Med

  The bovine papillomavirus type 1 E2 protein is a multifunctional early viral protein with roles in all phases of the cell cycle. E2 is… (more)

Subjects/Keywords: DNA-Binding Proteins; Nuclear Proteins; Transcription Factors; Viral Proteins; Bovine papillomavirus; Amino Acids, Peptides, and Proteins; Cells; Genetic Phenomena; Viruses

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APA (6th Edition):

Melanson, S. M. (2009). Functional Interaction of BPV-1 E2 with the Papillomavirus Genome: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/410

Chicago Manual of Style (16th Edition):

Melanson, Suzanne Marie. “Functional Interaction of BPV-1 E2 with the Papillomavirus Genome: A Dissertation.” 2009. Doctoral Dissertation, U of Massachusetts : Med. Accessed July 15, 2020. https://escholarship.umassmed.edu/gsbs_diss/410.

MLA Handbook (7th Edition):

Melanson, Suzanne Marie. “Functional Interaction of BPV-1 E2 with the Papillomavirus Genome: A Dissertation.” 2009. Web. 15 Jul 2020.

Vancouver:

Melanson SM. Functional Interaction of BPV-1 E2 with the Papillomavirus Genome: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2009. [cited 2020 Jul 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/410.

Council of Science Editors:

Melanson SM. Functional Interaction of BPV-1 E2 with the Papillomavirus Genome: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2009. Available from: https://escholarship.umassmed.edu/gsbs_diss/410


Universidade Nova

8. Freire, Filipe Miguel dos Santos. Integrated study by NMR and X-ray Crystallography on the analysis of the molecular interactions in heme-binding proteins.

Degree: 2012, Universidade Nova

Dissertação para obtenção do Grau de Doutor em Bioquímica, Especialidade Bioquímica Estrutural

Heme is essential to all aerobic organisms, as it is involved in several… (more)

Subjects/Keywords: Heme-binding proteins; BH3-only proteins; Biomolecular Crystallography; Nuclear magnetic resonance; Fluorescence quenching

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APA (6th Edition):

Freire, F. M. d. S. (2012). Integrated study by NMR and X-ray Crystallography on the analysis of the molecular interactions in heme-binding proteins. (Thesis). Universidade Nova. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/8775

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):

Freire, Filipe Miguel dos Santos. “Integrated study by NMR and X-ray Crystallography on the analysis of the molecular interactions in heme-binding proteins.” 2012. Thesis, Universidade Nova. Accessed July 15, 2020. http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/8775.

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

MLA Handbook (7th Edition):

Freire, Filipe Miguel dos Santos. “Integrated study by NMR and X-ray Crystallography on the analysis of the molecular interactions in heme-binding proteins.” 2012. Web. 15 Jul 2020.

Vancouver:

Freire FMdS. Integrated study by NMR and X-ray Crystallography on the analysis of the molecular interactions in heme-binding proteins. [Internet] [Thesis]. Universidade Nova; 2012. [cited 2020 Jul 15]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/8775.

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

Council of Science Editors:

Freire FMdS. Integrated study by NMR and X-ray Crystallography on the analysis of the molecular interactions in heme-binding proteins. [Thesis]. Universidade Nova; 2012. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/8775

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

9. Zahm, Jacob Aaron. Physical Studies of Actin Nucleation and Conformational Dynamics.

Degree: 2017, University of Texas Southwestern Medical Center

 Actin is a 42 kilodalton ATPase that exists ubiquitously in eukaryotic cells. Unlike other ATPases, however, actin, under suitable conditions, can polymerize, forming helical filaments.… (more)

Subjects/Keywords: Actins; Bacterial Proteins; Carbon Isotopes; Nuclear Magnetic Resonance, Biomolecular; Recombinant Proteins; Vibrio parahaemolyticus

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APA (6th Edition):

Zahm, J. A. (2017). Physical Studies of Actin Nucleation and Conformational Dynamics. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/7732

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):

Zahm, Jacob Aaron. “Physical Studies of Actin Nucleation and Conformational Dynamics.” 2017. Thesis, University of Texas Southwestern Medical Center. Accessed July 15, 2020. http://hdl.handle.net/2152.5/7732.

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

MLA Handbook (7th Edition):

Zahm, Jacob Aaron. “Physical Studies of Actin Nucleation and Conformational Dynamics.” 2017. Web. 15 Jul 2020.

Vancouver:

Zahm JA. Physical Studies of Actin Nucleation and Conformational Dynamics. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2017. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/2152.5/7732.

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

Council of Science Editors:

Zahm JA. Physical Studies of Actin Nucleation and Conformational Dynamics. [Thesis]. University of Texas Southwestern Medical Center; 2017. Available from: http://hdl.handle.net/2152.5/7732

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

10. Brulotte, Melissa Lynn. Spindle Checkpoint Silencing by TRIP13.

Degree: 2017, University of Texas Southwestern Medical Center

 The spindle checkpoint is important for maintaining genomic stability and preventing aneuploidy, a hallmark of cancer. The checkpoint ensures that chromosome segregation does not occur… (more)

Subjects/Keywords: Adaptor Proteins, Signal Transducing; ATPases Associated with Diverse Cellular Activities; Cdc20 Proteins; Cell Cycle Proteins; M Phase Cell Cycle Checkpoints; Mad2 Proteins; Nuclear Proteins

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APA (6th Edition):

Brulotte, M. L. (2017). Spindle Checkpoint Silencing by TRIP13. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/7734

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):

Brulotte, Melissa Lynn. “Spindle Checkpoint Silencing by TRIP13.” 2017. Thesis, University of Texas Southwestern Medical Center. Accessed July 15, 2020. http://hdl.handle.net/2152.5/7734.

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

MLA Handbook (7th Edition):

Brulotte, Melissa Lynn. “Spindle Checkpoint Silencing by TRIP13.” 2017. Web. 15 Jul 2020.

Vancouver:

Brulotte ML. Spindle Checkpoint Silencing by TRIP13. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2017. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/2152.5/7734.

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

Council of Science Editors:

Brulotte ML. Spindle Checkpoint Silencing by TRIP13. [Thesis]. University of Texas Southwestern Medical Center; 2017. Available from: http://hdl.handle.net/2152.5/7734

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


Wright State University

11. Delman, Emily. Effects of Synthetic Ligands onHeterodimer Pairs Regarding Full-Length Human PPARa, RXRa and LXRa.

Degree: MS, Biochemistry and Molecular Biology, 2016, Wright State University

Nuclear receptor study is critically relevant in therapeutic medicine since the intricate details of disease states pertaining to atherosclerosis and diabetes are poorly understood. Three… (more)

Subjects/Keywords: Biochemistry; nuclear receptor proteins; PPAR; LXR; RXR; synthetic ligands

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APA (6th Edition):

Delman, E. (2016). Effects of Synthetic Ligands onHeterodimer Pairs Regarding Full-Length Human PPARa, RXRa and LXRa. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1472204976

Chicago Manual of Style (16th Edition):

Delman, Emily. “Effects of Synthetic Ligands onHeterodimer Pairs Regarding Full-Length Human PPARa, RXRa and LXRa.” 2016. Masters Thesis, Wright State University. Accessed July 15, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=wright1472204976.

MLA Handbook (7th Edition):

Delman, Emily. “Effects of Synthetic Ligands onHeterodimer Pairs Regarding Full-Length Human PPARa, RXRa and LXRa.” 2016. Web. 15 Jul 2020.

Vancouver:

Delman E. Effects of Synthetic Ligands onHeterodimer Pairs Regarding Full-Length Human PPARa, RXRa and LXRa. [Internet] [Masters thesis]. Wright State University; 2016. [cited 2020 Jul 15]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1472204976.

Council of Science Editors:

Delman E. Effects of Synthetic Ligands onHeterodimer Pairs Regarding Full-Length Human PPARa, RXRa and LXRa. [Masters Thesis]. Wright State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1472204976


Louisiana State University

12. Jackson, Emily Ann. 14-3-3 sigma interacts with liver X receptor beta.

Degree: MS, 2010, Louisiana State University

 Atherosclerosis is the leading cause of mortality in developed countries accounting for 50% of all deaths. Atherosclerosis develops when macrophages in the artery wall accumulate… (more)

Subjects/Keywords: protein-protein interaction; export; 14-3-3 proteins; nuclear receptors

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APA (6th Edition):

Jackson, E. A. (2010). 14-3-3 sigma interacts with liver X receptor beta. (Masters Thesis). Louisiana State University. Retrieved from etd-04292010-185535 ; https://digitalcommons.lsu.edu/gradschool_theses/4251

Chicago Manual of Style (16th Edition):

Jackson, Emily Ann. “14-3-3 sigma interacts with liver X receptor beta.” 2010. Masters Thesis, Louisiana State University. Accessed July 15, 2020. etd-04292010-185535 ; https://digitalcommons.lsu.edu/gradschool_theses/4251.

MLA Handbook (7th Edition):

Jackson, Emily Ann. “14-3-3 sigma interacts with liver X receptor beta.” 2010. Web. 15 Jul 2020.

Vancouver:

Jackson EA. 14-3-3 sigma interacts with liver X receptor beta. [Internet] [Masters thesis]. Louisiana State University; 2010. [cited 2020 Jul 15]. Available from: etd-04292010-185535 ; https://digitalcommons.lsu.edu/gradschool_theses/4251.

Council of Science Editors:

Jackson EA. 14-3-3 sigma interacts with liver X receptor beta. [Masters Thesis]. Louisiana State University; 2010. Available from: etd-04292010-185535 ; https://digitalcommons.lsu.edu/gradschool_theses/4251


University of Saskatchewan

13. Savada, Raghavendra Prasad. Characterization of regulation of expression and nuclear/nucleolar localization of Arabidopsis ribsomal proteins.

Degree: 2011, University of Saskatchewan

 Ribosomal proteins (RPs), synthesized in the cytoplasm, need to be transported from the cytoplasm to the nucleolus (a nuclear compartment), where a single molecule of… (more)

Subjects/Keywords: Nuclear/Nucleolar localization; Transcriptional regulation; Arabidopsis; Ribosomal proteins; Ribosomes

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APA (6th Edition):

Savada, R. P. (2011). Characterization of regulation of expression and nuclear/nucleolar localization of Arabidopsis ribsomal proteins. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/etd-06242011-185044

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):

Savada, Raghavendra Prasad. “Characterization of regulation of expression and nuclear/nucleolar localization of Arabidopsis ribsomal proteins.” 2011. Thesis, University of Saskatchewan. Accessed July 15, 2020. http://hdl.handle.net/10388/etd-06242011-185044.

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

MLA Handbook (7th Edition):

Savada, Raghavendra Prasad. “Characterization of regulation of expression and nuclear/nucleolar localization of Arabidopsis ribsomal proteins.” 2011. Web. 15 Jul 2020.

Vancouver:

Savada RP. Characterization of regulation of expression and nuclear/nucleolar localization of Arabidopsis ribsomal proteins. [Internet] [Thesis]. University of Saskatchewan; 2011. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/10388/etd-06242011-185044.

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

Council of Science Editors:

Savada RP. Characterization of regulation of expression and nuclear/nucleolar localization of Arabidopsis ribsomal proteins. [Thesis]. University of Saskatchewan; 2011. Available from: http://hdl.handle.net/10388/etd-06242011-185044

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


University of Toronto

14. Zilberman, Emma. ARGLU1 is an RNA-binding Protein that has a Fundamental Role in Modulating Global Alternative Splicing Patterns.

Degree: 2017, University of Toronto

Alternative splicing (AS) is a key step of RNA maturation. More emerging evidence demonstrates RNA synthesis and processing are coupled, thus transcriptional coregulatory proteins are… (more)

Subjects/Keywords: Alternative splicing; Nuclear receptor coregulators; RNA-binding proteins; RNA processing; 0307

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APA (6th Edition):

Zilberman, E. (2017). ARGLU1 is an RNA-binding Protein that has a Fundamental Role in Modulating Global Alternative Splicing Patterns. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/97233

Chicago Manual of Style (16th Edition):

Zilberman, Emma. “ARGLU1 is an RNA-binding Protein that has a Fundamental Role in Modulating Global Alternative Splicing Patterns.” 2017. Masters Thesis, University of Toronto. Accessed July 15, 2020. http://hdl.handle.net/1807/97233.

MLA Handbook (7th Edition):

Zilberman, Emma. “ARGLU1 is an RNA-binding Protein that has a Fundamental Role in Modulating Global Alternative Splicing Patterns.” 2017. Web. 15 Jul 2020.

Vancouver:

Zilberman E. ARGLU1 is an RNA-binding Protein that has a Fundamental Role in Modulating Global Alternative Splicing Patterns. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/1807/97233.

Council of Science Editors:

Zilberman E. ARGLU1 is an RNA-binding Protein that has a Fundamental Role in Modulating Global Alternative Splicing Patterns. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/97233


Columbia University

15. O'Brien, Paul. Biomolecular NMR spectroscopy: Application to the study of the piRNA-pathway protein GTSF1, and backbone and side-chain spin relaxation methods development.

Degree: 2019, Columbia University

 The structural dynamics of proteins and other macromolecules typically serve crucial roles for their respective biological function. While rigid protein structures are used in classic… (more)

Subjects/Keywords: Biophysics; Biochemistry; Nuclear magnetic resonance spectroscopy; Proteins – Structure; Molecular dynamics

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APA (6th Edition):

O'Brien, P. (2019). Biomolecular NMR spectroscopy: Application to the study of the piRNA-pathway protein GTSF1, and backbone and side-chain spin relaxation methods development. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/d8-rg5e-gf61

Chicago Manual of Style (16th Edition):

O'Brien, Paul. “Biomolecular NMR spectroscopy: Application to the study of the piRNA-pathway protein GTSF1, and backbone and side-chain spin relaxation methods development.” 2019. Doctoral Dissertation, Columbia University. Accessed July 15, 2020. https://doi.org/10.7916/d8-rg5e-gf61.

MLA Handbook (7th Edition):

O'Brien, Paul. “Biomolecular NMR spectroscopy: Application to the study of the piRNA-pathway protein GTSF1, and backbone and side-chain spin relaxation methods development.” 2019. Web. 15 Jul 2020.

Vancouver:

O'Brien P. Biomolecular NMR spectroscopy: Application to the study of the piRNA-pathway protein GTSF1, and backbone and side-chain spin relaxation methods development. [Internet] [Doctoral dissertation]. Columbia University; 2019. [cited 2020 Jul 15]. Available from: https://doi.org/10.7916/d8-rg5e-gf61.

Council of Science Editors:

O'Brien P. Biomolecular NMR spectroscopy: Application to the study of the piRNA-pathway protein GTSF1, and backbone and side-chain spin relaxation methods development. [Doctoral Dissertation]. Columbia University; 2019. Available from: https://doi.org/10.7916/d8-rg5e-gf61


University of Texas Southwestern Medical Center

16. Guo, Wei. Roles of MicroRNAs in Fetal Lung Development.

Degree: 2016, University of Texas Southwestern Medical Center

 Lung alveolar type II cells uniquely synthesize surfactant, a developmentally-regulated lipoprotein that is essential for breathing. Expression of the major surfactant protein, SP-A, in midgestation… (more)

Subjects/Keywords: Alveolar Epithelial Cells; Lung; MicroRNAs; Nuclear Proteins; Transcription Factors

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APA (6th Edition):

Guo, W. (2016). Roles of MicroRNAs in Fetal Lung Development. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5729

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):

Guo, Wei. “Roles of MicroRNAs in Fetal Lung Development.” 2016. Thesis, University of Texas Southwestern Medical Center. Accessed July 15, 2020. http://hdl.handle.net/2152.5/5729.

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

MLA Handbook (7th Edition):

Guo, Wei. “Roles of MicroRNAs in Fetal Lung Development.” 2016. Web. 15 Jul 2020.

Vancouver:

Guo W. Roles of MicroRNAs in Fetal Lung Development. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2016. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/2152.5/5729.

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

Council of Science Editors:

Guo W. Roles of MicroRNAs in Fetal Lung Development. [Thesis]. University of Texas Southwestern Medical Center; 2016. Available from: http://hdl.handle.net/2152.5/5729

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

17. Zhou, Amy 1986-. Analysis of Synaptotagmin-SNARE Complex Interactions by One-Dimensional NMR Spectroscopy.

Degree: 2013, University of Texas Southwestern Medical Center

 The mechanism of calcium-triggered neurotransmitter release is mediated by numerous proteins at the neuronal synapse. The SNARE proteins form a complex that mediates fusion between… (more)

Subjects/Keywords: Nuclear Magnetic Resonance, Biomolecular; SNARE Proteins; Synaptotagmin I

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APA (6th Edition):

Zhou, A. 1. (2013). Analysis of Synaptotagmin-SNARE Complex Interactions by One-Dimensional NMR Spectroscopy. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1598

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):

Zhou, Amy 1986-. “Analysis of Synaptotagmin-SNARE Complex Interactions by One-Dimensional NMR Spectroscopy.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed July 15, 2020. http://hdl.handle.net/2152.5/1598.

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

MLA Handbook (7th Edition):

Zhou, Amy 1986-. “Analysis of Synaptotagmin-SNARE Complex Interactions by One-Dimensional NMR Spectroscopy.” 2013. Web. 15 Jul 2020.

Vancouver:

Zhou A1. Analysis of Synaptotagmin-SNARE Complex Interactions by One-Dimensional NMR Spectroscopy. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/2152.5/1598.

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

Council of Science Editors:

Zhou A1. Analysis of Synaptotagmin-SNARE Complex Interactions by One-Dimensional NMR Spectroscopy. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/1598

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

18. Patel, Amish Jayantibhai. Mechanistic and Therapeutic Insights for Epigenetic Regulation in Cancer Development.

Degree: 2014, University of Texas Southwestern Medical Center

 Malignant Peripheral Nerve Sheath Tumors (MPNSTs) are highly aggressive sarcomas that develop sporadically or in patients with Neurofibromatosis type 1 (NF1). Effective treatment options are… (more)

Subjects/Keywords: Apoptosis; Nerve Sheath Neoplasms; Neurofibromatosis 1; Nuclear Proteins; Transcription Factors

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APA (6th Edition):

Patel, A. J. (2014). Mechanistic and Therapeutic Insights for Epigenetic Regulation in Cancer Development. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/3944

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):

Patel, Amish Jayantibhai. “Mechanistic and Therapeutic Insights for Epigenetic Regulation in Cancer Development.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed July 15, 2020. http://hdl.handle.net/2152.5/3944.

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

MLA Handbook (7th Edition):

Patel, Amish Jayantibhai. “Mechanistic and Therapeutic Insights for Epigenetic Regulation in Cancer Development.” 2014. Web. 15 Jul 2020.

Vancouver:

Patel AJ. Mechanistic and Therapeutic Insights for Epigenetic Regulation in Cancer Development. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/2152.5/3944.

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

Council of Science Editors:

Patel AJ. Mechanistic and Therapeutic Insights for Epigenetic Regulation in Cancer Development. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/3944

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

19. Liu, Haoming. HP1BP3, A Chromatin Retention Factor for Co-Transcriptional MicroRNA Processing.

Degree: 2016, University of Texas Southwestern Medical Center

 RNA interference (RNAi) is a post-transcriptional gene silencing mechanism found in all eukaryotic organisms. It is characterized by a family of small non-coding RNAs, either… (more)

Subjects/Keywords: Chromatin; MicroRNAs; Nuclear Proteins; RNA Processing, Post-Transcriptional; Transcription, Genetic

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APA (6th Edition):

Liu, H. (2016). HP1BP3, A Chromatin Retention Factor for Co-Transcriptional MicroRNA Processing. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5732

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):

Liu, Haoming. “HP1BP3, A Chromatin Retention Factor for Co-Transcriptional MicroRNA Processing.” 2016. Thesis, University of Texas Southwestern Medical Center. Accessed July 15, 2020. http://hdl.handle.net/2152.5/5732.

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

MLA Handbook (7th Edition):

Liu, Haoming. “HP1BP3, A Chromatin Retention Factor for Co-Transcriptional MicroRNA Processing.” 2016. Web. 15 Jul 2020.

Vancouver:

Liu H. HP1BP3, A Chromatin Retention Factor for Co-Transcriptional MicroRNA Processing. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2016. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/2152.5/5732.

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

Council of Science Editors:

Liu H. HP1BP3, A Chromatin Retention Factor for Co-Transcriptional MicroRNA Processing. [Thesis]. University of Texas Southwestern Medical Center; 2016. Available from: http://hdl.handle.net/2152.5/5732

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

20. Rodriguez, Andrea Christine. Development of New Photocrosslinking Approaches to Discover Binding Partners of O-GlcNAc-Modified Proteins.

Degree: 2015, University of Texas Southwestern Medical Center

 O-linked β-N-acetylglucosamine (O-GlcNAc) is an abundant post-translational modification that is regulated by two enzymes, O-GlcNAc transferase (OGT) and O-GlcNAc hydrolase (OGA). While it is elusive… (more)

Subjects/Keywords: Acetylglucosamine; Mutation, Missense; N-Acetylglucosaminyltransferases; Nuclear Pore Complex Proteins

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APA (6th Edition):

Rodriguez, A. C. (2015). Development of New Photocrosslinking Approaches to Discover Binding Partners of O-GlcNAc-Modified Proteins. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4449

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):

Rodriguez, Andrea Christine. “Development of New Photocrosslinking Approaches to Discover Binding Partners of O-GlcNAc-Modified Proteins.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed July 15, 2020. http://hdl.handle.net/2152.5/4449.

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

MLA Handbook (7th Edition):

Rodriguez, Andrea Christine. “Development of New Photocrosslinking Approaches to Discover Binding Partners of O-GlcNAc-Modified Proteins.” 2015. Web. 15 Jul 2020.

Vancouver:

Rodriguez AC. Development of New Photocrosslinking Approaches to Discover Binding Partners of O-GlcNAc-Modified Proteins. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/2152.5/4449.

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

Council of Science Editors:

Rodriguez AC. Development of New Photocrosslinking Approaches to Discover Binding Partners of O-GlcNAc-Modified Proteins. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4449

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

21. D'Brot, Alejandro. Of Apoptosomes and Oncogenes: Repurposing a Death Machine & Deconstructing the Action of P53 Mutations.

Degree: 2014, University of Texas Southwestern Medical Center

 It is now well appreciated that the apoptosome, which governs caspase-dependent cell death, also drives nonapoptotic caspase activation to remodel cells. However, determinants that specify… (more)

Subjects/Keywords: Apoptosomes; Aryl Hydrocarbon Receptor Nuclear Translocator; Caspases; Drosophila melanogaster; Drosophila Proteins

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APA (6th Edition):

D'Brot, A. (2014). Of Apoptosomes and Oncogenes: Repurposing a Death Machine & Deconstructing the Action of P53 Mutations. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/3311

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):

D'Brot, Alejandro. “Of Apoptosomes and Oncogenes: Repurposing a Death Machine & Deconstructing the Action of P53 Mutations.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed July 15, 2020. http://hdl.handle.net/2152.5/3311.

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

MLA Handbook (7th Edition):

D'Brot, Alejandro. “Of Apoptosomes and Oncogenes: Repurposing a Death Machine & Deconstructing the Action of P53 Mutations.” 2014. Web. 15 Jul 2020.

Vancouver:

D'Brot A. Of Apoptosomes and Oncogenes: Repurposing a Death Machine & Deconstructing the Action of P53 Mutations. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/2152.5/3311.

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

Council of Science Editors:

D'Brot A. Of Apoptosomes and Oncogenes: Repurposing a Death Machine & Deconstructing the Action of P53 Mutations. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/3311

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

22. Stubblefield, Jeremy Joseph. Nocturnin Regulates Metabolic Flux Through Maintenance of Poly(A) Tail Length Dynamics.

Degree: 2016, University of Texas Southwestern Medical Center

Pages 32-126 are incorrectly numbered as pages 31-125.

Cyclic processes in both behavior and physiology are aligned to the external environment through the circadian clock.… (more)

Subjects/Keywords: Circadian Rhythm; Nuclear Proteins; Poly A; Transcription Factors

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APA (6th Edition):

Stubblefield, J. J. (2016). Nocturnin Regulates Metabolic Flux Through Maintenance of Poly(A) Tail Length Dynamics. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5738

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):

Stubblefield, Jeremy Joseph. “Nocturnin Regulates Metabolic Flux Through Maintenance of Poly(A) Tail Length Dynamics.” 2016. Thesis, University of Texas Southwestern Medical Center. Accessed July 15, 2020. http://hdl.handle.net/2152.5/5738.

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

MLA Handbook (7th Edition):

Stubblefield, Jeremy Joseph. “Nocturnin Regulates Metabolic Flux Through Maintenance of Poly(A) Tail Length Dynamics.” 2016. Web. 15 Jul 2020.

Vancouver:

Stubblefield JJ. Nocturnin Regulates Metabolic Flux Through Maintenance of Poly(A) Tail Length Dynamics. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2016. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/2152.5/5738.

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

Council of Science Editors:

Stubblefield JJ. Nocturnin Regulates Metabolic Flux Through Maintenance of Poly(A) Tail Length Dynamics. [Thesis]. University of Texas Southwestern Medical Center; 2016. Available from: http://hdl.handle.net/2152.5/5738

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


Rutgers University

23. Mao, Binchen, 1981-. Improving the quality of protein NMR structures by Rosetta refinement and its application in molecular replacement.

Degree: Biochemistry, 2012, Rutgers University

Subjects/Keywords: Nuclear magnetic resonance; Proteins – Spectra

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APA (6th Edition):

Mao, Binchen, 1. (2012). Improving the quality of protein NMR structures by Rosetta refinement and its application in molecular replacement. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066907

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):

Mao, Binchen, 1981-. “Improving the quality of protein NMR structures by Rosetta refinement and its application in molecular replacement.” 2012. Thesis, Rutgers University. Accessed July 15, 2020. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066907.

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

MLA Handbook (7th Edition):

Mao, Binchen, 1981-. “Improving the quality of protein NMR structures by Rosetta refinement and its application in molecular replacement.” 2012. Web. 15 Jul 2020.

Vancouver:

Mao, Binchen 1. Improving the quality of protein NMR structures by Rosetta refinement and its application in molecular replacement. [Internet] [Thesis]. Rutgers University; 2012. [cited 2020 Jul 15]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066907.

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

Council of Science Editors:

Mao, Binchen 1. Improving the quality of protein NMR structures by Rosetta refinement and its application in molecular replacement. [Thesis]. Rutgers University; 2012. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066907

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


Michigan State University

24. Xie, Li. Solid state nuclear magnetic resonance studies of structures and membrane locations of peptides.

Degree: 2014, Michigan State University

Thesis Ph. D. Michigan State University. Chemistry 2014.

Solid state nuclear magnetic resonance (SSNMR) can be used to study the structures of molecules such as… (more)

Subjects/Keywords: Nuclear magnetic resonance spectroscopy; Peptides – Analysis; Membrane proteins – Structure; Chemistry

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APA (6th Edition):

Xie, L. (2014). Solid state nuclear magnetic resonance studies of structures and membrane locations of peptides. (Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:3120

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):

Xie, Li. “Solid state nuclear magnetic resonance studies of structures and membrane locations of peptides.” 2014. Thesis, Michigan State University. Accessed July 15, 2020. http://etd.lib.msu.edu/islandora/object/etd:3120.

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

MLA Handbook (7th Edition):

Xie, Li. “Solid state nuclear magnetic resonance studies of structures and membrane locations of peptides.” 2014. Web. 15 Jul 2020.

Vancouver:

Xie L. Solid state nuclear magnetic resonance studies of structures and membrane locations of peptides. [Internet] [Thesis]. Michigan State University; 2014. [cited 2020 Jul 15]. Available from: http://etd.lib.msu.edu/islandora/object/etd:3120.

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

Council of Science Editors:

Xie L. Solid state nuclear magnetic resonance studies of structures and membrane locations of peptides. [Thesis]. Michigan State University; 2014. Available from: http://etd.lib.msu.edu/islandora/object/etd:3120

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


University of Missouri – Columbia

25. Oshokoya, Olayinka. Development of advanced chemometric methods for analysis of deep-ultraviolet resonance Raman and circular dichroism spectroscopic data for protein secondary structure determination.

Degree: 2015, University of Missouri – Columbia

 Determination of protein secondary structure has become an area of great importance in biochemistry and biophysics as protein secondary structure is directly related to protein… (more)

Subjects/Keywords: Proteins  – Structure; Nuclear magnetic resonance spectroscopy; Raman spectroscopy

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APA (6th Edition):

Oshokoya, O. (2015). Development of advanced chemometric methods for analysis of deep-ultraviolet resonance Raman and circular dichroism spectroscopic data for protein secondary structure determination. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/46886

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):

Oshokoya, Olayinka. “Development of advanced chemometric methods for analysis of deep-ultraviolet resonance Raman and circular dichroism spectroscopic data for protein secondary structure determination.” 2015. Thesis, University of Missouri – Columbia. Accessed July 15, 2020. http://hdl.handle.net/10355/46886.

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

MLA Handbook (7th Edition):

Oshokoya, Olayinka. “Development of advanced chemometric methods for analysis of deep-ultraviolet resonance Raman and circular dichroism spectroscopic data for protein secondary structure determination.” 2015. Web. 15 Jul 2020.

Vancouver:

Oshokoya O. Development of advanced chemometric methods for analysis of deep-ultraviolet resonance Raman and circular dichroism spectroscopic data for protein secondary structure determination. [Internet] [Thesis]. University of Missouri – Columbia; 2015. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/10355/46886.

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

Council of Science Editors:

Oshokoya O. Development of advanced chemometric methods for analysis of deep-ultraviolet resonance Raman and circular dichroism spectroscopic data for protein secondary structure determination. [Thesis]. University of Missouri – Columbia; 2015. Available from: http://hdl.handle.net/10355/46886

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

26. Onder, Yasemin. A Multi-Organ Role for Nocturnin in Post-Transcriptional Regulation of RNA.

Degree: 2018, University of Texas Southwestern Medical Center

 Nocturnin is an RNA-specific nuclease, a circadian deadenylase first discovered in the retina of Xenopus laevis, and is conserved among eukaryotes. Nocturnin is widely expressed… (more)

Subjects/Keywords: Adipose Tissue, Brown; Circadian Rhythm; Nuclear Proteins; RNA, Messenger; Transcription Factors

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APA (6th Edition):

Onder, Y. (2018). A Multi-Organ Role for Nocturnin in Post-Transcriptional Regulation of RNA. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/8308

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):

Onder, Yasemin. “A Multi-Organ Role for Nocturnin in Post-Transcriptional Regulation of RNA.” 2018. Thesis, University of Texas Southwestern Medical Center. Accessed July 15, 2020. http://hdl.handle.net/2152.5/8308.

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

MLA Handbook (7th Edition):

Onder, Yasemin. “A Multi-Organ Role for Nocturnin in Post-Transcriptional Regulation of RNA.” 2018. Web. 15 Jul 2020.

Vancouver:

Onder Y. A Multi-Organ Role for Nocturnin in Post-Transcriptional Regulation of RNA. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2018. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/2152.5/8308.

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

Council of Science Editors:

Onder Y. A Multi-Organ Role for Nocturnin in Post-Transcriptional Regulation of RNA. [Thesis]. University of Texas Southwestern Medical Center; 2018. Available from: http://hdl.handle.net/2152.5/8308

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


University of Toronto

27. Vovk, Andrei Igorevitch. Coarse Grained Modeling of Intrinsically Disordered Protein Structures and Dynamics.

Degree: PhD, 2019, University of Toronto

 Contrary to natively folded proteins, which often have a single stable 3D structure, Intrinsically Disordered Protein (IDP) structures dynamically fluctuate between many conformations. This complexity… (more)

Subjects/Keywords: IDP; intrinsically disordered proteins; NPC; nuclear pore complex; polymer physics; 0786

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APA (6th Edition):

Vovk, A. I. (2019). Coarse Grained Modeling of Intrinsically Disordered Protein Structures and Dynamics. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/97732

Chicago Manual of Style (16th Edition):

Vovk, Andrei Igorevitch. “Coarse Grained Modeling of Intrinsically Disordered Protein Structures and Dynamics.” 2019. Doctoral Dissertation, University of Toronto. Accessed July 15, 2020. http://hdl.handle.net/1807/97732.

MLA Handbook (7th Edition):

Vovk, Andrei Igorevitch. “Coarse Grained Modeling of Intrinsically Disordered Protein Structures and Dynamics.” 2019. Web. 15 Jul 2020.

Vancouver:

Vovk AI. Coarse Grained Modeling of Intrinsically Disordered Protein Structures and Dynamics. [Internet] [Doctoral dissertation]. University of Toronto; 2019. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/1807/97732.

Council of Science Editors:

Vovk AI. Coarse Grained Modeling of Intrinsically Disordered Protein Structures and Dynamics. [Doctoral Dissertation]. University of Toronto; 2019. Available from: http://hdl.handle.net/1807/97732


University of Toronto

28. Gu, Chad. Coarse-grained Theory and Simulation of Assemblies of Intrinsically-disordered Nucleoporins.

Degree: PhD, 2019, University of Toronto

 Selective import and export through the nuclear envelope in the eukaryotic cell is solely regulated by the transporter known as Nuclear Pore Complex (NPC). The… (more)

Subjects/Keywords: Intrinsically disordered proteins; Nuclear Pore Complex; Nucleoporins; Polymers; 0786

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

APA (6th Edition):

Gu, C. (2019). Coarse-grained Theory and Simulation of Assemblies of Intrinsically-disordered Nucleoporins. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/95846

Chicago Manual of Style (16th Edition):

Gu, Chad. “Coarse-grained Theory and Simulation of Assemblies of Intrinsically-disordered Nucleoporins.” 2019. Doctoral Dissertation, University of Toronto. Accessed July 15, 2020. http://hdl.handle.net/1807/95846.

MLA Handbook (7th Edition):

Gu, Chad. “Coarse-grained Theory and Simulation of Assemblies of Intrinsically-disordered Nucleoporins.” 2019. Web. 15 Jul 2020.

Vancouver:

Gu C. Coarse-grained Theory and Simulation of Assemblies of Intrinsically-disordered Nucleoporins. [Internet] [Doctoral dissertation]. University of Toronto; 2019. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/1807/95846.

Council of Science Editors:

Gu C. Coarse-grained Theory and Simulation of Assemblies of Intrinsically-disordered Nucleoporins. [Doctoral Dissertation]. University of Toronto; 2019. Available from: http://hdl.handle.net/1807/95846


University of Texas Southwestern Medical Center

29. House, Amy Elizabeth. Formation of an Exon-Defined A Complex Spliceosome Intermediate Results in Cd45 Exon Repression.

Degree: PhD, Biological Chemistry, 2007, University of Texas Southwestern Medical Center

 Alternative splicing is a common means for genetic regulation in higher eukaryotes, and variability in splicing patterns results in a significant increase in protein diversity.… (more)

Subjects/Keywords: Alternative Splicing; Spliceosomes; Nuclear Proteins

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APA (6th Edition):

House, A. E. (2007). Formation of an Exon-Defined A Complex Spliceosome Intermediate Results in Cd45 Exon Repression. (Doctoral Dissertation). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/496

Chicago Manual of Style (16th Edition):

House, Amy Elizabeth. “Formation of an Exon-Defined A Complex Spliceosome Intermediate Results in Cd45 Exon Repression.” 2007. Doctoral Dissertation, University of Texas Southwestern Medical Center. Accessed July 15, 2020. http://hdl.handle.net/2152.5/496.

MLA Handbook (7th Edition):

House, Amy Elizabeth. “Formation of an Exon-Defined A Complex Spliceosome Intermediate Results in Cd45 Exon Repression.” 2007. Web. 15 Jul 2020.

Vancouver:

House AE. Formation of an Exon-Defined A Complex Spliceosome Intermediate Results in Cd45 Exon Repression. [Internet] [Doctoral dissertation]. University of Texas Southwestern Medical Center; 2007. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/2152.5/496.

Council of Science Editors:

House AE. Formation of an Exon-Defined A Complex Spliceosome Intermediate Results in Cd45 Exon Repression. [Doctoral Dissertation]. University of Texas Southwestern Medical Center; 2007. Available from: http://hdl.handle.net/2152.5/496


University of Texas Southwestern Medical Center

30. Wang, Zhu. Nuclear Receptor Controls Nematode Metabolism And Development: Insight Into Man’s Nemesis, the Conqueror Worm.

Degree: PhD, Biological Chemistry, 2011, University of Texas Southwestern Medical Center

 The nuclear receptor DAF-12 plays a central role in controlling the larval development of C. elegans. Activation of DAF-12 by its ligands called dafachronic acids… (more)

Subjects/Keywords: Receptors, Cytoplasmic and Nuclear; Growth and Development; Caenorhabditis elegans Proteins

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

APA (6th Edition):

Wang, Z. (2011). Nuclear Receptor Controls Nematode Metabolism And Development: Insight Into Man’s Nemesis, the Conqueror Worm. (Doctoral Dissertation). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/855

Chicago Manual of Style (16th Edition):

Wang, Zhu. “Nuclear Receptor Controls Nematode Metabolism And Development: Insight Into Man’s Nemesis, the Conqueror Worm.” 2011. Doctoral Dissertation, University of Texas Southwestern Medical Center. Accessed July 15, 2020. http://hdl.handle.net/2152.5/855.

MLA Handbook (7th Edition):

Wang, Zhu. “Nuclear Receptor Controls Nematode Metabolism And Development: Insight Into Man’s Nemesis, the Conqueror Worm.” 2011. Web. 15 Jul 2020.

Vancouver:

Wang Z. Nuclear Receptor Controls Nematode Metabolism And Development: Insight Into Man’s Nemesis, the Conqueror Worm. [Internet] [Doctoral dissertation]. University of Texas Southwestern Medical Center; 2011. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/2152.5/855.

Council of Science Editors:

Wang Z. Nuclear Receptor Controls Nematode Metabolism And Development: Insight Into Man’s Nemesis, the Conqueror Worm. [Doctoral Dissertation]. University of Texas Southwestern Medical Center; 2011. Available from: http://hdl.handle.net/2152.5/855

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