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Dept: Microbiology and Physiological Systems  Level: doctoral

You searched for subject:( GTPase Activating Proteins metabolism 60). Showing records 1 – 30 of 36 total matches.

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1. Yu, Lijian. The Role of PC4 in Oxidative Stress: A Dissertation.

Degree: Molecular Genetics and Microbiology, Microbiology and Physiological Systems, 2011, U of Massachusetts : Med

  Oxidative stress is a cellular condition where cells are challenged by elevated levels of reactive oxygen species (ROS) that are produced endogenously or exogenously.… (more)

Subjects/Keywords: Oxidative Stress; DNA Damage; DNA-Binding Proteins; Subtilisins; Proprotein Convertases; Polyadenylation; Biochemical Phenomena, Metabolism, and Nutrition; Biochemistry, Biophysics, and Structural Biology; Cells; Enzymes and Coenzymes; Genetic Phenomena

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APA (6th Edition):

Yu, L. (2011). The Role of PC4 in Oxidative Stress: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/545

Chicago Manual of Style (16th Edition):

Yu, Lijian. “The Role of PC4 in Oxidative Stress: A Dissertation.” 2011. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/545.

MLA Handbook (7th Edition):

Yu, Lijian. “The Role of PC4 in Oxidative Stress: A Dissertation.” 2011. Web. 13 Dec 2019.

Vancouver:

Yu L. The Role of PC4 in Oxidative Stress: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2011. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/545.

Council of Science Editors:

Yu L. The Role of PC4 in Oxidative Stress: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2011. Available from: https://escholarship.umassmed.edu/gsbs_diss/545

2. Hallstrom, Kelly N. The Epithelial Transmembrane Protein PERP Is Required for Inflammatory Responses to S. typhimurium Infection: A Dissertation.

Degree: Immunology and Microbiology, Microbiology and Physiological Systems, 2015, U of Massachusetts : Med

  Salmonella enterica subtype Typhimurium (S. Typhimurium) is one of many non-typhoidal Salmonella enterica strains responsible for over one million cases of salmonellosis in the… (more)

Subjects/Keywords: Bacterial Proteins; Caspase 3; Epithelial Cells; Inflammation; Membrane Proteins; Microfilament Proteins; Neutrophils; Salmonella Infections; Salmonella enterica; Salmonella typhimurium; Bacterial Infections and Mycoses; Bacteriology; Immunology of Infectious Disease; Immunopathology; Pathogenic Microbiology

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APA (6th Edition):

Hallstrom, K. N. (2015). The Epithelial Transmembrane Protein PERP Is Required for Inflammatory Responses to S. typhimurium Infection: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/807

Chicago Manual of Style (16th Edition):

Hallstrom, Kelly N. “The Epithelial Transmembrane Protein PERP Is Required for Inflammatory Responses to S. typhimurium Infection: A Dissertation.” 2015. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. http://escholarship.umassmed.edu/gsbs_diss/807.

MLA Handbook (7th Edition):

Hallstrom, Kelly N. “The Epithelial Transmembrane Protein PERP Is Required for Inflammatory Responses to S. typhimurium Infection: A Dissertation.” 2015. Web. 13 Dec 2019.

Vancouver:

Hallstrom KN. The Epithelial Transmembrane Protein PERP Is Required for Inflammatory Responses to S. typhimurium Infection: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2015. [cited 2019 Dec 13]. Available from: http://escholarship.umassmed.edu/gsbs_diss/807.

Council of Science Editors:

Hallstrom KN. The Epithelial Transmembrane Protein PERP Is Required for Inflammatory Responses to S. typhimurium Infection: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2015. Available from: http://escholarship.umassmed.edu/gsbs_diss/807

3. Hoe, Nancy Palme. Analysis of Temperature Sensing in Yersinia pestis: A Dissertation.

Degree: Molecular Genetics and Microbiology, Microbiology and Physiological Systems, 1994, U of Massachusetts : Med

  The lcrF gene of Yersinia pestis, the etiological agent of plague, encodes a transcription activator responsible for inducing expression of several virulence-related proteins (Yops)… (more)

Subjects/Keywords: Bacterial Proteins; Yersinia pestis; Amino Acids, Peptides, and Proteins; Bacteria; Genetic Phenomena

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APA (6th Edition):

Hoe, N. P. (1994). Analysis of Temperature Sensing in Yersinia pestis: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/98

Chicago Manual of Style (16th Edition):

Hoe, Nancy Palme. “Analysis of Temperature Sensing in Yersinia pestis: A Dissertation.” 1994. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/98.

MLA Handbook (7th Edition):

Hoe, Nancy Palme. “Analysis of Temperature Sensing in Yersinia pestis: A Dissertation.” 1994. Web. 13 Dec 2019.

Vancouver:

Hoe NP. Analysis of Temperature Sensing in Yersinia pestis: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1994. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/98.

Council of Science Editors:

Hoe NP. Analysis of Temperature Sensing in Yersinia pestis: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 1994. Available from: https://escholarship.umassmed.edu/gsbs_diss/98

4. Willems, Kristen N. Regulation of Humoral Immunity by Pim Kinases: A Dissertation.

Degree: Immunology and Microbiology, Microbiology and Physiological Systems, 2011, U of Massachusetts : Med

  Pim (Provirus Integration site for Moloney murine leukemia virus) kinases are a family of three serine/threonine kinases involved in cell cycle, survival and metabolism.… (more)

Subjects/Keywords: Proto-Oncogene Proteins c-pim-1; Proto-Oncogene Proteins; Protein-Serine-Threonine Kinases; Immunity; Humoral; Amino Acids, Peptides, and Proteins; Enzymes and Coenzymes; Hemic and Immune Systems; Immunology and Infectious Disease; Viruses

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APA (6th Edition):

Willems, K. N. (2011). Regulation of Humoral Immunity by Pim Kinases: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/567

Chicago Manual of Style (16th Edition):

Willems, Kristen N. “Regulation of Humoral Immunity by Pim Kinases: A Dissertation.” 2011. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/567.

MLA Handbook (7th Edition):

Willems, Kristen N. “Regulation of Humoral Immunity by Pim Kinases: A Dissertation.” 2011. Web. 13 Dec 2019.

Vancouver:

Willems KN. Regulation of Humoral Immunity by Pim Kinases: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2011. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/567.

Council of Science Editors:

Willems KN. Regulation of Humoral Immunity by Pim Kinases: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2011. Available from: https://escholarship.umassmed.edu/gsbs_diss/567

5. Rittershaus, Emily S. C. Identification of Essential Metabolic and Genetic Adaptations to the Quiescent State in Mycobacterium Tuberculosis: A Dissertation.

Degree: Molecular Genetics and Microbiology, Microbiology and Physiological Systems, 2016, U of Massachusetts : Med

  Mycobacterium tuberculosis stably adapts to respiratory limited environments by entering into a nongrowing but metabolically active state termed quiescence. This state is inherently tolerant… (more)

Subjects/Keywords: Mycobacterium tuberculosis; quiescence; metabolism; drug resistance; Bacteriology; Cellular and Molecular Physiology; Immunology of Infectious Disease; Microbial Physiology

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APA (6th Edition):

Rittershaus, E. S. C. (2016). Identification of Essential Metabolic and Genetic Adaptations to the Quiescent State in Mycobacterium Tuberculosis: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/876

Chicago Manual of Style (16th Edition):

Rittershaus, Emily S C. “Identification of Essential Metabolic and Genetic Adaptations to the Quiescent State in Mycobacterium Tuberculosis: A Dissertation.” 2016. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. http://escholarship.umassmed.edu/gsbs_diss/876.

MLA Handbook (7th Edition):

Rittershaus, Emily S C. “Identification of Essential Metabolic and Genetic Adaptations to the Quiescent State in Mycobacterium Tuberculosis: A Dissertation.” 2016. Web. 13 Dec 2019.

Vancouver:

Rittershaus ESC. Identification of Essential Metabolic and Genetic Adaptations to the Quiescent State in Mycobacterium Tuberculosis: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2016. [cited 2019 Dec 13]. Available from: http://escholarship.umassmed.edu/gsbs_diss/876.

Council of Science Editors:

Rittershaus ESC. Identification of Essential Metabolic and Genetic Adaptations to the Quiescent State in Mycobacterium Tuberculosis: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2016. Available from: http://escholarship.umassmed.edu/gsbs_diss/876

6. Corey, Elizabeth Ann. Characterization of the Relationship Between Measles Virus Fusion, Receptor Binding, and the Virus-Specific Interaction Between the Hemagglutinin and Fusion Glycoproteins: a Dissertation.

Degree: Molecular Genetics and Microbiology, Microbiology and Physiological Systems, 2006, U of Massachusetts : Med

  Measles (MV) virions, like those of other enveloped viruses, enter cells by fusing their lipid membranes with those of the target host cells. Additionally,… (more)

Subjects/Keywords: Measles; HN Protein; Membrane Fusion; Hemagglutinins; Viral Fusion Proteins; Viral Proteins; Amino Acids, Peptides, and Proteins; Cells; Chemical Actions and Uses; Lipids; Virus Diseases

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APA (6th Edition):

Corey, E. A. (2006). Characterization of the Relationship Between Measles Virus Fusion, Receptor Binding, and the Virus-Specific Interaction Between the Hemagglutinin and Fusion Glycoproteins: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/221

Chicago Manual of Style (16th Edition):

Corey, Elizabeth Ann. “Characterization of the Relationship Between Measles Virus Fusion, Receptor Binding, and the Virus-Specific Interaction Between the Hemagglutinin and Fusion Glycoproteins: a Dissertation.” 2006. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/221.

MLA Handbook (7th Edition):

Corey, Elizabeth Ann. “Characterization of the Relationship Between Measles Virus Fusion, Receptor Binding, and the Virus-Specific Interaction Between the Hemagglutinin and Fusion Glycoproteins: a Dissertation.” 2006. Web. 13 Dec 2019.

Vancouver:

Corey EA. Characterization of the Relationship Between Measles Virus Fusion, Receptor Binding, and the Virus-Specific Interaction Between the Hemagglutinin and Fusion Glycoproteins: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2006. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/221.

Council of Science Editors:

Corey EA. Characterization of the Relationship Between Measles Virus Fusion, Receptor Binding, and the Virus-Specific Interaction Between the Hemagglutinin and Fusion Glycoproteins: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2006. Available from: https://escholarship.umassmed.edu/gsbs_diss/221

7. Pantua, Homer Dadios. Requirements for Assembly and Release of Newcastle Disease Virus-Like Particles: A Dissertation.

Degree: Immunology and Microbiology, Microbiology and Physiological Systems, 2006, U of Massachusetts : Med

  The final step of paramyxovirus infection requires the assembly of viral structural components at the plasma membrane of infected cells followed by budding of… (more)

Subjects/Keywords: Newcastle disease virus; Viral Structural Proteins; Viral Fusion Proteins; Virus Assembly; Virion; Chickens; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Viruses

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APA (6th Edition):

Pantua, H. D. (2006). Requirements for Assembly and Release of Newcastle Disease Virus-Like Particles: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/242

Chicago Manual of Style (16th Edition):

Pantua, Homer Dadios. “Requirements for Assembly and Release of Newcastle Disease Virus-Like Particles: A Dissertation.” 2006. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/242.

MLA Handbook (7th Edition):

Pantua, Homer Dadios. “Requirements for Assembly and Release of Newcastle Disease Virus-Like Particles: A Dissertation.” 2006. Web. 13 Dec 2019.

Vancouver:

Pantua HD. Requirements for Assembly and Release of Newcastle Disease Virus-Like Particles: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2006. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/242.

Council of Science Editors:

Pantua HD. Requirements for Assembly and Release of Newcastle Disease Virus-Like Particles: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2006. Available from: https://escholarship.umassmed.edu/gsbs_diss/242

8. Belk, Jonathan Philip. A Characterization of Substrates and Factors Involved in Yeast Nonsense-Mediated mRNA Decay: A Dissertation.

Degree: Molecular Genetics and Microbiology, Microbiology and Physiological Systems, 2002, U of Massachusetts : Med

  Many intricate and highly conserved mechanisms have evolved to safeguard organisms against errors in gene expression. The nonsense-mediated mRNA decay pathway (NMD) exemplifies one… (more)

Subjects/Keywords: RNA-Binding Proteins; RNA Stability; Saccharomyces cerevisiae Proteins; Trans-Activators; Translation; Genetic; Amino Acids, Peptides, and Proteins; Cells; Fungi; Nucleic Acids, Nucleotides, and Nucleosides

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APA (6th Edition):

Belk, J. P. (2002). A Characterization of Substrates and Factors Involved in Yeast Nonsense-Mediated mRNA Decay: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/65

Chicago Manual of Style (16th Edition):

Belk, Jonathan Philip. “A Characterization of Substrates and Factors Involved in Yeast Nonsense-Mediated mRNA Decay: A Dissertation.” 2002. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/65.

MLA Handbook (7th Edition):

Belk, Jonathan Philip. “A Characterization of Substrates and Factors Involved in Yeast Nonsense-Mediated mRNA Decay: A Dissertation.” 2002. Web. 13 Dec 2019.

Vancouver:

Belk JP. A Characterization of Substrates and Factors Involved in Yeast Nonsense-Mediated mRNA Decay: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2002. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/65.

Council of Science Editors:

Belk JP. A Characterization of Substrates and Factors Involved in Yeast Nonsense-Mediated mRNA Decay: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2002. Available from: https://escholarship.umassmed.edu/gsbs_diss/65

9. Rogoff, Harry A. Pathways Linking Deregulated Proliferation to Apoptosis: a Dissertation.

Degree: Immunology and Microbiology, Microbiology and Physiological Systems, 2004, U of Massachusetts : Med

  Proper regulation of cellular proliferation is critical for normal development and cancer prevention. Most, if not all, cancers contain mutations in the Rb/E2F pathway,… (more)

Subjects/Keywords: Apoptosis; Cell Cycle Proteins; Retinoblastoma Protein; Signal Transduction; Transcription Factors; Tumor Suppressor Proteins; Amino Acids, Peptides, and Proteins; Cells; Eye Diseases; Neoplasms

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APA (6th Edition):

Rogoff, H. A. (2004). Pathways Linking Deregulated Proliferation to Apoptosis: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/63

Chicago Manual of Style (16th Edition):

Rogoff, Harry A. “Pathways Linking Deregulated Proliferation to Apoptosis: a Dissertation.” 2004. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/63.

MLA Handbook (7th Edition):

Rogoff, Harry A. “Pathways Linking Deregulated Proliferation to Apoptosis: a Dissertation.” 2004. Web. 13 Dec 2019.

Vancouver:

Rogoff HA. Pathways Linking Deregulated Proliferation to Apoptosis: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2004. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/63.

Council of Science Editors:

Rogoff HA. Pathways Linking Deregulated Proliferation to Apoptosis: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2004. Available from: https://escholarship.umassmed.edu/gsbs_diss/63

10. Ghosh, Shubhendu. Cross-Talk Between Factors Involved in mRNA Translation and Decay: A Dissertation.

Degree: Molecular Genetics and Microbiology, Microbiology and Physiological Systems, 2010, U of Massachusetts : Med

  The proper workings of an organism rely on the accurate expression of genes throughout its lifetime. An important determinant for protein production is the… (more)

Subjects/Keywords: RNA; Messenger; RNA Stability; Protein Biosynthesis; Amino Acids, Peptides, and Proteins; Cells; Genetic Phenomena; Nucleic Acids, Nucleotides, and Nucleosides

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APA (6th Edition):

Ghosh, S. (2010). Cross-Talk Between Factors Involved in mRNA Translation and Decay: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/454

Chicago Manual of Style (16th Edition):

Ghosh, Shubhendu. “Cross-Talk Between Factors Involved in mRNA Translation and Decay: A Dissertation.” 2010. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/454.

MLA Handbook (7th Edition):

Ghosh, Shubhendu. “Cross-Talk Between Factors Involved in mRNA Translation and Decay: A Dissertation.” 2010. Web. 13 Dec 2019.

Vancouver:

Ghosh S. Cross-Talk Between Factors Involved in mRNA Translation and Decay: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2010. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/454.

Council of Science Editors:

Ghosh S. Cross-Talk Between Factors Involved in mRNA Translation and Decay: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2010. Available from: https://escholarship.umassmed.edu/gsbs_diss/454

11. Elliott, Nathan Andrew. Prevention of Oxidative Damage by Yeast and Human OXR1: A Dissertation.

Degree: Molecular Genetics and Microbiology, Microbiology and Physiological Systems, 2004, U of Massachusetts : Med

Author did not provide abstract. Advisors/Committee Members: Michael Volkert, Ph.D..

Subjects/Keywords: Oxidation-Reduction; Oxidative Stress; Proteins; Reactive Oxygen Species; Saccharomyces cerevisiae; Amino Acids, Peptides, and Proteins; Fungi; Inorganic Chemicals

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APA (6th Edition):

Elliott, N. A. (2004). Prevention of Oxidative Damage by Yeast and Human OXR1: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/96

Chicago Manual of Style (16th Edition):

Elliott, Nathan Andrew. “Prevention of Oxidative Damage by Yeast and Human OXR1: A Dissertation.” 2004. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/96.

MLA Handbook (7th Edition):

Elliott, Nathan Andrew. “Prevention of Oxidative Damage by Yeast and Human OXR1: A Dissertation.” 2004. Web. 13 Dec 2019.

Vancouver:

Elliott NA. Prevention of Oxidative Damage by Yeast and Human OXR1: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2004. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/96.

Council of Science Editors:

Elliott NA. Prevention of Oxidative Damage by Yeast and Human OXR1: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2004. Available from: https://escholarship.umassmed.edu/gsbs_diss/96

12. Masison, Daniel C. Genetic Analysis of the Saccharomyces Cerevisiae Centromere-Binding Protein CP1: a Thesis.

Degree: Molecular Genetics and Microbiology, Microbiology and Physiological Systems, 1993, U of Massachusetts : Med

  CP1 is a sequence specific DNA-binding protein of the yeast Saccharomyces cerevisiae which recognizes the highly conserved centromere DNA element I (CDEI) of yeast… (more)

Subjects/Keywords: Centromere; DNA-Binding Proteins; Saccharomyces cerevisiae; Amino Acids, Peptides, and Proteins; Cells; Fungi; Genetic Phenomena

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APA (6th Edition):

Masison, D. C. (1993). Genetic Analysis of the Saccharomyces Cerevisiae Centromere-Binding Protein CP1: a Thesis. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/62

Chicago Manual of Style (16th Edition):

Masison, Daniel C. “Genetic Analysis of the Saccharomyces Cerevisiae Centromere-Binding Protein CP1: a Thesis.” 1993. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/62.

MLA Handbook (7th Edition):

Masison, Daniel C. “Genetic Analysis of the Saccharomyces Cerevisiae Centromere-Binding Protein CP1: a Thesis.” 1993. Web. 13 Dec 2019.

Vancouver:

Masison DC. Genetic Analysis of the Saccharomyces Cerevisiae Centromere-Binding Protein CP1: a Thesis. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1993. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/62.

Council of Science Editors:

Masison DC. Genetic Analysis of the Saccharomyces Cerevisiae Centromere-Binding Protein CP1: a Thesis. [Doctoral Dissertation]. U of Massachusetts : Med; 1993. Available from: https://escholarship.umassmed.edu/gsbs_diss/62

13. Reitter, Julie N. A Mutational Analysis of Structural Determinants Within the Newcastle Disease Virus Fusion Protein: a Dissertation.

Degree: Molecular Genetics and Microbiology, Microbiology and Physiological Systems, 1994, U of Massachusetts : Med

  The fusion protein of the Newcastle Disease Virus (NDV) contains three hydrophobic domains. To explore the topogenic signals of these domains, mutants were constructed… (more)

Subjects/Keywords: Newcastle Disease Virus; Viral Fusion Proteins; Amino Acids, Peptides, and Proteins; Animal Diseases; Animal Experimentation and Research; Genetic Phenomena; Virus Diseases

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APA (6th Edition):

Reitter, J. N. (1994). A Mutational Analysis of Structural Determinants Within the Newcastle Disease Virus Fusion Protein: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/78

Chicago Manual of Style (16th Edition):

Reitter, Julie N. “A Mutational Analysis of Structural Determinants Within the Newcastle Disease Virus Fusion Protein: a Dissertation.” 1994. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/78.

MLA Handbook (7th Edition):

Reitter, Julie N. “A Mutational Analysis of Structural Determinants Within the Newcastle Disease Virus Fusion Protein: a Dissertation.” 1994. Web. 13 Dec 2019.

Vancouver:

Reitter JN. A Mutational Analysis of Structural Determinants Within the Newcastle Disease Virus Fusion Protein: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1994. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/78.

Council of Science Editors:

Reitter JN. A Mutational Analysis of Structural Determinants Within the Newcastle Disease Virus Fusion Protein: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 1994. Available from: https://escholarship.umassmed.edu/gsbs_diss/78

14. O'Connell, Kevin F. Transcriptional Regulation by the SACCHAROMYCES CEREVISIAE Centromere-Binding Protein CP1: a Dissertation.

Degree: Molecular Genetics and Microbiology, Microbiology and Physiological Systems, 1994, U of Massachusetts : Med

  CP1 (encoded by the gene CEP1) is a sequence-specific DNA-binding protein of Saccharomyces cerevisiae that recognizes a sequence element (CDEI) found in both yeast… (more)

Subjects/Keywords: Centromere; DNA-Binding Proteins; Saccharomyces cerevisiae; Amino Acids, Peptides, and Proteins; Cells; Fungi; Genetic Phenomena

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APA (6th Edition):

O'Connell, K. F. (1994). Transcriptional Regulation by the SACCHAROMYCES CEREVISIAE Centromere-Binding Protein CP1: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/41

Chicago Manual of Style (16th Edition):

O'Connell, Kevin F. “Transcriptional Regulation by the SACCHAROMYCES CEREVISIAE Centromere-Binding Protein CP1: a Dissertation.” 1994. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/41.

MLA Handbook (7th Edition):

O'Connell, Kevin F. “Transcriptional Regulation by the SACCHAROMYCES CEREVISIAE Centromere-Binding Protein CP1: a Dissertation.” 1994. Web. 13 Dec 2019.

Vancouver:

O'Connell KF. Transcriptional Regulation by the SACCHAROMYCES CEREVISIAE Centromere-Binding Protein CP1: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1994. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/41.

Council of Science Editors:

O'Connell KF. Transcriptional Regulation by the SACCHAROMYCES CEREVISIAE Centromere-Binding Protein CP1: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 1994. Available from: https://escholarship.umassmed.edu/gsbs_diss/41

15. Castillo, Jonathan Patrick. The Role of Human Cytomegalovirus Immediate Early Proteins in Cell Growth Control: A Dissertation.

Degree: Immunology and Microbiology, Microbiology and Physiological Systems, 2002, U of Massachusetts : Med

  The proper maintenance of the pathways governing cell growth is critical to ensure cell survival and DNA fidelity. Much of our understanding of how… (more)

Subjects/Keywords: Cytomegalovirus; Immediate-Early Proteins; Protein p53; Retinoblastoma Protein; DNA Replication; S Phase; Amino Acids, Peptides, and Proteins; Cells; Genetic Phenomena; Viruses

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APA (6th Edition):

Castillo, J. P. (2002). The Role of Human Cytomegalovirus Immediate Early Proteins in Cell Growth Control: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/49

Chicago Manual of Style (16th Edition):

Castillo, Jonathan Patrick. “The Role of Human Cytomegalovirus Immediate Early Proteins in Cell Growth Control: A Dissertation.” 2002. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/49.

MLA Handbook (7th Edition):

Castillo, Jonathan Patrick. “The Role of Human Cytomegalovirus Immediate Early Proteins in Cell Growth Control: A Dissertation.” 2002. Web. 13 Dec 2019.

Vancouver:

Castillo JP. The Role of Human Cytomegalovirus Immediate Early Proteins in Cell Growth Control: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2002. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/49.

Council of Science Editors:

Castillo JP. The Role of Human Cytomegalovirus Immediate Early Proteins in Cell Growth Control: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2002. Available from: https://escholarship.umassmed.edu/gsbs_diss/49

16. Stone-Hulslander, Judith. Mechanisms of Newcastle Disease Virus-Mediated Membrane Fusion: A Dissertation.

Degree: Molecular Genetics and Microbiology, Microbiology and Physiological Systems, 1999, U of Massachusetts : Med

  For many paramyxoviruses, including Newcastle disease virus (NDV), syncytia formation requires the expression of both surface glycoproteins (HN and F) in the same cell,… (more)

Subjects/Keywords: Newcastle disease virus; Membrane Fusion; Amino Acids, Peptides, and Proteins; Carbohydrates; Viruses

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APA (6th Edition):

Stone-Hulslander, J. (1999). Mechanisms of Newcastle Disease Virus-Mediated Membrane Fusion: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/131

Chicago Manual of Style (16th Edition):

Stone-Hulslander, Judith. “Mechanisms of Newcastle Disease Virus-Mediated Membrane Fusion: A Dissertation.” 1999. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/131.

MLA Handbook (7th Edition):

Stone-Hulslander, Judith. “Mechanisms of Newcastle Disease Virus-Mediated Membrane Fusion: A Dissertation.” 1999. Web. 13 Dec 2019.

Vancouver:

Stone-Hulslander J. Mechanisms of Newcastle Disease Virus-Mediated Membrane Fusion: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1999. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/131.

Council of Science Editors:

Stone-Hulslander J. Mechanisms of Newcastle Disease Virus-Mediated Membrane Fusion: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 1999. Available from: https://escholarship.umassmed.edu/gsbs_diss/131

17. Laliberte, Jason P. Role of Host Cellular Membrane Raft Domains in the Assembly and Release of Newcastle Disease Virus: A Dissertation.

Degree: Immunology and Microbiology, Microbiology and Physiological Systems, 2008, U of Massachusetts : Med

  Newcastle disease virus (NDV) belongs to the Paramyxoviridae, a family of enveloped RNA viruses that includes many important human and animal pathogens. Although many… (more)

Subjects/Keywords: Cholesterol; HN Protein; Membrane Microdomains; Newcastle disease virus; Viral Fusion Proteins; Virus Assembly; Amino Acids, Peptides, and Proteins; Lipids; Nucleic Acids, Nucleotides, and Nucleosides; Polycyclic Compounds; Viruses

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APA (6th Edition):

Laliberte, J. P. (2008). Role of Host Cellular Membrane Raft Domains in the Assembly and Release of Newcastle Disease Virus: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/360

Chicago Manual of Style (16th Edition):

Laliberte, Jason P. “Role of Host Cellular Membrane Raft Domains in the Assembly and Release of Newcastle Disease Virus: A Dissertation.” 2008. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/360.

MLA Handbook (7th Edition):

Laliberte, Jason P. “Role of Host Cellular Membrane Raft Domains in the Assembly and Release of Newcastle Disease Virus: A Dissertation.” 2008. Web. 13 Dec 2019.

Vancouver:

Laliberte JP. Role of Host Cellular Membrane Raft Domains in the Assembly and Release of Newcastle Disease Virus: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2008. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/360.

Council of Science Editors:

Laliberte JP. Role of Host Cellular Membrane Raft Domains in the Assembly and Release of Newcastle Disease Virus: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2008. Available from: https://escholarship.umassmed.edu/gsbs_diss/360

18. Barrett, Curtis F. Modulation of N-type Calcium Channels in Rat Superior Cervical Ganglion Neurons: A Dissertation.

Degree: Cell Biology, Microbiology and Physiological Systems, 2001, U of Massachusetts : Med

  This thesis details my examination of several mechanisms for modulation of N-type calcium channels in neonatal rat superior cervical ganglion (SCG) neurons. The first… (more)

Subjects/Keywords: Calcium Channels; GTP-Binding Proteins; Superior Cervical Ganglion; Rats; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Biological Factors; Cells; Enzymes and Coenzymes; Nervous System

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APA (6th Edition):

Barrett, C. F. (2001). Modulation of N-type Calcium Channels in Rat Superior Cervical Ganglion Neurons: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/144

Chicago Manual of Style (16th Edition):

Barrett, Curtis F. “Modulation of N-type Calcium Channels in Rat Superior Cervical Ganglion Neurons: A Dissertation.” 2001. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/144.

MLA Handbook (7th Edition):

Barrett, Curtis F. “Modulation of N-type Calcium Channels in Rat Superior Cervical Ganglion Neurons: A Dissertation.” 2001. Web. 13 Dec 2019.

Vancouver:

Barrett CF. Modulation of N-type Calcium Channels in Rat Superior Cervical Ganglion Neurons: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2001. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/144.

Council of Science Editors:

Barrett CF. Modulation of N-type Calcium Channels in Rat Superior Cervical Ganglion Neurons: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2001. Available from: https://escholarship.umassmed.edu/gsbs_diss/144

19. Melanson, Vanessa R. Characterization of the Interaction Between the Attachment and Fusion Glycoproteins Required for Paramyxovirus Fusion: a Dissertation.

Degree: Molecular Genetics and Microbiology, Microbiology and Physiological Systems, 2005, U of Massachusetts : Med

  The first step of viral infection requires the binding of the viral attachment protein to cell surface receptors. Following binding, viruses penetrate the cellular… (more)

Subjects/Keywords: Paramyxovirinae; Antibodies; Monoclonal; HN Protein; Membrane Fusion; Receptors; Virus; Viral Fusion Proteins; Newcastle disease virus; Amino Acids, Peptides, and Proteins; Carbohydrates; Nucleic Acids, Nucleotides, and Nucleosides; Viruses

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APA (6th Edition):

Melanson, V. R. (2005). Characterization of the Interaction Between the Attachment and Fusion Glycoproteins Required for Paramyxovirus Fusion: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/24

Chicago Manual of Style (16th Edition):

Melanson, Vanessa R. “Characterization of the Interaction Between the Attachment and Fusion Glycoproteins Required for Paramyxovirus Fusion: a Dissertation.” 2005. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/24.

MLA Handbook (7th Edition):

Melanson, Vanessa R. “Characterization of the Interaction Between the Attachment and Fusion Glycoproteins Required for Paramyxovirus Fusion: a Dissertation.” 2005. Web. 13 Dec 2019.

Vancouver:

Melanson VR. Characterization of the Interaction Between the Attachment and Fusion Glycoproteins Required for Paramyxovirus Fusion: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2005. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/24.

Council of Science Editors:

Melanson VR. Characterization of the Interaction Between the Attachment and Fusion Glycoproteins Required for Paramyxovirus Fusion: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2005. Available from: https://escholarship.umassmed.edu/gsbs_diss/24

20. Alamares, Judith G. Newcastle Disease Virus Virulence: Mechanism of the Interferon Antagonistic Activity of the V Protein and Characterization of a Putative Virulence-Specific Antibody to the Attachment Protein: a dissertation.

Degree: Molecular Genetics and Microbiology, Microbiology and Physiological Systems, 2008, U of Massachusetts : Med

  Newcastle disease virus (NDV) is a member of the genus Avulavirus of the Paramyxoviridaefamily of enveloped negative-stranded RNA viruses. The virus causes respiratory, neurological,… (more)

Subjects/Keywords: Newcastle disease virus; Virulence; Viral Fusion Protein; Viral Proteins; HN Protein; Interferons; Amino Acids, Peptides, and Proteins; Biological Factors; Investigative Techniques; Neoplasms; Therapeutics; Viruses

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APA (6th Edition):

Alamares, J. G. (2008). Newcastle Disease Virus Virulence: Mechanism of the Interferon Antagonistic Activity of the V Protein and Characterization of a Putative Virulence-Specific Antibody to the Attachment Protein: a dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/372

Chicago Manual of Style (16th Edition):

Alamares, Judith G. “Newcastle Disease Virus Virulence: Mechanism of the Interferon Antagonistic Activity of the V Protein and Characterization of a Putative Virulence-Specific Antibody to the Attachment Protein: a dissertation.” 2008. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/372.

MLA Handbook (7th Edition):

Alamares, Judith G. “Newcastle Disease Virus Virulence: Mechanism of the Interferon Antagonistic Activity of the V Protein and Characterization of a Putative Virulence-Specific Antibody to the Attachment Protein: a dissertation.” 2008. Web. 13 Dec 2019.

Vancouver:

Alamares JG. Newcastle Disease Virus Virulence: Mechanism of the Interferon Antagonistic Activity of the V Protein and Characterization of a Putative Virulence-Specific Antibody to the Attachment Protein: a dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2008. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/372.

Council of Science Editors:

Alamares JG. Newcastle Disease Virus Virulence: Mechanism of the Interferon Antagonistic Activity of the V Protein and Characterization of a Putative Virulence-Specific Antibody to the Attachment Protein: a dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2008. Available from: https://escholarship.umassmed.edu/gsbs_diss/372

21. Jain, Surbhi. Role of Disulfide Bond Rearrangement in Newcastle Disease Virus Entry: A Dissertation.

Degree: Molecular Genetics and Microbiology, Microbiology and Physiological Systems, 2008, U of Massachusetts : Med

  Newcastle disease virus (NDV), an avian paramyxovirus, enters the host cell by fusion of viral and host cell membranes. The fusion of two membranes… (more)

Subjects/Keywords: Viral Fusion Proteins; Disulfides; Newcastle disease virus; Membrane Fusion; Protein Disulfide-Isomerase; Amino Acids, Peptides, and Proteins; Chemical Actions and Uses; Inorganic Chemicals; Organic Chemicals; Viruses

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APA (6th Edition):

Jain, S. (2008). Role of Disulfide Bond Rearrangement in Newcastle Disease Virus Entry: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/379

Chicago Manual of Style (16th Edition):

Jain, Surbhi. “Role of Disulfide Bond Rearrangement in Newcastle Disease Virus Entry: A Dissertation.” 2008. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/379.

MLA Handbook (7th Edition):

Jain, Surbhi. “Role of Disulfide Bond Rearrangement in Newcastle Disease Virus Entry: A Dissertation.” 2008. Web. 13 Dec 2019.

Vancouver:

Jain S. Role of Disulfide Bond Rearrangement in Newcastle Disease Virus Entry: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2008. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/379.

Council of Science Editors:

Jain S. Role of Disulfide Bond Rearrangement in Newcastle Disease Virus Entry: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2008. Available from: https://escholarship.umassmed.edu/gsbs_diss/379

22. Du, Ling. CIS/SOCS Proteins in Growth Hormone Action: A Dissertation.

Degree: Cell Biology, Microbiology and Physiological Systems, 2000, U of Massachusetts : Med

  CIS/SOCS (cytokine-inducible SH2 protein/suppressor of cytokine signaling) are a family of proteins that are thought to act as negative regulators of signaling by erythropoetin,… (more)

Subjects/Keywords: Immediate-Early Proteins; Suppressor of Cytokine Signaling Proteins; Human Growth Hormone; Human Growth Hormone; Cytokines; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Biological Factors; Cells; Hormones, Hormone Substitutes, and Hormone Antagonists; Nucleic Acids, Nucleotides, and Nucleosides

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APA (6th Edition):

Du, L. (2000). CIS/SOCS Proteins in Growth Hormone Action: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/92

Chicago Manual of Style (16th Edition):

Du, Ling. “CIS/SOCS Proteins in Growth Hormone Action: A Dissertation.” 2000. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/92.

MLA Handbook (7th Edition):

Du, Ling. “CIS/SOCS Proteins in Growth Hormone Action: A Dissertation.” 2000. Web. 13 Dec 2019.

Vancouver:

Du L. CIS/SOCS Proteins in Growth Hormone Action: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2000. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/92.

Council of Science Editors:

Du L. CIS/SOCS Proteins in Growth Hormone Action: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2000. Available from: https://escholarship.umassmed.edu/gsbs_diss/92

23. Dong, Shuyun. Transcript-Specific Cytoplasmic Degradation of YRA1 Pre-mRNA Mediated by the Yeast EDC3 Protein: A Dissertation.

Degree: Molecular Genetics and Microbiology, Microbiology and Physiological Systems, 2007, U of Massachusetts : Med

  mRNA degradation is a fundamental process that controls both the level and the fidelity of gene expression. Using a combination of bioinformatic, genomic, genetic,… (more)

Subjects/Keywords: Gene Expression; Cell Nucleus; Feedback; Biochemical; Nuclear Proteins; RNA Stability; RNA Precursors; RNA-Binding Proteins; Saccharomyces cerevisiae; Amino Acids, Peptides, and Proteins; Biochemistry; Bioinformatics; Cells; Computational Biology; Fungi; Genetic Phenomena; Genetics; Genetics and Genomics; Genomics; Molecular Biology; Molecular Genetics; Nucleic Acids, Nucleotides, and Nucleosides

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APA (6th Edition):

Dong, S. (2007). Transcript-Specific Cytoplasmic Degradation of YRA1 Pre-mRNA Mediated by the Yeast EDC3 Protein: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/352

Chicago Manual of Style (16th Edition):

Dong, Shuyun. “Transcript-Specific Cytoplasmic Degradation of YRA1 Pre-mRNA Mediated by the Yeast EDC3 Protein: A Dissertation.” 2007. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/352.

MLA Handbook (7th Edition):

Dong, Shuyun. “Transcript-Specific Cytoplasmic Degradation of YRA1 Pre-mRNA Mediated by the Yeast EDC3 Protein: A Dissertation.” 2007. Web. 13 Dec 2019.

Vancouver:

Dong S. Transcript-Specific Cytoplasmic Degradation of YRA1 Pre-mRNA Mediated by the Yeast EDC3 Protein: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2007. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/352.

Council of Science Editors:

Dong S. Transcript-Specific Cytoplasmic Degradation of YRA1 Pre-mRNA Mediated by the Yeast EDC3 Protein: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2007. Available from: https://escholarship.umassmed.edu/gsbs_diss/352

24. Pouliot, Kimberly Lea. Surface of Yersinia pestis: LCRV, F1 Production, Invasion and Oxygen: A Dissertation.

Degree: Molecular Genetics and Microbiology, Microbiology and Physiological Systems, 2007, U of Massachusetts : Med

  Of the eleven species of bacteria that comprise the genus Yersinia of the family Enterobacteriaceae, three species are pathogenic for humans. Yersinia pseudotuberculosis and… (more)

Subjects/Keywords: Yersinia pestis; Plague; Antigens; Bacterial; Pore Forming Cytotoxic Proteins; Toll-Like Receptor 2; Signal Transduction; Virulence Factors; Oxygen; Amino Acids, Peptides, and Proteins; Bacteria; Bacterial Infections and Mycoses; Biological Factors; Inorganic Chemicals

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APA (6th Edition):

Pouliot, K. L. (2007). Surface of Yersinia pestis: LCRV, F1 Production, Invasion and Oxygen: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/358

Chicago Manual of Style (16th Edition):

Pouliot, Kimberly Lea. “Surface of Yersinia pestis: LCRV, F1 Production, Invasion and Oxygen: A Dissertation.” 2007. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/358.

MLA Handbook (7th Edition):

Pouliot, Kimberly Lea. “Surface of Yersinia pestis: LCRV, F1 Production, Invasion and Oxygen: A Dissertation.” 2007. Web. 13 Dec 2019.

Vancouver:

Pouliot KL. Surface of Yersinia pestis: LCRV, F1 Production, Invasion and Oxygen: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2007. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/358.

Council of Science Editors:

Pouliot KL. Surface of Yersinia pestis: LCRV, F1 Production, Invasion and Oxygen: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2007. Available from: https://escholarship.umassmed.edu/gsbs_diss/358

25. Maderazo, Alan Baer. A Study on the Cellular Localization of Factors Involved in Yeast Nonsense-Mediated mRNA Decay and their Mechanisms of Control on Nonsense mRNA Translation: a Dissertation.

Degree: Molecular Genetics and Microbiology, Microbiology and Physiological Systems, 2000, U of Massachusetts : Med

  Nonsense-mediated mRNA decay (NMD) is an important mRNA surveillance mechanism conserved in eukaryotes. This thesis explores several interesting aspects of the NMD pathway. One… (more)

Subjects/Keywords: Saccharomyces cerevisiae; RNA; Messenger; Protein Biosynthesis; Amino Acids, Peptides, and Proteins; Bacteria; Cells; Nucleic Acids, Nucleotides, and Nucleosides

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APA (6th Edition):

Maderazo, A. B. (2000). A Study on the Cellular Localization of Factors Involved in Yeast Nonsense-Mediated mRNA Decay and their Mechanisms of Control on Nonsense mRNA Translation: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/105

Chicago Manual of Style (16th Edition):

Maderazo, Alan Baer. “A Study on the Cellular Localization of Factors Involved in Yeast Nonsense-Mediated mRNA Decay and their Mechanisms of Control on Nonsense mRNA Translation: a Dissertation.” 2000. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/105.

MLA Handbook (7th Edition):

Maderazo, Alan Baer. “A Study on the Cellular Localization of Factors Involved in Yeast Nonsense-Mediated mRNA Decay and their Mechanisms of Control on Nonsense mRNA Translation: a Dissertation.” 2000. Web. 13 Dec 2019.

Vancouver:

Maderazo AB. A Study on the Cellular Localization of Factors Involved in Yeast Nonsense-Mediated mRNA Decay and their Mechanisms of Control on Nonsense mRNA Translation: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2000. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/105.

Council of Science Editors:

Maderazo AB. A Study on the Cellular Localization of Factors Involved in Yeast Nonsense-Mediated mRNA Decay and their Mechanisms of Control on Nonsense mRNA Translation: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2000. Available from: https://escholarship.umassmed.edu/gsbs_diss/105

26. Pickering, Mary Theresa. Rb Inactivation Leads to E2F1-mediated DNA Double Strand Break Accumulation: A Dissertation.

Degree: Molecular Genetics and Microbiology, Microbiology and Physiological Systems, 2006, U of Massachusetts : Med

  Although it is unclear which cellular factor(s) is responsible for the genetic instability associated with initiating and sustaining cell transformation, it is known that… (more)

Subjects/Keywords: DNA Damage; E2F1 Transcription Factor; Genes; Retinoblastoma; Mutation; Amino Acids, Peptides, and Proteins; Genetic Phenomena; Neoplasms; Virus Diseases

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APA (6th Edition):

Pickering, M. T. (2006). Rb Inactivation Leads to E2F1-mediated DNA Double Strand Break Accumulation: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/26

Chicago Manual of Style (16th Edition):

Pickering, Mary Theresa. “Rb Inactivation Leads to E2F1-mediated DNA Double Strand Break Accumulation: A Dissertation.” 2006. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/26.

MLA Handbook (7th Edition):

Pickering, Mary Theresa. “Rb Inactivation Leads to E2F1-mediated DNA Double Strand Break Accumulation: A Dissertation.” 2006. Web. 13 Dec 2019.

Vancouver:

Pickering MT. Rb Inactivation Leads to E2F1-mediated DNA Double Strand Break Accumulation: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2006. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/26.

Council of Science Editors:

Pickering MT. Rb Inactivation Leads to E2F1-mediated DNA Double Strand Break Accumulation: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2006. Available from: https://escholarship.umassmed.edu/gsbs_diss/26

27. McNally, James M. Molecular Mechanisms of Neuropeptide Secretion from Neurohypophysial Terminals: a Dissertation.

Degree: Neuroscience, Microbiology and Physiological Systems, 2008, U of Massachusetts : Med

  A clear definition of the mechanisms involved in synaptic transmission is of paramount importance for the understanding of the processes governing synaptic efficacy. Despite… (more)

Subjects/Keywords: Synaptic Transmission; Presynaptic Terminals; Neurosecretory Systems; Neuropeptides; Calcium Channels; Amino Acids, Peptides, and Proteins; Nervous System

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APA (6th Edition):

McNally, J. M. (2008). Molecular Mechanisms of Neuropeptide Secretion from Neurohypophysial Terminals: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/383

Chicago Manual of Style (16th Edition):

McNally, James M. “Molecular Mechanisms of Neuropeptide Secretion from Neurohypophysial Terminals: a Dissertation.” 2008. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/383.

MLA Handbook (7th Edition):

McNally, James M. “Molecular Mechanisms of Neuropeptide Secretion from Neurohypophysial Terminals: a Dissertation.” 2008. Web. 13 Dec 2019.

Vancouver:

McNally JM. Molecular Mechanisms of Neuropeptide Secretion from Neurohypophysial Terminals: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2008. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/383.

Council of Science Editors:

McNally JM. Molecular Mechanisms of Neuropeptide Secretion from Neurohypophysial Terminals: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2008. Available from: https://escholarship.umassmed.edu/gsbs_diss/383

28. Yip, Rupert G. Signal Transduction Mechanisms for the Stimulation of Lipolysis by Growth Hormone: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Microbiology and Physiological Systems, 1994, U of Massachusetts : Med

  The purpose of this study was to investigate the mechanism of action of lipolysis by growth hormone in rat adipocytes. GH-induced lipolysis, in contrast… (more)

Subjects/Keywords: Lipolysis; Hormones; Adipocytes; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Cellular and Molecular Physiology; Hormones, Hormone Substitutes, and Hormone Antagonists

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APA (6th Edition):

Yip, R. G. (1994). Signal Transduction Mechanisms for the Stimulation of Lipolysis by Growth Hormone: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/108

Chicago Manual of Style (16th Edition):

Yip, Rupert G. “Signal Transduction Mechanisms for the Stimulation of Lipolysis by Growth Hormone: A Dissertation.” 1994. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/108.

MLA Handbook (7th Edition):

Yip, Rupert G. “Signal Transduction Mechanisms for the Stimulation of Lipolysis by Growth Hormone: A Dissertation.” 1994. Web. 13 Dec 2019.

Vancouver:

Yip RG. Signal Transduction Mechanisms for the Stimulation of Lipolysis by Growth Hormone: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1994. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/108.

Council of Science Editors:

Yip RG. Signal Transduction Mechanisms for the Stimulation of Lipolysis by Growth Hormone: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 1994. Available from: https://escholarship.umassmed.edu/gsbs_diss/108

29. Schmidt, Madelyn R. Virus-Lymphocyte Interactions: Virus Expression Is Differentially Modulated by B Cell Activation Signals: A Dissertation.

Degree: Molecular Genetics and Microbiology, Microbiology and Physiological Systems, 1991, U of Massachusetts : Med

  It is shown here that the ability of B lymphocytes to act as supportive host cells for virus infections requires they be activated from… (more)

Subjects/Keywords: Cell Communication; B-Lymphocytes; Viruses; Newcastle Disease Virus; Amino Acids, Peptides, and Proteins; Animal Diseases; Cells; Hemic and Immune Systems; Stomatognathic Diseases; Virus Diseases

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

APA (6th Edition):

Schmidt, M. R. (1991). Virus-Lymphocyte Interactions: Virus Expression Is Differentially Modulated by B Cell Activation Signals: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/51

Chicago Manual of Style (16th Edition):

Schmidt, Madelyn R. “Virus-Lymphocyte Interactions: Virus Expression Is Differentially Modulated by B Cell Activation Signals: A Dissertation.” 1991. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/51.

MLA Handbook (7th Edition):

Schmidt, Madelyn R. “Virus-Lymphocyte Interactions: Virus Expression Is Differentially Modulated by B Cell Activation Signals: A Dissertation.” 1991. Web. 13 Dec 2019.

Vancouver:

Schmidt MR. Virus-Lymphocyte Interactions: Virus Expression Is Differentially Modulated by B Cell Activation Signals: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1991. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/51.

Council of Science Editors:

Schmidt MR. Virus-Lymphocyte Interactions: Virus Expression Is Differentially Modulated by B Cell Activation Signals: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 1991. Available from: https://escholarship.umassmed.edu/gsbs_diss/51

30. George, Edward E. Regulation of β-Adrenergic-Induced Protein Phosphorylation in the Myocardium: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Microbiology and Physiological Systems, 1990, U of Massachusetts : Med

  The purpose of this investigation was to examine selected biochemical mechanisms known to influence contractility and energy metabolism in the myocardium, with particular emphasis… (more)

Subjects/Keywords: Myocardial Contraction; Myocardium; Heart; beta-Adrenergic Receptor Kinase; Phosphorylation; Rats; Sprague-Dawley; Biochemical Phenomena, Metabolism, and Nutrition; Circulatory and Respiratory Physiology; Enzymes and Coenzymes; Musculoskeletal, Neural, and Ocular Physiology

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

APA (6th Edition):

George, E. E. (1990). Regulation of β-Adrenergic-Induced Protein Phosphorylation in the Myocardium: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/228

Chicago Manual of Style (16th Edition):

George, Edward E. “Regulation of β-Adrenergic-Induced Protein Phosphorylation in the Myocardium: A Dissertation.” 1990. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 13, 2019. https://escholarship.umassmed.edu/gsbs_diss/228.

MLA Handbook (7th Edition):

George, Edward E. “Regulation of β-Adrenergic-Induced Protein Phosphorylation in the Myocardium: A Dissertation.” 1990. Web. 13 Dec 2019.

Vancouver:

George EE. Regulation of β-Adrenergic-Induced Protein Phosphorylation in the Myocardium: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1990. [cited 2019 Dec 13]. Available from: https://escholarship.umassmed.edu/gsbs_diss/228.

Council of Science Editors:

George EE. Regulation of β-Adrenergic-Induced Protein Phosphorylation in the Myocardium: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 1990. Available from: https://escholarship.umassmed.edu/gsbs_diss/228

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