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Dept: Biochemistry and Molecular Pharmacology  Level: doctoral

You searched for subject:( GTPase Activating Proteins metabolism 60). Showing records 1 – 30 of 64 total matches.

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1. Cura, Anthony J. Acute Modulation of Endothelial Cell Glucose Transport: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2010, U of Massachusetts : Med

  Studies have demonstrated that under conditions of chronic metabolic stress, GLUT1-mediated sugar transport is upregulated at the blood-brain barrier by a number of mechanisms.… (more)

Subjects/Keywords: Glucose Transporter Type 1; Endothelial Cells; Metabolism; Stress; Physiological; Amino Acids, Peptides, and Proteins; Biochemical Phenomena, Metabolism, and Nutrition; Biochemistry, Biophysics, and Structural Biology; Carbohydrates; Cells

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APA (6th Edition):

Cura, A. J. (2010). Acute Modulation of Endothelial Cell Glucose Transport: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/507

Chicago Manual of Style (16th Edition):

Cura, Anthony J. “Acute Modulation of Endothelial Cell Glucose Transport: A Dissertation.” 2010. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. https://escholarship.umassmed.edu/gsbs_diss/507.

MLA Handbook (7th Edition):

Cura, Anthony J. “Acute Modulation of Endothelial Cell Glucose Transport: A Dissertation.” 2010. Web. 06 Dec 2019.

Vancouver:

Cura AJ. Acute Modulation of Endothelial Cell Glucose Transport: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2010. [cited 2019 Dec 06]. Available from: https://escholarship.umassmed.edu/gsbs_diss/507.

Council of Science Editors:

Cura AJ. Acute Modulation of Endothelial Cell Glucose Transport: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2010. Available from: https://escholarship.umassmed.edu/gsbs_diss/507

2. Choi, Sung Hugh. The Role of Dynamic Cdk1 Phosphorylation in Chromosome Segregation in Schizosaccharomyces pombe: A Dissertation.

Degree: Interdisciplinary Graduate Program, Biochemistry and Molecular Pharmacology, 2010, U of Massachusetts : Med

  The proper transmission of genetic materials into progeny cells is crucial for maintenance of genetic integrity in eukaryotes and fundamental for reproduction of organisms.… (more)

Subjects/Keywords: Schizosaccharomyces pombe Proteins; Phosphorylation; Chromosome Segregation; Mitotic Spindle Apparatus; CDC2 Protein Kinase; Anaphase; Metaphase; Amino Acids, Peptides, and Proteins; Biochemical Phenomena, Metabolism, and Nutrition; Enzymes and Coenzymes; Fungi

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APA (6th Edition):

Choi, S. H. (2010). The Role of Dynamic Cdk1 Phosphorylation in Chromosome Segregation in Schizosaccharomyces pombe: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/453

Chicago Manual of Style (16th Edition):

Choi, Sung Hugh. “The Role of Dynamic Cdk1 Phosphorylation in Chromosome Segregation in Schizosaccharomyces pombe: A Dissertation.” 2010. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. https://escholarship.umassmed.edu/gsbs_diss/453.

MLA Handbook (7th Edition):

Choi, Sung Hugh. “The Role of Dynamic Cdk1 Phosphorylation in Chromosome Segregation in Schizosaccharomyces pombe: A Dissertation.” 2010. Web. 06 Dec 2019.

Vancouver:

Choi SH. The Role of Dynamic Cdk1 Phosphorylation in Chromosome Segregation in Schizosaccharomyces pombe: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2010. [cited 2019 Dec 06]. Available from: https://escholarship.umassmed.edu/gsbs_diss/453.

Council of Science Editors:

Choi SH. The Role of Dynamic Cdk1 Phosphorylation in Chromosome Segregation in Schizosaccharomyces pombe: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2010. Available from: https://escholarship.umassmed.edu/gsbs_diss/453

3. Bas, Tuba. Co– and Post–Translational N–Linked Glycosylation of Cardiac Potassium Channel Subunits: A Dissertation.

Degree: Interdisciplinary Graduate Program, Biochemistry and Molecular Pharmacology, 2010, U of Massachusetts : Med

  KCNE1 (E1) peptide is the founding member of the KCNE family (1-5), which is a class of type I transmembrane ß-subunits. KCNE1 peptides assemble… (more)

Subjects/Keywords: Potassium Channels; Potassium Channels; Voltage-Gated; Glycosylation; N-Glycosyl Hydrolases; Amino Acids, Peptides, and Proteins; Biochemical Phenomena, Metabolism, and Nutrition; Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Enzymes and Coenzymes; Genetic Phenomena; Inorganic Chemicals; Pathological Conditions, Signs and Symptoms

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APA (6th Edition):

Bas, T. (2010). Co– and Post–Translational N–Linked Glycosylation of Cardiac Potassium Channel Subunits: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/490

Chicago Manual of Style (16th Edition):

Bas, Tuba. “Co– and Post–Translational N–Linked Glycosylation of Cardiac Potassium Channel Subunits: A Dissertation.” 2010. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. https://escholarship.umassmed.edu/gsbs_diss/490.

MLA Handbook (7th Edition):

Bas, Tuba. “Co– and Post–Translational N–Linked Glycosylation of Cardiac Potassium Channel Subunits: A Dissertation.” 2010. Web. 06 Dec 2019.

Vancouver:

Bas T. Co– and Post–Translational N–Linked Glycosylation of Cardiac Potassium Channel Subunits: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2010. [cited 2019 Dec 06]. Available from: https://escholarship.umassmed.edu/gsbs_diss/490.

Council of Science Editors:

Bas T. Co– and Post–Translational N–Linked Glycosylation of Cardiac Potassium Channel Subunits: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2010. Available from: https://escholarship.umassmed.edu/gsbs_diss/490

4. Kayatekin, Can. The Coupling Between Folding, Zinc Binding, and Disulfide Bond Status of Human Cu, Zn Superoxide Dismutase: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2010, U of Massachusetts : Med

  Cu, Zn superoxide dismutase (SOD1) is a dimeric, β-sandwich, metalloenzyme responsible for the dismutation of superoxide. Mutations covering nearly 50% of the amino acid… (more)

Subjects/Keywords: Superoxide Dismutase; Amyotrophic Lateral Sclerosis; Zinc; Protein Folding; Proteostasis Deficiencies; Disulfides; Amino Acids, Peptides, and Proteins; Biochemical Phenomena, Metabolism, and Nutrition; Biochemistry, Biophysics, and Structural Biology; Enzymes and Coenzymes; Genetic Phenomena; Inorganic Chemicals; Nervous System Diseases; Nutritional and Metabolic Diseases; Organic Chemicals

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APA (6th Edition):

Kayatekin, C. (2010). The Coupling Between Folding, Zinc Binding, and Disulfide Bond Status of Human Cu, Zn Superoxide Dismutase: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/515

Chicago Manual of Style (16th Edition):

Kayatekin, Can. “The Coupling Between Folding, Zinc Binding, and Disulfide Bond Status of Human Cu, Zn Superoxide Dismutase: A Dissertation.” 2010. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. https://escholarship.umassmed.edu/gsbs_diss/515.

MLA Handbook (7th Edition):

Kayatekin, Can. “The Coupling Between Folding, Zinc Binding, and Disulfide Bond Status of Human Cu, Zn Superoxide Dismutase: A Dissertation.” 2010. Web. 06 Dec 2019.

Vancouver:

Kayatekin C. The Coupling Between Folding, Zinc Binding, and Disulfide Bond Status of Human Cu, Zn Superoxide Dismutase: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2010. [cited 2019 Dec 06]. Available from: https://escholarship.umassmed.edu/gsbs_diss/515.

Council of Science Editors:

Kayatekin C. The Coupling Between Folding, Zinc Binding, and Disulfide Bond Status of Human Cu, Zn Superoxide Dismutase: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2010. Available from: https://escholarship.umassmed.edu/gsbs_diss/515

5. Chacko, Benoy M. The Structural Basis for the Phosphorylation-Induced Activation of Smad Proteins: a Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2004, U of Massachusetts : Med

  The Smad proteins transduce the signal of transforming growth factor-β (TGF-β) and related factors from the cell surface to the nucleus. Following C-terminal phosphorylation… (more)

Subjects/Keywords: DNA-Binding Proteins; Phosphorylation; Signal Transduction; Trans-Activators; Transforming Growth Factor beta; Amino Acids, Peptides, and Proteins; Biochemical Phenomena, Metabolism, and Nutrition; Cells; Enzymes and Coenzymes; Genetic Phenomena; Investigative Techniques

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APA (6th Edition):

Chacko, B. M. (2004). The Structural Basis for the Phosphorylation-Induced Activation of Smad Proteins: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/161

Chicago Manual of Style (16th Edition):

Chacko, Benoy M. “The Structural Basis for the Phosphorylation-Induced Activation of Smad Proteins: a Dissertation.” 2004. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. https://escholarship.umassmed.edu/gsbs_diss/161.

MLA Handbook (7th Edition):

Chacko, Benoy M. “The Structural Basis for the Phosphorylation-Induced Activation of Smad Proteins: a Dissertation.” 2004. Web. 06 Dec 2019.

Vancouver:

Chacko BM. The Structural Basis for the Phosphorylation-Induced Activation of Smad Proteins: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2004. [cited 2019 Dec 06]. Available from: https://escholarship.umassmed.edu/gsbs_diss/161.

Council of Science Editors:

Chacko BM. The Structural Basis for the Phosphorylation-Induced Activation of Smad Proteins: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2004. Available from: https://escholarship.umassmed.edu/gsbs_diss/161

6. Brewer, Daniel Niron. Elucidation of the Role of the Exocyst Subunit Sec6p in Exocytosis: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2009, U of Massachusetts : Med

  Trafficking of protein and lipid cargo through the secretory pathway in eukaryotic cells is mediated by membrane-bound vesicles. Secretory vesicles are targeted to sites… (more)

Subjects/Keywords: SNARE Proteins; Vesicular Transport Proteins; Exocytosis; Amino Acids, Peptides, and Proteins; Cells; Genetic Phenomena

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APA (6th Edition):

Brewer, D. N. (2009). Elucidation of the Role of the Exocyst Subunit Sec6p in Exocytosis: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/446

Chicago Manual of Style (16th Edition):

Brewer, Daniel Niron. “Elucidation of the Role of the Exocyst Subunit Sec6p in Exocytosis: A Dissertation.” 2009. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. https://escholarship.umassmed.edu/gsbs_diss/446.

MLA Handbook (7th Edition):

Brewer, Daniel Niron. “Elucidation of the Role of the Exocyst Subunit Sec6p in Exocytosis: A Dissertation.” 2009. Web. 06 Dec 2019.

Vancouver:

Brewer DN. Elucidation of the Role of the Exocyst Subunit Sec6p in Exocytosis: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2009. [cited 2019 Dec 06]. Available from: https://escholarship.umassmed.edu/gsbs_diss/446.

Council of Science Editors:

Brewer DN. Elucidation of the Role of the Exocyst Subunit Sec6p in Exocytosis: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2009. Available from: https://escholarship.umassmed.edu/gsbs_diss/446

7. Kaymak, Ebru. Understanding the Sequence-Specificity and RNA Target Recognition Properties of the Oocyte Maturation Factor, OMA-1, in Caenorhabditis elegans: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2016, U of Massachusetts : Med

  Maternally supplied mRNAs encode for necessary developmental regulators that pattern early embryos in many species until zygotic transcription is activated. In Caenorhabditis elegans, post-transcriptional… (more)

Subjects/Keywords: Caenorhabditis elegans Proteins; Carrier Proteins; Oocytes; Oogenesis; Messenger RNA; RNA-Binding Proteins; Oocyte Maturation Factors; OMA-1; Cell Biology; Developmental Biology

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APA (6th Edition):

Kaymak, E. (2016). Understanding the Sequence-Specificity and RNA Target Recognition Properties of the Oocyte Maturation Factor, OMA-1, in Caenorhabditis elegans: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/852

Chicago Manual of Style (16th Edition):

Kaymak, Ebru. “Understanding the Sequence-Specificity and RNA Target Recognition Properties of the Oocyte Maturation Factor, OMA-1, in Caenorhabditis elegans: A Dissertation.” 2016. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. http://escholarship.umassmed.edu/gsbs_diss/852.

MLA Handbook (7th Edition):

Kaymak, Ebru. “Understanding the Sequence-Specificity and RNA Target Recognition Properties of the Oocyte Maturation Factor, OMA-1, in Caenorhabditis elegans: A Dissertation.” 2016. Web. 06 Dec 2019.

Vancouver:

Kaymak E. Understanding the Sequence-Specificity and RNA Target Recognition Properties of the Oocyte Maturation Factor, OMA-1, in Caenorhabditis elegans: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2016. [cited 2019 Dec 06]. Available from: http://escholarship.umassmed.edu/gsbs_diss/852.

Council of Science Editors:

Kaymak E. Understanding the Sequence-Specificity and RNA Target Recognition Properties of the Oocyte Maturation Factor, OMA-1, in Caenorhabditis elegans: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2016. Available from: http://escholarship.umassmed.edu/gsbs_diss/852

8. Gupta, Sneha. Understanding Regulation of the Cytoskeleton during Cell Cycle Transitions through Examination of Crosstalk between Homologous Fission Yeast Pathways, Septation Initiation Network and Morphogenesis ORB6 Network: A Dissertation.

Degree: Interdisciplinary Graduate Program, Biochemistry and Molecular Pharmacology, 2013, U of Massachusetts : Med

  The fission yeast Schizosaccharomyces pombe has become a powerful model system for studying cytokinesis, a process of cytoplasmic division by which one cell divides… (more)

Subjects/Keywords: Cytokinesis; Cell Cycle; Cell Cycle Proteins; Cytoskeleton; Cytoskeletal Proteins; Schizosaccharomyces; Schizosaccharomyces pombe Proteins; Cellular and Molecular Physiology

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APA (6th Edition):

Gupta, S. (2013). Understanding Regulation of the Cytoskeleton during Cell Cycle Transitions through Examination of Crosstalk between Homologous Fission Yeast Pathways, Septation Initiation Network and Morphogenesis ORB6 Network: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/693

Chicago Manual of Style (16th Edition):

Gupta, Sneha. “Understanding Regulation of the Cytoskeleton during Cell Cycle Transitions through Examination of Crosstalk between Homologous Fission Yeast Pathways, Septation Initiation Network and Morphogenesis ORB6 Network: A Dissertation.” 2013. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. http://escholarship.umassmed.edu/gsbs_diss/693.

MLA Handbook (7th Edition):

Gupta, Sneha. “Understanding Regulation of the Cytoskeleton during Cell Cycle Transitions through Examination of Crosstalk between Homologous Fission Yeast Pathways, Septation Initiation Network and Morphogenesis ORB6 Network: A Dissertation.” 2013. Web. 06 Dec 2019.

Vancouver:

Gupta S. Understanding Regulation of the Cytoskeleton during Cell Cycle Transitions through Examination of Crosstalk between Homologous Fission Yeast Pathways, Septation Initiation Network and Morphogenesis ORB6 Network: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2013. [cited 2019 Dec 06]. Available from: http://escholarship.umassmed.edu/gsbs_diss/693.

Council of Science Editors:

Gupta S. Understanding Regulation of the Cytoskeleton during Cell Cycle Transitions through Examination of Crosstalk between Homologous Fission Yeast Pathways, Septation Initiation Network and Morphogenesis ORB6 Network: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2013. Available from: http://escholarship.umassmed.edu/gsbs_diss/693

9. Dubuke, Michelle L. The Exocyst Subunit Sec6 Interacts with Assembled Exocytic Snare Complexes: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2015, U of Massachusetts : Med

  In eukaryotic cells, membrane-bound vesicles carry cargo between intracellular compartments, to and from the cell surface, and to the extracellular environment. Many conserved families… (more)

Subjects/Keywords: SNARE Proteins; Saccharomyces cerevisiae Proteins; Vesicular Transport Proteins; Exocysts; Exocyst Subunit Sec6; Biochemistry; Cell and Developmental Biology; Molecular Biology

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APA (6th Edition):

Dubuke, M. L. (2015). The Exocyst Subunit Sec6 Interacts with Assembled Exocytic Snare Complexes: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/868

Chicago Manual of Style (16th Edition):

Dubuke, Michelle L. “The Exocyst Subunit Sec6 Interacts with Assembled Exocytic Snare Complexes: A Dissertation.” 2015. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. http://escholarship.umassmed.edu/gsbs_diss/868.

MLA Handbook (7th Edition):

Dubuke, Michelle L. “The Exocyst Subunit Sec6 Interacts with Assembled Exocytic Snare Complexes: A Dissertation.” 2015. Web. 06 Dec 2019.

Vancouver:

Dubuke ML. The Exocyst Subunit Sec6 Interacts with Assembled Exocytic Snare Complexes: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2015. [cited 2019 Dec 06]. Available from: http://escholarship.umassmed.edu/gsbs_diss/868.

Council of Science Editors:

Dubuke ML. The Exocyst Subunit Sec6 Interacts with Assembled Exocytic Snare Complexes: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2015. Available from: http://escholarship.umassmed.edu/gsbs_diss/868

10. Miele, Adriana. Analysis of Long-Range Chromosomal Interactions in Saccharomyces cerevisiae: A Dissertation.

Degree: Interdisciplinary Graduate Program, Biochemistry and Molecular Pharmacology, 2009, U of Massachusetts : Med

  Long-range chromosomal interactions have been discovered in a number of organisms, suggesting that gene regulation through direct physical association with regulatory elements and/or other… (more)

Subjects/Keywords: Gene Expression Regulation; Chromosomes; Nuclear Proteins; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins; Transcription; Genetic; Amino Acids, Peptides, and Proteins; Cells; Fungi; Genetic Phenomena

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APA (6th Edition):

Miele, A. (2009). Analysis of Long-Range Chromosomal Interactions in Saccharomyces cerevisiae: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/413

Chicago Manual of Style (16th Edition):

Miele, Adriana. “Analysis of Long-Range Chromosomal Interactions in Saccharomyces cerevisiae: A Dissertation.” 2009. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. https://escholarship.umassmed.edu/gsbs_diss/413.

MLA Handbook (7th Edition):

Miele, Adriana. “Analysis of Long-Range Chromosomal Interactions in Saccharomyces cerevisiae: A Dissertation.” 2009. Web. 06 Dec 2019.

Vancouver:

Miele A. Analysis of Long-Range Chromosomal Interactions in Saccharomyces cerevisiae: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2009. [cited 2019 Dec 06]. Available from: https://escholarship.umassmed.edu/gsbs_diss/413.

Council of Science Editors:

Miele A. Analysis of Long-Range Chromosomal Interactions in Saccharomyces cerevisiae: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2009. Available from: https://escholarship.umassmed.edu/gsbs_diss/413

11. Willis, Nicholas Adrian. Checkpoint Regulation of Replication Forks in Response to DNA Damage: A Dissertation.

Degree: Interdisciplinary Graduate Program, Biochemistry and Molecular Pharmacology, 2009, U of Massachusetts : Med

  Faithful duplication and segregation of undamaged DNA is critical to the survival of all organisms and prevention of oncogenesis in multicellular organisms. To ensure… (more)

Subjects/Keywords: DNA Damage; DNA Helicases; DNA-Binding Proteins; Endonucleases; S Phase; Schizosaccharomyces; Schizosaccharomyces pombe Proteins; RecQ Helicases; Amino Acids, Peptides, and Proteins; Enzymes and Coenzymes; Fungi; Genetic Phenomena

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APA (6th Edition):

Willis, N. A. (2009). Checkpoint Regulation of Replication Forks in Response to DNA Damage: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/427

Chicago Manual of Style (16th Edition):

Willis, Nicholas Adrian. “Checkpoint Regulation of Replication Forks in Response to DNA Damage: A Dissertation.” 2009. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. https://escholarship.umassmed.edu/gsbs_diss/427.

MLA Handbook (7th Edition):

Willis, Nicholas Adrian. “Checkpoint Regulation of Replication Forks in Response to DNA Damage: A Dissertation.” 2009. Web. 06 Dec 2019.

Vancouver:

Willis NA. Checkpoint Regulation of Replication Forks in Response to DNA Damage: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2009. [cited 2019 Dec 06]. Available from: https://escholarship.umassmed.edu/gsbs_diss/427.

Council of Science Editors:

Willis NA. Checkpoint Regulation of Replication Forks in Response to DNA Damage: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2009. Available from: https://escholarship.umassmed.edu/gsbs_diss/427

12. Clingman, Carina C. A Feedback Loop Couples Musashi-1 Activity to Omega-9 Fatty Acid Biosynthesis: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2014, U of Massachusetts : Med

  All living creatures change their gene expression program in response to nutrient availability and metabolic demands. Nutrients and metabolites can directly control transcription and… (more)

Subjects/Keywords: Fatty Acids; Gene Expression Regulation; RNA; RNA-Binding Proteins; Stem Cells; Amino Acids, Peptides, and Proteins; Biochemistry; Molecular Biology

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APA (6th Edition):

Clingman, C. C. (2014). A Feedback Loop Couples Musashi-1 Activity to Omega-9 Fatty Acid Biosynthesis: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/718

Chicago Manual of Style (16th Edition):

Clingman, Carina C. “A Feedback Loop Couples Musashi-1 Activity to Omega-9 Fatty Acid Biosynthesis: A Dissertation.” 2014. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. http://escholarship.umassmed.edu/gsbs_diss/718.

MLA Handbook (7th Edition):

Clingman, Carina C. “A Feedback Loop Couples Musashi-1 Activity to Omega-9 Fatty Acid Biosynthesis: A Dissertation.” 2014. Web. 06 Dec 2019.

Vancouver:

Clingman CC. A Feedback Loop Couples Musashi-1 Activity to Omega-9 Fatty Acid Biosynthesis: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2014. [cited 2019 Dec 06]. Available from: http://escholarship.umassmed.edu/gsbs_diss/718.

Council of Science Editors:

Clingman CC. A Feedback Loop Couples Musashi-1 Activity to Omega-9 Fatty Acid Biosynthesis: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2014. Available from: http://escholarship.umassmed.edu/gsbs_diss/718

13. Duffy, Caroline M. Structural Mechanisms of the Sliding Clamp and Sliding Clamp Loader: Insights into Disease and Function: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2016, U of Massachusetts : Med

  Chromosomal replication is an essential process in all life. This dissertation highlights regulatory roles for two critical protein complexes at the heart of the… (more)

Subjects/Keywords: DNA Replication; DNA-Binding Proteins; DNA Primers; Amino Acids, Peptides, and Proteins; Biochemistry; Molecular Biology; Structural Biology

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APA (6th Edition):

Duffy, C. M. (2016). Structural Mechanisms of the Sliding Clamp and Sliding Clamp Loader: Insights into Disease and Function: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/844

Chicago Manual of Style (16th Edition):

Duffy, Caroline M. “Structural Mechanisms of the Sliding Clamp and Sliding Clamp Loader: Insights into Disease and Function: A Dissertation.” 2016. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. http://escholarship.umassmed.edu/gsbs_diss/844.

MLA Handbook (7th Edition):

Duffy, Caroline M. “Structural Mechanisms of the Sliding Clamp and Sliding Clamp Loader: Insights into Disease and Function: A Dissertation.” 2016. Web. 06 Dec 2019.

Vancouver:

Duffy CM. Structural Mechanisms of the Sliding Clamp and Sliding Clamp Loader: Insights into Disease and Function: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2016. [cited 2019 Dec 06]. Available from: http://escholarship.umassmed.edu/gsbs_diss/844.

Council of Science Editors:

Duffy CM. Structural Mechanisms of the Sliding Clamp and Sliding Clamp Loader: Insights into Disease and Function: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2016. Available from: http://escholarship.umassmed.edu/gsbs_diss/844

14. Weicksel, Steven E. hox Gene Regulation and Function During Zebrafish Embryogenesis: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2013, U of Massachusetts : Med

  Hox genes encode a conserved family of homeodomain containing transcription factors essential for metazoan development. The establishment of overlapping Hox expression domains specifies tissue… (more)

Subjects/Keywords: Homeobox Genes; Homeodomain Proteins; Zebrafish; Zebrafish Proteins; Embryonic Development; Nucleosomes; Developmental Gene Expression Regulation; Developmental Biology; Genetics; Genomics; Molecular Genetics

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APA (6th Edition):

Weicksel, S. E. (2013). hox Gene Regulation and Function During Zebrafish Embryogenesis: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/692

Chicago Manual of Style (16th Edition):

Weicksel, Steven E. “hox Gene Regulation and Function During Zebrafish Embryogenesis: A Dissertation.” 2013. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. http://escholarship.umassmed.edu/gsbs_diss/692.

MLA Handbook (7th Edition):

Weicksel, Steven E. “hox Gene Regulation and Function During Zebrafish Embryogenesis: A Dissertation.” 2013. Web. 06 Dec 2019.

Vancouver:

Weicksel SE. hox Gene Regulation and Function During Zebrafish Embryogenesis: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2013. [cited 2019 Dec 06]. Available from: http://escholarship.umassmed.edu/gsbs_diss/692.

Council of Science Editors:

Weicksel SE. hox Gene Regulation and Function During Zebrafish Embryogenesis: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2013. Available from: http://escholarship.umassmed.edu/gsbs_diss/692

15. Alexa, Kristen M. Endoderm Patterning in Zebrafish: Pancreas Development: A Dissertation.

Degree: Interdisciplinary Graduate Program, Biochemistry and Molecular Pharmacology, 2009, U of Massachusetts : Med

  The pancreas is located below the liver and adjacent to the small intestine where it connects to the duodenum. It consists of exocrine and… (more)

Subjects/Keywords: Zebrafish; Zebrafish Proteins; Pancreas; Endoderm; SOX Transcription Factors; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Digestive System; Embryonic Structures

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APA (6th Edition):

Alexa, K. M. (2009). Endoderm Patterning in Zebrafish: Pancreas Development: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/450

Chicago Manual of Style (16th Edition):

Alexa, Kristen M. “Endoderm Patterning in Zebrafish: Pancreas Development: A Dissertation.” 2009. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. https://escholarship.umassmed.edu/gsbs_diss/450.

MLA Handbook (7th Edition):

Alexa, Kristen M. “Endoderm Patterning in Zebrafish: Pancreas Development: A Dissertation.” 2009. Web. 06 Dec 2019.

Vancouver:

Alexa KM. Endoderm Patterning in Zebrafish: Pancreas Development: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2009. [cited 2019 Dec 06]. Available from: https://escholarship.umassmed.edu/gsbs_diss/450.

Council of Science Editors:

Alexa KM. Endoderm Patterning in Zebrafish: Pancreas Development: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2009. Available from: https://escholarship.umassmed.edu/gsbs_diss/450

16. Ray, Samriddha. Elucidation of the Multi-Faceted Roles of the SIN (Septation Initiation Network); Understanding How the SIN Promotes Cytokinesis and Inhibits Interphase Growth in the Fission Yeast Schizosaccharomyces pombe: A Dissertation.

Degree: Interdisciplinary Graduate Program, Biochemistry and Molecular Pharmacology, 2010, U of Massachusetts : Med

  Cytokinesis is the cytoplasmic division of one cell into two independent daughter cells. Precise regulation of cytokinesis during cell cycle is essential for healthy… (more)

Subjects/Keywords: Cytokinesis; Schizosaccharomyces pombe Proteins; Signal Transduction; Amino Acids, Peptides, and Proteins; Cell and Developmental Biology; Cells; Fungi; Genetic Phenomena

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APA (6th Edition):

Ray, S. (2010). Elucidation of the Multi-Faceted Roles of the SIN (Septation Initiation Network); Understanding How the SIN Promotes Cytokinesis and Inhibits Interphase Growth in the Fission Yeast Schizosaccharomyces pombe: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/482

Chicago Manual of Style (16th Edition):

Ray, Samriddha. “Elucidation of the Multi-Faceted Roles of the SIN (Septation Initiation Network); Understanding How the SIN Promotes Cytokinesis and Inhibits Interphase Growth in the Fission Yeast Schizosaccharomyces pombe: A Dissertation.” 2010. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. https://escholarship.umassmed.edu/gsbs_diss/482.

MLA Handbook (7th Edition):

Ray, Samriddha. “Elucidation of the Multi-Faceted Roles of the SIN (Septation Initiation Network); Understanding How the SIN Promotes Cytokinesis and Inhibits Interphase Growth in the Fission Yeast Schizosaccharomyces pombe: A Dissertation.” 2010. Web. 06 Dec 2019.

Vancouver:

Ray S. Elucidation of the Multi-Faceted Roles of the SIN (Septation Initiation Network); Understanding How the SIN Promotes Cytokinesis and Inhibits Interphase Growth in the Fission Yeast Schizosaccharomyces pombe: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2010. [cited 2019 Dec 06]. Available from: https://escholarship.umassmed.edu/gsbs_diss/482.

Council of Science Editors:

Ray S. Elucidation of the Multi-Faceted Roles of the SIN (Septation Initiation Network); Understanding How the SIN Promotes Cytokinesis and Inhibits Interphase Growth in the Fission Yeast Schizosaccharomyces pombe: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2010. Available from: https://escholarship.umassmed.edu/gsbs_diss/482

17. Mofford, David M. Pushing The Boundaries of Bioluminescence Using Synthetic Luciferins: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2015, U of Massachusetts : Med

  Fireflies are beetles that generate yellow-green light when their luciferase enzyme activates and oxidizes its substrate, D-luciferin. This bioluminescent reaction is widely used as… (more)

Subjects/Keywords: Fireflies; Luciferases; Luminescent Proteins; Benzothiazoles; Biochemistry; Biology; Molecular Biology

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APA (6th Edition):

Mofford, D. M. (2015). Pushing The Boundaries of Bioluminescence Using Synthetic Luciferins: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/794

Chicago Manual of Style (16th Edition):

Mofford, David M. “Pushing The Boundaries of Bioluminescence Using Synthetic Luciferins: A Dissertation.” 2015. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. http://escholarship.umassmed.edu/gsbs_diss/794.

MLA Handbook (7th Edition):

Mofford, David M. “Pushing The Boundaries of Bioluminescence Using Synthetic Luciferins: A Dissertation.” 2015. Web. 06 Dec 2019.

Vancouver:

Mofford DM. Pushing The Boundaries of Bioluminescence Using Synthetic Luciferins: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2015. [cited 2019 Dec 06]. Available from: http://escholarship.umassmed.edu/gsbs_diss/794.

Council of Science Editors:

Mofford DM. Pushing The Boundaries of Bioluminescence Using Synthetic Luciferins: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2015. Available from: http://escholarship.umassmed.edu/gsbs_diss/794

18. Choe, Seong-Kyu. Essential Roles of the Meis Family Proteins During Segmentation of the Zebrafish Hindbrain : a Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2003, U of Massachusetts : Med

  Hindbrain patterning requires many factors involved in early segmentation and later segment identity of the specific domains of the hindbrain. Hox proteins and their… (more)

Subjects/Keywords: Zebrafish; Rhombencephalon; Gene Expression Regulation; Developmental; Zebrafish Proteins; Homeodomain Proteins; Homeodomain Proteins; Amino Acids, Peptides, and Proteins; Biochemistry; Nervous System

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APA (6th Edition):

Choe, S. (2003). Essential Roles of the Meis Family Proteins During Segmentation of the Zebrafish Hindbrain : a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/7

Chicago Manual of Style (16th Edition):

Choe, Seong-Kyu. “Essential Roles of the Meis Family Proteins During Segmentation of the Zebrafish Hindbrain : a Dissertation.” 2003. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. https://escholarship.umassmed.edu/gsbs_diss/7.

MLA Handbook (7th Edition):

Choe, Seong-Kyu. “Essential Roles of the Meis Family Proteins During Segmentation of the Zebrafish Hindbrain : a Dissertation.” 2003. Web. 06 Dec 2019.

Vancouver:

Choe S. Essential Roles of the Meis Family Proteins During Segmentation of the Zebrafish Hindbrain : a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2003. [cited 2019 Dec 06]. Available from: https://escholarship.umassmed.edu/gsbs_diss/7.

Council of Science Editors:

Choe S. Essential Roles of the Meis Family Proteins During Segmentation of the Zebrafish Hindbrain : a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2003. Available from: https://escholarship.umassmed.edu/gsbs_diss/7

19. Deveau, Laura M. Characterizing the Disorder in Tristetraprolin and its Contribution to Post-Transcriptional Gene Regulation: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2016, U of Massachusetts : Med

  RNA-binding proteins (RBPs) are important for a wide variety of biological processes involved in gene regulation. However, the structural and dynamic contributions to their… (more)

Subjects/Keywords: RNA-Binding Proteins; Tristetraprolin; Zinc Fingers; Messenger RNA; Post-Transcriptional Gene Regulation; Amino Acids, Peptides, and Proteins; Biochemistry; Biophysics; Molecular Biology; Structural Biology

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APA (6th Edition):

Deveau, L. M. (2016). Characterizing the Disorder in Tristetraprolin and its Contribution to Post-Transcriptional Gene Regulation: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/855

Chicago Manual of Style (16th Edition):

Deveau, Laura M. “Characterizing the Disorder in Tristetraprolin and its Contribution to Post-Transcriptional Gene Regulation: A Dissertation.” 2016. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. http://escholarship.umassmed.edu/gsbs_diss/855.

MLA Handbook (7th Edition):

Deveau, Laura M. “Characterizing the Disorder in Tristetraprolin and its Contribution to Post-Transcriptional Gene Regulation: A Dissertation.” 2016. Web. 06 Dec 2019.

Vancouver:

Deveau LM. Characterizing the Disorder in Tristetraprolin and its Contribution to Post-Transcriptional Gene Regulation: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2016. [cited 2019 Dec 06]. Available from: http://escholarship.umassmed.edu/gsbs_diss/855.

Council of Science Editors:

Deveau LM. Characterizing the Disorder in Tristetraprolin and its Contribution to Post-Transcriptional Gene Regulation: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2016. Available from: http://escholarship.umassmed.edu/gsbs_diss/855

20. Bhaduri, Samyabrata. Regulation of CDK1 Activity during the G1/S Transition in S. cerevisiae through Specific Cyclin-Substrate Docking: A Dissertation.

Degree: Interdisciplinary Graduate Program, Biochemistry and Molecular Pharmacology, 2014, U of Massachusetts : Med

  Several cell cycle events require specific forms of the cyclin-CDK complexes. It has been known for some time that cyclins not only contribute by… (more)

Subjects/Keywords: Cell Cycle; Cell Cycle Proteins; Saccharomyces cerevisiae Proteins; Cyclin B; Cyclin G1; Cyclins; Cyclin-Dependent Kinases; CDC2 Protein; Biochemistry; Cell Biology; Molecular Biology

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APA (6th Edition):

Bhaduri, S. (2014). Regulation of CDK1 Activity during the G1/S Transition in S. cerevisiae through Specific Cyclin-Substrate Docking: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/871

Chicago Manual of Style (16th Edition):

Bhaduri, Samyabrata. “Regulation of CDK1 Activity during the G1/S Transition in S. cerevisiae through Specific Cyclin-Substrate Docking: A Dissertation.” 2014. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. http://escholarship.umassmed.edu/gsbs_diss/871.

MLA Handbook (7th Edition):

Bhaduri, Samyabrata. “Regulation of CDK1 Activity during the G1/S Transition in S. cerevisiae through Specific Cyclin-Substrate Docking: A Dissertation.” 2014. Web. 06 Dec 2019.

Vancouver:

Bhaduri S. Regulation of CDK1 Activity during the G1/S Transition in S. cerevisiae through Specific Cyclin-Substrate Docking: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2014. [cited 2019 Dec 06]. Available from: http://escholarship.umassmed.edu/gsbs_diss/871.

Council of Science Editors:

Bhaduri S. Regulation of CDK1 Activity during the G1/S Transition in S. cerevisiae through Specific Cyclin-Substrate Docking: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2014. Available from: http://escholarship.umassmed.edu/gsbs_diss/871

21. Nobrega, Robert P. Early Folding Biases in the Folding Free-Energy Surface of βα-Repeat Proteins: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2014, U of Massachusetts : Med

  Early events in folding can determine if a protein is going to fold, misfold, or aggregate. Understanding these deterministic events is paramount for de… (more)

Subjects/Keywords: Protein Folding; Protein Engineering; Proteins; Biochemistry; Biophysics; Computational Biology; Molecular Biology; Structural Biology

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APA (6th Edition):

Nobrega, R. P. (2014). Early Folding Biases in the Folding Free-Energy Surface of βα-Repeat Proteins: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/723

Chicago Manual of Style (16th Edition):

Nobrega, Robert P. “Early Folding Biases in the Folding Free-Energy Surface of βα-Repeat Proteins: A Dissertation.” 2014. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. http://escholarship.umassmed.edu/gsbs_diss/723.

MLA Handbook (7th Edition):

Nobrega, Robert P. “Early Folding Biases in the Folding Free-Energy Surface of βα-Repeat Proteins: A Dissertation.” 2014. Web. 06 Dec 2019.

Vancouver:

Nobrega RP. Early Folding Biases in the Folding Free-Energy Surface of βα-Repeat Proteins: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2014. [cited 2019 Dec 06]. Available from: http://escholarship.umassmed.edu/gsbs_diss/723.

Council of Science Editors:

Nobrega RP. Early Folding Biases in the Folding Free-Energy Surface of βα-Repeat Proteins: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2014. Available from: http://escholarship.umassmed.edu/gsbs_diss/723

22. Runko, Alexander Peter. Function of the Zinc-Finger Repressor NLZ in the Developing Zebrafish Hindbrain: a Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2003, U of Massachusetts : Med

  Generation of the primitive neuroectoderm into specialized brain subdivisions, such as the hindbrain primordium, involves the regulated coordination of complex morphogenetic and molecular mechanisms.… (more)

Subjects/Keywords: DNA-Binding Proteins; Repressor Proteins; Rhombencephalon; Zebrafish; Zebrafish Proteins; Zinc Fingers; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Genetic Phenomena; Nervous System

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APA (6th Edition):

Runko, A. P. (2003). Function of the Zinc-Finger Repressor NLZ in the Developing Zebrafish Hindbrain: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/74

Chicago Manual of Style (16th Edition):

Runko, Alexander Peter. “Function of the Zinc-Finger Repressor NLZ in the Developing Zebrafish Hindbrain: a Dissertation.” 2003. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. https://escholarship.umassmed.edu/gsbs_diss/74.

MLA Handbook (7th Edition):

Runko, Alexander Peter. “Function of the Zinc-Finger Repressor NLZ in the Developing Zebrafish Hindbrain: a Dissertation.” 2003. Web. 06 Dec 2019.

Vancouver:

Runko AP. Function of the Zinc-Finger Repressor NLZ in the Developing Zebrafish Hindbrain: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2003. [cited 2019 Dec 06]. Available from: https://escholarship.umassmed.edu/gsbs_diss/74.

Council of Science Editors:

Runko AP. Function of the Zinc-Finger Repressor NLZ in the Developing Zebrafish Hindbrain: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2003. Available from: https://escholarship.umassmed.edu/gsbs_diss/74

23. Cheng, Wei. From Neurodegeneration to Infertility and Back - Exploring Functions of Two Genes: ARMC4 and TARDBP: A Dissertation.

Degree: Interdisciplinary Graduate Program, Biochemistry and Molecular Pharmacology, 2014, U of Massachusetts : Med

  Amyotrophic Lateral Sclerosis (ALS) is an adult-onset progressive neurodegenerative disease that causes degeneration in both upper and lower motor neurons. ALS progresses relentlessly after… (more)

Subjects/Keywords: Amyotrophic Lateral Sclerosis; DNA-Binding Proteins; Armadillo Domain Proteins; Drosophila Gudu protein; Drosophila Proteins; Spermatogenesis; Biochemistry; Cellular and Molecular Physiology; Developmental Biology; Developmental Neuroscience; Nervous System Diseases; Reproductive and Urinary Physiology

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APA (6th Edition):

Cheng, W. (2014). From Neurodegeneration to Infertility and Back - Exploring Functions of Two Genes: ARMC4 and TARDBP: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/695

Chicago Manual of Style (16th Edition):

Cheng, Wei. “From Neurodegeneration to Infertility and Back - Exploring Functions of Two Genes: ARMC4 and TARDBP: A Dissertation.” 2014. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. http://escholarship.umassmed.edu/gsbs_diss/695.

MLA Handbook (7th Edition):

Cheng, Wei. “From Neurodegeneration to Infertility and Back - Exploring Functions of Two Genes: ARMC4 and TARDBP: A Dissertation.” 2014. Web. 06 Dec 2019.

Vancouver:

Cheng W. From Neurodegeneration to Infertility and Back - Exploring Functions of Two Genes: ARMC4 and TARDBP: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2014. [cited 2019 Dec 06]. Available from: http://escholarship.umassmed.edu/gsbs_diss/695.

Council of Science Editors:

Cheng W. From Neurodegeneration to Infertility and Back - Exploring Functions of Two Genes: ARMC4 and TARDBP: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2014. Available from: http://escholarship.umassmed.edu/gsbs_diss/695

24. Farley, Brian M. Sequence and Target Specificity of the C. elegans Cell Fate Specification Factor POS-1: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2012, U of Massachusetts : Med

  In most metazoans, early embryogenesis is controlled by the translational regulation of maternally supplied mRNA. Sequence-specific RNA-binding proteins play an important role in regulating… (more)

Subjects/Keywords: Caenorhabditis elegans Proteins; Carrier Proteins; 3' Untranslated Regions; RNA; Messenger; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Biochemistry, Biophysics, and Structural Biology; Cell and Developmental Biology; Cells; Embryonic Structures; Nucleic Acids, Nucleotides, and Nucleosides

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APA (6th Edition):

Farley, B. M. (2012). Sequence and Target Specificity of the C. elegans Cell Fate Specification Factor POS-1: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/629

Chicago Manual of Style (16th Edition):

Farley, Brian M. “Sequence and Target Specificity of the C. elegans Cell Fate Specification Factor POS-1: A Dissertation.” 2012. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. https://escholarship.umassmed.edu/gsbs_diss/629.

MLA Handbook (7th Edition):

Farley, Brian M. “Sequence and Target Specificity of the C. elegans Cell Fate Specification Factor POS-1: A Dissertation.” 2012. Web. 06 Dec 2019.

Vancouver:

Farley BM. Sequence and Target Specificity of the C. elegans Cell Fate Specification Factor POS-1: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2012. [cited 2019 Dec 06]. Available from: https://escholarship.umassmed.edu/gsbs_diss/629.

Council of Science Editors:

Farley BM. Sequence and Target Specificity of the C. elegans Cell Fate Specification Factor POS-1: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2012. Available from: https://escholarship.umassmed.edu/gsbs_diss/629

25. Dutta, Chaitali. Checkpoint Regulation of S-Phase Transcription: A Dissertation.

Degree: Interdisciplinary Graduate Program, Biochemistry and Molecular Pharmacology, 2008, U of Massachusetts : Med

  The DNA replication checkpoint transcriptionally up-regulates genes that allow cells to adapt to and survive replication stress. Our results show that, in the fission… (more)

Subjects/Keywords: Cell Cycle Proteins; DNA Replication; Schizosaccharomyces; Schizosaccharomyces pombe Proteins; Transcription Factors; Amino Acids, Peptides, and Proteins; Cells; Fungi; Genetic Phenomena

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APA (6th Edition):

Dutta, C. (2008). Checkpoint Regulation of S-Phase Transcription: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/391

Chicago Manual of Style (16th Edition):

Dutta, Chaitali. “Checkpoint Regulation of S-Phase Transcription: A Dissertation.” 2008. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. https://escholarship.umassmed.edu/gsbs_diss/391.

MLA Handbook (7th Edition):

Dutta, Chaitali. “Checkpoint Regulation of S-Phase Transcription: A Dissertation.” 2008. Web. 06 Dec 2019.

Vancouver:

Dutta C. Checkpoint Regulation of S-Phase Transcription: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2008. [cited 2019 Dec 06]. Available from: https://escholarship.umassmed.edu/gsbs_diss/391.

Council of Science Editors:

Dutta C. Checkpoint Regulation of S-Phase Transcription: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2008. Available from: https://escholarship.umassmed.edu/gsbs_diss/391

26. Kommajosyula, Naveen. Regulation of DNA Replication Origins in Fission Yeast: A Dissertation.

Degree: Interdisciplinary Graduate Program, Biochemistry and Molecular Pharmacology, 2009, U of Massachusetts : Med

  Cells need to complete DNA replication in a timely and error-free manner. To ensure that replication is completed efficiently and in a finite amount… (more)

Subjects/Keywords: DNA Replication; Schizosaccharomyces pombe Proteins; Protein-Serine-Threonine Kinases; Replication Origin; Cell Cycle Proteins; CDC2 Protein Kinase; Gene Expression Regulation; Fungal; DNA Damage; Amino Acids, Peptides, and Proteins; Enzymes and Coenzymes; Fungi; Genetic Phenomena

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APA (6th Edition):

Kommajosyula, N. (2009). Regulation of DNA Replication Origins in Fission Yeast: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/436

Chicago Manual of Style (16th Edition):

Kommajosyula, Naveen. “Regulation of DNA Replication Origins in Fission Yeast: A Dissertation.” 2009. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. https://escholarship.umassmed.edu/gsbs_diss/436.

MLA Handbook (7th Edition):

Kommajosyula, Naveen. “Regulation of DNA Replication Origins in Fission Yeast: A Dissertation.” 2009. Web. 06 Dec 2019.

Vancouver:

Kommajosyula N. Regulation of DNA Replication Origins in Fission Yeast: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2009. [cited 2019 Dec 06]. Available from: https://escholarship.umassmed.edu/gsbs_diss/436.

Council of Science Editors:

Kommajosyula N. Regulation of DNA Replication Origins in Fission Yeast: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2009. Available from: https://escholarship.umassmed.edu/gsbs_diss/436

27. Forget, Anthony L. Homologous Recombinational DNA Repair: from Prokaryotes to Eukaryotes: a Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2004, U of Massachusetts : Med

  The error free repair of DNA double strand breaks through the homologous recombinational repair pathway is essential for organisms of all types to sustain… (more)

Subjects/Keywords: DNA-Binding Proteins; DNA Repair; Rec A Recombinases; Recombinant Proteins; Amino Acids, Peptides, and Proteins; Genetic Phenomena

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APA (6th Edition):

Forget, A. L. (2004). Homologous Recombinational DNA Repair: from Prokaryotes to Eukaryotes: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/68

Chicago Manual of Style (16th Edition):

Forget, Anthony L. “Homologous Recombinational DNA Repair: from Prokaryotes to Eukaryotes: a Dissertation.” 2004. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. https://escholarship.umassmed.edu/gsbs_diss/68.

MLA Handbook (7th Edition):

Forget, Anthony L. “Homologous Recombinational DNA Repair: from Prokaryotes to Eukaryotes: a Dissertation.” 2004. Web. 06 Dec 2019.

Vancouver:

Forget AL. Homologous Recombinational DNA Repair: from Prokaryotes to Eukaryotes: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2004. [cited 2019 Dec 06]. Available from: https://escholarship.umassmed.edu/gsbs_diss/68.

Council of Science Editors:

Forget AL. Homologous Recombinational DNA Repair: from Prokaryotes to Eukaryotes: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2004. Available from: https://escholarship.umassmed.edu/gsbs_diss/68

28. Ozen, Aysegul. Structure and Dynamics of Viral Substrate Recognition and Drug Resistance: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2013, U of Massachusetts : Med

  Drug resistance is a major problem in quickly evolving diseases, including the human immunodeficiency (HIV) and hepatitis C viral (HCV) infections. The viral proteases… (more)

Subjects/Keywords: Viral Drug Resistance; HIV Protease; HIV Protease Inhibitors; Hepacivirus; Viral Nonstructural Proteins; Immunology and Infectious Disease; Molecular Biology; Structural Biology; Virology

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

APA (6th Edition):

Ozen, A. (2013). Structure and Dynamics of Viral Substrate Recognition and Drug Resistance: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/677

Chicago Manual of Style (16th Edition):

Ozen, Aysegul. “Structure and Dynamics of Viral Substrate Recognition and Drug Resistance: A Dissertation.” 2013. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. http://escholarship.umassmed.edu/gsbs_diss/677.

MLA Handbook (7th Edition):

Ozen, Aysegul. “Structure and Dynamics of Viral Substrate Recognition and Drug Resistance: A Dissertation.” 2013. Web. 06 Dec 2019.

Vancouver:

Ozen A. Structure and Dynamics of Viral Substrate Recognition and Drug Resistance: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2013. [cited 2019 Dec 06]. Available from: http://escholarship.umassmed.edu/gsbs_diss/677.

Council of Science Editors:

Ozen A. Structure and Dynamics of Viral Substrate Recognition and Drug Resistance: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2013. Available from: http://escholarship.umassmed.edu/gsbs_diss/677

29. Hietpas, Ryan T. Experimental Illumination of Comprehensive Fitness Landscapes: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2013, U of Massachusetts : Med

  Evolution is the single cohesive logical framework in which all biological processes may exist simultaneously. Incremental changes in phenotype over imperceptibly large timescales have… (more)

Subjects/Keywords: Molecular Evolution; Mutation; Genetic Fitness; Genetic Techniques; Point Mutation; Saccharomyces cerevisiae Proteins; Computational Biology; Evolution; Molecular Genetics

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

APA (6th Edition):

Hietpas, R. T. (2013). Experimental Illumination of Comprehensive Fitness Landscapes: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/667

Chicago Manual of Style (16th Edition):

Hietpas, Ryan T. “Experimental Illumination of Comprehensive Fitness Landscapes: A Dissertation.” 2013. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. http://escholarship.umassmed.edu/gsbs_diss/667.

MLA Handbook (7th Edition):

Hietpas, Ryan T. “Experimental Illumination of Comprehensive Fitness Landscapes: A Dissertation.” 2013. Web. 06 Dec 2019.

Vancouver:

Hietpas RT. Experimental Illumination of Comprehensive Fitness Landscapes: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2013. [cited 2019 Dec 06]. Available from: http://escholarship.umassmed.edu/gsbs_diss/667.

Council of Science Editors:

Hietpas RT. Experimental Illumination of Comprehensive Fitness Landscapes: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2013. Available from: http://escholarship.umassmed.edu/gsbs_diss/667

30. Malaby, Heidi L. H. Identification of Molecular Determinants that Shift Co- and Post-Translational N-Glycosylation Kinetics in Type I Transmembrane Peptides: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2014, U of Massachusetts : Med

  Asparagine (N)-linked glycosylation occurs on 90% of membrane and secretory proteins and drives folding and trafficking along the secretory pathway. The N-glycan can be… (more)

Subjects/Keywords: Asparagine; Consensus Sequence; Glycosylation; Kinetics; Membrane Proteins; Voltage-Gated Potassium Channels; RNA; Small Interfering; Biochemistry; Molecular Biology; Organic Chemistry

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

APA (6th Edition):

Malaby, H. L. H. (2014). Identification of Molecular Determinants that Shift Co- and Post-Translational N-Glycosylation Kinetics in Type I Transmembrane Peptides: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/702

Chicago Manual of Style (16th Edition):

Malaby, Heidi L H. “Identification of Molecular Determinants that Shift Co- and Post-Translational N-Glycosylation Kinetics in Type I Transmembrane Peptides: A Dissertation.” 2014. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. http://escholarship.umassmed.edu/gsbs_diss/702.

MLA Handbook (7th Edition):

Malaby, Heidi L H. “Identification of Molecular Determinants that Shift Co- and Post-Translational N-Glycosylation Kinetics in Type I Transmembrane Peptides: A Dissertation.” 2014. Web. 06 Dec 2019.

Vancouver:

Malaby HLH. Identification of Molecular Determinants that Shift Co- and Post-Translational N-Glycosylation Kinetics in Type I Transmembrane Peptides: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2014. [cited 2019 Dec 06]. Available from: http://escholarship.umassmed.edu/gsbs_diss/702.

Council of Science Editors:

Malaby HLH. Identification of Molecular Determinants that Shift Co- and Post-Translational N-Glycosylation Kinetics in Type I Transmembrane Peptides: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2014. Available from: http://escholarship.umassmed.edu/gsbs_diss/702

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