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University: U of Massachusetts : Med

You searched for subject:(Genes). Showing records 1 – 30 of 31 total matches.

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1. Guillemette, Shawna S. Investigating Tumor Suppressors in the DNA Damage Response: Caretakers of the Genome and Biomarkers to Predict Therapeutic Response: A Dissertation.

Degree: Cancer Biology, Molecular, Cell and Cancer Biology Department, 2014, U of Massachusetts : Med

  Our genome is constantly challenged by sources that cause DNA damage. To repair DNA damage and maintain genomic stability eukaryotes have evolved a complex… (more)

Subjects/Keywords: BRCA2 Protein; Carcinogenesis; Cell Cycle; DNA Damage; DNA Repair; BRCA2 Genes; Tumor Suppressor Genes; RNA Interference; Cancer Biology

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APA (6th Edition):

Guillemette, S. S. (2014). Investigating Tumor Suppressors in the DNA Damage Response: Caretakers of the Genome and Biomarkers to Predict Therapeutic Response: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/712

Chicago Manual of Style (16th Edition):

Guillemette, Shawna S. “Investigating Tumor Suppressors in the DNA Damage Response: Caretakers of the Genome and Biomarkers to Predict Therapeutic Response: A Dissertation.” 2014. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. http://escholarship.umassmed.edu/gsbs_diss/712.

MLA Handbook (7th Edition):

Guillemette, Shawna S. “Investigating Tumor Suppressors in the DNA Damage Response: Caretakers of the Genome and Biomarkers to Predict Therapeutic Response: A Dissertation.” 2014. Web. 19 Oct 2019.

Vancouver:

Guillemette SS. Investigating Tumor Suppressors in the DNA Damage Response: Caretakers of the Genome and Biomarkers to Predict Therapeutic Response: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2014. [cited 2019 Oct 19]. Available from: http://escholarship.umassmed.edu/gsbs_diss/712.

Council of Science Editors:

Guillemette SS. Investigating Tumor Suppressors in the DNA Damage Response: Caretakers of the Genome and Biomarkers to Predict Therapeutic Response: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2014. Available from: http://escholarship.umassmed.edu/gsbs_diss/712

2. Tesell, Jessica M. The Notch1-c-Myc Pathway Mediates Leukemia-Initiating Cell Activity in Mouse T-ALL Models: A Dissertation.

Degree: Cancer Biology, Molecular, Cell and Cancer Biology Department, 2013, U of Massachusetts : Med

  Although cure rates have significantly improved for children with T-cell acute lymphoblastic leukemia (T-ALL), 20-30% undergo induction failure or relapse with most succumbing to… (more)

Subjects/Keywords: Notch1 Receptor; Precursor T-Cell Lymphoblastic Leukemia-Lymphoma; myc Genes; Cancer Biology

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APA (6th Edition):

Tesell, J. M. (2013). The Notch1-c-Myc Pathway Mediates Leukemia-Initiating Cell Activity in Mouse T-ALL Models: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/671

Chicago Manual of Style (16th Edition):

Tesell, Jessica M. “The Notch1-c-Myc Pathway Mediates Leukemia-Initiating Cell Activity in Mouse T-ALL Models: A Dissertation.” 2013. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. http://escholarship.umassmed.edu/gsbs_diss/671.

MLA Handbook (7th Edition):

Tesell, Jessica M. “The Notch1-c-Myc Pathway Mediates Leukemia-Initiating Cell Activity in Mouse T-ALL Models: A Dissertation.” 2013. Web. 19 Oct 2019.

Vancouver:

Tesell JM. The Notch1-c-Myc Pathway Mediates Leukemia-Initiating Cell Activity in Mouse T-ALL Models: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2013. [cited 2019 Oct 19]. Available from: http://escholarship.umassmed.edu/gsbs_diss/671.

Council of Science Editors:

Tesell JM. The Notch1-c-Myc Pathway Mediates Leukemia-Initiating Cell Activity in Mouse T-ALL Models: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2013. Available from: http://escholarship.umassmed.edu/gsbs_diss/671

3. Serra, Ryan W. Investigating Cancer Molecular Genetics using Genome-wide RNA Interference Screens: A Dissertation.

Degree: Cancer Biology, Molecular, Cell, and Cancer Biology Department, 2013, U of Massachusetts : Med

  The development of RNAi based technologies has given researchers the tools to interrogate processes as diverse as cancer biology, metabolism and organ development. Here… (more)

Subjects/Keywords: Carcinogenesis; RNA Interference; Tumor Suppressor Genes; Cell Aging; Transcription Factors; Cancer Biology; Molecular Genetics

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APA (6th Edition):

Serra, R. W. (2013). Investigating Cancer Molecular Genetics using Genome-wide RNA Interference Screens: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/676

Chicago Manual of Style (16th Edition):

Serra, Ryan W. “Investigating Cancer Molecular Genetics using Genome-wide RNA Interference Screens: A Dissertation.” 2013. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. http://escholarship.umassmed.edu/gsbs_diss/676.

MLA Handbook (7th Edition):

Serra, Ryan W. “Investigating Cancer Molecular Genetics using Genome-wide RNA Interference Screens: A Dissertation.” 2013. Web. 19 Oct 2019.

Vancouver:

Serra RW. Investigating Cancer Molecular Genetics using Genome-wide RNA Interference Screens: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2013. [cited 2019 Oct 19]. Available from: http://escholarship.umassmed.edu/gsbs_diss/676.

Council of Science Editors:

Serra RW. Investigating Cancer Molecular Genetics using Genome-wide RNA Interference Screens: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2013. Available from: http://escholarship.umassmed.edu/gsbs_diss/676

4. Belton, Jon-Matthew. The Recombination Enhancer Modulates the Conformation of Chr. III in Budding Yeast: A Dissertation.

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

  A hierarchy of different chromosome conformations plays a role in many biological systems. These conformations contribute to the regulation of gene expression, cellular development,… (more)

Subjects/Keywords: Chromosomes; Protein Conformation; Fungal Mating Type Genes; Saccharomycetales; Genetic Recombination; Genetics and Genomics; Genomics; Structural Biology

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APA (6th Edition):

Belton, J. (2014). The Recombination Enhancer Modulates the Conformation of Chr. III in Budding Yeast: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/762

Chicago Manual of Style (16th Edition):

Belton, Jon-Matthew. “The Recombination Enhancer Modulates the Conformation of Chr. III in Budding Yeast: A Dissertation.” 2014. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. http://escholarship.umassmed.edu/gsbs_diss/762.

MLA Handbook (7th Edition):

Belton, Jon-Matthew. “The Recombination Enhancer Modulates the Conformation of Chr. III in Budding Yeast: A Dissertation.” 2014. Web. 19 Oct 2019.

Vancouver:

Belton J. The Recombination Enhancer Modulates the Conformation of Chr. III in Budding Yeast: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2014. [cited 2019 Oct 19]. Available from: http://escholarship.umassmed.edu/gsbs_diss/762.

Council of Science Editors:

Belton J. The Recombination Enhancer Modulates the Conformation of Chr. III in Budding Yeast: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2014. Available from: http://escholarship.umassmed.edu/gsbs_diss/762

5. 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 October 19, 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. 19 Oct 2019.

Vancouver:

Weicksel SE. hox Gene Regulation and Function During Zebrafish Embryogenesis: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2013. [cited 2019 Oct 19]. 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

6. Lin, Ling. Genetic Approaches to Study Transcriptional Activation and Tumor Suppression: A Dissertation.

Degree: Interdisciplinary Graduate Program, Molecular, Cell and Cancer Biology, 2012, U of Massachusetts : Med

  The development of methods and techniques is the driving force of scientific research. In this work, we described two large-scale screens in studying transcriptional… (more)

Subjects/Keywords: Transcriptional Activation; Genes; Tumor Suppressor; Cells; Genetic Phenomena; Genetics and Genomics; Neoplasms; Nucleic Acids, Nucleotides, and Nucleosides; Respiratory Tract Diseases

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APA (6th Edition):

Lin, L. (2012). Genetic Approaches to Study Transcriptional Activation and Tumor Suppression: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/610

Chicago Manual of Style (16th Edition):

Lin, Ling. “Genetic Approaches to Study Transcriptional Activation and Tumor Suppression: A Dissertation.” 2012. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. https://escholarship.umassmed.edu/gsbs_diss/610.

MLA Handbook (7th Edition):

Lin, Ling. “Genetic Approaches to Study Transcriptional Activation and Tumor Suppression: A Dissertation.” 2012. Web. 19 Oct 2019.

Vancouver:

Lin L. Genetic Approaches to Study Transcriptional Activation and Tumor Suppression: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2012. [cited 2019 Oct 19]. Available from: https://escholarship.umassmed.edu/gsbs_diss/610.

Council of Science Editors:

Lin L. Genetic Approaches to Study Transcriptional Activation and Tumor Suppression: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2012. Available from: https://escholarship.umassmed.edu/gsbs_diss/610

7. Nguyen, Tina T. Structural and Functional Studies of Proteins Involved in Antigen Processing: A Dissertation.

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

  This thesis is comprised of studies of proteins involved in class I and class II major histocompatibility complex (MHC) antigen procressing. In class I… (more)

Subjects/Keywords: Major Histocompatibility Complex; Histocompatibility Antigens Class I; Histocompatibility Antigens Class II; Genes; MHC Class I; Genes; MHC Class II; Amino Acids, Peptides, and Proteins; Biological Factors; Cells; Genetic Phenomena; Genetics and Genomics; Immunology and Infectious Disease

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APA (6th Edition):

Nguyen, T. T. (2010). Structural and Functional Studies of Proteins Involved in Antigen Processing: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/503

Chicago Manual of Style (16th Edition):

Nguyen, Tina T. “Structural and Functional Studies of Proteins Involved in Antigen Processing: A Dissertation.” 2010. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. https://escholarship.umassmed.edu/gsbs_diss/503.

MLA Handbook (7th Edition):

Nguyen, Tina T. “Structural and Functional Studies of Proteins Involved in Antigen Processing: A Dissertation.” 2010. Web. 19 Oct 2019.

Vancouver:

Nguyen TT. Structural and Functional Studies of Proteins Involved in Antigen Processing: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2010. [cited 2019 Oct 19]. Available from: https://escholarship.umassmed.edu/gsbs_diss/503.

Council of Science Editors:

Nguyen TT. Structural and Functional Studies of Proteins Involved in Antigen Processing: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2010. Available from: https://escholarship.umassmed.edu/gsbs_diss/503

8. Quattrochi, Brian J. Subtle Controllers: MicroRNAs Drive Pancreatic Tumorigenesis and Progression: A Dissertation.

Degree: PhD, Molecular, Cell and Cancer Biology Department, 2015, U of Massachusetts : Med

  Pancreatic ductal adenocarcinoma (PDAC) is among the most lethal malignancies in the United States, with an average five-year survival rate of just 6.7%. One… (more)

Subjects/Keywords: Pancreatic Ductal Carcinoma; Carcinogenesis; Neoplastic Cell Transformation; ras Genes; MicroRNAs; Oncogenes; Proto-Oncogene Proteins; Cancer Biology; Genetics and Genomics; Neoplasms; Nucleic Acids, Nucleotides, and Nucleosides; Oncology

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APA (6th Edition):

Quattrochi, B. J. (2015). Subtle Controllers: MicroRNAs Drive Pancreatic Tumorigenesis and Progression: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/776

Chicago Manual of Style (16th Edition):

Quattrochi, Brian J. “Subtle Controllers: MicroRNAs Drive Pancreatic Tumorigenesis and Progression: A Dissertation.” 2015. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. http://escholarship.umassmed.edu/gsbs_diss/776.

MLA Handbook (7th Edition):

Quattrochi, Brian J. “Subtle Controllers: MicroRNAs Drive Pancreatic Tumorigenesis and Progression: A Dissertation.” 2015. Web. 19 Oct 2019.

Vancouver:

Quattrochi BJ. Subtle Controllers: MicroRNAs Drive Pancreatic Tumorigenesis and Progression: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2015. [cited 2019 Oct 19]. Available from: http://escholarship.umassmed.edu/gsbs_diss/776.

Council of Science Editors:

Quattrochi BJ. Subtle Controllers: MicroRNAs Drive Pancreatic Tumorigenesis and Progression: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2015. Available from: http://escholarship.umassmed.edu/gsbs_diss/776

9. Chen, Hsiuyi V. Systematic Dissection of Roles for Chromatin Regulators in Dynamics of Transcriptional Response to Stress in Yeast: A Dissertation.

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

  The following work demonstrates that chromatin regulators play far more pronounced roles in dynamic gene expression than they do in steady-state. Histone modifications have… (more)

Subjects/Keywords: Chromatin; Gene Expression Regulation; Regulator Genes; Histones; Saccharomyces cerevisiae Proteins; Histone-Lysine N-Methyltransferase; Biochemistry; Cell Biology; Cellular and Molecular Physiology; Genetics; Genomics

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APA (6th Edition):

Chen, H. V. (2015). Systematic Dissection of Roles for Chromatin Regulators in Dynamics of Transcriptional Response to Stress in Yeast: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/808

Chicago Manual of Style (16th Edition):

Chen, Hsiuyi V. “Systematic Dissection of Roles for Chromatin Regulators in Dynamics of Transcriptional Response to Stress in Yeast: A Dissertation.” 2015. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. http://escholarship.umassmed.edu/gsbs_diss/808.

MLA Handbook (7th Edition):

Chen, Hsiuyi V. “Systematic Dissection of Roles for Chromatin Regulators in Dynamics of Transcriptional Response to Stress in Yeast: A Dissertation.” 2015. Web. 19 Oct 2019.

Vancouver:

Chen HV. Systematic Dissection of Roles for Chromatin Regulators in Dynamics of Transcriptional Response to Stress in Yeast: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2015. [cited 2019 Oct 19]. Available from: http://escholarship.umassmed.edu/gsbs_diss/808.

Council of Science Editors:

Chen HV. Systematic Dissection of Roles for Chromatin Regulators in Dynamics of Transcriptional Response to Stress in Yeast: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2015. Available from: http://escholarship.umassmed.edu/gsbs_diss/808

10. Porter-Goff, Mary Elizabeth. The Role of the MRN Complex in the S-Phase DNA Damage Checkpoint: A Dissertation.

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

  The main focus of my work has been the role of the MRN in the S-phase DNA damage checkpoint. The MRN plays many roles… (more)

Subjects/Keywords: Methyl Methane sulfonate; DNA Damage; Cell Cycle Proteins; Intracellular Signaling Peptides and Proteins; Genes; cdc; S Phase; Amino Acids, Peptides, and Proteins; Cells; Enzymes and Coenzymes; Fungi; Genetic Phenomena; Viruses

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APA (6th Edition):

Porter-Goff, M. E. (2009). The Role of the MRN Complex in the S-Phase DNA Damage Checkpoint: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/405

Chicago Manual of Style (16th Edition):

Porter-Goff, Mary Elizabeth. “The Role of the MRN Complex in the S-Phase DNA Damage Checkpoint: A Dissertation.” 2009. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. https://escholarship.umassmed.edu/gsbs_diss/405.

MLA Handbook (7th Edition):

Porter-Goff, Mary Elizabeth. “The Role of the MRN Complex in the S-Phase DNA Damage Checkpoint: A Dissertation.” 2009. Web. 19 Oct 2019.

Vancouver:

Porter-Goff ME. The Role of the MRN Complex in the S-Phase DNA Damage Checkpoint: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2009. [cited 2019 Oct 19]. Available from: https://escholarship.umassmed.edu/gsbs_diss/405.

Council of Science Editors:

Porter-Goff ME. The Role of the MRN Complex in the S-Phase DNA Damage Checkpoint: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2009. Available from: https://escholarship.umassmed.edu/gsbs_diss/405

11. Martinez, Natalia Julia. Delineating the C. elegans MicroRNA Regulatory Network: A Dissertation.

Degree: Interdisciplinary Graduate Program, Program in Molecular Medicine, 2009, U of Massachusetts : Med

  Metazoan genomes contain thousands of protein-coding and non-coding RNA genes, most of which are differentially expressed, i.e., at different locations, at different times during… (more)

Subjects/Keywords: Transcription Factors; MicroRNAs; Gene Expression Regulation; Caenorhabditis elegans; Genes; Helminth; Transcription; Genetic; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Genetic Phenomena; Nucleic Acids, Nucleotides, and Nucleosides

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APA (6th Edition):

Martinez, N. J. (2009). Delineating the C. elegans MicroRNA Regulatory Network: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/411

Chicago Manual of Style (16th Edition):

Martinez, Natalia Julia. “Delineating the C. elegans MicroRNA Regulatory Network: A Dissertation.” 2009. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. https://escholarship.umassmed.edu/gsbs_diss/411.

MLA Handbook (7th Edition):

Martinez, Natalia Julia. “Delineating the C. elegans MicroRNA Regulatory Network: A Dissertation.” 2009. Web. 19 Oct 2019.

Vancouver:

Martinez NJ. Delineating the C. elegans MicroRNA Regulatory Network: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2009. [cited 2019 Oct 19]. Available from: https://escholarship.umassmed.edu/gsbs_diss/411.

Council of Science Editors:

Martinez NJ. Delineating the C. elegans MicroRNA Regulatory Network: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2009. Available from: https://escholarship.umassmed.edu/gsbs_diss/411

12. Kovi, Ramesh C. Defining the Role of CtBP2 in p53-Independent Tumor Suppressor Function of ARF: A Dissertation.

Degree: Cancer Biology, Department of Medicine; Department of Cancer Biology, 2009, U of Massachusetts : Med

  ARF, a potent tumor suppressor, positively regulates p53 by antagonizing MDM2, a negative regulator of p53, which in turn, results in either apoptosis or… (more)

Subjects/Keywords: ADP-Ribosylation Factors; Apoptosis; Tumor Suppressor Protein p53; Phosphoproteins; DNA-Binding Proteins; Tumor Suppressor Protein p14ARF; Colorectal Neoplasms; Genes; Tumor Suppressor; Amino Acids, Peptides, and Proteins; Cells; Genetic Phenomena; Neoplasms

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APA (6th Edition):

Kovi, R. C. (2009). Defining the Role of CtBP2 in p53-Independent Tumor Suppressor Function of ARF: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/433

Chicago Manual of Style (16th Edition):

Kovi, Ramesh C. “Defining the Role of CtBP2 in p53-Independent Tumor Suppressor Function of ARF: A Dissertation.” 2009. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. https://escholarship.umassmed.edu/gsbs_diss/433.

MLA Handbook (7th Edition):

Kovi, Ramesh C. “Defining the Role of CtBP2 in p53-Independent Tumor Suppressor Function of ARF: A Dissertation.” 2009. Web. 19 Oct 2019.

Vancouver:

Kovi RC. Defining the Role of CtBP2 in p53-Independent Tumor Suppressor Function of ARF: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2009. [cited 2019 Oct 19]. Available from: https://escholarship.umassmed.edu/gsbs_diss/433.

Council of Science Editors:

Kovi RC. Defining the Role of CtBP2 in p53-Independent Tumor Suppressor Function of ARF: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2009. Available from: https://escholarship.umassmed.edu/gsbs_diss/433

13. Narayan, Kavitha. The Function of Innate γδ T Cell Subsets is Molecularly Programmed in the Thymus in Three Stages: A Dissertation.

Degree: Immunology and Microbiology, Pathology, 2011, U of Massachusetts : Med

  The immune system generates discrete lineages of cells that are designed to respond optimally to environmental cues and infectious agents. Two distinct lineages of… (more)

Subjects/Keywords: Immunity; Innate; T-Lymphocytes; T-Lymphocyte Subsets; Genes; T-Cell Receptor; Cells; Genetic Phenomena; Hemic and Immune Systems; Immunology and Infectious Disease

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APA (6th Edition):

Narayan, K. (2011). The Function of Innate γδ T Cell Subsets is Molecularly Programmed in the Thymus in Three Stages: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/527

Chicago Manual of Style (16th Edition):

Narayan, Kavitha. “The Function of Innate γδ T Cell Subsets is Molecularly Programmed in the Thymus in Three Stages: A Dissertation.” 2011. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. https://escholarship.umassmed.edu/gsbs_diss/527.

MLA Handbook (7th Edition):

Narayan, Kavitha. “The Function of Innate γδ T Cell Subsets is Molecularly Programmed in the Thymus in Three Stages: A Dissertation.” 2011. Web. 19 Oct 2019.

Vancouver:

Narayan K. The Function of Innate γδ T Cell Subsets is Molecularly Programmed in the Thymus in Three Stages: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2011. [cited 2019 Oct 19]. Available from: https://escholarship.umassmed.edu/gsbs_diss/527.

Council of Science Editors:

Narayan K. The Function of Innate γδ T Cell Subsets is Molecularly Programmed in the Thymus in Three Stages: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2011. Available from: https://escholarship.umassmed.edu/gsbs_diss/527

14. Painter, Corrie A. Conformational Lability in MHC II Proteins: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Pathology, 2011, U of Massachusetts : Med

  MHC II proteins are heterodimeric glycoproteins that form complexes with antigenic peptides in order to elicit a CD4+ adaptive immune response. Even though there… (more)

Subjects/Keywords: Genes; MHC Class II; Protein Conformation; HLA-D Antigens; Amino Acids, Peptides, and Proteins; Biochemistry, Biophysics, and Structural Biology; Biological Factors; Genetic Phenomena

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APA (6th Edition):

Painter, C. A. (2011). Conformational Lability in MHC II Proteins: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/539

Chicago Manual of Style (16th Edition):

Painter, Corrie A. “Conformational Lability in MHC II Proteins: A Dissertation.” 2011. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. https://escholarship.umassmed.edu/gsbs_diss/539.

MLA Handbook (7th Edition):

Painter, Corrie A. “Conformational Lability in MHC II Proteins: A Dissertation.” 2011. Web. 19 Oct 2019.

Vancouver:

Painter CA. Conformational Lability in MHC II Proteins: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2011. [cited 2019 Oct 19]. Available from: https://escholarship.umassmed.edu/gsbs_diss/539.

Council of Science Editors:

Painter CA. Conformational Lability in MHC II Proteins: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2011. Available from: https://escholarship.umassmed.edu/gsbs_diss/539

15. Melichar, Heather J. SOX13, A γδ T Cell-Specific Gene, Is a WNT-Signaling Antagonist Regulating T Cell Development: A Dissertation.

Degree: Immunology and Microbiology, Pathology, 2006, U of Massachusetts : Med

  Mature αβ and γδ T cells arise from a common precursor population in the thymus. Much debate has focused on the mechanism of T… (more)

Subjects/Keywords: T-Lymphocytes; Genes; T-Cell Receptor gamma; Genes; T-Cell Receptor delta; Stem Cells; Cell Differentiation; Autoantigens; High Mobility Group Proteins; Transcription Factors; Amino Acids, Peptides, and Proteins; Cells; Genetic Phenomena; Hemic and Immune Systems

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APA (6th Edition):

Melichar, H. J. (2006). SOX13, A γδ T Cell-Specific Gene, Is a WNT-Signaling Antagonist Regulating T Cell Development: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/251

Chicago Manual of Style (16th Edition):

Melichar, Heather J. “SOX13, A γδ T Cell-Specific Gene, Is a WNT-Signaling Antagonist Regulating T Cell Development: A Dissertation.” 2006. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. https://escholarship.umassmed.edu/gsbs_diss/251.

MLA Handbook (7th Edition):

Melichar, Heather J. “SOX13, A γδ T Cell-Specific Gene, Is a WNT-Signaling Antagonist Regulating T Cell Development: A Dissertation.” 2006. Web. 19 Oct 2019.

Vancouver:

Melichar HJ. SOX13, A γδ T Cell-Specific Gene, Is a WNT-Signaling Antagonist Regulating T Cell Development: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2006. [cited 2019 Oct 19]. Available from: https://escholarship.umassmed.edu/gsbs_diss/251.

Council of Science Editors:

Melichar HJ. SOX13, A γδ T Cell-Specific Gene, Is a WNT-Signaling Antagonist Regulating T Cell Development: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2006. Available from: https://escholarship.umassmed.edu/gsbs_diss/251

16. Brown, David Spaulding. CD4+ T Cell Responses: A Complex Network of Activating and Tolerizing Signals as Revealed by Gene Expression Analysis: A Dissertation.

Degree: PhD, Department of Pathology, 2005, U of Massachusetts : Med

  Immunologic self-tolerance is maintained by both central and peripheral mechanisms. Furthermore, regulation of mature lymphocyte responses is governed by inhibitory as well as stimulatory… (more)

Subjects/Keywords: CD4-Positive T-Lymphocytes; Genes; T-Cell Receptor; Antigens; CD28; Antigens; Differentiation; Gene Expression; Signal Transduction; Self Tolerance; Genes; MHC Class II; Biological Factors; Cells; Genetic Phenomena; Hemic and Immune Systems

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APA (6th Edition):

Brown, D. S. (2005). CD4+ T Cell Responses: A Complex Network of Activating and Tolerizing Signals as Revealed by Gene Expression Analysis: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/230

Chicago Manual of Style (16th Edition):

Brown, David Spaulding. “CD4+ T Cell Responses: A Complex Network of Activating and Tolerizing Signals as Revealed by Gene Expression Analysis: A Dissertation.” 2005. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. https://escholarship.umassmed.edu/gsbs_diss/230.

MLA Handbook (7th Edition):

Brown, David Spaulding. “CD4+ T Cell Responses: A Complex Network of Activating and Tolerizing Signals as Revealed by Gene Expression Analysis: A Dissertation.” 2005. Web. 19 Oct 2019.

Vancouver:

Brown DS. CD4+ T Cell Responses: A Complex Network of Activating and Tolerizing Signals as Revealed by Gene Expression Analysis: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2005. [cited 2019 Oct 19]. Available from: https://escholarship.umassmed.edu/gsbs_diss/230.

Council of Science Editors:

Brown DS. CD4+ T Cell Responses: A Complex Network of Activating and Tolerizing Signals as Revealed by Gene Expression Analysis: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2005. Available from: https://escholarship.umassmed.edu/gsbs_diss/230

17. Vallaster, Markus Parzival. Intergenerational Effects of Nicotine in an Animal Model of Paternal Nicotine Exposure.

Degree: Interdisciplinary Graduate Program, Biochemistry and Molecular Pharmacology, 2017, U of Massachusetts : Med

  Environmental conditions imposed onto organisms during certain phases of their life cycles such as embryogenesis or puberty can not only impact the organisms’ own… (more)

Subjects/Keywords: chromosomes; epigenetics; genes; mouse; paternal effects; substance abuse; neuroscience; Behavioral Neurobiology; Biochemical Phenomena, Metabolism, and Nutrition; Cell Biology; Cellular and Molecular Physiology; Developmental Neuroscience; Genetics; Molecular Genetics; Other Pharmacology, Toxicology and Environmental Health

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APA (6th Edition):

Vallaster, M. P. (2017). Intergenerational Effects of Nicotine in an Animal Model of Paternal Nicotine Exposure. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/913

Chicago Manual of Style (16th Edition):

Vallaster, Markus Parzival. “Intergenerational Effects of Nicotine in an Animal Model of Paternal Nicotine Exposure.” 2017. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. http://escholarship.umassmed.edu/gsbs_diss/913.

MLA Handbook (7th Edition):

Vallaster, Markus Parzival. “Intergenerational Effects of Nicotine in an Animal Model of Paternal Nicotine Exposure.” 2017. Web. 19 Oct 2019.

Vancouver:

Vallaster MP. Intergenerational Effects of Nicotine in an Animal Model of Paternal Nicotine Exposure. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2017. [cited 2019 Oct 19]. Available from: http://escholarship.umassmed.edu/gsbs_diss/913.

Council of Science Editors:

Vallaster MP. Intergenerational Effects of Nicotine in an Animal Model of Paternal Nicotine Exposure. [Doctoral Dissertation]. U of Massachusetts : Med; 2017. Available from: http://escholarship.umassmed.edu/gsbs_diss/913

18. Ahronian, Leanne G. Identification and Characteristics of Factors Regulating Hepatocellular Carcinoma Progression and Metastasis: A Dissertation.

Degree: Cancer Biology, Molecular, Cell and Cancer Biology Department, 2014, U of Massachusetts : Med

  Hepatocellular carcinoma (HCC) is a common malignancy of the liver that is one of the most frequent causes of cancer-related death in the world.… (more)

Subjects/Keywords: Hepatocellular Carcinoma; Gene Expression Profiling; p53 Genes; Kruppel-Like Transcription Factors; Liver Neoplasms; Point Mutation; rho GTP-Binding Proteins; Transcription Factors; Tumor Suppressor Protein p53; Cancer Biology; Digestive System Diseases; Molecular Genetics; Neoplasms

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APA (6th Edition):

Ahronian, L. G. (2014). Identification and Characteristics of Factors Regulating Hepatocellular Carcinoma Progression and Metastasis: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/705

Chicago Manual of Style (16th Edition):

Ahronian, Leanne G. “Identification and Characteristics of Factors Regulating Hepatocellular Carcinoma Progression and Metastasis: A Dissertation.” 2014. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. http://escholarship.umassmed.edu/gsbs_diss/705.

MLA Handbook (7th Edition):

Ahronian, Leanne G. “Identification and Characteristics of Factors Regulating Hepatocellular Carcinoma Progression and Metastasis: A Dissertation.” 2014. Web. 19 Oct 2019.

Vancouver:

Ahronian LG. Identification and Characteristics of Factors Regulating Hepatocellular Carcinoma Progression and Metastasis: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2014. [cited 2019 Oct 19]. Available from: http://escholarship.umassmed.edu/gsbs_diss/705.

Council of Science Editors:

Ahronian LG. Identification and Characteristics of Factors Regulating Hepatocellular Carcinoma Progression and Metastasis: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2014. Available from: http://escholarship.umassmed.edu/gsbs_diss/705

19. 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 October 19, 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. 19 Oct 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 Oct 19]. 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

20. McNamee, Laura Michelle. DNA Damage-Induced Apoptosis in the Presence and Absence of the Tumor Suppressor p53: A Dissertation.

Degree: Interdisciplinary Graduate Program, Molecular, Cell and Cancer Biology, 2008, U of Massachusetts : Med

  A key regulator of DNA damage-induced apoptosis is the tumor suppressor gene, p53. p53 is a transcription factor that upregulates genes involved in cell… (more)

Subjects/Keywords: Apoptosis; Genes; p53; DNA Damage; Drosophila; Drosophila Proteins; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Cells; Genetic Phenomena; Neoplasms

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APA (6th Edition):

McNamee, L. M. (2008). DNA Damage-Induced Apoptosis in the Presence and Absence of the Tumor Suppressor p53: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/396

Chicago Manual of Style (16th Edition):

McNamee, Laura Michelle. “DNA Damage-Induced Apoptosis in the Presence and Absence of the Tumor Suppressor p53: A Dissertation.” 2008. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. https://escholarship.umassmed.edu/gsbs_diss/396.

MLA Handbook (7th Edition):

McNamee, Laura Michelle. “DNA Damage-Induced Apoptosis in the Presence and Absence of the Tumor Suppressor p53: A Dissertation.” 2008. Web. 19 Oct 2019.

Vancouver:

McNamee LM. DNA Damage-Induced Apoptosis in the Presence and Absence of the Tumor Suppressor p53: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2008. [cited 2019 Oct 19]. Available from: https://escholarship.umassmed.edu/gsbs_diss/396.

Council of Science Editors:

McNamee LM. DNA Damage-Induced Apoptosis in the Presence and Absence of the Tumor Suppressor p53: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2008. Available from: https://escholarship.umassmed.edu/gsbs_diss/396

21. Shi, Dingding. Defining the Roles of p300/CBP (CREB Binding Protein) and S5a in p53 Polyubiquitination, Degradation and DNA Damage Responses: A Dissertation.

Degree: Cancer Biology, Program in Cancer Biology; Medicine, 2010, U of Massachusetts : Med

  p53, known as the “guardian of the genome”, is the most well-characterized tumor suppressor gene. The central role of p53 is to prevent genome… (more)

Subjects/Keywords: Genes; p53; Tumor Suppressor Protein p53; p300-CBP Transcription Factors; CREB-Binding Protein; E1A-Associated p300 Protein; Proteasome Endopeptidase Complex; DNA Damage; Ubiquitination; Amino Acids, Peptides, and Proteins; Cancer Biology; Genetic Phenomena; Neoplasms; Pharmaceutical Preparations; Therapeutics

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APA (6th Edition):

Shi, D. (2010). Defining the Roles of p300/CBP (CREB Binding Protein) and S5a in p53 Polyubiquitination, Degradation and DNA Damage Responses: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/452

Chicago Manual of Style (16th Edition):

Shi, Dingding. “Defining the Roles of p300/CBP (CREB Binding Protein) and S5a in p53 Polyubiquitination, Degradation and DNA Damage Responses: A Dissertation.” 2010. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. https://escholarship.umassmed.edu/gsbs_diss/452.

MLA Handbook (7th Edition):

Shi, Dingding. “Defining the Roles of p300/CBP (CREB Binding Protein) and S5a in p53 Polyubiquitination, Degradation and DNA Damage Responses: A Dissertation.” 2010. Web. 19 Oct 2019.

Vancouver:

Shi D. Defining the Roles of p300/CBP (CREB Binding Protein) and S5a in p53 Polyubiquitination, Degradation and DNA Damage Responses: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2010. [cited 2019 Oct 19]. Available from: https://escholarship.umassmed.edu/gsbs_diss/452.

Council of Science Editors:

Shi D. Defining the Roles of p300/CBP (CREB Binding Protein) and S5a in p53 Polyubiquitination, Degradation and DNA Damage Responses: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2010. Available from: https://escholarship.umassmed.edu/gsbs_diss/452

22. Younan, Patrick. Identification and Characterization of SNAPIN as a Novel Antagonist of HIV-1 Egress: A Dissertation.

Degree: Immunology and Microbiology, Molecular Medicine, 2010, U of Massachusetts : Med

  Vpu has been shown to possess two distinct roles in the pathogenesis of HIV. First, Vpu has been shown to down-regulate the expression of… (more)

Subjects/Keywords: Human Immunodeficiency Virus Proteins; Viral Regulatory and Accessory Proteins; Vesicular Transport Proteins; Genes; vpu; HIV-1; Virus Release; Gene Products; gag; Amino Acids, Peptides, and Proteins; Cells; Genetic Phenomena; Pathology; Viruses

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APA (6th Edition):

Younan, P. (2010). Identification and Characterization of SNAPIN as a Novel Antagonist of HIV-1 Egress: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/460

Chicago Manual of Style (16th Edition):

Younan, Patrick. “Identification and Characterization of SNAPIN as a Novel Antagonist of HIV-1 Egress: A Dissertation.” 2010. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. https://escholarship.umassmed.edu/gsbs_diss/460.

MLA Handbook (7th Edition):

Younan, Patrick. “Identification and Characterization of SNAPIN as a Novel Antagonist of HIV-1 Egress: A Dissertation.” 2010. Web. 19 Oct 2019.

Vancouver:

Younan P. Identification and Characterization of SNAPIN as a Novel Antagonist of HIV-1 Egress: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2010. [cited 2019 Oct 19]. Available from: https://escholarship.umassmed.edu/gsbs_diss/460.

Council of Science Editors:

Younan P. Identification and Characterization of SNAPIN as a Novel Antagonist of HIV-1 Egress: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2010. Available from: https://escholarship.umassmed.edu/gsbs_diss/460

23. Dai, Lue. A Novel Motif in HIV-1 Nef that Regulates MIP-1β Chemokine Release in Macrophages: A Dissertation.

Degree: Immunology and Microbiology, Molecular Medicine, 2010, U of Massachusetts : Med

  Nef is an accessory protein encoded by human and simian immunodeficiency viruses (HIV and SIV), and is critical for viral pathogenicity in vivo.The structure… (more)

Subjects/Keywords: nef Gene Products; Human Immunodeficiency Virus; Genes; nef; Chemokine CCL3; Chemokine CCL4; Amino Acids, Peptides, and Proteins; Biological Factors; Cells; Genetic Phenomena; Immunology and Infectious Disease; Life Sciences; Medicine and Health Sciences; Pathology; Viruses

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APA (6th Edition):

Dai, L. (2010). A Novel Motif in HIV-1 Nef that Regulates MIP-1β Chemokine Release in Macrophages: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/485

Chicago Manual of Style (16th Edition):

Dai, Lue. “A Novel Motif in HIV-1 Nef that Regulates MIP-1β Chemokine Release in Macrophages: A Dissertation.” 2010. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. https://escholarship.umassmed.edu/gsbs_diss/485.

MLA Handbook (7th Edition):

Dai, Lue. “A Novel Motif in HIV-1 Nef that Regulates MIP-1β Chemokine Release in Macrophages: A Dissertation.” 2010. Web. 19 Oct 2019.

Vancouver:

Dai L. A Novel Motif in HIV-1 Nef that Regulates MIP-1β Chemokine Release in Macrophages: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2010. [cited 2019 Oct 19]. Available from: https://escholarship.umassmed.edu/gsbs_diss/485.

Council of Science Editors:

Dai L. A Novel Motif in HIV-1 Nef that Regulates MIP-1β Chemokine Release in Macrophages: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2010. Available from: https://escholarship.umassmed.edu/gsbs_diss/485

24. Malhotra, Nidhi. Distinct Gene Circuits Control the Differentiation of Innate Versus Adaptive IL-17 Producing T Cells: A Dissertation.

Degree: Immunology and Microbiology, Pathology, 2012, U of Massachusetts : Med

  T lymphocytes are distinguished by the expression of αβ TCR or γδ TCR on their cell surface. The kinetic differences in the effector functions… (more)

Subjects/Keywords: Cell Differentiation; Interleukin-17; T-Lymphocytes; Th17 Cells; Genes; T-Cell Receptor; Smad2 Protein; Transforming Growth Factor beta; Amino Acids, Peptides, and Proteins; Biological Factors; Cell and Developmental Biology; Cells; Genetic Phenomena; Hemic and Immune Systems; Immunology and Infectious Disease

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APA (6th Edition):

Malhotra, N. (2012). Distinct Gene Circuits Control the Differentiation of Innate Versus Adaptive IL-17 Producing T Cells: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/579

Chicago Manual of Style (16th Edition):

Malhotra, Nidhi. “Distinct Gene Circuits Control the Differentiation of Innate Versus Adaptive IL-17 Producing T Cells: A Dissertation.” 2012. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. https://escholarship.umassmed.edu/gsbs_diss/579.

MLA Handbook (7th Edition):

Malhotra, Nidhi. “Distinct Gene Circuits Control the Differentiation of Innate Versus Adaptive IL-17 Producing T Cells: A Dissertation.” 2012. Web. 19 Oct 2019.

Vancouver:

Malhotra N. Distinct Gene Circuits Control the Differentiation of Innate Versus Adaptive IL-17 Producing T Cells: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2012. [cited 2019 Oct 19]. Available from: https://escholarship.umassmed.edu/gsbs_diss/579.

Council of Science Editors:

Malhotra N. Distinct Gene Circuits Control the Differentiation of Innate Versus Adaptive IL-17 Producing T Cells: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2012. Available from: https://escholarship.umassmed.edu/gsbs_diss/579

25. Chatterjee, Madhurima. Intestine Homeostasis and the Role of Tumor Suppressor Gene 101 in Drosophila Melanogaster: A Dissertation.

Degree: Interdisciplinary Graduate Program, Program in Molecular Medicine, 2011, U of Massachusetts : Med

  Tissue homeostasis in the adult Drosophila melanogaster intestine is maintained by controlling the proper balance of stem cell self-renewal and differentiation. In the adult… (more)

Subjects/Keywords: Genes; Tumor Suppressor; DNA-Binding Proteins; Transcription Factors; Endosomal Sorting Complexes Required for Transport; Homeostasis; Intestines; Drosophila melanogaster; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Cell and Developmental Biology; Digestive System; Genetic Phenomena; Neoplasms; Physiology

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APA (6th Edition):

Chatterjee, M. (2011). Intestine Homeostasis and the Role of Tumor Suppressor Gene 101 in Drosophila Melanogaster: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/597

Chicago Manual of Style (16th Edition):

Chatterjee, Madhurima. “Intestine Homeostasis and the Role of Tumor Suppressor Gene 101 in Drosophila Melanogaster: A Dissertation.” 2011. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. https://escholarship.umassmed.edu/gsbs_diss/597.

MLA Handbook (7th Edition):

Chatterjee, Madhurima. “Intestine Homeostasis and the Role of Tumor Suppressor Gene 101 in Drosophila Melanogaster: A Dissertation.” 2011. Web. 19 Oct 2019.

Vancouver:

Chatterjee M. Intestine Homeostasis and the Role of Tumor Suppressor Gene 101 in Drosophila Melanogaster: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2011. [cited 2019 Oct 19]. Available from: https://escholarship.umassmed.edu/gsbs_diss/597.

Council of Science Editors:

Chatterjee M. Intestine Homeostasis and the Role of Tumor Suppressor Gene 101 in Drosophila Melanogaster: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2011. Available from: https://escholarship.umassmed.edu/gsbs_diss/597

26. Trautmann, Susanne. Functions of the Cdc14-Family Phosphatase Clp1p in the Cell Cycle Regulation of Schizosaccharomyces pombe: A Dissertation.

Degree: Interdisciplinary Graduate Program, Biochemistry and Molecular Pharmacology, 2005, U of Massachusetts : Med

  In order to generate healthy daughter cells, nuclear division and cytokinesis need to be coordinated. Premature division of the cytoplasm in the absence of… (more)

Subjects/Keywords: Cytokinesis; Cell Cycle Proteins; Gene Expression Regulation; Enzymologic; Protein-Serine-Threonine Kinases; Schizosaccharomyces pombe Proteins; Genes; cdc; Enzymes and Coenzymes; Fungi

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APA (6th Edition):

Trautmann, S. (2005). Functions of the Cdc14-Family Phosphatase Clp1p in the Cell Cycle Regulation of Schizosaccharomyces pombe: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/10

Chicago Manual of Style (16th Edition):

Trautmann, Susanne. “Functions of the Cdc14-Family Phosphatase Clp1p in the Cell Cycle Regulation of Schizosaccharomyces pombe: A Dissertation.” 2005. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. https://escholarship.umassmed.edu/gsbs_diss/10.

MLA Handbook (7th Edition):

Trautmann, Susanne. “Functions of the Cdc14-Family Phosphatase Clp1p in the Cell Cycle Regulation of Schizosaccharomyces pombe: A Dissertation.” 2005. Web. 19 Oct 2019.

Vancouver:

Trautmann S. Functions of the Cdc14-Family Phosphatase Clp1p in the Cell Cycle Regulation of Schizosaccharomyces pombe: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2005. [cited 2019 Oct 19]. Available from: https://escholarship.umassmed.edu/gsbs_diss/10.

Council of Science Editors:

Trautmann S. Functions of the Cdc14-Family Phosphatase Clp1p in the Cell Cycle Regulation of Schizosaccharomyces pombe: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2005. Available from: https://escholarship.umassmed.edu/gsbs_diss/10

27. Shen, Yuelei. MHC Class I Antigen Presentation is Regulated by the SUMO-Conjugating Enzyme UBC9: a Dissertation.

Degree: Immunology and Microbiology, Pathology, 2003, U of Massachusetts : Med

  CD8 T cells recognize complexes of MHC class I and peptide on the surface of target cells. MHC class I antigen presentation is a… (more)

Subjects/Keywords: Genes; MHC Class I; Histocompatibility Antigens Class I; Small Ubiquitin-Related Modifier Proteins; Ubiquitin-Conjugating Enzymes; Amino Acids, Peptides, and Proteins; Biological Factors; Cells; Enzymes and Coenzymes; Genetic Phenomena

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APA (6th Edition):

Shen, Y. (2003). MHC Class I Antigen Presentation is Regulated by the SUMO-Conjugating Enzyme UBC9: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/111

Chicago Manual of Style (16th Edition):

Shen, Yuelei. “MHC Class I Antigen Presentation is Regulated by the SUMO-Conjugating Enzyme UBC9: a Dissertation.” 2003. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. https://escholarship.umassmed.edu/gsbs_diss/111.

MLA Handbook (7th Edition):

Shen, Yuelei. “MHC Class I Antigen Presentation is Regulated by the SUMO-Conjugating Enzyme UBC9: a Dissertation.” 2003. Web. 19 Oct 2019.

Vancouver:

Shen Y. MHC Class I Antigen Presentation is Regulated by the SUMO-Conjugating Enzyme UBC9: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2003. [cited 2019 Oct 19]. Available from: https://escholarship.umassmed.edu/gsbs_diss/111.

Council of Science Editors:

Shen Y. MHC Class I Antigen Presentation is Regulated by the SUMO-Conjugating Enzyme UBC9: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2003. Available from: https://escholarship.umassmed.edu/gsbs_diss/111

28. Xu, Minzhen. Regulation of Transcription of Mouse Immunoglobulin Germ-Line γ1 RNA: Structural Characterization of Germ-Line γ1 RNA and Molecular Analysis of the Promoter: A Dissertation.

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

  The antibody class switch is achieved by DNA recombination between the sequences called switch (S) regions located 5' to immunoglobulin (Ig) heavy chain constant… (more)

Subjects/Keywords: Genes; Immunoglobulin Heavy Chain; Promoter Regions (Genetics); Regulatory Sequences; Ribonucleic Acid; Mice; Germ Cells; Molecular Probes; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Biological Factors; Cells; Genetic Phenomena

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APA (6th Edition):

Xu, M. (1991). Regulation of Transcription of Mouse Immunoglobulin Germ-Line γ1 RNA: Structural Characterization of Germ-Line γ1 RNA and Molecular Analysis of the Promoter: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/99

Chicago Manual of Style (16th Edition):

Xu, Minzhen. “Regulation of Transcription of Mouse Immunoglobulin Germ-Line γ1 RNA: Structural Characterization of Germ-Line γ1 RNA and Molecular Analysis of the Promoter: A Dissertation.” 1991. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. https://escholarship.umassmed.edu/gsbs_diss/99.

MLA Handbook (7th Edition):

Xu, Minzhen. “Regulation of Transcription of Mouse Immunoglobulin Germ-Line γ1 RNA: Structural Characterization of Germ-Line γ1 RNA and Molecular Analysis of the Promoter: A Dissertation.” 1991. Web. 19 Oct 2019.

Vancouver:

Xu M. Regulation of Transcription of Mouse Immunoglobulin Germ-Line γ1 RNA: Structural Characterization of Germ-Line γ1 RNA and Molecular Analysis of the Promoter: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1991. [cited 2019 Oct 19]. Available from: https://escholarship.umassmed.edu/gsbs_diss/99.

Council of Science Editors:

Xu M. Regulation of Transcription of Mouse Immunoglobulin Germ-Line γ1 RNA: Structural Characterization of Germ-Line γ1 RNA and Molecular Analysis of the Promoter: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 1991. Available from: https://escholarship.umassmed.edu/gsbs_diss/99

29. Hess, Patricia M. Role of c-Jun NH-terminal Kinase in Bcr/Abl Induced Cell Transformation: a dissertation.

Degree: Interdisciplinary Graduate Program, Program in Molecular Medicine, 2003, U of Massachusetts : Med

  The c-Jun NH2-terminal kinase (JNK) group of kinases include ten members that are created by alternative splicing of transcripts derived from Jnk1, Jnk2 and… (more)

Subjects/Keywords: Mitogen-Activated Protein Kinase Kinases; Fusion Proteins; bcr-abl; Genes; abl; Cell Transformation; Neoplastic; Leukemia; Amino Acids, Peptides, and Proteins; Cells; Enzymes and Coenzymes; Genetic Phenomena; Neoplasms; Pathology

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

APA (6th Edition):

Hess, P. M. (2003). Role of c-Jun NH-terminal Kinase in Bcr/Abl Induced Cell Transformation: a dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/88

Chicago Manual of Style (16th Edition):

Hess, Patricia M. “Role of c-Jun NH-terminal Kinase in Bcr/Abl Induced Cell Transformation: a dissertation.” 2003. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. https://escholarship.umassmed.edu/gsbs_diss/88.

MLA Handbook (7th Edition):

Hess, Patricia M. “Role of c-Jun NH-terminal Kinase in Bcr/Abl Induced Cell Transformation: a dissertation.” 2003. Web. 19 Oct 2019.

Vancouver:

Hess PM. Role of c-Jun NH-terminal Kinase in Bcr/Abl Induced Cell Transformation: a dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2003. [cited 2019 Oct 19]. Available from: https://escholarship.umassmed.edu/gsbs_diss/88.

Council of Science Editors:

Hess PM. Role of c-Jun NH-terminal Kinase in Bcr/Abl Induced Cell Transformation: a dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2003. Available from: https://escholarship.umassmed.edu/gsbs_diss/88

30. Guidi, Cynthia J. The Role of the SWI/SNF Component INI1 in Mammalian Development and Tumorigenesis: a Dissertation.

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

  In vivo DNA is compacted tightly, via its association with histones and non-histone proteins, into higher-order chromatin structure. In this state, the DNA is… (more)

Subjects/Keywords: Chromosomal Proteins; Non-Histone; DNA-Binding Proteins; Genes; Tumor Suppressor; Mammals – growth & development; Mice; Transgenic; Tumor Suppressor Proteins; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Genetic Phenomena; Neoplasms

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

APA (6th Edition):

Guidi, C. J. (2003). The Role of the SWI/SNF Component INI1 in Mammalian Development and Tumorigenesis: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/69

Chicago Manual of Style (16th Edition):

Guidi, Cynthia J. “The Role of the SWI/SNF Component INI1 in Mammalian Development and Tumorigenesis: a Dissertation.” 2003. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 19, 2019. https://escholarship.umassmed.edu/gsbs_diss/69.

MLA Handbook (7th Edition):

Guidi, Cynthia J. “The Role of the SWI/SNF Component INI1 in Mammalian Development and Tumorigenesis: a Dissertation.” 2003. Web. 19 Oct 2019.

Vancouver:

Guidi CJ. The Role of the SWI/SNF Component INI1 in Mammalian Development and Tumorigenesis: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2003. [cited 2019 Oct 19]. Available from: https://escholarship.umassmed.edu/gsbs_diss/69.

Council of Science Editors:

Guidi CJ. The Role of the SWI/SNF Component INI1 in Mammalian Development and Tumorigenesis: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2003. Available from: https://escholarship.umassmed.edu/gsbs_diss/69

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