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Degree: Cell Biology

You searched for subject:( Epistasis Genetic 60). Showing records 1 – 30 of 31 total matches.

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1. Ramkumar, Charusheila. Antagonistic Pleiotropy: The Role of Smurf2 in Cancer and Aging: A Dissertation.

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

  In response to telomere shortening, oxidative stress, DNA damage or aberrant activation of oncogenes, normal somatic cells exit the cell cycle and enter an… (more)

Subjects/Keywords: Cell Aging; Genetic Pleiotropy; Ubiquitin-Protein Ligases; Cell Transformation; Neoplastic; Tumor Suppressor Proteins; Amino Acids, Peptides, and Proteins; Cancer Biology; Cell and Developmental Biology; Cells; Enzymes and Coenzymes; Genetic Phenomena; Neoplasms

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APA (6th Edition):

Ramkumar, C. (2012). Antagonistic Pleiotropy: The Role of Smurf2 in Cancer and Aging: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/634

Chicago Manual of Style (16th Edition):

Ramkumar, Charusheila. “Antagonistic Pleiotropy: The Role of Smurf2 in Cancer and Aging: A Dissertation.” 2012. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/634.

MLA Handbook (7th Edition):

Ramkumar, Charusheila. “Antagonistic Pleiotropy: The Role of Smurf2 in Cancer and Aging: A Dissertation.” 2012. Web. 15 Sep 2019.

Vancouver:

Ramkumar C. Antagonistic Pleiotropy: The Role of Smurf2 in Cancer and Aging: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2012. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/634.

Council of Science Editors:

Ramkumar C. Antagonistic Pleiotropy: The Role of Smurf2 in Cancer and Aging: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2012. Available from: https://escholarship.umassmed.edu/gsbs_diss/634

2. van Wijnen, Andre John. Transcriptional Control of Human Histone Gene Expression: Delineation and Regulation of Protein/DNA Interactions: A Thesis.

Degree: Cell Biology, Radiology, 1991, U of Massachusetts : Med

  Transcriptional regulation of cell cycle controlled genes is fundamental to cell division in eukaryotes and a broad spectrum of physiological processes directly related to… (more)

Subjects/Keywords: Histones; Gene Expression Regulation; Transcription; Genetic; Amino Acids, Peptides, and Proteins; Cells; Genetic Phenomena; Nucleic Acids, Nucleotides, and Nucleosides

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APA (6th Edition):

van Wijnen, A. J. (1991). Transcriptional Control of Human Histone Gene Expression: Delineation and Regulation of Protein/DNA Interactions: A Thesis. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/237

Chicago Manual of Style (16th Edition):

van Wijnen, Andre John. “Transcriptional Control of Human Histone Gene Expression: Delineation and Regulation of Protein/DNA Interactions: A Thesis.” 1991. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/237.

MLA Handbook (7th Edition):

van Wijnen, Andre John. “Transcriptional Control of Human Histone Gene Expression: Delineation and Regulation of Protein/DNA Interactions: A Thesis.” 1991. Web. 15 Sep 2019.

Vancouver:

van Wijnen AJ. Transcriptional Control of Human Histone Gene Expression: Delineation and Regulation of Protein/DNA Interactions: A Thesis. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1991. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/237.

Council of Science Editors:

van Wijnen AJ. Transcriptional Control of Human Histone Gene Expression: Delineation and Regulation of Protein/DNA Interactions: A Thesis. [Doctoral Dissertation]. U of Massachusetts : Med; 1991. Available from: https://escholarship.umassmed.edu/gsbs_diss/237

3. Swanson, Eric C. Higher-Order Unfolding of Peri/Centric Satellite Heterochromatin is an Early and Consistent Event in Cell Senescence: A Dissertation.

Degree: Cell Biology, NeuroNexus Neuroscience Institute, 2014, U of Massachusetts : Med

  Cellular senescence is thought to play an essential role in many biological functions including tumor suppression and organismal aging. Senescent cells, which are permanently… (more)

Subjects/Keywords: Cell Aging; Chromatin; Heterochromatin; Satellite DNA; Down Syndrome; Genetic Epigenesis; Protein Unfolding; Cell and Developmental Biology; Cell Biology; Cellular and Molecular Physiology; Genetics and Genomics

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APA (6th Edition):

Swanson, E. C. (2014). Higher-Order Unfolding of Peri/Centric Satellite Heterochromatin is an Early and Consistent Event in Cell Senescence: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/765

Chicago Manual of Style (16th Edition):

Swanson, Eric C. “Higher-Order Unfolding of Peri/Centric Satellite Heterochromatin is an Early and Consistent Event in Cell Senescence: A Dissertation.” 2014. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. http://escholarship.umassmed.edu/gsbs_diss/765.

MLA Handbook (7th Edition):

Swanson, Eric C. “Higher-Order Unfolding of Peri/Centric Satellite Heterochromatin is an Early and Consistent Event in Cell Senescence: A Dissertation.” 2014. Web. 15 Sep 2019.

Vancouver:

Swanson EC. Higher-Order Unfolding of Peri/Centric Satellite Heterochromatin is an Early and Consistent Event in Cell Senescence: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2014. [cited 2019 Sep 15]. Available from: http://escholarship.umassmed.edu/gsbs_diss/765.

Council of Science Editors:

Swanson EC. Higher-Order Unfolding of Peri/Centric Satellite Heterochromatin is an Early and Consistent Event in Cell Senescence: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2014. Available from: http://escholarship.umassmed.edu/gsbs_diss/765

4. Wright, Kenneth Lynn. Functional and Structural Characterization of a Human H4 Histone Gene Promoter: a Thesis.

Degree: Cell Biology, Radiology, 1990, U of Massachusetts : Med

  Expression of the cell cycle dependent FO10S human H4 histone gene is regulated at both the transcriptional and post-transcriptional levels. We have investigated the… (more)

Subjects/Keywords: Molecular Biology; Histones; Amino Acids, Peptides, and Proteins; Cells; Genetic Phenomena; Molecular Biology

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APA (6th Edition):

Wright, K. L. (1990). Functional and Structural Characterization of a Human H4 Histone Gene Promoter: a Thesis. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/52

Chicago Manual of Style (16th Edition):

Wright, Kenneth Lynn. “Functional and Structural Characterization of a Human H4 Histone Gene Promoter: a Thesis.” 1990. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/52.

MLA Handbook (7th Edition):

Wright, Kenneth Lynn. “Functional and Structural Characterization of a Human H4 Histone Gene Promoter: a Thesis.” 1990. Web. 15 Sep 2019.

Vancouver:

Wright KL. Functional and Structural Characterization of a Human H4 Histone Gene Promoter: a Thesis. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1990. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/52.

Council of Science Editors:

Wright KL. Functional and Structural Characterization of a Human H4 Histone Gene Promoter: a Thesis. [Doctoral Dissertation]. U of Massachusetts : Med; 1990. Available from: https://escholarship.umassmed.edu/gsbs_diss/52

5. Dowdy, Christopher R. Runx1 C-terminal Domains During Hematopoietic Development and Leukemogenesis: A Dissertation.

Degree: Cell Biology, Radiology, 2012, U of Massachusetts : Med

  Runx1 is a master regulator of hematopoiesis, required for the initiation of definitive hematopoiesis in the embryo and essential for appropriate differentiation of many… (more)

Subjects/Keywords: Hematopoiesis; Core Binding Factor Alpha 2 Subunit; Leukemia; Amino Acids, Peptides, and Proteins; Cell and Developmental Biology; Cells; Circulatory and Respiratory Physiology; Genetic Phenomena; Neoplasms

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APA (6th Edition):

Dowdy, C. R. (2012). Runx1 C-terminal Domains During Hematopoietic Development and Leukemogenesis: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/604

Chicago Manual of Style (16th Edition):

Dowdy, Christopher R. “Runx1 C-terminal Domains During Hematopoietic Development and Leukemogenesis: A Dissertation.” 2012. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/604.

MLA Handbook (7th Edition):

Dowdy, Christopher R. “Runx1 C-terminal Domains During Hematopoietic Development and Leukemogenesis: A Dissertation.” 2012. Web. 15 Sep 2019.

Vancouver:

Dowdy CR. Runx1 C-terminal Domains During Hematopoietic Development and Leukemogenesis: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2012. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/604.

Council of Science Editors:

Dowdy CR. Runx1 C-terminal Domains During Hematopoietic Development and Leukemogenesis: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2012. Available from: https://escholarship.umassmed.edu/gsbs_diss/604

6. Gutierrez Gallegos, Soraya Elisa. Mechanisms Contributing to Transcriptional Regulation and Chromatin Remodeling of the Bone Specific Osteocalcin Gene.

Degree: Cell Biology, Radiology, 2002, U of Massachusetts : Med

  Activation of tissue-specific genes is a tightly controlled process that normally involves the combined action of several transcription factors and transcriptional co-regulators. The bone-specific… (more)

Subjects/Keywords: Bone Development; Transcription; Genetic; Transcription Factors; Chromatin; Osteoblasts; Osteocalcin; CCAAT-Enhancer-Binding Proteins; Core Binding Factor Alpha 1 Subunit; Cells; Genetic Phenomena; Polycyclic Compounds; Tissues

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APA (6th Edition):

Gutierrez Gallegos, S. E. (2002). Mechanisms Contributing to Transcriptional Regulation and Chromatin Remodeling of the Bone Specific Osteocalcin Gene. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/12

Chicago Manual of Style (16th Edition):

Gutierrez Gallegos, Soraya Elisa. “Mechanisms Contributing to Transcriptional Regulation and Chromatin Remodeling of the Bone Specific Osteocalcin Gene.” 2002. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/12.

MLA Handbook (7th Edition):

Gutierrez Gallegos, Soraya Elisa. “Mechanisms Contributing to Transcriptional Regulation and Chromatin Remodeling of the Bone Specific Osteocalcin Gene.” 2002. Web. 15 Sep 2019.

Vancouver:

Gutierrez Gallegos SE. Mechanisms Contributing to Transcriptional Regulation and Chromatin Remodeling of the Bone Specific Osteocalcin Gene. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2002. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/12.

Council of Science Editors:

Gutierrez Gallegos SE. Mechanisms Contributing to Transcriptional Regulation and Chromatin Remodeling of the Bone Specific Osteocalcin Gene. [Doctoral Dissertation]. U of Massachusetts : Med; 2002. Available from: https://escholarship.umassmed.edu/gsbs_diss/12

7. Gannon, Hugh S. Mdm2-p53 Signaling in Tissue Homeostasis and the DNA Damage Response: A Dissertation.

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

  The p53 transcription factor responds to various cellular stressors by regulating the expression of numerous target genes involved in cellular processes such as cell… (more)

Subjects/Keywords: Proto-Oncogene Proteins c-mdm2; Tumor Suppressor Protein p53; Homeostasis; DNA Damage; Cell Transformation; Neoplastic; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Cancer Biology; Cell and Developmental Biology; Cells; Genetic Phenomena; Neoplasms; Tissues

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APA (6th Edition):

Gannon, H. S. (2012). Mdm2-p53 Signaling in Tissue Homeostasis and the DNA Damage Response: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/631

Chicago Manual of Style (16th Edition):

Gannon, Hugh S. “Mdm2-p53 Signaling in Tissue Homeostasis and the DNA Damage Response: A Dissertation.” 2012. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/631.

MLA Handbook (7th Edition):

Gannon, Hugh S. “Mdm2-p53 Signaling in Tissue Homeostasis and the DNA Damage Response: A Dissertation.” 2012. Web. 15 Sep 2019.

Vancouver:

Gannon HS. Mdm2-p53 Signaling in Tissue Homeostasis and the DNA Damage Response: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2012. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/631.

Council of Science Editors:

Gannon HS. Mdm2-p53 Signaling in Tissue Homeostasis and the DNA Damage Response: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2012. Available from: https://escholarship.umassmed.edu/gsbs_diss/631

8. Melloni, Richard H. Dynamics of Neuron-Specific Gene Expression During Development and in Response to Selective Lesions of the Rat Central Nervous System: A Dissertation.

Degree: Cell Biology, Neurology, Cell Biology and Anesthesiology, 1993, U of Massachusetts : Med

  Synapse development and injury-induced reorganization in the nervous system have been extensively characterized morphologically, although, relatively little is known regarding the molecular and biochemical… (more)

Subjects/Keywords: Central Nervous System; Gene Expression Regulation; Rats; Synaptins; Animal Experimentation and Research; Developmental Biology; Developmental Neuroscience; Genetic Phenomena; Nervous System

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APA (6th Edition):

Melloni, R. H. (1993). Dynamics of Neuron-Specific Gene Expression During Development and in Response to Selective Lesions of the Rat Central Nervous System: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/204

Chicago Manual of Style (16th Edition):

Melloni, Richard H. “Dynamics of Neuron-Specific Gene Expression During Development and in Response to Selective Lesions of the Rat Central Nervous System: A Dissertation.” 1993. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/204.

MLA Handbook (7th Edition):

Melloni, Richard H. “Dynamics of Neuron-Specific Gene Expression During Development and in Response to Selective Lesions of the Rat Central Nervous System: A Dissertation.” 1993. Web. 15 Sep 2019.

Vancouver:

Melloni RH. Dynamics of Neuron-Specific Gene Expression During Development and in Response to Selective Lesions of the Rat Central Nervous System: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1993. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/204.

Council of Science Editors:

Melloni RH. Dynamics of Neuron-Specific Gene Expression During Development and in Response to Selective Lesions of the Rat Central Nervous System: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 1993. Available from: https://escholarship.umassmed.edu/gsbs_diss/204

9. Tynan, Sharon H. The Role of the Light Intermediate Chains in Cytoplasmic Dynein Function: a Dissertation.

Degree: Cell Biology, Cell Biology, 2000, U of Massachusetts : Med

  Cytoplasmic dynein is a multisubunit complex involved in retrograde transport of cellular components along microtubules. The heavy chains (HC) are very large catalytic subunits… (more)

Subjects/Keywords: Dynein ATPase; Cytoplasm; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Cells; Enzymes and Coenzymes; Genetic Phenomena

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APA (6th Edition):

Tynan, S. H. (2000). The Role of the Light Intermediate Chains in Cytoplasmic Dynein Function: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/85

Chicago Manual of Style (16th Edition):

Tynan, Sharon H. “The Role of the Light Intermediate Chains in Cytoplasmic Dynein Function: a Dissertation.” 2000. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/85.

MLA Handbook (7th Edition):

Tynan, Sharon H. “The Role of the Light Intermediate Chains in Cytoplasmic Dynein Function: a Dissertation.” 2000. Web. 15 Sep 2019.

Vancouver:

Tynan SH. The Role of the Light Intermediate Chains in Cytoplasmic Dynein Function: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2000. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/85.

Council of Science Editors:

Tynan SH. The Role of the Light Intermediate Chains in Cytoplasmic Dynein Function: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2000. Available from: https://escholarship.umassmed.edu/gsbs_diss/85

10. Bassell, Gary J. Development and Application of Ultrastructural in Situ Hybridization to Visualize the Spatial Organization of mRNA: a Dissertation.

Degree: Cell Biology, Cell Biology, 1992, U of Massachusetts : Med

  It has been well documented that mRNA is associated with the cytoskeleton, and that this relationship is involved in translation and mRNA sorting. The… (more)

Subjects/Keywords: Hybridization; Genetic; RNA; Messenger; Amino Acids, Peptides, and Proteins; Cells; Investigative Techniques; Macromolecular Substances; Nucleic Acids, Nucleotides, and Nucleosides

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APA (6th Edition):

Bassell, G. J. (1992). Development and Application of Ultrastructural in Situ Hybridization to Visualize the Spatial Organization of mRNA: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/153

Chicago Manual of Style (16th Edition):

Bassell, Gary J. “Development and Application of Ultrastructural in Situ Hybridization to Visualize the Spatial Organization of mRNA: a Dissertation.” 1992. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/153.

MLA Handbook (7th Edition):

Bassell, Gary J. “Development and Application of Ultrastructural in Situ Hybridization to Visualize the Spatial Organization of mRNA: a Dissertation.” 1992. Web. 15 Sep 2019.

Vancouver:

Bassell GJ. Development and Application of Ultrastructural in Situ Hybridization to Visualize the Spatial Organization of mRNA: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1992. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/153.

Council of Science Editors:

Bassell GJ. Development and Application of Ultrastructural in Situ Hybridization to Visualize the Spatial Organization of mRNA: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 1992. Available from: https://escholarship.umassmed.edu/gsbs_diss/153

11. Cielinski, Matthew Joseph. Osteoclast Ontogeny-Experimental Studies in Two Osteopetrotic Mutations in the Rat: A Dissertation.

Degree: Cell Biology, Cell Biology, 1994, U of Massachusetts : Med

  Osteopetrosis is a metabolic bone disease in mammals characterized by a generalized skeletal sclerosis caused by reduced bone resorption. This reduced bone resorption is… (more)

Subjects/Keywords: Osteopetrosis; Bone Resorption; Tooth Eruption; Rats; Mutant Strains; Animal Experimentation and Research; Digestive System; Genetic Phenomena; Musculoskeletal Diseases; Stomatognathic System

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APA (6th Edition):

Cielinski, M. J. (1994). Osteoclast Ontogeny-Experimental Studies in Two Osteopetrotic Mutations in the Rat: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/141

Chicago Manual of Style (16th Edition):

Cielinski, Matthew Joseph. “Osteoclast Ontogeny-Experimental Studies in Two Osteopetrotic Mutations in the Rat: A Dissertation.” 1994. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/141.

MLA Handbook (7th Edition):

Cielinski, Matthew Joseph. “Osteoclast Ontogeny-Experimental Studies in Two Osteopetrotic Mutations in the Rat: A Dissertation.” 1994. Web. 15 Sep 2019.

Vancouver:

Cielinski MJ. Osteoclast Ontogeny-Experimental Studies in Two Osteopetrotic Mutations in the Rat: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1994. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/141.

Council of Science Editors:

Cielinski MJ. Osteoclast Ontogeny-Experimental Studies in Two Osteopetrotic Mutations in the Rat: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 1994. Available from: https://escholarship.umassmed.edu/gsbs_diss/141

12. Paschal, Bryce M. Structure and Function of Cytoplasmic Dynein: a Thesis.

Degree: Cell Biology, Cell Biology, 1992, U of Massachusetts : Med

  In previous work I described the purification and properties of the microtubule-based mechanochemical ATPase cytoplasmic dynein. Cytoplasmic dynein was found to produce force along… (more)

Subjects/Keywords: Cell Movement; Amino Acids, Peptides, and Proteins; Cells; Enzymes and Coenzymes; Genetic Phenomena; Nucleic Acids, Nucleotides, and Nucleosides

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APA (6th Edition):

Paschal, B. M. (1992). Structure and Function of Cytoplasmic Dynein: a Thesis. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/82

Chicago Manual of Style (16th Edition):

Paschal, Bryce M. “Structure and Function of Cytoplasmic Dynein: a Thesis.” 1992. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/82.

MLA Handbook (7th Edition):

Paschal, Bryce M. “Structure and Function of Cytoplasmic Dynein: a Thesis.” 1992. Web. 15 Sep 2019.

Vancouver:

Paschal BM. Structure and Function of Cytoplasmic Dynein: a Thesis. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1992. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/82.

Council of Science Editors:

Paschal BM. Structure and Function of Cytoplasmic Dynein: a Thesis. [Doctoral Dissertation]. U of Massachusetts : Med; 1992. Available from: https://escholarship.umassmed.edu/gsbs_diss/82

13. Clemson, Christine Moulton. Structural Association of XIST RNA with Inactive Chromosomes in Somatic Cells : a Key Step in the Process that Establishes and Faithfully Maintains X-inactivation.

Degree: Cell Biology, Neurology, 1998, U of Massachusetts : Med

  The XIST gene is implicated in X-chromosome inactivation, yet the RNA contains no apparent open reading frame. An accumulation of XIST RNA is observed… (more)

Subjects/Keywords: Gene Expression Regulation; Dosage Compensation (Genetics); RNA; Genetic Phenomena; Nucleic Acids, Nucleotides, and Nucleosides

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APA (6th Edition):

Clemson, C. M. (1998). Structural Association of XIST RNA with Inactive Chromosomes in Somatic Cells : a Key Step in the Process that Establishes and Faithfully Maintains X-inactivation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/8

Chicago Manual of Style (16th Edition):

Clemson, Christine Moulton. “Structural Association of XIST RNA with Inactive Chromosomes in Somatic Cells : a Key Step in the Process that Establishes and Faithfully Maintains X-inactivation.” 1998. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/8.

MLA Handbook (7th Edition):

Clemson, Christine Moulton. “Structural Association of XIST RNA with Inactive Chromosomes in Somatic Cells : a Key Step in the Process that Establishes and Faithfully Maintains X-inactivation.” 1998. Web. 15 Sep 2019.

Vancouver:

Clemson CM. Structural Association of XIST RNA with Inactive Chromosomes in Somatic Cells : a Key Step in the Process that Establishes and Faithfully Maintains X-inactivation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1998. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/8.

Council of Science Editors:

Clemson CM. Structural Association of XIST RNA with Inactive Chromosomes in Somatic Cells : a Key Step in the Process that Establishes and Faithfully Maintains X-inactivation. [Doctoral Dissertation]. U of Massachusetts : Med; 1998. Available from: https://escholarship.umassmed.edu/gsbs_diss/8

14. Last, Thomas J. Transcriptional Regulation of a Human H4 Histone Gene is Mediated by Multiple Elements Interacting with Similar Transcription Factors: A Dissertation.

Degree: Cell Biology, Radiology, 1998, U of Massachusetts : Med

  Synthesis of histone proteins occurs largely during the S phase of the cell cycle and coincides with DNA replication to provide adequate amounts of… (more)

Subjects/Keywords: Histones; Gene Expression Regulation; Cells; Amino Acids, Peptides, and Proteins; Biochemistry; Cell Biology; Genetic Phenomena; Molecular Biology

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APA (6th Edition):

Last, T. J. (1998). Transcriptional Regulation of a Human H4 Histone Gene is Mediated by Multiple Elements Interacting with Similar Transcription Factors: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/15

Chicago Manual of Style (16th Edition):

Last, Thomas J. “Transcriptional Regulation of a Human H4 Histone Gene is Mediated by Multiple Elements Interacting with Similar Transcription Factors: A Dissertation.” 1998. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/15.

MLA Handbook (7th Edition):

Last, Thomas J. “Transcriptional Regulation of a Human H4 Histone Gene is Mediated by Multiple Elements Interacting with Similar Transcription Factors: A Dissertation.” 1998. Web. 15 Sep 2019.

Vancouver:

Last TJ. Transcriptional Regulation of a Human H4 Histone Gene is Mediated by Multiple Elements Interacting with Similar Transcription Factors: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1998. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/15.

Council of Science Editors:

Last TJ. Transcriptional Regulation of a Human H4 Histone Gene is Mediated by Multiple Elements Interacting with Similar Transcription Factors: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 1998. Available from: https://escholarship.umassmed.edu/gsbs_diss/15

15. Wirschell, Maureen. Chlamydomonas Reinhardtii ODA5 Encodes an Axonemal Protein Required for Assembly of the Outer Dynein Arm and an Associated Flagellar Adenylate Kinase: A Dissertation.

Degree: Cell Biology, Radiology, 2004, U of Massachusetts : Med

  The first type of dynein identified, axonemel dynein (Gibbons and Rowe, 1965), slides adjacent microtubules within the axoneme, generating the force necessary for ciliary… (more)

Subjects/Keywords: Chlamydomonas reinhardtii; Dynein ATPase; Flagella; Adenylate Kinase; Gene Expression; Amino Acids, Peptides, and Proteins; Enzymes and Coenzymes; Genetic Phenomena

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APA (6th Edition):

Wirschell, M. (2004). Chlamydomonas Reinhardtii ODA5 Encodes an Axonemal Protein Required for Assembly of the Outer Dynein Arm and an Associated Flagellar Adenylate Kinase: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/25

Chicago Manual of Style (16th Edition):

Wirschell, Maureen. “Chlamydomonas Reinhardtii ODA5 Encodes an Axonemal Protein Required for Assembly of the Outer Dynein Arm and an Associated Flagellar Adenylate Kinase: A Dissertation.” 2004. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/25.

MLA Handbook (7th Edition):

Wirschell, Maureen. “Chlamydomonas Reinhardtii ODA5 Encodes an Axonemal Protein Required for Assembly of the Outer Dynein Arm and an Associated Flagellar Adenylate Kinase: A Dissertation.” 2004. Web. 15 Sep 2019.

Vancouver:

Wirschell M. Chlamydomonas Reinhardtii ODA5 Encodes an Axonemal Protein Required for Assembly of the Outer Dynein Arm and an Associated Flagellar Adenylate Kinase: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2004. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/25.

Council of Science Editors:

Wirschell M. Chlamydomonas Reinhardtii ODA5 Encodes an Axonemal Protein Required for Assembly of the Outer Dynein Arm and an Associated Flagellar Adenylate Kinase: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2004. Available from: https://escholarship.umassmed.edu/gsbs_diss/25

16. Tai, Chin-Yin. Roles of Lissencephaly Gene, LIS1, in Regulating Cytoplasmic Dynein Functions: a Dissertation.

Degree: Cell Biology, Cell Biology, 2002, U of Massachusetts : Med

  Spontaneous mutations in the human LIS1 gene are responsible for Type I lissencephaly ("smooth brain"). The distribution of neurons within the cerebral cortex of… (more)

Subjects/Keywords: Brain Diseases; Dynein ATPase; Microtubule Proteins; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Genetic Phenomena; Nervous System Diseases

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APA (6th Edition):

Tai, C. (2002). Roles of Lissencephaly Gene, LIS1, in Regulating Cytoplasmic Dynein Functions: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/31

Chicago Manual of Style (16th Edition):

Tai, Chin-Yin. “Roles of Lissencephaly Gene, LIS1, in Regulating Cytoplasmic Dynein Functions: a Dissertation.” 2002. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/31.

MLA Handbook (7th Edition):

Tai, Chin-Yin. “Roles of Lissencephaly Gene, LIS1, in Regulating Cytoplasmic Dynein Functions: a Dissertation.” 2002. Web. 15 Sep 2019.

Vancouver:

Tai C. Roles of Lissencephaly Gene, LIS1, in Regulating Cytoplasmic Dynein Functions: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2002. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/31.

Council of Science Editors:

Tai C. Roles of Lissencephaly Gene, LIS1, in Regulating Cytoplasmic Dynein Functions: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2002. Available from: https://escholarship.umassmed.edu/gsbs_diss/31

17. Montecino, Martin A. Chromatin Structure of the Rat Osteocalcin Gene Promoter in Bone-Derived Cells.

Degree: Cell Biology, Radiology, 1995, U of Massachusetts : Med

  Transcription of the osteocalcin gene, which encodes a bone-specific 10 kDa protein, is controlled by the coordinated utilization of modularly organized basal and hormone-responsive… (more)

Subjects/Keywords: Osteocalcin; Promoter Regions; Rats; Gene Expression; Cells; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Cells; Genetic Phenomena

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APA (6th Edition):

Montecino, M. A. (1995). Chromatin Structure of the Rat Osteocalcin Gene Promoter in Bone-Derived Cells. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/33

Chicago Manual of Style (16th Edition):

Montecino, Martin A. “Chromatin Structure of the Rat Osteocalcin Gene Promoter in Bone-Derived Cells.” 1995. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/33.

MLA Handbook (7th Edition):

Montecino, Martin A. “Chromatin Structure of the Rat Osteocalcin Gene Promoter in Bone-Derived Cells.” 1995. Web. 15 Sep 2019.

Vancouver:

Montecino MA. Chromatin Structure of the Rat Osteocalcin Gene Promoter in Bone-Derived Cells. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1995. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/33.

Council of Science Editors:

Montecino MA. Chromatin Structure of the Rat Osteocalcin Gene Promoter in Bone-Derived Cells. [Doctoral Dissertation]. U of Massachusetts : Med; 1995. Available from: https://escholarship.umassmed.edu/gsbs_diss/33

18. Luong, Mai X. Involvement of CDP/Cux in the Regulation of Histone H4 Gene Expression, Proliferation and Differentiation: a Dissertation.

Degree: Cell Biology, Radiology, 2003, U of Massachusetts : Med

  Proliferation and differentiation are essential processes for the growth and development of higher eukaryotic organisms. Regulation of gene expression is essential for control of… (more)

Subjects/Keywords: Gene Expression Regulation; Histones; Nuclear Proteins; Repressor Proteins; Amino Acids, Peptides, and Proteins; Cells; Genetic Phenomena

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APA (6th Edition):

Luong, M. X. (2003). Involvement of CDP/Cux in the Regulation of Histone H4 Gene Expression, Proliferation and Differentiation: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/34

Chicago Manual of Style (16th Edition):

Luong, Mai X. “Involvement of CDP/Cux in the Regulation of Histone H4 Gene Expression, Proliferation and Differentiation: a Dissertation.” 2003. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/34.

MLA Handbook (7th Edition):

Luong, Mai X. “Involvement of CDP/Cux in the Regulation of Histone H4 Gene Expression, Proliferation and Differentiation: a Dissertation.” 2003. Web. 15 Sep 2019.

Vancouver:

Luong MX. Involvement of CDP/Cux in the Regulation of Histone H4 Gene Expression, Proliferation and Differentiation: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2003. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/34.

Council of Science Editors:

Luong MX. Involvement of CDP/Cux in the Regulation of Histone H4 Gene Expression, Proliferation and Differentiation: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2003. Available from: https://escholarship.umassmed.edu/gsbs_diss/34

19. Xing, Yigong P. Nuclear Structure Studied by Fluorescence Hybridization: Visualization of Individual Gene Transcription and RNA Splicing: A Thesis.

Degree: Cell Biology, Neurology, 1993, U of Massachusetts : Med

  The overall objective of this study has been to address some of the longstanding questions concerning functional organization of the interphase nucleus. This was… (more)

Subjects/Keywords: Gene Expression Regulation; In Situ Hybridization; Fluorescence; RNA Splicing; Genetic Phenomena; Neoplasms; Nucleic Acids, Nucleotides, and Nucleosides

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APA (6th Edition):

Xing, Y. P. (1993). Nuclear Structure Studied by Fluorescence Hybridization: Visualization of Individual Gene Transcription and RNA Splicing: A Thesis. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/48

Chicago Manual of Style (16th Edition):

Xing, Yigong P. “Nuclear Structure Studied by Fluorescence Hybridization: Visualization of Individual Gene Transcription and RNA Splicing: A Thesis.” 1993. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/48.

MLA Handbook (7th Edition):

Xing, Yigong P. “Nuclear Structure Studied by Fluorescence Hybridization: Visualization of Individual Gene Transcription and RNA Splicing: A Thesis.” 1993. Web. 15 Sep 2019.

Vancouver:

Xing YP. Nuclear Structure Studied by Fluorescence Hybridization: Visualization of Individual Gene Transcription and RNA Splicing: A Thesis. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1993. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/48.

Council of Science Editors:

Xing YP. Nuclear Structure Studied by Fluorescence Hybridization: Visualization of Individual Gene Transcription and RNA Splicing: A Thesis. [Doctoral Dissertation]. U of Massachusetts : Med; 1993. Available from: https://escholarship.umassmed.edu/gsbs_diss/48

20. Dacwag, Caroline S. Analysis of Protein Arginine Methyltransferase Function during Myogenic Gene Transcription: A Dissertation.

Degree: Cell Biology, Biochemistry and Molecular Pharmacology, 2008, U of Massachusetts : Med

  Skeletal muscle differentiation requires synergy between tissue-specific transcription factors, chromatin remodeling enzymes and the general transcription machinery. Here we demonstrate that two distinct protein… (more)

Subjects/Keywords: Protein-Arginine N-Methyltransferase; Myogenic Regulatory Factors; Muscle Development; Muscle; Skeletal; Amino Acids, Peptides, and Proteins; Genetic Phenomena; Musculoskeletal System

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APA (6th Edition):

Dacwag, C. S. (2008). Analysis of Protein Arginine Methyltransferase Function during Myogenic Gene Transcription: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/402

Chicago Manual of Style (16th Edition):

Dacwag, Caroline S. “Analysis of Protein Arginine Methyltransferase Function during Myogenic Gene Transcription: A Dissertation.” 2008. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/402.

MLA Handbook (7th Edition):

Dacwag, Caroline S. “Analysis of Protein Arginine Methyltransferase Function during Myogenic Gene Transcription: A Dissertation.” 2008. Web. 15 Sep 2019.

Vancouver:

Dacwag CS. Analysis of Protein Arginine Methyltransferase Function during Myogenic Gene Transcription: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2008. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/402.

Council of Science Editors:

Dacwag CS. Analysis of Protein Arginine Methyltransferase Function during Myogenic Gene Transcription: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2008. Available from: https://escholarship.umassmed.edu/gsbs_diss/402

21. Pande, Sandhya. Regulation of Runx Proteins in Human Cancers: A Dissertation.

Degree: Cell Biology, Radiology, 2011, U of Massachusetts : Med

  Runt related transcription factors (Runx) play an important role in mammalian development by regulating the expression of key genes involved in cell proliferation, differentiation… (more)

Subjects/Keywords: Core Binding Factor alpha Subunits; Core Binding Factor Alpha 2 Subunit; Core Binding Factor Alpha 3 Subunit; Gene Expression Regulation; Neoplasms; Amino Acids, Peptides, and Proteins; Cell and Developmental Biology; Cells; Genetic Phenomena; Neoplasms

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APA (6th Edition):

Pande, S. (2011). Regulation of Runx Proteins in Human Cancers: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/559

Chicago Manual of Style (16th Edition):

Pande, Sandhya. “Regulation of Runx Proteins in Human Cancers: A Dissertation.” 2011. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/559.

MLA Handbook (7th Edition):

Pande, Sandhya. “Regulation of Runx Proteins in Human Cancers: A Dissertation.” 2011. Web. 15 Sep 2019.

Vancouver:

Pande S. Regulation of Runx Proteins in Human Cancers: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2011. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/559.

Council of Science Editors:

Pande S. Regulation of Runx Proteins in Human Cancers: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2011. Available from: https://escholarship.umassmed.edu/gsbs_diss/559

22. Harrington, Kimberly Stacy. Intranuclear Trafficking of RUNX/AML/CBFA/PEBP2 Transcription Factors in Living Cells: A Dissertation.

Degree: Cell Biology, Radiology, 2003, U of Massachusetts : Med

  The family of runt related transcription factors (RUNX/Cbfa/AML/PEBP2) are essential for cellular differentiation and fetal development. RUNX factors are distributed throughout the nucleus in… (more)

Subjects/Keywords: Transcription; Genetic; Transcription Factors; DNA-Binding Proteins; Focal Adhesions; Cell Nucleus; Nuclear Localization Signals; Osteocalcin; Osteocytes; Osteoblasts; Bone Diseases; Models; Animal; Microscopy; Fluorescence; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Cell and Developmental Biology; Cells; Genetic Phenomena; Investigative Techniques; Musculoskeletal Diseases; Tissues

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APA (6th Edition):

Harrington, K. S. (2003). Intranuclear Trafficking of RUNX/AML/CBFA/PEBP2 Transcription Factors in Living Cells: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/104

Chicago Manual of Style (16th Edition):

Harrington, Kimberly Stacy. “Intranuclear Trafficking of RUNX/AML/CBFA/PEBP2 Transcription Factors in Living Cells: A Dissertation.” 2003. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/104.

MLA Handbook (7th Edition):

Harrington, Kimberly Stacy. “Intranuclear Trafficking of RUNX/AML/CBFA/PEBP2 Transcription Factors in Living Cells: A Dissertation.” 2003. Web. 15 Sep 2019.

Vancouver:

Harrington KS. Intranuclear Trafficking of RUNX/AML/CBFA/PEBP2 Transcription Factors in Living Cells: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2003. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/104.

Council of Science Editors:

Harrington KS. Intranuclear Trafficking of RUNX/AML/CBFA/PEBP2 Transcription Factors in Living Cells: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2003. Available from: https://escholarship.umassmed.edu/gsbs_diss/104

23. Echeverri, Christophe de Jesus. Cloning and Characterization of Dynamitin, the 50 kDa Subunit of Dynactin: A Study of Dynactin and Cytoplasmic Dynein Function in Vertebrates.

Degree: Cell Biology, Cell Biology, 1998, U of Massachusetts : Med

  Dynactin is a multi-subunit complex which was initially identified in 1991 as an activator of cytoplasmic dynein-driven microtubule-based organelle motility in vitro. Although genetic(more)

Subjects/Keywords: Microtubule-Associated Proteins; Dynein ATPase; Cytoplasmic Streaming; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Cells; Enzymes and Coenzymes; Genetic Phenomena; Tissues

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APA (6th Edition):

Echeverri, C. d. J. (1998). Cloning and Characterization of Dynamitin, the 50 kDa Subunit of Dynactin: A Study of Dynactin and Cytoplasmic Dynein Function in Vertebrates. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/86

Chicago Manual of Style (16th Edition):

Echeverri, Christophe de Jesus. “Cloning and Characterization of Dynamitin, the 50 kDa Subunit of Dynactin: A Study of Dynactin and Cytoplasmic Dynein Function in Vertebrates.” 1998. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/86.

MLA Handbook (7th Edition):

Echeverri, Christophe de Jesus. “Cloning and Characterization of Dynamitin, the 50 kDa Subunit of Dynactin: A Study of Dynactin and Cytoplasmic Dynein Function in Vertebrates.” 1998. Web. 15 Sep 2019.

Vancouver:

Echeverri CdJ. Cloning and Characterization of Dynamitin, the 50 kDa Subunit of Dynactin: A Study of Dynactin and Cytoplasmic Dynein Function in Vertebrates. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1998. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/86.

Council of Science Editors:

Echeverri CdJ. Cloning and Characterization of Dynamitin, the 50 kDa Subunit of Dynactin: A Study of Dynactin and Cytoplasmic Dynein Function in Vertebrates. [Doctoral Dissertation]. U of Massachusetts : Med; 1998. Available from: https://escholarship.umassmed.edu/gsbs_diss/86

24. Grishok, Alla. Analysis of RNA Interference in C. elegans: A Dissertation.

Degree: Cell Biology, RNA Therapeutics Institute, 2001, U of Massachusetts : Med

  RNA interference (RNAi) in the nematode Caenorhabditis elegans is a type of homology-dependent post-transcriptional gene silencing induced by dsRNA. This dissertation describes the genetic(more)

Subjects/Keywords: Caenorhabditis elegans; RNA Interference; RNA; Small Interfering; Animal Experimentation and Research; Genetic Phenomena; Hemic and Immune Systems; Nucleic Acids, Nucleotides, and Nucleosides

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APA (6th Edition):

Grishok, A. (2001). Analysis of RNA Interference in C. elegans: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/139

Chicago Manual of Style (16th Edition):

Grishok, Alla. “Analysis of RNA Interference in C. elegans: A Dissertation.” 2001. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/139.

MLA Handbook (7th Edition):

Grishok, Alla. “Analysis of RNA Interference in C. elegans: A Dissertation.” 2001. Web. 15 Sep 2019.

Vancouver:

Grishok A. Analysis of RNA Interference in C. elegans: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2001. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/139.

Council of Science Editors:

Grishok A. Analysis of RNA Interference in C. elegans: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2001. Available from: https://escholarship.umassmed.edu/gsbs_diss/139

25. Sparks, Cynthia A. Cloning and Cell Cycle Analysis of NuMA, a Phosphoprotein That Oscillates Between the Nucleus and the Mitotic Spindle.

Degree: Cell Biology, Cell Biology, 1995, U of Massachusetts : Med

  The overall objective of this study was to identify novel proteins of the nuclear matrix in order to contribute to a better understanding of… (more)

Subjects/Keywords: Nuclear Matrix-Associated Proteins; Phosphoproteins; Nuclear Matrix; Mitotic Spindle Apparatus; Amino Acids, Peptides, and Proteins; Cell Biology; Cells; Genetic Phenomena; Nucleic Acids, Nucleotides, and Nucleosides

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APA (6th Edition):

Sparks, C. A. (1995). Cloning and Cell Cycle Analysis of NuMA, a Phosphoprotein That Oscillates Between the Nucleus and the Mitotic Spindle. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/35

Chicago Manual of Style (16th Edition):

Sparks, Cynthia A. “Cloning and Cell Cycle Analysis of NuMA, a Phosphoprotein That Oscillates Between the Nucleus and the Mitotic Spindle.” 1995. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/35.

MLA Handbook (7th Edition):

Sparks, Cynthia A. “Cloning and Cell Cycle Analysis of NuMA, a Phosphoprotein That Oscillates Between the Nucleus and the Mitotic Spindle.” 1995. Web. 15 Sep 2019.

Vancouver:

Sparks CA. Cloning and Cell Cycle Analysis of NuMA, a Phosphoprotein That Oscillates Between the Nucleus and the Mitotic Spindle. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1995. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/35.

Council of Science Editors:

Sparks CA. Cloning and Cell Cycle Analysis of NuMA, a Phosphoprotein That Oscillates Between the Nucleus and the Mitotic Spindle. [Doctoral Dissertation]. U of Massachusetts : Med; 1995. Available from: https://escholarship.umassmed.edu/gsbs_diss/35

26. Salma, Nunciada. Transcriptional Regulation During Adipocyte Differentiation: A Role for SWI/SNF Chromatin Remodeling Enzymes: A Dissertation.

Degree: Cell Biology, Biochemistry and Molecular Pharmacology, 2006, U of Massachusetts : Med

  Chromatin has a compact organization in which most DNA sequences are structurally inaccessible and functionally inactive. Reconfiguration of thechromatir required to activate transcription. This… (more)

Subjects/Keywords: Transcription Factors; Chromatin Assembly and Disassembly; Cell Differentiation; Adipogenesis; PPAR gamma; CCAAT-Enhancer-Binding Proteins; Amino Acids, Peptides, and Proteins; Cells; Enzymes and Coenzymes; Genetic Phenomena

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APA (6th Edition):

Salma, N. (2006). Transcriptional Regulation During Adipocyte Differentiation: A Role for SWI/SNF Chromatin Remodeling Enzymes: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/50

Chicago Manual of Style (16th Edition):

Salma, Nunciada. “Transcriptional Regulation During Adipocyte Differentiation: A Role for SWI/SNF Chromatin Remodeling Enzymes: A Dissertation.” 2006. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/50.

MLA Handbook (7th Edition):

Salma, Nunciada. “Transcriptional Regulation During Adipocyte Differentiation: A Role for SWI/SNF Chromatin Remodeling Enzymes: A Dissertation.” 2006. Web. 15 Sep 2019.

Vancouver:

Salma N. Transcriptional Regulation During Adipocyte Differentiation: A Role for SWI/SNF Chromatin Remodeling Enzymes: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2006. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/50.

Council of Science Editors:

Salma N. Transcriptional Regulation During Adipocyte Differentiation: A Role for SWI/SNF Chromatin Remodeling Enzymes: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2006. Available from: https://escholarship.umassmed.edu/gsbs_diss/50

27. Ashraf, Shovon I. Snail Protein Family in Drosophila Neurogenesis: a Dissertation.

Degree: Cell Biology, Program in Molecular Medicine, 2001, U of Massachusetts : Med

  The Snail protein functions as a transcriptional regulator to establish early mesodermal cell fate in Drosophila. Later, in germ band-extended embryos, Snail is considered… (more)

Subjects/Keywords: Central Nervous System; Drosophila; Drosophila Proteins; Transcription Factors; Zinc Fingers; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Embryonic Structures; Genetic Phenomena; Nervous System; Nucleic Acids, Nucleotides, and Nucleosides

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APA (6th Edition):

Ashraf, S. I. (2001). Snail Protein Family in Drosophila Neurogenesis: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/53

Chicago Manual of Style (16th Edition):

Ashraf, Shovon I. “Snail Protein Family in Drosophila Neurogenesis: a Dissertation.” 2001. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/53.

MLA Handbook (7th Edition):

Ashraf, Shovon I. “Snail Protein Family in Drosophila Neurogenesis: a Dissertation.” 2001. Web. 15 Sep 2019.

Vancouver:

Ashraf SI. Snail Protein Family in Drosophila Neurogenesis: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2001. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/53.

Council of Science Editors:

Ashraf SI. Snail Protein Family in Drosophila Neurogenesis: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2001. Available from: https://escholarship.umassmed.edu/gsbs_diss/53

28. 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 (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 September 15, 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. 15 Sep 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 Sep 15]. 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

29. Lengner, Christopher J. Regulation and Function of Runx2 During Chondrogenic and Osteogenic Differentiation: a Dissertation.

Degree: Cell Biology, Radiology, 2004, U of Massachusetts : Med

  Members of the Runx family of transcription factors play essential roles in the differentiation and development of several organ systems. Here we address the… (more)

Subjects/Keywords: Cell Proliferation; Transcription Factors; Bone and Bones; Chondrocytes; DNA-Binding Proteins; Proto-Oncogene Proteins; Nuclear Proteins; Bone Morphogenetic Proteins; Amino Acids, Peptides, and Proteins; Cells; Genetic Phenomena; Musculoskeletal System; Tissues

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

APA (6th Edition):

Lengner, C. J. (2004). Regulation and Function of Runx2 During Chondrogenic and Osteogenic Differentiation: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/80

Chicago Manual of Style (16th Edition):

Lengner, Christopher J. “Regulation and Function of Runx2 During Chondrogenic and Osteogenic Differentiation: a Dissertation.” 2004. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/80.

MLA Handbook (7th Edition):

Lengner, Christopher J. “Regulation and Function of Runx2 During Chondrogenic and Osteogenic Differentiation: a Dissertation.” 2004. Web. 15 Sep 2019.

Vancouver:

Lengner CJ. Regulation and Function of Runx2 During Chondrogenic and Osteogenic Differentiation: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2004. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/80.

Council of Science Editors:

Lengner CJ. Regulation and Function of Runx2 During Chondrogenic and Osteogenic Differentiation: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2004. Available from: https://escholarship.umassmed.edu/gsbs_diss/80

30. Young, Daniel W. Regulation of Cell Growth and Differentiation within the Context of Nuclear Architecture by the Runx2 Transcription Factor: a Dissertation.

Degree: Cell Biology, Orthopedics and Physical Rehabilitation, 2005, U of Massachusetts : Med

  The Runx family of transcription factors performs an essential role in animal development by controlling gene expression programs that mediate cell proliferation, growth and… (more)

Subjects/Keywords: Transcription Factors; Cell Differentiation; Gene Expression Regulation; DNA-Binding Proteins; Core Binding Factor Alpha 1 Subunit; Chromatin Assembly and Disassembly; Computational Biology; Amino Acids, Peptides, and Proteins; Cells; Genetic Phenomena

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

APA (6th Edition):

Young, D. W. (2005). Regulation of Cell Growth and Differentiation within the Context of Nuclear Architecture by the Runx2 Transcription Factor: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/19

Chicago Manual of Style (16th Edition):

Young, Daniel W. “Regulation of Cell Growth and Differentiation within the Context of Nuclear Architecture by the Runx2 Transcription Factor: a Dissertation.” 2005. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 15, 2019. https://escholarship.umassmed.edu/gsbs_diss/19.

MLA Handbook (7th Edition):

Young, Daniel W. “Regulation of Cell Growth and Differentiation within the Context of Nuclear Architecture by the Runx2 Transcription Factor: a Dissertation.” 2005. Web. 15 Sep 2019.

Vancouver:

Young DW. Regulation of Cell Growth and Differentiation within the Context of Nuclear Architecture by the Runx2 Transcription Factor: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2005. [cited 2019 Sep 15]. Available from: https://escholarship.umassmed.edu/gsbs_diss/19.

Council of Science Editors:

Young DW. Regulation of Cell Growth and Differentiation within the Context of Nuclear Architecture by the Runx2 Transcription Factor: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2005. Available from: https://escholarship.umassmed.edu/gsbs_diss/19

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