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Degree: Cell Biology

You searched for subject:(AMINO SUGARS BIOCHEMISTRY ). Showing records 1 – 30 of 42 total matches.

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1. 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 December 09, 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. 09 Dec 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 Dec 09]. 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

2. Odgren, Paul R. Molecular Characterization of Mitofilin, a Novel, Mitochondrial, Coiled Coil Protein, and the Relationship Between Organism Complexity and Coiled Coil Protein-Mediated Structure: A Dissertation.

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

  In the course of experiments designed to identify and characterize structural proteins of the nuclear matrix, one antibody was generated which recognized an extraction-resistant… (more)

Subjects/Keywords: Recombinant Protein; Nuclear Matrix; Antibodies; Amino Acids, Peptides, and Proteins; Biochemistry; Cell Biology; Molecular Biology; Structural Biology

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APA (6th Edition):

Odgren, P. R. (1995). Molecular Characterization of Mitofilin, a Novel, Mitochondrial, Coiled Coil Protein, and the Relationship Between Organism Complexity and Coiled Coil Protein-Mediated Structure: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/28

Chicago Manual of Style (16th Edition):

Odgren, Paul R. “Molecular Characterization of Mitofilin, a Novel, Mitochondrial, Coiled Coil Protein, and the Relationship Between Organism Complexity and Coiled Coil Protein-Mediated Structure: A Dissertation.” 1995. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 09, 2019. https://escholarship.umassmed.edu/gsbs_diss/28.

MLA Handbook (7th Edition):

Odgren, Paul R. “Molecular Characterization of Mitofilin, a Novel, Mitochondrial, Coiled Coil Protein, and the Relationship Between Organism Complexity and Coiled Coil Protein-Mediated Structure: A Dissertation.” 1995. Web. 09 Dec 2019.

Vancouver:

Odgren PR. Molecular Characterization of Mitofilin, a Novel, Mitochondrial, Coiled Coil Protein, and the Relationship Between Organism Complexity and Coiled Coil Protein-Mediated Structure: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1995. [cited 2019 Dec 09]. Available from: https://escholarship.umassmed.edu/gsbs_diss/28.

Council of Science Editors:

Odgren PR. Molecular Characterization of Mitofilin, a Novel, Mitochondrial, Coiled Coil Protein, and the Relationship Between Organism Complexity and Coiled Coil Protein-Mediated Structure: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 1995. Available from: https://escholarship.umassmed.edu/gsbs_diss/28

3. Tortelote, Giovane G. An Extra-Embryonic Wnt Signaling Event Controls Gastrulation in Mice: A Dissertation.

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

  The formation of the anterior-posterior axis requires a symmetry-breaking event that starts gastrulation. Ultimately, the morphogenetic movements of gastrulation reshape the embryo to its… (more)

Subjects/Keywords: Wnt3 Protein; Gastrulation; Mice; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Cell and Developmental Biology; Embryonic Structures

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APA (6th Edition):

Tortelote, G. G. (2012). An Extra-Embryonic Wnt Signaling Event Controls Gastrulation in Mice: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/643

Chicago Manual of Style (16th Edition):

Tortelote, Giovane G. “An Extra-Embryonic Wnt Signaling Event Controls Gastrulation in Mice: A Dissertation.” 2012. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 09, 2019. https://escholarship.umassmed.edu/gsbs_diss/643.

MLA Handbook (7th Edition):

Tortelote, Giovane G. “An Extra-Embryonic Wnt Signaling Event Controls Gastrulation in Mice: A Dissertation.” 2012. Web. 09 Dec 2019.

Vancouver:

Tortelote GG. An Extra-Embryonic Wnt Signaling Event Controls Gastrulation in Mice: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2012. [cited 2019 Dec 09]. Available from: https://escholarship.umassmed.edu/gsbs_diss/643.

Council of Science Editors:

Tortelote GG. An Extra-Embryonic Wnt Signaling Event Controls Gastrulation in Mice: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2012. Available from: https://escholarship.umassmed.edu/gsbs_diss/643

4. Megeath, Laura Jalso. Characterization of the Molecular Mechanisms Regulating the Agrin Signaling Pathway: a Dissertation.

Degree: Cell Biology, Cell Biology, 1999, U of Massachusetts : Med

  The nervous system requires rapid, efficient, and accurate transmission between cells for proper functioning. Synapses are the predominant structures through which such vital communication… (more)

Subjects/Keywords: Neuromuscular Junction; Agrin; Synaptic Transmission; Amino Acids, Peptides, and Proteins; Nervous System

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APA (6th Edition):

Megeath, L. J. (1999). Characterization of the Molecular Mechanisms Regulating the Agrin Signaling Pathway: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/29

Chicago Manual of Style (16th Edition):

Megeath, Laura Jalso. “Characterization of the Molecular Mechanisms Regulating the Agrin Signaling Pathway: a Dissertation.” 1999. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 09, 2019. https://escholarship.umassmed.edu/gsbs_diss/29.

MLA Handbook (7th Edition):

Megeath, Laura Jalso. “Characterization of the Molecular Mechanisms Regulating the Agrin Signaling Pathway: a Dissertation.” 1999. Web. 09 Dec 2019.

Vancouver:

Megeath LJ. Characterization of the Molecular Mechanisms Regulating the Agrin Signaling Pathway: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1999. [cited 2019 Dec 09]. Available from: https://escholarship.umassmed.edu/gsbs_diss/29.

Council of Science Editors:

Megeath LJ. Characterization of the Molecular Mechanisms Regulating the Agrin Signaling Pathway: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 1999. Available from: https://escholarship.umassmed.edu/gsbs_diss/29

5. 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 December 09, 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. 09 Dec 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 Dec 09]. 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

6. 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 December 09, 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. 09 Dec 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 Dec 09]. 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

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 December 09, 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. 09 Dec 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 Dec 09]. 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. 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 December 09, 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. 09 Dec 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 Dec 09]. 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

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 December 09, 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. 09 Dec 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 Dec 09]. 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 December 09, 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. 09 Dec 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 Dec 09]. 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. Levine, Kara B. Identification of the Human Erythrocyte Glucose Transporter (GLUT1) ATP Binding Domain: A Dissertation.

Degree: Cell Biology, Biochemistry and Molecular Pharmacology, 1999, U of Massachusetts : Med

  The human erythrocyte glucose transport protein (GLUT1) interacts with, and is regulated by, cytosolic ATP. This study asks the following questions concerning ATP modulation… (more)

Subjects/Keywords: Monosaccharide Transport Proteins; Adenosine Triphosphate; Amino Acids, Peptides, and Proteins; Carbohydrates; Heterocyclic Compounds; Nucleic Acids, Nucleotides, and Nucleosides

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APA (6th Edition):

Levine, K. B. (1999). Identification of the Human Erythrocyte Glucose Transporter (GLUT1) ATP Binding Domain: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/247

Chicago Manual of Style (16th Edition):

Levine, Kara B. “Identification of the Human Erythrocyte Glucose Transporter (GLUT1) ATP Binding Domain: A Dissertation.” 1999. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 09, 2019. https://escholarship.umassmed.edu/gsbs_diss/247.

MLA Handbook (7th Edition):

Levine, Kara B. “Identification of the Human Erythrocyte Glucose Transporter (GLUT1) ATP Binding Domain: A Dissertation.” 1999. Web. 09 Dec 2019.

Vancouver:

Levine KB. Identification of the Human Erythrocyte Glucose Transporter (GLUT1) ATP Binding Domain: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1999. [cited 2019 Dec 09]. Available from: https://escholarship.umassmed.edu/gsbs_diss/247.

Council of Science Editors:

Levine KB. Identification of the Human Erythrocyte Glucose Transporter (GLUT1) ATP Binding Domain: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 1999. Available from: https://escholarship.umassmed.edu/gsbs_diss/247

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 December 09, 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. 09 Dec 2019.

Vancouver:

Paschal BM. Structure and Function of Cytoplasmic Dynein: a Thesis. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1992. [cited 2019 Dec 09]. 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. 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 December 09, 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. 09 Dec 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 Dec 09]. 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

14. 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 December 09, 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. 09 Dec 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 Dec 09]. 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

15. 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 December 09, 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. 09 Dec 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 Dec 09]. 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

16. Munevar, Steven. Mechanics of Fibroblast Migration: a Dissertation.

Degree: Cell Biology, Department of Physiology, 2003, U of Massachusetts : Med

  Cell migration involves complex mechanical interactions between cells or between cells and the underlying substrate. Using a newly developed technique, "traction force microscopy", I… (more)

Subjects/Keywords: Cell Movement; Microscopy; Fibroblasts; 3T3 Cells; Biomechanics; Amino Acids, Peptides, and Proteins; Cells; Investigative Techniques; Macromolecular Substances

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APA (6th Edition):

Munevar, S. (2003). Mechanics of Fibroblast Migration: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/36

Chicago Manual of Style (16th Edition):

Munevar, Steven. “Mechanics of Fibroblast Migration: a Dissertation.” 2003. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 09, 2019. https://escholarship.umassmed.edu/gsbs_diss/36.

MLA Handbook (7th Edition):

Munevar, Steven. “Mechanics of Fibroblast Migration: a Dissertation.” 2003. Web. 09 Dec 2019.

Vancouver:

Munevar S. Mechanics of Fibroblast Migration: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2003. [cited 2019 Dec 09]. Available from: https://escholarship.umassmed.edu/gsbs_diss/36.

Council of Science Editors:

Munevar S. Mechanics of Fibroblast Migration: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2003. Available from: https://escholarship.umassmed.edu/gsbs_diss/36

17. Rocheleau, Christian Ernest. Analysis of Cell Polarity Signaling in C. elegans: A Dissertation.

Degree: Cell Biology, RNA Therapeutics Institute, 1999, U of Massachusetts : Med

  During embryonic development of the nematode Caenorhabditis elegans, cell fates are specified by asymmetric segregation of cell fate determinants and via cell-cell signaling events.… (more)

Subjects/Keywords: Cell Polarity; Caenorhabditis elegans; Cell Differentiation; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Cells; Embryonic Structures; Enzymes and Coenzymes

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APA (6th Edition):

Rocheleau, C. E. (1999). Analysis of Cell Polarity Signaling in C. elegans: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/46

Chicago Manual of Style (16th Edition):

Rocheleau, Christian Ernest. “Analysis of Cell Polarity Signaling in C. elegans: A Dissertation.” 1999. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 09, 2019. https://escholarship.umassmed.edu/gsbs_diss/46.

MLA Handbook (7th Edition):

Rocheleau, Christian Ernest. “Analysis of Cell Polarity Signaling in C. elegans: A Dissertation.” 1999. Web. 09 Dec 2019.

Vancouver:

Rocheleau CE. Analysis of Cell Polarity Signaling in C. elegans: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1999. [cited 2019 Dec 09]. Available from: https://escholarship.umassmed.edu/gsbs_diss/46.

Council of Science Editors:

Rocheleau CE. Analysis of Cell Polarity Signaling in C. elegans: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 1999. Available from: https://escholarship.umassmed.edu/gsbs_diss/46

18. 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 December 09, 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. 09 Dec 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 Dec 09]. 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

19. 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 December 09, 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. 09 Dec 2019.

Vancouver:

Pande S. Regulation of Runx Proteins in Human Cancers: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2011. [cited 2019 Dec 09]. 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

20. 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 December 09, 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. 09 Dec 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 Dec 09]. 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

21. Matzelle, Melissa M. Inflammation Inhibits Osteoblast-Mediated Bone Formation in Rheumatoid Arthritis and Regulates the Wnt and BMP Signaling Pathways: A Dissertation.

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

  Osteoclast-mediated focal articular bone erosion is a hallmark of rheumatoid arthritis, a disease of inflammation-induced bone loss. Inflammation in the bone microenvironment enhances osteoclast… (more)

Subjects/Keywords: Inflammation; Osteogenesis; Arthritis; Rheumatoid; Wnt Signaling Pathway; Bone Morphogenetic Protein Receptors; Amino Acids, Peptides, and Proteins; Cell and Developmental Biology; Immune System Diseases; Musculoskeletal Diseases; Musculoskeletal, Neural, and Ocular Physiology; Musculoskeletal System; Pathological Conditions, Signs and Symptoms; Rheumatology; Skin and Connective Tissue Diseases

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APA (6th Edition):

Matzelle, M. M. (2012). Inflammation Inhibits Osteoblast-Mediated Bone Formation in Rheumatoid Arthritis and Regulates the Wnt and BMP Signaling Pathways: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/596

Chicago Manual of Style (16th Edition):

Matzelle, Melissa M. “Inflammation Inhibits Osteoblast-Mediated Bone Formation in Rheumatoid Arthritis and Regulates the Wnt and BMP Signaling Pathways: A Dissertation.” 2012. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 09, 2019. https://escholarship.umassmed.edu/gsbs_diss/596.

MLA Handbook (7th Edition):

Matzelle, Melissa M. “Inflammation Inhibits Osteoblast-Mediated Bone Formation in Rheumatoid Arthritis and Regulates the Wnt and BMP Signaling Pathways: A Dissertation.” 2012. Web. 09 Dec 2019.

Vancouver:

Matzelle MM. Inflammation Inhibits Osteoblast-Mediated Bone Formation in Rheumatoid Arthritis and Regulates the Wnt and BMP Signaling Pathways: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2012. [cited 2019 Dec 09]. Available from: https://escholarship.umassmed.edu/gsbs_diss/596.

Council of Science Editors:

Matzelle MM. Inflammation Inhibits Osteoblast-Mediated Bone Formation in Rheumatoid Arthritis and Regulates the Wnt and BMP Signaling Pathways: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2012. Available from: https://escholarship.umassmed.edu/gsbs_diss/596

22. Carr, Michael I. The Role of MDM2 Phosphorylation in P53 Responses to DNA Damage and Tumor Suppression: A Dissertation.

Degree: Cell Biology, Radiology, 2016, U of Massachusetts : Med

  The p53 tumor suppressor protein is upregulated in response to DNA damage and other stress signals. The upregulation of p53 involves freeing it from… (more)

Subjects/Keywords: Tumor Suppressor Protein p53; Proto-Oncogene Proteins c-mdm2; DNA Damage; Phosphorylation; Biochemistry; Cancer Biology; Cell Biology

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APA (6th Edition):

Carr, M. I. (2016). The Role of MDM2 Phosphorylation in P53 Responses to DNA Damage and Tumor Suppression: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/847

Chicago Manual of Style (16th Edition):

Carr, Michael I. “The Role of MDM2 Phosphorylation in P53 Responses to DNA Damage and Tumor Suppression: A Dissertation.” 2016. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 09, 2019. http://escholarship.umassmed.edu/gsbs_diss/847.

MLA Handbook (7th Edition):

Carr, Michael I. “The Role of MDM2 Phosphorylation in P53 Responses to DNA Damage and Tumor Suppression: A Dissertation.” 2016. Web. 09 Dec 2019.

Vancouver:

Carr MI. The Role of MDM2 Phosphorylation in P53 Responses to DNA Damage and Tumor Suppression: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2016. [cited 2019 Dec 09]. Available from: http://escholarship.umassmed.edu/gsbs_diss/847.

Council of Science Editors:

Carr MI. The Role of MDM2 Phosphorylation in P53 Responses to DNA Damage and Tumor Suppression: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2016. Available from: http://escholarship.umassmed.edu/gsbs_diss/847

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 December 09, 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. 09 Dec 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 Dec 09]. 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. Unhavaithaya, Yingdee. Conserved Nucleosome Remodeling/Histone Deacetylase Complex and Germ/Soma Distinction in C. elegans: A Dissertation.

Degree: Cell Biology, RNA Therapeutics Institute, 2003, U of Massachusetts : Med

  A rapid cascade of regulatory events defines the differentiated fates of embryonic cells, however, once established, these differentiated fates and the underlying transcriptional programs… (more)

Subjects/Keywords: Caenorhabditis elegans Proteins; Cell Differentiation; Germ Cells; Histone Deacetylases; Nuclear Proteins; Transcription Factors; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Cells

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APA (6th Edition):

Unhavaithaya, Y. (2003). Conserved Nucleosome Remodeling/Histone Deacetylase Complex and Germ/Soma Distinction in C. elegans: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/239

Chicago Manual of Style (16th Edition):

Unhavaithaya, Yingdee. “Conserved Nucleosome Remodeling/Histone Deacetylase Complex and Germ/Soma Distinction in C. elegans: A Dissertation.” 2003. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 09, 2019. https://escholarship.umassmed.edu/gsbs_diss/239.

MLA Handbook (7th Edition):

Unhavaithaya, Yingdee. “Conserved Nucleosome Remodeling/Histone Deacetylase Complex and Germ/Soma Distinction in C. elegans: A Dissertation.” 2003. Web. 09 Dec 2019.

Vancouver:

Unhavaithaya Y. Conserved Nucleosome Remodeling/Histone Deacetylase Complex and Germ/Soma Distinction in C. elegans: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2003. [cited 2019 Dec 09]. Available from: https://escholarship.umassmed.edu/gsbs_diss/239.

Council of Science Editors:

Unhavaithaya Y. Conserved Nucleosome Remodeling/Histone Deacetylase Complex and Germ/Soma Distinction in C. elegans: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2003. Available from: https://escholarship.umassmed.edu/gsbs_diss/239

25. Abbott, Mary-Alice. Structural and Signaling Proteins at the Synapse: Dystroglycan & Insulin Receptor Tyrosine Kinase Substrate p58/53: a Dissertation.

Degree: Cell Biology, Cell Biology, 1999, U of Massachusetts : Med

  The synapse is the primary locus of cell-cell communication in the nervous system. The elaboration of a functional synapse requires both a specialized structure… (more)

Subjects/Keywords: Synaptic Transmission; Protein-Tyrosine Kinase; Dystrophin; Receptor; Insulin; Amino Acids, Peptides, and Proteins; Cells; Enzymes and Coenzymes; Hormones, Hormone Substitutes, and Hormone Antagonists; Nervous System

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APA (6th Edition):

Abbott, M. (1999). Structural and Signaling Proteins at the Synapse: Dystroglycan & Insulin Receptor Tyrosine Kinase Substrate p58/53: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/124

Chicago Manual of Style (16th Edition):

Abbott, Mary-Alice. “Structural and Signaling Proteins at the Synapse: Dystroglycan & Insulin Receptor Tyrosine Kinase Substrate p58/53: a Dissertation.” 1999. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 09, 2019. https://escholarship.umassmed.edu/gsbs_diss/124.

MLA Handbook (7th Edition):

Abbott, Mary-Alice. “Structural and Signaling Proteins at the Synapse: Dystroglycan & Insulin Receptor Tyrosine Kinase Substrate p58/53: a Dissertation.” 1999. Web. 09 Dec 2019.

Vancouver:

Abbott M. Structural and Signaling Proteins at the Synapse: Dystroglycan & Insulin Receptor Tyrosine Kinase Substrate p58/53: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1999. [cited 2019 Dec 09]. Available from: https://escholarship.umassmed.edu/gsbs_diss/124.

Council of Science Editors:

Abbott M. Structural and Signaling Proteins at the Synapse: Dystroglycan & Insulin Receptor Tyrosine Kinase Substrate p58/53: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 1999. Available from: https://escholarship.umassmed.edu/gsbs_diss/124

26. Hou, Yuqing. Identification and Characterization of Components of the Intraflagellar transport (IFT) Machinery: a Dissertation.

Degree: Cell Biology, Radiology, 2007, U of Massachusetts : Med

  Intraflagellar transport (IFT), the bi-directional movement of particles along the length of flagella, is required for flagellar assembly. The IFT particles are moved by… (more)

Subjects/Keywords: Intracellular Signaling Peptides and Proteins; Protein Transport; Dynein ATPase; Chlamydomonas; Flagella; Protozoan Proteins; Molecular Motor Proteins; Amino Acids, Peptides, and Proteins; Cells

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APA (6th Edition):

Hou, Y. (2007). Identification and Characterization of Components of the Intraflagellar transport (IFT) Machinery: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/323

Chicago Manual of Style (16th Edition):

Hou, Yuqing. “Identification and Characterization of Components of the Intraflagellar transport (IFT) Machinery: a Dissertation.” 2007. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 09, 2019. https://escholarship.umassmed.edu/gsbs_diss/323.

MLA Handbook (7th Edition):

Hou, Yuqing. “Identification and Characterization of Components of the Intraflagellar transport (IFT) Machinery: a Dissertation.” 2007. Web. 09 Dec 2019.

Vancouver:

Hou Y. Identification and Characterization of Components of the Intraflagellar transport (IFT) Machinery: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2007. [cited 2019 Dec 09]. Available from: https://escholarship.umassmed.edu/gsbs_diss/323.

Council of Science Editors:

Hou Y. Identification and Characterization of Components of the Intraflagellar transport (IFT) Machinery: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2007. Available from: https://escholarship.umassmed.edu/gsbs_diss/323

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

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

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Barrett, Curtis F. “Modulation of N-type Calcium Channels in Rat Superior Cervical Ganglion Neurons: A Dissertation.” 2001. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 09, 2019. https://escholarship.umassmed.edu/gsbs_diss/144.

MLA Handbook (7th Edition):

Barrett, Curtis F. “Modulation of N-type Calcium Channels in Rat Superior Cervical Ganglion Neurons: A Dissertation.” 2001. Web. 09 Dec 2019.

Vancouver:

Barrett CF. Modulation of N-type Calcium Channels in Rat Superior Cervical Ganglion Neurons: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2001. [cited 2019 Dec 09]. Available from: https://escholarship.umassmed.edu/gsbs_diss/144.

Council of Science Editors:

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

28. 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 December 09, 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. 09 Dec 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 Dec 09]. 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

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

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 December 09, 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. 09 Dec 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 Dec 09]. 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

30. Gatto, Cheryl Lynn. Novel Insights into Schwann Cell Dynamics in Peripheral Nervous System Myelination: a dissertation.

Degree: Cell Biology, Department of Cell Biology, Program in Neuroscience, 2004, U of Massachusetts : Med

  This body of work details the exploitation of an incredibly powerful neural culture system, which enables the in vitrostudy of events involved in peripheral… (more)

Subjects/Keywords: Peripheral Nervous System; Ankyrins; Ganglia; Spinal; Myelin Sheath; Ranvier's Nodes; Schwann Cells; Amino Acids, Peptides, and Proteins; Cells; Nervous System; Neuroscience and Neurobiology; Tissues

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

APA (6th Edition):

Gatto, C. L. (2004). Novel Insights into Schwann Cell Dynamics in Peripheral Nervous System Myelination: a dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/213

Chicago Manual of Style (16th Edition):

Gatto, Cheryl Lynn. “Novel Insights into Schwann Cell Dynamics in Peripheral Nervous System Myelination: a dissertation.” 2004. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 09, 2019. https://escholarship.umassmed.edu/gsbs_diss/213.

MLA Handbook (7th Edition):

Gatto, Cheryl Lynn. “Novel Insights into Schwann Cell Dynamics in Peripheral Nervous System Myelination: a dissertation.” 2004. Web. 09 Dec 2019.

Vancouver:

Gatto CL. Novel Insights into Schwann Cell Dynamics in Peripheral Nervous System Myelination: a dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2004. [cited 2019 Dec 09]. Available from: https://escholarship.umassmed.edu/gsbs_diss/213.

Council of Science Editors:

Gatto CL. Novel Insights into Schwann Cell Dynamics in Peripheral Nervous System Myelination: a dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2004. Available from: https://escholarship.umassmed.edu/gsbs_diss/213

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