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You searched for subject:(Molecular Genetics). Showing records 1 – 30 of 1596 total matches.

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University of Nevada – Las Vegas

1. Bond, Nichole Dinell. The Role of ecdysone signaling in fat-body tissue remodeling and pupal metabolism.

Degree: PhD, Biological Science, 2010, University of Nevada – Las Vegas

 Holometabolous insects undergo an astonishing transition during their development. During metamorphosis, the larva dramatically changes form and becomes an adult fly. During this process obsolete… (more)

Subjects/Keywords: Genetics; Molecular Genetics

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APA (6th Edition):

Bond, N. D. (2010). The Role of ecdysone signaling in fat-body tissue remodeling and pupal metabolism. (Doctoral Dissertation). University of Nevada – Las Vegas. Retrieved from https://digitalscholarship.unlv.edu/thesesdissertations/250

Chicago Manual of Style (16th Edition):

Bond, Nichole Dinell. “The Role of ecdysone signaling in fat-body tissue remodeling and pupal metabolism.” 2010. Doctoral Dissertation, University of Nevada – Las Vegas. Accessed July 15, 2020. https://digitalscholarship.unlv.edu/thesesdissertations/250.

MLA Handbook (7th Edition):

Bond, Nichole Dinell. “The Role of ecdysone signaling in fat-body tissue remodeling and pupal metabolism.” 2010. Web. 15 Jul 2020.

Vancouver:

Bond ND. The Role of ecdysone signaling in fat-body tissue remodeling and pupal metabolism. [Internet] [Doctoral dissertation]. University of Nevada – Las Vegas; 2010. [cited 2020 Jul 15]. Available from: https://digitalscholarship.unlv.edu/thesesdissertations/250.

Council of Science Editors:

Bond ND. The Role of ecdysone signaling in fat-body tissue remodeling and pupal metabolism. [Doctoral Dissertation]. University of Nevada – Las Vegas; 2010. Available from: https://digitalscholarship.unlv.edu/thesesdissertations/250


Universitat de Valencia

2. Peris Navarro, David. Genome Characterization of natural Saccharomyces hybrids of biotechnological interest .

Degree: 2012, Universitat de Valencia

 At present, the genus Saccharomyces comprises seven species according to their patterns of breeding. The species boundaries are not clear due to the description of… (more)

Subjects/Keywords: yeasts; molecular genetics; Saccharomyces; molecular genetics; saccharomyces

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APA (6th Edition):

Peris Navarro, D. (2012). Genome Characterization of natural Saccharomyces hybrids of biotechnological interest . (Doctoral Dissertation). Universitat de Valencia. Retrieved from http://hdl.handle.net/10550/24743

Chicago Manual of Style (16th Edition):

Peris Navarro, David. “Genome Characterization of natural Saccharomyces hybrids of biotechnological interest .” 2012. Doctoral Dissertation, Universitat de Valencia. Accessed July 15, 2020. http://hdl.handle.net/10550/24743.

MLA Handbook (7th Edition):

Peris Navarro, David. “Genome Characterization of natural Saccharomyces hybrids of biotechnological interest .” 2012. Web. 15 Jul 2020.

Vancouver:

Peris Navarro D. Genome Characterization of natural Saccharomyces hybrids of biotechnological interest . [Internet] [Doctoral dissertation]. Universitat de Valencia; 2012. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/10550/24743.

Council of Science Editors:

Peris Navarro D. Genome Characterization of natural Saccharomyces hybrids of biotechnological interest . [Doctoral Dissertation]. Universitat de Valencia; 2012. Available from: http://hdl.handle.net/10550/24743


Temple University

3. Madireddi, Priyanka. THE ROLE OF CIS- AND TRANS-ACTING FACTORS IN REGULATION OF DNA METHYLATION.

Degree: PhD, 2015, Temple University

Molecular Biology and Genetics

High level DNA methylation of promoter CpG islands (CGIs) represses gene expression. However, low-level CGI methylation is currently not distinguished from… (more)

Subjects/Keywords: Molecular biology; Genetics

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APA (6th Edition):

Madireddi, P. (2015). THE ROLE OF CIS- AND TRANS-ACTING FACTORS IN REGULATION OF DNA METHYLATION. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,376391

Chicago Manual of Style (16th Edition):

Madireddi, Priyanka. “THE ROLE OF CIS- AND TRANS-ACTING FACTORS IN REGULATION OF DNA METHYLATION.” 2015. Doctoral Dissertation, Temple University. Accessed July 15, 2020. http://digital.library.temple.edu/u?/p245801coll10,376391.

MLA Handbook (7th Edition):

Madireddi, Priyanka. “THE ROLE OF CIS- AND TRANS-ACTING FACTORS IN REGULATION OF DNA METHYLATION.” 2015. Web. 15 Jul 2020.

Vancouver:

Madireddi P. THE ROLE OF CIS- AND TRANS-ACTING FACTORS IN REGULATION OF DNA METHYLATION. [Internet] [Doctoral dissertation]. Temple University; 2015. [cited 2020 Jul 15]. Available from: http://digital.library.temple.edu/u?/p245801coll10,376391.

Council of Science Editors:

Madireddi P. THE ROLE OF CIS- AND TRANS-ACTING FACTORS IN REGULATION OF DNA METHYLATION. [Doctoral Dissertation]. Temple University; 2015. Available from: http://digital.library.temple.edu/u?/p245801coll10,376391


The Ohio State University

4. Ouseph, Madhu Micheal. Atypical E2F repressors E2F7 and E2F8: Balancing E2F activity in normal and variant cell cycles.

Degree: PhD, Biochemistry Program, Ohio State, 2012, The Ohio State University

  Coordinated activation and repression of E2F-responsive genes is believed to be pivotal for progression of normal cell cycle. Studies using lower organisms and mammalian… (more)

Subjects/Keywords: Genetics; Molecular Biology

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APA (6th Edition):

Ouseph, M. M. (2012). Atypical E2F repressors E2F7 and E2F8: Balancing E2F activity in normal and variant cell cycles. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1331055740

Chicago Manual of Style (16th Edition):

Ouseph, Madhu Micheal. “Atypical E2F repressors E2F7 and E2F8: Balancing E2F activity in normal and variant cell cycles.” 2012. Doctoral Dissertation, The Ohio State University. Accessed July 15, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1331055740.

MLA Handbook (7th Edition):

Ouseph, Madhu Micheal. “Atypical E2F repressors E2F7 and E2F8: Balancing E2F activity in normal and variant cell cycles.” 2012. Web. 15 Jul 2020.

Vancouver:

Ouseph MM. Atypical E2F repressors E2F7 and E2F8: Balancing E2F activity in normal and variant cell cycles. [Internet] [Doctoral dissertation]. The Ohio State University; 2012. [cited 2020 Jul 15]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1331055740.

Council of Science Editors:

Ouseph MM. Atypical E2F repressors E2F7 and E2F8: Balancing E2F activity in normal and variant cell cycles. [Doctoral Dissertation]. The Ohio State University; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1331055740


The Ohio State University

5. Stephan, Joseph. An Evolutionary Proteomics Approach For The Identification Of Pka Targets In Saccharomyces Cerevisiae Identifies Atg1 And Atg13, Two Proteins That Play A Central Role In The Regulation Of Autophagy By The Ras/Pka Pathway And The Tor Pathway.

Degree: PhD, Molecular, Cellular, and Developmental Biology, 2008, The Ohio State University

  A cell in its natural environment spends its time in a quiescent state known as G0. A challenge the cell faces is to determine… (more)

Subjects/Keywords: Genetics; Molecular Biology

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APA (6th Edition):

Stephan, J. (2008). An Evolutionary Proteomics Approach For The Identification Of Pka Targets In Saccharomyces Cerevisiae Identifies Atg1 And Atg13, Two Proteins That Play A Central Role In The Regulation Of Autophagy By The Ras/Pka Pathway And The Tor Pathway. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1218042573

Chicago Manual of Style (16th Edition):

Stephan, Joseph. “An Evolutionary Proteomics Approach For The Identification Of Pka Targets In Saccharomyces Cerevisiae Identifies Atg1 And Atg13, Two Proteins That Play A Central Role In The Regulation Of Autophagy By The Ras/Pka Pathway And The Tor Pathway.” 2008. Doctoral Dissertation, The Ohio State University. Accessed July 15, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1218042573.

MLA Handbook (7th Edition):

Stephan, Joseph. “An Evolutionary Proteomics Approach For The Identification Of Pka Targets In Saccharomyces Cerevisiae Identifies Atg1 And Atg13, Two Proteins That Play A Central Role In The Regulation Of Autophagy By The Ras/Pka Pathway And The Tor Pathway.” 2008. Web. 15 Jul 2020.

Vancouver:

Stephan J. An Evolutionary Proteomics Approach For The Identification Of Pka Targets In Saccharomyces Cerevisiae Identifies Atg1 And Atg13, Two Proteins That Play A Central Role In The Regulation Of Autophagy By The Ras/Pka Pathway And The Tor Pathway. [Internet] [Doctoral dissertation]. The Ohio State University; 2008. [cited 2020 Jul 15]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1218042573.

Council of Science Editors:

Stephan J. An Evolutionary Proteomics Approach For The Identification Of Pka Targets In Saccharomyces Cerevisiae Identifies Atg1 And Atg13, Two Proteins That Play A Central Role In The Regulation Of Autophagy By The Ras/Pka Pathway And The Tor Pathway. [Doctoral Dissertation]. The Ohio State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1218042573


Columbia University

6. Washkowitz, Andrew. The Role of Mga in the Survival of Pluripotent Cells During Peri-implantation Development.

Degree: 2013, Columbia University

 The dual specificity transcription factor Mga contains both a T-box binding domain and a basic helix-loop-helix zipper (bHLHZip) domain. Loss of Mga leads to embryonic… (more)

Subjects/Keywords: Genetics; Molecular biology

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APA (6th Edition):

Washkowitz, A. (2013). The Role of Mga in the Survival of Pluripotent Cells During Peri-implantation Development. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8M61JMR

Chicago Manual of Style (16th Edition):

Washkowitz, Andrew. “The Role of Mga in the Survival of Pluripotent Cells During Peri-implantation Development.” 2013. Doctoral Dissertation, Columbia University. Accessed July 15, 2020. https://doi.org/10.7916/D8M61JMR.

MLA Handbook (7th Edition):

Washkowitz, Andrew. “The Role of Mga in the Survival of Pluripotent Cells During Peri-implantation Development.” 2013. Web. 15 Jul 2020.

Vancouver:

Washkowitz A. The Role of Mga in the Survival of Pluripotent Cells During Peri-implantation Development. [Internet] [Doctoral dissertation]. Columbia University; 2013. [cited 2020 Jul 15]. Available from: https://doi.org/10.7916/D8M61JMR.

Council of Science Editors:

Washkowitz A. The Role of Mga in the Survival of Pluripotent Cells During Peri-implantation Development. [Doctoral Dissertation]. Columbia University; 2013. Available from: https://doi.org/10.7916/D8M61JMR


Columbia University

7. Vargas, Marcus L. Studies of a Site-Specific Recombination System and Analysis of New Modulators of Notch Signaling in C. elegans.

Degree: 2012, Columbia University

 The ability to make transgenic animals has been a great tool for biologists to study living organisms. In C. elegans, the way transgenes are generated… (more)

Subjects/Keywords: Genetics; Molecular biology

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APA (6th Edition):

Vargas, M. L. (2012). Studies of a Site-Specific Recombination System and Analysis of New Modulators of Notch Signaling in C. elegans. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D81R6NKP

Chicago Manual of Style (16th Edition):

Vargas, Marcus L. “Studies of a Site-Specific Recombination System and Analysis of New Modulators of Notch Signaling in C. elegans.” 2012. Doctoral Dissertation, Columbia University. Accessed July 15, 2020. https://doi.org/10.7916/D81R6NKP.

MLA Handbook (7th Edition):

Vargas, Marcus L. “Studies of a Site-Specific Recombination System and Analysis of New Modulators of Notch Signaling in C. elegans.” 2012. Web. 15 Jul 2020.

Vancouver:

Vargas ML. Studies of a Site-Specific Recombination System and Analysis of New Modulators of Notch Signaling in C. elegans. [Internet] [Doctoral dissertation]. Columbia University; 2012. [cited 2020 Jul 15]. Available from: https://doi.org/10.7916/D81R6NKP.

Council of Science Editors:

Vargas ML. Studies of a Site-Specific Recombination System and Analysis of New Modulators of Notch Signaling in C. elegans. [Doctoral Dissertation]. Columbia University; 2012. Available from: https://doi.org/10.7916/D81R6NKP


Columbia University

8. Kratz, John Ernest. Prohibitin Homology Domain Proteins in Caenorhabditis elegans.

Degree: 2010, Columbia University

 The PHB-d protein family is an evolutionarily ancient family of integral membrane proteins with members in all taxa that are involved in a wide variety… (more)

Subjects/Keywords: Molecular biology; Genetics

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APA (6th Edition):

Kratz, J. E. (2010). Prohibitin Homology Domain Proteins in Caenorhabditis elegans. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D88051FN

Chicago Manual of Style (16th Edition):

Kratz, John Ernest. “Prohibitin Homology Domain Proteins in Caenorhabditis elegans.” 2010. Doctoral Dissertation, Columbia University. Accessed July 15, 2020. https://doi.org/10.7916/D88051FN.

MLA Handbook (7th Edition):

Kratz, John Ernest. “Prohibitin Homology Domain Proteins in Caenorhabditis elegans.” 2010. Web. 15 Jul 2020.

Vancouver:

Kratz JE. Prohibitin Homology Domain Proteins in Caenorhabditis elegans. [Internet] [Doctoral dissertation]. Columbia University; 2010. [cited 2020 Jul 15]. Available from: https://doi.org/10.7916/D88051FN.

Council of Science Editors:

Kratz JE. Prohibitin Homology Domain Proteins in Caenorhabditis elegans. [Doctoral Dissertation]. Columbia University; 2010. Available from: https://doi.org/10.7916/D88051FN


University of Nevada – Las Vegas

9. Constantino, Benjamin. The Larval salivary gland of Drosophila melangogaster: A model system for temporal and spatial steroid hormone regulation.

Degree: PhD, Life Sciences, 2010, University of Nevada – Las Vegas

  Drosophila melanogaster provides an ideal model organism to test genetic and molecular biological mechanisms within the context of a living animal. For over one… (more)

Subjects/Keywords: Genetics; Molecular Biology

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APA (6th Edition):

Constantino, B. (2010). The Larval salivary gland of Drosophila melangogaster: A model system for temporal and spatial steroid hormone regulation. (Doctoral Dissertation). University of Nevada – Las Vegas. Retrieved from https://digitalscholarship.unlv.edu/thesesdissertations/833

Chicago Manual of Style (16th Edition):

Constantino, Benjamin. “The Larval salivary gland of Drosophila melangogaster: A model system for temporal and spatial steroid hormone regulation.” 2010. Doctoral Dissertation, University of Nevada – Las Vegas. Accessed July 15, 2020. https://digitalscholarship.unlv.edu/thesesdissertations/833.

MLA Handbook (7th Edition):

Constantino, Benjamin. “The Larval salivary gland of Drosophila melangogaster: A model system for temporal and spatial steroid hormone regulation.” 2010. Web. 15 Jul 2020.

Vancouver:

Constantino B. The Larval salivary gland of Drosophila melangogaster: A model system for temporal and spatial steroid hormone regulation. [Internet] [Doctoral dissertation]. University of Nevada – Las Vegas; 2010. [cited 2020 Jul 15]. Available from: https://digitalscholarship.unlv.edu/thesesdissertations/833.

Council of Science Editors:

Constantino B. The Larval salivary gland of Drosophila melangogaster: A model system for temporal and spatial steroid hormone regulation. [Doctoral Dissertation]. University of Nevada – Las Vegas; 2010. Available from: https://digitalscholarship.unlv.edu/thesesdissertations/833


Wayne State University

10. Kalita, Cynthia Ann. Validating Functional Mechanisms For Non-Coding Genetic Variants Associated With Complex Traits.

Degree: PhD, Molecular Biology and Genetics, 2018, Wayne State University

  Genome-wide association studies (GWAS) have identified a large number of genetic variants associated with disease as well as normal phenotypic variation for complex traits.… (more)

Subjects/Keywords: Genetics; Molecular Biology

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APA (6th Edition):

Kalita, C. A. (2018). Validating Functional Mechanisms For Non-Coding Genetic Variants Associated With Complex Traits. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/2169

Chicago Manual of Style (16th Edition):

Kalita, Cynthia Ann. “Validating Functional Mechanisms For Non-Coding Genetic Variants Associated With Complex Traits.” 2018. Doctoral Dissertation, Wayne State University. Accessed July 15, 2020. https://digitalcommons.wayne.edu/oa_dissertations/2169.

MLA Handbook (7th Edition):

Kalita, Cynthia Ann. “Validating Functional Mechanisms For Non-Coding Genetic Variants Associated With Complex Traits.” 2018. Web. 15 Jul 2020.

Vancouver:

Kalita CA. Validating Functional Mechanisms For Non-Coding Genetic Variants Associated With Complex Traits. [Internet] [Doctoral dissertation]. Wayne State University; 2018. [cited 2020 Jul 15]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/2169.

Council of Science Editors:

Kalita CA. Validating Functional Mechanisms For Non-Coding Genetic Variants Associated With Complex Traits. [Doctoral Dissertation]. Wayne State University; 2018. Available from: https://digitalcommons.wayne.edu/oa_dissertations/2169

11. Shao, Lin. Characterization of the expression profile of polyamine biosynthetic genes (Spermidine synthase) and polyamine metabolic regulation in arabidopsis.

Degree: PhD, 2013, University of New Hampshire

  Polyamines are ubiquitously distributed cationic compounds, which play important roles in numerous cellular functions in plants. This study was aimed at elaborating the regulation… (more)

Subjects/Keywords: Biology; Genetics; Biology; Molecular; Biology; Botany; Genetics

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APA (6th Edition):

Shao, L. (2013). Characterization of the expression profile of polyamine biosynthetic genes (Spermidine synthase) and polyamine metabolic regulation in arabidopsis. (Doctoral Dissertation). University of New Hampshire. Retrieved from https://scholars.unh.edu/dissertation/722

Chicago Manual of Style (16th Edition):

Shao, Lin. “Characterization of the expression profile of polyamine biosynthetic genes (Spermidine synthase) and polyamine metabolic regulation in arabidopsis.” 2013. Doctoral Dissertation, University of New Hampshire. Accessed July 15, 2020. https://scholars.unh.edu/dissertation/722.

MLA Handbook (7th Edition):

Shao, Lin. “Characterization of the expression profile of polyamine biosynthetic genes (Spermidine synthase) and polyamine metabolic regulation in arabidopsis.” 2013. Web. 15 Jul 2020.

Vancouver:

Shao L. Characterization of the expression profile of polyamine biosynthetic genes (Spermidine synthase) and polyamine metabolic regulation in arabidopsis. [Internet] [Doctoral dissertation]. University of New Hampshire; 2013. [cited 2020 Jul 15]. Available from: https://scholars.unh.edu/dissertation/722.

Council of Science Editors:

Shao L. Characterization of the expression profile of polyamine biosynthetic genes (Spermidine synthase) and polyamine metabolic regulation in arabidopsis. [Doctoral Dissertation]. University of New Hampshire; 2013. Available from: https://scholars.unh.edu/dissertation/722


The Ohio State University

12. Ghosh, Sankha. REGULATION OF ACTIVATION PHASE OF ANGIOGENESIS BY TRANCRIPTION FACTORS ETS1 AND ETS2.

Degree: PhD, Molecular, Cellular and Developmental Biology, 2014, The Ohio State University

 Vascular remodeling is a necessary process not only for embryonic development but also for specific physiological and pathological conditions in adult. Several growth factors are… (more)

Subjects/Keywords: Molecular Biology; Developmental Biology; Genetics

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APA (6th Edition):

Ghosh, S. (2014). REGULATION OF ACTIVATION PHASE OF ANGIOGENESIS BY TRANCRIPTION FACTORS ETS1 AND ETS2. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1409052955

Chicago Manual of Style (16th Edition):

Ghosh, Sankha. “REGULATION OF ACTIVATION PHASE OF ANGIOGENESIS BY TRANCRIPTION FACTORS ETS1 AND ETS2.” 2014. Doctoral Dissertation, The Ohio State University. Accessed July 15, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1409052955.

MLA Handbook (7th Edition):

Ghosh, Sankha. “REGULATION OF ACTIVATION PHASE OF ANGIOGENESIS BY TRANCRIPTION FACTORS ETS1 AND ETS2.” 2014. Web. 15 Jul 2020.

Vancouver:

Ghosh S. REGULATION OF ACTIVATION PHASE OF ANGIOGENESIS BY TRANCRIPTION FACTORS ETS1 AND ETS2. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2020 Jul 15]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1409052955.

Council of Science Editors:

Ghosh S. REGULATION OF ACTIVATION PHASE OF ANGIOGENESIS BY TRANCRIPTION FACTORS ETS1 AND ETS2. [Doctoral Dissertation]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1409052955


Texas Medical Center

13. Chen, Haoyi. RMI1 is Essential for Early Embryonic Development and Attenuation of Tumor Development.

Degree: PhD, 2010, Texas Medical Center

 RMI1 (BLM-Associated Protein 75 or Blap75) is highly conserved from yeast to human. Previous studies have shown that hRMI1 is required for BLM/TopoIIIα/RMI1 complex stability… (more)

Subjects/Keywords: RMI1; HR; DSB.; Molecular Genetics

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APA (6th Edition):

Chen, H. (2010). RMI1 is Essential for Early Embryonic Development and Attenuation of Tumor Development. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/94

Chicago Manual of Style (16th Edition):

Chen, Haoyi. “RMI1 is Essential for Early Embryonic Development and Attenuation of Tumor Development.” 2010. Doctoral Dissertation, Texas Medical Center. Accessed July 15, 2020. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/94.

MLA Handbook (7th Edition):

Chen, Haoyi. “RMI1 is Essential for Early Embryonic Development and Attenuation of Tumor Development.” 2010. Web. 15 Jul 2020.

Vancouver:

Chen H. RMI1 is Essential for Early Embryonic Development and Attenuation of Tumor Development. [Internet] [Doctoral dissertation]. Texas Medical Center; 2010. [cited 2020 Jul 15]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/94.

Council of Science Editors:

Chen H. RMI1 is Essential for Early Embryonic Development and Attenuation of Tumor Development. [Doctoral Dissertation]. Texas Medical Center; 2010. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/94


The Ohio State University

14. Jowdy, Casey C. The Regulation of Commissureless in the Embryonic CNS of Drosophila melanogaster.

Degree: PhD, Molecular Genetics, 2010, The Ohio State University

  During development the precise wiring of the nervous system is dependent on thecorrect repertoire of axon guidance molecules being expressed at the right time… (more)

Subjects/Keywords: Biology; Genetics; Molecular Biology

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APA (6th Edition):

Jowdy, C. C. (2010). The Regulation of Commissureless in the Embryonic CNS of Drosophila melanogaster. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1284172382

Chicago Manual of Style (16th Edition):

Jowdy, Casey C. “The Regulation of Commissureless in the Embryonic CNS of Drosophila melanogaster.” 2010. Doctoral Dissertation, The Ohio State University. Accessed July 15, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1284172382.

MLA Handbook (7th Edition):

Jowdy, Casey C. “The Regulation of Commissureless in the Embryonic CNS of Drosophila melanogaster.” 2010. Web. 15 Jul 2020.

Vancouver:

Jowdy CC. The Regulation of Commissureless in the Embryonic CNS of Drosophila melanogaster. [Internet] [Doctoral dissertation]. The Ohio State University; 2010. [cited 2020 Jul 15]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1284172382.

Council of Science Editors:

Jowdy CC. The Regulation of Commissureless in the Embryonic CNS of Drosophila melanogaster. [Doctoral Dissertation]. The Ohio State University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1284172382


Harvard University

15. Cai, Xuyu. Single-Neuron Sequencing to Explore Somatic Genetic Variants in Normal and Pathological Human Brain Development.

Degree: PhD, Biological and Biomedical Sciences, 2013, Harvard University

 The human brain is one of the most exquisite structures in nature, featuring extreme functional complexity and capacities that allow for advanced cognitive abilities. During… (more)

Subjects/Keywords: Molecular biology; Neurosciences; Genetics

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APA (6th Edition):

Cai, X. (2013). Single-Neuron Sequencing to Explore Somatic Genetic Variants in Normal and Pathological Human Brain Development. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:11129105

Chicago Manual of Style (16th Edition):

Cai, Xuyu. “Single-Neuron Sequencing to Explore Somatic Genetic Variants in Normal and Pathological Human Brain Development.” 2013. Doctoral Dissertation, Harvard University. Accessed July 15, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:11129105.

MLA Handbook (7th Edition):

Cai, Xuyu. “Single-Neuron Sequencing to Explore Somatic Genetic Variants in Normal and Pathological Human Brain Development.” 2013. Web. 15 Jul 2020.

Vancouver:

Cai X. Single-Neuron Sequencing to Explore Somatic Genetic Variants in Normal and Pathological Human Brain Development. [Internet] [Doctoral dissertation]. Harvard University; 2013. [cited 2020 Jul 15]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:11129105.

Council of Science Editors:

Cai X. Single-Neuron Sequencing to Explore Somatic Genetic Variants in Normal and Pathological Human Brain Development. [Doctoral Dissertation]. Harvard University; 2013. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:11129105


Harvard University

16. Manning, Lauren Brooke. Experimental Evaluation of Discoid Domain Receptor 2 as an Ideal Target for Development of Disease-Modifying Osteoarthritis Drugs.

Degree: DMSc, 2015, Harvard University

 Osteoarthritis (OA) affects 250 million people worldwide. Currently, no targets for disease-modifying osteoarthritis drugs exist. Matrix metalloproteinase-13 (MMP-13) would make it an ideal target; however,… (more)

Subjects/Keywords: Biology, Molecular; Biology, Genetics

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APA (6th Edition):

Manning, L. B. (2015). Experimental Evaluation of Discoid Domain Receptor 2 as an Ideal Target for Development of Disease-Modifying Osteoarthritis Drugs. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:17331959

Chicago Manual of Style (16th Edition):

Manning, Lauren Brooke. “Experimental Evaluation of Discoid Domain Receptor 2 as an Ideal Target for Development of Disease-Modifying Osteoarthritis Drugs.” 2015. Doctoral Dissertation, Harvard University. Accessed July 15, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:17331959.

MLA Handbook (7th Edition):

Manning, Lauren Brooke. “Experimental Evaluation of Discoid Domain Receptor 2 as an Ideal Target for Development of Disease-Modifying Osteoarthritis Drugs.” 2015. Web. 15 Jul 2020.

Vancouver:

Manning LB. Experimental Evaluation of Discoid Domain Receptor 2 as an Ideal Target for Development of Disease-Modifying Osteoarthritis Drugs. [Internet] [Doctoral dissertation]. Harvard University; 2015. [cited 2020 Jul 15]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:17331959.

Council of Science Editors:

Manning LB. Experimental Evaluation of Discoid Domain Receptor 2 as an Ideal Target for Development of Disease-Modifying Osteoarthritis Drugs. [Doctoral Dissertation]. Harvard University; 2015. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:17331959


Harvard University

17. Wang, Yifan. A Gain of Function Senescence Bypass Screen Identifies the Homeobox Transcription Factor DLX2 as a Regulator of ATM-P53 Signaling.

Degree: PhD, 2016, Harvard University

Senescence stimuli activate multiple tumor suppressor pathways to initiate cycle arrest and a differentiation program characteristic of senescent cells. We performed a two-stage, gain-of function… (more)

Subjects/Keywords: Biology, Genetics; Biology, Molecular

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APA (6th Edition):

Wang, Y. (2016). A Gain of Function Senescence Bypass Screen Identifies the Homeobox Transcription Factor DLX2 as a Regulator of ATM-P53 Signaling. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:26718730

Chicago Manual of Style (16th Edition):

Wang, Yifan. “A Gain of Function Senescence Bypass Screen Identifies the Homeobox Transcription Factor DLX2 as a Regulator of ATM-P53 Signaling.” 2016. Doctoral Dissertation, Harvard University. Accessed July 15, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:26718730.

MLA Handbook (7th Edition):

Wang, Yifan. “A Gain of Function Senescence Bypass Screen Identifies the Homeobox Transcription Factor DLX2 as a Regulator of ATM-P53 Signaling.” 2016. Web. 15 Jul 2020.

Vancouver:

Wang Y. A Gain of Function Senescence Bypass Screen Identifies the Homeobox Transcription Factor DLX2 as a Regulator of ATM-P53 Signaling. [Internet] [Doctoral dissertation]. Harvard University; 2016. [cited 2020 Jul 15]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:26718730.

Council of Science Editors:

Wang Y. A Gain of Function Senescence Bypass Screen Identifies the Homeobox Transcription Factor DLX2 as a Regulator of ATM-P53 Signaling. [Doctoral Dissertation]. Harvard University; 2016. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:26718730


Harvard University

18. Panchakshari, Rohit. Investigating Mechanisms of DNA Double Strand Break Joining of Switch Regions During IgH Class Switch Recombination.

Degree: PhD, 2016, Harvard University

During B cell development, RAG endonuclease cleaves immunoglobulin heavy chain (IgH) V, D, and J gene segments and orchestrates their fusion as deletional events that… (more)

Subjects/Keywords: Biology, Molecular; Biology, Genetics

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APA (6th Edition):

Panchakshari, R. (2016). Investigating Mechanisms of DNA Double Strand Break Joining of Switch Regions During IgH Class Switch Recombination. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493369

Chicago Manual of Style (16th Edition):

Panchakshari, Rohit. “Investigating Mechanisms of DNA Double Strand Break Joining of Switch Regions During IgH Class Switch Recombination.” 2016. Doctoral Dissertation, Harvard University. Accessed July 15, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493369.

MLA Handbook (7th Edition):

Panchakshari, Rohit. “Investigating Mechanisms of DNA Double Strand Break Joining of Switch Regions During IgH Class Switch Recombination.” 2016. Web. 15 Jul 2020.

Vancouver:

Panchakshari R. Investigating Mechanisms of DNA Double Strand Break Joining of Switch Regions During IgH Class Switch Recombination. [Internet] [Doctoral dissertation]. Harvard University; 2016. [cited 2020 Jul 15]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493369.

Council of Science Editors:

Panchakshari R. Investigating Mechanisms of DNA Double Strand Break Joining of Switch Regions During IgH Class Switch Recombination. [Doctoral Dissertation]. Harvard University; 2016. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493369


Harvard University

19. Canver, Matthew. Elucidation of Mechanisms of Fetal Hemoglobin Regulation by CRISPR/Cas9 Mediated Genome Editing.

Degree: PhD, 2016, Harvard University

Despite nearly complete understanding of the genetics of the β-hemoglobinopathies for several decades, definitive treatment options have lagged behind. Fetal hemoglobin (HbF) reinduction represents a… (more)

Subjects/Keywords: Biology, Genetics; Biology, Molecular

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APA (6th Edition):

Canver, M. (2016). Elucidation of Mechanisms of Fetal Hemoglobin Regulation by CRISPR/Cas9 Mediated Genome Editing. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493407

Chicago Manual of Style (16th Edition):

Canver, Matthew. “Elucidation of Mechanisms of Fetal Hemoglobin Regulation by CRISPR/Cas9 Mediated Genome Editing.” 2016. Doctoral Dissertation, Harvard University. Accessed July 15, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493407.

MLA Handbook (7th Edition):

Canver, Matthew. “Elucidation of Mechanisms of Fetal Hemoglobin Regulation by CRISPR/Cas9 Mediated Genome Editing.” 2016. Web. 15 Jul 2020.

Vancouver:

Canver M. Elucidation of Mechanisms of Fetal Hemoglobin Regulation by CRISPR/Cas9 Mediated Genome Editing. [Internet] [Doctoral dissertation]. Harvard University; 2016. [cited 2020 Jul 15]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493407.

Council of Science Editors:

Canver M. Elucidation of Mechanisms of Fetal Hemoglobin Regulation by CRISPR/Cas9 Mediated Genome Editing. [Doctoral Dissertation]. Harvard University; 2016. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493407


Harvard University

20. McElroy, Kyle A. Balancing transcriptional activity in Drosophila through protein-protein interactions on chromatin.

Degree: PhD, 2016, Harvard University

 Chromatin plays a vital role in the implementation of gene expression programs. Several disparate groups of regulatory proteins alter chromatin state through post-translational modification of… (more)

Subjects/Keywords: Biology, Molecular; Biology, Genetics

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APA (6th Edition):

McElroy, K. A. (2016). Balancing transcriptional activity in Drosophila through protein-protein interactions on chromatin. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493492

Chicago Manual of Style (16th Edition):

McElroy, Kyle A. “Balancing transcriptional activity in Drosophila through protein-protein interactions on chromatin.” 2016. Doctoral Dissertation, Harvard University. Accessed July 15, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493492.

MLA Handbook (7th Edition):

McElroy, Kyle A. “Balancing transcriptional activity in Drosophila through protein-protein interactions on chromatin.” 2016. Web. 15 Jul 2020.

Vancouver:

McElroy KA. Balancing transcriptional activity in Drosophila through protein-protein interactions on chromatin. [Internet] [Doctoral dissertation]. Harvard University; 2016. [cited 2020 Jul 15]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493492.

Council of Science Editors:

McElroy KA. Balancing transcriptional activity in Drosophila through protein-protein interactions on chromatin. [Doctoral Dissertation]. Harvard University; 2016. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493492


Harvard University

21. Akhmetova, Laila. Transcriptional Regulation of Nodal Target Genes in Early Zebrafish Development.

Degree: PhD, 2016, Harvard University

Nodal signaling is one of the principal players in the process of gastrulation, during which the primary germ layers (endoderm, mesoderm, and ectoderm) are formed… (more)

Subjects/Keywords: Biology, Molecular; Biology, Genetics

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APA (6th Edition):

Akhmetova, L. (2016). Transcriptional Regulation of Nodal Target Genes in Early Zebrafish Development. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493493

Chicago Manual of Style (16th Edition):

Akhmetova, Laila. “Transcriptional Regulation of Nodal Target Genes in Early Zebrafish Development.” 2016. Doctoral Dissertation, Harvard University. Accessed July 15, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493493.

MLA Handbook (7th Edition):

Akhmetova, Laila. “Transcriptional Regulation of Nodal Target Genes in Early Zebrafish Development.” 2016. Web. 15 Jul 2020.

Vancouver:

Akhmetova L. Transcriptional Regulation of Nodal Target Genes in Early Zebrafish Development. [Internet] [Doctoral dissertation]. Harvard University; 2016. [cited 2020 Jul 15]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493493.

Council of Science Editors:

Akhmetova L. Transcriptional Regulation of Nodal Target Genes in Early Zebrafish Development. [Doctoral Dissertation]. Harvard University; 2016. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493493


Harvard University

22. Lau, Mei Sheng. Mutations in the Charged Domain of CBX2 Disrupt PRC1 Function in Vivo.

Degree: PhD, 2016, Harvard University

Epigenetics inheritance is a phenomenon where a cell state is inherited across cellular divisions. It is important for maintaining differentiated cells types, and thus is… (more)

Subjects/Keywords: Biology, Genetics; Biology, Molecular

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APA (6th Edition):

Lau, M. S. (2016). Mutations in the Charged Domain of CBX2 Disrupt PRC1 Function in Vivo. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493506

Chicago Manual of Style (16th Edition):

Lau, Mei Sheng. “Mutations in the Charged Domain of CBX2 Disrupt PRC1 Function in Vivo.” 2016. Doctoral Dissertation, Harvard University. Accessed July 15, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493506.

MLA Handbook (7th Edition):

Lau, Mei Sheng. “Mutations in the Charged Domain of CBX2 Disrupt PRC1 Function in Vivo.” 2016. Web. 15 Jul 2020.

Vancouver:

Lau MS. Mutations in the Charged Domain of CBX2 Disrupt PRC1 Function in Vivo. [Internet] [Doctoral dissertation]. Harvard University; 2016. [cited 2020 Jul 15]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493506.

Council of Science Editors:

Lau MS. Mutations in the Charged Domain of CBX2 Disrupt PRC1 Function in Vivo. [Doctoral Dissertation]. Harvard University; 2016. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493506


Harvard University

23. Daugharthy, Evan. Towards Perfect Molecular Measurement.

Degree: PhD, 2016, Harvard University

The rapid pace of technological innovation has profoundly transformed life sciences research. Whereas less than 100 years ago researchers were often confined to descriptive and… (more)

Subjects/Keywords: Biology, Genetics; Biology, Molecular

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APA (6th Edition):

Daugharthy, E. (2016). Towards Perfect Molecular Measurement. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33840753

Chicago Manual of Style (16th Edition):

Daugharthy, Evan. “Towards Perfect Molecular Measurement.” 2016. Doctoral Dissertation, Harvard University. Accessed July 15, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33840753.

MLA Handbook (7th Edition):

Daugharthy, Evan. “Towards Perfect Molecular Measurement.” 2016. Web. 15 Jul 2020.

Vancouver:

Daugharthy E. Towards Perfect Molecular Measurement. [Internet] [Doctoral dissertation]. Harvard University; 2016. [cited 2020 Jul 15]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33840753.

Council of Science Editors:

Daugharthy E. Towards Perfect Molecular Measurement. [Doctoral Dissertation]. Harvard University; 2016. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33840753


Oregon State University

24. Zhao, Yuqi. Molecular genetic characterization of a pathogenicity-attenuated mutant of Pseudomonas syringae pathovar syringae.

Degree: PhD, Genetics, 1991, Oregon State University

 A pathogenicity locus of Pseudomonas syringae pv. syringae identified by Tn5 mutagenesis was investigated. The mutant strain PS9024 is attenuated for disease expression in its… (more)

Subjects/Keywords: Molecular genetics

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APA (6th Edition):

Zhao, Y. (1991). Molecular genetic characterization of a pathogenicity-attenuated mutant of Pseudomonas syringae pathovar syringae. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/37468

Chicago Manual of Style (16th Edition):

Zhao, Yuqi. “Molecular genetic characterization of a pathogenicity-attenuated mutant of Pseudomonas syringae pathovar syringae.” 1991. Doctoral Dissertation, Oregon State University. Accessed July 15, 2020. http://hdl.handle.net/1957/37468.

MLA Handbook (7th Edition):

Zhao, Yuqi. “Molecular genetic characterization of a pathogenicity-attenuated mutant of Pseudomonas syringae pathovar syringae.” 1991. Web. 15 Jul 2020.

Vancouver:

Zhao Y. Molecular genetic characterization of a pathogenicity-attenuated mutant of Pseudomonas syringae pathovar syringae. [Internet] [Doctoral dissertation]. Oregon State University; 1991. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/1957/37468.

Council of Science Editors:

Zhao Y. Molecular genetic characterization of a pathogenicity-attenuated mutant of Pseudomonas syringae pathovar syringae. [Doctoral Dissertation]. Oregon State University; 1991. Available from: http://hdl.handle.net/1957/37468


Oregon State University

25. Parks, Matthew Benjamin. Plastome phylogenomics in the genus Pinus using massively parallel sequencing technology.

Degree: PhD, Botany and Plant Pathology, 2011, Oregon State University

 This thesis summarizes work completed over the previous four years primarily focusing on chloroplast phylogenomic inquiry into the genus Pinus and related Pinaceae outgroups using… (more)

Subjects/Keywords: Pinus; Pine  – Molecular genetics

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APA (6th Edition):

Parks, M. B. (2011). Plastome phylogenomics in the genus Pinus using massively parallel sequencing technology. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/21691

Chicago Manual of Style (16th Edition):

Parks, Matthew Benjamin. “Plastome phylogenomics in the genus Pinus using massively parallel sequencing technology.” 2011. Doctoral Dissertation, Oregon State University. Accessed July 15, 2020. http://hdl.handle.net/1957/21691.

MLA Handbook (7th Edition):

Parks, Matthew Benjamin. “Plastome phylogenomics in the genus Pinus using massively parallel sequencing technology.” 2011. Web. 15 Jul 2020.

Vancouver:

Parks MB. Plastome phylogenomics in the genus Pinus using massively parallel sequencing technology. [Internet] [Doctoral dissertation]. Oregon State University; 2011. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/1957/21691.

Council of Science Editors:

Parks MB. Plastome phylogenomics in the genus Pinus using massively parallel sequencing technology. [Doctoral Dissertation]. Oregon State University; 2011. Available from: http://hdl.handle.net/1957/21691


Columbia University

26. Quibria, Naureen. Characterization of Gf a Drosophila trimeric G protein alpha subunit.

Degree: 2012, Columbia University

 In the morphogenesis of tissue development, how coordination of patterning and growth achieve the correct organ size and shape is a principal question in biology.… (more)

Subjects/Keywords: Genetics; Cytology; Molecular biology

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APA (6th Edition):

Quibria, N. (2012). Characterization of Gf a Drosophila trimeric G protein alpha subunit. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8WQ09RX

Chicago Manual of Style (16th Edition):

Quibria, Naureen. “Characterization of Gf a Drosophila trimeric G protein alpha subunit.” 2012. Doctoral Dissertation, Columbia University. Accessed July 15, 2020. https://doi.org/10.7916/D8WQ09RX.

MLA Handbook (7th Edition):

Quibria, Naureen. “Characterization of Gf a Drosophila trimeric G protein alpha subunit.” 2012. Web. 15 Jul 2020.

Vancouver:

Quibria N. Characterization of Gf a Drosophila trimeric G protein alpha subunit. [Internet] [Doctoral dissertation]. Columbia University; 2012. [cited 2020 Jul 15]. Available from: https://doi.org/10.7916/D8WQ09RX.

Council of Science Editors:

Quibria N. Characterization of Gf a Drosophila trimeric G protein alpha subunit. [Doctoral Dissertation]. Columbia University; 2012. Available from: https://doi.org/10.7916/D8WQ09RX


Columbia University

27. Zee, Tiffany. Non-autonomous regulation of bone mass accrual and the role of T-cell protein tyrosine phosphatase in the bone regulation of insulin sensitivity.

Degree: 2013, Columbia University

 The skeleton is a highly dynamic organ that undergoes constant remodeling to renew itself and maintain bone mass. It is subject to regulation from both… (more)

Subjects/Keywords: Molecular biology; Physiology; Genetics

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APA (6th Edition):

Zee, T. (2013). Non-autonomous regulation of bone mass accrual and the role of T-cell protein tyrosine phosphatase in the bone regulation of insulin sensitivity. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8F47W70

Chicago Manual of Style (16th Edition):

Zee, Tiffany. “Non-autonomous regulation of bone mass accrual and the role of T-cell protein tyrosine phosphatase in the bone regulation of insulin sensitivity.” 2013. Doctoral Dissertation, Columbia University. Accessed July 15, 2020. https://doi.org/10.7916/D8F47W70.

MLA Handbook (7th Edition):

Zee, Tiffany. “Non-autonomous regulation of bone mass accrual and the role of T-cell protein tyrosine phosphatase in the bone regulation of insulin sensitivity.” 2013. Web. 15 Jul 2020.

Vancouver:

Zee T. Non-autonomous regulation of bone mass accrual and the role of T-cell protein tyrosine phosphatase in the bone regulation of insulin sensitivity. [Internet] [Doctoral dissertation]. Columbia University; 2013. [cited 2020 Jul 15]. Available from: https://doi.org/10.7916/D8F47W70.

Council of Science Editors:

Zee T. Non-autonomous regulation of bone mass accrual and the role of T-cell protein tyrosine phosphatase in the bone regulation of insulin sensitivity. [Doctoral Dissertation]. Columbia University; 2013. Available from: https://doi.org/10.7916/D8F47W70


Columbia University

28. Kuo, Chao-Ling. Characterization ofAthsq1, an Atherosclerosis Modifier Locus on Mouse Chromosome 4:.

Degree: 2011, Columbia University

 Atherosclerosis, the primary cause of heart attack, stroke, and peripheral vascular disease, is genetically complex and the genes that confer cardiovascular risk remain largely unknown.… (more)

Subjects/Keywords: Medical sciences; Genetics; Molecular biology

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APA (6th Edition):

Kuo, C. (2011). Characterization ofAthsq1, an Atherosclerosis Modifier Locus on Mouse Chromosome 4:. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8CV4QXC

Chicago Manual of Style (16th Edition):

Kuo, Chao-Ling. “Characterization ofAthsq1, an Atherosclerosis Modifier Locus on Mouse Chromosome 4:.” 2011. Doctoral Dissertation, Columbia University. Accessed July 15, 2020. https://doi.org/10.7916/D8CV4QXC.

MLA Handbook (7th Edition):

Kuo, Chao-Ling. “Characterization ofAthsq1, an Atherosclerosis Modifier Locus on Mouse Chromosome 4:.” 2011. Web. 15 Jul 2020.

Vancouver:

Kuo C. Characterization ofAthsq1, an Atherosclerosis Modifier Locus on Mouse Chromosome 4:. [Internet] [Doctoral dissertation]. Columbia University; 2011. [cited 2020 Jul 15]. Available from: https://doi.org/10.7916/D8CV4QXC.

Council of Science Editors:

Kuo C. Characterization ofAthsq1, an Atherosclerosis Modifier Locus on Mouse Chromosome 4:. [Doctoral Dissertation]. Columbia University; 2011. Available from: https://doi.org/10.7916/D8CV4QXC


Columbia University

29. Reid, Latarsha. Analysis of The RING Domain And BRCT Repeats of BRCA1.

Degree: 2011, Columbia University

 Mutations within BRCA1 often contribute to breast cancer susceptibility. Many of these mutations cluster within two highly conserved regions that may be important for BRCA1's… (more)

Subjects/Keywords: Biology; Molecular biology; Genetics

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APA (6th Edition):

Reid, L. (2011). Analysis of The RING Domain And BRCT Repeats of BRCA1. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8KH0VG3

Chicago Manual of Style (16th Edition):

Reid, Latarsha. “Analysis of The RING Domain And BRCT Repeats of BRCA1.” 2011. Doctoral Dissertation, Columbia University. Accessed July 15, 2020. https://doi.org/10.7916/D8KH0VG3.

MLA Handbook (7th Edition):

Reid, Latarsha. “Analysis of The RING Domain And BRCT Repeats of BRCA1.” 2011. Web. 15 Jul 2020.

Vancouver:

Reid L. Analysis of The RING Domain And BRCT Repeats of BRCA1. [Internet] [Doctoral dissertation]. Columbia University; 2011. [cited 2020 Jul 15]. Available from: https://doi.org/10.7916/D8KH0VG3.

Council of Science Editors:

Reid L. Analysis of The RING Domain And BRCT Repeats of BRCA1. [Doctoral Dissertation]. Columbia University; 2011. Available from: https://doi.org/10.7916/D8KH0VG3


Columbia University

30. Reddy, Bharat. Elucidating the Biological Function of PWWP-Domain Containing Protein Complexes.

Degree: 2013, Columbia University

 In eukaryotes, nuclear DNA is folded with histone proteins in the form of chromatin, and this structure plays a critical role in multiple biological processes,… (more)

Subjects/Keywords: Biology; Genetics; Molecular biology

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APA (6th Edition):

Reddy, B. (2013). Elucidating the Biological Function of PWWP-Domain Containing Protein Complexes. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D81V5N5Z

Chicago Manual of Style (16th Edition):

Reddy, Bharat. “Elucidating the Biological Function of PWWP-Domain Containing Protein Complexes.” 2013. Doctoral Dissertation, Columbia University. Accessed July 15, 2020. https://doi.org/10.7916/D81V5N5Z.

MLA Handbook (7th Edition):

Reddy, Bharat. “Elucidating the Biological Function of PWWP-Domain Containing Protein Complexes.” 2013. Web. 15 Jul 2020.

Vancouver:

Reddy B. Elucidating the Biological Function of PWWP-Domain Containing Protein Complexes. [Internet] [Doctoral dissertation]. Columbia University; 2013. [cited 2020 Jul 15]. Available from: https://doi.org/10.7916/D81V5N5Z.

Council of Science Editors:

Reddy B. Elucidating the Biological Function of PWWP-Domain Containing Protein Complexes. [Doctoral Dissertation]. Columbia University; 2013. Available from: https://doi.org/10.7916/D81V5N5Z

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