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You searched for +publisher:"Cornell University" +contributor:("Soloway,Paul"). Showing records 1 – 24 of 24 total matches.

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Cornell University

1. Wei, Heng Chin Kevin. Natural Variation And Divergence Of Repetitive Dna In Drosophila .

Degree: 2016, Cornell University

 Most eukaryotic genomes harbor substantial amounts of transposable elements and satellite DNA, collectively known as repetitive sequences. They are characterized as genomic parasites as they… (more)

Subjects/Keywords: Repetitive DNA; Divergence; Variation

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

APA (6th Edition):

Wei, H. C. K. (2016). Natural Variation And Divergence Of Repetitive Dna In Drosophila . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/43621

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wei, Heng Chin Kevin. “Natural Variation And Divergence Of Repetitive Dna In Drosophila .” 2016. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/43621.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wei, Heng Chin Kevin. “Natural Variation And Divergence Of Repetitive Dna In Drosophila .” 2016. Web. 07 Jul 2020.

Vancouver:

Wei HCK. Natural Variation And Divergence Of Repetitive Dna In Drosophila . [Internet] [Thesis]. Cornell University; 2016. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/43621.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wei HCK. Natural Variation And Divergence Of Repetitive Dna In Drosophila . [Thesis]. Cornell University; 2016. Available from: http://hdl.handle.net/1813/43621

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Cornell University

2. Wallin, Christopher. Single Cell And Single Molecule Techniques For The Analysis Of The Epigenome .

Degree: 2016, Cornell University

 Epigenetic regulation is a critical biological process for the health and development of a cell. Epigenetic regulation is facilitated by covalent modifications to the underlying… (more)

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APA (6th Edition):

Wallin, C. (2016). Single Cell And Single Molecule Techniques For The Analysis Of The Epigenome . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/43572

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wallin, Christopher. “Single Cell And Single Molecule Techniques For The Analysis Of The Epigenome .” 2016. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/43572.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wallin, Christopher. “Single Cell And Single Molecule Techniques For The Analysis Of The Epigenome .” 2016. Web. 07 Jul 2020.

Vancouver:

Wallin C. Single Cell And Single Molecule Techniques For The Analysis Of The Epigenome . [Internet] [Thesis]. Cornell University; 2016. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/43572.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wallin C. Single Cell And Single Molecule Techniques For The Analysis Of The Epigenome . [Thesis]. Cornell University; 2016. Available from: http://hdl.handle.net/1813/43572

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Cornell University

3. Shibata, Maho. Regulation Of Mouse Embryonic And Extraembryonic Morphogenesis By Zfp568 And Trim28 .

Degree: 2011, Cornell University

 In mammals, extraembryonic tissues are critical for sustaining embryonic life inside the uterus, providing nourishment and secreting factors to maintain pregnancy. However, our understanding of… (more)

Subjects/Keywords: Yolk sac; Extraembryonic mesoderm; KRAB zinc finger protein

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APA (6th Edition):

Shibata, M. (2011). Regulation Of Mouse Embryonic And Extraembryonic Morphogenesis By Zfp568 And Trim28 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/33584

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Shibata, Maho. “Regulation Of Mouse Embryonic And Extraembryonic Morphogenesis By Zfp568 And Trim28 .” 2011. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/33584.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Shibata, Maho. “Regulation Of Mouse Embryonic And Extraembryonic Morphogenesis By Zfp568 And Trim28 .” 2011. Web. 07 Jul 2020.

Vancouver:

Shibata M. Regulation Of Mouse Embryonic And Extraembryonic Morphogenesis By Zfp568 And Trim28 . [Internet] [Thesis]. Cornell University; 2011. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/33584.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Shibata M. Regulation Of Mouse Embryonic And Extraembryonic Morphogenesis By Zfp568 And Trim28 . [Thesis]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/33584

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Cornell University

4. Yao, Li. Dissecting The Function Of Drosophila Melanogaster Insulators Using Rna Aptamers .

Degree: 2015, Cornell University

 Heat shock response in Drosophila melanogaster is a complex process causing changes of the cellular environment in reaction to the heat shock induction. RNA transcription… (more)

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APA (6th Edition):

Yao, L. (2015). Dissecting The Function Of Drosophila Melanogaster Insulators Using Rna Aptamers . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/40679

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Yao, Li. “Dissecting The Function Of Drosophila Melanogaster Insulators Using Rna Aptamers .” 2015. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/40679.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Yao, Li. “Dissecting The Function Of Drosophila Melanogaster Insulators Using Rna Aptamers .” 2015. Web. 07 Jul 2020.

Vancouver:

Yao L. Dissecting The Function Of Drosophila Melanogaster Insulators Using Rna Aptamers . [Internet] [Thesis]. Cornell University; 2015. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/40679.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Yao L. Dissecting The Function Of Drosophila Melanogaster Insulators Using Rna Aptamers . [Thesis]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/40679

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Cornell University

5. Lee, Jayhun. Understanding The Molecular Mechanisms Of Hair Follicle Stem Cell Quiescence And Genome Plasticity .

Degree: 2013, Cornell University

 Adult stem cells (SCs) utilize their abilities of self-renewal and differentiation to maintain proper homeostasis of their residing tissue. Malfunctioning of tissue SCs can result… (more)

Subjects/Keywords: stem cell; quiescence; plasticity

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APA (6th Edition):

Lee, J. (2013). Understanding The Molecular Mechanisms Of Hair Follicle Stem Cell Quiescence And Genome Plasticity . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/34267

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Lee, Jayhun. “Understanding The Molecular Mechanisms Of Hair Follicle Stem Cell Quiescence And Genome Plasticity .” 2013. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/34267.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Lee, Jayhun. “Understanding The Molecular Mechanisms Of Hair Follicle Stem Cell Quiescence And Genome Plasticity .” 2013. Web. 07 Jul 2020.

Vancouver:

Lee J. Understanding The Molecular Mechanisms Of Hair Follicle Stem Cell Quiescence And Genome Plasticity . [Internet] [Thesis]. Cornell University; 2013. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/34267.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Lee J. Understanding The Molecular Mechanisms Of Hair Follicle Stem Cell Quiescence And Genome Plasticity . [Thesis]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/34267

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Cornell University

6. Strong, Edward. Towards The Understanding Of Ccnb1Ip1 As A Co-Regulator Of Meiotic Crossing-Over In The Mouse .

Degree: 2014, Cornell University

 It is clear that there are many genes required for meiosis in mammals that are not present in the more tractable model organisms. To identify… (more)

Subjects/Keywords: Meiosis; Sumoylation; CCNB1IP1

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APA (6th Edition):

Strong, E. (2014). Towards The Understanding Of Ccnb1Ip1 As A Co-Regulator Of Meiotic Crossing-Over In The Mouse . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/36075

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Strong, Edward. “Towards The Understanding Of Ccnb1Ip1 As A Co-Regulator Of Meiotic Crossing-Over In The Mouse .” 2014. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/36075.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Strong, Edward. “Towards The Understanding Of Ccnb1Ip1 As A Co-Regulator Of Meiotic Crossing-Over In The Mouse .” 2014. Web. 07 Jul 2020.

Vancouver:

Strong E. Towards The Understanding Of Ccnb1Ip1 As A Co-Regulator Of Meiotic Crossing-Over In The Mouse . [Internet] [Thesis]. Cornell University; 2014. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/36075.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Strong E. Towards The Understanding Of Ccnb1Ip1 As A Co-Regulator Of Meiotic Crossing-Over In The Mouse . [Thesis]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/36075

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Cornell University

7. Henkhaus, Natalie. Natural Genetic And Epigenetic Variation At Retroposon Loci In Arabidopsis .

Degree: 2015, Cornell University

 In both plants and animals, transposable elements are epigenetically regulated to maintain genomic integrity. DNA methylation (5-methylcytosine) is an important epigenetic modification that maintains transcriptional… (more)

Subjects/Keywords: Epigenetics; Natural variation; Arabidopsis

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APA (6th Edition):

Henkhaus, N. (2015). Natural Genetic And Epigenetic Variation At Retroposon Loci In Arabidopsis . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/40692

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Henkhaus, Natalie. “Natural Genetic And Epigenetic Variation At Retroposon Loci In Arabidopsis .” 2015. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/40692.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Henkhaus, Natalie. “Natural Genetic And Epigenetic Variation At Retroposon Loci In Arabidopsis .” 2015. Web. 07 Jul 2020.

Vancouver:

Henkhaus N. Natural Genetic And Epigenetic Variation At Retroposon Loci In Arabidopsis . [Internet] [Thesis]. Cornell University; 2015. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/40692.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Henkhaus N. Natural Genetic And Epigenetic Variation At Retroposon Loci In Arabidopsis . [Thesis]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/40692

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Cornell University

8. Rajavasireddy, Satyaki. The Hybrid Incompatibility Gene Lethal Hybrid Rescue Represses Repetitive Dna .

Degree: 2014, Cornell University

 Heterochromatin keeps in check selfish elements such as transposable elements (TEs) and satellite DNAs, which can wreak havoc on a genome by mobilizing and increasing… (more)

Subjects/Keywords: Heterochromatin Lhr Drosophila; Hybrid Incompatibility; Satellites Transposable elements

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APA (6th Edition):

Rajavasireddy, S. (2014). The Hybrid Incompatibility Gene Lethal Hybrid Rescue Represses Repetitive Dna . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/36181

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Rajavasireddy, Satyaki. “The Hybrid Incompatibility Gene Lethal Hybrid Rescue Represses Repetitive Dna .” 2014. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/36181.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Rajavasireddy, Satyaki. “The Hybrid Incompatibility Gene Lethal Hybrid Rescue Represses Repetitive Dna .” 2014. Web. 07 Jul 2020.

Vancouver:

Rajavasireddy S. The Hybrid Incompatibility Gene Lethal Hybrid Rescue Represses Repetitive Dna . [Internet] [Thesis]. Cornell University; 2014. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/36181.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Rajavasireddy S. The Hybrid Incompatibility Gene Lethal Hybrid Rescue Represses Repetitive Dna . [Thesis]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/36181

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

9. McGurk, Michael Peter. Uncovering variation in the repetitive portions of genomes to elucidate transposable element and satellite evolution .

Degree: 2019, Cornell University

 Eukaryotic genomes are replete with repeated sequence, in the form of transposable elements (TEs) dispersed throughout genomes and as large stretches of tandem repeats (satellite… (more)

Subjects/Keywords: Repetitive DNA; Satellite DNA; Transposable elements; Evolution & development; Genetics; Bioinformatics

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APA (6th Edition):

McGurk, M. P. (2019). Uncovering variation in the repetitive portions of genomes to elucidate transposable element and satellite evolution . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/67819

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

McGurk, Michael Peter. “Uncovering variation in the repetitive portions of genomes to elucidate transposable element and satellite evolution .” 2019. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/67819.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

McGurk, Michael Peter. “Uncovering variation in the repetitive portions of genomes to elucidate transposable element and satellite evolution .” 2019. Web. 07 Jul 2020.

Vancouver:

McGurk MP. Uncovering variation in the repetitive portions of genomes to elucidate transposable element and satellite evolution . [Internet] [Thesis]. Cornell University; 2019. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/67819.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

McGurk MP. Uncovering variation in the repetitive portions of genomes to elucidate transposable element and satellite evolution . [Thesis]. Cornell University; 2019. Available from: http://hdl.handle.net/1813/67819

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Cornell University

10. Wang, Wenke. THE ROLES OF SET-9 AND SET-26 IN LONGEVITY, GERMLINE FUNCTION AND RNAI PATHWAY May 2018 .

Degree: 2018, Cornell University

 Aging, germline function and RNA interference are three distinct biological processes that associate with alterations in epigenetic state, including histone modifications. Our lab discovered two… (more)

Subjects/Keywords: Molecular biology

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APA (6th Edition):

Wang, W. (2018). THE ROLES OF SET-9 AND SET-26 IN LONGEVITY, GERMLINE FUNCTION AND RNAI PATHWAY May 2018 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/59299

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wang, Wenke. “THE ROLES OF SET-9 AND SET-26 IN LONGEVITY, GERMLINE FUNCTION AND RNAI PATHWAY May 2018 .” 2018. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/59299.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wang, Wenke. “THE ROLES OF SET-9 AND SET-26 IN LONGEVITY, GERMLINE FUNCTION AND RNAI PATHWAY May 2018 .” 2018. Web. 07 Jul 2020.

Vancouver:

Wang W. THE ROLES OF SET-9 AND SET-26 IN LONGEVITY, GERMLINE FUNCTION AND RNAI PATHWAY May 2018 . [Internet] [Thesis]. Cornell University; 2018. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/59299.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wang W. THE ROLES OF SET-9 AND SET-26 IN LONGEVITY, GERMLINE FUNCTION AND RNAI PATHWAY May 2018 . [Thesis]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59299

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Cornell University

11. Wang, Mengqiao. A Histone Deacetylase Hos3 Establishes Crosslink Between The Morphogenesis And Spindle Positioning Checkpoints .

Degree: 2013, Cornell University

 An increasing number of cellular activities are under the regulation of lysine acetylation. This post-translational modification (PTM) is reversibly catalyzed by histone acetyltransferases (HATs) and… (more)

Subjects/Keywords: Histone deacetylase Hos3; Morphogenesis checkpoint; Spindle positioning checkpoint

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APA (6th Edition):

Wang, M. (2013). A Histone Deacetylase Hos3 Establishes Crosslink Between The Morphogenesis And Spindle Positioning Checkpoints . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/33908

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wang, Mengqiao. “A Histone Deacetylase Hos3 Establishes Crosslink Between The Morphogenesis And Spindle Positioning Checkpoints .” 2013. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/33908.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wang, Mengqiao. “A Histone Deacetylase Hos3 Establishes Crosslink Between The Morphogenesis And Spindle Positioning Checkpoints .” 2013. Web. 07 Jul 2020.

Vancouver:

Wang M. A Histone Deacetylase Hos3 Establishes Crosslink Between The Morphogenesis And Spindle Positioning Checkpoints . [Internet] [Thesis]. Cornell University; 2013. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/33908.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wang M. A Histone Deacetylase Hos3 Establishes Crosslink Between The Morphogenesis And Spindle Positioning Checkpoints . [Thesis]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/33908

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Cornell University

12. Li, Minxing. Effects Of Mammalian Ribonucleotide Reductase Deregulation On Redox Homeostasis And Genomic Integrity .

Degree: 2013, Cornell University

 Ribonucleotide reductase catalyzes the rate-limiting step in de novo deoxyribonucleoside triphosphate (dNTPs) biosynthesis and is essential for providing balanced dNTP pools for nuclear and mitochondrial… (more)

Subjects/Keywords: Ribonucleotide Reductase; Redox Homeostasis; Genomic Integrity

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APA (6th Edition):

Li, M. (2013). Effects Of Mammalian Ribonucleotide Reductase Deregulation On Redox Homeostasis And Genomic Integrity . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/34053

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Li, Minxing. “Effects Of Mammalian Ribonucleotide Reductase Deregulation On Redox Homeostasis And Genomic Integrity .” 2013. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/34053.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Li, Minxing. “Effects Of Mammalian Ribonucleotide Reductase Deregulation On Redox Homeostasis And Genomic Integrity .” 2013. Web. 07 Jul 2020.

Vancouver:

Li M. Effects Of Mammalian Ribonucleotide Reductase Deregulation On Redox Homeostasis And Genomic Integrity . [Internet] [Thesis]. Cornell University; 2013. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/34053.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Li M. Effects Of Mammalian Ribonucleotide Reductase Deregulation On Redox Homeostasis And Genomic Integrity . [Thesis]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/34053

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Cornell University

13. Xu, Yitian. MODULATING LOCAL IMMUNE ENVIRONMENT TO DETER TUBERCULOSIS PROGRESSION .

Degree: 2018, Cornell University

 Mycobacterium tuberculosis (Mtb) remains a grave threat to world health with emerging drug resistant strains. One prominent feature of Mtb infection is the extensive reprogramming… (more)

Subjects/Keywords: Biology; Enhanced TB drug efficacy; Immune cell modulation; Immune cell recruitment; Matrix metalloproteinase inhibitor; Mycobacterium tuberculosis; Synthetic mRNA; Bioengineering

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APA (6th Edition):

Xu, Y. (2018). MODULATING LOCAL IMMUNE ENVIRONMENT TO DETER TUBERCULOSIS PROGRESSION . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/59451

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Xu, Yitian. “MODULATING LOCAL IMMUNE ENVIRONMENT TO DETER TUBERCULOSIS PROGRESSION .” 2018. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/59451.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Xu, Yitian. “MODULATING LOCAL IMMUNE ENVIRONMENT TO DETER TUBERCULOSIS PROGRESSION .” 2018. Web. 07 Jul 2020.

Vancouver:

Xu Y. MODULATING LOCAL IMMUNE ENVIRONMENT TO DETER TUBERCULOSIS PROGRESSION . [Internet] [Thesis]. Cornell University; 2018. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/59451.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Xu Y. MODULATING LOCAL IMMUNE ENVIRONMENT TO DETER TUBERCULOSIS PROGRESSION . [Thesis]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59451

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Cornell University

14. Lynch, Amanda. "Making It Work:" The Role Of Goals, Strategies, And Self-Monitoring In Dietary Change And Weight Management After Gastric Bypass Surgery .

Degree: 2011, Cornell University

 Dietary practices following gastric bypass surgery must encompass new restrictions on eating, prevention of nutrient deficiencies, and weight maintenanc e. Using a mixedmethods approach, this… (more)

Subjects/Keywords: Gastric bypass surgery; Goals; Strategies

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APA (6th Edition):

Lynch, A. (2011). "Making It Work:" The Role Of Goals, Strategies, And Self-Monitoring In Dietary Change And Weight Management After Gastric Bypass Surgery . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/30602

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Lynch, Amanda. “"Making It Work:" The Role Of Goals, Strategies, And Self-Monitoring In Dietary Change And Weight Management After Gastric Bypass Surgery .” 2011. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/30602.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Lynch, Amanda. “"Making It Work:" The Role Of Goals, Strategies, And Self-Monitoring In Dietary Change And Weight Management After Gastric Bypass Surgery .” 2011. Web. 07 Jul 2020.

Vancouver:

Lynch A. "Making It Work:" The Role Of Goals, Strategies, And Self-Monitoring In Dietary Change And Weight Management After Gastric Bypass Surgery . [Internet] [Thesis]. Cornell University; 2011. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/30602.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Lynch A. "Making It Work:" The Role Of Goals, Strategies, And Self-Monitoring In Dietary Change And Weight Management After Gastric Bypass Surgery . [Thesis]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/30602

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Cornell University

15. Jiang, Xinyin. Influence Of Choline Intake During Pregnancy On Maternal And Fetal Genomic Markers In Humans .

Degree: 2013, Cornell University

 Choline is an essential nutrient, which functions in cellular membrane structure, neurotransmission and methyl group donation. The need for choline increases substantially during pregnancy. An… (more)

Subjects/Keywords: choline; genomics; epigenetics

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APA (6th Edition):

Jiang, X. (2013). Influence Of Choline Intake During Pregnancy On Maternal And Fetal Genomic Markers In Humans . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/34096

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Jiang, Xinyin. “Influence Of Choline Intake During Pregnancy On Maternal And Fetal Genomic Markers In Humans .” 2013. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/34096.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Jiang, Xinyin. “Influence Of Choline Intake During Pregnancy On Maternal And Fetal Genomic Markers In Humans .” 2013. Web. 07 Jul 2020.

Vancouver:

Jiang X. Influence Of Choline Intake During Pregnancy On Maternal And Fetal Genomic Markers In Humans . [Internet] [Thesis]. Cornell University; 2013. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/34096.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Jiang X. Influence Of Choline Intake During Pregnancy On Maternal And Fetal Genomic Markers In Humans . [Thesis]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/34096

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Cornell University

16. Hwang, Chang-il. The Role Of P53/Mir34/Met Pathway In Epithelial Ovarian Cancer Pathogenesis .

Degree: 2012, Cornell University

 The miR-34 family is directly transactivated by tumor suppressor p53, which is frequently mutated in the majority of human cancers, including epithelial ovarian cancer (EOC).… (more)

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APA (6th Edition):

Hwang, C. (2012). The Role Of P53/Mir34/Met Pathway In Epithelial Ovarian Cancer Pathogenesis . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/29260

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Hwang, Chang-il. “The Role Of P53/Mir34/Met Pathway In Epithelial Ovarian Cancer Pathogenesis .” 2012. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/29260.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Hwang, Chang-il. “The Role Of P53/Mir34/Met Pathway In Epithelial Ovarian Cancer Pathogenesis .” 2012. Web. 07 Jul 2020.

Vancouver:

Hwang C. The Role Of P53/Mir34/Met Pathway In Epithelial Ovarian Cancer Pathogenesis . [Internet] [Thesis]. Cornell University; 2012. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/29260.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Hwang C. The Role Of P53/Mir34/Met Pathway In Epithelial Ovarian Cancer Pathogenesis . [Thesis]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/29260

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Cornell University

17. Wissink, Erin. Post-Transcriptional Gene Regulation: Roles For Micrornas In Cd8+ T Cells And Discovery Of Novel Cis-Regulatory Elements .

Degree: 2016, Cornell University

 Post-transcriptional events control the amount of protein produced by an mRNA transcript. In mammals, the sequences that regulate post-transcriptional events are predominantly located within a… (more)

Subjects/Keywords: gene regulation; immunology; development

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APA (6th Edition):

Wissink, E. (2016). Post-Transcriptional Gene Regulation: Roles For Micrornas In Cd8+ T Cells And Discovery Of Novel Cis-Regulatory Elements . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/43605

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wissink, Erin. “Post-Transcriptional Gene Regulation: Roles For Micrornas In Cd8+ T Cells And Discovery Of Novel Cis-Regulatory Elements .” 2016. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/43605.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wissink, Erin. “Post-Transcriptional Gene Regulation: Roles For Micrornas In Cd8+ T Cells And Discovery Of Novel Cis-Regulatory Elements .” 2016. Web. 07 Jul 2020.

Vancouver:

Wissink E. Post-Transcriptional Gene Regulation: Roles For Micrornas In Cd8+ T Cells And Discovery Of Novel Cis-Regulatory Elements . [Internet] [Thesis]. Cornell University; 2016. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/43605.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wissink E. Post-Transcriptional Gene Regulation: Roles For Micrornas In Cd8+ T Cells And Discovery Of Novel Cis-Regulatory Elements . [Thesis]. Cornell University; 2016. Available from: http://hdl.handle.net/1813/43605

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Cornell University

18. McElwee, John. Identification Of Peptidylarginine Deiminase-2 (Padi2) As A Potential Oncogene And Therapeutic Target .

Degree: 2014, Cornell University

 Breast cancer is the most frequently diagnosed cancer in women, with over 1 million new cases in the world each year. Recently, in addition to… (more)

Subjects/Keywords: Peptidylarginine deiminase; Cl-amidine; PADI2

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APA (6th Edition):

McElwee, J. (2014). Identification Of Peptidylarginine Deiminase-2 (Padi2) As A Potential Oncogene And Therapeutic Target . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/36093

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

McElwee, John. “Identification Of Peptidylarginine Deiminase-2 (Padi2) As A Potential Oncogene And Therapeutic Target .” 2014. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/36093.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

McElwee, John. “Identification Of Peptidylarginine Deiminase-2 (Padi2) As A Potential Oncogene And Therapeutic Target .” 2014. Web. 07 Jul 2020.

Vancouver:

McElwee J. Identification Of Peptidylarginine Deiminase-2 (Padi2) As A Potential Oncogene And Therapeutic Target . [Internet] [Thesis]. Cornell University; 2014. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/36093.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

McElwee J. Identification Of Peptidylarginine Deiminase-2 (Padi2) As A Potential Oncogene And Therapeutic Target . [Thesis]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/36093

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Cornell University

19. Taesuwan, Siraphat. RELATIONSHIP OF CHOLINE AND TRIMETHYLAMINE-N-OXIDE INTAKE WITH METABOLIC AND HEALTH OUTCOMES IN HUMANS .

Degree: 2018, Cornell University

 This dissertation is focused on dietary choline and its derivative trimethylamine-N-oxide (TMAO). Recent discoveries have implicated circulating TMAO as a candidate risk factor for cardiovascular… (more)

Subjects/Keywords: Choline; Nutrition; Gut microbiota; Hypertension; NHANES; Randomized controlled trial; Trimethylamine-N-oxide

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APA (6th Edition):

Taesuwan, S. (2018). RELATIONSHIP OF CHOLINE AND TRIMETHYLAMINE-N-OXIDE INTAKE WITH METABOLIC AND HEALTH OUTCOMES IN HUMANS . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/59272

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Taesuwan, Siraphat. “RELATIONSHIP OF CHOLINE AND TRIMETHYLAMINE-N-OXIDE INTAKE WITH METABOLIC AND HEALTH OUTCOMES IN HUMANS .” 2018. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/59272.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Taesuwan, Siraphat. “RELATIONSHIP OF CHOLINE AND TRIMETHYLAMINE-N-OXIDE INTAKE WITH METABOLIC AND HEALTH OUTCOMES IN HUMANS .” 2018. Web. 07 Jul 2020.

Vancouver:

Taesuwan S. RELATIONSHIP OF CHOLINE AND TRIMETHYLAMINE-N-OXIDE INTAKE WITH METABOLIC AND HEALTH OUTCOMES IN HUMANS . [Internet] [Thesis]. Cornell University; 2018. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/59272.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Taesuwan S. RELATIONSHIP OF CHOLINE AND TRIMETHYLAMINE-N-OXIDE INTAKE WITH METABOLIC AND HEALTH OUTCOMES IN HUMANS . [Thesis]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59272

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

20. Fair, Benjamin Jung. IDENTIFICATION OF SPLICING PATHWAY MUTATIONS VIA TARGETED SEQUENCING .

Degree: 2018, Cornell University

 The identification of splice sites and catalytic removal of introns via the spliceosome is an essential and regulated component of eukaryotic gene expression. While ever-increasing… (more)

Subjects/Keywords: screen; Sequencing; splicing; Genetics; Molecular biology; Yeast; Transcription

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APA (6th Edition):

Fair, B. J. (2018). IDENTIFICATION OF SPLICING PATHWAY MUTATIONS VIA TARGETED SEQUENCING . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/59753

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Fair, Benjamin Jung. “IDENTIFICATION OF SPLICING PATHWAY MUTATIONS VIA TARGETED SEQUENCING .” 2018. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/59753.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Fair, Benjamin Jung. “IDENTIFICATION OF SPLICING PATHWAY MUTATIONS VIA TARGETED SEQUENCING .” 2018. Web. 07 Jul 2020.

Vancouver:

Fair BJ. IDENTIFICATION OF SPLICING PATHWAY MUTATIONS VIA TARGETED SEQUENCING . [Internet] [Thesis]. Cornell University; 2018. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/59753.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Fair BJ. IDENTIFICATION OF SPLICING PATHWAY MUTATIONS VIA TARGETED SEQUENCING . [Thesis]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59753

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Cornell University

21. Chen, Frances. GENOMIC REGULATORY ELEMENTS IN TRANSCRIPTION, DEVELOPMENT, AND DISEASE: GENERATING MOUSE MODELS FOR LATERALITY DEFECTS USING CRISPR/CAS9 GENOME ENGINEERING AT THE PITX2 LOCUS .

Degree: 2018, Cornell University

 The genome contains the code of life: conservation of DNA sequence ensures proper stereotypical patterning and precise formation of the body’s tissues replicated in members… (more)

Subjects/Keywords: LR asymmetry; Pitx2; transcriptional regulation; Developmental biology; Genetics; atrial fibrillation; intestinal morphogenesis; lncRNA

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APA (6th Edition):

Chen, F. (2018). GENOMIC REGULATORY ELEMENTS IN TRANSCRIPTION, DEVELOPMENT, AND DISEASE: GENERATING MOUSE MODELS FOR LATERALITY DEFECTS USING CRISPR/CAS9 GENOME ENGINEERING AT THE PITX2 LOCUS . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/59710

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Chen, Frances. “GENOMIC REGULATORY ELEMENTS IN TRANSCRIPTION, DEVELOPMENT, AND DISEASE: GENERATING MOUSE MODELS FOR LATERALITY DEFECTS USING CRISPR/CAS9 GENOME ENGINEERING AT THE PITX2 LOCUS .” 2018. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/59710.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Chen, Frances. “GENOMIC REGULATORY ELEMENTS IN TRANSCRIPTION, DEVELOPMENT, AND DISEASE: GENERATING MOUSE MODELS FOR LATERALITY DEFECTS USING CRISPR/CAS9 GENOME ENGINEERING AT THE PITX2 LOCUS .” 2018. Web. 07 Jul 2020.

Vancouver:

Chen F. GENOMIC REGULATORY ELEMENTS IN TRANSCRIPTION, DEVELOPMENT, AND DISEASE: GENERATING MOUSE MODELS FOR LATERALITY DEFECTS USING CRISPR/CAS9 GENOME ENGINEERING AT THE PITX2 LOCUS . [Internet] [Thesis]. Cornell University; 2018. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/59710.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Chen F. GENOMIC REGULATORY ELEMENTS IN TRANSCRIPTION, DEVELOPMENT, AND DISEASE: GENERATING MOUSE MODELS FOR LATERALITY DEFECTS USING CRISPR/CAS9 GENOME ENGINEERING AT THE PITX2 LOCUS . [Thesis]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59710

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Cornell University

22. Hart, James Charles. A characterization of orofacial phenotypes resulting from tissue specific deletion of Pbx genes within the cranial neural crest cell population or the cephalic epithelium of the developing murine embryo .

Degree: 2018, Cornell University

 Affecting approximately 1-in-700 live births, “orofacial clefting” represents the most common class of craniofacial birth defect. Although not a major cause of mortality, these conditions… (more)

Subjects/Keywords: Veterinary science; Palate; Cleft; Cranial Neural Crest; Developmental biology; Pbx; Mouse; Molecular biology

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APA (6th Edition):

Hart, J. C. (2018). A characterization of orofacial phenotypes resulting from tissue specific deletion of Pbx genes within the cranial neural crest cell population or the cephalic epithelium of the developing murine embryo . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/59292

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Hart, James Charles. “A characterization of orofacial phenotypes resulting from tissue specific deletion of Pbx genes within the cranial neural crest cell population or the cephalic epithelium of the developing murine embryo .” 2018. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/59292.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Hart, James Charles. “A characterization of orofacial phenotypes resulting from tissue specific deletion of Pbx genes within the cranial neural crest cell population or the cephalic epithelium of the developing murine embryo .” 2018. Web. 07 Jul 2020.

Vancouver:

Hart JC. A characterization of orofacial phenotypes resulting from tissue specific deletion of Pbx genes within the cranial neural crest cell population or the cephalic epithelium of the developing murine embryo . [Internet] [Thesis]. Cornell University; 2018. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/59292.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Hart JC. A characterization of orofacial phenotypes resulting from tissue specific deletion of Pbx genes within the cranial neural crest cell population or the cephalic epithelium of the developing murine embryo . [Thesis]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59292

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

23. Duarte, Fabiana de Melo. Genome-Wide Characterization of the Roles of Transcription Factors GAF and HSF in the Transcriptional Heat Shock Response .

Degree: 2017, Cornell University

 In eukaryotes, RNA polymerase II (Pol II) is responsible for the transcription of all protein-coding genes, and regulation of its activity is fundamental for cellular… (more)

Subjects/Keywords: Genetics; Biochemistry; Molecular biology; Heat shock; Pol II pausing; RNA aptamers; Transcription factors; Transcription regulation

…transcriptional HS response is regulated. Among these groups, the Lis laboratory at Cornell University… …that eventually led to my acceptance to the Genetics and Development program at Cornell… …University. Over my years in the Lis lab, I have had the opportunity to interact and learn from an… 

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APA (6th Edition):

Duarte, F. d. M. (2017). Genome-Wide Characterization of the Roles of Transcription Factors GAF and HSF in the Transcriptional Heat Shock Response . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/51554

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Duarte, Fabiana de Melo. “Genome-Wide Characterization of the Roles of Transcription Factors GAF and HSF in the Transcriptional Heat Shock Response .” 2017. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/51554.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Duarte, Fabiana de Melo. “Genome-Wide Characterization of the Roles of Transcription Factors GAF and HSF in the Transcriptional Heat Shock Response .” 2017. Web. 07 Jul 2020.

Vancouver:

Duarte FdM. Genome-Wide Characterization of the Roles of Transcription Factors GAF and HSF in the Transcriptional Heat Shock Response . [Internet] [Thesis]. Cornell University; 2017. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/51554.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Duarte FdM. Genome-Wide Characterization of the Roles of Transcription Factors GAF and HSF in the Transcriptional Heat Shock Response . [Thesis]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/51554

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

24. King, Julia Heather. Maternal Choline Supplementation in a Mouse Model of Placental Insufficiency .

Degree: 2017, Cornell University

 Placental insufficiency is commonly associated with intrauterine growth restriction, preeclampsia, and spontaneous abortion. The essential nutrient choline may mitigate some of these impairments, as suggested… (more)

Subjects/Keywords: Choline; Dlx3; Fetal Growth; Pregnancy; Placenta; vitamin B12; Nutrition

…approved by the Institutional Animal Care and Use Committees at Cornell University and conducted… 

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APA (6th Edition):

King, J. H. (2017). Maternal Choline Supplementation in a Mouse Model of Placental Insufficiency . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/59133

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

King, Julia Heather. “Maternal Choline Supplementation in a Mouse Model of Placental Insufficiency .” 2017. Thesis, Cornell University. Accessed July 07, 2020. http://hdl.handle.net/1813/59133.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

King, Julia Heather. “Maternal Choline Supplementation in a Mouse Model of Placental Insufficiency .” 2017. Web. 07 Jul 2020.

Vancouver:

King JH. Maternal Choline Supplementation in a Mouse Model of Placental Insufficiency . [Internet] [Thesis]. Cornell University; 2017. [cited 2020 Jul 07]. Available from: http://hdl.handle.net/1813/59133.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

King JH. Maternal Choline Supplementation in a Mouse Model of Placental Insufficiency . [Thesis]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/59133

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

.