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

Degree: PhD, Genetics, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/33584

Chicago Manual of Style (16th Edition):

Shibata, Maho. “Regulation Of Mouse Embryonic And Extraembryonic Morphogenesis By Zfp568 And Trim28.” 2011. Doctoral Dissertation, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/33584.

MLA Handbook (7th Edition):

Shibata, Maho. “Regulation Of Mouse Embryonic And Extraembryonic Morphogenesis By Zfp568 And Trim28.” 2011. Web. 05 Mar 2021.

Vancouver:

Shibata M. Regulation Of Mouse Embryonic And Extraembryonic Morphogenesis By Zfp568 And Trim28. [Internet] [Doctoral dissertation]. Cornell University; 2011. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/33584.

Council of Science Editors:

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


Cornell University

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

Degree: M.S., Genetics, Genetics, 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. (Masters Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/40679

Chicago Manual of Style (16th Edition):

Yao, Li. “Dissecting The Function Of Drosophila Melanogaster Insulators Using Rna Aptamers.” 2015. Masters Thesis, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/40679.

MLA Handbook (7th Edition):

Yao, Li. “Dissecting The Function Of Drosophila Melanogaster Insulators Using Rna Aptamers.” 2015. Web. 05 Mar 2021.

Vancouver:

Yao L. Dissecting The Function Of Drosophila Melanogaster Insulators Using Rna Aptamers. [Internet] [Masters thesis]. Cornell University; 2015. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/40679.

Council of Science Editors:

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


Cornell University

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

Degree: PhD, Molecular and Cell Biology, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/36181

Chicago Manual of Style (16th Edition):

Rajavasireddy, Satyaki. “The Hybrid Incompatibility Gene Lethal Hybrid Rescue Represses Repetitive Dna.” 2014. Doctoral Dissertation, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/36181.

MLA Handbook (7th Edition):

Rajavasireddy, Satyaki. “The Hybrid Incompatibility Gene Lethal Hybrid Rescue Represses Repetitive Dna.” 2014. Web. 05 Mar 2021.

Vancouver:

Rajavasireddy S. The Hybrid Incompatibility Gene Lethal Hybrid Rescue Represses Repetitive Dna. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/36181.

Council of Science Editors:

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


Cornell University

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

Degree: PhD, Molecular and Cell Biology, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/33908

Chicago Manual of Style (16th Edition):

Wang, Mengqiao. “A Histone Deacetylase Hos3 Establishes Crosslink Between The Morphogenesis And Spindle Positioning Checkpoints.” 2013. Doctoral Dissertation, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/33908.

MLA Handbook (7th Edition):

Wang, Mengqiao. “A Histone Deacetylase Hos3 Establishes Crosslink Between The Morphogenesis And Spindle Positioning Checkpoints.” 2013. Web. 05 Mar 2021.

Vancouver:

Wang M. A Histone Deacetylase Hos3 Establishes Crosslink Between The Morphogenesis And Spindle Positioning Checkpoints. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/33908.

Council of Science Editors:

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


Cornell University

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

Degree: PhD, Molecular and Cell Biology, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/34053

Chicago Manual of Style (16th Edition):

Li, Minxing. “Effects Of Mammalian Ribonucleotide Reductase Deregulation On Redox Homeostasis And Genomic Integrity.” 2013. Doctoral Dissertation, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/34053.

MLA Handbook (7th Edition):

Li, Minxing. “Effects Of Mammalian Ribonucleotide Reductase Deregulation On Redox Homeostasis And Genomic Integrity.” 2013. Web. 05 Mar 2021.

Vancouver:

Li M. Effects Of Mammalian Ribonucleotide Reductase Deregulation On Redox Homeostasis And Genomic Integrity. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/34053.

Council of Science Editors:

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


Cornell University

6. Chu, Erin Tsi-Jia. MECHANISMS AND CONSEQUENCES OF DNA METHYLATION IN TWO MODEL SPECIES.

Degree: PhD, Comparative Biomedical Sciences, 2017, Cornell University

 Epigenetic modifications are known to regulate gene expression in a heritable manner, and can broadly be divided into three interacting classes: DNA methylation, histone modifications,… (more)

Subjects/Keywords: Genetics; Molecular biology

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APA (6th Edition):

Chu, E. T. (2017). MECHANISMS AND CONSEQUENCES OF DNA METHYLATION IN TWO MODEL SPECIES. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59013

Chicago Manual of Style (16th Edition):

Chu, Erin Tsi-Jia. “MECHANISMS AND CONSEQUENCES OF DNA METHYLATION IN TWO MODEL SPECIES.” 2017. Doctoral Dissertation, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/59013.

MLA Handbook (7th Edition):

Chu, Erin Tsi-Jia. “MECHANISMS AND CONSEQUENCES OF DNA METHYLATION IN TWO MODEL SPECIES.” 2017. Web. 05 Mar 2021.

Vancouver:

Chu ET. MECHANISMS AND CONSEQUENCES OF DNA METHYLATION IN TWO MODEL SPECIES. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/59013.

Council of Science Editors:

Chu ET. MECHANISMS AND CONSEQUENCES OF DNA METHYLATION IN TWO MODEL SPECIES. [Doctoral Dissertation]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/59013


Cornell University

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

Degree: PhD, Biological and Environmental Engineering, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59451

Chicago Manual of Style (16th Edition):

Xu, Yitian. “MODULATING LOCAL IMMUNE ENVIRONMENT TO DETER TUBERCULOSIS PROGRESSION.” 2018. Doctoral Dissertation, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/59451.

MLA Handbook (7th Edition):

Xu, Yitian. “MODULATING LOCAL IMMUNE ENVIRONMENT TO DETER TUBERCULOSIS PROGRESSION.” 2018. Web. 05 Mar 2021.

Vancouver:

Xu Y. MODULATING LOCAL IMMUNE ENVIRONMENT TO DETER TUBERCULOSIS PROGRESSION. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/59451.

Council of Science Editors:

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


Cornell University

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

Degree: PhD, Biochemistry, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/34267

Chicago Manual of Style (16th Edition):

Lee, Jayhun. “Understanding The Molecular Mechanisms Of Hair Follicle Stem Cell Quiescence And Genome Plasticity.” 2013. Doctoral Dissertation, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/34267.

MLA Handbook (7th Edition):

Lee, Jayhun. “Understanding The Molecular Mechanisms Of Hair Follicle Stem Cell Quiescence And Genome Plasticity.” 2013. Web. 05 Mar 2021.

Vancouver:

Lee J. Understanding The Molecular Mechanisms Of Hair Follicle Stem Cell Quiescence And Genome Plasticity. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/34267.

Council of Science Editors:

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


Cornell University

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

Degree: PhD, Genetics, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/36075

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. Doctoral Dissertation, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/36075.

MLA Handbook (7th Edition):

Strong, Edward. “Towards The Understanding Of Ccnb1Ip1 As A Co-Regulator Of Meiotic Crossing-Over In The Mouse.” 2014. Web. 05 Mar 2021.

Vancouver:

Strong E. Towards The Understanding Of Ccnb1Ip1 As A Co-Regulator Of Meiotic Crossing-Over In The Mouse. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/36075.

Council of Science Editors:

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


Cornell University

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

Degree: PhD, Genetics, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/40692

Chicago Manual of Style (16th Edition):

Henkhaus, Natalie. “Natural Genetic And Epigenetic Variation At Retroposon Loci In Arabidopsis.” 2015. Doctoral Dissertation, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/40692.

MLA Handbook (7th Edition):

Henkhaus, Natalie. “Natural Genetic And Epigenetic Variation At Retroposon Loci In Arabidopsis.” 2015. Web. 05 Mar 2021.

Vancouver:

Henkhaus N. Natural Genetic And Epigenetic Variation At Retroposon Loci In Arabidopsis. [Internet] [Doctoral dissertation]. Cornell University; 2015. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/40692.

Council of Science Editors:

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

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

Degree: PhD, Biochemistry, Molecular and Cell Biology, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/67819

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. Doctoral Dissertation, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/67819.

MLA Handbook (7th Edition):

McGurk, Michael Peter. “Uncovering variation in the repetitive portions of genomes to elucidate transposable element and satellite evolution.” 2019. Web. 05 Mar 2021.

Vancouver:

McGurk MP. Uncovering variation in the repetitive portions of genomes to elucidate transposable element and satellite evolution. [Internet] [Doctoral dissertation]. Cornell University; 2019. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/67819.

Council of Science Editors:

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


Cornell University

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

Degree: PhD, Biochemistry, Molecular and Cell Biology, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59299

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. Doctoral Dissertation, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/59299.

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. 05 Mar 2021.

Vancouver:

Wang W. THE ROLES OF SET-9 AND SET-26 IN LONGEVITY, GERMLINE FUNCTION AND RNAI PATHWAY May 2018. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/59299.

Council of Science Editors:

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


Cornell University

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

Degree: PhD, Veterinary Medicine, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/29260

Chicago Manual of Style (16th Edition):

Hwang, Chang-il. “The Role Of P53/Mir34/Met Pathway In Epithelial Ovarian Cancer Pathogenesis.” 2012. Doctoral Dissertation, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/29260.

MLA Handbook (7th Edition):

Hwang, Chang-il. “The Role Of P53/Mir34/Met Pathway In Epithelial Ovarian Cancer Pathogenesis.” 2012. Web. 05 Mar 2021.

Vancouver:

Hwang C. The Role Of P53/Mir34/Met Pathway In Epithelial Ovarian Cancer Pathogenesis. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/29260.

Council of Science Editors:

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

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

Degree: PhD, Biochemistry, Molecular and Cell Biology, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59753

Chicago Manual of Style (16th Edition):

Fair, Benjamin Jung. “IDENTIFICATION OF SPLICING PATHWAY MUTATIONS VIA TARGETED SEQUENCING.” 2018. Doctoral Dissertation, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/59753.

MLA Handbook (7th Edition):

Fair, Benjamin Jung. “IDENTIFICATION OF SPLICING PATHWAY MUTATIONS VIA TARGETED SEQUENCING.” 2018. Web. 05 Mar 2021.

Vancouver:

Fair BJ. IDENTIFICATION OF SPLICING PATHWAY MUTATIONS VIA TARGETED SEQUENCING. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/59753.

Council of Science Editors:

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


Cornell University

15. 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: PhD, Comparative Biomedical Sciences, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59710

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. Doctoral Dissertation, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/59710.

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. 05 Mar 2021.

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] [Doctoral dissertation]. Cornell University; 2018. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/59710.

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. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59710


Cornell University

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

Degree: PhD, Nutrition, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/30602

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. Doctoral Dissertation, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/30602.

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. 05 Mar 2021.

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] [Doctoral dissertation]. Cornell University; 2011. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/30602.

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. [Doctoral Dissertation]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/30602


Cornell University

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

Degree: PhD, Nutrition, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/34096

Chicago Manual of Style (16th Edition):

Jiang, Xinyin. “Influence Of Choline Intake During Pregnancy On Maternal And Fetal Genomic Markers In Humans.” 2013. Doctoral Dissertation, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/34096.

MLA Handbook (7th Edition):

Jiang, Xinyin. “Influence Of Choline Intake During Pregnancy On Maternal And Fetal Genomic Markers In Humans.” 2013. Web. 05 Mar 2021.

Vancouver:

Jiang X. Influence Of Choline Intake During Pregnancy On Maternal And Fetal Genomic Markers In Humans. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/34096.

Council of Science Editors:

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


Cornell University

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

Degree: PhD, Veterinary Medicine, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/36093

Chicago Manual of Style (16th Edition):

McElwee, John. “Identification Of Peptidylarginine Deiminase-2 (Padi2) As A Potential Oncogene And Therapeutic Target.” 2014. Doctoral Dissertation, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/36093.

MLA Handbook (7th Edition):

McElwee, John. “Identification Of Peptidylarginine Deiminase-2 (Padi2) As A Potential Oncogene And Therapeutic Target.” 2014. Web. 05 Mar 2021.

Vancouver:

McElwee J. Identification Of Peptidylarginine Deiminase-2 (Padi2) As A Potential Oncogene And Therapeutic Target. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/36093.

Council of Science Editors:

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


Cornell University

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

Degree: PhD, Nutrition, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59272

Chicago Manual of Style (16th Edition):

Taesuwan, Siraphat. “RELATIONSHIP OF CHOLINE AND TRIMETHYLAMINE-N-OXIDE INTAKE WITH METABOLIC AND HEALTH OUTCOMES IN HUMANS.” 2018. Doctoral Dissertation, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/59272.

MLA Handbook (7th Edition):

Taesuwan, Siraphat. “RELATIONSHIP OF CHOLINE AND TRIMETHYLAMINE-N-OXIDE INTAKE WITH METABOLIC AND HEALTH OUTCOMES IN HUMANS.” 2018. Web. 05 Mar 2021.

Vancouver:

Taesuwan S. RELATIONSHIP OF CHOLINE AND TRIMETHYLAMINE-N-OXIDE INTAKE WITH METABOLIC AND HEALTH OUTCOMES IN HUMANS. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/59272.

Council of Science Editors:

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


Cornell University

20. 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: PhD, Comparative Biomedical Sciences, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59292

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. Doctoral Dissertation, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/59292.

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. 05 Mar 2021.

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] [Doctoral dissertation]. Cornell University; 2018. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/59292.

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. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59292

21. Spektor, Roman. Single Cell and Combinatorial Analyses of Chromatin Accessibility.

Degree: PhD, Genetics, Genomics and Development, 2019, Cornell University

 The study of chromatin accessibility and DNA methylation have been fundamentally important to the understanding of gene regulation and disease. I developed methyl-ATAC-seq to query… (more)

Subjects/Keywords: Genetics

…Biology and Medicine, Cornell University, Ithaca, New York 14853, USA. 3 College of Agricultural… …and Life Sciences, Cornell University, Ithaca, New York 14853, USA 4 College of Veterinary… …Medicine, Department of Biomedical Sciences, Cornell University, Ithaca, New York 14853, USA. 5… …College of Agriculture and Life Sciences, Division of Nutritional Sciences, Cornell University… …of Molecular Biology and Genetics, Field of Genetics, Genomics, and Development, Cornell… 

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APA (6th Edition):

Spektor, R. (2019). Single Cell and Combinatorial Analyses of Chromatin Accessibility. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/67467

Chicago Manual of Style (16th Edition):

Spektor, Roman. “Single Cell and Combinatorial Analyses of Chromatin Accessibility.” 2019. Doctoral Dissertation, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/67467.

MLA Handbook (7th Edition):

Spektor, Roman. “Single Cell and Combinatorial Analyses of Chromatin Accessibility.” 2019. Web. 05 Mar 2021.

Vancouver:

Spektor R. Single Cell and Combinatorial Analyses of Chromatin Accessibility. [Internet] [Doctoral dissertation]. Cornell University; 2019. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/67467.

Council of Science Editors:

Spektor R. Single Cell and Combinatorial Analyses of Chromatin Accessibility. [Doctoral Dissertation]. Cornell University; 2019. Available from: http://hdl.handle.net/1813/67467

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

Degree: PhD, Genetics and Development, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/51554

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. Doctoral Dissertation, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/51554.

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. 05 Mar 2021.

Vancouver:

Duarte FdM. Genome-Wide Characterization of the Roles of Transcription Factors GAF and HSF in the Transcriptional Heat Shock Response. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/51554.

Council of Science Editors:

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

23. Murphy, Patrick. Mechanisms Of Epigenetic Regulation Characterized Using Novel Single Molecule And Traditional Methods.

Degree: PhD, Genetics, 2013, Cornell University

Subjects/Keywords: Epigenetics; Cancer; Single Molecule Nanofluidics

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APA (6th Edition):

Murphy, P. (2013). Mechanisms Of Epigenetic Regulation Characterized Using Novel Single Molecule And Traditional Methods. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/33788

Chicago Manual of Style (16th Edition):

Murphy, Patrick. “Mechanisms Of Epigenetic Regulation Characterized Using Novel Single Molecule And Traditional Methods.” 2013. Doctoral Dissertation, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/33788.

MLA Handbook (7th Edition):

Murphy, Patrick. “Mechanisms Of Epigenetic Regulation Characterized Using Novel Single Molecule And Traditional Methods.” 2013. Web. 05 Mar 2021.

Vancouver:

Murphy P. Mechanisms Of Epigenetic Regulation Characterized Using Novel Single Molecule And Traditional Methods. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/33788.

Council of Science Editors:

Murphy P. Mechanisms Of Epigenetic Regulation Characterized Using Novel Single Molecule And Traditional Methods. [Doctoral Dissertation]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/33788

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

Degree: PhD, Nutrition, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59133

Chicago Manual of Style (16th Edition):

King, Julia Heather. “Maternal Choline Supplementation in a Mouse Model of Placental Insufficiency.” 2017. Doctoral Dissertation, Cornell University. Accessed March 05, 2021. http://hdl.handle.net/1813/59133.

MLA Handbook (7th Edition):

King, Julia Heather. “Maternal Choline Supplementation in a Mouse Model of Placental Insufficiency.” 2017. Web. 05 Mar 2021.

Vancouver:

King JH. Maternal Choline Supplementation in a Mouse Model of Placental Insufficiency. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1813/59133.

Council of Science Editors:

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

.