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You searched for +publisher:"Cornell University" +contributor:("Schimenti, John C."). Showing records 1 – 30 of 41 total matches.

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Cornell University

1. Wang, Alex. Molecular Regulation of Hair Follicle Stem and Progenitor Cell Homeostasis .

Degree: 2017, Cornell University

 Maintenance of adult stem cells and their progenitor cells is critical for proper homeostasis of their resident tissues. Defects in tissue stem or progenitor cell… (more)

Subjects/Keywords: Hair Follicle; Stem Cell; Molecular biology

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APA (6th Edition):

Wang, A. (2017). Molecular Regulation of Hair Follicle Stem and Progenitor Cell Homeostasis . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/47750

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, Alex. “Molecular Regulation of Hair Follicle Stem and Progenitor Cell Homeostasis .” 2017. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/47750.

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

MLA Handbook (7th Edition):

Wang, Alex. “Molecular Regulation of Hair Follicle Stem and Progenitor Cell Homeostasis .” 2017. Web. 02 Jul 2020.

Vancouver:

Wang A. Molecular Regulation of Hair Follicle Stem and Progenitor Cell Homeostasis . [Internet] [Thesis]. Cornell University; 2017. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/47750.

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

Council of Science Editors:

Wang A. Molecular Regulation of Hair Follicle Stem and Progenitor Cell Homeostasis . [Thesis]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/47750

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


Cornell University

2. Al-Sweel, Najla Abdulaziz. THE MISMATCH REPAIR AND MEIOTIC RECOMBINATION ENDONUCLEASE MLH1-MLH3 IS DIRECTED BY PROTEIN-PROTEIN INTERACTIONS .

Degree: 2017, Cornell University

 During meiosis, diploid germ cells that will become eggs or sperm undergo a single round of DNA replication followed by two consecutive chromosomal divisions. The… (more)

Subjects/Keywords: meiosis; Molecular biology; Genetics; Biochemistry; crossing over; genome integrity; homologous recombination; mismatch repair

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APA (6th Edition):

Al-Sweel, N. A. (2017). THE MISMATCH REPAIR AND MEIOTIC RECOMBINATION ENDONUCLEASE MLH1-MLH3 IS DIRECTED BY PROTEIN-PROTEIN INTERACTIONS . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/59043

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):

Al-Sweel, Najla Abdulaziz. “THE MISMATCH REPAIR AND MEIOTIC RECOMBINATION ENDONUCLEASE MLH1-MLH3 IS DIRECTED BY PROTEIN-PROTEIN INTERACTIONS .” 2017. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/59043.

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

MLA Handbook (7th Edition):

Al-Sweel, Najla Abdulaziz. “THE MISMATCH REPAIR AND MEIOTIC RECOMBINATION ENDONUCLEASE MLH1-MLH3 IS DIRECTED BY PROTEIN-PROTEIN INTERACTIONS .” 2017. Web. 02 Jul 2020.

Vancouver:

Al-Sweel NA. THE MISMATCH REPAIR AND MEIOTIC RECOMBINATION ENDONUCLEASE MLH1-MLH3 IS DIRECTED BY PROTEIN-PROTEIN INTERACTIONS . [Internet] [Thesis]. Cornell University; 2017. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/59043.

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

Council of Science Editors:

Al-Sweel NA. THE MISMATCH REPAIR AND MEIOTIC RECOMBINATION ENDONUCLEASE MLH1-MLH3 IS DIRECTED BY PROTEIN-PROTEIN INTERACTIONS . [Thesis]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/59043

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


Cornell University

3. Murphy, Kristin. Understanding The Molecular Mechanisms Of Transcriptional Repression Mediated By Krab Zinc Finger Proteins And Trim28 .

Degree: 2013, Cornell University

 KRAB domain Zinc Finger proteins make up the largest family of transcription factors in mammals. Previous studies on a handful of KRAB Zinc Finger proteins… (more)

Subjects/Keywords: embryogenesis; repression; transcription

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APA (6th Edition):

Murphy, K. (2013). Understanding The Molecular Mechanisms Of Transcriptional Repression Mediated By Krab Zinc Finger Proteins And Trim28 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/34035

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):

Murphy, Kristin. “Understanding The Molecular Mechanisms Of Transcriptional Repression Mediated By Krab Zinc Finger Proteins And Trim28 .” 2013. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/34035.

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

MLA Handbook (7th Edition):

Murphy, Kristin. “Understanding The Molecular Mechanisms Of Transcriptional Repression Mediated By Krab Zinc Finger Proteins And Trim28 .” 2013. Web. 02 Jul 2020.

Vancouver:

Murphy K. Understanding The Molecular Mechanisms Of Transcriptional Repression Mediated By Krab Zinc Finger Proteins And Trim28 . [Internet] [Thesis]. Cornell University; 2013. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/34035.

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

Council of Science Editors:

Murphy K. Understanding The Molecular Mechanisms Of Transcriptional Repression Mediated By Krab Zinc Finger Proteins And Trim28 . [Thesis]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/34035

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


Cornell University

4. Zhang, Zijing. FUNCTION AND REGULATION OF MATERNAL PROTEINS THAT ARE PHOSPHOREGULATED DURING EGG ACTIVATION .

Degree: 2018, Cornell University

 Egg activation is the essential transition through which a mature oocyte becomes a developmentally competent egg. During this transition, the oocyte completes meiosis and remodels… (more)

Subjects/Keywords: egg activation; protein phosphorylation; proteomics; Cellular biology; Developmental biology; Genetics; oocyte; Drosophila melanogaster; reproduction

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APA (6th Edition):

Zhang, Z. (2018). FUNCTION AND REGULATION OF MATERNAL PROTEINS THAT ARE PHOSPHOREGULATED DURING EGG ACTIVATION . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/59752

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):

Zhang, Zijing. “FUNCTION AND REGULATION OF MATERNAL PROTEINS THAT ARE PHOSPHOREGULATED DURING EGG ACTIVATION .” 2018. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/59752.

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

MLA Handbook (7th Edition):

Zhang, Zijing. “FUNCTION AND REGULATION OF MATERNAL PROTEINS THAT ARE PHOSPHOREGULATED DURING EGG ACTIVATION .” 2018. Web. 02 Jul 2020.

Vancouver:

Zhang Z. FUNCTION AND REGULATION OF MATERNAL PROTEINS THAT ARE PHOSPHOREGULATED DURING EGG ACTIVATION . [Internet] [Thesis]. Cornell University; 2018. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/59752.

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

Council of Science Editors:

Zhang Z. FUNCTION AND REGULATION OF MATERNAL PROTEINS THAT ARE PHOSPHOREGULATED DURING EGG ACTIVATION . [Thesis]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59752

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


Cornell University

5. Peiffer, Jason. An Analysis Of Genetic Variation In Complex Traits Of Maize .

Degree: 2012, Cornell University

 Maize (Zea mays L.) is a complex crop. Governed by the universal processes of evolution that dictate the differential reproduction of all life, maize germplasm… (more)

Subjects/Keywords: Quantitative Genetics of Maize; Maize Rhizosphere Metagenomics; Genetics of Plant Height

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APA (6th Edition):

Peiffer, J. (2012). An Analysis Of Genetic Variation In Complex Traits Of Maize . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/31049

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):

Peiffer, Jason. “An Analysis Of Genetic Variation In Complex Traits Of Maize .” 2012. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/31049.

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

MLA Handbook (7th Edition):

Peiffer, Jason. “An Analysis Of Genetic Variation In Complex Traits Of Maize .” 2012. Web. 02 Jul 2020.

Vancouver:

Peiffer J. An Analysis Of Genetic Variation In Complex Traits Of Maize . [Internet] [Thesis]. Cornell University; 2012. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/31049.

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

Council of Science Editors:

Peiffer J. An Analysis Of Genetic Variation In Complex Traits Of Maize . [Thesis]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/31049

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


Cornell University

6. Cheng, Chieh-Yang. Understanding Prostate Cancer Pathogenesis .

Degree: 2014, Cornell University

 Prostate cancer is the most prevalent type of cancer in men. However, there is no cure for relapsed androgen withdrawal-refractory prostate cancer which is fatal… (more)

Subjects/Keywords: prostate cancer; miR-34; Neuroendocrine

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APA (6th Edition):

Cheng, C. (2014). Understanding Prostate Cancer Pathogenesis . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/38772

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):

Cheng, Chieh-Yang. “Understanding Prostate Cancer Pathogenesis .” 2014. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/38772.

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

MLA Handbook (7th Edition):

Cheng, Chieh-Yang. “Understanding Prostate Cancer Pathogenesis .” 2014. Web. 02 Jul 2020.

Vancouver:

Cheng C. Understanding Prostate Cancer Pathogenesis . [Internet] [Thesis]. Cornell University; 2014. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/38772.

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

Council of Science Editors:

Cheng C. Understanding Prostate Cancer Pathogenesis . [Thesis]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/38772

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


Cornell University

7. Patel, Darshil R. MOLECULAR FUNCTIONS OF THE RAD9A-RAD1-HUS1 DNA DAMAGE CHECKPOINT CLAMP IN GENOME MAINTENANCE AND TUMORIGENESIS .

Degree: 2018, Cornell University

 DNA damage checkpoint pathways are part of the broader cellular DNA damage response (DDR) that promotes genome maintenance when cells experience DNA damage. The RAD9A-HUS1-RAD1… (more)

Subjects/Keywords: Biochemistry; Cellular biology; Molecular biology; Checkpoint; DNA Damage Response; DNA Repair; Genomic Stability; Replication Fork Stability; Tumorigenesis

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APA (6th Edition):

Patel, D. R. (2018). MOLECULAR FUNCTIONS OF THE RAD9A-RAD1-HUS1 DNA DAMAGE CHECKPOINT CLAMP IN GENOME MAINTENANCE AND TUMORIGENESIS . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/59785

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):

Patel, Darshil R. “MOLECULAR FUNCTIONS OF THE RAD9A-RAD1-HUS1 DNA DAMAGE CHECKPOINT CLAMP IN GENOME MAINTENANCE AND TUMORIGENESIS .” 2018. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/59785.

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

MLA Handbook (7th Edition):

Patel, Darshil R. “MOLECULAR FUNCTIONS OF THE RAD9A-RAD1-HUS1 DNA DAMAGE CHECKPOINT CLAMP IN GENOME MAINTENANCE AND TUMORIGENESIS .” 2018. Web. 02 Jul 2020.

Vancouver:

Patel DR. MOLECULAR FUNCTIONS OF THE RAD9A-RAD1-HUS1 DNA DAMAGE CHECKPOINT CLAMP IN GENOME MAINTENANCE AND TUMORIGENESIS . [Internet] [Thesis]. Cornell University; 2018. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/59785.

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

Council of Science Editors:

Patel DR. MOLECULAR FUNCTIONS OF THE RAD9A-RAD1-HUS1 DNA DAMAGE CHECKPOINT CLAMP IN GENOME MAINTENANCE AND TUMORIGENESIS . [Thesis]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59785

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


Cornell University

8. Kim, Dongsung. ATR SIGNALING IN GENOME REPLICATION AND MAINTENANCE .

Degree: 2018, Cornell University

 DNA replication is essential for cell survival. During DNA replication, cells encounter many challenges, such as dNTP depletion, transcription intermediates, chemical adducts, double strand breaks,… (more)

Subjects/Keywords: Genetics; DNA replication; Biochemistry; ATR/ATM; DNA Repair; Mass Spec; DNA damage

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APA (6th Edition):

Kim, D. (2018). ATR SIGNALING IN GENOME REPLICATION AND MAINTENANCE . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/64929

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):

Kim, Dongsung. “ATR SIGNALING IN GENOME REPLICATION AND MAINTENANCE .” 2018. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/64929.

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

MLA Handbook (7th Edition):

Kim, Dongsung. “ATR SIGNALING IN GENOME REPLICATION AND MAINTENANCE .” 2018. Web. 02 Jul 2020.

Vancouver:

Kim D. ATR SIGNALING IN GENOME REPLICATION AND MAINTENANCE . [Internet] [Thesis]. Cornell University; 2018. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/64929.

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

Council of Science Editors:

Kim D. ATR SIGNALING IN GENOME REPLICATION AND MAINTENANCE . [Thesis]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/64929

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


Cornell University

9. Lim, Pei Xin. Mechanistic Functions Of The 9-1-1 Complex Subunit Hus1 In The Maintenance Of Genomic Integrity .

Degree: 2015, Cornell University

 The mammalian RAD9A-HUS1-RAD1 (9-1-1) complex is a heterotrimeric clamp that promotes checkpoint signaling and DNA repair by functioning as a scaffold at DNA damage sites.… (more)

Subjects/Keywords: RAD9-HUS1-RAD1; DNA damage response; checkpoint-repair coordination

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APA (6th Edition):

Lim, P. X. (2015). Mechanistic Functions Of The 9-1-1 Complex Subunit Hus1 In The Maintenance Of Genomic Integrity . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/40589

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):

Lim, Pei Xin. “Mechanistic Functions Of The 9-1-1 Complex Subunit Hus1 In The Maintenance Of Genomic Integrity .” 2015. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/40589.

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

MLA Handbook (7th Edition):

Lim, Pei Xin. “Mechanistic Functions Of The 9-1-1 Complex Subunit Hus1 In The Maintenance Of Genomic Integrity .” 2015. Web. 02 Jul 2020.

Vancouver:

Lim PX. Mechanistic Functions Of The 9-1-1 Complex Subunit Hus1 In The Maintenance Of Genomic Integrity . [Internet] [Thesis]. Cornell University; 2015. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/40589.

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

Council of Science Editors:

Lim PX. Mechanistic Functions Of The 9-1-1 Complex Subunit Hus1 In The Maintenance Of Genomic Integrity . [Thesis]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/40589

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


Cornell University

10. Lai, Yun Wei. Genetic And Molecular Analysis Of Calcium Signaling Pathways And The Prage Gene In Drosophila Egg Activation .

Degree: 2011, Cornell University

 Egg activation, the transition of mature oocytes into developing embryos, is initiated by different external signals in different animals. The signals include sperm entry, mechanical… (more)

Subjects/Keywords: egg activation; calcium; Drosophila

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APA (6th Edition):

Lai, Y. W. (2011). Genetic And Molecular Analysis Of Calcium Signaling Pathways And The Prage Gene In Drosophila Egg Activation . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/29524

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):

Lai, Yun Wei. “Genetic And Molecular Analysis Of Calcium Signaling Pathways And The Prage Gene In Drosophila Egg Activation .” 2011. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/29524.

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

MLA Handbook (7th Edition):

Lai, Yun Wei. “Genetic And Molecular Analysis Of Calcium Signaling Pathways And The Prage Gene In Drosophila Egg Activation .” 2011. Web. 02 Jul 2020.

Vancouver:

Lai YW. Genetic And Molecular Analysis Of Calcium Signaling Pathways And The Prage Gene In Drosophila Egg Activation . [Internet] [Thesis]. Cornell University; 2011. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/29524.

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

Council of Science Editors:

Lai YW. Genetic And Molecular Analysis Of Calcium Signaling Pathways And The Prage Gene In Drosophila Egg Activation . [Thesis]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/29524

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


Cornell University

11. Brown, Megan. Roles For Telomere-Led Chromosome Motion And Crossover Resolution During Meiosis In Saccharomyces Cerevisiae .

Degree: 2013, Cornell University

 During meiosis, multiple mechanisms act to promote accurate segregation of chromosomes, ensuring that all progeny receive exactly one copy of each chromosome. To achieve this… (more)

Subjects/Keywords: meiosis; crossing over; Csm4; Mlh3; telomere-led chromosome motion

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APA (6th Edition):

Brown, M. (2013). Roles For Telomere-Led Chromosome Motion And Crossover Resolution During Meiosis In Saccharomyces Cerevisiae . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/33899

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):

Brown, Megan. “Roles For Telomere-Led Chromosome Motion And Crossover Resolution During Meiosis In Saccharomyces Cerevisiae .” 2013. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/33899.

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

MLA Handbook (7th Edition):

Brown, Megan. “Roles For Telomere-Led Chromosome Motion And Crossover Resolution During Meiosis In Saccharomyces Cerevisiae .” 2013. Web. 02 Jul 2020.

Vancouver:

Brown M. Roles For Telomere-Led Chromosome Motion And Crossover Resolution During Meiosis In Saccharomyces Cerevisiae . [Internet] [Thesis]. Cornell University; 2013. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/33899.

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

Council of Science Editors:

Brown M. Roles For Telomere-Led Chromosome Motion And Crossover Resolution During Meiosis In Saccharomyces Cerevisiae . [Thesis]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/33899

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


Cornell University

12. Melville, Katherine. Estrogen Receptor Alpha In Osteoblasts Mediates Bone Mass And Bone’S Response To In Vivo Loading .

Degree: 2014, Cornell University

 Decreased bioavailable estrogen levels are a major cause of bone loss in postmenopausal women, but sex hormones are important regulators of bone mass in both… (more)

Subjects/Keywords: estrogen receptor alpha; bone; loading

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APA (6th Edition):

Melville, K. (2014). Estrogen Receptor Alpha In Osteoblasts Mediates Bone Mass And Bone’S Response To In Vivo Loading . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/38857

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):

Melville, Katherine. “Estrogen Receptor Alpha In Osteoblasts Mediates Bone Mass And Bone’S Response To In Vivo Loading .” 2014. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/38857.

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

MLA Handbook (7th Edition):

Melville, Katherine. “Estrogen Receptor Alpha In Osteoblasts Mediates Bone Mass And Bone’S Response To In Vivo Loading .” 2014. Web. 02 Jul 2020.

Vancouver:

Melville K. Estrogen Receptor Alpha In Osteoblasts Mediates Bone Mass And Bone’S Response To In Vivo Loading . [Internet] [Thesis]. Cornell University; 2014. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/38857.

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

Council of Science Editors:

Melville K. Estrogen Receptor Alpha In Osteoblasts Mediates Bone Mass And Bone’S Response To In Vivo Loading . [Thesis]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/38857

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


Cornell University

13. Kelly, Natalie H. Transcriptomic analysis of cortical versus cancellous bone in response to mechanical loading and estrogen signaling .

Degree: 2017, Cornell University

 Osteoporosis is a skeletal disease characterized by low bone mass that often results in fracture. Mechanical loading of the skeleton is a promising approach to… (more)

Subjects/Keywords: bone; mechanobiology; Biomedical engineering; RNA-sequencing; Biomechanics; Molecular biology; osteoporosis

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APA (6th Edition):

Kelly, N. H. (2017). Transcriptomic analysis of cortical versus cancellous bone in response to mechanical loading and estrogen signaling . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/47742

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):

Kelly, Natalie H. “Transcriptomic analysis of cortical versus cancellous bone in response to mechanical loading and estrogen signaling .” 2017. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/47742.

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

MLA Handbook (7th Edition):

Kelly, Natalie H. “Transcriptomic analysis of cortical versus cancellous bone in response to mechanical loading and estrogen signaling .” 2017. Web. 02 Jul 2020.

Vancouver:

Kelly NH. Transcriptomic analysis of cortical versus cancellous bone in response to mechanical loading and estrogen signaling . [Internet] [Thesis]. Cornell University; 2017. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/47742.

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

Council of Science Editors:

Kelly NH. Transcriptomic analysis of cortical versus cancellous bone in response to mechanical loading and estrogen signaling . [Thesis]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/47742

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


Cornell University

14. 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 02, 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. 02 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 02]. 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

15. Brown, Joel. INVESTIGATING MAMMALIAN DEVELOPMENT USING MOUSE FORWARD GENETICS .

Degree: 2018, Cornell University

 Forward genetics allows the identification of novel genes involved in a particular biological process. We performed an ENU forward mutagenesis screen in mice aimed at… (more)

Subjects/Keywords: calcium; Actomyosin; Apical Constriction; Cofilin 1; Neural Tube; SPCA1; Developmental biology; Genetics; Molecular biology

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APA (6th Edition):

Brown, J. (2018). INVESTIGATING MAMMALIAN DEVELOPMENT USING MOUSE FORWARD GENETICS . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/59291

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):

Brown, Joel. “INVESTIGATING MAMMALIAN DEVELOPMENT USING MOUSE FORWARD GENETICS .” 2018. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/59291.

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

MLA Handbook (7th Edition):

Brown, Joel. “INVESTIGATING MAMMALIAN DEVELOPMENT USING MOUSE FORWARD GENETICS .” 2018. Web. 02 Jul 2020.

Vancouver:

Brown J. INVESTIGATING MAMMALIAN DEVELOPMENT USING MOUSE FORWARD GENETICS . [Internet] [Thesis]. Cornell University; 2018. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/59291.

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

Council of Science Editors:

Brown J. INVESTIGATING MAMMALIAN DEVELOPMENT USING MOUSE FORWARD GENETICS . [Thesis]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59291

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


Cornell University

16. Migone, Fernando. Vasoconstriction At The Apex Of The Follicle Is Essential For Follicle Rupture At Ovulation: Findings From Studies In Vivo Using Multiphoton Microscopy And Power Doppler Ultrasound In Anovulatory Mouse Models .

Degree: 2015, Cornell University

 In the effort to elucidate the role of the hedgehog (HH) signaling pathway in reproduction, mice were created in which HH signaling was overactivated in… (more)

Subjects/Keywords: Ovulation; Ovary; Vasoconstriction

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APA (6th Edition):

Migone, F. (2015). Vasoconstriction At The Apex Of The Follicle Is Essential For Follicle Rupture At Ovulation: Findings From Studies In Vivo Using Multiphoton Microscopy And Power Doppler Ultrasound In Anovulatory Mouse Models . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/39331

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):

Migone, Fernando. “Vasoconstriction At The Apex Of The Follicle Is Essential For Follicle Rupture At Ovulation: Findings From Studies In Vivo Using Multiphoton Microscopy And Power Doppler Ultrasound In Anovulatory Mouse Models .” 2015. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/39331.

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

MLA Handbook (7th Edition):

Migone, Fernando. “Vasoconstriction At The Apex Of The Follicle Is Essential For Follicle Rupture At Ovulation: Findings From Studies In Vivo Using Multiphoton Microscopy And Power Doppler Ultrasound In Anovulatory Mouse Models .” 2015. Web. 02 Jul 2020.

Vancouver:

Migone F. Vasoconstriction At The Apex Of The Follicle Is Essential For Follicle Rupture At Ovulation: Findings From Studies In Vivo Using Multiphoton Microscopy And Power Doppler Ultrasound In Anovulatory Mouse Models . [Internet] [Thesis]. Cornell University; 2015. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/39331.

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

Council of Science Editors:

Migone F. Vasoconstriction At The Apex Of The Follicle Is Essential For Follicle Rupture At Ovulation: Findings From Studies In Vivo Using Multiphoton Microscopy And Power Doppler Ultrasound In Anovulatory Mouse Models . [Thesis]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/39331

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


Cornell University

17. Page, Jennifer. Effects Of Deregulation Of Ribonucleotide Reductase In Mice .

Degree: 2011, Cornell University

 Nucleotide levels play a critical role in genome stability, and proper regulation of these pools is crucial for survival. Ribonucleotide reductase (RNR) catalyzes the rate-… (more)

Subjects/Keywords: ribonucleotide reductase; nucleotide metabolism; DNA replication

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

APA (6th Edition):

Page, J. (2011). Effects Of Deregulation Of Ribonucleotide Reductase In Mice . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/29350

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):

Page, Jennifer. “Effects Of Deregulation Of Ribonucleotide Reductase In Mice .” 2011. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/29350.

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

MLA Handbook (7th Edition):

Page, Jennifer. “Effects Of Deregulation Of Ribonucleotide Reductase In Mice .” 2011. Web. 02 Jul 2020.

Vancouver:

Page J. Effects Of Deregulation Of Ribonucleotide Reductase In Mice . [Internet] [Thesis]. Cornell University; 2011. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/29350.

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

Council of Science Editors:

Page J. Effects Of Deregulation Of Ribonucleotide Reductase In Mice . [Thesis]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/29350

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


Cornell University

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

Degree: 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 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/59013

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):

Chu, Erin Tsi-Jia. “MECHANISMS AND CONSEQUENCES OF DNA METHYLATION IN TWO MODEL SPECIES .” 2017. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/59013.

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

MLA Handbook (7th Edition):

Chu, Erin Tsi-Jia. “MECHANISMS AND CONSEQUENCES OF DNA METHYLATION IN TWO MODEL SPECIES .” 2017. Web. 02 Jul 2020.

Vancouver:

Chu ET. MECHANISMS AND CONSEQUENCES OF DNA METHYLATION IN TWO MODEL SPECIES . [Internet] [Thesis]. Cornell University; 2017. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/59013.

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

Council of Science Editors:

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

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


Cornell University

19. 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 02, 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. 02 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 02]. 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

20. White, Michelle Elizabeth. GENETIC MAPPING OF NOVEL LOCI AFFECTING CLINICAL PHENOTYPES OF THE DOMESTIC DOG AND CAT .

Degree: 2019, Cornell University

 Domestic dogs and cats present a unique opportunity for research in precision medicine: they receive comparable medical surveillance, share our environment, and have similar resources… (more)

Subjects/Keywords: Genetics; Canine genomics; Canine lymphoma; Feline genomics; Personalized medicine; Precision medicine; Translational medicine; Translation studies; Medicine

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APA (6th Edition):

White, M. E. (2019). GENETIC MAPPING OF NOVEL LOCI AFFECTING CLINICAL PHENOTYPES OF THE DOMESTIC DOG AND CAT . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/67781

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):

White, Michelle Elizabeth. “GENETIC MAPPING OF NOVEL LOCI AFFECTING CLINICAL PHENOTYPES OF THE DOMESTIC DOG AND CAT .” 2019. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/67781.

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

MLA Handbook (7th Edition):

White, Michelle Elizabeth. “GENETIC MAPPING OF NOVEL LOCI AFFECTING CLINICAL PHENOTYPES OF THE DOMESTIC DOG AND CAT .” 2019. Web. 02 Jul 2020.

Vancouver:

White ME. GENETIC MAPPING OF NOVEL LOCI AFFECTING CLINICAL PHENOTYPES OF THE DOMESTIC DOG AND CAT . [Internet] [Thesis]. Cornell University; 2019. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/67781.

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

Council of Science Editors:

White ME. GENETIC MAPPING OF NOVEL LOCI AFFECTING CLINICAL PHENOTYPES OF THE DOMESTIC DOG AND CAT . [Thesis]. Cornell University; 2019. Available from: http://hdl.handle.net/1813/67781

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 02, 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. 02 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 02]. 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. Balmus, Gabriel. Roles For The Dna Damage Checkpoint Gene Hus1 In Responding To Endogenous And Exogenous Stresses In Vivo .

Degree: 2013, Cornell University

 The DNA damage response (DDR) represents the primary line of defense against exogenous and endogenous genotoxic agents that threaten the stability of our genomes. The… (more)

Subjects/Keywords: DNA damage; ATM; ATR; HUS1; cell cycle checkpoints; cancer; development; genomic instability

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APA (6th Edition):

Balmus, G. (2013). Roles For The Dna Damage Checkpoint Gene Hus1 In Responding To Endogenous And Exogenous Stresses In Vivo . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/33855

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):

Balmus, Gabriel. “Roles For The Dna Damage Checkpoint Gene Hus1 In Responding To Endogenous And Exogenous Stresses In Vivo .” 2013. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/33855.

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

MLA Handbook (7th Edition):

Balmus, Gabriel. “Roles For The Dna Damage Checkpoint Gene Hus1 In Responding To Endogenous And Exogenous Stresses In Vivo .” 2013. Web. 02 Jul 2020.

Vancouver:

Balmus G. Roles For The Dna Damage Checkpoint Gene Hus1 In Responding To Endogenous And Exogenous Stresses In Vivo . [Internet] [Thesis]. Cornell University; 2013. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/33855.

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

Council of Science Editors:

Balmus G. Roles For The Dna Damage Checkpoint Gene Hus1 In Responding To Endogenous And Exogenous Stresses In Vivo . [Thesis]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/33855

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


Cornell University

23. Migone, Fernando. Dominant Activation Of Hedgehog Signaling Alters Development Of The Female Reproductive Tract .

Degree: 2011, Cornell University

 The hedgehog (HH) signaling pathway regulates the development of multiple organs in the embryo as well as remodeling in adult tissues. Signaling occurs through binding… (more)

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APA (6th Edition):

Migone, F. (2011). Dominant Activation Of Hedgehog Signaling Alters Development Of The Female Reproductive Tract . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/29303

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):

Migone, Fernando. “Dominant Activation Of Hedgehog Signaling Alters Development Of The Female Reproductive Tract .” 2011. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/29303.

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

MLA Handbook (7th Edition):

Migone, Fernando. “Dominant Activation Of Hedgehog Signaling Alters Development Of The Female Reproductive Tract .” 2011. Web. 02 Jul 2020.

Vancouver:

Migone F. Dominant Activation Of Hedgehog Signaling Alters Development Of The Female Reproductive Tract . [Internet] [Thesis]. Cornell University; 2011. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/29303.

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

Council of Science Editors:

Migone F. Dominant Activation Of Hedgehog Signaling Alters Development Of The Female Reproductive Tract . [Thesis]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/29303

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


Cornell University

24. Cota, Christina. Phenotypic, Molecular And Genetic Characterization Of Developmental Defects In Ddx11 And Mgrn1 Mutant Mice .

Degree: 2012, Cornell University

 Early stages in the development of the mouse embryo are characterized by rapid growth and dynamic changes in patterning and morphology. However, technical challenges in… (more)

Subjects/Keywords: mgrn1; ddx11; Left-right patterning; DEAD/H Helicase; mesoderm

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APA (6th Edition):

Cota, C. (2012). Phenotypic, Molecular And Genetic Characterization Of Developmental Defects In Ddx11 And Mgrn1 Mutant Mice . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/31404

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):

Cota, Christina. “Phenotypic, Molecular And Genetic Characterization Of Developmental Defects In Ddx11 And Mgrn1 Mutant Mice .” 2012. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/31404.

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

MLA Handbook (7th Edition):

Cota, Christina. “Phenotypic, Molecular And Genetic Characterization Of Developmental Defects In Ddx11 And Mgrn1 Mutant Mice .” 2012. Web. 02 Jul 2020.

Vancouver:

Cota C. Phenotypic, Molecular And Genetic Characterization Of Developmental Defects In Ddx11 And Mgrn1 Mutant Mice . [Internet] [Thesis]. Cornell University; 2012. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/31404.

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

Council of Science Editors:

Cota C. Phenotypic, Molecular And Genetic Characterization Of Developmental Defects In Ddx11 And Mgrn1 Mutant Mice . [Thesis]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/31404

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


Cornell University

25. Welsh, Ian. Giving Shape To Genomic Regulatory Networks Controlling Craniofacial And Asymmetric Organ Morphogenesis .

Degree: 2016, Cornell University

 Morphogenesis is the most critical and dynamic utilization of genomic information in the life history of an organism and a powerful system for advancing our… (more)

Subjects/Keywords: genomics; morphogenesis; transcriptional regulation

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APA (6th Edition):

Welsh, I. (2016). Giving Shape To Genomic Regulatory Networks Controlling Craniofacial And Asymmetric Organ Morphogenesis . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/43625

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):

Welsh, Ian. “Giving Shape To Genomic Regulatory Networks Controlling Craniofacial And Asymmetric Organ Morphogenesis .” 2016. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/43625.

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

MLA Handbook (7th Edition):

Welsh, Ian. “Giving Shape To Genomic Regulatory Networks Controlling Craniofacial And Asymmetric Organ Morphogenesis .” 2016. Web. 02 Jul 2020.

Vancouver:

Welsh I. Giving Shape To Genomic Regulatory Networks Controlling Craniofacial And Asymmetric Organ Morphogenesis . [Internet] [Thesis]. Cornell University; 2016. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/43625.

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

Council of Science Editors:

Welsh I. Giving Shape To Genomic Regulatory Networks Controlling Craniofacial And Asymmetric Organ Morphogenesis . [Thesis]. Cornell University; 2016. Available from: http://hdl.handle.net/1813/43625

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


Cornell University

26. Ren, Yi. The Hedgehog Signaling Pathway In The Mouse Ovary .

Degree: 2012, Cornell University

 The hedgehog (HH) signaling pathway plays critical roles in the Drosophila ovary. Previous studies have provided basic information on the pattern of expression of genes… (more)

Subjects/Keywords: hedgehog signaling; ovary; development

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APA (6th Edition):

Ren, Y. (2012). The Hedgehog Signaling Pathway In The Mouse Ovary . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/29526

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):

Ren, Yi. “The Hedgehog Signaling Pathway In The Mouse Ovary .” 2012. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/29526.

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

MLA Handbook (7th Edition):

Ren, Yi. “The Hedgehog Signaling Pathway In The Mouse Ovary .” 2012. Web. 02 Jul 2020.

Vancouver:

Ren Y. The Hedgehog Signaling Pathway In The Mouse Ovary . [Internet] [Thesis]. Cornell University; 2012. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/29526.

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

Council of Science Editors:

Ren Y. The Hedgehog Signaling Pathway In The Mouse Ovary . [Thesis]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/29526

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


Cornell University

27. Goldstein, Orly. Insight Into Sight: Deciphering The Heterogeneity Of Hereditary Retinal Degeneration In The Canine Population .

Degree: 2014, Cornell University

 As of October 2013, around 285 million people are visually impaired worldwide. For an important subset of these, this visual impairment is genetic. That is,… (more)

Subjects/Keywords: Retinal degeneration; Genetic mutation; Canine PRA

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APA (6th Edition):

Goldstein, O. (2014). Insight Into Sight: Deciphering The Heterogeneity Of Hereditary Retinal Degeneration In The Canine Population . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/36147

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):

Goldstein, Orly. “Insight Into Sight: Deciphering The Heterogeneity Of Hereditary Retinal Degeneration In The Canine Population .” 2014. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/36147.

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

MLA Handbook (7th Edition):

Goldstein, Orly. “Insight Into Sight: Deciphering The Heterogeneity Of Hereditary Retinal Degeneration In The Canine Population .” 2014. Web. 02 Jul 2020.

Vancouver:

Goldstein O. Insight Into Sight: Deciphering The Heterogeneity Of Hereditary Retinal Degeneration In The Canine Population . [Internet] [Thesis]. Cornell University; 2014. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/36147.

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

Council of Science Editors:

Goldstein O. Insight Into Sight: Deciphering The Heterogeneity Of Hereditary Retinal Degeneration In The Canine Population . [Thesis]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/36147

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


Cornell University

28. Tu, Lan Ngoc Ly. MOLECULAR FUNCTION OF MAMMALIAN TRANSLOCATOR PROTEIN (TSPO) .

Degree: 2017, Cornell University

 Translocator protein (TSPO), previously known as the peripheral benzodiazepine receptor (PBR), is a mitochondrial outer membrane protein highly conserved from bacteria to humans. TSPO is… (more)

Subjects/Keywords: physiology

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APA (6th Edition):

Tu, L. N. L. (2017). MOLECULAR FUNCTION OF MAMMALIAN TRANSLOCATOR PROTEIN (TSPO) . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/56808

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):

Tu, Lan Ngoc Ly. “MOLECULAR FUNCTION OF MAMMALIAN TRANSLOCATOR PROTEIN (TSPO) .” 2017. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/56808.

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

MLA Handbook (7th Edition):

Tu, Lan Ngoc Ly. “MOLECULAR FUNCTION OF MAMMALIAN TRANSLOCATOR PROTEIN (TSPO) .” 2017. Web. 02 Jul 2020.

Vancouver:

Tu LNL. MOLECULAR FUNCTION OF MAMMALIAN TRANSLOCATOR PROTEIN (TSPO) . [Internet] [Thesis]. Cornell University; 2017. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/56808.

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

Council of Science Editors:

Tu LNL. MOLECULAR FUNCTION OF MAMMALIAN TRANSLOCATOR PROTEIN (TSPO) . [Thesis]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/56808

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


Cornell University

29. Kim, Boram. The Role Of Mater In Cytoplasmic Lattice Formation, Endoplasmic Reticulum Distribution, And Calcium Homeostasis In Mouse Oocytes .

Degree: 2013, Cornell University

 Ca2+ oscillation is hallmark of mammalian fertilization that is thought to mediate egg activation process, and dramatic targeting of the endoplasmic reticulum (ER) to the… (more)

Subjects/Keywords: MATER; cytoplasmic lattice; calcium homeostasis

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

APA (6th Edition):

Kim, B. (2013). The Role Of Mater In Cytoplasmic Lattice Formation, Endoplasmic Reticulum Distribution, And Calcium Homeostasis In Mouse Oocytes . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/33817

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):

Kim, Boram. “The Role Of Mater In Cytoplasmic Lattice Formation, Endoplasmic Reticulum Distribution, And Calcium Homeostasis In Mouse Oocytes .” 2013. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/33817.

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

MLA Handbook (7th Edition):

Kim, Boram. “The Role Of Mater In Cytoplasmic Lattice Formation, Endoplasmic Reticulum Distribution, And Calcium Homeostasis In Mouse Oocytes .” 2013. Web. 02 Jul 2020.

Vancouver:

Kim B. The Role Of Mater In Cytoplasmic Lattice Formation, Endoplasmic Reticulum Distribution, And Calcium Homeostasis In Mouse Oocytes . [Internet] [Thesis]. Cornell University; 2013. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/33817.

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

Council of Science Editors:

Kim B. The Role Of Mater In Cytoplasmic Lattice Formation, Endoplasmic Reticulum Distribution, And Calcium Homeostasis In Mouse Oocytes . [Thesis]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/33817

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


Cornell University

30. Prieto, Jennifer. Equine B Lymphopoiesis And Cd5+ B Lymphocytes .

Degree: 2015, Cornell University

 The development of the humoral immune system starts during gestation with the production of two major types of B cells: B1 and B2. B2 cells… (more)

Subjects/Keywords: Equine; B Lymphocytes; Development

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

APA (6th Edition):

Prieto, J. (2015). Equine B Lymphopoiesis And Cd5+ B Lymphocytes . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/41107

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):

Prieto, Jennifer. “Equine B Lymphopoiesis And Cd5+ B Lymphocytes .” 2015. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/41107.

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

MLA Handbook (7th Edition):

Prieto, Jennifer. “Equine B Lymphopoiesis And Cd5+ B Lymphocytes .” 2015. Web. 02 Jul 2020.

Vancouver:

Prieto J. Equine B Lymphopoiesis And Cd5+ B Lymphocytes . [Internet] [Thesis]. Cornell University; 2015. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/41107.

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

Council of Science Editors:

Prieto J. Equine B Lymphopoiesis And Cd5+ B Lymphocytes . [Thesis]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/41107

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

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