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You searched for +publisher:"Cornell University" +contributor:("Weiss, Robert S."). Showing records 1 – 30 of 45 total matches.

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Cornell University

1. Daugherity, Erin. The Dna Damage Checkpoint Protein Atm Promotes Hepatocellular Apoptosis And Fibrosis In A Mouse Model Of Non-Alcoholic Fatty Liver Disease.

Degree: M.S., Veterinary Medicine, Veterinary Medicine, 2013, Cornell University

 Steatoapoptosis is a hallmark of non-alcoholic fatty liver disease (NAFLD) and is an important factor in liver disease progression. We hypothesized that increased reactive oxygen… (more)

Subjects/Keywords: Ataxia Telangiectasia Mutated (ATM); Steatoapoptosis; Non-alcoholic fatty liver disease

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APA (6th Edition):

Daugherity, E. (2013). The Dna Damage Checkpoint Protein Atm Promotes Hepatocellular Apoptosis And Fibrosis In A Mouse Model Of Non-Alcoholic Fatty Liver Disease. (Masters Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/33847

Chicago Manual of Style (16th Edition):

Daugherity, Erin. “The Dna Damage Checkpoint Protein Atm Promotes Hepatocellular Apoptosis And Fibrosis In A Mouse Model Of Non-Alcoholic Fatty Liver Disease.” 2013. Masters Thesis, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/33847.

MLA Handbook (7th Edition):

Daugherity, Erin. “The Dna Damage Checkpoint Protein Atm Promotes Hepatocellular Apoptosis And Fibrosis In A Mouse Model Of Non-Alcoholic Fatty Liver Disease.” 2013. Web. 27 Feb 2021.

Vancouver:

Daugherity E. The Dna Damage Checkpoint Protein Atm Promotes Hepatocellular Apoptosis And Fibrosis In A Mouse Model Of Non-Alcoholic Fatty Liver Disease. [Internet] [Masters thesis]. Cornell University; 2013. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/33847.

Council of Science Editors:

Daugherity E. The Dna Damage Checkpoint Protein Atm Promotes Hepatocellular Apoptosis And Fibrosis In A Mouse Model Of Non-Alcoholic Fatty Liver Disease. [Masters Thesis]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/33847


Cornell University

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

Degree: PhD, Biochemistry, Molecular and Cell Biology, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59785

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. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/59785.

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. 27 Feb 2021.

Vancouver:

Patel DR. MOLECULAR FUNCTIONS OF THE RAD9A-RAD1-HUS1 DNA DAMAGE CHECKPOINT CLAMP IN GENOME MAINTENANCE AND TUMORIGENESIS. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/59785.

Council of Science Editors:

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


Cornell University

3. Negron Abril, Yashira Liz. TUMOR PROMOTING FUNCTIONS FOR THE METABOLIC REGULATOR SIRT5.

Degree: PhD, Chemistry and Chemical Biology, 2018, Cornell University

 Cancer is among the leading causes of death worldwide, highlighting the urgent need for identification of new targets and the development of new strategies to… (more)

Subjects/Keywords: Mice; Post-translational modifications; SIRT5; Sirtuins; Small molecules; Biology; Molecular biology; Chemistry; cancer

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APA (6th Edition):

Negron Abril, Y. L. (2018). TUMOR PROMOTING FUNCTIONS FOR THE METABOLIC REGULATOR SIRT5. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59440

Chicago Manual of Style (16th Edition):

Negron Abril, Yashira Liz. “TUMOR PROMOTING FUNCTIONS FOR THE METABOLIC REGULATOR SIRT5.” 2018. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/59440.

MLA Handbook (7th Edition):

Negron Abril, Yashira Liz. “TUMOR PROMOTING FUNCTIONS FOR THE METABOLIC REGULATOR SIRT5.” 2018. Web. 27 Feb 2021.

Vancouver:

Negron Abril YL. TUMOR PROMOTING FUNCTIONS FOR THE METABOLIC REGULATOR SIRT5. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/59440.

Council of Science Editors:

Negron Abril YL. TUMOR PROMOTING FUNCTIONS FOR THE METABOLIC REGULATOR SIRT5. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59440


Cornell University

4. Rivera, David. Multiphoton Endoscopy.

Degree: PhD, Applied Physics, 2013, Cornell University

 Multiphoton microscopy has the potential to be a versatile tool for clinical disease diagnosis and treatment, providing numerous benefits over current practices involving the histopathological… (more)

Subjects/Keywords: Multiphoton Endoscopy; Scanning Fiber Endoscopy; Endogenous Fluorescence

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APA (6th Edition):

Rivera, D. (2013). Multiphoton Endoscopy. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/33844

Chicago Manual of Style (16th Edition):

Rivera, David. “Multiphoton Endoscopy.” 2013. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/33844.

MLA Handbook (7th Edition):

Rivera, David. “Multiphoton Endoscopy.” 2013. Web. 27 Feb 2021.

Vancouver:

Rivera D. Multiphoton Endoscopy. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/33844.

Council of Science Editors:

Rivera D. Multiphoton Endoscopy. [Doctoral Dissertation]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/33844


Cornell University

5. Sinha, Siddhartha. Role Of Substrate Stiffness In Driving Atherogenic Behavior In Macrophages.

Degree: M.S., Physiology, Physiology, 2014, Cornell University

 Atherosclerosis is a decades-long process whose patients often remain asymptomatic until after a heart attack or stroke. Novel therapeutic approaches focus on tuning the body's(more)

Subjects/Keywords: Atherosclerosis; Inflammation; Macrophage

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APA (6th Edition):

Sinha, S. (2014). Role Of Substrate Stiffness In Driving Atherogenic Behavior In Macrophages. (Masters Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/37128

Chicago Manual of Style (16th Edition):

Sinha, Siddhartha. “Role Of Substrate Stiffness In Driving Atherogenic Behavior In Macrophages.” 2014. Masters Thesis, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/37128.

MLA Handbook (7th Edition):

Sinha, Siddhartha. “Role Of Substrate Stiffness In Driving Atherogenic Behavior In Macrophages.” 2014. Web. 27 Feb 2021.

Vancouver:

Sinha S. Role Of Substrate Stiffness In Driving Atherogenic Behavior In Macrophages. [Internet] [Masters thesis]. Cornell University; 2014. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/37128.

Council of Science Editors:

Sinha S. Role Of Substrate Stiffness In Driving Atherogenic Behavior In Macrophages. [Masters Thesis]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/37128


Cornell University

6. Wallace, Marsha. Elucidation Of Mechanisms In Mammary Tumorigenesis And Identification Of Driving Events And Susceptibility Loci.

Degree: PhD, Genetics, 2012, Cornell University

 Human breast cancer research faces limitations necessitating a comparative oncogenomic approach and use of models, in which the environment and genetic background can be controlled.… (more)

Subjects/Keywords: Breast Cancer; Cancer Drivers and Susceptibility Loci; Chaos3; mcm; nf1; tln1

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APA (6th Edition):

Wallace, M. (2012). Elucidation Of Mechanisms In Mammary Tumorigenesis And Identification Of Driving Events And Susceptibility Loci. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/31103

Chicago Manual of Style (16th Edition):

Wallace, Marsha. “Elucidation Of Mechanisms In Mammary Tumorigenesis And Identification Of Driving Events And Susceptibility Loci.” 2012. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/31103.

MLA Handbook (7th Edition):

Wallace, Marsha. “Elucidation Of Mechanisms In Mammary Tumorigenesis And Identification Of Driving Events And Susceptibility Loci.” 2012. Web. 27 Feb 2021.

Vancouver:

Wallace M. Elucidation Of Mechanisms In Mammary Tumorigenesis And Identification Of Driving Events And Susceptibility Loci. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/31103.

Council of Science Editors:

Wallace M. Elucidation Of Mechanisms In Mammary Tumorigenesis And Identification Of Driving Events And Susceptibility Loci. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/31103


Cornell University

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

Degree: PhD, Genetics, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/40589

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. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/40589.

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. 27 Feb 2021.

Vancouver:

Lim PX. Mechanistic Functions Of The 9-1-1 Complex Subunit Hus1 In The Maintenance Of Genomic Integrity. [Internet] [Doctoral dissertation]. Cornell University; 2015. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/40589.

Council of Science Editors:

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


Cornell University

8. Dowicki, Michael. The Wing Helix Domain Of Orc4 Is The Primary Determinant Of Dna Binding Specificity Of The Origin Recognition Complex.

Degree: PhD, Genetics, 2015, Cornell University

 The process of DNA replication is regulated to ensure that the entire genome is replicated only once during every cell division cycle. Eukaryotic DNA replication… (more)

Subjects/Keywords: DNA Replication; Origin Recognition Complex

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APA (6th Edition):

Dowicki, M. (2015). The Wing Helix Domain Of Orc4 Is The Primary Determinant Of Dna Binding Specificity Of The Origin Recognition Complex. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/40691

Chicago Manual of Style (16th Edition):

Dowicki, Michael. “The Wing Helix Domain Of Orc4 Is The Primary Determinant Of Dna Binding Specificity Of The Origin Recognition Complex.” 2015. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/40691.

MLA Handbook (7th Edition):

Dowicki, Michael. “The Wing Helix Domain Of Orc4 Is The Primary Determinant Of Dna Binding Specificity Of The Origin Recognition Complex.” 2015. Web. 27 Feb 2021.

Vancouver:

Dowicki M. The Wing Helix Domain Of Orc4 Is The Primary Determinant Of Dna Binding Specificity Of The Origin Recognition Complex. [Internet] [Doctoral dissertation]. Cornell University; 2015. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/40691.

Council of Science Editors:

Dowicki M. The Wing Helix Domain Of Orc4 Is The Primary Determinant Of Dna Binding Specificity Of The Origin Recognition Complex. [Doctoral Dissertation]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/40691


Cornell University

9. Jing, Hui. MULTIPLE ENZYMATIC FUNCTIONS OF SIRT2 AND ITS INVOLVEMENT IN CANCER.

Degree: PhD, Chemistry and Chemical Biology, 2017, Cornell University

 SIRT2 belongs to the mammalian sirtuin or NAD-dependent lysine deacylase family. Growing evidence suggests that SIRT2 plays important roles in cell cycle regulation, stress response,… (more)

Subjects/Keywords: c-Myc; K-Ras; Lysine fatty acylation; SIRT2; Sirtuin; Chemistry; cancer

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APA (6th Edition):

Jing, H. (2017). MULTIPLE ENZYMATIC FUNCTIONS OF SIRT2 AND ITS INVOLVEMENT IN CANCER. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59083

Chicago Manual of Style (16th Edition):

Jing, Hui. “MULTIPLE ENZYMATIC FUNCTIONS OF SIRT2 AND ITS INVOLVEMENT IN CANCER.” 2017. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/59083.

MLA Handbook (7th Edition):

Jing, Hui. “MULTIPLE ENZYMATIC FUNCTIONS OF SIRT2 AND ITS INVOLVEMENT IN CANCER.” 2017. Web. 27 Feb 2021.

Vancouver:

Jing H. MULTIPLE ENZYMATIC FUNCTIONS OF SIRT2 AND ITS INVOLVEMENT IN CANCER. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/59083.

Council of Science Editors:

Jing H. MULTIPLE ENZYMATIC FUNCTIONS OF SIRT2 AND ITS INVOLVEMENT IN CANCER. [Doctoral Dissertation]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/59083


Cornell University

10. 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 February 27, 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. 27 Feb 2021.

Vancouver:

Li M. Effects Of Mammalian Ribonucleotide Reductase Deregulation On Redox Homeostasis And Genomic Integrity. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2021 Feb 27]. 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

11. Luo, Yunhai. Genetic Dissection Of Checkpoint Signaling In Mouse Primordial Germ Cells.

Degree: PhD, Genetics, 2015, Cornell University

 Although mutations are the force of evolution, most mutations are deleterious. Faithful inheritance of genetic information is the key to evolutionary success. The only cell… (more)

Subjects/Keywords: Checkpoint signaling; Primordial germ cells; Mouse genetics

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APA (6th Edition):

Luo, Y. (2015). Genetic Dissection Of Checkpoint Signaling In Mouse Primordial Germ Cells. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/39436

Chicago Manual of Style (16th Edition):

Luo, Yunhai. “Genetic Dissection Of Checkpoint Signaling In Mouse Primordial Germ Cells.” 2015. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/39436.

MLA Handbook (7th Edition):

Luo, Yunhai. “Genetic Dissection Of Checkpoint Signaling In Mouse Primordial Germ Cells.” 2015. Web. 27 Feb 2021.

Vancouver:

Luo Y. Genetic Dissection Of Checkpoint Signaling In Mouse Primordial Germ Cells. [Internet] [Doctoral dissertation]. Cornell University; 2015. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/39436.

Council of Science Editors:

Luo Y. Genetic Dissection Of Checkpoint Signaling In Mouse Primordial Germ Cells. [Doctoral Dissertation]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/39436


Cornell University

12. Wayt, Jessica. Actin Nucleators In Microvillar Assembly: Cordon Bleu As A Novel Microvillar Protein.

Degree: PhD, Molecular and Cell Biology, 2015, Cornell University

 Epithelial cells polarize through reorganization of the actin cytoskeleton which results in distinct apical and basolateral domains. At the apical domain are structures called microvilli,… (more)

Subjects/Keywords: Polarity; Actin Cytoskeleton; Microvilli

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APA (6th Edition):

Wayt, J. (2015). Actin Nucleators In Microvillar Assembly: Cordon Bleu As A Novel Microvillar Protein. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/39365

Chicago Manual of Style (16th Edition):

Wayt, Jessica. “Actin Nucleators In Microvillar Assembly: Cordon Bleu As A Novel Microvillar Protein.” 2015. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/39365.

MLA Handbook (7th Edition):

Wayt, Jessica. “Actin Nucleators In Microvillar Assembly: Cordon Bleu As A Novel Microvillar Protein.” 2015. Web. 27 Feb 2021.

Vancouver:

Wayt J. Actin Nucleators In Microvillar Assembly: Cordon Bleu As A Novel Microvillar Protein. [Internet] [Doctoral dissertation]. Cornell University; 2015. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/39365.

Council of Science Editors:

Wayt J. Actin Nucleators In Microvillar Assembly: Cordon Bleu As A Novel Microvillar Protein. [Doctoral Dissertation]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/39365


Cornell University

13. Alonzo, Judith Raquel. Dysregulation of Folate-Dependent Mitochondrial de novo Thymidylate Biosynthesis Affects Mitohcondrial DNA Integrity.

Degree: PhD, Biochemistry, Molecular and Cell Biology, 2018, Cornell University

 Mitochondrial DNA (mtDNA) Depletion Syndrome (MDS) is a genetic disorder caused by mutations in nuclear-encoded mitochondrial proteins involved primarily in nucleotide or mtDNA synthesis. Folate-dependent… (more)

Subjects/Keywords: Nutrition; dTMP synthesis; Folate metabolism; Mitochondrial DNA integrity; Mitochondrial inner membrane protein Mpv17; serine hydroxymethyltransferase 2 SHMT2; uracil; Biochemistry; Molecular biology

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APA (6th Edition):

Alonzo, J. R. (2018). Dysregulation of Folate-Dependent Mitochondrial de novo Thymidylate Biosynthesis Affects Mitohcondrial DNA Integrity. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59495

Chicago Manual of Style (16th Edition):

Alonzo, Judith Raquel. “Dysregulation of Folate-Dependent Mitochondrial de novo Thymidylate Biosynthesis Affects Mitohcondrial DNA Integrity.” 2018. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/59495.

MLA Handbook (7th Edition):

Alonzo, Judith Raquel. “Dysregulation of Folate-Dependent Mitochondrial de novo Thymidylate Biosynthesis Affects Mitohcondrial DNA Integrity.” 2018. Web. 27 Feb 2021.

Vancouver:

Alonzo JR. Dysregulation of Folate-Dependent Mitochondrial de novo Thymidylate Biosynthesis Affects Mitohcondrial DNA Integrity. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/59495.

Council of Science Editors:

Alonzo JR. Dysregulation of Folate-Dependent Mitochondrial de novo Thymidylate Biosynthesis Affects Mitohcondrial DNA Integrity. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59495


Cornell University

14. Wang, Lihua. NON-CODING RNA REGULATION OF COLON CANCER STEM CELL FATE AND METASTASIS.

Degree: PhD, Biological and Environmental Engineering, 2017, Cornell University

 Colorectal cancer (CRC) is a leading cause of cancer related death. Colon cancer stem cells (CCSCs) play important roles in CRC tumorigenesis and metastasis. The… (more)

Subjects/Keywords: Cellular biology; colon cancer; lnc34a; miR-1269; miR-34a; non-coding RNA; Biology; Stem Cell; Biomedical engineering

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APA (6th Edition):

Wang, L. (2017). NON-CODING RNA REGULATION OF COLON CANCER STEM CELL FATE AND METASTASIS. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/56823

Chicago Manual of Style (16th Edition):

Wang, Lihua. “NON-CODING RNA REGULATION OF COLON CANCER STEM CELL FATE AND METASTASIS.” 2017. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/56823.

MLA Handbook (7th Edition):

Wang, Lihua. “NON-CODING RNA REGULATION OF COLON CANCER STEM CELL FATE AND METASTASIS.” 2017. Web. 27 Feb 2021.

Vancouver:

Wang L. NON-CODING RNA REGULATION OF COLON CANCER STEM CELL FATE AND METASTASIS. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/56823.

Council of Science Editors:

Wang L. NON-CODING RNA REGULATION OF COLON CANCER STEM CELL FATE AND METASTASIS. [Doctoral Dissertation]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/56823


Cornell University

15. Hartford, Suzanne. The Role For Dna Replication And Repair Genes In Germ-Line Maintenance And Tumor Suppression.

Degree: PhD, Genetics, 2012, Cornell University

 : Faithful DNA replication and repair of DNA damage is important for prevention of disease and birth defects. My thesis work utilized reverse and forward… (more)

Subjects/Keywords: DNA Replication; DNA Repair; mcm9

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APA (6th Edition):

Hartford, S. (2012). The Role For Dna Replication And Repair Genes In Germ-Line Maintenance And Tumor Suppression. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/29477

Chicago Manual of Style (16th Edition):

Hartford, Suzanne. “The Role For Dna Replication And Repair Genes In Germ-Line Maintenance And Tumor Suppression.” 2012. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/29477.

MLA Handbook (7th Edition):

Hartford, Suzanne. “The Role For Dna Replication And Repair Genes In Germ-Line Maintenance And Tumor Suppression.” 2012. Web. 27 Feb 2021.

Vancouver:

Hartford S. The Role For Dna Replication And Repair Genes In Germ-Line Maintenance And Tumor Suppression. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/29477.

Council of Science Editors:

Hartford S. The Role For Dna Replication And Repair Genes In Germ-Line Maintenance And Tumor Suppression. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/29477


Cornell University

16. Plys, Aaron. Analysis Of The Movement Of Saccharomyces Cerevisiae Mismatch Repair Proteins On Dna.

Degree: PhD, Biochemistry, 2011, Cornell University

 Replication errors that escape DNA polymerase proof-reading activity are efficientl y recognized and repaired by conserved DNA mismatch repair factors. The overall result is a… (more)

Subjects/Keywords: DNA mismatch repair; Replication; Cancer

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APA (6th Edition):

Plys, A. (2011). Analysis Of The Movement Of Saccharomyces Cerevisiae Mismatch Repair Proteins On Dna. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/30604

Chicago Manual of Style (16th Edition):

Plys, Aaron. “Analysis Of The Movement Of Saccharomyces Cerevisiae Mismatch Repair Proteins On Dna.” 2011. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/30604.

MLA Handbook (7th Edition):

Plys, Aaron. “Analysis Of The Movement Of Saccharomyces Cerevisiae Mismatch Repair Proteins On Dna.” 2011. Web. 27 Feb 2021.

Vancouver:

Plys A. Analysis Of The Movement Of Saccharomyces Cerevisiae Mismatch Repair Proteins On Dna. [Internet] [Doctoral dissertation]. Cornell University; 2011. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/30604.

Council of Science Editors:

Plys A. Analysis Of The Movement Of Saccharomyces Cerevisiae Mismatch Repair Proteins On Dna. [Doctoral Dissertation]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/30604


Cornell University

17. Liberti, Maria Volpe. STRATEGIES FOR SELECTIVE TARGETING OF THE WARBURG EFFECT IN CANCER.

Degree: PhD, Biochemistry, Molecular and Cell Biology, 2018, Cornell University

 Cancer cells undergo numerous adaptive processes to sustain rapid growth and survival. One notable mechanism is by rewiring their metabolism, most prominently through a phenomenon… (more)

Subjects/Keywords: Cancer metabolism; Glycolysis; Biochemistry; Warburg effect; metabolomics

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APA (6th Edition):

Liberti, M. V. (2018). STRATEGIES FOR SELECTIVE TARGETING OF THE WARBURG EFFECT IN CANCER. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/64974

Chicago Manual of Style (16th Edition):

Liberti, Maria Volpe. “STRATEGIES FOR SELECTIVE TARGETING OF THE WARBURG EFFECT IN CANCER.” 2018. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/64974.

MLA Handbook (7th Edition):

Liberti, Maria Volpe. “STRATEGIES FOR SELECTIVE TARGETING OF THE WARBURG EFFECT IN CANCER.” 2018. Web. 27 Feb 2021.

Vancouver:

Liberti MV. STRATEGIES FOR SELECTIVE TARGETING OF THE WARBURG EFFECT IN CANCER. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/64974.

Council of Science Editors:

Liberti MV. STRATEGIES FOR SELECTIVE TARGETING OF THE WARBURG EFFECT IN CANCER. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/64974


Cornell University

18. Fu, Dah-Jiun. Understanding gastric squamous-columnar junction carcinogenesis.

Degree: PhD, Comparative Biomedical Sciences, 2018, Cornell University

 Areas of a junction between two types of epithelia are known to be cancer-prone in many organ systems. In some cases, this is attributed to… (more)

Subjects/Keywords: CD44; gastroesophageal carcinoma; junction between epithelia; osteopontin; Biology; Stem Cell; Oncology; Medicine

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APA (6th Edition):

Fu, D. (2018). Understanding gastric squamous-columnar junction carcinogenesis. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/64949

Chicago Manual of Style (16th Edition):

Fu, Dah-Jiun. “Understanding gastric squamous-columnar junction carcinogenesis.” 2018. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/64949.

MLA Handbook (7th Edition):

Fu, Dah-Jiun. “Understanding gastric squamous-columnar junction carcinogenesis.” 2018. Web. 27 Feb 2021.

Vancouver:

Fu D. Understanding gastric squamous-columnar junction carcinogenesis. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/64949.

Council of Science Editors:

Fu D. Understanding gastric squamous-columnar junction carcinogenesis. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/64949


Cornell University

19. McGregor, Alexandra L. A NUCLEAR SQUEEZE: THE ROLE OF THE NUCLEUS IN CONFINED CANCER CELL MIGRATION.

Degree: PhD, Biomedical Engineering, 2018, Cornell University

 Metastasis is the leading cause of breast cancer deaths worldwide. During cancer metastasis, cells must squeeze through small spaces in the basement membrane, interstitium, and… (more)

Subjects/Keywords: Breast cancer; microfluidic devices; Biomedical engineering; Cell Migration; Nucleus; Lamins; Nuclear envelope

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APA (6th Edition):

McGregor, A. L. (2018). A NUCLEAR SQUEEZE: THE ROLE OF THE NUCLEUS IN CONFINED CANCER CELL MIGRATION. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/64962

Chicago Manual of Style (16th Edition):

McGregor, Alexandra L. “A NUCLEAR SQUEEZE: THE ROLE OF THE NUCLEUS IN CONFINED CANCER CELL MIGRATION.” 2018. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/64962.

MLA Handbook (7th Edition):

McGregor, Alexandra L. “A NUCLEAR SQUEEZE: THE ROLE OF THE NUCLEUS IN CONFINED CANCER CELL MIGRATION.” 2018. Web. 27 Feb 2021.

Vancouver:

McGregor AL. A NUCLEAR SQUEEZE: THE ROLE OF THE NUCLEUS IN CONFINED CANCER CELL MIGRATION. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/64962.

Council of Science Editors:

McGregor AL. A NUCLEAR SQUEEZE: THE ROLE OF THE NUCLEUS IN CONFINED CANCER CELL MIGRATION. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/64962


Cornell University

20. Krumm, Christopher Steven. Tales of Metabolic Regulation: Adiponectin in the Cow and Sel1L in the Mouse.

Degree: PhD, Animal Science, 2017, Cornell University

 The first part of this dissertation assessed factors regulating the insulin sensitizing hormone adiponectin in dairy cows. Plasma adiponectin is reduced during the transition from… (more)

Subjects/Keywords: Endocrinology; Biology; Adiponectin; endoplasmic reticulum stress; Metabolism; Sel1L; Transition Dairy Cow; Animal sciences

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APA (6th Edition):

Krumm, C. S. (2017). Tales of Metabolic Regulation: Adiponectin in the Cow and Sel1L in the Mouse. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/47862

Chicago Manual of Style (16th Edition):

Krumm, Christopher Steven. “Tales of Metabolic Regulation: Adiponectin in the Cow and Sel1L in the Mouse.” 2017. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/47862.

MLA Handbook (7th Edition):

Krumm, Christopher Steven. “Tales of Metabolic Regulation: Adiponectin in the Cow and Sel1L in the Mouse.” 2017. Web. 27 Feb 2021.

Vancouver:

Krumm CS. Tales of Metabolic Regulation: Adiponectin in the Cow and Sel1L in the Mouse. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/47862.

Council of Science Editors:

Krumm CS. Tales of Metabolic Regulation: Adiponectin in the Cow and Sel1L in the Mouse. [Doctoral Dissertation]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/47862


Cornell University

21. Lee, Yoon Jung. Ca2+ Channel Independent Functions Of An Alternatively Spliced ß4 Subunit.

Degree: PhD, Physiology, 2014, Cornell University

 The [beta] subunits of voltage-gated Ca2+ channels are multifunctional proteins, which act primarily as a Ca2+ channel regulatory subunit to regulate trafficking and gating properties… (more)

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APA (6th Edition):

Lee, Y. J. (2014). Ca2+ Channel Independent Functions Of An Alternatively Spliced ß4 Subunit. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/38955

Chicago Manual of Style (16th Edition):

Lee, Yoon Jung. “Ca2+ Channel Independent Functions Of An Alternatively Spliced ß4 Subunit.” 2014. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/38955.

MLA Handbook (7th Edition):

Lee, Yoon Jung. “Ca2+ Channel Independent Functions Of An Alternatively Spliced ß4 Subunit.” 2014. Web. 27 Feb 2021.

Vancouver:

Lee YJ. Ca2+ Channel Independent Functions Of An Alternatively Spliced ß4 Subunit. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/38955.

Council of Science Editors:

Lee YJ. Ca2+ Channel Independent Functions Of An Alternatively Spliced ß4 Subunit. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/38955


Cornell University

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

Degree: PhD, Molecular and Integrative Physiology, 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). (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/56808

Chicago Manual of Style (16th Edition):

Tu, Lan Ngoc Ly. “MOLECULAR FUNCTION OF MAMMALIAN TRANSLOCATOR PROTEIN (TSPO).” 2017. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/56808.

MLA Handbook (7th Edition):

Tu, Lan Ngoc Ly. “MOLECULAR FUNCTION OF MAMMALIAN TRANSLOCATOR PROTEIN (TSPO).” 2017. Web. 27 Feb 2021.

Vancouver:

Tu LNL. MOLECULAR FUNCTION OF MAMMALIAN TRANSLOCATOR PROTEIN (TSPO). [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/56808.

Council of Science Editors:

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


Cornell University

23. Jinadasa, Rasika. Molecular Mechanisms Of Cycle Arrest And Apoptosis In Lymphoid Cells Elicited By Cytolethal Distending Toxin, A Genotoxin Produced By Campylobacter Jejuni And Helicobacter Hepaticus.

Degree: PhD, Veterinary Medicine, 2012, Cornell University

 It is well-established that the genotoxin, cytolethal distending toxin (CDT) which is produced by nearly two dozens of clinically-important bacterial pathogens causes DNA damage in… (more)

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APA (6th Edition):

Jinadasa, R. (2012). Molecular Mechanisms Of Cycle Arrest And Apoptosis In Lymphoid Cells Elicited By Cytolethal Distending Toxin, A Genotoxin Produced By Campylobacter Jejuni And Helicobacter Hepaticus. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/29467

Chicago Manual of Style (16th Edition):

Jinadasa, Rasika. “Molecular Mechanisms Of Cycle Arrest And Apoptosis In Lymphoid Cells Elicited By Cytolethal Distending Toxin, A Genotoxin Produced By Campylobacter Jejuni And Helicobacter Hepaticus.” 2012. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/29467.

MLA Handbook (7th Edition):

Jinadasa, Rasika. “Molecular Mechanisms Of Cycle Arrest And Apoptosis In Lymphoid Cells Elicited By Cytolethal Distending Toxin, A Genotoxin Produced By Campylobacter Jejuni And Helicobacter Hepaticus.” 2012. Web. 27 Feb 2021.

Vancouver:

Jinadasa R. Molecular Mechanisms Of Cycle Arrest And Apoptosis In Lymphoid Cells Elicited By Cytolethal Distending Toxin, A Genotoxin Produced By Campylobacter Jejuni And Helicobacter Hepaticus. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/29467.

Council of Science Editors:

Jinadasa R. Molecular Mechanisms Of Cycle Arrest And Apoptosis In Lymphoid Cells Elicited By Cytolethal Distending Toxin, A Genotoxin Produced By Campylobacter Jejuni And Helicobacter Hepaticus. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/29467


Cornell University

24. Moore, Elizabeth Susanne. DNA damage response pathways in DNA double strand break repair and hepatic metabolism.

Degree: PhD, Biomedical and Biological Sciences, 2019, Cornell University

 The maintenance of genomic integrity and cellular homeostasis relies upon the appropriate selection and coordination of signaling and effector pathways in response to damage or… (more)

Subjects/Keywords: Genetics; Molecular biology; Biology

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APA (6th Edition):

Moore, E. S. (2019). DNA damage response pathways in DNA double strand break repair and hepatic metabolism. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/67325

Chicago Manual of Style (16th Edition):

Moore, Elizabeth Susanne. “DNA damage response pathways in DNA double strand break repair and hepatic metabolism.” 2019. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/67325.

MLA Handbook (7th Edition):

Moore, Elizabeth Susanne. “DNA damage response pathways in DNA double strand break repair and hepatic metabolism.” 2019. Web. 27 Feb 2021.

Vancouver:

Moore ES. DNA damage response pathways in DNA double strand break repair and hepatic metabolism. [Internet] [Doctoral dissertation]. Cornell University; 2019. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/67325.

Council of Science Editors:

Moore ES. DNA damage response pathways in DNA double strand break repair and hepatic metabolism. [Doctoral Dissertation]. Cornell University; 2019. Available from: http://hdl.handle.net/1813/67325


Cornell University

25. Mohanan Nair Padmini, Sunish. Role Of Peptidylarginine Deiminase 2 (Pad2) In Epithelial Carcinogenesis And Tumor-Associated Inflammation.

Degree: PhD, Veterinary Medicine, 2014, Cornell University

 Numerous recent studies have shown that epigenetic modifications play a significant role in cancer pathogenesis. The PADs are a family of epigenetic enzymes that catalyze… (more)

Subjects/Keywords: Peptidylarginine deiminase 2 (PAD2); Cancer progression; Extracellular chromatin traps (ETosis)

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APA (6th Edition):

Mohanan Nair Padmini, S. (2014). Role Of Peptidylarginine Deiminase 2 (Pad2) In Epithelial Carcinogenesis And Tumor-Associated Inflammation. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/36176

Chicago Manual of Style (16th Edition):

Mohanan Nair Padmini, Sunish. “Role Of Peptidylarginine Deiminase 2 (Pad2) In Epithelial Carcinogenesis And Tumor-Associated Inflammation.” 2014. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/36176.

MLA Handbook (7th Edition):

Mohanan Nair Padmini, Sunish. “Role Of Peptidylarginine Deiminase 2 (Pad2) In Epithelial Carcinogenesis And Tumor-Associated Inflammation.” 2014. Web. 27 Feb 2021.

Vancouver:

Mohanan Nair Padmini S. Role Of Peptidylarginine Deiminase 2 (Pad2) In Epithelial Carcinogenesis And Tumor-Associated Inflammation. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/36176.

Council of Science Editors:

Mohanan Nair Padmini S. Role Of Peptidylarginine Deiminase 2 (Pad2) In Epithelial Carcinogenesis And Tumor-Associated Inflammation. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/36176


Cornell University

26. Chuang, Chen-hua. Unique Regulatory Mechanisms For Dna Replication And Genome Maintenance In Mammals.

Degree: PhD, Physiology, 2012, Cornell University

 DNA replication is a fundamental process in all organisms. Using single stranded DNA (ssDNA) as a template, DNA polymerase synthesizes new DNA to produce an… (more)

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APA (6th Edition):

Chuang, C. (2012). Unique Regulatory Mechanisms For Dna Replication And Genome Maintenance In Mammals. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/29249

Chicago Manual of Style (16th Edition):

Chuang, Chen-hua. “Unique Regulatory Mechanisms For Dna Replication And Genome Maintenance In Mammals.” 2012. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/29249.

MLA Handbook (7th Edition):

Chuang, Chen-hua. “Unique Regulatory Mechanisms For Dna Replication And Genome Maintenance In Mammals.” 2012. Web. 27 Feb 2021.

Vancouver:

Chuang C. Unique Regulatory Mechanisms For Dna Replication And Genome Maintenance In Mammals. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/29249.

Council of Science Editors:

Chuang C. Unique Regulatory Mechanisms For Dna Replication And Genome Maintenance In Mammals. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/29249


Cornell University

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

Degree: PhD, Physiology, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/33855

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. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/33855.

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. 27 Feb 2021.

Vancouver:

Balmus G. Roles For The Dna Damage Checkpoint Gene Hus1 In Responding To Endogenous And Exogenous Stresses In Vivo. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/33855.

Council of Science Editors:

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


Cornell University

28. Chen, Huanhuan. Engineering Colorectal Cancer Models For Mechanistic Studies And Therapeutics.

Degree: PhD, Biomedical Engineering, 2014, Cornell University

 Current orthotopic xenograft models of colorectal cancer (CRC) require survival surgery and do not robustly form tumors in liver, the most common site of metastasis… (more)

Subjects/Keywords: Colorectal cancer; Modeling oncology; Forward genetics screen

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APA (6th Edition):

Chen, H. (2014). Engineering Colorectal Cancer Models For Mechanistic Studies And Therapeutics. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/38822

Chicago Manual of Style (16th Edition):

Chen, Huanhuan. “Engineering Colorectal Cancer Models For Mechanistic Studies And Therapeutics.” 2014. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/38822.

MLA Handbook (7th Edition):

Chen, Huanhuan. “Engineering Colorectal Cancer Models For Mechanistic Studies And Therapeutics.” 2014. Web. 27 Feb 2021.

Vancouver:

Chen H. Engineering Colorectal Cancer Models For Mechanistic Studies And Therapeutics. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/38822.

Council of Science Editors:

Chen H. Engineering Colorectal Cancer Models For Mechanistic Studies And Therapeutics. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/38822


Cornell University

29. Sun, Xianfei. Investigating Mammalian Meiosis: The Role Of Mismatch Repair Proteins And Their Interactors.

Degree: PhD, Physiology, 2012, Cornell University

 Prophase I is the defining stage of meiosis when chromosomes must first pair with their homologous partner, then synapse, and undergo precisely controlled reciprocal recombination.… (more)

Subjects/Keywords: Mouse meiosis; mismatch repair protein; meiotic recombination; mlh3; cntd1

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APA (6th Edition):

Sun, X. (2012). Investigating Mammalian Meiosis: The Role Of Mismatch Repair Proteins And Their Interactors. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/31179

Chicago Manual of Style (16th Edition):

Sun, Xianfei. “Investigating Mammalian Meiosis: The Role Of Mismatch Repair Proteins And Their Interactors.” 2012. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/31179.

MLA Handbook (7th Edition):

Sun, Xianfei. “Investigating Mammalian Meiosis: The Role Of Mismatch Repair Proteins And Their Interactors.” 2012. Web. 27 Feb 2021.

Vancouver:

Sun X. Investigating Mammalian Meiosis: The Role Of Mismatch Repair Proteins And Their Interactors. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/31179.

Council of Science Editors:

Sun X. Investigating Mammalian Meiosis: The Role Of Mismatch Repair Proteins And Their Interactors. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/31179


Cornell University

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

Degree: PhD, Genetics, 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 (6th Edition):

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

Chicago Manual of Style (16th Edition):

Page, Jennifer. “Effects Of Deregulation Of Ribonucleotide Reductase In Mice.” 2011. Doctoral Dissertation, Cornell University. Accessed February 27, 2021. http://hdl.handle.net/1813/29350.

MLA Handbook (7th Edition):

Page, Jennifer. “Effects Of Deregulation Of Ribonucleotide Reductase In Mice.” 2011. Web. 27 Feb 2021.

Vancouver:

Page J. Effects Of Deregulation Of Ribonucleotide Reductase In Mice. [Internet] [Doctoral dissertation]. Cornell University; 2011. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1813/29350.

Council of Science Editors:

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

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