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You searched for +publisher:"Cornell University" +contributor:("Weiss, Robert S."). Showing records 1 – 30 of 43 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: 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 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/33847

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):

Daugherity, Erin. “The Dna Damage Checkpoint Protein Atm Promotes Hepatocellular Apoptosis And Fibrosis In A Mouse Model Of Non-Alcoholic Fatty Liver Disease .” 2013. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/33847.

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

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. 18 Oct 2019.

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] [Thesis]. Cornell University; 2013. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/33847.

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

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 . [Thesis]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/33847

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


Cornell University

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

Degree: 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 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/30604

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):

Plys, Aaron. “Analysis Of The Movement Of Saccharomyces Cerevisiae Mismatch Repair Proteins On Dna .” 2011. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/30604.

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

MLA Handbook (7th Edition):

Plys, Aaron. “Analysis Of The Movement Of Saccharomyces Cerevisiae Mismatch Repair Proteins On Dna .” 2011. Web. 18 Oct 2019.

Vancouver:

Plys A. Analysis Of The Movement Of Saccharomyces Cerevisiae Mismatch Repair Proteins On Dna . [Internet] [Thesis]. Cornell University; 2011. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/30604.

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

Council of Science Editors:

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

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


Cornell University

3. Kartha, Nithya. CHARACTERIZING THE ROLE OF THE CHROMATIN REMODELING COMPONENT ARID1A AS A SUPPRESSOR OF SPORADIC MAMMARY TUMORS IN MICE .

Degree: 2017, Cornell University

 The American Cancer Society estimates that in the year 2017, approximately 40,000 women will die from breast cancer. The vast majority of these breast cancer… (more)

Subjects/Keywords: Genetics; Breast cancer; Molecular biology; Arid1a; Chromatin remodelers; Mouse model; SWI/SNF; Biochemistry

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APA (6th Edition):

Kartha, N. (2017). CHARACTERIZING THE ROLE OF THE CHROMATIN REMODELING COMPONENT ARID1A AS A SUPPRESSOR OF SPORADIC MAMMARY TUMORS IN MICE . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/56907

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):

Kartha, Nithya. “CHARACTERIZING THE ROLE OF THE CHROMATIN REMODELING COMPONENT ARID1A AS A SUPPRESSOR OF SPORADIC MAMMARY TUMORS IN MICE .” 2017. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/56907.

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

MLA Handbook (7th Edition):

Kartha, Nithya. “CHARACTERIZING THE ROLE OF THE CHROMATIN REMODELING COMPONENT ARID1A AS A SUPPRESSOR OF SPORADIC MAMMARY TUMORS IN MICE .” 2017. Web. 18 Oct 2019.

Vancouver:

Kartha N. CHARACTERIZING THE ROLE OF THE CHROMATIN REMODELING COMPONENT ARID1A AS A SUPPRESSOR OF SPORADIC MAMMARY TUMORS IN MICE . [Internet] [Thesis]. Cornell University; 2017. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/56907.

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

Council of Science Editors:

Kartha N. CHARACTERIZING THE ROLE OF THE CHROMATIN REMODELING COMPONENT ARID1A AS A SUPPRESSOR OF SPORADIC MAMMARY TUMORS IN MICE . [Thesis]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/56907

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


Cornell University

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

Degree: 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 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/56823

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, Lihua. “NON-CODING RNA REGULATION OF COLON CANCER STEM CELL FATE AND METASTASIS .” 2017. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/56823.

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

MLA Handbook (7th Edition):

Wang, Lihua. “NON-CODING RNA REGULATION OF COLON CANCER STEM CELL FATE AND METASTASIS .” 2017. Web. 18 Oct 2019.

Vancouver:

Wang L. NON-CODING RNA REGULATION OF COLON CANCER STEM CELL FATE AND METASTASIS . [Internet] [Thesis]. Cornell University; 2017. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/56823.

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

Council of Science Editors:

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

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


Cornell University

5. Rivera, David. Multiphoton Endoscopy .

Degree: 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 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/33844

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):

Rivera, David. “Multiphoton Endoscopy .” 2013. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/33844.

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

MLA Handbook (7th Edition):

Rivera, David. “Multiphoton Endoscopy .” 2013. Web. 18 Oct 2019.

Vancouver:

Rivera D. Multiphoton Endoscopy . [Internet] [Thesis]. Cornell University; 2013. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/33844.

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

Council of Science Editors:

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

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


Cornell University

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

Degree: 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 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/31103

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):

Wallace, Marsha. “Elucidation Of Mechanisms In Mammary Tumorigenesis And Identification Of Driving Events And Susceptibility Loci .” 2012. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/31103.

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

MLA Handbook (7th Edition):

Wallace, Marsha. “Elucidation Of Mechanisms In Mammary Tumorigenesis And Identification Of Driving Events And Susceptibility Loci .” 2012. Web. 18 Oct 2019.

Vancouver:

Wallace M. Elucidation Of Mechanisms In Mammary Tumorigenesis And Identification Of Driving Events And Susceptibility Loci . [Internet] [Thesis]. Cornell University; 2012. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/31103.

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

Council of Science Editors:

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

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


Cornell University

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

Degree: 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 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/29477

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):

Hartford, Suzanne. “The Role For Dna Replication And Repair Genes In Germ-Line Maintenance And Tumor Suppression .” 2012. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/29477.

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

MLA Handbook (7th Edition):

Hartford, Suzanne. “The Role For Dna Replication And Repair Genes In Germ-Line Maintenance And Tumor Suppression .” 2012. Web. 18 Oct 2019.

Vancouver:

Hartford S. The Role For Dna Replication And Repair Genes In Germ-Line Maintenance And Tumor Suppression . [Internet] [Thesis]. Cornell University; 2012. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/29477.

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

Council of Science Editors:

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

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


Cornell University

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

Degree: 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. (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/37128

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):

Sinha, Siddhartha. “Role Of Substrate Stiffness In Driving Atherogenic Behavior In Macrophages. ” 2014. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/37128.

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

MLA Handbook (7th Edition):

Sinha, Siddhartha. “Role Of Substrate Stiffness In Driving Atherogenic Behavior In Macrophages. ” 2014. Web. 18 Oct 2019.

Vancouver:

Sinha S. Role Of Substrate Stiffness In Driving Atherogenic Behavior In Macrophages. [Internet] [Thesis]. Cornell University; 2014. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/37128.

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

Council of Science Editors:

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

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


Cornell University

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

Degree: 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 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/39365

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):

Wayt, Jessica. “Actin Nucleators In Microvillar Assembly: Cordon Bleu As A Novel Microvillar Protein .” 2015. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/39365.

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

MLA Handbook (7th Edition):

Wayt, Jessica. “Actin Nucleators In Microvillar Assembly: Cordon Bleu As A Novel Microvillar Protein .” 2015. Web. 18 Oct 2019.

Vancouver:

Wayt J. Actin Nucleators In Microvillar Assembly: Cordon Bleu As A Novel Microvillar Protein . [Internet] [Thesis]. Cornell University; 2015. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/39365.

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

Council of Science Editors:

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

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


Cornell University

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

Degree: 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 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/39436

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):

Luo, Yunhai. “Genetic Dissection Of Checkpoint Signaling In Mouse Primordial Germ Cells .” 2015. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/39436.

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

MLA Handbook (7th Edition):

Luo, Yunhai. “Genetic Dissection Of Checkpoint Signaling In Mouse Primordial Germ Cells .” 2015. Web. 18 Oct 2019.

Vancouver:

Luo Y. Genetic Dissection Of Checkpoint Signaling In Mouse Primordial Germ Cells . [Internet] [Thesis]. Cornell University; 2015. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/39436.

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

Council of Science Editors:

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

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


Cornell University

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

Degree: 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 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/40691

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):

Dowicki, Michael. “The Wing Helix Domain Of Orc4 Is The Primary Determinant Of Dna Binding Specificity Of The Origin Recognition Complex .” 2015. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/40691.

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

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. 18 Oct 2019.

Vancouver:

Dowicki M. The Wing Helix Domain Of Orc4 Is The Primary Determinant Of Dna Binding Specificity Of The Origin Recognition Complex . [Internet] [Thesis]. Cornell University; 2015. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/40691.

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

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 . [Thesis]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/40691

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


Cornell University

12. Bai, Gongshi. Tumor Suppression By Regulation Of Mini-Chromosome Maintenance Expression In Response To Dna Replication Stress .

Degree: 2016, Cornell University

 DNA replication is an essential process during cell proliferation, when genomic information is completely and precisely duplicated. DNA replication machinery (replisome) is responsible for the… (more)

Subjects/Keywords: DNA replication and replication stress; Mini-chromosome maintenance (MCM); Genome integrity maintenance

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APA (6th Edition):

Bai, G. (2016). Tumor Suppression By Regulation Of Mini-Chromosome Maintenance Expression In Response To Dna Replication Stress . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/44309

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):

Bai, Gongshi. “Tumor Suppression By Regulation Of Mini-Chromosome Maintenance Expression In Response To Dna Replication Stress .” 2016. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/44309.

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

MLA Handbook (7th Edition):

Bai, Gongshi. “Tumor Suppression By Regulation Of Mini-Chromosome Maintenance Expression In Response To Dna Replication Stress .” 2016. Web. 18 Oct 2019.

Vancouver:

Bai G. Tumor Suppression By Regulation Of Mini-Chromosome Maintenance Expression In Response To Dna Replication Stress . [Internet] [Thesis]. Cornell University; 2016. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/44309.

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

Council of Science Editors:

Bai G. Tumor Suppression By Regulation Of Mini-Chromosome Maintenance Expression In Response To Dna Replication Stress . [Thesis]. Cornell University; 2016. Available from: http://hdl.handle.net/1813/44309

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


Cornell University

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

Degree: 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 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/59440

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):

Negron Abril, Yashira Liz. “TUMOR PROMOTING FUNCTIONS FOR THE METABOLIC REGULATOR SIRT5 .” 2018. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/59440.

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

MLA Handbook (7th Edition):

Negron Abril, Yashira Liz. “TUMOR PROMOTING FUNCTIONS FOR THE METABOLIC REGULATOR SIRT5 .” 2018. Web. 18 Oct 2019.

Vancouver:

Negron Abril YL. TUMOR PROMOTING FUNCTIONS FOR THE METABOLIC REGULATOR SIRT5 . [Internet] [Thesis]. Cornell University; 2018. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/59440.

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

Council of Science Editors:

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

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


Cornell University

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

Degree: 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 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/59083

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):

Jing, Hui. “MULTIPLE ENZYMATIC FUNCTIONS OF SIRT2 AND ITS INVOLVEMENT IN CANCER .” 2017. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/59083.

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

MLA Handbook (7th Edition):

Jing, Hui. “MULTIPLE ENZYMATIC FUNCTIONS OF SIRT2 AND ITS INVOLVEMENT IN CANCER .” 2017. Web. 18 Oct 2019.

Vancouver:

Jing H. MULTIPLE ENZYMATIC FUNCTIONS OF SIRT2 AND ITS INVOLVEMENT IN CANCER . [Internet] [Thesis]. Cornell University; 2017. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/59083.

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

Council of Science Editors:

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

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


Cornell University

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

Degree: 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 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/59495

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):

Alonzo, Judith Raquel. “Dysregulation of Folate-Dependent Mitochondrial de novo Thymidylate Biosynthesis Affects Mitohcondrial DNA Integrity .” 2018. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/59495.

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

MLA Handbook (7th Edition):

Alonzo, Judith Raquel. “Dysregulation of Folate-Dependent Mitochondrial de novo Thymidylate Biosynthesis Affects Mitohcondrial DNA Integrity .” 2018. Web. 18 Oct 2019.

Vancouver:

Alonzo JR. Dysregulation of Folate-Dependent Mitochondrial de novo Thymidylate Biosynthesis Affects Mitohcondrial DNA Integrity . [Internet] [Thesis]. Cornell University; 2018. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/59495.

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

Council of Science Editors:

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

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


Cornell University

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

Degree: 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 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/64974

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):

Liberti, Maria Volpe. “STRATEGIES FOR SELECTIVE TARGETING OF THE WARBURG EFFECT IN CANCER .” 2018. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/64974.

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

MLA Handbook (7th Edition):

Liberti, Maria Volpe. “STRATEGIES FOR SELECTIVE TARGETING OF THE WARBURG EFFECT IN CANCER .” 2018. Web. 18 Oct 2019.

Vancouver:

Liberti MV. STRATEGIES FOR SELECTIVE TARGETING OF THE WARBURG EFFECT IN CANCER . [Internet] [Thesis]. Cornell University; 2018. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/64974.

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

Council of Science Editors:

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

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


Cornell University

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

Degree: 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 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/64949

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):

Fu, Dah-Jiun. “Understanding gastric squamous-columnar junction carcinogenesis .” 2018. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/64949.

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

MLA Handbook (7th Edition):

Fu, Dah-Jiun. “Understanding gastric squamous-columnar junction carcinogenesis .” 2018. Web. 18 Oct 2019.

Vancouver:

Fu D. Understanding gastric squamous-columnar junction carcinogenesis . [Internet] [Thesis]. Cornell University; 2018. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/64949.

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

Council of Science Editors:

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

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


Cornell University

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

Degree: 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 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/64962

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):

McGregor, Alexandra L. “A NUCLEAR SQUEEZE: THE ROLE OF THE NUCLEUS IN CONFINED CANCER CELL MIGRATION .” 2018. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/64962.

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

MLA Handbook (7th Edition):

McGregor, Alexandra L. “A NUCLEAR SQUEEZE: THE ROLE OF THE NUCLEUS IN CONFINED CANCER CELL MIGRATION .” 2018. Web. 18 Oct 2019.

Vancouver:

McGregor AL. A NUCLEAR SQUEEZE: THE ROLE OF THE NUCLEUS IN CONFINED CANCER CELL MIGRATION . [Internet] [Thesis]. Cornell University; 2018. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/64962.

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

Council of Science Editors:

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

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


Cornell University

19. 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: 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 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/29467

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):

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. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/29467.

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

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. 18 Oct 2019.

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] [Thesis]. Cornell University; 2012. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/29467.

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

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 . [Thesis]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/29467

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


Cornell University

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

Degree: 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 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/29249

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):

Chuang, Chen-hua. “Unique Regulatory Mechanisms For Dna Replication And Genome Maintenance In Mammals .” 2012. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/29249.

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

MLA Handbook (7th Edition):

Chuang, Chen-hua. “Unique Regulatory Mechanisms For Dna Replication And Genome Maintenance In Mammals .” 2012. Web. 18 Oct 2019.

Vancouver:

Chuang C. Unique Regulatory Mechanisms For Dna Replication And Genome Maintenance In Mammals . [Internet] [Thesis]. Cornell University; 2012. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/29249.

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

Council of Science Editors:

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

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


Cornell University

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

Degree: 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 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/36176

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):

Mohanan Nair Padmini, Sunish. “Role Of Peptidylarginine Deiminase 2 (Pad2) In Epithelial Carcinogenesis And Tumor-Associated Inflammation .” 2014. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/36176.

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

MLA Handbook (7th Edition):

Mohanan Nair Padmini, Sunish. “Role Of Peptidylarginine Deiminase 2 (Pad2) In Epithelial Carcinogenesis And Tumor-Associated Inflammation .” 2014. Web. 18 Oct 2019.

Vancouver:

Mohanan Nair Padmini S. Role Of Peptidylarginine Deiminase 2 (Pad2) In Epithelial Carcinogenesis And Tumor-Associated Inflammation . [Internet] [Thesis]. Cornell University; 2014. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/36176.

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

Council of Science Editors:

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

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


Cornell University

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

Degree: 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 . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/38822

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, Huanhuan. “Engineering Colorectal Cancer Models For Mechanistic Studies And Therapeutics .” 2014. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/38822.

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

MLA Handbook (7th Edition):

Chen, Huanhuan. “Engineering Colorectal Cancer Models For Mechanistic Studies And Therapeutics .” 2014. Web. 18 Oct 2019.

Vancouver:

Chen H. Engineering Colorectal Cancer Models For Mechanistic Studies And Therapeutics . [Internet] [Thesis]. Cornell University; 2014. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/38822.

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

Council of Science Editors:

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

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


Cornell University

23. Davis, Kristen. Endoplasmic Reticulum Homeostasis In The Mouse Mammary Epithelium During Lactation .

Degree: 2015, Cornell University

 Lactation is an essential stage of mammalian life. Milk is a complex fluid that provides complete nutrition for neonates in the early stages of postnatal… (more)

Subjects/Keywords: endoplasmic reticulum; mammary gland; lactation

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APA (6th Edition):

Davis, K. (2015). Endoplasmic Reticulum Homeostasis In The Mouse Mammary Epithelium During Lactation . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/40669

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):

Davis, Kristen. “Endoplasmic Reticulum Homeostasis In The Mouse Mammary Epithelium During Lactation .” 2015. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/40669.

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

MLA Handbook (7th Edition):

Davis, Kristen. “Endoplasmic Reticulum Homeostasis In The Mouse Mammary Epithelium During Lactation .” 2015. Web. 18 Oct 2019.

Vancouver:

Davis K. Endoplasmic Reticulum Homeostasis In The Mouse Mammary Epithelium During Lactation . [Internet] [Thesis]. Cornell University; 2015. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/40669.

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

Council of Science Editors:

Davis K. Endoplasmic Reticulum Homeostasis In The Mouse Mammary Epithelium During Lactation . [Thesis]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/40669

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


Cornell University

24. Srinivasan, Tara. Notch Signaling: Mechanistic And Functional Studies In Intestinal Stem Cells And Colorectal Cancer Cells .

Degree: 2016, Cornell University

 : The study of stem cell regulation in intestinal and colonic tissues is an area of significant focus within the scientific community, providing mechanistic insight… (more)

Subjects/Keywords: colorectal cancer; stem cell; NOTCH signaling

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APA (6th Edition):

Srinivasan, T. (2016). Notch Signaling: Mechanistic And Functional Studies In Intestinal Stem Cells And Colorectal Cancer Cells . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/44394

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):

Srinivasan, Tara. “Notch Signaling: Mechanistic And Functional Studies In Intestinal Stem Cells And Colorectal Cancer Cells .” 2016. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/44394.

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

MLA Handbook (7th Edition):

Srinivasan, Tara. “Notch Signaling: Mechanistic And Functional Studies In Intestinal Stem Cells And Colorectal Cancer Cells .” 2016. Web. 18 Oct 2019.

Vancouver:

Srinivasan T. Notch Signaling: Mechanistic And Functional Studies In Intestinal Stem Cells And Colorectal Cancer Cells . [Internet] [Thesis]. Cornell University; 2016. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/44394.

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

Council of Science Editors:

Srinivasan T. Notch Signaling: Mechanistic And Functional Studies In Intestinal Stem Cells And Colorectal Cancer Cells . [Thesis]. Cornell University; 2016. Available from: http://hdl.handle.net/1813/44394

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


Cornell University

25. Thege, Fredrik Ivar. The effect of phenotypic heterogeneity on pancreatic circulating tumor cell capture and tumor spheroids .

Degree: 2017, Cornell University

 Pancreatic cancer is the third-leading cause of cancer-related death in the US and represents a difficult challenge to modern medicine, with increasing incidence and modest… (more)

Subjects/Keywords: Pancreatic cancer; Chemoresistance; EMT; Heterogeneity; Circulating tumor cells; Spheroids; Biomedical engineering

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APA (6th Edition):

Thege, F. I. (2017). The effect of phenotypic heterogeneity on pancreatic circulating tumor cell capture and tumor spheroids . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/47848

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):

Thege, Fredrik Ivar. “The effect of phenotypic heterogeneity on pancreatic circulating tumor cell capture and tumor spheroids .” 2017. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/47848.

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

MLA Handbook (7th Edition):

Thege, Fredrik Ivar. “The effect of phenotypic heterogeneity on pancreatic circulating tumor cell capture and tumor spheroids .” 2017. Web. 18 Oct 2019.

Vancouver:

Thege FI. The effect of phenotypic heterogeneity on pancreatic circulating tumor cell capture and tumor spheroids . [Internet] [Thesis]. Cornell University; 2017. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/47848.

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

Council of Science Editors:

Thege FI. The effect of phenotypic heterogeneity on pancreatic circulating tumor cell capture and tumor spheroids . [Thesis]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/47848

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


Cornell University

26. LaValley, Danielle Judith. Effects of Tumor Microenvironmental Cues on Endothelial Cell Behavior and Chemotherapeutic Efficiency .

Degree: 2018, Cornell University

 Cancer is a leading cause of death worldwide and within the US. While cancer initially arises from genetic mutations that transform otherwise healthy cells into… (more)

Subjects/Keywords: Biomedical engineering

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APA (6th Edition):

LaValley, D. J. (2018). Effects of Tumor Microenvironmental Cues on Endothelial Cell Behavior and Chemotherapeutic Efficiency . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/64986

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):

LaValley, Danielle Judith. “Effects of Tumor Microenvironmental Cues on Endothelial Cell Behavior and Chemotherapeutic Efficiency .” 2018. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/64986.

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

MLA Handbook (7th Edition):

LaValley, Danielle Judith. “Effects of Tumor Microenvironmental Cues on Endothelial Cell Behavior and Chemotherapeutic Efficiency .” 2018. Web. 18 Oct 2019.

Vancouver:

LaValley DJ. Effects of Tumor Microenvironmental Cues on Endothelial Cell Behavior and Chemotherapeutic Efficiency . [Internet] [Thesis]. Cornell University; 2018. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/64986.

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

Council of Science Editors:

LaValley DJ. Effects of Tumor Microenvironmental Cues on Endothelial Cell Behavior and Chemotherapeutic Efficiency . [Thesis]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/64986

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


Cornell University

27. Purwada, Alberto. Bioengineered Immune Organoids for Controlling B Cell Development .

Degree: 2017, Cornell University

 The humoral arm of the adaptive immune system works by producing antigen-specific antibody to clear pathogens from the extracellular spaces in the body. The humoral… (more)

Subjects/Keywords: Biomedical engineering; 3D Cell Culture; B Cells; Germinal Center; Lymphoid Tissues; Tissue Engineering

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APA (6th Edition):

Purwada, A. (2017). Bioengineered Immune Organoids for Controlling B Cell Development . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/56816

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):

Purwada, Alberto. “Bioengineered Immune Organoids for Controlling B Cell Development .” 2017. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/56816.

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

MLA Handbook (7th Edition):

Purwada, Alberto. “Bioengineered Immune Organoids for Controlling B Cell Development .” 2017. Web. 18 Oct 2019.

Vancouver:

Purwada A. Bioengineered Immune Organoids for Controlling B Cell Development . [Internet] [Thesis]. Cornell University; 2017. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/56816.

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

Council of Science Editors:

Purwada A. Bioengineered Immune Organoids for Controlling B Cell Development . [Thesis]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/56816

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


Cornell University

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

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

APA (6th Edition):

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

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):

Sun, Xianfei. “Investigating Mammalian Meiosis: The Role Of Mismatch Repair Proteins And Their Interactors .” 2012. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/31179.

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

MLA Handbook (7th Edition):

Sun, Xianfei. “Investigating Mammalian Meiosis: The Role Of Mismatch Repair Proteins And Their Interactors .” 2012. Web. 18 Oct 2019.

Vancouver:

Sun X. Investigating Mammalian Meiosis: The Role Of Mismatch Repair Proteins And Their Interactors . [Internet] [Thesis]. Cornell University; 2012. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/31179.

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

Council of Science Editors:

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

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


Cornell University

29. Hope, Kristine. The Development And Application Of A Zebrafish Infection Model For Viral Hemorrhagic Septicemia Virus Ivb .

Degree: 2012, Cornell University

 Viral hemorrhagic septicemia virus (VHSV) is the causative agent of a highly lethal, World Organization for Animal Health (OIE) reportable fish disease. With a broad… (more)

Subjects/Keywords: Viral hemorrhagic septicemia virus; Zebrafish; Infection model

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

APA (6th Edition):

Hope, K. (2012). The Development And Application Of A Zebrafish Infection Model For Viral Hemorrhagic Septicemia Virus Ivb . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/29379

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):

Hope, Kristine. “The Development And Application Of A Zebrafish Infection Model For Viral Hemorrhagic Septicemia Virus Ivb .” 2012. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/29379.

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

MLA Handbook (7th Edition):

Hope, Kristine. “The Development And Application Of A Zebrafish Infection Model For Viral Hemorrhagic Septicemia Virus Ivb .” 2012. Web. 18 Oct 2019.

Vancouver:

Hope K. The Development And Application Of A Zebrafish Infection Model For Viral Hemorrhagic Septicemia Virus Ivb . [Internet] [Thesis]. Cornell University; 2012. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/29379.

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

Council of Science Editors:

Hope K. The Development And Application Of A Zebrafish Infection Model For Viral Hemorrhagic Septicemia Virus Ivb . [Thesis]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/29379

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


Cornell University

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

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

APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Lee, Yoon Jung. “Ca2+ Channel Independent Functions Of An Alternatively Spliced ß4 Subunit .” 2014. Thesis, Cornell University. Accessed October 18, 2019. http://hdl.handle.net/1813/38955.

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

MLA Handbook (7th Edition):

Lee, Yoon Jung. “Ca2+ Channel Independent Functions Of An Alternatively Spliced ß4 Subunit .” 2014. Web. 18 Oct 2019.

Vancouver:

Lee YJ. Ca2+ Channel Independent Functions Of An Alternatively Spliced ß4 Subunit . [Internet] [Thesis]. Cornell University; 2014. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1813/38955.

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

Council of Science Editors:

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

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

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