Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for +publisher:"Cornell University" +contributor:("Alani, Eric"). Showing records 1 – 30 of 36 total matches.

[1] [2]

Search Limiters

Last 2 Years | English Only

▼ Search Limiters


Cornell University

1. West, Timothy. THE MEIOSIS SPECIFIC AAA+ ATPASE PCH2 INTERACTS WITH THE SYNAPTONEMAL COMPLEX PROTEIN HOP1 THROUGH THE HOP1 HORMA DOMAIN.

Degree: M.S., Molecular and Cell Biology, Molecular and Cell Biology, 2016, Cornell University

 In most sexually reproducing organisms physical linkages are required between homologous chromosome pairs in order to properly segregate them in the first meiotic division. Crossovers… (more)

Subjects/Keywords: Hop1; Pch2; HORMA

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

West, T. (2016). THE MEIOSIS SPECIFIC AAA+ ATPASE PCH2 INTERACTS WITH THE SYNAPTONEMAL COMPLEX PROTEIN HOP1 THROUGH THE HOP1 HORMA DOMAIN. (Masters Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/44115

Chicago Manual of Style (16th Edition):

West, Timothy. “THE MEIOSIS SPECIFIC AAA+ ATPASE PCH2 INTERACTS WITH THE SYNAPTONEMAL COMPLEX PROTEIN HOP1 THROUGH THE HOP1 HORMA DOMAIN.” 2016. Masters Thesis, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/44115.

MLA Handbook (7th Edition):

West, Timothy. “THE MEIOSIS SPECIFIC AAA+ ATPASE PCH2 INTERACTS WITH THE SYNAPTONEMAL COMPLEX PROTEIN HOP1 THROUGH THE HOP1 HORMA DOMAIN.” 2016. Web. 26 Nov 2020.

Vancouver:

West T. THE MEIOSIS SPECIFIC AAA+ ATPASE PCH2 INTERACTS WITH THE SYNAPTONEMAL COMPLEX PROTEIN HOP1 THROUGH THE HOP1 HORMA DOMAIN. [Internet] [Masters thesis]. Cornell University; 2016. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/44115.

Council of Science Editors:

West T. THE MEIOSIS SPECIFIC AAA+ ATPASE PCH2 INTERACTS WITH THE SYNAPTONEMAL COMPLEX PROTEIN HOP1 THROUGH THE HOP1 HORMA DOMAIN. [Masters Thesis]. Cornell University; 2016. Available from: http://hdl.handle.net/1813/44115


Cornell University

2. Patel, Vaidehi. Characterizing the role of central carbon metabolism and cell wall stress responses in Bacillus subtilis cell wall synthesis.

Degree: PhD, Microbiology, 2018, Cornell University

 The cell wall is an essential organelle for many bacteria since it provides mechanical strength and prevents bacterial cell lysis due to internal turgor pressure.… (more)

Subjects/Keywords: Beta-lactam; Gluconeogenesis; moonlighting enzyme; Genetics; Microbiology; Molecular biology; Metabolism; Bacillus subtilis; Peptidoglycan

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Patel, V. (2018). Characterizing the role of central carbon metabolism and cell wall stress responses in Bacillus subtilis cell wall synthesis. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/64848

Chicago Manual of Style (16th Edition):

Patel, Vaidehi. “Characterizing the role of central carbon metabolism and cell wall stress responses in Bacillus subtilis cell wall synthesis.” 2018. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/64848.

MLA Handbook (7th Edition):

Patel, Vaidehi. “Characterizing the role of central carbon metabolism and cell wall stress responses in Bacillus subtilis cell wall synthesis.” 2018. Web. 26 Nov 2020.

Vancouver:

Patel V. Characterizing the role of central carbon metabolism and cell wall stress responses in Bacillus subtilis cell wall synthesis. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/64848.

Council of Science Editors:

Patel V. Characterizing the role of central carbon metabolism and cell wall stress responses in Bacillus subtilis cell wall synthesis. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/64848


Cornell University

3. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 November 26, 2020. 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. 26 Nov 2020.

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 2020 Nov 26]. 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

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

Degree: PhD, Biochemistry, 2013, Cornell University

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

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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Brown, Megan. “Roles For Telomere-Led Chromosome Motion And Crossover Resolution During Meiosis In Saccharomyces Cerevisiae.” 2013. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/33899.

MLA Handbook (7th Edition):

Brown, Megan. “Roles For Telomere-Led Chromosome Motion And Crossover Resolution During Meiosis In Saccharomyces Cerevisiae.” 2013. Web. 26 Nov 2020.

Vancouver:

Brown M. Roles For Telomere-Led Chromosome Motion And Crossover Resolution During Meiosis In Saccharomyces Cerevisiae. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/33899.

Council of Science Editors:

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


Cornell University

5. Larson, Amy. Genomic Approaches to Understanding Pre-mRNA Splicing Regulation in Schizosaccharomyces Pombe.

Degree: PhD, Biochemistry, Molecular and Cell Biology, 2017, Cornell University

 The protein-coding regions of most eukaryotic genes are interrupted by non-coding introns, which must be excised from the pre-messenger RNA (pre-mRNA) prior to translation. Pre-mRNA… (more)

Subjects/Keywords: Biochemistry; Fission Yeast; Multi-intronic; Pre-mRNA Splicing; Spliceosome Structure; Splicing Regulation; Genetics; Molecular biology; Genomics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Larson, A. (2017). Genomic Approaches to Understanding Pre-mRNA Splicing Regulation in Schizosaccharomyces Pombe. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/51553

Chicago Manual of Style (16th Edition):

Larson, Amy. “Genomic Approaches to Understanding Pre-mRNA Splicing Regulation in Schizosaccharomyces Pombe.” 2017. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/51553.

MLA Handbook (7th Edition):

Larson, Amy. “Genomic Approaches to Understanding Pre-mRNA Splicing Regulation in Schizosaccharomyces Pombe.” 2017. Web. 26 Nov 2020.

Vancouver:

Larson A. Genomic Approaches to Understanding Pre-mRNA Splicing Regulation in Schizosaccharomyces Pombe. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/51553.

Council of Science Editors:

Larson A. Genomic Approaches to Understanding Pre-mRNA Splicing Regulation in Schizosaccharomyces Pombe. [Doctoral Dissertation]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/51553

6. Gustafson, Margaret Ann. The Arf-GEFs Gea1 and Gea2 integrate signals to coordinate vesicle trafficking at the Golgi complex.

Degree: PhD, Biochemistry, Molecular and Cell Biology, 2017, Cornell University

 At the Golgi complex, the biosynthetic sorting center of the cell, the Arf GTPases are responsible for coordinating vesicle formation. The Arf-GEFs activate Arf GTPases… (more)

Subjects/Keywords: Cellular biology; Molecular biology; Biochemistry; Arf; Arf-GEF; Gea1; Gea2; Golgi complex; membrane trafficking

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Gustafson, M. A. (2017). The Arf-GEFs Gea1 and Gea2 integrate signals to coordinate vesicle trafficking at the Golgi complex. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/56834

Chicago Manual of Style (16th Edition):

Gustafson, Margaret Ann. “The Arf-GEFs Gea1 and Gea2 integrate signals to coordinate vesicle trafficking at the Golgi complex.” 2017. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/56834.

MLA Handbook (7th Edition):

Gustafson, Margaret Ann. “The Arf-GEFs Gea1 and Gea2 integrate signals to coordinate vesicle trafficking at the Golgi complex.” 2017. Web. 26 Nov 2020.

Vancouver:

Gustafson MA. The Arf-GEFs Gea1 and Gea2 integrate signals to coordinate vesicle trafficking at the Golgi complex. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/56834.

Council of Science Editors:

Gustafson MA. The Arf-GEFs Gea1 and Gea2 integrate signals to coordinate vesicle trafficking at the Golgi complex. [Doctoral Dissertation]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/56834


Cornell University

7. Chen, Cheng. Pch2 Is A Hexameric Ring Atpase That Remodels The Meiotic Chromosome Axis Protein Hop1.

Degree: PhD, Genetics, 2014, Cornell University

 In most organisms, the accurate segregation of chromosomes during the first meiotic division requires at least one crossover between each pair of homologous chromosomes. Crossovers… (more)

Subjects/Keywords: meiosis; AAA proteins; hexameric ATPase

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Chen, C. (2014). Pch2 Is A Hexameric Ring Atpase That Remodels The Meiotic Chromosome Axis Protein Hop1. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/37032

Chicago Manual of Style (16th Edition):

Chen, Cheng. “Pch2 Is A Hexameric Ring Atpase That Remodels The Meiotic Chromosome Axis Protein Hop1.” 2014. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/37032.

MLA Handbook (7th Edition):

Chen, Cheng. “Pch2 Is A Hexameric Ring Atpase That Remodels The Meiotic Chromosome Axis Protein Hop1.” 2014. Web. 26 Nov 2020.

Vancouver:

Chen C. Pch2 Is A Hexameric Ring Atpase That Remodels The Meiotic Chromosome Axis Protein Hop1. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/37032.

Council of Science Editors:

Chen C. Pch2 Is A Hexameric Ring Atpase That Remodels The Meiotic Chromosome Axis Protein Hop1. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/37032


Cornell University

8. Dolan, Adam Emin. CHARACTERIZATION OF THE TYPE I-E CRISPR SYSTEM OF T. FUSCA AND ITS APPLICATION TO GENOME EDITING.

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

 Genome editing techniques and platforms for nucleic acid targeting have been revolutionized by the discovery and technological adaptation of bacterial immune systems called CRISPR systems.… (more)

Subjects/Keywords: Biochemistry; Molecular biology; Cas3; Cascade; CRISPR; Genome Editing; Bioengineering

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Dolan, A. E. (2018). CHARACTERIZATION OF THE TYPE I-E CRISPR SYSTEM OF T. FUSCA AND ITS APPLICATION TO GENOME EDITING. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/64835

Chicago Manual of Style (16th Edition):

Dolan, Adam Emin. “CHARACTERIZATION OF THE TYPE I-E CRISPR SYSTEM OF T. FUSCA AND ITS APPLICATION TO GENOME EDITING.” 2018. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/64835.

MLA Handbook (7th Edition):

Dolan, Adam Emin. “CHARACTERIZATION OF THE TYPE I-E CRISPR SYSTEM OF T. FUSCA AND ITS APPLICATION TO GENOME EDITING.” 2018. Web. 26 Nov 2020.

Vancouver:

Dolan AE. CHARACTERIZATION OF THE TYPE I-E CRISPR SYSTEM OF T. FUSCA AND ITS APPLICATION TO GENOME EDITING. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/64835.

Council of Science Editors:

Dolan AE. CHARACTERIZATION OF THE TYPE I-E CRISPR SYSTEM OF T. FUSCA AND ITS APPLICATION TO GENOME EDITING. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/64835


Cornell University

9. Lanz, Michael. MEC1 KINASE SIGNALING IN THE MAINTENANCE AND REPLICATION OF THE GENOME.

Degree: PhD, Biochemistry, Molecular and Cell Biology, 2019, Cornell University

 From bacteria to mammalian cells, damaged DNA is sensed and targeted by DNA repair pathways. A distinguishing feature of eukaryotes is that kinases play central… (more)

Subjects/Keywords: Genetics; DNA replication; Molecular biology; ATR; Genetic instability; Gross Chromosomal Rearrangement; Mec1; Phosphoproteomics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lanz, M. (2019). MEC1 KINASE SIGNALING IN THE MAINTENANCE AND REPLICATION OF THE GENOME. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/67447

Chicago Manual of Style (16th Edition):

Lanz, Michael. “MEC1 KINASE SIGNALING IN THE MAINTENANCE AND REPLICATION OF THE GENOME.” 2019. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/67447.

MLA Handbook (7th Edition):

Lanz, Michael. “MEC1 KINASE SIGNALING IN THE MAINTENANCE AND REPLICATION OF THE GENOME.” 2019. Web. 26 Nov 2020.

Vancouver:

Lanz M. MEC1 KINASE SIGNALING IN THE MAINTENANCE AND REPLICATION OF THE GENOME. [Internet] [Doctoral dissertation]. Cornell University; 2019. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/67447.

Council of Science Editors:

Lanz M. MEC1 KINASE SIGNALING IN THE MAINTENANCE AND REPLICATION OF THE GENOME. [Doctoral Dissertation]. Cornell University; 2019. Available from: http://hdl.handle.net/1813/67447


Cornell University

10. Pinto, Uelinton. Quorum Sensing, Entry Exclusion And Replication Of The Ti Plasmid Of Agrobacterium Tumefaciens.

Degree: PhD, Microbiology, 2011, Cornell University

 Agrobacterium tumefaciens contains the tumor inducing (Ti) plasmid that stimulates tumor formation in wounded plant tissues. Replication, partitioning, conjugation and entry exclusion of this plasmid… (more)

Subjects/Keywords: quorum sensing; entry exclusion; replication

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Pinto, U. (2011). Quorum Sensing, Entry Exclusion And Replication Of The Ti Plasmid Of Agrobacterium Tumefaciens. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/33639

Chicago Manual of Style (16th Edition):

Pinto, Uelinton. “Quorum Sensing, Entry Exclusion And Replication Of The Ti Plasmid Of Agrobacterium Tumefaciens.” 2011. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/33639.

MLA Handbook (7th Edition):

Pinto, Uelinton. “Quorum Sensing, Entry Exclusion And Replication Of The Ti Plasmid Of Agrobacterium Tumefaciens.” 2011. Web. 26 Nov 2020.

Vancouver:

Pinto U. Quorum Sensing, Entry Exclusion And Replication Of The Ti Plasmid Of Agrobacterium Tumefaciens. [Internet] [Doctoral dissertation]. Cornell University; 2011. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/33639.

Council of Science Editors:

Pinto U. Quorum Sensing, Entry Exclusion And Replication Of The Ti Plasmid Of Agrobacterium Tumefaciens. [Doctoral Dissertation]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/33639


Cornell University

11. Bird, Jeremy. Characterization Of Novel Dna Elements Necessary For Sigma-Dependent Promoter Proximal Transcriptional Pausing.

Degree: PhD, Biochemistry, 2013, Cornell University

 Transcription is not necessarily uniform in rate, but instead consists of multiple periods of continuous elongation by RNA polymerase (RNAP) interrupted by occasional pausing events.… (more)

Subjects/Keywords: Transcription; Pausing; Phage

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bird, J. (2013). Characterization Of Novel Dna Elements Necessary For Sigma-Dependent Promoter Proximal Transcriptional Pausing. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/34019

Chicago Manual of Style (16th Edition):

Bird, Jeremy. “Characterization Of Novel Dna Elements Necessary For Sigma-Dependent Promoter Proximal Transcriptional Pausing.” 2013. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/34019.

MLA Handbook (7th Edition):

Bird, Jeremy. “Characterization Of Novel Dna Elements Necessary For Sigma-Dependent Promoter Proximal Transcriptional Pausing.” 2013. Web. 26 Nov 2020.

Vancouver:

Bird J. Characterization Of Novel Dna Elements Necessary For Sigma-Dependent Promoter Proximal Transcriptional Pausing. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/34019.

Council of Science Editors:

Bird J. Characterization Of Novel Dna Elements Necessary For Sigma-Dependent Promoter Proximal Transcriptional Pausing. [Doctoral Dissertation]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/34019


Cornell University

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

Degree: PhD, Biochemistry, Molecular and Cell Biology, 2017, Cornell University

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

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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Al-Sweel, Najla Abdulaziz. “THE MISMATCH REPAIR AND MEIOTIC RECOMBINATION ENDONUCLEASE MLH1-MLH3 IS DIRECTED BY PROTEIN-PROTEIN INTERACTIONS.” 2017. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/59043.

MLA Handbook (7th Edition):

Al-Sweel, Najla Abdulaziz. “THE MISMATCH REPAIR AND MEIOTIC RECOMBINATION ENDONUCLEASE MLH1-MLH3 IS DIRECTED BY PROTEIN-PROTEIN INTERACTIONS.” 2017. Web. 26 Nov 2020.

Vancouver:

Al-Sweel NA. THE MISMATCH REPAIR AND MEIOTIC RECOMBINATION ENDONUCLEASE MLH1-MLH3 IS DIRECTED BY PROTEIN-PROTEIN INTERACTIONS. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/59043.

Council of Science Editors:

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


Cornell University

13. Santiago-Tirado, Felipe. Investigating The Association Of The Myosin Motor Myo2P With Its Secretory Cargo.

Degree: PhD, Molecular and Cell Biology, 2011, Cornell University

 Cell polarity involves transport of specific membranes and macromolecules at the right time to the right place. In budding yeast, growth is highly asymmetric and… (more)

Subjects/Keywords: myosin motors; phosphoinositides; myo2; sec4; yeast

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Santiago-Tirado, F. (2011). Investigating The Association Of The Myosin Motor Myo2P With Its Secretory Cargo. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/30651

Chicago Manual of Style (16th Edition):

Santiago-Tirado, Felipe. “Investigating The Association Of The Myosin Motor Myo2P With Its Secretory Cargo.” 2011. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/30651.

MLA Handbook (7th Edition):

Santiago-Tirado, Felipe. “Investigating The Association Of The Myosin Motor Myo2P With Its Secretory Cargo.” 2011. Web. 26 Nov 2020.

Vancouver:

Santiago-Tirado F. Investigating The Association Of The Myosin Motor Myo2P With Its Secretory Cargo. [Internet] [Doctoral dissertation]. Cornell University; 2011. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/30651.

Council of Science Editors:

Santiago-Tirado F. Investigating The Association Of The Myosin Motor Myo2P With Its Secretory Cargo. [Doctoral Dissertation]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/30651


Cornell University

14. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 November 26, 2020. 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. 26 Nov 2020.

Vancouver:

Alonzo JR. Dysregulation of Folate-Dependent Mitochondrial de novo Thymidylate Biosynthesis Affects Mitohcondrial DNA Integrity. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2020 Nov 26]. 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

15. Sidhu, Gaganpreet. Analysis Of Natural Variation In Recombination In Maize.

Degree: PhD, Plant Breeding, 2012, Cornell University

 Meiotic recombination is a major source of genetic variation in plants. Understanding factors that affect the recombination rates in plants is important for general genetic… (more)

Subjects/Keywords: natural variation; recombination

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sidhu, G. (2012). Analysis Of Natural Variation In Recombination In Maize. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/29310

Chicago Manual of Style (16th Edition):

Sidhu, Gaganpreet. “Analysis Of Natural Variation In Recombination In Maize.” 2012. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/29310.

MLA Handbook (7th Edition):

Sidhu, Gaganpreet. “Analysis Of Natural Variation In Recombination In Maize.” 2012. Web. 26 Nov 2020.

Vancouver:

Sidhu G. Analysis Of Natural Variation In Recombination In Maize. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/29310.

Council of Science Editors:

Sidhu G. Analysis Of Natural Variation In Recombination In Maize. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/29310

16. Hosford, Chris John. ASSESSING SPECIES SPECIFIC DETERMINANTS OF DNA BINDING IN MCRB HOMOLOGS.

Degree: PhD, Biochemistry, Molecular and Cell Biology, 2019, Cornell University

 Antibiotic resistance poses a significant threat to human health. The lagging development of new antibiotics and the rapid exchange of resistance genes have created a… (more)

Subjects/Keywords: Biophysics; B3 Domain; DNA Binding; EVE Domain; McrBC; Restriction System; YTH Domain; Biochemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hosford, C. J. (2019). ASSESSING SPECIES SPECIFIC DETERMINANTS OF DNA BINDING IN MCRB HOMOLOGS. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/67310

Chicago Manual of Style (16th Edition):

Hosford, Chris John. “ASSESSING SPECIES SPECIFIC DETERMINANTS OF DNA BINDING IN MCRB HOMOLOGS.” 2019. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/67310.

MLA Handbook (7th Edition):

Hosford, Chris John. “ASSESSING SPECIES SPECIFIC DETERMINANTS OF DNA BINDING IN MCRB HOMOLOGS.” 2019. Web. 26 Nov 2020.

Vancouver:

Hosford CJ. ASSESSING SPECIES SPECIFIC DETERMINANTS OF DNA BINDING IN MCRB HOMOLOGS. [Internet] [Doctoral dissertation]. Cornell University; 2019. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/67310.

Council of Science Editors:

Hosford CJ. ASSESSING SPECIES SPECIFIC DETERMINANTS OF DNA BINDING IN MCRB HOMOLOGS. [Doctoral Dissertation]. Cornell University; 2019. Available from: http://hdl.handle.net/1813/67310


Cornell University

17. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 November 26, 2020. 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. 26 Nov 2020.

Vancouver:

Plys A. Analysis Of The Movement Of Saccharomyces Cerevisiae Mismatch Repair Proteins On Dna. [Internet] [Doctoral dissertation]. Cornell University; 2011. [cited 2020 Nov 26]. 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

18. Sitnik, Jessica. Male And Female Derived Reproductive Proteins That Contribute To The Regulation Of The Long-Term Post-Mating Response In Female Drosophila Melanogaster.

Degree: PhD, Genetics, 2014, Cornell University

 In organisms with internal fertilization, seminal fluid proteins (Sfps) are essential for the reproductive success of both sexes. In Drosophila melanogaster, Sfps are required to… (more)

Subjects/Keywords: Drosophila melanogaster; Seminal fluid; Reproduction

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sitnik, J. (2014). Male And Female Derived Reproductive Proteins That Contribute To The Regulation Of The Long-Term Post-Mating Response In Female Drosophila Melanogaster. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/36095

Chicago Manual of Style (16th Edition):

Sitnik, Jessica. “Male And Female Derived Reproductive Proteins That Contribute To The Regulation Of The Long-Term Post-Mating Response In Female Drosophila Melanogaster.” 2014. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/36095.

MLA Handbook (7th Edition):

Sitnik, Jessica. “Male And Female Derived Reproductive Proteins That Contribute To The Regulation Of The Long-Term Post-Mating Response In Female Drosophila Melanogaster.” 2014. Web. 26 Nov 2020.

Vancouver:

Sitnik J. Male And Female Derived Reproductive Proteins That Contribute To The Regulation Of The Long-Term Post-Mating Response In Female Drosophila Melanogaster. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/36095.

Council of Science Editors:

Sitnik J. Male And Female Derived Reproductive Proteins That Contribute To The Regulation Of The Long-Term Post-Mating Response In Female Drosophila Melanogaster. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/36095


Cornell University

19. Awan, Ali. Discovering Alternative Splicing Of Deeply Conserved Exons And Characterizing The Intronome In The Unicellular Yeast S. Pombe Using Lariat Sequencing.

Degree: PhD, Genetics, 2013, Cornell University

 Alternative splicing is a potent regulator of gene expression that vastly increases proteomic diversity in multi-cellular eukaryotes. Although it is widespread in vertebrates, little is… (more)

Subjects/Keywords: Alternative Splicing; Sequencing; pombe

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Awan, A. (2013). Discovering Alternative Splicing Of Deeply Conserved Exons And Characterizing The Intronome In The Unicellular Yeast S. Pombe Using Lariat Sequencing. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/34200

Chicago Manual of Style (16th Edition):

Awan, Ali. “Discovering Alternative Splicing Of Deeply Conserved Exons And Characterizing The Intronome In The Unicellular Yeast S. Pombe Using Lariat Sequencing.” 2013. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/34200.

MLA Handbook (7th Edition):

Awan, Ali. “Discovering Alternative Splicing Of Deeply Conserved Exons And Characterizing The Intronome In The Unicellular Yeast S. Pombe Using Lariat Sequencing.” 2013. Web. 26 Nov 2020.

Vancouver:

Awan A. Discovering Alternative Splicing Of Deeply Conserved Exons And Characterizing The Intronome In The Unicellular Yeast S. Pombe Using Lariat Sequencing. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/34200.

Council of Science Editors:

Awan A. Discovering Alternative Splicing Of Deeply Conserved Exons And Characterizing The Intronome In The Unicellular Yeast S. Pombe Using Lariat Sequencing. [Doctoral Dissertation]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/34200


Cornell University

20. Chakraborty, Ujani. A DELICATE BALANCE IN MISMATCH REPAIR FACTORS IS CRITICAL FOR MAINTAINING GENOME STABILITY.

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

 Mismatch repair (MMR) proteins act to correct DNA polymerase errors that arise during DNA replication. They also play vital roles maintaining homologous recombination fidelity during… (more)

Subjects/Keywords: Genome stability; Heteroduplex rejection; Biochemistry; Genetics; chromatin; Molecular biology; homologous recombination; mismatch repair

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Chakraborty, U. (2018). A DELICATE BALANCE IN MISMATCH REPAIR FACTORS IS CRITICAL FOR MAINTAINING GENOME STABILITY. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59525

Chicago Manual of Style (16th Edition):

Chakraborty, Ujani. “A DELICATE BALANCE IN MISMATCH REPAIR FACTORS IS CRITICAL FOR MAINTAINING GENOME STABILITY.” 2018. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/59525.

MLA Handbook (7th Edition):

Chakraborty, Ujani. “A DELICATE BALANCE IN MISMATCH REPAIR FACTORS IS CRITICAL FOR MAINTAINING GENOME STABILITY.” 2018. Web. 26 Nov 2020.

Vancouver:

Chakraborty U. A DELICATE BALANCE IN MISMATCH REPAIR FACTORS IS CRITICAL FOR MAINTAINING GENOME STABILITY. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/59525.

Council of Science Editors:

Chakraborty U. A DELICATE BALANCE IN MISMATCH REPAIR FACTORS IS CRITICAL FOR MAINTAINING GENOME STABILITY. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59525


Cornell University

21. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 November 26, 2020. 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. 26 Nov 2020.

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 2020 Nov 26]. 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

22. Rinaldi, Vera Da Silva Garcia. Genetically dissecting the meiotic checkpoint active during prophase I in female mice.

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

 Females have a non-renewable number of gametes at birth. These oocytes are extremely sensitive to environmental factors that generate DNA damage. Oocyte death due to… (more)

Subjects/Keywords: teaching; Developmental biology; meiosis; Biology; Genetics; reproduction; DNA-damage checkpoint; fertility; gametogenesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Rinaldi, V. D. S. G. (2017). Genetically dissecting the meiotic checkpoint active during prophase I in female mice. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/56716

Chicago Manual of Style (16th Edition):

Rinaldi, Vera Da Silva Garcia. “Genetically dissecting the meiotic checkpoint active during prophase I in female mice.” 2017. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/56716.

MLA Handbook (7th Edition):

Rinaldi, Vera Da Silva Garcia. “Genetically dissecting the meiotic checkpoint active during prophase I in female mice.” 2017. Web. 26 Nov 2020.

Vancouver:

Rinaldi VDSG. Genetically dissecting the meiotic checkpoint active during prophase I in female mice. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/56716.

Council of Science Editors:

Rinaldi VDSG. Genetically dissecting the meiotic checkpoint active during prophase I in female mice. [Doctoral Dissertation]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/56716


Cornell University

23. Raghavan, Madhura. Balancing Splicing Speed with Fidelity: Role of a Structural Toggle in the RNaseH Domain of Prp8.

Degree: PhD, Genetics and Development, 2018, Cornell University

 The molecular mechanisms by which the spliceosome achieves high fidelity during pre-mRNA splicing while simultaneously maintaining a high rate remain poorly understood. Here, I show… (more)

Subjects/Keywords: Genetics; RNA; Molecular biology; Prp8; splicing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Raghavan, M. (2018). Balancing Splicing Speed with Fidelity: Role of a Structural Toggle in the RNaseH Domain of Prp8. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59715

Chicago Manual of Style (16th Edition):

Raghavan, Madhura. “Balancing Splicing Speed with Fidelity: Role of a Structural Toggle in the RNaseH Domain of Prp8.” 2018. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/59715.

MLA Handbook (7th Edition):

Raghavan, Madhura. “Balancing Splicing Speed with Fidelity: Role of a Structural Toggle in the RNaseH Domain of Prp8.” 2018. Web. 26 Nov 2020.

Vancouver:

Raghavan M. Balancing Splicing Speed with Fidelity: Role of a Structural Toggle in the RNaseH Domain of Prp8. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/59715.

Council of Science Editors:

Raghavan M. Balancing Splicing Speed with Fidelity: Role of a Structural Toggle in the RNaseH Domain of Prp8. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59715

24. Haught, Katrina. SEX SPECIFIC DIFFERENCES IN THE GENOMIC LANDSCAPES OF NAÏVE MALE AND FEMALE CD8+ T-CELLS.

Degree: M.S., Biochemistry, Molecular and Cell Biology, Biochemistry, Molecular and Cell Biology, 2018, Cornell University

 Sex specific differences in the immune response have been demonstrated in organisms from sea urchins to humans. In mammals, these differences have been linked to… (more)

Subjects/Keywords: Molecular biology

…Laboratory, Cornell University). 200,000 cells from n=3 males and n=3 females were immediately… …100ng of RNA by the RNA Sequencing Core (Cornell University). The resulting… 

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Haught, K. (2018). SEX SPECIFIC DIFFERENCES IN THE GENOMIC LANDSCAPES OF NAÏVE MALE AND FEMALE CD8+ T-CELLS. (Masters Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/59537

Chicago Manual of Style (16th Edition):

Haught, Katrina. “SEX SPECIFIC DIFFERENCES IN THE GENOMIC LANDSCAPES OF NAÏVE MALE AND FEMALE CD8+ T-CELLS.” 2018. Masters Thesis, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/59537.

MLA Handbook (7th Edition):

Haught, Katrina. “SEX SPECIFIC DIFFERENCES IN THE GENOMIC LANDSCAPES OF NAÏVE MALE AND FEMALE CD8+ T-CELLS.” 2018. Web. 26 Nov 2020.

Vancouver:

Haught K. SEX SPECIFIC DIFFERENCES IN THE GENOMIC LANDSCAPES OF NAÏVE MALE AND FEMALE CD8+ T-CELLS. [Internet] [Masters thesis]. Cornell University; 2018. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/59537.

Council of Science Editors:

Haught K. SEX SPECIFIC DIFFERENCES IN THE GENOMIC LANDSCAPES OF NAÏVE MALE AND FEMALE CD8+ T-CELLS. [Masters Thesis]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59537

25. Petesch, Steven. Identification Of A Novel, Rapid Mechanism To Alleviate The Nucleosome Barrier To Transcription.

Degree: PhD, Biochemistry, 2012, Cornell University

 To efficiently transcribe genes, RNA Polymerase II (Pol II) must overcome the barrier imposed by nucleosomes and higher order chromatin structure. Many genes, including Drosophila… (more)

Subjects/Keywords: chromatin; transcription; nucleosomes; heat shock; RNA Polymerase II; Poly(ADP-Ribose) Polymerase

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Petesch, S. (2012). Identification Of A Novel, Rapid Mechanism To Alleviate The Nucleosome Barrier To Transcription. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/31387

Chicago Manual of Style (16th Edition):

Petesch, Steven. “Identification Of A Novel, Rapid Mechanism To Alleviate The Nucleosome Barrier To Transcription.” 2012. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/31387.

MLA Handbook (7th Edition):

Petesch, Steven. “Identification Of A Novel, Rapid Mechanism To Alleviate The Nucleosome Barrier To Transcription.” 2012. Web. 26 Nov 2020.

Vancouver:

Petesch S. Identification Of A Novel, Rapid Mechanism To Alleviate The Nucleosome Barrier To Transcription. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/31387.

Council of Science Editors:

Petesch S. Identification Of A Novel, Rapid Mechanism To Alleviate The Nucleosome Barrier To Transcription. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/31387

26. Raghavan, Vandana. INCOMPATIBILITIES IN MISMATCH REPAIR GENES MLH1-PMS1 CONTRIBUTE TO A WIDE RANGE OF MUTATION RATES IN HUMAN ISOLATES OF BAKER'S YEAST.

Degree: PhD, Biochemistry, Molecular and Cell Biology, 2019, Cornell University

 The mismatch repair (MMR) pathway maintains genome stability by repairing mutations incorporated in the genome during replication and recombination. While most microorganisms tend to have… (more)

Subjects/Keywords: Molecular biology; Genetics; Biochemistry; Adaptation; mismatch repair; baker's yeast; clinical isolates; genetic incompatibility; Saccharomyces cerevisiae

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Raghavan, V. (2019). INCOMPATIBILITIES IN MISMATCH REPAIR GENES MLH1-PMS1 CONTRIBUTE TO A WIDE RANGE OF MUTATION RATES IN HUMAN ISOLATES OF BAKER'S YEAST. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/67771

Chicago Manual of Style (16th Edition):

Raghavan, Vandana. “INCOMPATIBILITIES IN MISMATCH REPAIR GENES MLH1-PMS1 CONTRIBUTE TO A WIDE RANGE OF MUTATION RATES IN HUMAN ISOLATES OF BAKER'S YEAST.” 2019. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/67771.

MLA Handbook (7th Edition):

Raghavan, Vandana. “INCOMPATIBILITIES IN MISMATCH REPAIR GENES MLH1-PMS1 CONTRIBUTE TO A WIDE RANGE OF MUTATION RATES IN HUMAN ISOLATES OF BAKER'S YEAST.” 2019. Web. 26 Nov 2020.

Vancouver:

Raghavan V. INCOMPATIBILITIES IN MISMATCH REPAIR GENES MLH1-PMS1 CONTRIBUTE TO A WIDE RANGE OF MUTATION RATES IN HUMAN ISOLATES OF BAKER'S YEAST. [Internet] [Doctoral dissertation]. Cornell University; 2019. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/67771.

Council of Science Editors:

Raghavan V. INCOMPATIBILITIES IN MISMATCH REPAIR GENES MLH1-PMS1 CONTRIBUTE TO A WIDE RANGE OF MUTATION RATES IN HUMAN ISOLATES OF BAKER'S YEAST. [Doctoral Dissertation]. Cornell University; 2019. Available from: http://hdl.handle.net/1813/67771

27. George, Carolyn. Investigation Of Mechanisms That Suppress Non-Allelic Homologous Recombination.

Degree: PhD, Biochemistry, 2013, Cornell University

 Homologous recombination (HR) is a conserved pathway for repair of DNA double strand breaks (DSBs) and stalled or collapsed replication forks, and depends upon recognition… (more)

Subjects/Keywords: genomic instability; non-allelic homologous recombination; heteroduplex rejection

…NIH awarded to Eric Alani and to Cornell University. vii TABLE OF CONTENTS BIOGRAPHICAL… 

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

George, C. (2013). Investigation Of Mechanisms That Suppress Non-Allelic Homologous Recombination. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/34110

Chicago Manual of Style (16th Edition):

George, Carolyn. “Investigation Of Mechanisms That Suppress Non-Allelic Homologous Recombination.” 2013. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/34110.

MLA Handbook (7th Edition):

George, Carolyn. “Investigation Of Mechanisms That Suppress Non-Allelic Homologous Recombination.” 2013. Web. 26 Nov 2020.

Vancouver:

George C. Investigation Of Mechanisms That Suppress Non-Allelic Homologous Recombination. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/34110.

Council of Science Editors:

George C. Investigation Of Mechanisms That Suppress Non-Allelic Homologous Recombination. [Doctoral Dissertation]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/34110

28. Ma, Xin. Statistical Methods For Genome Variant Calling And Population Genetic Inference From Next-Generation Sequencing Data.

Degree: PhD, Statistics, 2012, Cornell University

 Next Generation Sequencing (NGS) technology has been widely adopted as a platform for DNA sequence variation detection and hence, accurate and rapid detection of genome… (more)

Subjects/Keywords: Next Generation Sequencing; SNP Calling Algorithm; Bayesian Model; Statistics Genomics; Population Genetics

…was admitted as a graduate student in department of Statistics of Cornell university in New… …Professor Eric Alani in the Molecular Biology department of Cornell University, who is always… …of Cornell University, for his friendship, encouragement, and numerous fruitful discussions… …from Eric Alani’s group at Cornell University. I am grateful for their fantastic experimental… …Another thank-you note goes out to Adam Siepel and Andre Martins at Cornell University, Ryan… 

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ma, X. (2012). Statistical Methods For Genome Variant Calling And Population Genetic Inference From Next-Generation Sequencing Data. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/29182

Chicago Manual of Style (16th Edition):

Ma, Xin. “Statistical Methods For Genome Variant Calling And Population Genetic Inference From Next-Generation Sequencing Data.” 2012. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/29182.

MLA Handbook (7th Edition):

Ma, Xin. “Statistical Methods For Genome Variant Calling And Population Genetic Inference From Next-Generation Sequencing Data.” 2012. Web. 26 Nov 2020.

Vancouver:

Ma X. Statistical Methods For Genome Variant Calling And Population Genetic Inference From Next-Generation Sequencing Data. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/29182.

Council of Science Editors:

Ma X. Statistical Methods For Genome Variant Calling And Population Genetic Inference From Next-Generation Sequencing Data. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/29182

29. Kingston, Anthony. Membrane Stress Resistance Mechanisms In Bacillus Subtilis.

Degree: PhD, Biochemistry, 2014, Cornell University

 Bacteria exist in environments that can inflict a variety of stresses upon the cell, many of which target the cell membrane. As a result, bacterial… (more)

Subjects/Keywords: cell envelope stress response; extracytoplasmic function sigma factors; antibiotic resistance

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kingston, A. (2014). Membrane Stress Resistance Mechanisms In Bacillus Subtilis. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/36005

Chicago Manual of Style (16th Edition):

Kingston, Anthony. “Membrane Stress Resistance Mechanisms In Bacillus Subtilis.” 2014. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/36005.

MLA Handbook (7th Edition):

Kingston, Anthony. “Membrane Stress Resistance Mechanisms In Bacillus Subtilis.” 2014. Web. 26 Nov 2020.

Vancouver:

Kingston A. Membrane Stress Resistance Mechanisms In Bacillus Subtilis. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/36005.

Council of Science Editors:

Kingston A. Membrane Stress Resistance Mechanisms In Bacillus Subtilis. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/36005

30. Mccloskey, Richard. The Deubiquitylation Enzymes Math-33, Usp-47, And Usp-46 Are Required For Polarity Establishment In Caenorhabditis Elegans.

Degree: PhD, Molecular and Cell Biology, 2012, Cornell University

Subjects/Keywords: polarity; deubiquitylation; deubiquitination

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Mccloskey, R. (2012). The Deubiquitylation Enzymes Math-33, Usp-47, And Usp-46 Are Required For Polarity Establishment In Caenorhabditis Elegans. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/31232

Chicago Manual of Style (16th Edition):

Mccloskey, Richard. “The Deubiquitylation Enzymes Math-33, Usp-47, And Usp-46 Are Required For Polarity Establishment In Caenorhabditis Elegans.” 2012. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/31232.

MLA Handbook (7th Edition):

Mccloskey, Richard. “The Deubiquitylation Enzymes Math-33, Usp-47, And Usp-46 Are Required For Polarity Establishment In Caenorhabditis Elegans.” 2012. Web. 26 Nov 2020.

Vancouver:

Mccloskey R. The Deubiquitylation Enzymes Math-33, Usp-47, And Usp-46 Are Required For Polarity Establishment In Caenorhabditis Elegans. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/31232.

Council of Science Editors:

Mccloskey R. The Deubiquitylation Enzymes Math-33, Usp-47, And Usp-46 Are Required For Polarity Establishment In Caenorhabditis Elegans. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/31232

[1] [2]

.