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A Pater

Showing results (111-120 of 125) with videos related to

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Frontiers in Genetics|September 6, 2023
Unraveling haplotype errors in the DFNA33 locusBarbara Vona, Sabrina Regele, Aboulfazl Rad, et al.
Biorxiv : the Preprint Server for Biology|February 20, 2025
An HIV-1 Reference EpitranscriptomeMichael S Bosmeny, Adrian A Pater, Li Zhang, et al.
The Journal of Biological Chemistry|April 14, 2023
Binding to the conserved and stably folded guide RNA pseudoknot induces Cas12a conformational changes during ribonucleoprotein assemblySruthi Sudhakar, Christopher L Barkau, Ramadevi Chilamkurthy, et al.
Nucleic Acids Research|March 19, 2026
A nanopore-based HIV-1 reference epitranscriptomeMichael S Bosmeny, Adrian A Pater, Li Zhang, et al.
European Journal of Human Genetics : EJHG|May 30, 2020
The genetic architecture of Stargardt macular dystrophy (STGD1): a longitudinal 40-year study in a genetic isolateJane S Green, Darren D O'Rielly, Justin A Pater, et al.
BMC Medical Genetics|May 4, 2019
Novel Usher syndrome pathogenic variants identified in cases with hearing and vision lossJustin A Pater, Jane Green, Darren D O'Rielly, et al.
Human Genetics|November 14, 2016
A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effectJustin A Pater, Tammy Benteau, Anne Griffin, et al.
Biorxiv : the Preprint Server for Biology|January 23, 2026
A guide RNA repeat checkpoint steers CRISPR-Cas9 catalysisRamadevi Chilamkurthy, Sruthi Sudhakar, Adrian A Pater, et al.
Molecular Genetics & Genomic Medicine|November 30, 2019
A dominant RAD51C pathogenic splicing variant predisposes to breast and ovarian cancer in the Newfoundland population due to founder effectLesa M Dawson, Kerri N Smith, Salem Werdyani, et al.
Antioxidants (Basel, Switzerland)|November 27, 2021
Tryptophan Metabolism in Bipolar Disorder in a Longitudinal SettingFrederike T Fellendorf, Johanna M Gostner, Melanie Lenger, et al.
Pageof 13

Showing results (111-120 of 125) with videos related to

Sort By:
Pageof 13
Frontiers in Genetics|September 6, 2023
Unraveling haplotype errors in the DFNA33 locusBarbara Vona, Sabrina Regele, Aboulfazl Rad, et al.
Biorxiv : the Preprint Server for Biology|February 20, 2025
An HIV-1 Reference EpitranscriptomeMichael S Bosmeny, Adrian A Pater, Li Zhang, et al.
The Journal of Biological Chemistry|April 14, 2023
Binding to the conserved and stably folded guide RNA pseudoknot induces Cas12a conformational changes during ribonucleoprotein assemblySruthi Sudhakar, Christopher L Barkau, Ramadevi Chilamkurthy, et al.
Nucleic Acids Research|March 19, 2026
A nanopore-based HIV-1 reference epitranscriptomeMichael S Bosmeny, Adrian A Pater, Li Zhang, et al.
European Journal of Human Genetics : EJHG|May 30, 2020
The genetic architecture of Stargardt macular dystrophy (STGD1): a longitudinal 40-year study in a genetic isolateJane S Green, Darren D O'Rielly, Justin A Pater, et al.
BMC Medical Genetics|May 4, 2019
Novel Usher syndrome pathogenic variants identified in cases with hearing and vision lossJustin A Pater, Jane Green, Darren D O'Rielly, et al.
Human Genetics|November 14, 2016
A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effectJustin A Pater, Tammy Benteau, Anne Griffin, et al.
Biorxiv : the Preprint Server for Biology|January 23, 2026
A guide RNA repeat checkpoint steers CRISPR-Cas9 catalysisRamadevi Chilamkurthy, Sruthi Sudhakar, Adrian A Pater, et al.
Molecular Genetics & Genomic Medicine|November 30, 2019
A dominant RAD51C pathogenic splicing variant predisposes to breast and ovarian cancer in the Newfoundland population due to founder effectLesa M Dawson, Kerri N Smith, Salem Werdyani, et al.
Antioxidants (Basel, Switzerland)|November 27, 2021
Tryptophan Metabolism in Bipolar Disorder in a Longitudinal SettingFrederike T Fellendorf, Johanna M Gostner, Melanie Lenger, et al.
Pageof 13