Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

D Huff

Showing results (201-210 of 225) with videos related to

Pageof 23
Sort By:
Proceedings of the National Academy of Sciences of the United States of America|April 12, 2022
Hereditary retinoblastoma iPSC model reveals aberrant spliceosome function driving bone malignanciesJian Tu, Zijun Huo, Yao Yu, et al.
Human Molecular Genetics|January 10, 2019
Functionally oriented analysis of cardiometabolic traits in a trans-ethnic sampleLauren E Petty, Heather M Highland, Eric R Gamazon, et al.
JAMA Oncology|June 21, 2019
Association Between Birth Defects and Cancer Risk Among Children and Adolescents in a Population-Based Assessment of 10 Million Live BirthsPhilip J Lupo, Jeremy M Schraw, Tania A Desrosiers, et al.
American Journal of Human Genetics|June 25, 2011
Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiencyAlan F Rope, Kai Wang, Rune Evjenth, et al.
Plos One|July 25, 2019
Climate vulnerability assessment for Pacific salmon and steelhead in the California Current Large Marine EcosystemLisa G Crozier, Michelle M McClure, Tim Beechie, et al.
Medrxiv : the Preprint Server for Health Sciences|March 27, 2026
Local ancestry modulates gene expression: shifting our understanding of genetic regulation and disease association within and across populationsHung-Hsin Chen, Yanwei Cai, MariaElisa Graff, et al.
Nature Communications|March 27, 2023
Rewired m<sup>6</sup>A epitranscriptomic networks link mutant p53 to neoplastic transformationAn Xu, Mo Liu, Mo-Fan Huang, et al.
Blood|May 24, 2013
Mutational and structural analysis of diffuse large B-cell lymphoma using whole-genome sequencingRyan D Morin, Karen Mungall, Erin Pleasance, et al.
Cancer Discovery|July 23, 2014
Rare mutations in RINT1 predispose carriers to breast and Lynch syndrome-spectrum cancersDaniel J Park, Kayoko Tao, Florence Le Calvez-Kelm, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 11, 2019
ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorderLloyd B Williams, Asif Javed, Amin Sabri, et al.
Pageof 23

Showing results (201-210 of 225) with videos related to

Sort By:
Pageof 23
Proceedings of the National Academy of Sciences of the United States of America|April 12, 2022
Hereditary retinoblastoma iPSC model reveals aberrant spliceosome function driving bone malignanciesJian Tu, Zijun Huo, Yao Yu, et al.
Human Molecular Genetics|January 10, 2019
Functionally oriented analysis of cardiometabolic traits in a trans-ethnic sampleLauren E Petty, Heather M Highland, Eric R Gamazon, et al.
JAMA Oncology|June 21, 2019
Association Between Birth Defects and Cancer Risk Among Children and Adolescents in a Population-Based Assessment of 10 Million Live BirthsPhilip J Lupo, Jeremy M Schraw, Tania A Desrosiers, et al.
American Journal of Human Genetics|June 25, 2011
Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiencyAlan F Rope, Kai Wang, Rune Evjenth, et al.
Plos One|July 25, 2019
Climate vulnerability assessment for Pacific salmon and steelhead in the California Current Large Marine EcosystemLisa G Crozier, Michelle M McClure, Tim Beechie, et al.
Medrxiv : the Preprint Server for Health Sciences|March 27, 2026
Local ancestry modulates gene expression: shifting our understanding of genetic regulation and disease association within and across populationsHung-Hsin Chen, Yanwei Cai, MariaElisa Graff, et al.
Nature Communications|March 27, 2023
Rewired m<sup>6</sup>A epitranscriptomic networks link mutant p53 to neoplastic transformationAn Xu, Mo Liu, Mo-Fan Huang, et al.
Blood|May 24, 2013
Mutational and structural analysis of diffuse large B-cell lymphoma using whole-genome sequencingRyan D Morin, Karen Mungall, Erin Pleasance, et al.
Cancer Discovery|July 23, 2014
Rare mutations in RINT1 predispose carriers to breast and Lynch syndrome-spectrum cancersDaniel J Park, Kayoko Tao, Florence Le Calvez-Kelm, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 11, 2019
ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorderLloyd B Williams, Asif Javed, Amin Sabri, et al.
Pageof 23