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

Chad A Shaw

Showing results (41-50 of 171) with videos related to

Pageof 18
Sort By:
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 19, 2023
Clinical genome sequencing: Three years' experience at a tertiary children's hospitalRunjun D Kumar, Lisa F Saba, Haley Streff, et al.
American Journal of Human Genetics|May 3, 2016
Integrative Multi-omic Analysis of Human Platelet eQTLs Reveals Alternative Start Site in Mitofusin 2Lukas M Simon, Edward S Chen, Leonard C Edelstein, et al.
Plos Genetics|April 5, 2013
Ataxin1L is a regulator of HSC function highlighting the utility of cross-tissue comparisons for gene discoveryJuliette J Kahle, George P Souroullas, Peng Yu, et al.
Plos One|March 15, 2014
Gene sequence variability of the three surface proteins of human respiratory syncytial virus (HRSV) in TexasLorena I Tapia, Chad A Shaw, Letisha O Aideyan, et al.
European Journal of Human Genetics : EJHG|September 5, 2025
Clinical exome sequencing efficacy and phenotypic expansions involving non-isolated congenital anomalies of kidney and urinary tract (CAKUT+)E Andres Rivera-Munoz, Xiaonan E Zhao, Jill A Rosenfeld, et al.
American Journal of Human Genetics|August 19, 2007
Oral curcumin mitigates the clinical and neuropathologic phenotype of the Trembler-J mouse: a potential therapy for inherited neuropathyMehrdad Khajavi, Kensuke Shiga, Wojciech Wiszniewski, et al.
Journal of Cellular Physiology|May 1, 2008
Brachy-syndactyly caused by loss of Sfrp2 functionRoy Morello, Terry K Bertin, Silke Schlaubitz, et al.
Science (New York, N.Y.)|August 15, 2015
DNA REPAIR. Mus81 and converging forks limit the mutagenicity of replication fork breakageRyan Mayle, Ian M Campbell, Christine R Beck, et al.
American Journal of Medical Genetics. Part A|April 17, 2008
Low-level mosaicism of trisomy 14: phenotypic and molecular characterizationMarwan Shinawi, Lina Shao, Linda Jo Bone Jeng, et al.
BMC Medical Genomics|April 24, 2014
Testicular sex cord-stromal tumor in a boy with 2q37 deletion syndromeYasunari Sakai, Ryota Souzaki, Hidetaka Yamamoto, et al.
Pageof 18

Showing results (41-50 of 171) with videos related to

Sort By:
Pageof 18
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 19, 2023
Clinical genome sequencing: Three years' experience at a tertiary children's hospitalRunjun D Kumar, Lisa F Saba, Haley Streff, et al.
American Journal of Human Genetics|May 3, 2016
Integrative Multi-omic Analysis of Human Platelet eQTLs Reveals Alternative Start Site in Mitofusin 2Lukas M Simon, Edward S Chen, Leonard C Edelstein, et al.
Plos Genetics|April 5, 2013
Ataxin1L is a regulator of HSC function highlighting the utility of cross-tissue comparisons for gene discoveryJuliette J Kahle, George P Souroullas, Peng Yu, et al.
Plos One|March 15, 2014
Gene sequence variability of the three surface proteins of human respiratory syncytial virus (HRSV) in TexasLorena I Tapia, Chad A Shaw, Letisha O Aideyan, et al.
European Journal of Human Genetics : EJHG|September 5, 2025
Clinical exome sequencing efficacy and phenotypic expansions involving non-isolated congenital anomalies of kidney and urinary tract (CAKUT+)E Andres Rivera-Munoz, Xiaonan E Zhao, Jill A Rosenfeld, et al.
American Journal of Human Genetics|August 19, 2007
Oral curcumin mitigates the clinical and neuropathologic phenotype of the Trembler-J mouse: a potential therapy for inherited neuropathyMehrdad Khajavi, Kensuke Shiga, Wojciech Wiszniewski, et al.
Journal of Cellular Physiology|May 1, 2008
Brachy-syndactyly caused by loss of Sfrp2 functionRoy Morello, Terry K Bertin, Silke Schlaubitz, et al.
Science (New York, N.Y.)|August 15, 2015
DNA REPAIR. Mus81 and converging forks limit the mutagenicity of replication fork breakageRyan Mayle, Ian M Campbell, Christine R Beck, et al.
American Journal of Medical Genetics. Part A|April 17, 2008
Low-level mosaicism of trisomy 14: phenotypic and molecular characterizationMarwan Shinawi, Lina Shao, Linda Jo Bone Jeng, et al.
BMC Medical Genomics|April 24, 2014
Testicular sex cord-stromal tumor in a boy with 2q37 deletion syndromeYasunari Sakai, Ryota Souzaki, Hidetaka Yamamoto, et al.
Pageof 18