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

C Gabriel

Showing results (261-270 of 267) with videos related to

Pageof 27
Sort By:
You have reached the last page of results.This site can display upto 267 results.
Nature Genetics|October 6, 2015
MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebratesAnne Guimier, George C Gabriel, Fanny Bajolle, et al.
Cell Reports. Medicine|March 4, 2022
Genetic resiliency associated with dominant lethal <i>TPM1</i> mutation causing atrial septal defect with high heritabilityPolakit Teekakirikul, Wenjuan Zhu, Xinxiu Xu, et al.
American Journal of Human Genetics|September 6, 2014
CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formationRim Hjeij, Alexandros Onoufriadis, Christopher M Watson, et al.
Kidney International|March 1, 2022
Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tractJohannes Münch, Marie Engesser, Ria Schönauer, et al.
HGG Advances|December 10, 2021
Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart diseasePolakit Teekakirikul, Wenjuan Zhu, George C Gabriel, et al.
Vox Sanguinis|March 25, 2014
Bacterial contamination in platelet concentratesR N I Pietersz, H W Reesink, S Panzer, et al.
Genome Biology|July 18, 2018
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6Bram P Prins, Timothy J Mead, Jennifer A Brody, et al.
Pageof 27

Showing results (261-270 of 267) with videos related to

Sort By:
Pageof 27
You have reached the last page of results.This site can display upto 267 results.
Nature Genetics|October 6, 2015
MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebratesAnne Guimier, George C Gabriel, Fanny Bajolle, et al.
Cell Reports. Medicine|March 4, 2022
Genetic resiliency associated with dominant lethal <i>TPM1</i> mutation causing atrial septal defect with high heritabilityPolakit Teekakirikul, Wenjuan Zhu, Xinxiu Xu, et al.
American Journal of Human Genetics|September 6, 2014
CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formationRim Hjeij, Alexandros Onoufriadis, Christopher M Watson, et al.
Kidney International|March 1, 2022
Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tractJohannes Münch, Marie Engesser, Ria Schönauer, et al.
HGG Advances|December 10, 2021
Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart diseasePolakit Teekakirikul, Wenjuan Zhu, George C Gabriel, et al.
Vox Sanguinis|March 25, 2014
Bacterial contamination in platelet concentratesR N I Pietersz, H W Reesink, S Panzer, et al.
Genome Biology|July 18, 2018
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6Bram P Prins, Timothy J Mead, Jennifer A Brody, et al.
Pageof 27