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

R Barton

Showing results (631-640 of 672) with videos related to

Pageof 68
Sort By:
Cold Spring Harbor Molecular Case Studies|January 5, 2017
Histiocytoid cardiomyopathy and microphthalmia with linear skin defects syndrome: phenotypes linked by truncating variants in <i>NDUFB11</i>Gillian Rea, Tessa Homfray, Jan Till, et al.
Science (New York, N.Y.)|December 9, 2017
Aging and neurodegeneration are associated with increased mutations in single human neuronsMichael A Lodato, Rachel E Rodin, Craig L Bohrson, et al.
Circulation|August 30, 2021
New Variant With a Previously Unrecognized Mechanism of Pathogenicity in Hypertrophic CardiomyopathyYasmine Aguib, Mona Allouba, Roddy Walsh, et al.
Cardiovascular Research|October 9, 2024
Interleukin 11 therapy causes acute left ventricular dysfunctionMark Sweeney, Katie O'Fee, Chelsie Villanueva-Hayes, et al.
American Journal of Obstetrics and Gynecology|April 29, 2023
Care plan for individuals at risk for preeclampsia: shared approach to education, strategies for prevention, surveillance, and follow-upJames M Roberts, Tekoa L King, John R Barton, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 26, 2018
CardioClassifier: disease- and gene-specific computational decision support for clinical genome interpretationNicola Whiffin, Roddy Walsh, Risha Govind, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2018
A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathyClaire Horvat, Renee Johnson, Lien Lam, et al.
The Journal of Clinical Investigation|August 8, 2017
NBEAL2 is required for neutrophil and NK cell function and pathogen defenseJohn M Sowerby, David C Thomas, Simon Clare, et al.
American Journal of Human Genetics|August 31, 2023
The penetrance of rare variants in cardiomyopathy-associated genes: A cross-sectional approach to estimating penetrance for secondary findingsKathryn A McGurk, Xiaolei Zhang, Pantazis Theotokis, et al.
Physical Review Letters|August 2, 2014
Comley et al. replyA J Comley, B R Maddox, R E Rudd, et al.
Pageof 68

Showing results (631-640 of 672) with videos related to

Sort By:
Pageof 68
Cold Spring Harbor Molecular Case Studies|January 5, 2017
Histiocytoid cardiomyopathy and microphthalmia with linear skin defects syndrome: phenotypes linked by truncating variants in <i>NDUFB11</i>Gillian Rea, Tessa Homfray, Jan Till, et al.
Science (New York, N.Y.)|December 9, 2017
Aging and neurodegeneration are associated with increased mutations in single human neuronsMichael A Lodato, Rachel E Rodin, Craig L Bohrson, et al.
Circulation|August 30, 2021
New Variant With a Previously Unrecognized Mechanism of Pathogenicity in Hypertrophic CardiomyopathyYasmine Aguib, Mona Allouba, Roddy Walsh, et al.
Cardiovascular Research|October 9, 2024
Interleukin 11 therapy causes acute left ventricular dysfunctionMark Sweeney, Katie O'Fee, Chelsie Villanueva-Hayes, et al.
American Journal of Obstetrics and Gynecology|April 29, 2023
Care plan for individuals at risk for preeclampsia: shared approach to education, strategies for prevention, surveillance, and follow-upJames M Roberts, Tekoa L King, John R Barton, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 26, 2018
CardioClassifier: disease- and gene-specific computational decision support for clinical genome interpretationNicola Whiffin, Roddy Walsh, Risha Govind, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2018
A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathyClaire Horvat, Renee Johnson, Lien Lam, et al.
The Journal of Clinical Investigation|August 8, 2017
NBEAL2 is required for neutrophil and NK cell function and pathogen defenseJohn M Sowerby, David C Thomas, Simon Clare, et al.
American Journal of Human Genetics|August 31, 2023
The penetrance of rare variants in cardiomyopathy-associated genes: A cross-sectional approach to estimating penetrance for secondary findingsKathryn A McGurk, Xiaolei Zhang, Pantazis Theotokis, et al.
Physical Review Letters|August 2, 2014
Comley et al. replyA J Comley, B R Maddox, R E Rudd, et al.
Pageof 68