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

Thomas Meitinger

Showing results (211-220 of 508) with videos related to

Pageof 51
Sort By:
Human Molecular Genetics|May 5, 2022
Suleiman-El-Hattab syndrome: a histone modification disorder caused by TASP1 deficiencyKorbinian M Riedhammer, Anna L Burgemeister, Vincent Cantagrel, et al.
Plos Biology|June 23, 2004
Integrative analysis of the mitochondrial proteome in yeastHolger Prokisch, Curt Scharfe, David G Camp, et al.
European Heart Journal|January 21, 2011
Mutations in the mitochondrial thioredoxin reductase gene TXNRD2 cause dilated cardiomyopathyDirk Sibbing, Arne Pfeufer, Tamara Perisic, et al.
Annals of Neurology|May 29, 2009
Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic strokeAndreas Gschwendtner, Steve Bevan, John W Cole, et al.
International Journal of Cancer|October 27, 2009
Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patientsKari Hemminki, Bertram Müller-Myhsok, Peter Lichtner, et al.
American Journal of Human Genetics|September 13, 2016
NAXE Mutations Disrupt the Cellular NAD(P)HX Repair System and Cause a Lethal Neurometabolic Disorder of Early ChildhoodLaura S Kremer, Katharina Danhauser, Diran Herebian, et al.
Clinical Epigenetics|December 28, 2018
Analysis of repeated leukocyte DNA methylation assessments reveals persistent epigenetic alterations after an incident myocardial infarctionCavin K Ward-Caviness, Golareh Agha, Brian H Chen, et al.
Brain : a Journal of Neurology|December 14, 2020
De novo stop-loss variants in CLDN11 cause hypomyelinating leukodystrophyKorbinian M Riedhammer, Sylvia Stockler, Rafal Ploski, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN projectFabio Marroni, Arne Pfeufer, Yurii S Aulchenko, et al.
Brain : a Journal of Neurology|December 24, 2016
CAD mutations and uridine-responsive epileptic encephalopathyJohannes Koch, Johannes A Mayr, Bader Alhaddad, et al.
Pageof 51

Showing results (211-220 of 508) with videos related to

Sort By:
Pageof 51
Human Molecular Genetics|May 5, 2022
Suleiman-El-Hattab syndrome: a histone modification disorder caused by TASP1 deficiencyKorbinian M Riedhammer, Anna L Burgemeister, Vincent Cantagrel, et al.
Plos Biology|June 23, 2004
Integrative analysis of the mitochondrial proteome in yeastHolger Prokisch, Curt Scharfe, David G Camp, et al.
European Heart Journal|January 21, 2011
Mutations in the mitochondrial thioredoxin reductase gene TXNRD2 cause dilated cardiomyopathyDirk Sibbing, Arne Pfeufer, Tamara Perisic, et al.
Annals of Neurology|May 29, 2009
Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic strokeAndreas Gschwendtner, Steve Bevan, John W Cole, et al.
International Journal of Cancer|October 27, 2009
Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patientsKari Hemminki, Bertram Müller-Myhsok, Peter Lichtner, et al.
American Journal of Human Genetics|September 13, 2016
NAXE Mutations Disrupt the Cellular NAD(P)HX Repair System and Cause a Lethal Neurometabolic Disorder of Early ChildhoodLaura S Kremer, Katharina Danhauser, Diran Herebian, et al.
Clinical Epigenetics|December 28, 2018
Analysis of repeated leukocyte DNA methylation assessments reveals persistent epigenetic alterations after an incident myocardial infarctionCavin K Ward-Caviness, Golareh Agha, Brian H Chen, et al.
Brain : a Journal of Neurology|December 14, 2020
De novo stop-loss variants in CLDN11 cause hypomyelinating leukodystrophyKorbinian M Riedhammer, Sylvia Stockler, Rafal Ploski, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN projectFabio Marroni, Arne Pfeufer, Yurii S Aulchenko, et al.
Brain : a Journal of Neurology|December 24, 2016
CAD mutations and uridine-responsive epileptic encephalopathyJohannes Koch, Johannes A Mayr, Bader Alhaddad, et al.
Pageof 51