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Thomas Meitinger

Showing results (191-200 of 508) with videos related to

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Nature Communications|January 12, 2022
MicroRNA-365 regulates human cardiac action potential durationDena Esfandyari, Bio Maria Ghéo Idrissou, Konstantin Hennis, et al.
American Journal of Human Genetics|July 5, 2014
Targeted resequencing and systematic in vivo functional testing identifies rare variants in MEIS1 as significant contributors to restless legs syndromeEva C Schulte, Maria Kousi, Perciliz L Tan, et al.
BMC Medical Genetics|June 7, 2007
The genetic study of three population microisolates in South Tyrol (MICROS): study design and epidemiological perspectivesCristian Pattaro, Fabio Marroni, Alice Riegler, et al.
American Journal of Human Genetics|January 26, 2016
Bi-allelic Truncating Mutations in TANGO2 Cause Infancy-Onset Recurrent Metabolic Crises with EncephalocardiomyopathyLaura S Kremer, Felix Distelmaier, Bader Alhaddad, et al.
American Journal of Human Genetics|July 16, 2013
ELAC2 mutations cause a mitochondrial RNA processing defect associated with hypertrophic cardiomyopathyTobias B Haack, Robert Kopajtich, Peter Freisinger, et al.
Heart Rhythm|November 9, 2010
Lack of replication in polymorphisms reported to be associated with atrial fibrillationMoritz F Sinner, Steven A Lubitz, Arne Pfeufer, et al.
Circulation. Cardiovascular Genetics|March 11, 2017
Identification of Cadherin 2 (<i>CDH2</i>) Mutations in Arrhythmogenic Right Ventricular CardiomyopathyBongani M Mayosi, Maryam Fish, Gasnat Shaboodien, et al.
American Journal of Human Genetics|December 27, 2008
A genome-wide association study identifies three loci associated with mean platelet volumeChrista Meisinger, Holger Prokisch, Christian Gieger, et al.
Oxidative Medicine and Cellular Longevity|August 15, 2017
Combined Respiratory Chain Deficiency and <i>UQCC2</i> Mutations in Neonatal Encephalomyopathy: Defective Supercomplex Assembly in Complex III DeficienciesRené G Feichtinger, Michaela Brunner-Krainz, Bader Alhaddad, et al.
European Journal of Human Genetics : EJHG|January 19, 2018
Compound heterozygous SPATA5 variants in four families and functional studies of SPATA5 deficiencySanna Puusepp, Reka Kovacs-Nagy, Bader Alhaddad, et al.
Pageof 51

Showing results (191-200 of 508) with videos related to

Sort By:
Pageof 51
Nature Communications|January 12, 2022
MicroRNA-365 regulates human cardiac action potential durationDena Esfandyari, Bio Maria Ghéo Idrissou, Konstantin Hennis, et al.
American Journal of Human Genetics|July 5, 2014
Targeted resequencing and systematic in vivo functional testing identifies rare variants in MEIS1 as significant contributors to restless legs syndromeEva C Schulte, Maria Kousi, Perciliz L Tan, et al.
BMC Medical Genetics|June 7, 2007
The genetic study of three population microisolates in South Tyrol (MICROS): study design and epidemiological perspectivesCristian Pattaro, Fabio Marroni, Alice Riegler, et al.
American Journal of Human Genetics|January 26, 2016
Bi-allelic Truncating Mutations in TANGO2 Cause Infancy-Onset Recurrent Metabolic Crises with EncephalocardiomyopathyLaura S Kremer, Felix Distelmaier, Bader Alhaddad, et al.
American Journal of Human Genetics|July 16, 2013
ELAC2 mutations cause a mitochondrial RNA processing defect associated with hypertrophic cardiomyopathyTobias B Haack, Robert Kopajtich, Peter Freisinger, et al.
Heart Rhythm|November 9, 2010
Lack of replication in polymorphisms reported to be associated with atrial fibrillationMoritz F Sinner, Steven A Lubitz, Arne Pfeufer, et al.
Circulation. Cardiovascular Genetics|March 11, 2017
Identification of Cadherin 2 (<i>CDH2</i>) Mutations in Arrhythmogenic Right Ventricular CardiomyopathyBongani M Mayosi, Maryam Fish, Gasnat Shaboodien, et al.
American Journal of Human Genetics|December 27, 2008
A genome-wide association study identifies three loci associated with mean platelet volumeChrista Meisinger, Holger Prokisch, Christian Gieger, et al.
Oxidative Medicine and Cellular Longevity|August 15, 2017
Combined Respiratory Chain Deficiency and <i>UQCC2</i> Mutations in Neonatal Encephalomyopathy: Defective Supercomplex Assembly in Complex III DeficienciesRené G Feichtinger, Michaela Brunner-Krainz, Bader Alhaddad, et al.
European Journal of Human Genetics : EJHG|January 19, 2018
Compound heterozygous SPATA5 variants in four families and functional studies of SPATA5 deficiencySanna Puusepp, Reka Kovacs-Nagy, Bader Alhaddad, et al.
Pageof 51