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Nature Communications
|
January 12, 2022
MicroRNA-365 regulates human cardiac action potential duration
Dena 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 syndrome
Eva 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 perspectives
Cristian 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 Encephalocardiomyopathy
Laura 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 cardiomyopathy
Tobias B Haack, Robert Kopajtich, Peter Freisinger, et al.
Heart Rhythm
|
November 9, 2010
Lack of replication in polymorphisms reported to be associated with atrial fibrillation
Moritz 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 Cardiomyopathy
Bongani 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 volume
Christa 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 Deficiencies
René 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 deficiency
Sanna Puusepp, Reka Kovacs-Nagy, Bader Alhaddad, et al.
Page
of 51
Search research articles
Search
Showing results (191-200 of 508) with videos related to
Sort By:
Page
of 51
Nature Communications
|
January 12, 2022
MicroRNA-365 regulates human cardiac action potential duration
Dena 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 syndrome
Eva 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 perspectives
Cristian 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 Encephalocardiomyopathy
Laura 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 cardiomyopathy
Tobias B Haack, Robert Kopajtich, Peter Freisinger, et al.
Heart Rhythm
|
November 9, 2010
Lack of replication in polymorphisms reported to be associated with atrial fibrillation
Moritz 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 Cardiomyopathy
Bongani 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 volume
Christa 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 Deficiencies
René 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 deficiency
Sanna Puusepp, Reka Kovacs-Nagy, Bader Alhaddad, et al.
Page
of 51