Showing results (21-30 of 63) with videos related to
Sort By:
Pageof 7
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|January 14, 2014
Key role for CD4 T cells during mixed antibody-mediated rejection of renal allograftsA Gaughan, J Wang, R P Pelletier, et al.Journal of the American Heart Association|January 5, 2019
Systems Genetics Approaches in Rat Identify Novel Genes and Gene Networks Associated With Cardiac ConductionMichiel E Adriaens, Elisabeth M Lodder, Aida Moreno-Moral, et al.Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|August 13, 2009
Implication of long-distance regulation of the HOXA cluster in a patient with postaxial polydactylyElisabeth M Lodder, Bert H Eussen, Daniëlla A C M van Hassel, et al.European Journal of Human Genetics : EJHG|March 16, 2017
Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden deathNajim Lahrouchi, Elisabeth M Lodder, Maria Mansouri, et al.Plos Genetics|December 14, 2012
Dissection of a quantitative trait locus for PR interval duration identifies Tnni3k as a novel modulator of cardiac conductionElisabeth M Lodder, Brendon P Scicluna, Annalisa Milano, et al.The Journal of Pathology|February 10, 2022
The earliest events in BRAF-mutant colorectal cancer: exome sequencing of sessile serrated lesions with a tiny focus dysplasia or cancer reveals recurring mutations in two distinct progression pathwaysArne Gc Bleijenberg, Joep Eg IJspeert, Jos Bg Mulder, et al.Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|December 16, 2020
Two siblings with early repolarization syndrome: clinical and genetic characterization by whole-exome sequencingJohannes Steinfurt, Connie R Bezzina, Jürgen Biermann, et al.International Journal of Cardiology|March 7, 2017
Gain-of-function mutation in SCN5A causes ventricular arrhythmias and early onset atrial fibrillationKrystien V Lieve, Arie O Verkerk, Svitlana Podliesna, et al.Journal of the American Heart Association|July 26, 2017
Switch From Fetal to Adult SCN5A Isoform in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Unmasks the Cellular Phenotype of a Conduction Disease-Causing MutationChristiaan C Veerman, Isabella Mengarelli, Elisabeth M Lodder, et al.BMC Public Health|May 12, 2007
Referral patterns of children with poor growth in primary health careFloor K Grote, Wilma Oostdijk, Sabine M P F De Muinck Keizer-Schrama, et al.Pageof 7