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Genomics|May 1, 1993
Yeast artificial chromosome cloning in the glycerol kinase and adrenal hypoplasia congenita region of Xp21K C Worley, K A Ellison, Y H Zhang, et al.Physiological Genomics|May 19, 2025
Genetic mapping of electrocardiographic parameters in BXD strains reveals Chromosome 3 loci to be associated with cardiac repolarization abnormalitiesBuyan-Ochir Orgil, Fuyi Xu, Ning Li, et al.Journal of Affective Disorders|January 31, 2017
Test-retest reliability and validity of a frustration paradigm and irritability measuresWan-Ling Tseng, Elizabeth Moroney, Laura Machlin, et al.Blood|May 1, 2024
Impact of hematopoietic cell transplantation on myocardial fibrosis in young patients with sickle cell diseaseAkshay Sharma, Subodh Selukar, Yu Bi, et al.American Journal of Physiology. Heart and Circulatory Physiology|April 16, 2021
Deficiency in nebulin repeats of sarcomeric nebulette is detrimental for cardiomyocyte tolerance to exercise and biomechanical stressRamona M Vejandla, Buyan-Ochir Orgil, Neely R Alberson, et al.American Journal of Human Genetics|June 10, 2008
Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephalyErich Roessler, Maia V Ouspenskaia, Jayaprakash D Karkera, et al.Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc|February 15, 2002
Variable expression of long QT syndrome among gene carriers from families with five different HERG mutationsJesaia Benhorin, Arthur J Moss, Matthew Bak, et al.The Journal of Craniofacial Surgery|August 7, 1998
Intracranial volume in craniosynostotic rabbitsM P Mooney, A M Burrows, W Wigginton, et al.Journal of Molecular and Cellular Cardiology|May 30, 2020
Identifying modifier genes for hypertrophic cardiomyopathyYuanjian Chen, Fuyi Xu, Undral Munkhsaikhan, et al.BMC Medical Genetics|February 16, 2005
SNP genotyping to screen for a common deletion in CHARGE syndromeSeema R Lalani, Arsalan M Safiullah, Susan D Fernbach, et al.Pageof 44