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Journal of Inherited Metabolic Disease|May 23, 2022
A promoter variant in the OTC gene associated with late and variable age of onset hyperammonemiaSangwoo T Han, Katherine J Anderson, Hans T Bjornsson, et al.Mitochondrion|August 27, 2005
Cell cycle dependent morphology changes and associated mitochondrial DNA redistribution in mitochondria of human cell linesDaciana H Margineantu, W Gregory Cox, Linda Sundell, et al.Springerplus|May 17, 2014
The ATRX cDNA is prone to bacterial IS10 element insertions that alter its structureDavid Valle-García, Lyra M Griffiths, Michael A Dyer, et al.Nucleic Acids Research|December 26, 2001
Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disordersAda Hamosh, Alan F Scott, Joanna Amberger, et al.Molecular and Cellular Biology|May 25, 2002
PEX11 beta deficiency is lethal and impairs neuronal migration but does not abrogate peroxisome functionXiaoling Li, Eveline Baumgart, James C Morrell, et al.Proceedings of the National Academy of Sciences of the United States of America|May 16, 2007
The human disease networkKwang-Il Goh, Michael E Cusick, David Valle, et al.Amino Acids|May 29, 2008
Functional genomics and SNP analysis of human genes encoding proline metabolic enzymesChien-An A Hu, D Bart Williams, Siqin Zhaorigetu, et al.Frontiers in Pharmacology|March 22, 2017
Skeletal Dysplasias: Growing Therapy for Growing BonesAngie C Jelin, Elizabeth O'Hare, Karin Blakemore, et al.American Journal of Human Genetics|April 29, 2005
Alternative splicing suggests extended function of PEX26 in peroxisome biogenesisSabine Weller, Ivelisse Cajigas, James Morrell, et al.Journal of Occupational Medicine and Toxicology (London, England)|May 5, 2022
Forecasting the rate of hand injuries in SingaporeLiau Zi Qiang Glen, Joel Yat Seng Wong, Wei Xuan Tay, et al.Pageof 15