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Clinical Genetics|January 24, 2015
X-chromosomal inactivation directly influences the phenotypic manifestation of X-linked protoporphyriaV Brancaleoni, M Balwani, F Granata, et al.Human Gene Therapy|July 31, 1999
Correction of enzymatic and lysosomal storage defects in Fabry mice by adenovirus-mediated gene transferR J Ziegler, N S Yew, C Li, et al.Journal of Medical Genetics|May 3, 2005
A new syndrome, congenital extraocular muscle fibrosis with ulnar hand anomalies, maps to chromosome 21qterT Tukel, A Uzumcu, A Gezer, et al.The Biochemical Journal|December 15, 1989
Non-invasive detection of protein metabolism in vivo by n.m.r. spectroscopy. Application of a novel 19F-containing residualizing labelA Daugherty, N N Becker, L A Scherrer, et al.Diabetologia|July 16, 2003
Prevention of retinal capillary basement membrane thickening in diabetic dogs by a non-steroidal anti-inflammatory drugT A Gardiner, H R Anderson, T Degenhardt, et al.Proceedings of the National Academy of Sciences of the United States of America|April 1, 1990
Restoration of normal lysosomal function in mucopolysaccharidosis type VII cells by retroviral vector-mediated gene transferJ H Wolfe, E H Schuchman, L E Stramm, et al.Environmental Research|May 21, 1998
Effect of the delta-aminolevulinate dehydratase polymorphism on the accumulation of lead in bone and blood in lead smelter workersD E Fleming, D R Chettle, J G Wetmur, et al.Analytical Biochemistry|July 16, 1999
Quantification of N-(glucitol)ethanolamine and N-(carboxymethyl)serine: two products of nonenzymatic modification of aminophospholipids formed in vivoW C Fountain, J R Requena, A J Jenkins, et al.Prenatal Diagnosis|May 1, 1992
Cytogenetic results from the U.S. Collaborative Study on CVSD H Ledbetter, J M Zachary, J L Simpson, et al.The Journal of Clinical Investigation|June 1, 1993
Accumulation of Maillard reaction products in skin collagen in diabetes and agingD G Dyer, J A Dunn, S R Thorpe, et al.Pageof 40