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Somatic Cell and Molecular Genetics|November 1, 1996
Delivery of cytosolic liver arginase into the mitochondrial matrix space: a possible novel site for gene replacement therapyP B Wissmann, B K Goodman, J G Vockley, et al.Pediatrics|November 1, 1976
Ketonic diet in the management of pyruvate dehydrogenase deficiencyR E Falk, S D Cederbaum, J P Blass, et al.Pediatric Research|June 11, 1992
Deletion in blood mitochondrial DNA in Kearns-Sayre syndromeN Fischel-Ghodsian, M C Bohlman, T R Prezant, et al.Molecular Genetics and Metabolism|October 6, 1998
Molecular basis of hyperargininemia: structure-function consequences of mutations in human liver arginaseD E Ash, L R Scolnick, Z F Kanyo, et al.Archives of Biochemistry and Biophysics|July 1, 1987
Regulation of mRNA levels for five urea cycle enzymes in rat liver by diet, cyclic AMP, and glucocorticoidsS M Morris, C L Moncman, K D Rand, et al.American Journal of Medical Genetics|May 30, 1998
Bilateral radial ray hypoplasia with multiple epiphyseal dysplasiaM C Eddy, R D Steiner, W H McAlister, et al.American Journal of Medical Genetics|December 4, 1995
Klippel-Trenaunay-Weber syndrome associated with a 5:11 balanced translocationA J Whelan, M S Watson, F D Porter, et al.Molecular Genetics and Metabolism|June 28, 2000
Fructose-1,6-diphosphatase deficiency and glyceroluria: one possible etiology for GISM E Beatty, Y H Zhang, E R McCabe, et al.Human Genetics|March 1, 1993
Arginase deficiency manifesting delayed clinical sequelae and induction of a kidney arginase isozymeW W Grody, R M Kern, D Klein, et al.Human Genetics|March 1, 1995
Asp187Asn mutation of gelsolin in an American kindred with familial amyloidosis, Finnish type (FAP IV)R D Steiner, T Paunio, T Uemichi, et al.Pageof 10