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American Journal of Human Genetics|March 1, 1985
Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndromeU Francke, H D Ochs, B de Martinville, et al.Proceedings of the National Academy of Sciences of the United States of America|November 1, 1988
Physical linkage of a human immunoglobulin heavy chain variable region gene segment to diversity and joining region elementsH W Schroeder, M A Walter, M H Hofker, et al.The Journal of Biological Chemistry|May 15, 1993
Transgenic mice carrying the apolipoprotein E3-Leiden gene exhibit hyperlipoproteinemiaA M van den Maagdenberg, M H Hofker, P J Krimpenfort, et al.The Journal of Clinical Investigation|April 1, 1994
Diet-induced hyperlipoproteinemia and atherosclerosis in apolipoprotein E3-Leiden transgenic miceB J van Vlijmen, A M van den Maagdenberg, M J Gijbels, et al.Cell|November 21, 1986
A physical map of 4 million bp around the Duchenne muscular dystrophy gene on the human X-chromosomeG J van Ommen, J M Verkerk, M H Hofker, et al.European Journal of Human Genetics : EJHG|January 1, 1996
A 3-Mb region for the familial hemiplegic migraine locus on 19p13.1-p13.2: exclusion of PRKCSH as a candidate gene. Dutch Migraine Genetic Research GroupR A Ophoff, G M Terwindt, M N Vergouwe, et al.Human Molecular Genetics|August 1, 1995
Inactivation of Apoe and Apoc1 by two consecutive rounds of gene targeting: effects on mRNA expression levels of gene cluster membersJ H van Ree, W J van den Broek, A van der Zee, et al.The Biochemical Journal|February 20, 1999
Reversal of hyperlipidaemia in apolipoprotein C1 transgenic mice by adenovirus-mediated gene delivery of the low-density-lipoprotein receptor, but not by the very-low-density-lipoprotein receptorM C Jong, K W van Dijk, V E Dahlmans, et al.The Biochemical Journal|February 1, 1995
Increased response to cholesterol feeding in apolipoprotein C1-deficient miceJ H van Ree, M H Hofker, W J van den Broek, et al.Muscle & Nerve. Supplement|January 1, 1995
Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35J C van Deutekom, M H Hofker, S Romberg, et al.Pageof 11