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Nature|July 5, 1987
A cDNA clone from the Duchenne/Becker muscular dystrophy geneA H Burghes, C Logan, X Hu, et al.Genomics|June 1, 1991
Point mutation in the human dystrophin gene: identification through western blot analysisD E Bulman, S B Gangopadhyay, K G Bebchuck, et al.American Journal of Human Genetics|June 1, 1989
Evidence for mutation by unequal sister chromatid exchange in the Duchenne muscular dystrophy geneX Y Hu, A H Burghes, D E Bulman, et al.Journal of the National Cancer Institute|February 24, 2001
Arm edema in breast cancer patientsV S Erickson, M L Pearson, P A Ganz, et al.The Journal of Experimental Medicine|March 1, 1985
Analysis of human blood monocyte activation at the level of gene expression. Expression of alpha interferon genes during activation of human monocytes by poly IC/LC and muramyl dipeptideH C Stevenson, G A Dekaban, P J Miller, et al.Muscle & Nerve|May 1, 1990
Dystrophin is localized to the plasma membrane of human skeletal muscle fibers by electron-microscopic cytochemical studyS Carpenter, G Karpati, E Zubrzycka-Gaarn, et al.American Journal of Human Genetics|February 1, 1991
Differentiation of Duchenne and Becker muscular dystrophy phenotypes with amino- and carboxy-terminal antisera specific for dystrophinD E Bulman, E G Murphy, E E Zubrzycka-Gaarn, et al.Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|June 15, 1988
The problem of Duchenne muscular dystrophyR G Worton, P N Ray, S Bodrug, et al.American Journal of Medical Genetics|February 5, 1998
Impact of carrier status determination for Duchenne/Becker muscular dystrophy by computer-assisted laser densitometryD J Allingham-Hawkins, L K McGlynn-Steele, C A Brown, et al.Human Molecular Genetics|October 1, 1996
Identification of a transcriptional enhancer within muscle intron 1 of the human dystrophin geneH J Klamut, L O Bosnoyan-Collins, R G Worton, et al.Pageof 13