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Nature|February 18, 1993
Use of evolutionary limitations of HIV-1 multidrug resistance to optimize therapyY K Chow, M S Hirsch, D P Merrill, et al.Journal of Clinical Microbiology|October 1, 1987
Dot immunobinding assay for detection of human immunodeficiency virus-associated antigensR S Blumberg, K L Hartshorn, B Ardman, et al.Lancet (London, England)|March 16, 1985
Recombinant human interferon alfa-A suppresses HTLV-III replication in vitroD D Ho, K L Hartshorn, T R Rota, et al.Nature|February 18, 1993
Efficient adenovirus-mediated transfer of a human minidystrophin gene to skeletal muscle of mdx miceT Ragot, N Vincent, P Chafey, et al.Nature Genetics|October 1, 1993
Long-term correction of mouse dystrophic degeneration by adenovirus-mediated transfer of a minidystrophin geneN Vincent, T Ragot, H Gilgenkrantz, et al.Human Genetics|March 1, 1988
Deletion proximal to DXS68 locus (L1 probe site) in a boy with Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal hypoplasiaJ Chelly, F Marlhens, B Dutrillaux, et al.Neuromuscular Disorders : NMD|January 1, 1991
Immunolocalization and developmental expression of dystrophin related protein in skeletal muscleT S Khurana, S C Watkins, P Chafey, et al.Neuropediatrics|February 1, 1996
Neurosensory hearing loss in secondary adhalinopathyK Oexle, R Herrmann, C Dodé, et al.The Journal of Clinical Investigation|October 1, 1991
Illegitimate transcription. Application to the analysis of truncated transcripts of the dystrophin gene in nonmuscle cultured cells from Duchenne and Becker patientsJ Chelly, H Gilgenkrantz, J P Hugnot, et al.Human Genetics|May 1, 1994
Skewed inactivation of an X chromosome deleted at the dystrophin gene in an asymptomatic mother and her affected daughterF Tihy, N Vogt, D Recan, et al.Pageof 19