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Annales De Genetique|January 1, 1996
Sequence analysis of the CAG triplet repeats region in the Huntington disease gene (IT15) in several mammalian speciesC Pêcheux, A L Gall, J C Kaplan, et al.Proceedings of the National Academy of Sciences of the United States of America|April 1, 1989
Illegitimate transcription: transcription of any gene in any cell typeJ Chelly, J P Concordet, J C Kaplan, et al.The Journal of Infectious Diseases|July 1, 1985
Phenotypic properties of atypical lymphocytes in cytomegalovirus-induced mononucleosisD Felsenstein, W P Carney, V R Iacoviello, et al.Blood|April 15, 1995
Four new mutations in the NADH-cytochrome b5 reductase gene from patients with recessive congenital methemoglobinemia type IIL M Vieira, J C Kaplan, A Kahn, et al.Human Genetics|April 15, 1977
12pter to 12p12.2: possible assignment of human triose phosphate isomeraseM O Rethoré, J C Kaplan, C Junien, et al.The Journal of Infectious Diseases|November 1, 1992
Human immunodeficiency virus type 1 (HIV-1) inhibitory interactions between protease inhibitor Ro 31-8959 and zidovudine, 2',3'-dideoxycytidine, or recombinant interferon-alpha A against zidovudine-sensitive or -resistant HIV-1 in vitroV A Johnson, D P Merrill, T C Chou, et al.Clinical Immunology and Immunopathology|July 1, 1984
Effect of interferon alpha on natural killer cell cytotoxicity in kidney transplant recipientsA P Kelly, R T Schooley, R H Rubin, et al.Infection and Immunity|August 1, 1979
Persistent infection of human lymphoid and myeloid cell lines with herpes simplex virusC R Rinaldo, B S Richter, P H Black, et al.Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|November 1, 1995
Potential clinical implications of interlaboratory variability in CD4+ T-lymphocyte counts of patients infected with human immunodeficiency virusP E Sax, S L Boswell, M White-Guthro, et al.Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales|January 1, 1992
[Molecular pathology of Duchenne and Becker muscular dystrophy]H Gilgenkrantz, J Chelly, D Récan, et al.Pageof 33