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Journal of Human Virology|April 25, 2000
CXCR4 and CCR5 expression on CD4+ T cells in vivo and HIV-1 antigen beta-chemokine production in vitro after treatment with HIV-1 immunogen (REMUNE)R B Moss, W K Giermakowska, J P Diveley, et al.AIDS Research and Human Retroviruses|February 1, 1992
Quantitation of HIV viral burden by PCR in HIV seropositive Navy personnel representing Walter Reed stages 1 to 6F Ferre, A Marchese, P C Duffy, et al.The Journal of Infectious Diseases|August 1, 1996
Treatment of adult varicella with sorivudine: a randomized, placebo-controlled trialM R Wallace, C J Chamberlin, M H Sawyer, et al.Journal of Medical Genetics|June 27, 1998
Constitutional and mosaic large NF1 gene deletions in neurofibromatosis type 1S A Rasmussen, S D Colman, V T Ho, et al.The Journal of Infectious Diseases|October 1, 1992
Detection of varicella-zoster virus DNA in the oropharynx and blood of patients with varicellaM H Sawyer, Y N Wu, C J Chamberlin, et al.Proceedings of the National Academy of Sciences of the United States of America|July 1, 1989
Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome regionD H Ledbetter, S A Ledbetter, P vanTuinen, et al.American Journal of Human Genetics|June 1, 1995
Identification of a yeast artificial chromosome clone spanning a translocation breakpoint at 7q32.1 in a Smith-Lemli-Opitz syndrome patientT L Alley, B A Gray, S H Lee, et al.American Journal of Medical Genetics|August 26, 1998
Newly described form of X-linked arthrogryposis maps to the long arm of the human X chromosomeR T Zori, J L Gardner, J Zhang, et al.Psychosomatic Medicine|January 1, 1994
Neuropsychological impairment in human immunodeficiency virus-infection: implications for employment. HNRC Group. HIV Neurobehavioral Research CenterR K Heaton, R A Velin, J A McCutchan, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2001
Exon 10b of the NF1 gene represents a mutational hotspot and harbors a recurrent missense mutation Y489C associated with aberrant splicingL M Messiaen, T Callens, K J Roux, et al.Pageof 17