Showing results (481-490 of 532) with videos related to
Sort By:
Pageof 54
Annals of Neurology|October 8, 1999
Linkage and association analysis of susceptibility regions on chromosomes 5 and 6 in 106 Scandinavian sibling pair families with multiple sclerosisA Oturai, F Larsen, L P Ryder, et al.Genes and Immunity|February 24, 2001
Linkage analysis of a candidate region in Scandinavian sib pairs with multiple sclerosis reveals linkage to chromosome 17qF Larsen, A Oturai, L P Ryder, et al.Cancer Research|April 15, 1997
Gap junctions promote the bystander effect of herpes simplex virus thymidine kinase in vivoM S Dilber, M R Abedi, B Christensson, et al.Journal of Immunology (Baltimore, Md. : 1950)|July 1, 1992
Transcription of unrearranged Ig H chain genes in human B cell malignancies. Biased expression of genes encoded within the first duplication unit of the Ig H chain locusP Sideras, L Nilsson, K B Islam, et al.European Journal of Haematology|November 1, 1995
Retroviral-mediated gene transfer into human bone marrow stromal cells: studies of efficiency and in vivo survival in SCID miceK J Li, M S Dilber, M R Abedi, et al.The Journal of Chemical Physics|February 5, 2009
Determination of the structure of adenine monolayers adsorbed at Au(110)/electrolyte interfaces using reflection anisotropy spectroscopyC I Smith, A Bowfield, G J Dolan, et al.The American Journal of Gastroenterology|October 29, 2000
Prevalence and clinical significance of HFE gene mutations in patients with iron overloadD J Brandhagen, V F Fairbanks, W P Baldus, et al.Nucleic Acids Research|November 25, 1986
Cloning of cDNA for human T-cell replacing factor (interleukin-5) and comparison with the murine homologueC Azuma, T Tanabe, M Konishi, et al.Human Molecular Genetics|January 1, 1995
DNA-based mutation analysis of Bruton's tyrosine kinase gene in patients with X-linked agammaglobulinaemiaI Vorechovský, M Vihinen, G de Saint Basile, et al.Oncogene|December 1, 1994
BMX, a novel nonreceptor tyrosine kinase gene of the BTK/ITK/TEC/TXK family located in chromosome Xp22.2L Tamagnone, I Lahtinen, T Mustonen, et al.Pageof 54