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Nature|March 10, 1988
Haemophilia A resulting from de novo insertion of L1 sequences represents a novel mechanism for mutation in manH H Kazazian, C Wong, H Youssoufian, et al.Nature|July 12, 1984
Quantification of the close association between DNA haplotypes and specific beta-thalassaemia mutations in MediterraneansH H Kazazian, S H Orkin, A F Markham, et al.American Journal of Medical Genetics|May 8, 1999
Normal expression of the Fanconi anemia proteins FAA and FAC and sensitivity to mitomycin C in two patients with Seckel syndromeF Abou-Zahr, B Bejjani, F A Kruyt, et al.Blood|November 14, 1997
Cytoplasmic localization of a functionally active Fanconi anemia group A-green fluorescent protein chimera in human 293 cellsF A Kruyt, Q Waisfisz, L M Dijkmans, et al.Genomics|January 1, 1988
Mild hemophilia A associated with a cryptic donor splice site mutation in intron 4 of the factor VIII geneH Youssoufian, H H Kazazian, A Patel, et al.Nature|November 3, 1986
Recurrent mutations in haemophilia A give evidence for CpG mutation hotspotsH Youssoufian, H H Kazazian, D G Phillips, et al.Genetics|January 11, 2000
Cellular Werner phenotypes in mice expressing a putative dominant-negative human WRN geneL Wang, C E Ogburn, C B Ware, et al.Molecular Biology of the Cell|November 6, 2001
Cell cycle-dependent expression and nucleolar localization of hCAP-HO A Cabello, E Eliseeva, W G He, et al.Blood|May 30, 1998
Molecular chaperone GRP94 binds to the Fanconi anemia group C protein and regulates its intracellular expressionT Hoshino, J Wang, M P Devetten, et al.Nature Genetics|December 2, 2000
Cancer predisposition caused by elevated mitotic recombination in Bloom miceG Luo, I M Santoro, L D McDaniel, et al.Pageof 6