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Journal of Biological Regulators and Homeostatic Agents|January 6, 2012
SOS1 over-expression in genital skin fibroblasts from hirsute women: a putative role of the SOS1/RAS pathway in the pathogenesis of hirsutismD Minella, F Wannenes, M Biancolella, et al.
Human Molecular Genetics|February 1, 1997
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndromeA Pizzuti, G Novelli, A Ratti, et al.
Molecular Genetics and Metabolism|June 25, 1999
Isolation and characterization of a novel transcript embedded within HIRA, a gene deleted in DiGeorge syndromeA Pizzuti, G Novelli, A Ratti, et al.
American Journal of Medical Genetics|August 10, 2001
Association study of a promoter polymorphism of UFD1L gene with schizophreniaA De Luca, A Pasini, F Amati, et al.
Clinical and Experimental Immunology|April 18, 2003
Biased T-cell receptor repertoires in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)M Pierdominici, F Mazzetta, E Caprini, et al.
Human Molecular Genetics|July 1, 1996
cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity geneA Pizzuti, F Amati, G Calabrese, et al.
Biochimica Et Biophysica Acta|April 16, 1998
Structure and expression of the human ubiquitin fusion-degradation gene (UFD1L)G Novelli, A Mari, F Amati, et al.
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