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FEBS Letters|July 1, 1999
Localization of the human caveolin-3 gene to the D3S18/D3S4163/D3S4539 locus (3p25), in close proximity to the human oxytocin receptor gene. Identification of the caveolin-3 gene as a candidate for deletion in 3p-syndromeF Sotgia, C Minetti, M P LisantiNeurology|February 26, 2004
Caveolinopathies: mutations in caveolin-3 cause four distinct autosomal dominant muscle diseasesS E Woodman, F Sotgia, F Galbiati, et al.Biochemistry|November 29, 2001
Tyrosine phosphorylation of beta-dystroglycan at its WW domain binding motif, PPxY, recruits SH2 domain containing proteinsF Sotgia, H Lee, M T Bedford, et al.Human Genetics|April 17, 1998
Identification and characterization of a new human cDNA from chromosome 21q22.3 encoding a basic nuclear proteinA Egeo, M Mazzocco, F Sotgia, et al.Journal of Neurology, Neurosurgery, and Psychiatry|June 26, 2002
Familial isolated hyperCKaemia associated with a new mutation in the caveolin-3 (CAV-3) geneL Merlini, I Carbone, C Capanni, et al.Biochemical and Biophysical Research Communications|August 12, 1999
Increased number of caveolae and caveolin-3 overexpression in Duchenne muscular dystrophyS Repetto, M Bado, P Broda, et al.The Journal of Biological Chemistry|September 16, 2000
Caveolin-3 directly interacts with the C-terminal tail of beta -dystroglycan. Identification of a central WW-like domain within caveolin family membersF Sotgia, J K Lee, K Das, et al.Neurology|April 4, 2000
Mutation in the CAV3 gene causes partial caveolin-3 deficiency and hyperCKemiaI Carbone, C Bruno, F Sotgia, et al.Nature Genetics|April 16, 1998
Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophyC Minetti, F Sotgia, C Bruno, et al.Pageof 1