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Results: 1-7 |
Results: 7
Cloning of the mouse dysferlin gene and genomic characterization of the SJL-Dysf mutation
Authors: Vafiadaki, E Reis, A Keers, S Harrison, R Anderson, LVB Raffelsberger, T Ivanova, S Hoger, H Bittner, RE Bushby, K Bashir, R
Citation: E. Vafiadaki et al., Cloning of the mouse dysferlin gene and genomic characterization of the SJL-Dysf mutation, NEUROREPORT, 12(3), 2001, pp. 625-629
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)
Authors: Anderson, LVB Harrison, RM Pogue, R Vafiadaki, E Pollitt, C Davison, K Moss, JA Keers, S Pyle, A Shaw, PJ Mahjneh, I Argov, Z Greenberg, CR Wrogemann, K Bertorini, T Goebel, HH Beckmann, JS Bashir, R Bushby, KMD
Citation: Lvb. Anderson et al., Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies), NEUROMUSC D, 10(8), 2000, pp. 553-559
The third human FER-1-like protein is highly similar to dysferlin
Authors: Britton, S Freeman, T Vafiadaki, E Keers, S Harrison, R Bushby, K Bashir, R
Citation: S. Britton et al., The third human FER-1-like protein is highly similar to dysferlin, GENOMICS, 68(3), 2000, pp. 313-321
Muscular dystrophy due to dysferlin deficiency in Libyan Jews - Clinical and genetic features
Authors: Argov, Z Sadeh, M Mazor, K Soffer, D Kahana, E Eisenberg, I Mitrani-Rosenbaum, S Richard, I Beckmann, J Keers, S Bashir, R Bushby, K Rosenmann, H
Citation: Z. Argov et al., Muscular dystrophy due to dysferlin deficiency in Libyan Jews - Clinical and genetic features, BRAIN, 123, 2000, pp. 1229-1237
Dysferlin is a plasma membrane protein and is expressed early in human development (vol 8, pg 855, 1999)
Authors: Anderson, LVB Davison, K Moss, JA Young, C Cullen, MJ Walsh, J Johnson, MA Bashir, R Britton, S Keers, S Argov, Z Mahjneh, I Fougerousse, F Beckmann, JS Bushby, KMD
Citation: Lvb. Anderson et al., Dysferlin is a plasma membrane protein and is expressed early in human development (vol 8, pg 855, 1999), HUM MOL GEN, 8(6), 1999, pp. 1141-1141
Dysferlin is a plasma membrane protein and is expressed early in human development
Authors: Anderson, LVB Davison, K Moss, JA Young, C Cullen, MJ Walsh, J Johnson, MA Bashir, R Britton, S Keers, S Argov, Z Mahjneh, I Fougerousse, F Beckmann, JS Bushby, KMD
Citation: Lvb. Anderson et al., Dysferlin is a plasma membrane protein and is expressed early in human development, HUM MOL GEN, 8(5), 1999, pp. 855-861
Identical mutation in patients with limb girdle muscular dystrophy type 2Bor Miyoshi myopathy suggests a role for modifier gene(s)
Authors: Weiler, T Bashir, R Anderson, LVB Davison, K Moss, JA Britton, S Nylen, E Keers, S Vafiadaki, E Greenberg, CR Bushby, KMD Wrogemann, K
Citation: T. Weiler et al., Identical mutation in patients with limb girdle muscular dystrophy type 2Bor Miyoshi myopathy suggests a role for modifier gene(s), HUM MOL GEN, 8(5), 1999, pp. 871-877
Risultati: 1-7 |