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Results: 1-17 |
Results: 17
Dystrophin and muscular dystrophy: Past, present, and future
Authors: O'Brien, KF Kunkel, LM
Citation: Kf. O'Brien et Lm. Kunkel, Dystrophin and muscular dystrophy: Past, present, and future, MOL GEN MET, 74(1-2), 2001, pp. 75-88
Evaluation of the dystrophin-glycoprotein complex, alpha-actinin, dysferlin and calpain 3 in an autosomal recessive muscular dystrophy in Labrador retrievers
Authors: Olby, NJ Sharp, NJH Anderson, LVB Kunkel, LM Bonnemann, CG
Citation: Nj. Olby et al., Evaluation of the dystrophin-glycoprotein complex, alpha-actinin, dysferlin and calpain 3 in an autosomal recessive muscular dystrophy in Labrador retrievers, NEUROMUSC D, 11(1), 2001, pp. 41-49
Mutations in the caveolin-3 gene: When are they pathogenic?
Authors: de Paula, F Vainzof, M Bernardino, ALF McNally, E Kunkel, LM Zatz, M
Citation: F. De Paula et al., Mutations in the caveolin-3 gene: When are they pathogenic?, AM J MED G, 99(4), 2001, pp. 303-307
Myozenin: An alpha-actinin- and gamma-filamin-binding protein of skeletal muscle Z lines
Authors: Takada, F Vander Woude, DL Tong, HQ Thompson, TG Watkins, SC Kunkel, LM Beggs, AH
Citation: F. Takada et al., Myozenin: An alpha-actinin- and gamma-filamin-binding protein of skeletal muscle Z lines, P NAS US, 98(4), 2001, pp. 1595-1600
A genome-wide scan for linkage to human exceptional longevity identifies alocus on chromosome 4
Authors: Puca, AA Daly, MJ Brewster, SJ Matise, TC Barrett, J Shea-Drinkwater, M Kang, S Joyce, E Nicoli, J Benson, E Kunkel, LM Perls, T
Citation: Aa. Puca et al., A genome-wide scan for linkage to human exceptional longevity identifies alocus on chromosome 4, P NAS US, 98(18), 2001, pp. 10505-10508
Desmuslin, an intermediate filament protein that interacts with alpha-dystrobrevin and desmin
Authors: Mizuno, Y Thompson, TC Guyon, JR Lidov, HGW Brosius, M Imamura, M Ozawa, E Watkins, SC Kunkel, LM
Citation: Y. Mizuno et al., Desmuslin, an intermediate filament protein that interacts with alpha-dystrobrevin and desmin, P NAS US, 98(11), 2001, pp. 6156-6161
A homozygous nonsense mutation in delta-sarcoglycan exon 3 in a case of LGMD2F
Authors: Dincer, P Bonnemann, CG Aker, OE Akcoren, Z Nigro, V Kunkel, LM Topaloglu, H
Citation: P. Dincer et al., A homozygous nonsense mutation in delta-sarcoglycan exon 3 in a case of LGMD2F, NEUROMUSC D, 10(4-5), 2000, pp. 247-250
Evolutionary divergence of the mouse and human Lgn1/SMA repeat structures
Authors: Growney, JD Scharf, JM Kunkel, LM Dietrich, WF
Citation: Jd. Growney et al., Evolutionary divergence of the mouse and human Lgn1/SMA repeat structures, GENOMICS, 64(1), 2000, pp. 62-81
Intrafamilial phenotypic variation in limb-girdle muscular dystrophy type 2C with compound heterozygous mutations
Authors: Takano, A Bonnemann, CG Honda, H Sakai, M Feener, CA Kunkel, LM Sobue, G
Citation: A. Takano et al., Intrafamilial phenotypic variation in limb-girdle muscular dystrophy type 2C with compound heterozygous mutations, MUSCLE NERV, 23(5), 2000, pp. 807-810
A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathy
Authors: Bonnemann, CG Cox, GF Shapiro, F Wu, JJ Feener, CA Thompson, TG Anthony, DC Eyre, DR Darras, BT Kunkel, LM
Citation: Cg. Bonnemann et al., A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathy, P NAS US, 97(3), 2000, pp. 1212-1217
Filamin 2 (FLN2): A muscle-specific sarcoglycan interacting protein
Authors: Thompson, TG Chan, YM Hack, AA Brosius, M Rajala, M Lidov, HGW McNally, EM Watkins, S Kunkel, LM
Citation: Tg. Thompson et al., Filamin 2 (FLN2): A muscle-specific sarcoglycan interacting protein, J CELL BIOL, 148(1), 2000, pp. 115-126
Mutation detection in beta- and gamma-sarcoglycan (LGMD2E and LGMD2C)
Authors: Bonnemann, CG Kunkel, LM
Citation: Cg. Bonnemann et Lm. Kunkel, Mutation detection in beta- and gamma-sarcoglycan (LGMD2E and LGMD2C), METH MOL M, 43, 2000, pp. 227-255
Identification of FLRT1, FLRT2, and FLRT3: A novel family of transmembraneleucine-rich repeat proteins
Authors: Lacy, SE Bonnemann, CG Buzney, EA Kunkel, LM
Citation: Se. Lacy et al., Identification of FLRT1, FLRT2, and FLRT3: A novel family of transmembraneleucine-rich repeat proteins, GENOMICS, 62(3), 1999, pp. 417-426
Comparative sequence analysis of the mouse and human Lgn1/SMA interval
Authors: Endrizzi, M Huang, S Scharf, JM Kelter, AR Wirth, B Kunkel, LM Miller, W Dietrich, WF
Citation: M. Endrizzi et al., Comparative sequence analysis of the mouse and human Lgn1/SMA interval, GENOMICS, 60(2), 1999, pp. 137-151
Dystrophin expression in the mdx mouse restored by stem cell transplantation
Authors: Gussoni, E Soneoka, Y Strickland, CD Buzney, EA Khan, MK Flint, AF Kunkel, LM Mulligan, RC
Citation: E. Gussoni et al., Dystrophin expression in the mdx mouse restored by stem cell transplantation, NATURE, 401(6751), 1999, pp. 390-394
Dystrophin and Dp140 in the adult rodent kidney
Authors: Lidov, HGW Kunkel, LM
Citation: Hgw. Lidov et Lm. Kunkel, Dystrophin and Dp140 in the adult rodent kidney, LAB INV, 78(12), 1998, pp. 1543-1551
Molecular organization of sarcoglycan complex in mouse myotubes in culture
Authors: Chan, YM Bonnemann, CG Lidov, HGW Kunkel, LM
Citation: Ym. Chan et al., Molecular organization of sarcoglycan complex in mouse myotubes in culture, J CELL BIOL, 143(7), 1998, pp. 2033-2044
Risultati: 1-17 |