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The Journal of Biological Chemistry|June 27, 1998
Functional defects of a muscle-specific calpain, p94, caused by mutations associated with limb-girdle muscular dystrophy type 2AY Ono, H Shimada, H Sorimachi, et al.
Human Molecular Genetics|February 9, 1999
An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21M Mustapha, D Weil, S Chardenoux, et al.
Diabetologia|July 18, 2009
JNK3 is abundant in insulin-secreting cells and protects against cytokine-induced apoptosisS Abdelli, J Puyal, C Bielmann, et al.
Biostatistics (Oxford, England)|June 15, 2010
Methods for testing association between uncertain genotypes and quantitative traitsZoltán Kutalik, Toby Johnson, Murielle Bochud, et al.
Genomics|May 1, 1990
(TG)n uncovers a sex-specific hybridization pattern in cattleY Kashi, F Iraqi, Y Tikochinski, et al.
Pharmacology & Toxicology|July 15, 2000
Inhibitory effects of silibinin on cytochrome P-450 enzymes in human liver microsomesS Beckmann-Knopp, S Rietbrock, R Weyhenmeyer, et al.
Human Molecular Genetics|December 1, 1993
A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellitesJ S Beckmann, J Tomfohrde, R I Barnes, et al.
Genomics|April 2, 1998
Expression of genes (CAPN3, SGCA, SGCB, and TTN) involved in progressive muscular dystrophies during early human developmentF Fougerousse, M Durand, L Suel, et al.
Molecular and Cellular Endocrinology|October 19, 2004
Circadian regulation of islet genes involved in insulin production and secretionN Allaman-Pillet, R Roduit, A Oberson, et al.
Human Mutation|July 21, 2009
A single-base substitution within an intronic repetitive element causes dominant retinitis pigmentosa with reduced penetranceThomas Rio Frio, Terri L McGee, Nicholas M Wade, et al.
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