Leland E. Lim, Ph.D.
Affiliations: | 2000 | University of Iowa, Iowa City, IA |
Area:
Ion channels, muscle pathologyGoogle:
"Leland Lim"Mean distance: 20.18 (cluster 46) | S | N | B | C | P |
Parents
Sign in to add mentor| Kevin P. Campbell | grad student | 2000 | University of Iowa | |
| (Studies of the sarcoglycan complex in limb -girdle muscular dystrophy and the bio 14.6 hamster.) | ||||
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Publications
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| Lim LE, Rando TA. (2008) Technology insight: therapy for Duchenne muscular dystrophy-an opportunity for personalized medicine? Nature Clinical Practice. Neurology. 4: 149-58 |
| Lim LE, Thornton CA, Rando TA. (2007) Muscular dystrophies Neurobiology of Disease. 925-934 |
| Crosbie RH, Lim LE, Moore SA, et al. (2000) Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions. Human Molecular Genetics. 9: 2019-27 |
| Johnston JC, Gasmi M, Lim LE, et al. (1999) Minimum requirements for efficient transduction of dividing and nondividing cells by feline immunodeficiency virus vectors. Journal of Virology. 73: 4991-5000 |
| Lim LE, Campbell KP. (1998) The sarcoglycan complex in limb-girdle muscular dystrophy. Current Opinion in Neurology. 11: 443-52 |
| Duclos F, Straub V, Moore SA, et al. (1998) Progressive muscular dystrophy in alpha-sarcoglycan-deficient mice. The Journal of Cell Biology. 142: 1461-71 |
| Holt KH, Lim LE, Straub V, et al. (1998) Functional rescue of the sarcoglycan complex in the BIO 14.6 hamster using delta-sarcoglycan gene transfer. Molecular Cell. 1: 841-8 |
| Duclos F, Broux O, Bourg N, et al. (1998) Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate. Neuromuscular Disorders : Nmd. 8: 30-8 |
| Beckmann JS, Richard I, Broux O, et al. (1996) Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophies. Neuromuscular Disorders : Nmd. 6: 455-62 |
| Broux O, Duclos F, Lim LE, et al. (1996) β-sarcoglycan : Characterization and role in limb-girdle muscular dystrophy linked to 4q12 Neuromuscular Disorders. 6 |