| Year |
Citation |
Score |
| 2008 |
Lim LE, Rando TA. Technology insight: therapy for Duchenne muscular dystrophy-an opportunity for personalized medicine? Nature Clinical Practice. Neurology. 4: 149-58. PMID 18268530 DOI: 10.1038/ncpneuro0737 |
0.381 |
|
| 2007 |
Lim LE, Thornton CA, Rando TA. Muscular dystrophies Neurobiology of Disease. 925-934. DOI: 10.1016/B978-012088592-3/50086-4 |
0.315 |
|
| 2000 |
Crosbie RH, Lim LE, Moore SA, Hirano M, Hays AP, Maybaum SW, Collin H, Dovico SA, Stolle CA, Fardeau M, Tomé FM, Campbell KP. Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions. Human Molecular Genetics. 9: 2019-27. PMID 10942431 DOI: 10.1093/Hmg/9.13.2019 |
0.632 |
|
| 1999 |
Johnston JC, Gasmi M, Lim LE, Elder JH, Yee JK, Jolly DJ, Campbell KP, Davidson BL, Sauter SL. Minimum requirements for efficient transduction of dividing and nondividing cells by feline immunodeficiency virus vectors. Journal of Virology. 73: 4991-5000. PMID 10233961 DOI: 10.1128/Jvi.73.6.4991-5000.1999 |
0.463 |
|
| 1998 |
Lim LE, Campbell KP. The sarcoglycan complex in limb-girdle muscular dystrophy. Current Opinion in Neurology. 11: 443-52. PMID 9847993 DOI: 10.1097/00019052-199810000-00006 |
0.594 |
|
| 1998 |
Duclos F, Straub V, Moore SA, Venzke DP, Hrstka RF, Crosbie RH, Durbeej M, Lebakken CS, Ettinger AJ, van der Meulen J, Holt KH, Lim LE, Sanes JR, Davidson BL, Faulkner JA, et al. Progressive muscular dystrophy in alpha-sarcoglycan-deficient mice. The Journal of Cell Biology. 142: 1461-71. PMID 9744877 DOI: 10.1083/Jcb.142.6.1461 |
0.597 |
|
| 1998 |
Holt KH, Lim LE, Straub V, Venzke DP, Duclos F, Anderson RD, Davidson BL, Campbell KP. Functional rescue of the sarcoglycan complex in the BIO 14.6 hamster using delta-sarcoglycan gene transfer. Molecular Cell. 1: 841-8. PMID 9660967 DOI: 10.1016/S1097-2765(00)80083-0 |
0.637 |
|
| 1998 |
Duclos F, Broux O, Bourg N, Straub V, Feldman GL, Sunada Y, Lim LE, Piccolo F, Cutshall S, Gary F, Quetier F, Kaplan JC, Jackson CE, Beckmann JS, Campbell KP. Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate. Neuromuscular Disorders : Nmd. 8: 30-8. PMID 9565988 DOI: 10.1016/S0960-8966(97)00135-1 |
0.586 |
|
| 1996 |
Beckmann JS, Richard I, Broux O, Fougerousse F, Allamand V, Chiannilkulchai N, Lim LE, Duclos F, Bourg N, Brenguier L, Pasturaud P, Quétier F, Roudaut C, Sunada Y, Meyer J, et al. Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophies. Neuromuscular Disorders : Nmd. 6: 455-62. PMID 9027855 DOI: 10.1016/S0960-8966(96)00386-0 |
0.59 |
|
| 1996 |
Broux O, Duclos F, Lim LE, Bourg N, Sunada Y, Allamand V, Meyer J, Richard I, Moomaw C, Slaughter C, Tomé FMS, Fardeau M, Jackson CE, Campbell KP, Beckmann JS. β-sarcoglycan : Characterization and role in limb-girdle muscular dystrophy linked to 4q12 Neuromuscular Disorders. 6. DOI: 10.1016/0960-8966(96)88965-6 |
0.425 |
|
| 1995 |
Lim LE, Duclos F, Broux O, Bourg N, Sunada Y, Allamand V, Meyer J, Richard I, Moomaw C, Slaughter C. Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12. Nature Genetics. 11: 257-65. PMID 7581448 DOI: 10.1038/Ng1195-257 |
0.446 |
|
| 1994 |
Roberds SL, Leturcq F, Allamand V, Piccolo F, Jeanpierre M, Anderson RD, Lim LE, Lee JC, Tomé FM, Romero NB. Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy. Cell. 78: 625-33. PMID 8069911 DOI: 10.1016/0092-8674(94)90527-4 |
0.474 |
|
| 1994 |
Allamand V, Leturcq F, Piccolo F, Jeanpierre M, Azibi K, Roberds SL, Lim LE, Campbell KP, Beckmann JS, Kaplan JC. Adhalin gene polymorphism. Human Molecular Genetics. 3: 2269. PMID 7881446 DOI: 10.1093/Hmg/3.12.2269 |
0.476 |
|
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