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432 results
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Muscular dystrophies involving the dystrophin-glycoprotein complex: an overview of current mouse models.
Durbeej M, Campbell KP. Durbeej M, et al. Among authors: campbell kp. Curr Opin Genet Dev. 2002 Jun;12(3):349-61. doi: 10.1016/s0959-437x(02)00309-x. Curr Opin Genet Dev. 2002. PMID: 12076680 Review.
Assembly of the dystrophin-associated protein complex does not require the dystrophin COOH-terminal domain.
Crawford GE, Faulkner JA, Crosbie RH, Campbell KP, Froehner SC, Chamberlain JS. Crawford GE, et al. Among authors: campbell kp. J Cell Biol. 2000 Sep 18;150(6):1399-410. doi: 10.1083/jcb.150.6.1399. J Cell Biol. 2000. PMID: 10995444 Free PMC article.
Dystroglycan inside and out.
Henry MD, Campbell KP. Henry MD, et al. Among authors: campbell kp. Curr Opin Cell Biol. 1999 Oct;11(5):602-7. doi: 10.1016/s0955-0674(99)00024-1. Curr Opin Cell Biol. 1999. PMID: 10508656 Review.
Dystroglycan in development and disease.
Durbeej M, Henry MD, Campbell KP. Durbeej M, et al. Among authors: campbell kp. Curr Opin Cell Biol. 1998 Oct;10(5):594-601. doi: 10.1016/s0955-0674(98)80034-3. Curr Opin Cell Biol. 1998. PMID: 9818169 Review.
Dystrophin and the membrane skeleton.
Ervasti JM, Campbell KP. Ervasti JM, et al. Among authors: campbell kp. Curr Opin Cell Biol. 1993 Feb;5(1):82-7. doi: 10.1016/s0955-0674(05)80012-2. Curr Opin Cell Biol. 1993. PMID: 8448034 Review.
Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.
Campbell KP. Campbell KP. Cell. 1995 Mar 10;80(5):675-9. doi: 10.1016/0092-8674(95)90344-5. Cell. 1995. PMID: 7889563 Review. No abstract available.
Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions.
Crosbie RH, Lim LE, Moore SA, Hirano M, Hays AP, Maybaum SW, Collin H, Dovico SA, Stolle CA, Fardeau M, Tomé FM, Campbell KP. Crosbie RH, et al. Among authors: campbell kp. Hum Mol Genet. 2000 Aug 12;9(13):2019-27. doi: 10.1093/hmg/9.13.2019. Hum Mol Genet. 2000. PMID: 10942431
Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2E.
Durbeej M, Cohn RD, Hrstka RF, Moore SA, Allamand V, Davidson BL, Williamson RA, Campbell KP. Durbeej M, et al. Among authors: campbell kp. Mol Cell. 2000 Jan;5(1):141-51. doi: 10.1016/s1097-2765(00)80410-4. Mol Cell. 2000. PMID: 10678176
Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate.
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. Duclos F, et al. Among authors: campbell kp. Neuromuscul Disord. 1998 Feb;8(1):30-8. doi: 10.1016/s0960-8966(97)00135-1. Neuromuscul Disord. 1998. PMID: 9565988
mdx muscle pathology is independent of nNOS perturbation.
Crosbie RH, Straub V, Yun HY, Lee JC, Rafael JA, Chamberlain JS, Dawson VL, Dawson TM, Campbell KP. Crosbie RH, et al. Among authors: campbell kp. Hum Mol Genet. 1998 May;7(5):823-9. doi: 10.1093/hmg/7.5.823. Hum Mol Genet. 1998. PMID: 9536086
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