Campbell KP - Search Results

1

Merosin-negative congenital muscular dystrophy associated with extensive brain abnormalities.

Sunada Y, Edgar TS, Lotz BP, Rust RS, Campbell KP. Sunada Y, et al. Among authors: campbell kp. Neurology. 1995 Nov;45(11):2084-9. doi: 10.1212/wnl.45.11.2084. Neurology. 1995. PMID: 7501163

2

Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy.

Matsumura K, Tomé FM, Collin H, Azibi K, Chaouch M, Kaplan JC, Fardeau M, Campbell KP. Matsumura K, et al. Among authors: campbell kp. Nature. 1992 Sep 24;359(6393):320-2. doi: 10.1038/359320a0. Nature. 1992. PMID: 1406935

3

Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle.

Matsumura K, Ervasti JM, Ohlendieck K, Kahl SD, Campbell KP. Matsumura K, et al. Among authors: campbell kp. Nature. 1992 Dec 10;360(6404):588-91. doi: 10.1038/360588a0. Nature. 1992. PMID: 1461282

4

Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix.

Ibraghimov-Beskrovnaya O, Ervasti JM, Leveille CJ, Slaughter CA, Sernett SW, Campbell KP. Ibraghimov-Beskrovnaya O, et al. Among authors: campbell kp. Nature. 1992 Feb 20;355(6362):696-702. doi: 10.1038/355696a0. Nature. 1992. PMID: 1741056

5

Expression of dystrophin-associated proteins in dystrophin-positive muscle fibers (revertants) in Duchenne muscular dystrophy.

Matsumura K, Tomé FM, Collin H, Leturcq F, Jeanpierre M, Kaplan JC, Fardeau M, Campbell KP. Matsumura K, et al. Among authors: campbell kp. Neuromuscul Disord. 1994 Mar;4(2):115-20. doi: 10.1016/0960-8966(94)90002-7. Neuromuscul Disord. 1994. PMID: 7516752

6

Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy.

Wells DJ, Wells KE, Asante EA, Turner G, Sunada Y, Campbell KP, Walsh FS, Dickson G. Wells DJ, et al. Among authors: campbell kp. Hum Mol Genet. 1995 Aug;4(8):1245-50. doi: 10.1093/hmg/4.8.1245. Hum Mol Genet. 1995. PMID: 7581360

7

Identification of a novel mutant transcript of laminin alpha 2 chain gene responsible for muscular dystrophy and dysmyelination in dy2J mice.

Sunada Y, Bernier SM, Utani A, Yamada Y, Campbell KP. Sunada Y, et al. Among authors: campbell kp. Hum Mol Genet. 1995 Jun;4(6):1055-61. doi: 10.1093/hmg/4.6.1055. Hum Mol Genet. 1995. PMID: 7655459

8

[Complete deficiency of adhalin (50 kDa DAG) in skeletal muscle of malignant limb-girdle muscular dystrophy].

Kawai H, Inui T, Mitsui T, Campbell KP, Shimizu T, Matsumura K. Kawai H, et al. Among authors: campbell kp. Rinsho Shinkeigaku. 1995 Feb;35(2):184-9. Rinsho Shinkeigaku. 1995. PMID: 7781237 Japanese.

9

Prevention of dystrophic pathology in mdx mice by a truncated dystrophin isoform.

Rafael JA, Sunada Y, Cole NM, Campbell KP, Faulkner JA, Chamberlain JS. Rafael JA, et al. Among authors: campbell kp. Hum Mol Genet. 1994 Oct;3(10):1725-33. doi: 10.1093/hmg/3.10.1725. Hum Mol Genet. 1994. PMID: 7849695

10

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 Free article. Review. No abstract available.

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