Campbell KP - Search Results

1

Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin.

Higuchi I, Yamada H, Fukunaga H, Iwaki H, Okubo R, Nakagawa M, Osame M, Roberds SL, Shimizu T, Campbell KP, et al. Higuchi I, et al. Among authors: campbell kp. J Clin Invest. 1994 Aug;94(2):601-6. doi: 10.1172/JCI117375. J Clin Invest. 1994. PMID: 8040315 Free PMC article.

2

The expression of dystrophin-associated glycoproteins during skeletal muscle degeneration and regeneration. An immunofluorescence study.

Vater R, Harris JB, Anderson VB, Roberds SL, Campbell KP, Cullen MJ. Vater R, et al. Among authors: campbell kp. J Neuropathol Exp Neurol. 1995 Jul;54(4):557-69. doi: 10.1097/00005072-199507000-00010. J Neuropathol Exp Neurol. 1995. PMID: 7602329

3

Rapsyn may function as a link between the acetylcholine receptor and the agrin-binding dystrophin-associated glycoprotein complex.

Apel ED, Roberds SL, Campbell KP, Merlie JP. Apel ED, et al. Among authors: campbell kp. Neuron. 1995 Jul;15(1):115-26. doi: 10.1016/0896-6273(95)90069-1. Neuron. 1995. PMID: 7619516 Free article.

4

Expression of deletion-containing dystrophins in mdx muscle: implications for gene therapy and dystrophin function.

Fritz JD, Danko I, Roberds SL, Campbell KP, Latendresse JS, Wolff JA. Fritz JD, et al. Among authors: campbell kp. Pediatr Res. 1995 Jun;37(6):693-700. doi: 10.1203/00006450-199506000-00004. Pediatr Res. 1995. PMID: 7651751

5

Adhalin mRNA and cDNA sequence are normal in the cardiomyopathic hamster.

Roberds SL, Campbell KP. Roberds SL, et al. Among authors: campbell kp. FEBS Lett. 1995 May 15;364(3):245-9. doi: 10.1016/0014-5793(95)00395-p. FEBS Lett. 1995. PMID: 7758576 Free article.

6

[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.

7

Non-muscle alpha-dystroglycan is involved in epithelial development.

Durbeej M, Larsson E, Ibraghimov-Beskrovnaya O, Roberds SL, Campbell KP, Ekblom P. Durbeej M, et al. Among authors: campbell kp. J Cell Biol. 1995 Jul;130(1):79-91. doi: 10.1083/jcb.130.1.79. J Cell Biol. 1995. PMID: 7790379 Free PMC article.

8

Adhalin gene polymorphism.

Allamand V, Leturcq F, Piccolo F, Jeanpierre M, Azibi K, Roberds SL, Lim LE, Campbell KP, Beckmann JS, Kaplan JC. Allamand V, et al. Among authors: campbell kp. Hum Mol Genet. 1994 Dec;3(12):2269. doi: 10.1093/hmg/3.12.2269. Hum Mol Genet. 1994. PMID: 7881446 No abstract available.

9

Dystroglycan is a binding protein of laminin and merosin in peripheral nerve.

Yamada H, Shimizu T, Tanaka T, Campbell KP, Matsumura K. Yamada H, et al. Among authors: campbell kp. FEBS Lett. 1994 Sep 19;352(1):49-53. doi: 10.1016/0014-5793(94)00917-1. FEBS Lett. 1994. PMID: 7925941 Free article.

10

Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiency.

Romero NB, Tomé FM, Leturcq F, el Kerch FE, Azibi K, Bachner L, Anderson RD, Roberds SL, Campbell KP, Fardeau M, et al. Romero NB, et al. Among authors: campbell kp. C R Acad Sci III. 1994 Jan;317(1):70-6. C R Acad Sci III. 1994. PMID: 7987694

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