Anderson RD - Search Results

1

Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy.

Roberds SL, Leturcq F, Allamand V, Piccolo F, Jeanpierre M, Anderson RD, Lim LE, Lee JC, Tomé FM, Romero NB, et al. Roberds SL, et al. Among authors: anderson rd. Cell. 1994 Aug 26;78(4):625-33. doi: 10.1016/0092-8674(94)90527-4. Cell. 1994. PMID: 8069911

2

Primary structure and muscle-specific expression of the 50-kDa dystrophin-associated glycoprotein (adhalin).

Roberds SL, Anderson RD, Ibraghimov-Beskrovnaya O, Campbell KP. Roberds SL, et al. Among authors: anderson rd. J Biol Chem. 1993 Nov 15;268(32):23739-42. J Biol Chem. 1993. PMID: 8226900 Free article.

3

Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin.

Matsumura K, Tomé FM, Ionasescu V, Ervasti JM, Anderson RD, Romero NB, Simon D, Récan D, Kaplan JC, Fardeau M, et al. Matsumura K, et al. Among authors: anderson rd. J Clin Invest. 1993 Aug;92(2):866-71. doi: 10.1172/JCI116661. J Clin Invest. 1993. PMID: 8349821 Free PMC article.

4

Functional rescue of the sarcoglycan complex in the BIO 14.6 hamster using delta-sarcoglycan gene transfer.

Holt KH, Lim LE, Straub V, Venzke DP, Duclos F, Anderson RD, Davidson BL, Campbell KP. Holt KH, et al. Among authors: anderson rd. Mol Cell. 1998 May;1(6):841-8. doi: 10.1016/s1097-2765(00)80083-0. Mol Cell. 1998. PMID: 9660967 Free article.

5

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: anderson rd. C R Acad Sci III. 1994 Jan;317(1):70-6. C R Acad Sci III. 1994. PMID: 7987694

6

Disruption of the dystrophin-glycoprotein complex in the cardiomyopathic hamster.

Roberds SL, Ervasti JM, Anderson RD, Ohlendieck K, Kahl SD, Zoloto D, Campbell KP. Roberds SL, et al. Among authors: anderson rd. J Biol Chem. 1993 Jun 5;268(16):11496-9. J Biol Chem. 1993. PMID: 8505286 Free article.

7

Clinical and molecular pathological features of severe childhood autosomal recessive muscular dystrophy in Saudi Arabia.

Salih MA, Mahdi AH, al-Rikabi AC, al-Bunyan M, Roberds SL, Anderson RD, Campbell KP. Salih MA, et al. Among authors: anderson rd. Dev Med Child Neurol. 1996 Mar;38(3):262-70. doi: 10.1111/j.1469-8749.1996.tb15089.x. Dev Med Child Neurol. 1996. PMID: 8631523

8

Genetic heterogeneity for Duchenne-like muscular dystrophy (DLMD) based on linkage and 50 DAG analysis.

Passos-Bueno MR, Oliveira JR, Bakker E, Anderson RD, Marie SK, Vainzof M, Roberds S, Campbell KP, Zatz M. Passos-Bueno MR, et al. Among authors: anderson rd. Hum Mol Genet. 1993 Nov;2(11):1945-7. doi: 10.1093/hmg/2.11.1945. Hum Mol Genet. 1993. PMID: 8281158

9

Alpha-dystroglycan deficiency correlates with elevated serum creatine kinase and decreased muscle contraction tension in golden retriever muscular dystrophy.

Ervasti JM, Roberds SL, Anderson RD, Sharp NJ, Kornegay JN, Campbell KP. Ervasti JM, et al. Among authors: anderson rd. FEBS Lett. 1994 Aug 22;350(2-3):173-6. doi: 10.1016/0014-5793(94)00748-9. FEBS Lett. 1994. PMID: 8070559 Free article.

10

Absence of the skeletal muscle sarcolemma chloride channel ClC-1 in myotonic mice.

Gurnett CA, Kahl SD, Anderson RD, Campbell KP. Gurnett CA, et al. Among authors: anderson rd. J Biol Chem. 1995 Apr 21;270(16):9035-8. doi: 10.1074/jbc.270.16.9035. J Biol Chem. 1995. PMID: 7721815 Free article.

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