Harris JB - Search Results

1

Very mild muscular dystrophy associated with the deletion of 46% of dystrophin.

England SB, Nicholson LV, Johnson MA, Forrest SM, Love DR, Zubrzycka-Gaarn EE, Bulman DE, Harris JB, Davies KE. England SB, et al. Among authors: harris jb. Nature. 1990 Jan 11;343(6254):180-2. doi: 10.1038/343180a0. Nature. 1990. PMID: 2404210

2

Identification of a mutation in the promoter region of the dystrophin gene in a patient with atypical Becker muscular dystrophy.

Bushby KM, Cleghorn NJ, Curtis A, Haggerty ID, Nicholson LV, Johnson MA, Harris JB, Bhattacharya SS. Bushby KM, et al. Among authors: harris jb. Hum Genet. 1991 Dec;88(2):195-9. doi: 10.1007/BF00206071. Hum Genet. 1991. PMID: 1757094

3

The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy. II. Correlation of phenotype with genetic and protein abnormalities.

Bushby KM, Gardner-Medwin D, Nicholson LV, Johnson MA, Haggerty ID, Cleghorn NJ, Harris JB, Bhattacharya SS. Bushby KM, et al. Among authors: harris jb. J Neurol. 1993 Feb;240(2):105-12. doi: 10.1007/BF00858726. J Neurol. 1993. PMID: 8437017

4

Heterogeneity of dystrophin expression in patients with Duchenne and Becker muscular dystrophy.

Nicholson LV, Johnson MA, Gardner-Medwin D, Bhattacharya S, Harris JB. Nicholson LV, et al. Among authors: harris jb. Acta Neuropathol. 1990;80(3):239-50. doi: 10.1007/BF00294640. Acta Neuropathol. 1990. PMID: 2205076

5

Dystrophin in skeletal muscle. II. Immunoreactivity in patients with Xp21 muscular dystrophy.

Nicholson LV, Davison K, Johnson MA, Slater CR, Young C, Bhattacharya S, Gardner-Medwin D, Harris JB. Nicholson LV, et al. Among authors: harris jb. J Neurol Sci. 1989 Dec;94(1-3):137-46. doi: 10.1016/0022-510x(89)90224-4. J Neurol Sci. 1989. PMID: 2693618

6

Dystrophin or a "related protein" in Duchenne muscular dystrophy?

Nicholson LV, Johnson MA, Davison K, O'Donnell E, Falkous G, Barron M, Harris JB. Nicholson LV, et al. Among authors: harris jb. Acta Neurol Scand. 1992 Jul;86(1):8-14. doi: 10.1111/j.1600-0404.1992.tb08046.x. Acta Neurol Scand. 1992. PMID: 1519480

7

Immunogold labelling of dystrophin in human muscle, using an antibody to the last 17 amino acids of the C-terminus.

Cullen MJ, Walsh J, Nicholson LV, Harris JB, Zubrzycka-Gaarn EE, Ray PN, Worton RG. Cullen MJ, et al. Among authors: harris jb. Neuromuscul Disord. 1991;1(2):113-9. doi: 10.1016/0960-8966(91)90058-z. Neuromuscul Disord. 1991. PMID: 1822781

8

Ultrastructural localization of dystrophin in human muscle by using gold immunolabelling.

Cullen MJ, Walsh J, Nicholson LV, Harris JB. Cullen MJ, et al. Among authors: harris jb. Proc R Soc Lond B Biol Sci. 1990 May 22;240(1297):197-210. doi: 10.1098/rspb.1990.0034. Proc R Soc Lond B Biol Sci. 1990. PMID: 1972991

9

Improved diagnosis of Becker muscular dystrophy by dystrophin testing.

Hoffman EP, Kunkel LM, Angelini C, Clarke A, Johnson M, Harris JB. Hoffman EP, et al. Among authors: harris jb. Neurology. 1989 Aug;39(8):1011-7. doi: 10.1212/wnl.39.8.1011. Neurology. 1989. PMID: 2668783

10

Dystrophin in skeletal muscle. I. Western blot analysis using a monoclonal antibody.

Nicholson LV, Davison K, Falkous G, Harwood C, O'Donnell E, Slater CR, Harris JB. Nicholson LV, et al. Among authors: harris jb. J Neurol Sci. 1989 Dec;94(1-3):125-36. doi: 10.1016/0022-510x(89)90223-2. J Neurol Sci. 1989. PMID: 2693617

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