Dubowitz V - Search Results

1

Exon skipping and translation in patients with frameshift deletions in the dystrophin gene.

Sherratt TG, Vulliamy T, Dubowitz V, Sewry CA, Strong PN. Sherratt TG, et al. Among authors: dubowitz v. Am J Hum Genet. 1993 Nov;53(5):1007-15. Am J Hum Genet. 1993. PMID: 8213828 Free PMC article.

2

Dystrophin and nebulin in the muscular dystrophies.

Patel K, Voit T, Dunn MJ, Strong PN, Dubowitz V. Patel K, et al. Among authors: dubowitz v. J Neurol Sci. 1988 Nov;87(2-3):315-26. doi: 10.1016/0022-510x(88)90256-0. J Neurol Sci. 1988. PMID: 3062133

3

Calmodulin-binding profiles for nebulin and dystrophin in human skeletal muscle.

Patel K, Strong PN, Dubowitz V, Dunn MJ. Patel K, et al. Among authors: dubowitz v. FEBS Lett. 1988 Jul 18;234(2):267-71. doi: 10.1016/0014-5793(88)80095-4. FEBS Lett. 1988. PMID: 3292289 Free article.

4

Expression of dystrophin-associated glycoproteins and utrophin in carriers of Duchenne muscular dystrophy.

Sewry CA, Matsumura K, Campbell KP, Dubowitz V. Sewry CA, et al. Among authors: dubowitz v. Neuromuscul Disord. 1994 Sep-Nov;4(5-6):401-9. doi: 10.1016/0960-8966(94)90079-5. Neuromuscul Disord. 1994. PMID: 7881285 Clinical Trial.

5

Manifesting carriers of Xp21 muscular dystrophy; lack of correlation between dystrophin expression and clinical weakness.

Sewry CA, Sansome A, Clerk A, Sherratt TG, Hasson N, Rodillo E, Heckmatt JZ, Strong PN, Dubowitz V. Sewry CA, et al. Among authors: dubowitz v. Neuromuscul Disord. 1993 Mar;3(2):141-8. doi: 10.1016/0960-8966(93)90006-6. Neuromuscul Disord. 1993. PMID: 8358239

6

Dystrophin-related protein, utrophin, in normal and dystrophic human fetal skeletal muscle.

Clerk A, Morris GE, Dubowitz V, Davies KE, Sewry CA. Clerk A, et al. Among authors: dubowitz v. Histochem J. 1993 Aug;25(8):554-61. Histochem J. 1993. PMID: 8407365

7

Is there selection in favour of heterozygotes in families with merosin-deficient congenital muscular dystrophy?

D'Alessandro M, Naom I, Ferlini A, Sewry C, Dubowitz V, Muntoni F. D'Alessandro M, et al. Among authors: dubowitz v. Hum Genet. 1999 Oct;105(4):308-13. doi: 10.1007/s004399900093. Hum Genet. 1999. PMID: 10543397

8

Characterisation of dystrophin in fetuses at risk for Duchenne muscular dystrophy.

Clerk A, Sewry CA, Dubowitz V, Strong PN. Clerk A, et al. Among authors: dubowitz v. J Neurol Sci. 1992 Aug;111(1):82-91. doi: 10.1016/0022-510x(92)90116-3. J Neurol Sci. 1992. PMID: 1403002

9

Dystrophin in frameshift deletion patients with Becker muscular dystrophy.

Gangopadhyay SB, Sherratt TG, Heckmatt JZ, Dubowitz V, Miller G, Shokeir M, Ray PN, Strong PN, Worton RG. Gangopadhyay SB, et al. Among authors: dubowitz v. Am J Hum Genet. 1992 Sep;51(3):562-70. Am J Hum Genet. 1992. PMID: 1496988 Free PMC article.

10

Dystrophin abnormalities in polymyositis and dermatomyositis.

Sewry CA, Clerk A, Heckmatt JZ, Vyse T, Dubowitz V, Strong PN. Sewry CA, et al. Among authors: dubowitz v. Neuromuscul Disord. 1991;1(5):333-9. doi: 10.1016/0960-8966(91)90119-d. Neuromuscul Disord. 1991. PMID: 1822343

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