Wilton SD - Search Results

1

Personalized exon skipping strategies to address clustered non-deletion dystrophin mutations.

Forrest S, Meloni PL, Muntoni F, Kim J, Fletcher S, Wilton SD. Forrest S, et al. Among authors: wilton sd. Neuromuscul Disord. 2010 Dec;20(12):810-6. doi: 10.1016/j.nmd.2010.07.276. Neuromuscul Disord. 2010. PMID: 20817455 Free PMC article.

2

Two distinct mutations in a single dystrophin gene: identification of an altered splice-site as the primary Becker muscular dystrophy mutation.

Wilton SD, Johnsen RD, Pedretti JR, Laing NG. Wilton SD, et al. Am J Med Genet. 1993 Jun 15;46(5):563-9. doi: 10.1002/ajmg.1320460521. Am J Med Genet. 1993. PMID: 8322822

3

Mutation segregation and rapid carrier detection of X-linked muscular dystrophy in dogs.

Bartlett RJ, Winand NJ, Secore SL, Singer JT, Fletcher S, Wilton S, Bogan DJ, Metcalf-Bogan JR, Bartlett WT, Howell JM, Cooper BJ, Kornegay JN. Bartlett RJ, et al. Am J Vet Res. 1996 May;57(5):650-4. Am J Vet Res. 1996. PMID: 8723876

4

Three novel mutations and two variants in the gene for Cu/Zn superoxide dismutase in familial amyotrophic lateral sclerosis.

Hosler BA, Nicholson GA, Sapp PC, Chin W, Orrell RW, de Belleroche JS, Esteban J, Hayward LJ, Mckenna-Yasek D, Yeung L, Cherryson AK, Dench JE, Wilton SD, Laing NG, Horvitz HR, Brown RH Jr. Hosler BA, et al. Among authors: wilton sd. Neuromuscul Disord. 1996 Oct;6(5):361-6. doi: 10.1016/0960-8966(96)00353-7. Neuromuscul Disord. 1996. PMID: 8938700

5

Dystrophin gene transcripts skipping the mdx mutation.

Wilton SD, Dye DE, Laing NG. Wilton SD, et al. Muscle Nerve. 1997 Jun;20(6):728-34. doi: 10.1002/(sici)1097-4598(199706)20:6<728::aid-mus10>3.0.co;2-q. Muscle Nerve. 1997. PMID: 9149080

6

Revertant fibres: a possible genetic therapy for Duchenne muscular dystrophy?

Wilton SD, Dye DE, Blechynden LM, Laing NG. Wilton SD, et al. Neuromuscul Disord. 1997 Jul;7(5):329-35. doi: 10.1016/s0960-8966(97)00058-8. Neuromuscul Disord. 1997. PMID: 9267847

7

A splice-site mutation causing ovine McArdle's disease.

Tan P, Allen JG, Wilton SD, Akkari PA, Huxtable CR, Laing NG. Tan P, et al. Among authors: wilton sd. Neuromuscul Disord. 1997 Jul;7(5):336-42. doi: 10.1016/s0960-8966(97)00062-x. Neuromuscul Disord. 1997. PMID: 9267848

8

Snapback SSCP analysis: engineered conformation changes for the rapid typing of known mutations.

Wilton SD, Honeyman K, Fletcher S, Laing NG. Wilton SD, et al. Hum Mutat. 1998;11(3):252-8. doi: 10.1002/(SICI)1098-1004(1998)11:3<252::AID-HUMU11>3.0.CO;2-Y. Hum Mutat. 1998. PMID: 9521428

9

Development of a snapback method of single-strand conformation polymorphism analysis for genotyping Golden Retrievers for the X-linked muscular dystrophy allele.

Honeyman K, Carville KS, Howell JM, Fletcher S, Wilton SD. Honeyman K, et al. Among authors: wilton sd. Am J Vet Res. 1999 Jun;60(6):734-7. Am J Vet Res. 1999. PMID: 10376903

10

Molecular analysis of a spontaneous dystrophin 'knockout' dog.

Schatzberg SJ, Olby NJ, Breen M, Anderson LV, Langford CF, Dickens HF, Wilton SD, Zeiss CJ, Binns MM, Kornegay JN, Morris GE, Sharp NJ. Schatzberg SJ, et al. Among authors: wilton sd. Neuromuscul Disord. 1999 Jul;9(5):289-95. doi: 10.1016/s0960-8966(99)00011-5. Neuromuscul Disord. 1999. PMID: 10407848

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