Wilton SD - Search Results

1

Multiple exon skipping strategies to by-pass dystrophin mutations.

Adkin CF, Meloni PL, Fletcher S, Adams AM, Muntoni F, Wong B, Wilton SD. Adkin CF, et al. Among authors: wilton sd. Neuromuscul Disord. 2012 Apr;22(4):297-305. doi: 10.1016/j.nmd.2011.10.007. Epub 2011 Dec 17. Neuromuscul Disord. 2012. PMID: 22182525 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

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

4

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

5

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

6

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

7

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

8

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

9

Specific removal of the nonsense mutation from the mdx dystrophin mRNA using antisense oligonucleotides.

Wilton SD, Lloyd F, Carville K, Fletcher S, Honeyman K, Agrawal S, Kole R. Wilton SD, et al. Neuromuscul Disord. 1999 Jul;9(5):330-8. doi: 10.1016/s0960-8966(99)00010-3. Neuromuscul Disord. 1999. PMID: 10407856

10

Homozygosity for a nonsense mutation in the alpha-tropomyosin slow gene TPM3 in a patient with severe infantile nemaline myopathy.

Tan P, Briner J, Boltshauser E, Davis MR, Wilton SD, North K, Wallgren-Pettersson C, Laing NG. Tan P, et al. Among authors: wilton sd. Neuromuscul Disord. 1999 Dec;9(8):573-9. doi: 10.1016/s0960-8966(99)00053-x. Neuromuscul Disord. 1999. PMID: 10619715

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