Fletcher S - 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: fletcher s. 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

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. Among authors: fletcher s. Am J Vet Res. 1996 May;57(5):650-4. Am J Vet Res. 1996. PMID: 8723876

3

Use of the dog model for Duchenne muscular dystrophy in gene therapy trials.

Howell JM, Fletcher S, Kakulas BA, O'Hara M, Lochmuller H, Karpati G. Howell JM, et al. Among authors: fletcher s. Neuromuscul Disord. 1997 Jul;7(5):325-8. doi: 10.1016/s0960-8966(97)00057-6. Neuromuscul Disord. 1997. PMID: 9267846

4

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. Among authors: fletcher s. 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

5

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: fletcher s. Am J Vet Res. 1999 Jun;60(6):734-7. Am J Vet Res. 1999. PMID: 10376903

6

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. Among authors: fletcher s. Neuromuscul Disord. 1999 Jul;9(5):330-8. doi: 10.1016/s0960-8966(99)00010-3. Neuromuscul Disord. 1999. PMID: 10407856

7

Gene therapy and molecular approaches to the treatment of hereditary muscular disorders.

Fletcher S, Wilton SD, Howell JM. Fletcher S, et al. Curr Opin Neurol. 2000 Oct;13(5):553-60. doi: 10.1097/00019052-200010000-00008. Curr Opin Neurol. 2000. PMID: 11073362 Review.

8

Antisense-induced exon skipping and synthesis of dystrophin in the mdx mouse.

Mann CJ, Honeyman K, Cheng AJ, Ly T, Lloyd F, Fletcher S, Morgan JE, Partridge TA, Wilton SD. Mann CJ, et al. Among authors: fletcher s. Proc Natl Acad Sci U S A. 2001 Jan 2;98(1):42-7. doi: 10.1073/pnas.98.1.42. Proc Natl Acad Sci U S A. 2001. PMID: 11120883 Free PMC article.

9

Cryptic splicing involving the splice site mutation in the canine model of Duchenne muscular dystrophy.

Fletcher S, Ly T, Duff RM, McC Howell J, Wilton SD. Fletcher S, et al. Neuromuscul Disord. 2001 Apr;11(3):239-43. doi: 10.1016/s0960-8966(00)00187-5. Neuromuscul Disord. 2001. PMID: 11297938

10

Evaluation of a short interspersed nucleotide element in the 3' untranslated region of the defective dystrophin gene of dogs with muscular dystrophy.

Fletcher S, Carville KS, Howell JM, Mann CJ, Wilton SD. Fletcher S, et al. Am J Vet Res. 2001 Dec;62(12):1964-8. doi: 10.2460/ajvr.2001.62.1964. Am J Vet Res. 2001. PMID: 11763189 Free article.

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