Wilton SD - Search Results

1

Single Stranded Fully Modified-Phosphorothioate Oligonucleotides can Induce Structured Nuclear Inclusions, Alter Nuclear Protein Localization and Disturb the Transcriptome In Vitro.

Flynn LL, Li R, Pitout IL, Aung-Htut MT, Larcher LM, Cooper JAL, Greer KL, Hubbard A, Griffiths L, Bond CS, Wilton SD, Fox AH, Fletcher S. Flynn LL, et al. Among authors: wilton sd. Front Genet. 2022 Apr 6;13:791416. doi: 10.3389/fgene.2022.791416. eCollection 2022. Front Genet. 2022. PMID: 35464859 Free PMC article.

2

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

3

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

4

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

5

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

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

6

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: wilton sd. 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.

7

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. Among authors: wilton sd. Neuromuscul Disord. 2001 Apr;11(3):239-43. doi: 10.1016/s0960-8966(00)00187-5. Neuromuscul Disord. 2001. PMID: 11297938

8

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. Among authors: wilton sd. 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.

9

Improved antisense oligonucleotide induced exon skipping in the mdx mouse model of muscular dystrophy.

Mann CJ, Honeyman K, McClorey G, Fletcher S, Wilton SD. Mann CJ, et al. Among authors: wilton sd. J Gene Med. 2002 Nov-Dec;4(6):644-54. doi: 10.1002/jgm.295. J Gene Med. 2002. PMID: 12439856

10

Target selection for antisense oligonucleotide induced exon skipping in the dystrophin gene.

Errington SJ, Mann CJ, Fletcher S, Wilton SD. Errington SJ, et al. Among authors: wilton sd. J Gene Med. 2003 Jun;5(6):518-27. doi: 10.1002/jgm.361. J Gene Med. 2003. PMID: 12797117

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