Wilton SD - Search Results

1

ALS Genetics, Mechanisms, and Therapeutics: Where Are We Now?

Mejzini R, Flynn LL, Pitout IL, Fletcher S, Wilton SD, Akkari PA. Mejzini R, et al. Among authors: wilton sd. Front Neurosci. 2019 Dec 6;13:1310. doi: 10.3389/fnins.2019.01310. eCollection 2019. Front Neurosci. 2019. PMID: 31866818 Free PMC article. Review.

2

Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisation.

Hunt CC, Eyre HJ, Akkari PA, Meredith C, Dorosz SM, Wilton SD, Callen DF, Laing NG, Baker E. Hunt CC, et al. Among authors: wilton sd. Cytogenet Cell Genet. 1995;71(1):94-5. doi: 10.1159/000134070. Cytogenet Cell Genet. 1995. PMID: 7606936

3

A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy.

Laing NG, Wilton SD, Akkari PA, Dorosz S, Boundy K, Kneebone C, Blumbergs P, White S, Watkins H, Love DR, et al. Laing NG, et al. Among authors: wilton sd. Nat Genet. 1995 Jan;9(1):75-9. doi: 10.1038/ng0195-75. Nat Genet. 1995. PMID: 7704029

4

Assignment of the human skeletal muscle alpha-tropomyosin gene (TPM1) to band 15q22 by fluorescence in situ hybridization.

Eyre H, Akkari PA, Wilton SD, Callen DC, Baker E, Laing NG. Eyre H, et al. Among authors: wilton sd. Cytogenet Cell Genet. 1995;69(1-2):15-7. doi: 10.1159/000133928. Cytogenet Cell Genet. 1995. PMID: 7835079

5

Assignment of the human a-tropomyosin gene TPM3 to 1q22-->q23 by fluorescence in situ hybridisation.

Wilton SD, Eyre H, Akkari PA, Watkins HC, MacRae C, Laing NG, Callen DC. Wilton SD, et al. Cytogenet Cell Genet. 1995;68(1-2):122-4. doi: 10.1159/000133905. Cytogenet Cell Genet. 1995. PMID: 7956350

6

Assignment of the human skeletal muscle alpha actin gene (ACTA1) to 1q42 by fluorescence in situ hybridisation.

Akkari PA, Eyre HJ, Wilton SD, Callen DF, Lane SA, Meredith C, Kedes L, Laing NG. Akkari PA, et al. Among authors: wilton sd. Cytogenet Cell Genet. 1994;65(4):265-7. doi: 10.1159/000133644. Cytogenet Cell Genet. 1994. PMID: 8258301

7

Assignment of the human slow skeletal muscle troponin gene (TNNI1) to 1q32 by fluorescence in situ hybridisation.

Eyre HJ, Akkari PA, Meredith C, Wilton SD, Callen DC, Kedes L, Laing NG. Eyre HJ, et al. Among authors: wilton sd. Cytogenet Cell Genet. 1993;62(2-3):181-2. doi: 10.1159/000133467. Cytogenet Cell Genet. 1993. PMID: 8428521

8

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

9

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

10

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

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