Laing NG - Search Results

1

Mutations and polymorphisms of the skeletal muscle alpha-actin gene (ACTA1).

Laing NG, Dye DE, Wallgren-Pettersson C, Richard G, Monnier N, Lillis S, Winder TL, Lochmüller H, Graziano C, Mitrani-Rosenbaum S, Twomey D, Sparrow JC, Beggs AH, Nowak KJ. Laing NG, et al. Hum Mutat. 2009 Sep;30(9):1267-77. doi: 10.1002/humu.21059. Hum Mutat. 2009. PMID: 19562689 Free PMC article.

2

Assignment of a gene (NEMI) for autosomal dominant nemaline myopathy to chromosome I.

Laing NG, Majda BT, Akkari PA, Layton MG, Mulley JC, Phillips H, Haan EA, White SJ, Beggs AH, Kunkel LM, et al. Laing NG, et al. Am J Hum Genet. 1992 Mar;50(3):576-83. Am J Hum Genet. 1992. PMID: 1347195 Free PMC article.

3

A (CA)n repeat polymorphism for the human skeletal muscle alpha-actinin gene ACTN2 and its localization on the linkage map of chromosome 1.

Beggs AH, Phillips HA, Kozman H, Mulley JC, Wilton SD, Kunkel LM, Laing NG. Beggs AH, et al. Among authors: laing ng. Genomics. 1992 Aug;13(4):1314-5. doi: 10.1016/0888-7543(92)90054-v. Genomics. 1992. PMID: 1505962

4

Identification of a point mutation and germinal mosaicism in a Duchenne muscular dystrophy family.

Wilton SD, Chandler DC, Kakulas BA, Laing NG. Wilton SD, et al. Among authors: laing ng. Hum Mutat. 1994;3(2):133-40. doi: 10.1002/humu.1380030208. Hum Mutat. 1994. PMID: 8199594

5

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: laing ng. Cytogenet Cell Genet. 1994;65(4):265-7. doi: 10.1159/000133644. Cytogenet Cell Genet. 1994. PMID: 8258301

6

Inherited disorders of contractile proteins in skeletal and cardiac muscle.

Laing NG. Laing NG. Curr Opin Neurol. 1995 Oct;8(5):391-6. doi: 10.1097/00019052-199510000-00012. Curr Opin Neurol. 1995. PMID: 8542046 Review.

7

40th ENMC Sponsored International Workshop: Nemaline Myopathy. 2-4 February 1996, Naarden, The Netherlands.

Wallgren-Pettersson C, Laing N. Wallgren-Pettersson C, et al. Neuromuscul Disord. 1996 Oct;6(5):389-91. doi: 10.1016/0960-8966(96)00354-9. Neuromuscul Disord. 1996. PMID: 8938704 Review. No abstract available.

8

Bandstab: a PCR-based alternative to cloning PCR products.

Wilton SD, Lim L, Dye D, Laing N. Wilton SD, et al. Biotechniques. 1997 Apr;22(4):642-5. doi: 10.2144/97224bm14. Biotechniques. 1997. PMID: 9105612 Free article. No abstract available.

9

Dystrophin gene transcripts skipping the mdx mutation.

Wilton SD, Dye DE, Laing NG. Wilton SD, et al. Among authors: laing ng. 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

10

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

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

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