Laing NG - Search Results

1

Novel application of flow cytometry: determination of muscle fiber types and protein levels in whole murine skeletal muscles and heart.

Jackaman C, Nowak KJ, Ravenscroft G, Lim EM, Clément S, Laing NG. Jackaman C, et al. Among authors: laing ng. Cell Motil Cytoskeleton. 2007 Dec;64(12):914-25. doi: 10.1002/cm.20239. Cell Motil Cytoskeleton. 2007. PMID: 17922482

2

Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy.

Mastaglia FL, Nowak KJ, Stell R, Phillips BA, Edmondston JE, Dorosz SM, Wilton SD, Hallmayer J, Kakulas BA, Laing NG. Mastaglia FL, et al. Among authors: laing ng. J Neurol Neurosurg Psychiatry. 1999 Aug;67(2):174-9. doi: 10.1136/jnnp.67.2.174. J Neurol Neurosurg Psychiatry. 1999. PMID: 10406984 Free PMC article.

3

Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy.

Nowak KJ, Wattanasirichaigoon D, Goebel HH, Wilce M, Pelin K, Donner K, Jacob RL, Hübner C, Oexle K, Anderson JR, Verity CM, North KN, Iannaccone ST, Müller CR, Nürnberg P, Muntoni F, Sewry C, Hughes I, Sutphen R, Lacson AG, Swoboda KJ, Vigneron J, Wallgren-Pettersson C, Beggs AH, Laing NG. Nowak KJ, et al. Among authors: laing ng. Nat Genet. 1999 Oct;23(2):208-12. doi: 10.1038/13837. Nat Genet. 1999. PMID: 10508519

4

Inherited disorders of sarcomeric proteins.

Laing NG. Laing NG. Curr Opin Neurol. 1999 Oct;12(5):513-8. doi: 10.1097/00019052-199910000-00004. Curr Opin Neurol. 1999. PMID: 10590887 Review.

5

Inherited skeletal muscle disorders.

Laing NG, Mastaglia FL. Laing NG, et al. Ann Hum Biol. 1999 Nov-Dec;26(6):507-25. doi: 10.1080/030144699282435. Ann Hum Biol. 1999. PMID: 10612262 Free article. Review.

6

Severe gamma-sarcoglycanopathy caused by a novel missense mutation and a large deletion.

Nowak KJ, Walsh P, Jacob RL, Johnsen RD, Peverall J, McNally EM, Wilton SD, Kakulas BA, Laing NG. Nowak KJ, et al. Among authors: laing ng. Neuromuscul Disord. 2000 Feb;10(2):100-7. doi: 10.1016/s0960-8966(99)00063-2. Neuromuscul Disord. 2000. PMID: 10714584

7

Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle alpha-actin (ACTA1) gene.

Jungbluth H, Sewry CA, Brown SC, Nowak KJ, Laing NG, Wallgren-Pettersson C, Pelin K, Manzur AY, Mercuri E, Dubowitz V, Muntoni F. Jungbluth H, et al. Among authors: laing ng. Neuromuscul Disord. 2001 Jan;11(1):35-40. doi: 10.1016/s0960-8966(00)00167-x. Neuromuscul Disord. 2001. PMID: 11166164

8

Nemaline myopathy caused by mutations in the muscle alpha-skeletal-actin gene.

Ilkovski B, Cooper ST, Nowak K, Ryan MM, Yang N, Schnell C, Durling HJ, Roddick LG, Wilkinson I, Kornberg AJ, Collins KJ, Wallace G, Gunning P, Hardeman EC, Laing NG, North KN. Ilkovski B, et al. Among authors: laing ng. Am J Hum Genet. 2001 Jun;68(6):1333-43. doi: 10.1086/320605. Epub 2001 Apr 27. Am J Hum Genet. 2001. PMID: 11333380 Free PMC article.

9

Characterization of human muscle type cofilin (CFL2) in normal and regenerating muscle.

Thirion C, Stucka R, Mendel B, Gruhler A, Jaksch M, Nowak KJ, Binz N, Laing NG, Lochmüller H. Thirion C, et al. Among authors: laing ng. Eur J Biochem. 2001 Jun;268(12):3473-82. doi: 10.1046/j.1432-1327.2001.02247.x. Eur J Biochem. 2001. PMID: 11422377 Free article.

10

Congenital nemaline myopathy due to ACTA1-gene mutation and carnitine insufficiency: a case report.

Buxmann H, Schlösser R, Schlote W, Sewell A, Nowak KJ, Laing NG, Loewenich V. Buxmann H, et al. Among authors: laing ng. Neuropediatrics. 2001 Oct;32(5):267-70. doi: 10.1055/s-2001-19122. Neuropediatrics. 2001. PMID: 11748499

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