Lek M - Search Results

1

Variants in SLC18A3, vesicular acetylcholine transporter, cause congenital myasthenic syndrome.

O'Grady GL, Verschuuren C, Yuen M, Webster R, Menezes M, Fock JM, Pride N, Best HA, Benavides Damm T, Turner C, Lek M, Engel AG, North KN, Clarke NF, MacArthur DG, Kamsteeg EJ, Cooper ST. O'Grady GL, et al. Among authors: lek m. Neurology. 2016 Oct 4;87(14):1442-1448. doi: 10.1212/WNL.0000000000003179. Epub 2016 Sep 2. Neurology. 2016. PMID: 27590285 Free PMC article.

2

Myoblast sensitivity and fibroblast insensitivity to osteogenic conversion by BMP-2 correlates with the expression of Bmpr-1a.

Liu R, Ginn SL, Lek M, North KN, Alexander IE, Little DG, Schindeler A. Liu R, et al. Among authors: lek m. BMC Musculoskelet Disord. 2009 May 15;10:51. doi: 10.1186/1471-2474-10-51. BMC Musculoskelet Disord. 2009. PMID: 19442313 Free PMC article.

3

Phylogenetic analysis of gene structure and alternative splicing in alpha-actinins.

Lek M, MacArthur DG, Yang N, North KN. Lek M, et al. Mol Biol Evol. 2010 Apr;27(4):773-80. doi: 10.1093/molbev/msp268. Epub 2009 Nov 6. Mol Biol Evol. 2010. PMID: 19897525 Free PMC article.

4

The evolution of skeletal muscle performance: gene duplication and divergence of human sarcomeric alpha-actinins.

Lek M, Quinlan KG, North KN. Lek M, et al. Bioessays. 2010 Jan;32(1):17-25. doi: 10.1002/bies.200900110. Bioessays. 2010. PMID: 19967710 Review.

5

Alpha-actinin-3 deficiency results in reduced glycogen phosphorylase activity and altered calcium handling in skeletal muscle.

Quinlan KG, Seto JT, Turner N, Vandebrouck A, Floetenmeyer M, Macarthur DG, Raftery JM, Lek M, Yang N, Parton RG, Cooney GJ, North KN. Quinlan KG, et al. Among authors: lek m. Hum Mol Genet. 2010 Apr 1;19(7):1335-46. doi: 10.1093/hmg/ddq010. Epub 2010 Jan 20. Hum Mol Genet. 2010. PMID: 20089531

6

Are biological sensors modulated by their structural scaffolds? The role of the structural muscle proteins alpha-actinin-2 and alpha-actinin-3 as modulators of biological sensors.

Lek M, North KN. Lek M, et al. FEBS Lett. 2010 Jul 16;584(14):2974-80. doi: 10.1016/j.febslet.2010.05.059. Epub 2010 May 31. FEBS Lett. 2010. PMID: 20515688 Free article. Review.

7

Phylogenetic analysis of ferlin genes reveals ancient eukaryotic origins.

Lek A, Lek M, North KN, Cooper ST. Lek A, et al. Among authors: lek m. BMC Evol Biol. 2010 Jul 29;10:231. doi: 10.1186/1471-2148-10-231. BMC Evol Biol. 2010. PMID: 20667140 Free PMC article.

8

Deficiency of α-actinin-3 is associated with increased susceptibility to contraction-induced damage and skeletal muscle remodeling.

Seto JT, Lek M, Quinlan KG, Houweling PJ, Zheng XF, Garton F, MacArthur DG, Raftery JM, Garvey SM, Hauser MA, Yang N, Head SI, North KN. Seto JT, et al. Among authors: lek m. Hum Mol Genet. 2011 Aug 1;20(15):2914-27. doi: 10.1093/hmg/ddr196. Epub 2011 May 2. Hum Mol Genet. 2011. PMID: 21536590

9

A study of FHL1, BAG3, MATR3, PTRF and TCAP in Australian muscular dystrophy patients.

Waddell LB, Tran J, Zheng XF, Bönnemann CG, Hu Y, Evesson FJ, Lek M, Arbuckle S, Wang MX, Smith RL, North KN, Clarke NF. Waddell LB, et al. Among authors: lek m. Neuromuscul Disord. 2011 Nov;21(11):776-81. doi: 10.1016/j.nmd.2011.05.007. Epub 2011 Jun 17. Neuromuscul Disord. 2011. PMID: 21683594 Free PMC article.

10

α-Actinin-3 deficiency is associated with reduced bone mass in human and mouse.

Yang N, Schindeler A, McDonald MM, Seto JT, Houweling PJ, Lek M, Hogarth M, Morse AR, Raftery JM, Balasuriya D, MacArthur DG, Berman Y, Quinlan KG, Eisman JA, Nguyen TV, Center JR, Prince RL, Wilson SG, Zhu K, Little DG, North KN. Yang N, et al. Among authors: lek m. Bone. 2011 Oct;49(4):790-8. doi: 10.1016/j.bone.2011.07.009. Epub 2011 Jul 19. Bone. 2011. PMID: 21784188

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