Wei L - Search Results

1

Mitochondrial superoxide flashes: metabolic biomarkers of skeletal muscle activity and disease.

Wei L, Salahura G, Boncompagni S, Kasischke KA, Protasi F, Sheu SS, Dirksen RT. Wei L, et al. FASEB J. 2011 Sep;25(9):3068-78. doi: 10.1096/fj.11-187252. Epub 2011 Jun 6. FASEB J. 2011. PMID: 21646399 Free PMC article.

2

Differential impact of mitochondrial positioning on mitochondrial Ca(2+) uptake and Ca(2+) spark suppression in skeletal muscle.

Rossi AE, Boncompagni S, Wei L, Protasi F, Dirksen RT. Rossi AE, et al. Among authors: wei l. Am J Physiol Cell Physiol. 2011 Nov;301(5):C1128-39. doi: 10.1152/ajpcell.00194.2011. Epub 2011 Aug 17. Am J Physiol Cell Physiol. 2011. PMID: 21849670 Free PMC article.

3

Perspectives on: SGP symposium on mitochondrial physiology and medicine: mitochondrial superoxide flashes: from discovery to new controversies.

Wei L, Dirksen RT. Wei L, et al. J Gen Physiol. 2012 Jun;139(6):425-34. doi: 10.1085/jgp.201210790. J Gen Physiol. 2012. PMID: 22641637 Free PMC article. No abstract available.

4

Muscle weakness in myotonic dystrophy associated with misregulated splicing and altered gating of Ca(V)1.1 calcium channel.

Tang ZZ, Yarotskyy V, Wei L, Sobczak K, Nakamori M, Eichinger K, Moxley RT, Dirksen RT, Thornton CA. Tang ZZ, et al. Among authors: wei l. Hum Mol Genet. 2012 Mar 15;21(6):1312-24. doi: 10.1093/hmg/ddr568. Epub 2011 Dec 2. Hum Mol Genet. 2012. PMID: 22140091 Free PMC article.

5

A variably spliced region in the type 1 ryanodine receptor may participate in an inter-domain interaction.

Kimura T, Pace SM, Wei L, Beard NA, Dirksen RT, Dulhunty AF. Kimura T, et al. Among authors: wei l. Biochem J. 2007 Jan 1;401(1):317-24. doi: 10.1042/BJ20060686. Biochem J. 2007. PMID: 16989644 Free PMC article.

6

The elusive role of the SPRY2 domain in RyR1.

Tae H, Wei L, Willemse H, Mirza S, Gallant EM, Board PG, Dirksen RT, Casarotto MG, Dulhunty A. Tae H, et al. Among authors: wei l. Channels (Austin). 2011 Mar-Apr;5(2):148-60. doi: 10.4161/chan.5.2.14407. Epub 2011 Mar 1. Channels (Austin). 2011. PMID: 21239886 Free PMC article.

7

Ryanodinopathies: RyR-Linked Muscle Diseases.

Wei L, Dirksen RT. Wei L, et al. Curr Top Membr. 2010;66:139-67. doi: 10.1016/S1063-5823(10)66007-3. Epub 2010 Jul 25. Curr Top Membr. 2010. PMID: 22353479 No abstract available.

8

Unique isoform-specific properties of calsequestrin in the heart and skeletal muscle.

Wei L, Hanna AD, Beard NA, Dulhunty AF. Wei L, et al. Cell Calcium. 2009 May;45(5):474-84. doi: 10.1016/j.ceca.2009.03.006. Epub 2009 Apr 18. Cell Calcium. 2009. PMID: 19376574

9

Phosphorylation of skeletal muscle calsequestrin enhances its Ca2+ binding capacity and promotes its association with junctin.

Beard NA, Wei L, Cheung SN, Kimura T, Varsányi M, Dulhunty AF. Beard NA, et al. Among authors: wei l. Cell Calcium. 2008 Oct;44(4):363-73. doi: 10.1016/j.ceca.2008.01.005. Cell Calcium. 2008. PMID: 19230141

10

Muscle-specific GSTM2-2 on the luminal side of the sarcoplasmic reticulum modifies RyR ion channel activity.

Wei L, Abdellatif YA, Liu D, Kimura T, Coggan M, Gallant EM, Beard NA, Board PG, Dulhunty AF. Wei L, et al. Int J Biochem Cell Biol. 2008;40(8):1616-28. doi: 10.1016/j.biocel.2007.12.019. Epub 2008 Jan 20. Int J Biochem Cell Biol. 2008. PMID: 18308613

The properties of hGSTM2-2 were compared with those of the calsequestrin (CSQ), a Ca(2+) binding protein also present in the lumen of the SR which, like GSTM2-2, contains a thioredoxin-fold structure and modifies RyR activity (Wei, L., Varsanyi, M., Dulhunty, A. F., …

The properties of hGSTM2-2 were compared with those of the calsequestrin (CSQ), a Ca(2+) binding protein also present in the lumen of the SR …

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