Zhou H - Search Results

1

Establishment of a human skeletal muscle-derived cell line: biochemical, cellular and electrophysiological characterization.

Rokach O, Ullrich ND, Rausch M, Mouly V, Zhou H, Muntoni F, Zorzato F, Treves S. Rokach O, et al. Among authors: zhou h. Biochem J. 2013 Oct 15;455(2):169-77. doi: 10.1042/BJ20130698. Biochem J. 2013. PMID: 23905709 Free article.

2

Characterization of recessive RYR1 mutations in core myopathies.

Zhou H, Yamaguchi N, Xu L, Wang Y, Sewry C, Jungbluth H, Zorzato F, Bertini E, Muntoni F, Meissner G, Treves S. Zhou H, et al. Hum Mol Genet. 2006 Sep 15;15(18):2791-803. doi: 10.1093/hmg/ddl221. Epub 2006 Aug 29. Hum Mol Genet. 2006. PMID: 16940308 Free article.

3

Epigenetic allele silencing unveils recessive RYR1 mutations in core myopathies.

Zhou H, Brockington M, Jungbluth H, Monk D, Stanier P, Sewry CA, Moore GE, Muntoni F. Zhou H, et al. Am J Hum Genet. 2006 Nov;79(5):859-68. doi: 10.1086/508500. Epub 2006 Sep 21. Am J Hum Genet. 2006. PMID: 17033962 Free PMC article.

4

Desmin immunolocalisation in autosomal dominant Emery-Dreifuss muscular dystrophy.

Piercy RJ, Zhou H, Feng L, Pombo A, Muntoni F, Brown SC. Piercy RJ, et al. Among authors: zhou h. Neuromuscul Disord. 2007 Apr;17(4):297-305. doi: 10.1016/j.nmd.2007.01.003. Epub 2007 Feb 27. Neuromuscul Disord. 2007. PMID: 17329105

5

Functional effects of mutations identified in patients with multiminicore disease.

Zorzato F, Jungbluth H, Zhou H, Muntoni F, Treves S. Zorzato F, et al. Among authors: zhou h. IUBMB Life. 2007 Jan;59(1):14-20. doi: 10.1080/15216540601187803. IUBMB Life. 2007. PMID: 17365175 Free article. Review.

6

Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene.

Jungbluth H, Zhou H, Sewry CA, Robb S, Treves S, Bitoun M, Guicheney P, Buj-Bello A, Bönnemann C, Muntoni F. Jungbluth H, et al. Among authors: zhou h. Neuromuscul Disord. 2007 Apr;17(4):338-45. doi: 10.1016/j.nmd.2007.01.016. Epub 2007 Mar 21. Neuromuscul Disord. 2007. PMID: 17376685

7

Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies.

Zhou H, Jungbluth H, Sewry CA, Feng L, Bertini E, Bushby K, Straub V, Roper H, Rose MR, Brockington M, Kinali M, Manzur A, Robb S, Appleton R, Messina S, D'Amico A, Quinlivan R, Swash M, Müller CR, Brown S, Treves S, Muntoni F. Zhou H, et al. Brain. 2007 Aug;130(Pt 8):2024-36. doi: 10.1093/brain/awm096. Epub 2007 May 4. Brain. 2007. PMID: 17483490 Free article.

8

A recessive ryanodine receptor 1 mutation in a CCD patient increases channel activity.

Ghassemi F, Vukcevic M, Xu L, Zhou H, Meissner G, Muntoni F, Jungbluth H, Zorzato F, Treves S. Ghassemi F, et al. Among authors: zhou h. Cell Calcium. 2009 Feb;45(2):192-7. doi: 10.1016/j.ceca.2008.10.001. Epub 2008 Nov 21. Cell Calcium. 2009. PMID: 19027160 Free PMC article.

9

Assessment of the transformation of equine skin-derived fibroblasts to multinucleated skeletal myotubes following lentiviral-induced expression of equine myogenic differentiation 1.

Fernandez-Fuente M, Ames EG, Wagner ML, Zhou H, Strom M, Zammit PS, Mickelson JR, Muntoni F, Brown SC, Piercy RJ. Fernandez-Fuente M, et al. Among authors: zhou h. Am J Vet Res. 2008 Dec;69(12):1637-45. doi: 10.2460/ajvr.69.12.1637. Am J Vet Res. 2008. PMID: 19046012 Free article.

10

Late-onset axial myopathy with cores due to a novel heterozygous dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene.

Jungbluth H, Lillis S, Zhou H, Abbs S, Sewry C, Swash M, Muntoni F. Jungbluth H, et al. Among authors: zhou h. Neuromuscul Disord. 2009 May;19(5):344-7. doi: 10.1016/j.nmd.2009.02.005. Epub 2009 Mar 19. Neuromuscul Disord. 2009. PMID: 19303294

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