Laval SH - Search Results

1

Attenuated muscle regeneration is a key factor in dysferlin-deficient muscular dystrophy.

Chiu YH, Hornsey MA, Klinge L, Jørgensen LH, Laval SH, Charlton R, Barresi R, Straub V, Lochmüller H, Bushby K. Chiu YH, et al. Among authors: laval sh. Hum Mol Genet. 2009 Jun 1;18(11):1976-89. doi: 10.1093/hmg/ddp121. Epub 2009 Mar 13. Hum Mol Genet. 2009. PMID: 19286669 Free PMC article.

2

Abnormal vascular development in zebrafish models for fukutin and FKRP deficiency.

Wood AJ, Müller JS, Jepson CD, Laval SH, Lochmüller H, Bushby K, Barresi R, Straub V. Wood AJ, et al. Among authors: laval sh. Hum Mol Genet. 2011 Dec 15;20(24):4879-90. doi: 10.1093/hmg/ddr426. Epub 2011 Sep 15. Hum Mol Genet. 2011. PMID: 21926082

3

The differential gene expression profiles of proximal and distal muscle groups are altered in pre-pathological dysferlin-deficient mice.

von der Hagen M, Laval SH, Cree LM, Haldane F, Pocock M, Wappler I, Peters H, Reitsamer HA, Hoger H, Wiedner M, Oberndorfer F, Anderson LV, Straub V, Bittner RE, Bushby KM. von der Hagen M, et al. Among authors: laval sh. Neuromuscul Disord. 2005 Dec;15(12):863-77. doi: 10.1016/j.nmd.2005.09.002. Epub 2005 Nov 8. Neuromuscul Disord. 2005. PMID: 16288871

4

Dok-7 promotes slow muscle integrity as well as neuromuscular junction formation in a zebrafish model of congenital myasthenic syndromes.

Müller JS, Jepson CD, Laval SH, Bushby K, Straub V, Lochmüller H. Müller JS, et al. Among authors: laval sh. Hum Mol Genet. 2010 May 1;19(9):1726-40. doi: 10.1093/hmg/ddq049. Epub 2010 Feb 10. Hum Mol Genet. 2010. PMID: 20147321

5

Muscular dystrophy in dysferlin-deficient mouse models.

Hornsey MA, Laval SH, Barresi R, Lochmüller H, Bushby K. Hornsey MA, et al. Among authors: laval sh. Neuromuscul Disord. 2013 May;23(5):377-87. doi: 10.1016/j.nmd.2013.02.004. Epub 2013 Mar 7. Neuromuscul Disord. 2013. PMID: 23473732 Review.

6

From T-tubule to sarcolemma: damage-induced dysferlin translocation in early myogenesis.

Klinge L, Laval S, Keers S, Haldane F, Straub V, Barresi R, Bushby K. Klinge L, et al. FASEB J. 2007 Jun;21(8):1768-76. doi: 10.1096/fj.06-7659com. Epub 2007 Mar 15. FASEB J. 2007. PMID: 17363620

7

Dysferlin associates with the developing T-tubule system in rodent and human skeletal muscle.

Klinge L, Harris J, Sewry C, Charlton R, Anderson L, Laval S, Chiu YH, Hornsey M, Straub V, Barresi R, Lochmüller H, Bushby K. Klinge L, et al. Muscle Nerve. 2010 Feb;41(2):166-73. doi: 10.1002/mus.21166. Muscle Nerve. 2010. PMID: 20082313

8

Intolerance to ß-blockade in a mouse model of δ-sarcoglycan-deficient muscular dystrophy cardiomyopathy.

Bauer R, Blain A, Greally E, Bushby K, Lochmüller H, Laval S, Straub V, MacGowan GA. Bauer R, et al. Eur J Heart Fail. 2010 Nov;12(11):1163-70. doi: 10.1093/eurjhf/hfq129. Epub 2010 Jul 30. Eur J Heart Fail. 2010. PMID: 20675662 Free article.

9

Characterisation of the dysferlin skeletal muscle promoter.

Foxton RM, Laval SH, Bushby KM. Foxton RM, et al. Among authors: laval sh. Eur J Hum Genet. 2004 Feb;12(2):127-31. doi: 10.1038/sj.ejhg.5201092. Eur J Hum Genet. 2004. PMID: 14560310

10

Limb-girdle muscular dystrophies--from genetics to molecular pathology.

Laval SH, Bushby KM. Laval SH, et al. Neuropathol Appl Neurobiol. 2004 Apr;30(2):91-105. doi: 10.1111/j.1365-2990.2004.00555.x. Neuropathol Appl Neurobiol. 2004. PMID: 15043707 Review.

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