Allamand V - Search Results

1

Selenoprotein N is dynamically expressed during mouse development and detected early in muscle precursors.

Castets P, Maugenre S, Gartioux C, Rederstorff M, Krol A, Lescure A, Tajbakhsh S, Allamand V, Guicheney P. Castets P, et al. Among authors: allamand v. BMC Dev Biol. 2009 Aug 22;9:46. doi: 10.1186/1471-213X-9-46. BMC Dev Biol. 2009. PMID: 19698141 Free PMC article.

2

Selenoprotein function and muscle disease.

Lescure A, Rederstorff M, Krol A, Guicheney P, Allamand V. Lescure A, et al. Among authors: allamand v. Biochim Biophys Acta. 2009 Nov;1790(11):1569-74. doi: 10.1016/j.bbagen.2009.03.002. Epub 2009 Mar 11. Biochim Biophys Acta. 2009. PMID: 19285112 Review.

3

Satellite cell loss and impaired muscle regeneration in selenoprotein N deficiency.

Castets P, Bertrand AT, Beuvin M, Ferry A, Le Grand F, Castets M, Chazot G, Rederstorff M, Krol A, Lescure A, Romero NB, Guicheney P, Allamand V. Castets P, et al. Among authors: allamand v. Hum Mol Genet. 2011 Feb 15;20(4):694-704. doi: 10.1093/hmg/ddq515. Epub 2010 Dec 2. Hum Mol Genet. 2011. PMID: 21131290

4

Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for alpha2 chain of laminin).

Allamand V, Guicheney P. Allamand V, et al. Eur J Hum Genet. 2002 Feb;10(2):91-4. doi: 10.1038/sj.ejhg.5200743. Eur J Hum Genet. 2002. PMID: 11938437

5

A single homozygous point mutation in a 3'untranslated region motif of selenoprotein N mRNA causes SEPN1-related myopathy.

Allamand V, Richard P, Lescure A, Ledeuil C, Desjardin D, Petit N, Gartioux C, Ferreiro A, Krol A, Pellegrini N, Urtizberea JA, Guicheney P. Allamand V, et al. EMBO Rep. 2006 Apr;7(4):450-4. doi: 10.1038/sj.embor.7400648. Epub 2006 Feb 24. EMBO Rep. 2006. PMID: 16498447 Free PMC article.

6

Early onset collagen VI myopathies: Genetic and clinical correlations.

Briñas L, Richard P, Quijano-Roy S, Gartioux C, Ledeuil C, Lacène E, Makri S, Ferreiro A, Maugenre S, Topaloglu H, Haliloglu G, Pénisson-Besnier I, Jeannet PY, Merlini L, Navarro C, Toutain A, Chaigne D, Desguerre I, de Die-Smulders C, Dunand M, Echenne B, Eymard B, Kuntzer T, Maincent K, Mayer M, Plessis G, Rivier F, Roelens F, Stojkovic T, Taratuto AL, Lubieniecki F, Monges S, Tranchant C, Viollet L, Romero NB, Estournet B, Guicheney P, Allamand V. Briñas L, et al. Among authors: allamand v. Ann Neurol. 2010 Oct;68(4):511-20. doi: 10.1002/ana.22087. Ann Neurol. 2010. PMID: 20976770

7

Increased muscle stress-sensitivity induced by selenoprotein N inactivation in mouse: a mammalian model for SEPN1-related myopathy.

Rederstorff M, Castets P, Arbogast S, Lainé J, Vassilopoulos S, Beuvin M, Dubourg O, Vignaud A, Ferry A, Krol A, Allamand V, Guicheney P, Ferreiro A, Lescure A. Rederstorff M, et al. Among authors: allamand v. PLoS One. 2011;6(8):e23094. doi: 10.1371/journal.pone.0023094. Epub 2011 Aug 8. PLoS One. 2011. PMID: 21858002 Free PMC article.

8

Selenoprotein N in skeletal muscle: from diseases to function.

Castets P, Lescure A, Guicheney P, Allamand V. Castets P, et al. Among authors: allamand v. J Mol Med (Berl). 2012 Oct;90(10):1095-107. doi: 10.1007/s00109-012-0896-x. Epub 2012 Apr 14. J Mol Med (Berl). 2012. PMID: 22527882 Review.

9

Drug-induced readthrough of premature stop codons leads to the stabilization of laminin alpha2 chain mRNA in CMD myotubes.

Allamand V, Bidou L, Arakawa M, Floquet C, Shiozuka M, Paturneau-Jouas M, Gartioux C, Butler-Browne GS, Mouly V, Rousset JP, Matsuda R, Ikeda D, Guicheney P. Allamand V, et al. J Gene Med. 2008 Feb;10(2):217-24. doi: 10.1002/jgm.1140. J Gene Med. 2008. PMID: 18074402

10

Two novel COLVI long chains in zebrafish that are essential for muscle development.

Ramanoudjame L, Rocancourt C, Lainé J, Klein A, Joassard L, Gartioux C, Fleury M, Lyphout L, Kabashi E, Ciura S, Cousin X, Allamand V. Ramanoudjame L, et al. Among authors: allamand v. Hum Mol Genet. 2015 Dec 1;24(23):6624-39. doi: 10.1093/hmg/ddv368. Epub 2015 Sep 11. Hum Mol Genet. 2015. PMID: 26362255

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