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Items: 1 to 20 of 96

1.

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.

PLoS One. 2011;6(8):e23094. doi: 10.1371/journal.pone.0023094. Epub 2011 Aug 8.

2.

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.

Hum Mol Genet. 2011 Feb 15;20(4):694-704. doi: 10.1093/hmg/ddq515. Epub 2010 Dec 2.

PMID:
21131290
3.

Oxidative stress in SEPN1-related myopathy: from pathophysiology to treatment.

Arbogast S, Beuvin M, Fraysse B, Zhou H, Muntoni F, Ferreiro A.

Ann Neurol. 2009 Jun;65(6):677-86. doi: 10.1002/ana.21644.

PMID:
19557870
4.

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.

BMC Dev Biol. 2009 Aug 22;9:46. doi: 10.1186/1471-213X-9-46.

5.

Selenoprotein N in skeletal muscle: from diseases to function.

Castets P, Lescure A, Guicheney P, Allamand V.

J Mol Med (Berl). 2012 Oct;90(10):1095-107. doi: 10.1007/s00109-012-0896-x. Epub 2012 Apr 14. Review.

PMID:
22527882
6.

Selenoprotein N deficiency in mice is associated with abnormal lung development.

Moghadaszadeh B, Rider BE, Lawlor MW, Childers MK, Grange RW, Gupta K, Boukedes SS, Owen CA, Beggs AH.

FASEB J. 2013 Apr;27(4):1585-99. doi: 10.1096/fj.12-212688. Epub 2013 Jan 16.

7.

Selenoprotein function and muscle disease.

Lescure A, Rederstorff M, Krol A, Guicheney P, Allamand V.

Biochim Biophys Acta. 2009 Nov;1790(11):1569-74. doi: 10.1016/j.bbagen.2009.03.002. Epub 2009 Mar 11. Review.

PMID:
19285112
8.

Ubiquitous expression of selenoprotein N transcripts in chicken tissues and early developmental expression pattern in skeletal muscles.

Zhang J, Li J, Zhang Z, Sun B, Wang R, Jiang Z, Li S, Xu S.

Biol Trace Elem Res. 2012 May;146(2):187-91. doi: 10.1007/s12011-011-9249-9. Epub 2011 Nov 16.

PMID:
22086647
9.

A mutation in the SEPN1 selenocysteine redefinition element (SRE) reduces selenocysteine incorporation and leads to SEPN1-related myopathy.

Maiti B, Arbogast S, Allamand V, Moyle MW, Anderson CB, Richard P, Guicheney P, Ferreiro A, Flanigan KM, Howard MT.

Hum Mutat. 2009 Mar;30(3):411-6. doi: 10.1002/humu.20879.

10.

Selenoproteins and protection against oxidative stress: selenoprotein N as a novel player at the crossroads of redox signaling and calcium homeostasis.

Arbogast S, Ferreiro A.

Antioxid Redox Signal. 2010 Apr 1;12(7):893-904. doi: 10.1089/ars.2009.2890. Review.

PMID:
19769461
11.

Loss of selenoprotein N function causes disruption of muscle architecture in the zebrafish embryo.

Deniziak M, Thisse C, Rederstorff M, Hindelang C, Thisse B, Lescure A.

Exp Cell Res. 2007 Jan 1;313(1):156-67. Epub 2006 Oct 13.

PMID:
17123513
12.

SEPN1, an endoplasmic reticulum-localized selenoprotein linked to skeletal muscle pathology, counteracts hyperoxidation by means of redox-regulating SERCA2 pump activity.

Marino M, Stoilova T, Giorgi C, Bachi A, Cattaneo A, Auricchio A, Pinton P, Zito E.

Hum Mol Genet. 2015 Apr 1;24(7):1843-55. doi: 10.1093/hmg/ddu602. Epub 2014 Dec 1.

PMID:
25452428
13.

A centronuclear myopathy-dynamin 2 mutation impairs skeletal muscle structure and function in mice.

Durieux AC, Vignaud A, Prudhon B, Viou MT, Beuvin M, Vassilopoulos S, Fraysse B, Ferry A, Lainé J, Romero NB, Guicheney P, Bitoun M.

Hum Mol Genet. 2010 Dec 15;19(24):4820-36. doi: 10.1093/hmg/ddq413. Epub 2010 Sep 21.

PMID:
20858595
14.

Abnormal distribution of calcium-handling proteins: a novel distinctive marker in core myopathies.

Herasse M, Parain K, Marty I, Monnier N, Kaindl AM, Leroy JP, Richard P, Lunardi J, Romero NB, Ferreiro A.

J Neuropathol Exp Neurol. 2007 Jan;66(1):57-65.

PMID:
17204937
15.

Dietary selenium regulation of transcript abundance of selenoprotein N and selenoprotein W in chicken muscle tissues.

Zhang JL, Li JL, Huang XD, Bo S, Rihua W, Li S, Xu SW.

Biometals. 2012 Apr;25(2):297-307. doi: 10.1007/s10534-011-9502-x. Epub 2011 Nov 2.

PMID:
22045056
16.

Endoplasmic Reticulum Oxidative Stress Triggers Tgf-Beta-Dependent Muscle Dysfunction by Accelerating Ascorbic Acid Turnover.

Pozzer D, Favellato M, Bolis M, Invernizzi RW, Solagna F, Blaauw B, Zito E.

Sci Rep. 2017 Jan 20;7:40993. doi: 10.1038/srep40993.

17.

Effects of dietary selenium deficiency or excess on gene expression of selenoprotein N in chicken muscle tissues.

Zhang JL, Zhang ZW, Shan AS, Xu SW.

Biol Trace Elem Res. 2014 Mar;157(3):234-41. doi: 10.1007/s12011-014-9893-y. Epub 2014 Feb 2.

PMID:
24488809
18.

The phenotype and long-term follow-up in 11 patients with juvenile selenoprotein N1-related myopathy.

Schara U, Kress W, Bönnemann CG, Breitbach-Faller N, Korenke CG, Schreiber G, Stoetter M, Ferreiro A, von der Hagen M.

Eur J Paediatr Neurol. 2008 May;12(3):224-30. Epub 2007 Oct 22.

PMID:
17951086
19.

SEPN1: associated with congenital fiber-type disproportion and insulin resistance.

Clarke NF, Kidson W, Quijano-Roy S, Estournet B, Ferreiro A, Guicheney P, Manson JI, Kornberg AJ, Shield LK, North KN.

Ann Neurol. 2006 Mar;59(3):546-52.

PMID:
16365872
20.

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.

EMBO Rep. 2006 Apr;7(4):450-4. Epub 2006 Feb 24.

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