Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

74 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Cyclosporine A treatment for Ullrich congenital muscular dystrophy: a cellular study of mitochondrial dysfunction and its rescue.
Hicks D, Lampe AK, Laval SH, Allamand V, Jimenez-Mallebrera C, Walter MC, Muntoni F, Quijano-Roy S, Richard P, Straub V, Lochmüller H, Bushby KM. Hicks D, et al. Brain. 2009 Jan;132(Pt 1):147-55. doi: 10.1093/brain/awn289. Epub 2008 Nov 16. Brain. 2009. PMID: 19015158
Autophagy is increased in laminin α2 chain-deficient muscle and its inhibition improves muscle morphology in a mouse model of MDC1A.
Carmignac V, Svensson M, Körner Z, Elowsson L, Matsumura C, Gawlik KI, Allamand V, Durbeej M. Carmignac V, et al. Hum Mol Genet. 2011 Dec 15;20(24):4891-902. doi: 10.1093/hmg/ddr427. Epub 2011 Sep 14. Hum Mol Genet. 2011. PMID: 21920942
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. 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
The transcription coactivator ASC-1 is a regulator of skeletal myogenesis, and its deficiency causes a novel form of congenital muscle disease.
Davignon L, Chauveau C, Julien C, Dill C, Duband-Goulet I, Cabet E, Buendia B, Lilienbaum A, Rendu J, Minot MC, Guichet A, Allamand V, Vadrot N, Fauré J, Odent S, Lazaro L, Leroy JP, Marcorelles P, Dubourg O, Ferreiro A. Davignon L, et al. Among authors: allamand v. Hum Mol Genet. 2016 Apr 15;25(8):1559-73. doi: 10.1093/hmg/ddw033. Epub 2016 Feb 9. Hum Mol Genet. 2016. PMID: 27008887
Spontaneous muscular dystrophy caused by a retrotransposal insertion in the mouse laminin alpha2 chain gene.
Besse S, Allamand V, Vilquin JT, Li Z, Poirier C, Vignier N, Hori H, Guénet JL, Guicheney P. Besse S, et al. Neuromuscul Disord. 2003 Mar;13(3):216-22. doi: 10.1016/s0960-8966(02)00278-x. Neuromuscul Disord. 2003. PMID: 12609503
Mutations in COL6A3 cause severe and mild phenotypes of Ullrich congenital muscular dystrophy.
Demir E, Sabatelli P, Allamand V, Ferreiro A, Moghadaszadeh B, Makrelouf M, Topaloglu H, Echenne B, Merlini L, Guicheney P. Demir E, et al. Am J Hum Genet. 2002 Jun;70(6):1446-58. doi: 10.1086/340608. Epub 2002 Apr 24. Am J Hum Genet. 2002. PMID: 11992252 Free PMC article.
Gene transfer establishes primacy of striated vs. smooth muscle sarcoglycan complex in limb-girdle muscular dystrophy.
Durbeej M, Sawatzki SM, Barresi R, Schmainda KM, Allamand V, Michele DE, Campbell KP. Durbeej M, et al. Proc Natl Acad Sci U S A. 2003 Jul 22;100(15):8910-5. doi: 10.1073/pnas.1537554100. Epub 2003 Jul 8. Proc Natl Acad Sci U S A. 2003. PMID: 12851463 Free PMC article.
Contrast agent-enhanced magnetic resonance imaging of skeletal muscle damage in animal models of muscular dystrophy.
Straub V, Donahue KM, Allamand V, Davisson RL, Kim YR, Campbell KP. Straub V, et al. Magn Reson Med. 2000 Oct;44(4):655-9. doi: 10.1002/1522-2594(200010)44:4<655::aid-mrm22>;2-t. Magn Reson Med. 2000. PMID: 11025524
74 results
Jump to page