Carinne Roudaut
Overview
Explore the profile of Carinne Roudaut including associated specialties, affiliations and a list of published articles.
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Articles
18
Citations
459
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0
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Recent Articles
11.
Laure L, Daniele N, Suel L, Marchand S, Aubert S, Bourg N, et al.
FEBS J
. 2010 Sep;
277(20):4322-37.
PMID: 20860623
A multiprotein complex encompassing a transcription regulator, cardiac ankyrin repeat protein (CARP), and the calpain 3 protease was identified in the N2A elastic region of the giant sarcomeric protein titin....
12.
Charton K, Daniele N, Vihola A, Roudaut C, Gicquel E, Monjaret F, et al.
Hum Mol Genet
. 2010 Sep;
19(23):4608-24.
PMID: 20855473
The dominant tibial muscular dystrophy (TMD) and recessive limb-girdle muscular dystrophy 2J are allelic disorders caused by mutations in the C-terminus of titin, a giant sarcomeric protein. Both clinical presentations...
13.
Lostal W, Bartoli M, Bourg N, Roudaut C, Bentaib A, Miyake K, et al.
Hum Mol Genet
. 2010 Feb;
19(10):1897-907.
PMID: 20154340
Deficiency of the dysferlin protein presents as two major clinical phenotypes: limb-girdle muscular dystrophy type 2B and Miyoshi myopathy. Dysferlin is known to participate in membrane repair, providing a potential...
14.
Laure L, Suel L, Roudaut C, Bourg N, Ouali A, Bartoli M, et al.
FEBS J
. 2009 Jan;
276(3):669-84.
PMID: 19143834
In an attempt to identify potential therapeutic targets for the correction of muscle wasting, the gene expression of several pivotal proteins involved in protein metabolism was investigated in experimental atrophy...
15.
Milic A, Daniele N, Lochmuller H, Mora M, Comi G, Moggio M, et al.
Neuromuscul Disord
. 2007 Jan;
17(2):148-56.
PMID: 17236769
Limb-girdle muscular dystrophy type 2A (LGMD2A) is an autosomal recessive muscular disorder caused by mutations in the gene coding for calpain 3, a calcium-dependent protease. We developed an in vitro...
16.
Bartoli M, Roudaut C, Martin S, Fougerousse F, Suel L, Poupiot J, et al.
Mol Ther
. 2005 Nov;
13(2):250-9.
PMID: 16290124
Calpainopathy (limb-girdle muscular dystrophy type 2A, LGMD2A) is a recessive muscular disorder caused by deficiency in the calcium-dependent cysteine protease calpain 3. To date, no treatment exists for this disease....
17.
Taveau M, Stockholm D, Marchand S, Roudaut C, Le Bert M, Richard I
Genomics
. 2004 Oct;
84(3):592-5.
PMID: 15498466
A calpain 3 (Capn3) deficiency model was created by targeted disruption of the mouse Capn3 gene through homologous recombination in ES cells. Analysis of the genotype of pups from heterozygous...
18.
Taveau M, Bourg N, Sillon G, Roudaut C, Bartoli M, Richard I
Mol Cell Biol
. 2003 Dec;
23(24):9127-35.
PMID: 14645524
Calpain 3 (Capn3) is known as the skeletal muscle-specific member of the calpains, a family of intracellular nonlysosomal cysteine proteases. This enigmatic protease has many unique features among the calpain...