C A Dechesne
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Explore the profile of C A Dechesne including associated specialties, affiliations and a list of published articles.
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Articles
19
Citations
399
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Recent Articles
1.
Moratal C, Raffort J, Arrighi N, Rekima S, Schaub S, Dechesne C, et al.
Sci Rep
. 2018 Nov;
8(1):17005.
PMID: 30451963
Intramuscular fat deposition represents a negative prognostic factor for several myopathies, metabolic diseases and aging. Fibro-adipogenic progenitors (FAPs) are considered as the main source of intramuscular adipocytes, but the mechanisms...
2.
Arrighi N, Lypovetska K, Moratal C, Giorgetti-Peraldi S, Dechesne C, Dani C, et al.
Sci Rep
. 2017 Nov;
7(1):15248.
PMID: 29127365
The primary cilium is an organelle, present at the cell surface, with various biological functions. We, and others, have shown that it plays a role in the differentiation of adipose...
3.
Arrighi N, Moratal C, Clement N, Giorgetti-Peraldi S, Peraldi P, Loubat A, et al.
Cell Death Dis
. 2015 Apr;
6:e1733.
PMID: 25906156
A population of fibro/adipogenic but non-myogenic progenitors located between skeletal muscle fibers was recently discovered. The aim of this study was to determine the extent to which these progenitors differentiate...
4.
Loseva P, Kostyuk S, Malinovskaya E, Clement N, Dechesne C, Dani C, et al.
Expert Opin Biol Ther
. 2012 May;
12 Suppl 1:S85-97.
PMID: 22594577
Introduction: Human blood normally contains circulating cell-free DNA (cirDNA). Cell-free DNA (cfDNA) present in cell culture medium is termed extracellular DNA (ecDNA). Its concentration, GC content and oxidation level depend...
5.
Pisani D, Cabane C, Derijard B, Dechesne C
Cell Death Differ
. 2004 Oct;
11(11):1157-65.
PMID: 15486563
DNA topoisomerase I (Topo1) contributes to vital biological functions, but its regulation is not clearly understood. The BTBD1 protein was recently cloned on the basis of its interaction with the...
6.
Cros N, Tkatchenko A, Pisani D, Leclerc L, Leger J, Marini J, et al.
J Cell Biochem
. 2001 Oct;
83(3):508-19.
PMID: 11596118
The present study involved a global analysis of genes whose expression was modified in rat soleus muscle atrophied after hindlimb suspension (HS). HS muscle unloading is a common model for...
7.
Tkatchenko A, Pietu G, Cros N, Auffray C, Leger J, Dechesne C
Neuromuscul Disord
. 2001 Apr;
11(3):269-77.
PMID: 11297942
Mutations in the dystrophin gene lead to dystrophin deficiency, which is the cause of Duchenne muscular dystrophy (DMD). This important discovery more than 10 years ago opened a new field...
8.
Tkatchenko A, Le Cam G, Leger J, Dechesne C
Biochim Biophys Acta
. 1999 Nov;
1500(1):17-30.
PMID: 10564714
The mdx mouse is an animal model for Duchenne muscular dystrophy (DMD), which is caused by the absence of dystrophin. Mdx limb muscles substantially compensate for the lack of dystrophin...
9.
Bouju S, Pietu G, Le Cunff M, Cros N, Malzac P, Pellissier J, et al.
Neuromuscul Disord
. 1999 Mar;
9(1):3-10.
PMID: 10063829
Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant disorder for which no candidate gene has yet been identified. The gene corresponding to one of the novel human cDNAs that we...
10.
Cros N, Muller J, Bouju S, Pietu G, Jacquet C, Leger J, et al.
Am J Physiol
. 1999 Feb;
276(2):R308-16.
PMID: 9950906
Muscle disuse induces substantial alterations in the highly plastic skeletal muscle tissues, which occur especially in antigravity slow muscles. We differentially screened a muscle cDNA array to identify modifications in...