C Aquaviva
Overview
Explore the profile of C Aquaviva including associated specialties, affiliations and a list of published articles.
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Articles
5
Citations
92
Followers
0
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Recent Articles
1.
Morel N, Corne C, Aquaviva C, Besson G
Rev Neurol (Paris)
. 2012 Feb;
168(3):296-7.
PMID: 22340867
No abstract available.
2.
Feillet F, Ogier H, Cheillan D, Aquaviva C, Labarthe F, Baruteau J, et al.
Arch Pediatr
. 2012 Jan;
19(2):184-93.
PMID: 22244319
MCAD deficiency is the most common fatty acid oxidation disorder, with the prevalence varying from 1/10,000 to 1/27,000 in the countries adjacent to France. As the High Authority for Health...
3.
Bienvenu T, Souville I, Poirier K, Aquaviva C, Burglen L, Amiel J, et al.
Hum Mutat
. 2001 Aug;
18(3):251-2.
PMID: 11524737
Rett syndrome (RTT) is a severe progressive neurological disorder that affects almost exclusively females. The gene responsible for this disorder, MECP2, was recently identified by candidate gene strategy. Mutations were...
4.
Couvert P, Bienvenu T, Aquaviva C, Poirier K, Moraine C, Gendrot C, et al.
Hum Mol Genet
. 2001 Apr;
10(9):941-6.
PMID: 11309367
Following the recent discovery that the methyl-CpG binding protein 2 (MECP2) gene located on Xq28 is involved in Rett syndrome (RTT), a wild spectrum of phenotypes, including mental handicap, has...
5.
Salvat C, Aquaviva C, Jariel-Encontre I, Ferrara P, Pariat M, Steff A, et al.
Mol Biol Rep
. 1999 Jun;
26(1-2):45-51.
PMID: 10363646
The c-Fos and c-Jun oncoproteins and the p53 tumor suppressor protein are short-lived transcription factors. Several catabolic pathways contribute to their degradation in vivo. c-Fos and c-Jun are thus mostly...