P Couvert
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Explore the profile of P Couvert including associated specialties, affiliations and a list of published articles.
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12
Citations
414
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Recent Articles
1.
Lhermusier T, Severin S, Van Rothem J, Garcia C, Bertrand-Michel J, Le Faouder P, et al.
J Thromb Haemost
. 2016 Jan;
14(3):585-95.
PMID: 26749169
Unlabelled: ESSENTIALS: The role of ATP-binding cassette transporter 1 (ABCA1) in platelet functions is poorly characterized. We studied the impact of ABCA1 deficiency on platelet responses in a mouse model...
2.
Pichit P, Quillard M, Couvert P, Senant J, Carrie A, Bittar R, et al.
Rev Neurol (Paris)
. 2010 Jan;
166(5):534-7.
PMID: 20070997
Introduction: Tangier disease (TD) is a rare autosomal recessive disorder characterized by a deficiency or absence of high-density lipoprotein (HDL) caused by mutations in the adenotriphosphate-binding cassette transporter-1 gene (ABCA1)....
3.
Couvert P, Poirier K, Carrie A, Chalas C, Jouannet P, Beldjord C, et al.
Biotechniques
. 2003 Mar;
34(2):356-62.
PMID: 12613258
The bisulfite genomic sequencing method is one of the most widely used techniques for methylation analysis in heterogeneous unbiased PCR, amplifying for both methylated and unmethylated alleles simultaneously. However, it...
4.
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...
5.
Girard M, Couvert P, Carrie A, Tardieu M, Chelly J, Beldjord C, et al.
Eur J Hum Genet
. 2001 Apr;
9(3):231-6.
PMID: 11313764
Rett syndrome (RTT) is a neurodevelopmental disorder occurring almost exclusively in females as sporadic cases. Recently, DNA mutations in the MECP2 gene have been detected in approximately 70% of patients...
6.
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...
7.
Bienvenu T, Portes V, McDonell N, Carrie A, Zemni R, Couvert P, et al.
Am J Med Genet
. 2000 Aug;
93(4):294-8.
PMID: 10946356
X-linked mental retardation is a very common condition that affects approximately 1 in 600 males. Despite recent progress, in most cases the molecular defects underlying this disorder remain unknown. Recently,...
8.
Billuart P, Chelly J, Carrie A, Vinet M, Couvert P, McDonell N, et al.
Ann Genet
. 2000 May;
43(1):5-9.
PMID: 10818214
We have recently shown that mutations in oligophrenin-1 (OPHN1) are responsible for non-specific X-linked mental retardation (MRX). The structure of the gene encoding the OPHN1 protein was determined by isolation...
9.
Bienvenu T, Carrie A, De Roux N, Vinet M, Jonveaux P, Couvert P, et al.
Hum Mol Genet
. 2000 May;
9(9):1377-84.
PMID: 10814719
Rett syndrome (RTT) is a severe progressive neurological disorder that affects almost exclusively females, with an estimated prevalence of approximately one in 10 000-15 000 female births. Most cases are...
10.
Zemni R, Bienvenu T, Vinet M, Sefiani A, Carrie A, Billuart P, et al.
Nat Genet
. 2000 Feb;
24(2):167-70.
PMID: 10655063
X-linked forms of mental retardation (MR) affect approximately 1 in 600 males and are likely to be highly heterogeneous. They can be categorized into syndromic (MRXS) and nonspecific (MRX) forms....