Catherine BARRIERE
Maitre de Conférences
BARRIERE
Catherine
Maitre de Conférences
MCF
Publications
L1 chimeric transcripts are expressed in healthy brain and their deregulation in glioma follows that of their host locus.
Publié le 17 Août 2022 dans Human molecular genetics , vol. 31 - pp 2606-2622
Pinson ME , Court F , Masson A , Renaud Y , Fantini A , Bacoeur-Ouzillou O, Barriere M, Pereira B, Guichet PO, Chautard E, Karayan-Tapon L, Verrelle P, Arnaud P , Vaurs-Barrière C
Widespread overexpression from the four DNA hypermethylated HOX clusters in aggressive (IDHwt) glioma is associated with H3K27me3 depletion and alternative promoter usage.
Publié le 30 Août 2021 dans Molecular oncology , vol. 15 - pp 1995-2010
Le Boiteux E , Court F , Guichet PO, Vaurs-Barrière C , Vaillant I , Chautard E, Verrelle P, Costa BM, Karayan-Tapon L, Fogli A , Arnaud P
Transcriptional alterations in glioma result primarily from DNA methylation-independent mechanisms.
Publié le 30 Oct 2019 dans Genome research , vol. 29 - pp 1605-1621
Court F , Le Boiteux E , Fogli A , Müller-Barthélémy M, Vaurs-Barrière C , Chautard E, Pereira B, Biau J, Kemeny JL, Khalil T, Karayan-Tapon L, Verrelle P, Arnaud P
Oxidative stress and mitochondrial dynamics malfunction are linked in Pelizaeus-Merzbacher disease.
Publié le 30 Sep 2018 dans Brain pathology (Zurich, Switzerland) , vol. 28 - pp 611-630
Ruiz M, Bégou M, Launay N, Ranea-Robles P, Bianchi P, López-Erauskin J, Morató L, Guilera C, Petit B, Vaurs-Barriere C , Guéret-Gonthier C, Bonnet-Dupeyron MN, Fourcade S, Auwerx J, Boespflug-Tanguy O, Pujol A
CLIFinder: identification of LINE-1 chimeric transcripts in RNA-seq data.
Publié le 15 Fév 2018 dans Bioinformatics (Oxford, England) , vol. 34 - pp 688-690
Pinson ME , Pogorelcnik R , Court F , Arnaud P , Vaurs-Barrière C
Detection of the alternative lengthening of telomeres pathway in malignant gliomas for improved molecular diagnosis.
Publié le 30 Nov 2017 dans Journal of neuro-oncology , vol. 135 - pp 381-390
Fogli A , Demattei MV, Corset L, Vaurs-Barrière C , Chautard E, Biau J, Kémény JL, Godfraind C, Pereira B, Khalil T, Grandin N , Arnaud P , Charbonneau M , Verrelle P
The tumoral A genotype of the MGMT rs34180180 single-nucleotide polymorphism in aggressive gliomas is associated with shorter patients’ survival.
Publié le 01 Mar 2016 dans Carcinogenesis , vol. 37 - pp 169-176
Fogli A , Chautard E, Vaurs-Barrière C , Pereira B, Müller-Barthélémy M, Court F , Biau J, Pinto AA, Kémény JL, Khalil T, Karayan-Tapon L, Verrelle P, Costa BM, Arnaud P
Fluorescent mRNA labeling through cytoplasmic FISH.
Publié le 30 Déc 2013 dans Nature protocols , vol. 8 - pp 2538-47
Sjögren-Larsson syndrome: novel mutations in the ALDH3A2 gene in a French cohort.
Publié le 15 Jan 2012 dans Journal of the neurological sciences , vol. 312 - pp 123-6
Sarret C, Rigal M , Vaurs-Barrière C , Dorboz I, Eymard-Pierre E, Combes P, Giraud G , Wanders RJ, Afenjar A, Francannet C, Boespflug-Tanguy O
Relevance of GJC2 promoter mutation in Pelizaeus-Merzbacher-like disease.
Publié le 30 Jan 2012 dans Annals of neurology , vol. 71 - pp 146-8
Combes P, Kammoun N, Monnier A, Gonthier-Guéret C, Giraud G , Bertini E, Chahnez T, Fakhfakh F, Boespflug-Tanguy O, Vaurs-Barrière C
Molecular genetic analysis of the PLP1 gene in 38 families with PLP1-related disorders: identification and functional characterization of 11 novel PLP1 mutations.
Publié le 16 Juin 2011 dans Orphanet journal of rare diseases , vol. 6 - pp 40
Grossi S, Regis S, Biancheri R, Mort M, Lualdi S, Bertini E, Uziel G, Boespflug-Tanguy O, Simonati A, Corsolini F, Demir E, Marchiani V, Percesepe A, Stanzial F, Rossi A, Vaurs-Barrière C , Cooper DN, Filocamo M
Neurodegenerative disorder related to AIMP1/p43 mutation is not a PMLD.
Publié le 11 Mar 2011 dans American journal of human genetics , vol. 88 - pp 392-3; author reply 393-5
Boespflug-Tanguy O, Aubourg P, Dorboz I, Bégou M, Giraud G , Sarret C, Vaurs-Barrière C
Pelizaeus-Merzbacher-Like disease presentation of MCT8 mutated male subjects.
Publié le 30 Jan 2009 dans Annals of neurology , vol. 65 - pp 114-8
Vaurs-Barrière C , Deville M, Sarret C, Giraud G , Des Portes V, Prats-Viñas JM, De Michele G, Dan B, Brady AF, Boespflug-Tanguy O, Touraine R
Absence of OLIG2 mutations in patients presenting with a severe Pelizaeus-Merzbacher-like leukodystrophy associated with motor neuron dysfunction.
Publié le 05 Juin 2008 dans American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics , vol. 147B - pp 538-9
Bonnet-Dupeyron MN, Combes P, Boespflug-Tanguy O, Vaurs-Barrière C
PLP1 splicing abnormalities identified in Pelizaeus-Merzbacher disease and SPG2 fibroblasts are associated with different types of mutations.
Publié le 30 Août 2008 dans Human mutation , vol. 29 - pp 1028-36
Bonnet-Dupeyron MN, Combes P, Santander P, Cailloux F, Boespflug-Tanguy O, Vaurs-Barrière C
