Výsledky vyhledávání - "Jp, Kerckaert"

High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2 alpha B gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21

Autor: Preudhomme C, Warot-Loze D, Roumier C, Grardel-Duflos N, Garand R, Jl, Lai, Dastugue N, Macintyre E, Denis C, Bauters F, Jp, Kerckaert, Cosson A, Fenaux P

Publikováno v: Europe PubMed Central

The AML1 gene, situated in 21q22, is often rearranged in acute leukemias through t(8;21) translocation, t(12;21) translocation, or less often t(3;21) translocation. Recently, point mutations in the Runt domain of the AML1 gene have also been reported

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::751794e43df32aea4359f3303772da2b
https://pubmed.ncbi.nlm.nih.gov/11023523

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The LAZ3/BCL6 oncogene encodes a sequence-specific transcriptional inhibitor: a novel function for the BTB/POZ domain as an autonomous repressing domain

Autor: Deweindt C, Albagli O, Bernardin F, Dhordain P, Quief S, Lantoine D, Jp, Kerckaert, Dominique Leprince

Publikováno v: Europe PubMed Central

Rearrangements and mutations of the LAZ3/BCL6 gene are the most frequent events associated with diffuse large-cell lymphoma, a particular class of non-Hodgkin's lymphomas. This gene encodes a putative regulatory protein with six COOH-terminal Krüppe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::e83ed8f3a7074df000b8f85e892f1427
https://pubmed.ncbi.nlm.nih.gov/9019154

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Polymorphism of the proto-oncogene ETS-1 in hematological malignancies

Autor: Jp, Kerckaert, Martine Duterque-Coquillaud, Collyn-d'Hooghe M, Morel P, Ma, Majérus, Jl, Laï, Fenaux P, Bauters F, Debuire B, Mh, Loucheux-Lefebvre

Publikováno v: Europe PubMed Central

We studied a novel restriction fragment length polymorphism (RFLP) of the proto-oncogenes ETS-1 that we detected in a patient with an acute monocytic leukemia by the presence of two, 3.7 and 10 kb, Xbal fragments on Southern blots of DNA from blast c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::25a404b13a0cb848082a377d9d26839d
http://europepmc.org/abstract/med/1967322

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Akademický článek

Colonic gene expression patterns of mucin Muc2 knockout mice reveal various phases in colitis development.

Autor: Lu P; Laboratory of Pediatrics, Division Neonatology, Erasmus MC-Sophia, Rotterdam, The Netherlands., Burger-van Paassen N, van der Sluis M, Witte-Bouma J, Kerckaert JP, van Goudoever JB, Van Seuningen I, Renes IB

Publikováno v: Inflammatory bowel diseases [Inflamm Bowel Dis] 2011 Oct; Vol. 17 (10), pp. 2047-57. Date of Electronic Publication: 2011 Jan 06.

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Akademický článek

Transcriptional profile of Parkinson blood mononuclear cells with LRRK2 mutation.

Autor: Mutez E; Univ Lille Nord de France, F-59000 Lille, France., Larvor L, Leprêtre F, Mouroux V, Hamalek D, Kerckaert JP, Pérez-Tur J, Waucquier N, Vanbesien-Mailliot C, Duflot A, Devos D, Defebvre L, Kreisler A, Frigard B, Destée A, Chartier-Harlin MC

Publikováno v: Neurobiology of aging [Neurobiol Aging] 2011 Oct; Vol. 32 (10), pp. 1839-48. Date of Electronic Publication: 2010 Jan 22.

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Akademický článek

Thrombocytopenia-absent radius (TAR) syndrome: a clinical genetic series of 14 further cases. impact of the associated 1q21.1 deletion on the genetic counselling.

Autor: Houeijeh A; Service de Génétique clinique Guy Fontaine, CHRU Lille, France., Andrieux J, Saugier-Veber P, David A, Goldenberg A, Bonneau D, Fouassier M, Journel H, Martinovic J, Escande F, Devisme L, Bisiaux S, Chaffiotte C, Baux M, Kerckaert JP, Holder-Espinasse M, Manouvrier-Hanu S

Publikováno v: European journal of medical genetics [Eur J Med Genet] 2011 Sep-Oct; Vol. 54 (5), pp. e471-7. Date of Electronic Publication: 2011 May 13.

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Akademický článek

Molecular characterization of 9p21 deletions shows a minimal common deleted region removing CDKN2A exon 1 and CDKN2B exon 2 in diffuse large B-cell lymphomas.

Autor: Guney S; INSERM U918, Groupe d'étude des Proliférations Lymphodes, Institut Fédératif de Recherches multidisciplinaires sur les Peptides 23 (IFRMP23), Rouen, France., Bertrand P, Jardin F, Ruminy P, Kerckaert JP, Tilly H, Bastard C

Publikováno v: Genes, chromosomes & cancer [Genes Chromosomes Cancer] 2011 Sep; Vol. 50 (9), pp. 715-25. Date of Electronic Publication: 2011 Jun 02.

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Akademický článek

Repression of the RHOH gene by JunD.

Autor: Delestré L; Institut National de la Santé et de la Recherche Médicale U.837, Centre Jean-Pierre Aubert, Institut pour la Recherche sur le Cancer de Lille and Université Lille Nord de France, UDSL, 59000 Lille, France., Berthon C, Quesnel B, Figeac M, Kerckaert JP, Galiègue-Zouitina S, Shelley CS

Publikováno v: The Biochemical journal [Biochem J] 2011 Jul 01; Vol. 437 (1), pp. 75-88.

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Akademický článek

SNCA locus duplication carriers: from genetics to Parkinson disease phenotypes.

Autor: Mutez E; UMR 837 INSERM, Team 6, JParc, IRCL, Lille, France., Leprêtre F, Le Rhun E, Larvor L, Duflot A, Mouroux V, Kerckaert JP, Figeac M, Dujardin K, Destée A, Chartier-Harlin MC

Publikováno v: Human mutation [Hum Mutat] 2011 Apr; Vol. 32 (4), pp. E2079-90. Date of Electronic Publication: 2011 Feb 08.

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