Search Results - "Laffaire, J"

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  1. 1

    IDH1 or IDH2 mutations predict longer survival and response to temozolomide in low-grade gliomas by HOUILLIER, C, WANG, X, HOANG-XUAN, K, SANSON, M, DELATTRE, J.-Y, KALOSHI, G, MOKHTARI, K, GUILLEVIN, R, LAFFAIRE, J, PARIS, S, BOISSELIER, B, IDBAIH, A, LAIGLE-DONADEY, F

    Published in Neurology (26-10-2010)
    “…Recent studies have shown that IDH1 and IDH2 mutations occur frequently in gliomas, including low-grade gliomas. However, their impact on the prognosis and…”
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    Journal Article
  2. 2

    All the 1p19q codeleted gliomas are mutated on IDH1 or IDH2 by LABUSSIERE, M, IDBAIH, A, DUCRAY, F, EL HALLANI, S, MOKHTARI, K, HOANG-XUAN, K, DELATTRE, J.-Y, SANSON, M, WANG, X.-W, MARIE, Y, BOISSELIER, B, FALET, C, PARIS, S, LAFFAIRE, J, CARPENTIER, C, CRINIERE, E

    Published in Neurology (08-06-2010)
    “…Recently, the gene encoding the human cytosolic NADPH-dependent isocitrate dehydrogenase (IDH1) was reported frequently mutated in gliomas. Rare mutations were…”
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    Journal Article
  3. 3

    Increased NR2A expression and prolonged decay of NMDA-induced calcium transient in cerebellum of TgDyrk1A mice, a mouse model of Down syndrome by Altafaj, X, Ortiz-Abalia, J, Fernández, M, Potier, M.C, Laffaire, J, Andreu, N, Dierssen, M, González-García, C, Ceña, V, Martí, E, Fillat, C

    Published in Neurobiology of disease (01-12-2008)
    “…Abstract Transgenic mice overexpressing Dyrk1A (TgDyrk1A), a Down syndrome (DS) candidate gene, exhibit motor and cognitive alterations similar to those…”
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    Journal Article
  4. 4

    Comparative analysis of two 14-3-3 homologues and their expression pattern in the root-knot nematode Meloidogyne incognita by Jaubert, S., Laffaire, J.-B., Ledger, T.N., Escoubas, P., Amri, E.-Z., Abad, P., Rosso, M.N.

    Published in International journal for parasitology (01-06-2004)
    “…14-3-3 proteins are highly conserved ubiquitous proteins found in all eukaryotic organisms. They are involved in various cellular processes including signal…”
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    Journal Article
  5. 5

    Transcriptional disruptions in Down syndrome: a case study in the Ts1Cje mouse cerebellum during post‐natal development by Potier, M.‐C., Rivals, I., Mercier, G., Ettwiller, L., Moldrich, R. X., Laffaire, J., Personnaz, L., Rossier, J., Dauphinot, L.

    Published in Journal of neurochemistry (01-04-2006)
    “…To understand the aetiology and the phenotypic severity of Down syndrome, we searched for transcriptional signatures in a substructure of the brain…”
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    Journal Article Conference Proceeding
  6. 6

    Transmembrane protein 50b ( C21orf4 ), a candidate for Down syndrome neurophenotypes, encodes an intracellular membrane protein expressed in the rodent brain by Moldrich, R.X, Lainé, J, Visel, A, Beart, P.M, Laffaire, J, Rossier, J, Potier, M.-C

    Published in Neuroscience (17-07-2008)
    “…Abstract Transmembrane protein 50b, Tmem50b , previously referred to as C21orf4 , encodes a predicted transmembrane protein and is one of few genes…”
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    Journal Article
  7. 7
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  9. 9

    Methylation profiling identifies 2 groups of gliomas according to their tumorigenesis by Laffaire, Julien, Everhard, Sibille, Idbaih, Ahmed, Crinière, Emmanuelle, Marie, Yannick, de Reyniès, Aurelien, Schiappa, Renaud, Mokhtari, Karima, Hoang-Xuan, Khê, Sanson, Marc, Delattre, Jean-Yves, Thillet, Joëlle, Ducray, François

    Published in Neuro-oncology (Charlottesville, Va.) (01-01-2011)
    “…Extensive genomic and gene expression studies have been performed in gliomas, but the epigenetic alterations that characterize different subtypes of gliomas…”
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    Journal Article
  10. 10
  11. 11

    Chromosome 9p and 10q losses predict unfavorable outcome in low-grade gliomas by Houillier, Caroline, Mokhtari, Karima, Carpentier, Catherine, Crinière, Emmanuelle, Marie, Yannick, Rousseau, Audrey, Kaloshi, Gentian, Dehais, Caroline, Laffaire, Julien, Laigle-Donadey, Florence, Hoang-Xuan, Khê, Sanson, Marc, Delattre, Jean-Yves

    Published in Neuro-oncology (Charlottesville, Va.) (01-01-2010)
    “…The loss of chromosomes 1p-19q is the only prognostic molecular alteration identified in low-grade gliomas (LGGs) to date. Search for loss of heterozygosity…”
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    Journal Article
  12. 12

    SPECIAL ISSUE: Transcriptional disruptions in Down syndrome: a case study in the Ts1Cje mouse cerebellum during post-natal development by M.-C. Potier, Rivals, I, Mercier, G, Ettwiller, L, Moldrich, R X, Laffaire, J, Personnaz, L, Rossier, J, Dauphinot, L

    Published in Journal of neurochemistry (01-04-2006)
    “…To understand the aetiology and the phenotypic severity of Down syndrome, we searched for transcriptional signatures in a substructure of the brain…”
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    Journal Article
  13. 13

    A polygalacturonase of animal origin isolated from the root-knot nematode Meloidogyne incognita by Jaubert, Stéphanie, Laffaire, Jean-Baptiste, Abad, Pierre, Rosso, Marie-Noëlle

    Published in FEBS letters (03-07-2002)
    “…The first animal polygalacturonase (PG, EC 2.1.15) encoding cDNA, Mi-pg-1, was cloned from the plant parasitic nematode Meloidogyne incognita. The enzymatic…”
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    Journal Article
  14. 14

    Direct identification of stylet secreted proteins from root-knot nematodes by a proteomic approach by Jaubert, Stéphanie, Laffaire, Jean Baptiste, Piotte, Christine, Abad, Pierre, Rosso, Marie-Noëlle, Ledger, Terence Neil

    Published in Molecular and biochemical parasitology (01-05-2002)
    “…The stylet secretions produced by plant parasitic root-knot nematodes are thought to be pathogenicity factors involved in the invasion of the root tissue and…”
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    Journal Article