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34
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for author:"Delabar J."
in Literature Citations
| DYRK1A, a novel determinant of the methionine-homocysteine cycle in different mouse models overexpressing this Down-syndrome-associated kinase. Noll C., Planque C., Ripoll C., Guedj F., Diez A., Ducros V., Belin N., Duchon A., Paul J.L., Badel A. et al. PLoS ONE 4:e7540-e7540(2009) · Mapped (1) |
| A quantitative assessment of gene expression (QAGE) reveals differential overexpression of DOPEY2, a candidate gene for mental retardation, in Down syndrome brain regions. Rachidi M., Delezoide A.L., Delabar J.M., Lopes C. Int. J. Dev. Neurosci. 27:393-398(2009) · Mapped (1) |
| Calpain activation is required for homocysteine-mediated hepatic degradation of inhibitor I kappa B alpha. Hamelet J., Couty J.P., Crain A.M., Noll C., Postic C., Paul J.L., Delabar J.M., Viguier M., Janel N. Mol. Genet. Metab. 97:114-120(2009) · Mapped (4) |
| Green tea polyphenols rescue of brain defects induced by overexpression of DYRK1A. Guedj F., Sebrie C., Rivals I., Ledru A., Paly E., Bizot J.C., Smith D., Rubin E., Gillet B., Arbones M. et al. PLoS ONE 4:e4606-e4606(2009) · Mapped (6) |
| DYRK1A interacts with the REST/NRSF-SWI/SNF chromatin remodelling complex to deregulate gene clusters involved in the neuronal phenotypic traits of Down syndrome. Lepagnol-Bestel A.M., Zvara A., Maussion G., Quignon F., Ngimbous B., Ramoz N., Imbeaud S., Loe-Mie Y., Benihoud K., Agier N. et al. Hum. Mol. Genet. 18:1405-1414(2009) · Mapped (10) |
| The protein kinase DYRK1A regulates caspase-9-mediated apoptosis during retina development. Laguna A., Aranda S., Barallobre M.J., Barhoum R., Fernandez E., Fotaki V., Delabar J.M., de la Luna S., de la Villa P., Arbones M.L. Dev. Cell 15:841-853(2008) · Mapped (55) |
| Effect of hyperhomocysteinemia on the protein kinase DYRK1A in liver of mice. Hamelet J., Noll C., Ripoll C., Paul J.L., Janel N., Delabar J.M. Biochem. Biophys. Res. Commun. 378:673-677(2009) · Mapped (7) |
| Cystathionine beta synthase deficiency induces catalase-mediated hydrogen peroxide detoxification in mice liver. Hamelet J., Seltzer V., Petit E., Noll C., Andreau K., Delabar J.M., Janel N. Biochim. Biophys. Acta 1782:482-488(2008) · Mapped (1) |
| Increased dosage of DYRK1A and brain volumetric alterations in a YAC model of partial trisomy 21. Sebrie C., Chabert C., Ledru A., Guedj F., Po C., Smith D.J., Rubin E., Rivals I., Beloeil J.C., Gillet B. et al. Anat Rec (Hoboken) 291:254-262(2008) · Mapped (6) |
| New cerebellar phenotypes in YAC transgenic mouse in vivo library of human Down syndrome critical region-1. Rachidi M., Lopes C., Vayssettes C., Smith D.J., Rubin E.M., Delabar J.M. Biochem. Biophys. Res. Commun. 364:488-494(2007) · Mapped (4) |
| Mice deficient in cystathionine beta synthase display altered homocysteine remethylation pathway. Alberto J.M., Hamelet J., Noll C., Blaise S., Bronowicki J.P., Gueant J.L., Delabar J.M., Janel N. Mol. Genet. Metab. 91:396-398(2007) · Mapped (1) |
| Effects of catechin on homocysteine metabolism in hyperhomocysteinemic mice. Hamelet J., Demuth K., Dairou J., Ledru A., Paul J.L., Dupret J.M., Delabar J.M., Rodrigues-Lima F., Janel N. Biochem. Biophys. Res. Commun. 355:221-227(2007) · Mapped (1) |
| Inhibition of extracellular signal-regulated kinase in liver of hyperhomocysteinemic mice. Hamelet J., Demuth K., Delabar J.M., Janel N. Arterioscler. Thromb. Vasc. Biol. 26:e126-7(2006) · Mapped (1) |
| C21orf5, a new member of Dopey family involved in morphogenesis, could participate in neurological alterations and mental retardation in Down syndrome. Rachidi M., Lopes C., Costantine M., Delabar J.M. DNA Res. 12:203-210(2005) · Mapped (2) |
| C21orf5, a human candidate gene for brain abnormalities and mental retardation in Down syndrome. Rachidi M., Lopes C., Delezoide A.-L., Delabar J.-M. Cytogenet. Genome Res. 112:16-22(2006) · UniProtKB (1) |
| Spatial and temporal localization during embryonic and fetal human development of the transcription factor SIM2 in brain regions altered in Down syndrome. Rachidi M., Lopes C., Charron G., Delezoide A.L., Paly E., Bloch B., Delabar J.M. Int. J. Dev. Neurosci. 23:475-484(2005) · Mapped (1) |
| Regulation of extracellular signal-regulated kinase by homocysteine in hippocampus. Robert K., Pages C., Ledru A., Delabar J., Caboche J., Janel N. Neuroscience 133:925-935(2005) · Mapped (1) |
| Cystathionine beta synthase deficiency promotes oxidative stress, fibrosis, and steatosis in mice liver. Robert K., Nehme J., Bourdon E., Pivert G., Friguet B., Delcayre C., Delabar J.M., Janel N. Gastroenterology 128:1405-1415(2005) · Mapped (1) |
| Hyperkeratosis in cystathionine beta synthase-deficient mice: an animal model of hyperhomocysteinemia. Robert K., Maurin N., Ledru A., Delabar J., Janel N. Anat Rec A Discov Mol Cell Evol Biol 280:1072-1076(2004) · Mapped (1) |
| Mouse liver paraoxonase-1 gene expression is downregulated in hyperhomocysteinemia. Janel N., Robert K., Chabert C., Ledru A., Gouedard C., Barouki R., Delabar J.M., Chasse J.F. Thromb. Haemost. 92:221-222(2004) · Mapped (2) |
| Transgenic mouse in vivo library of human Down syndrome critical region 1: association between DYRK1A overexpression, brain development abnormalities, and cell cycle protein alteration. Branchi I., Bichler Z., Minghetti L., Delabar J.M., Malchiodi-Albedi F., Gonzalez M.C., Chettouh Z., Nicolini A., Chabert C., Smith D.J. et al. J. Neuropathol. Exp. Neurol. 63:429-440(2004) · Mapped (7) |
| Chromosome 21 KIR channels in brain development. Thiery E., Thomas S., Vacher S., Delezoide A.L., Delabar J.M., Creau N. J. Neural Transm. Suppl. 2003:105-115(2003) · Mapped (4) |
| The differentially expressed C21orf5 gene in the medial temporal-lobe system could play a role in mental retardation in Down syndrome and transgenic mice. Lopes C., Chettouh Z., Delabar J.-M., Rachidi M. Biochem. Biophys. Res. Commun. 305:915-924(2003) · UniProtKB (2) · Mapped (3) |
| The CASK/Lin-2 Drosophila homologue, Camguk, could play a role in epithelial patterning and in neuronal targeting. Lopes C., Gassanova S., Delabar J.M., Rachidi M. Biochem. Biophys. Res. Commun. 284:1004-1010(2001) · Mapped (1) |
| C21orf5, a novel human chromosome 21 gene, has a Caenorhabditis elegans ortholog (pad-1) required for embryonic patterning. Guipponi M., Brunschwig K., Chamoun Z., Scott H.S., Shibuya K., Kudoh J., Delezoide A.-L., El Samadi S., Chettouh Z., Rossier C. et al. Genomics 68:30-40(2000) · UniProtKB (2) |
