Search Results - "Potier, M.C"

Modifications of the endo-lysosomal compartment in Down syndrome and Alzheimer’s disease: impact on amyloid deposition by Potier, M.C, Botté, A, Lainé, J, Franck, A, Fontaine, G, Lavaur, J

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P.1.h.045 Down syndrome model characterisation: gene expression after treatment with selective α5 GABAA modulator and quantification of metabolites by Albac, C, Dauphinot, L, Delatour, B, Santin, M.D, Potier, M.C

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Behavioural and psychological symptoms of dementia in Down syndrome: European development of the novel BPSD-DS evaluation scale by Dekker, A.D, Coppus, A.M.W, Strydom, A, Vermeiren, Y, Grefelman, S, Eleveld, J, Beugelsdijk, G, Schippers, M, Potier, M.C, Sacco, S, Rebillat, A.S, Benejam, B, Fortea, J, De Deyn, P.P

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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

“…Abstract Transgenic mice overexpressing Dyrk1A (TgDyrk1A), a Down syndrome (DS) candidate gene, exhibit motor and cognitive alterations similar to those…”
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S.16.04 A non convulsant alpha5 selective GABA-A inverse agonist restores cognitive deficits in a mouse model of Down syndrome by Delatour, B, Braudeau, J, Duchon, A, Dauphinot, L, Dodd, R.H, Hérault, Y, Potier, M.C

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Neurogenesis deficits in Down syndrome: testing recovery with GABAα5 negative allosteric modulator, β2 adrenergic agonist and IGF-1 in Ts65Dn mice by Albac, C., Stagni, F., Grilli, M., Salvalai, M.E., Bartesaghi, R., Potier, M.C.

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P.213 Specific polygenic risk scores discriminate asymptomatic at-risk individuals according to their brain amyloid load by Xicota, L., Lecoeur, A., Gyorgy, B., Danjou, F., Fontaine, G., Epelbaum, S., Villain, N., Dubois, B., Lambert, J.C., Potier, M.C.

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P.1.005 - Mutating the cholesterol binding site on amyloid precursor protein alters the processing and production of Aβ-amyloid peptides by Hanbouch, L., Marquer, C., Boussicault, L., Schaack, B., Perronet, K., Moreau, J., Gilles, N., Louis, C., Millan, M.J., Potier, M.C.

“…Levels of cholesterol are elevated in the brains of Alzheimer’s disease (AD) patients [1,2]. While the precise pathophysiological consequences remain unclear,…”
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S.02.04 - Modifications of the endo-lysosomal compartment in Down syndrome and Alzheimer’s disease: impact on amyloid deposition by Potier, M.C., Botté, A., Lainé, J., Franck, A., Fontaine, G., Lavaur, J.

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Classification of Human Chromosome 21 Gene-Expression Variations in Down Syndrome: Impact on Disease Phenotypes by Aït Yahya-Graison, E., Aubert, J., Dauphinot, L., Rivals, I., Prieur, M., Golfier, G., Rossier, J., Personnaz, L., Créau, N., Bléhaut, H., Robin, S., Delabar, J.M., Potier, M.-C.

“…Down syndrome caused by chromosome 21 trisomy is the most common genetic cause of mental retardation in humans. Disruption of the phenotype is thought to be…”
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Mutating the cholesterol binding site on amyloid precursor protein alters the processing and production of Aβ-amyloid peptides by Hanbouch, L., Marquer, C., Boussicault, L., Schaack, B., Perronet, K., Moreau, J., Gilles, N., Louis, C., Millan, M.J., Potier, M.C.

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P.5.b.003 - Behavioural and psychological symptoms of dementia in Down syndrome: European development of the novel BPSD-DS evaluation scale by Dekker, A.D., Coppus, A.M.W., Strydom, A., Vermeiren, Y., Grefelman, S., Eleveld, J., Beugelsdijk, G., Schippers, M., Potier, M.C., Sacco, S., Rebillat, A.S., Benejam, B., Fortea, J., De Deyn, P.P.

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Classification of variations of HSA21 gene expression in down syndrome lymphoblastoid cell lines : impact on disease phenotype by Aït Yahya-Graison, E., Aubert, Julie, Dauphinot, L., Rivals, Isabelle, Prieur, Marguerite, Golfier, G., Rossier, J., Personnaz, L., Créau, N, Robin, Stephane, Delabar, J., Potier, M.C

“…absent…”
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Transcription Profile Analysis Reveals That OBP-1F mRNA Is Downregulated in the Olfactory Mucosa Following Food Deprivation by Badonnel, K, Denis, J-B, Caillol, M, Monnerie, R, Piumi, F, Potier, M-C, Salesse, R, Baly, C

“…Neuroanatomical data show that olfactory mucosa (OM) is a possible place for interactions between nutrition and smell. A combination of differential display…”
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The Human Myosin Light Chain Kinase (MLCK) from Hippocampus: Cloning, Sequencing, Expression, and Localization to 3qcen–q21 by POTIER, M.-C., CHELOT, E., PEKARSKY, Y., GARDINER, K., ROSSIER, J., TURNELL, W.G.

“…Myosin light chain kinase (MLCK), a key enzyme in muscle contraction, has been shown by immunohistology to be present in neurons and glia. We describe here the…”
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Conservation of pericentromeric duplications of a 200-kb part of the human 21q22.1 region in primates by Orti, R, Potier, M C, Maunoury, C, Prieur, M, Créau, N, Delabar, J M

“…We analyzed the conservation of large paralogous regions (more than 200 kb) on human chromosome regions 21q22.1 and 21q11.2 and on pericentromeric regions of…”
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Cloning and characterization of a 135- to 500-kb region of homology on the long arm of human chromosome 21 by Dutriaux, A, Rossier, J, Van Hul, W, Nizetic, D, Theophille, D, Delabar, J M, Van Broeckhoven, C, Potier, M C

“…The polymorphic marker D21S190 was initially isolated from a chromosome 21 phage library and mapped to two loci: one in 21q11.1 (proximal locus) and the other…”
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Assignment of the human glutamate receptor gene GLUR5 to 21q22 by screening a chromosome 21 YAC library by Potier, M C, Dutriaux, A, Lambolez, B, Bochet, P, Rossier, J

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Construction and characterization of a yeast artificial chromosome library containing 1.5 equivalents of human chromosome 21 by Potier, M C, Kuo, W L, Dutriaux, A, Gray, J, Goedert, M

“…A library of yeast artificial chromosomes (YACs) was constructed from a human/hamster somatic cell hybrid containing human chromosome 21 (q11-qter). Cells were…”
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FRET detection in the plasma membrane using Total Internal Reflection Fluorescence Lifetime Imaging Microscopy by Blandin, P., Leveque-Fort, S., Lecart, S., Druon, F., Georges, P., Cossec, J.C., Potier, M.C., Lenkei, Z.

“…We developed a total internal reflection fluorescence lifetime imaging microscope to perform functional imaging of living cells membranes labeled with FRET…”
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