Search Results - Bauche, Isabelle B.

Overexpression of Adiponectin Targeted to Adipose Tissue in Transgenic Mice: Impaired Adipocyte Differentiation by Bauche, Isabelle B, El Mkadem, Samira Ait, Pottier, Anne-Marie, Senou, Maximin, Many, Marie-Christine, Rezsohazy, René, Penicaud, Luc, Maeda, Norikazu, Funahashi, Tohru, Brichard, Sonia M

“…Adiponectin (ApN) is an adipokine whose expression and plasma levels are inversely related to obesity and insulin-resistant states. Chronic repercussions of…”
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Adiponectin downregulates its own production and the expression of its AdipoR2 receptor in transgenic mice by Bauche, Isabelle B., Ait El Mkadem, Samira, Rezsohazy, René, Funahashi, Tohru, Maeda, Norikazu, Miranda, Lisa Miranda, Brichard, Sonia M.

“…Adiponectin (ApN) is an adipokine whose expression and plasma levels are inversely related to obesity and insulin-resistant states. The in vivo effects of a…”
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Induction of Adiponectin in Skeletal Muscle by Inflammatory Cytokines: in Vivo and in Vitro Studies by Delaigle, Aurélie M, Jonas, Jean-Christophe, Bauche, Isabelle B, Cornu, Olivier, Brichard, Sonia M

“…Adiponectin (ApN) is an adipocytokine that plays a fundamental role in energy homeostasis and counteracting inflammation. We examined whether ApN could be…”
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Multiexon deletions account for 15% of congenital myasthenic syndromes with RAPSN mutations after negative DNA sequencing by Gaudon, Karen, Pénisson-Besnier, Isabelle, Chabrol, Brigitte, Bouhour, Françoise, Demay, Laurence, Ben Ammar, Asma, Bauché, Stéphanie, Vial, Christophe, Nicolas, Guillaume, Eymard, Bruno, Hantaï, Daniel, Richard, Pascale

“…Congenital myasthenic syndromes (CMS) are a heterogeneous group of genetic disorders that give rise to a defect in neuromuscular transmission. We described…”
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New recessive mutations in SYT2 causing severe presynaptic congenital myasthenic syndromes by Bauché, Stéphanie, Sureau, Alain, Sternberg, Damien, Rendu, John, Buon, Céline, Messéant, Julien, Boëx, Myriam, Furling, Denis, Fauré, Julien, Latypova, Xénia, Gelot, Antoinette Bernabe, Mayer, Michèle, Mary, Pierre, Whalen, Sandra, Fournier, Emmanuel, Cloix, Isabelle, Remerand, Ganaelle, Laffargue, Fanny, Nougues, Marie-Christine, Fontaine, Bertrand, Eymard, Bruno, Isapof, Arnaud, Strochlic, Laure

“…To report the identification of 2 new homozygous recessive mutations in the synaptotagmin 2 ( ) gene as the genetic cause of severe and early presynaptic forms…”
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