Výsledky vyhledávání - "El Idrissi Abdeslem"

Akademický článek

Pharmacological characterization of GABAA receptors in taurine-fed mice

Autor: L’Amoreaux William J, Marsillo Alexandra, El Idrissi Abdeslem

Publikováno v: Journal of Biomedical Science, Vol 17, Iss Suppl 1, p S14 (2010)

Abstract Background Taurine is one of the most abundant free amino acids especially in excitable tissues, with wide physiological actions. Chronic supplementation of taurine in drinking water to mice increases brain excitability mainly through altera

Externí odkaz: https://doaj.org/article/e09e801e80124887bc3309b3fae50879

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Akademický článek

Neuro-endocrine basis for altered plasma glucose homeostasis in the Fragile X mouse

Autor: El Idrissi Abdeslem, Yan Xin, Sidime Francoise, L’Amoreaux William

Publikováno v: Journal of Biomedical Science, Vol 17, Iss Suppl 1, p S8 (2010)

Abstract Background The fragile X mouse model shows an increase in seizure susceptibility, indicating an involvement of the GABAergic system via an alteration in cellular excitability. In the brain, we have previously described a reduction in GABAA r

Externí odkaz: https://doaj.org/article/5d42499e665443f5b69deb9e6863a468

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Akademický článek

Taurine regulates insulin release from pancreatic beta cell lines

Autor: L’Amoreaux William J, Cuttitta Christina, Santora Allison, Blaize Jonathan F, Tachjadi Janto, El Idrissi Abdeslem

Publikováno v: Journal of Biomedical Science, Vol 17, Iss Suppl 1, p S11 (2010)

Abstract Background Pancreatic β-cells release insulin via an electrogenic response triggered by an increase in plasma glucose concentrations. The critical plasma glucose concentration has been determined to be ~3 mM, at which time both insulin and

Externí odkaz: https://doaj.org/article/ba980d5ed8b84a18b7179211ae34e933

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Akademický článek

Taurine regulation of short term synaptic plasticity in fragile X mice

Autor: El Idrissi Abdeslem, Neuwirth Lorenz S, L’Amoreaux William

Publikováno v: Journal of Biomedical Science, Vol 17, Iss Suppl 1, p S15 (2010)

Abstract Background Fragile X Syndrome is the most common known genetic cause of autism. The Fmr1-KO mouse, lacks the fragile X mental retardation protein (FMRP), and is used as a model of the syndrome. The core behavioral deficits of autism may be c

Externí odkaz: https://doaj.org/article/07b9c74cefa3424bb408a815178674ec

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