Hypoxanthine-guanine phosphoribosyl transferase regulates early developmental programming of dopamine neurons: implications for Lesch-Nyhan disease pathogenesis

Autor: Alvarez-Fischer, Daniel, Castagner, François, Stettler, Olivier, Massiani-Beaudoin, Olivia, Moya, Kenneth, Bouillot, Colette, Oertel, Wolfgang, Lombès, Anne, Faigle, Wolfgang, Joshi, Rajiv L, Hartmann, Andreas, Prochiantz, Alain, Ceballos-Picot, I., Mockel, L., Potier, M.-C., Dauphinot, L., Shirley, L., Torero-Ibad, R., Fuchs, Julia, Jinnah, H.A.

Publikováno v: Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2009, 18 (13), pp.2317-2327. ⟨10.1093/hmg/ddp164⟩
Journal of Inherited Metabolic Disease
Journal of Inherited Metabolic Disease, Springer Verlag, 2010, 33 (S1), pp.S175. ⟨10.1093/hmg/ddp164⟩
ResearcherID
Human Molecular Genetics, 2009, 18 (13), pp.2317-2327. ⟨10.1093/hmg/ddp164⟩

Hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency results in Lesch-Nyhan disease (LND), where affected individuals exhibit a characteristic neurobehavioral disorder that has been linked with dysfunction of dopaminergic pathways of the

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https://hal.archives-ouvertes.fr/hal-02156827

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Activation of the fibrinogen receptor on human platelets exposed to alpha chymotrypsin.

Autor: Pidard, Dominique, Frelinger, Andrew L., Bouillot, Colette, Nurden, Alan T.

Publikováno v: European Journal of Biochemistry; 9/1/91, Vol. 200 Issue 2, p437-447, 11p

Axonal Amyloid Precursor Protein Expressed by Neurons in VitroIs Present in a Membrane Fraction with Caveolae-like Properties (∗)

Autor: Bouillot, Colette, Prochiantz, Alain, Rougon, Geneviève, Allinquant, Bernadette

Publikováno v: Journal of Biological Chemistry; March 1996, Vol. 271 Issue: 13 p7640-7644, 5p