Critical Role of the D21S55 Region on Chromosome 21 in the Pathogenesis of Down Syndrome

Autor: Rahmani, Zohra, Blouin, Jean-Louis, Creau-Goldberg, Nicole, Watkins, Paul C., Mattei, Jean-François, Poissonnier, Marc, Prieur, Marguerite, Chettouh, Zoubida, Nicole, Annie, Aurias, Alain, Sinet, Pierre-Marie, Delabar, Jean-Maurice

Publikováno v: Proceedings of the National Academy of Sciences of the United States of America, 1989 Aug 01. 86(15), 5958-5962.

Externí odkaz: https://www.jstor.org/stable/34240

The amyloid peptide induces early genotoxic damage in human preneuron NT2

Autor: Santiard-Baron, Dominique, Lacoste, Aurélien, Ellouk-Achard, Sophie, Soulié, Cathia, Nicole, Annie, Sarasin, Alain, Ceballos-Picot, Irène ^*

Publikováno v: In Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis 2001 479(1):113-120

Cloning and sequencing of a rat CuZn superoxide dismutase cDNA.

Autor: Delabar, Jean-Maurice¹, Nicole, Annie, D'Auriol, Luc², Jacob, Yves¹, Meunier-Rotival, Michèle², Galibert, Francis², Sinet, Pierre-M.¹, Jérôme, Henri¹

Publikováno v: European Journal of Biochemistry. 7/1/87, Vol. 166 Issue 1, p181-187. 7p. 4 Diagrams, 1 Chart.

Myotonic dystrophy CTG expansion affects synaptic vesicle proteins, neurotransmission and mouse behaviour

Autor: Hernández-Hernández, Oscar, Guiraud-Dogan, Céline, Sicot, Géraldine, Huguet, Aline, Luilier, Sabrina, Steidl, Esther, Saenger, Stefanie, Marciniak, Elodie, Obriot, Hélène, Chevarin, Caroline, Nicole, Annie, Revillod, Lucile, Charizanis, Konstantinos, Lee, Kuang-Yung, Suzuki, Yasuhiro, Kimura, Takashi, Matsuura, Tohru, Cisneros, Bulmaro, Swanson, Maurice, Trovero, Fabrice, Buisson, Bruno, Bizot, Jean-Charles, Hamon, Michel, Humez, Sandrine, Bassez, Guillaume, Metzger, Friedrich, Buée, Luc, Munnich, Arnold, Sergeant, Nicolas, Gourdon, Geneviève, Gomes-Pereira, Mário

Publikováno v: Brain-A Journal of Neurology
Brain-A Journal of Neurology, Oxford University Press (OUP), 2013, 136 (Pt 3), pp.957-70. ⟨10.1093/brain/aws367⟩
Brain-A Journal of Neurology, 2013, 136 (Pt 3), pp.957-70. ⟨10.1093/brain/aws367⟩

International audience; Myotonic dystrophy type 1 is a complex multisystemic inherited disorder, which displays multiple debilitating neurological manifestations. Despite recent progress in the understanding of the molecular pathogenesis of myotonic

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b1ac78e8b9bf7d74fe6eee4cd89ce6cc
https://www.hal.inserm.fr/inserm-00795195/document

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