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Overexpression of mSim2 gene in the zona limitans of the diencephalon of segmental trisomy 16 Ts1Cje fetuses, a mouse model for trisomy 21: a novel whole-mount based RNA hybridization study.
Vialard, F; Toyama, K; Vernoux, S; Carlson, E J; Epstein, C J; Sinet, P M; Rahmani, Z.
Afiliación
  • Vialard F; CNRS UMR 8602, Faculté de Médecine Necker-Enfants Malades, 156 Rue de Vaugirard, 75730 Cedex 15, Paris, France.
Brain Res Dev Brain Res ; 121(1): 73-8, 2000 May 11.
Article en En | MEDLINE | ID: mdl-10837894
ABSTRACT
Trisomy 21 (Down syndrome) is the most common chromosomal abnormality associated with mental retardation in humans. Sim2, a human homologue of Drosophila sim gene, which acts as a master regulator of the early development of the fly central nervous system midline, is located on chromosome 21, in the Down syndrome critical region, and might therefore be involved in the pathogenesis of some of the morphological features and brain anomalies observed in Down syndrome. We report here the detailed expression pattern of murine mSim2 gene in Ts1Cje mice fetuses, a segmental trisomy 16 mouse model for trisomy 21, and its overexpression in the zona limitans of the diencephalon using a new quantitative method based on the whole-mount RNA hybridization technique.
Asunto(s)
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Nucleares / Síndrome de Down / Regulación del Desarrollo de la Expresión Génica / Diencéfalo / Proteínas de Unión al ADN Tipo de estudio: Prognostic_studies Límite: Animals / Female / Humans / Male Idioma: En Revista: Brain Res Dev Brain Res Asunto de la revista: CEREBRO / NEUROLOGIA Año: 2000 Tipo del documento: Article País de afiliación: Francia
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Nucleares / Síndrome de Down / Regulación del Desarrollo de la Expresión Génica / Diencéfalo / Proteínas de Unión al ADN Tipo de estudio: Prognostic_studies Límite: Animals / Female / Humans / Male Idioma: En Revista: Brain Res Dev Brain Res Asunto de la revista: CEREBRO / NEUROLOGIA Año: 2000 Tipo del documento: Article País de afiliación: Francia