Un deficit en noradrénaline à l’origine des troubles respiratoires dans un modèle animal du syndrome de Rett

Laurent Villard; Jean-Christophe Roux

doi:10.1051/medsci/200622181

Accès gratuit

Numéro		Med Sci (Paris) Volume 22, Numéro 1, Janvier 2006


Page(s)		81 - 83
Section		Dernière Heures
DOI		https://doi.org/10.1051/medsci/200622181
Publié en ligne		15 janvier 2006

Weaving LS, Ellaway CJ, Gecz J, et al. Rett syndrome : clinical review and genetic update. J Med Genet 2005; 42 : 1–7. [Google Scholar]
Hagberg B. Rett syndrome : clinical peculiarities and biological mysteries. Acta Paediatr 1995; 84 : 971–6. [Google Scholar]
Amir RE, Van den Veyver IB, Wan M, et al. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein2. Nat Genet 1999; 23 : 185–8. [Google Scholar]
Gilgenkrantz S, Bourdon V. MeCP2 et retard mental. Med Sci (Paris) 2001; 17 : 811–3. [Google Scholar]
Traynor J, Agarwal P, Lazzeroni L, et al. Gene expression patterns vary in clonal cell cultures from Rett syndrome females with eight different MECP2 mutations. BMC Med Genet 2002; 3 h 12. [Google Scholar]
Guy J, Hendrich B, Holmes M, et al. A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome. Nat Genet 2001; 27 : 322–6. [Google Scholar]
Chen RZ, Akbarian S, Tudor M, et al. Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice. Nat Genet 2001; 27 : 327–31. [Google Scholar]
Shahbazian M, Young J, Yuva-Paylor L, et al. Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3. Neuron 2002; 35 : 243–54. [Google Scholar]
Julu PO, Kerr AM, Apartopoulos F, et al. Characterisation of breathing and associated central autonomic dysfunction in the Rett disorder. Arch Dis Child 2001; 85 : 29–37. [Google Scholar]
Elian M, Rudolf ND. EEG and respiration in Rett syndrome. Acta Neurol Scand 1991; 83 : 123–8. [Google Scholar]
Viemari JC, Roux JC, Tryba AK, et al. Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice. J Neurosci 2005; 25 : 11521–30. [Google Scholar]

Les statistiques affichées correspondent au cumul d'une part des vues des résumés de l'article et d'autre part des vues et téléchargements de l'article plein-texte (PDF, Full-HTML, ePub... selon les formats disponibles) sur la platefome Vision4Press.

Les statistiques sont disponibles avec un délai de 48 à 96 heures et sont mises à jour quotidiennement en semaine.

Le chargement des statistiques peut être long.

[1] Weaving LS, Ellaway CJ, Gecz J, et al. Rett syndrome : clinical review and genetic update. J Med Genet 2005; 42 : 1–7. [Google Scholar]

[2] Hagberg B. Rett syndrome : clinical peculiarities and biological mysteries. Acta Paediatr 1995; 84 : 971–6. [Google Scholar]

[3] Amir RE, Van den Veyver IB, Wan M, et al. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein2. Nat Genet 1999; 23 : 185–8. [Google Scholar]

[4] Gilgenkrantz S, Bourdon V. MeCP2 et retard mental. Med Sci (Paris) 2001; 17 : 811–3. [Google Scholar]

[5] Traynor J, Agarwal P, Lazzeroni L, et al. Gene expression patterns vary in clonal cell cultures from Rett syndrome females with eight different MECP2 mutations. BMC Med Genet 2002; 3 h 12. [Google Scholar]

[6] Guy J, Hendrich B, Holmes M, et al. A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome. Nat Genet 2001; 27 : 322–6. [Google Scholar]

[7] Chen RZ, Akbarian S, Tudor M, et al. Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice. Nat Genet 2001; 27 : 327–31. [Google Scholar]

[8] Shahbazian M, Young J, Yuva-Paylor L, et al. Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3. Neuron 2002; 35 : 243–54. [Google Scholar]

[9] Julu PO, Kerr AM, Apartopoulos F, et al. Characterisation of breathing and associated central autonomic dysfunction in the Rett disorder. Arch Dis Child 2001; 85 : 29–37. [Google Scholar]

[10] Elian M, Rudolf ND. EEG and respiration in Rett syndrome. Acta Neurol Scand 1991; 83 : 123–8. [Google Scholar]

[11] Viemari JC, Roux JC, Tryba AK, et al. Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice. J Neurosci 2005; 25 : 11521–30. [Google Scholar]