Zoghbi HY - Search Results

1

Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome.

Moretti P, Bouwknecht JA, Teague R, Paylor R, Zoghbi HY. Moretti P, et al. Among authors: zoghbi hy. Hum Mol Genet. 2005 Jan 15;14(2):205-20. doi: 10.1093/hmg/ddi016. Epub 2004 Nov 17. Hum Mol Genet. 2005. PMID: 15548546

2

Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysis.

Ellison KA, Fill CP, Terwilliger J, DeGennaro LJ, Martin-Gallardo A, Anvret M, Percy AK, Ott J, Zoghbi H. Ellison KA, et al. Am J Hum Genet. 1992 Feb;50(2):278-87. Am J Hum Genet. 1992. PMID: 1734712 Free PMC article.

3

Genetic aspects of Rett syndrome.

Zoghbi H. Zoghbi H. J Child Neurol. 1988;3 Suppl:S76-8. doi: 10.1177/0883073888003001s15. J Child Neurol. 1988. PMID: 3058791 Review.

4

Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation.

Shahbazian MD, Antalffy B, Armstrong DL, Zoghbi HY. Shahbazian MD, et al. Among authors: zoghbi hy. Hum Mol Genet. 2002 Jan 15;11(2):115-24. doi: 10.1093/hmg/11.2.115. Hum Mol Genet. 2002. PMID: 11809720

5

Impaired conditioned fear and enhanced long-term potentiation in Fmr2 knock-out mice.

Gu Y, McIlwain KL, Weeber EJ, Yamagata T, Xu B, Antalffy BA, Reyes C, Yuva-Paylor L, Armstrong D, Zoghbi H, Sweatt JD, Paylor R, Nelson DL. Gu Y, et al. J Neurosci. 2002 Apr 1;22(7):2753-63. doi: 10.1523/JNEUROSCI.22-07-02753.2002. J Neurosci. 2002. PMID: 11923441 Free PMC article.

6

A long CAG repeat in the mouse Sca1 locus replicates SCA1 features and reveals the impact of protein solubility on selective neurodegeneration.

Watase K, Weeber EJ, Xu B, Antalffy B, Yuva-Paylor L, Hashimoto K, Kano M, Atkinson R, Sun Y, Armstrong DL, Sweatt JD, Orr HT, Paylor R, Zoghbi HY. Watase K, et al. Among authors: zoghbi hy. Neuron. 2002 Jun 13;34(6):905-19. doi: 10.1016/s0896-6273(02)00733-x. Neuron. 2002. PMID: 12086639 Free article.

7

Introduction: Rett syndrome.

Zoghbi HY. Zoghbi HY. Ment Retard Dev Disabil Res Rev. 2002;8(2):59-60. doi: 10.1002/mrdd.10028. Ment Retard Dev Disabil Res Rev. 2002. PMID: 12112727 No abstract available.

8

Genetic basis of Rett syndrome.

Van den Veyver IB, Zoghbi HY. Van den Veyver IB, et al. Among authors: zoghbi hy. Ment Retard Dev Disabil Res Rev. 2002;8(2):82-6. doi: 10.1002/mrdd.10025. Ment Retard Dev Disabil Res Rev. 2002. PMID: 12112732 Review.

9

Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3.

Shahbazian M, Young J, Yuva-Paylor L, Spencer C, Antalffy B, Noebels J, Armstrong D, Paylor R, Zoghbi H. Shahbazian M, et al. Neuron. 2002 Jul 18;35(2):243-54. doi: 10.1016/s0896-6273(02)00768-7. Neuron. 2002. PMID: 12160743 Free article.

10

Balanced X chromosome inactivation patterns in the Rett syndrome brain.

Shahbazian MD, Sun Y, Zoghbi HY. Shahbazian MD, et al. Among authors: zoghbi hy. Am J Med Genet. 2002 Aug 1;111(2):164-8. doi: 10.1002/ajmg.10557. Am J Med Genet. 2002. PMID: 12210344

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