Zoghbi HY - Search Results

1

Molecular genetics and neurobiology of neurodegenerative and neurodevelopmental disorders.

Zoghbi HY. Zoghbi HY. Pediatr Res. 1997 May;41(5):722-6. doi: 10.1203/00006450-199705000-00019. Pediatr Res. 1997. PMID: 9128297 Review. No abstract available.

2

Neurobiology of disease.

Zoghbi HY, Gage FH, Choi DW. Zoghbi HY, et al. Curr Opin Neurobiol. 2000 Oct;10(5):655-60. doi: 10.1016/s0959-4388(00)00135-5. Curr Opin Neurobiol. 2000. PMID: 11084329 Review.

3

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.

4

Regional differences of somatic CAG repeat instability do not account for selective neuronal vulnerability in a knock-in mouse model of SCA1.

Watase K, Venken KJ, Sun Y, Orr HT, Zoghbi HY. Watase K, et al. Among authors: zoghbi hy. Hum Mol Genet. 2003 Nov 1;12(21):2789-95. doi: 10.1093/hmg/ddg300. Epub 2003 Sep 2. Hum Mol Genet. 2003. PMID: 12952864

5

Postnatal neurodevelopmental disorders: meeting at the synapse?

Zoghbi HY. Zoghbi HY. Science. 2003 Oct 31;302(5646):826-30. doi: 10.1126/science.1089071. Science. 2003. PMID: 14593168

6

The story of Rett syndrome: from clinic to neurobiology.

Chahrour M, Zoghbi HY. Chahrour M, et al. Among authors: zoghbi hy. Neuron. 2007 Nov 8;56(3):422-37. doi: 10.1016/j.neuron.2007.10.001. Neuron. 2007. PMID: 17988628 Free article. Review.

7

Pathogenic mechanisms of a polyglutamine-mediated neurodegenerative disease, spinocerebellar ataxia type 1.

Zoghbi HY, Orr HT. Zoghbi HY, et al. J Biol Chem. 2009 Mar 20;284(12):7425-9. doi: 10.1074/jbc.R800041200. Epub 2008 Oct 28. J Biol Chem. 2009. PMID: 18957430 Free PMC article. Review.

8

Coexpression enrichment analysis at the single-cell level reveals convergent defects in neural progenitor cells and their cell-type transitions in neurodevelopmental disorders.

Pang K, Wang L, Wang W, Zhou J, Cheng C, Han K, Zoghbi HY, Liu Z. Pang K, et al. Among authors: zoghbi hy. Genome Res. 2020 Jun;30(6):835-848. doi: 10.1101/gr.254987.119. Epub 2020 Jun 18. Genome Res. 2020. PMID: 32554779 Free PMC article.

9

Spinocerebellar ataxias.

Zoghbi HY. Zoghbi HY. Neurobiol Dis. 2000 Oct;7(5):523-7. doi: 10.1006/nbdi.2000.0346. Neurobiol Dis. 2000. PMID: 11042068 No abstract available.

10

Loss of holocytochrome c-type synthetase causes the male lethality of X-linked dominant microphthalmia with linear skin defects (MLS) syndrome.

Prakash SK, Cormier TA, McCall AE, Garcia JJ, Sierra R, Haupt B, Zoghbi HY, Van Den Veyver IB. Prakash SK, et al. Among authors: zoghbi hy. Hum Mol Genet. 2002 Dec 1;11(25):3237-48. doi: 10.1093/hmg/11.25.3237. Hum Mol Genet. 2002. PMID: 12444108

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