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Literature DB >> 16492741

Profile of Huda Y. Zoghbi.

Regina Nuzzo.

Abstract

Entities: Chemical

Mesh：

Year: 2006 PMID： 16492741 PMCID： PMC1413894 DOI： 10.1073/pnas.0509604103

Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN： 0027-8424 Impact factor: 11.205

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References

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16 in total

1. Requirement of Math1 for secretory cell lineage commitment in the mouse intestine.

Authors: Q Yang; N A Bermingham; M J Finegold; H Y Zoghbi
Journal: Science Date: 2001-12-07 Impact factor: 47.728

2. Evolutionary conservation of sequence and expression of the bHLH protein Atonal suggests a conserved role in neurogenesis.

Authors: N Ben-Arie; A E McCall; S Berkman; G Eichele; H J Bellen; H Y Zoghbi
Journal: Hum Mol Genet Date: 1996-09 Impact factor: 6.150

3. [On a unusual brain atrophy syndrome in hyperammonemia in childhood].

Authors: A Rett
Journal: Wien Med Wochenschr Date: 1966-09-10

4. Math1: an essential gene for the generation of inner ear hair cells.

Authors: N A Bermingham; B A Hassan; S D Price; M A Vollrath; N Ben-Arie; R A Eatock; H J Bellen; A Lysakowski; H Y Zoghbi
Journal: Science Date: 1999-06-11 Impact factor: 47.728

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

Authors: Mona Shahbazian; Juan Young; Lisa Yuva-Paylor; Corinne Spencer; Barbara Antalffy; Jeffrey Noebels; Dawna Armstrong; Richard Paylor; Huda Zoghbi
Journal: Neuron Date: 2002-07-18 Impact factor: 17.173

6. Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1.

Authors: C J Cummings; M A Mancini; B Antalffy; D B DeFranco; H T Orr; H Y Zoghbi
Journal: Nat Genet Date: 1998-06 Impact factor: 38.330

Profile of Huda Y. Zoghbi.

1. Requirement of Math1 for secretory cell lineage commitment in the mouse intestine.

2. Evolutionary conservation of sequence and expression of the bHLH protein Atonal suggests a conserved role in neurogenesis.

3. [On a unusual brain atrophy syndrome in hyperammonemia in childhood].

4. Math1: an essential gene for the generation of inner ear hair cells.

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

6. Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1.

7. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

8. Math1 is essential for genesis of cerebellar granule neurons.

9. Reduction of biogenic amine levels in the Rett syndrome.

10. Serine 776 of ataxin-1 is critical for polyglutamine-induced disease in SCA1 transgenic mice.