NS27699/NS/NINDS NIH HHS/United States[Grant Number] - Search Results

Year	Number of Results
1990	1
1991	4
1992	3
1993	5
1994	1
1995	5
1996	3
1997	6
1998	5
1999	2
2000	4
2001	3
2002	3
2003	4
2005	2
2006	4
2007	4
2008	3
2009	2
2010	2
2011	4
2012	1
2013	3
2015	1
2021	0

1

Trinucleotide repeat disorders.

Orr HT, Zoghbi HY. Orr HT, et al. Annu Rev Neurosci. 2007;30:575-621. doi: 10.1146/annurev.neuro.29.051605.113042. Annu Rev Neurosci. 2007. PMID: 17417937 Review.

2

A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration.

Lim J, Hao T, Shaw C, Patel AJ, Szabó G, Rual JF, Fisk CJ, Li N, Smolyar A, Hill DE, Barabási AL, Vidal M, Zoghbi HY. Lim J, et al. Cell. 2006 May 19;125(4):801-14. doi: 10.1016/j.cell.2006.03.032. Cell. 2006. PMID: 16713569 Free article.

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. Neuron. 2002 Jun 13;34(6):905-19. doi: 10.1016/s0896-6273(02)00733-x. Neuron. 2002. PMID: 12086639 Free article.

4

Trinucleotide repeat disorders in pediatrics.

O'Donnell DM, Zoghbi HY. O'Donnell DM, et al. Curr Opin Pediatr. 1995 Dec;7(6):715-25. doi: 10.1097/00008480-199512000-00016. Curr Opin Pediatr. 1995. PMID: 8776025 Review.

5

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.

6

Deficiency of Capicua disrupts bile acid homeostasis.

Kim E, Park S, Choi N, Lee J, Yoe J, Kim S, Jung HY, Kim KT, Kang H, Fryer JD, Zoghbi HY, Hwang D, Lee Y. Kim E, et al. Sci Rep. 2015 Feb 5;5:8272. doi: 10.1038/srep08272. Sci Rep. 2015. PMID: 25653040 Free PMC article.

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

SCA1 molecular genetics: a history of a 13 year collaboration against glutamines.

Orr HT, Zoghbi HY. Orr HT, et al. Hum Mol Genet. 2001 Oct 1;10(20):2307-11. doi: 10.1093/hmg/10.20.2307. Hum Mol Genet. 2001. PMID: 11673415 Review.

9

The CAG/polyglutamine tract diseases: gene products and molecular pathogenesis.

Koshy BT, Zoghbi HY. Koshy BT, et al. Brain Pathol. 1997 Jul;7(3):927-42. doi: 10.1111/j.1750-3639.1997.tb00894.x. Brain Pathol. 1997. PMID: 9217976 Review.

10

Progress in pathogenesis studies of spinocerebellar ataxia type 1.

Cummings CJ, Orr HT, Zoghbi HY. Cummings CJ, et al. Philos Trans R Soc Lond B Biol Sci. 1999 Jun 29;354(1386):1079-81. doi: 10.1098/rstb.1999.0462. Philos Trans R Soc Lond B Biol Sci. 1999. PMID: 10434309 Free PMC article. Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

Search Page

Search Results