NS22920/NS/NINDS NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1990	2
1991	1
1993	4
1994	1
1995	1
1996	1
1997	2
1998	2
1999	2
2000	2
2001	4
2002	2
2003	3
2004	1
2005	2
2006	3
2007	1
2008	3
2009	1
2010	1
2024	0

1

Beyond the Qs in the polyglutamine diseases.

Orr HT. Orr HT. Genes Dev. 2001 Apr 15;15(8):925-32. doi: 10.1101/gad.888401. Genes Dev. 2001. PMID: 11316786 Free article. Review. No abstract available.

2

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.

3

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.

4

Polyglutamine neurodegenerative diseases and regulation of transcription: assembling the puzzle.

Riley BE, Orr HT. Riley BE, et al. Genes Dev. 2006 Aug 15;20(16):2183-92. doi: 10.1101/gad.1436506. Genes Dev. 2006. PMID: 16912271 Free article. Review.

5

Identification and characterization of the gene causing type 1 spinocerebellar ataxia.

Banfi S, Servadio A, Chung MY, Kwiatkowski TJ Jr, McCall AE, Duvick LA, Shen Y, Roth EJ, Orr HT, Zoghbi HY. Banfi S, et al. Nat Genet. 1994 Aug;7(4):513-20. doi: 10.1038/ng0894-513. Nat Genet. 1994. PMID: 7951322

6

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.

7

Altered trafficking of membrane proteins in purkinje cells of SCA1 transgenic mice.

Skinner PJ, Vierra-Green CA, Clark HB, Zoghbi HY, Orr HT. Skinner PJ, et al. Am J Pathol. 2001 Sep;159(3):905-13. doi: 10.1016/S0002-9440(10)61766-X. Am J Pathol. 2001. PMID: 11549583 Free PMC article.

8

Increased trinucleotide repeat instability with advanced maternal age.

Kaytor MD, Burright EN, Duvick LA, Zoghbi HY, Orr HT. Kaytor MD, et al. Hum Mol Genet. 1997 Nov;6(12):2135-9. doi: 10.1093/hmg/6.12.2135. Hum Mol Genet. 1997. PMID: 9328478

9

Spinocerebellar ataxia type-1 and spinobulbar muscular atrophy gene products interact with glyceraldehyde-3-phosphate dehydrogenase.

Koshy B, Matilla T, Burright EN, Merry DE, Fischbeck KH, Orr HT, Zoghbi HY. Koshy B, et al. Hum Mol Genet. 1996 Sep;5(9):1311-8. doi: 10.1093/hmg/5.9.1311. Hum Mol Genet. 1996. PMID: 8872471

10

Interaction of Akt-phosphorylated ataxin-1 with 14-3-3 mediates neurodegeneration in spinocerebellar ataxia type 1.

Chen HK, Fernandez-Funez P, Acevedo SF, Lam YC, Kaytor MD, Fernandez MH, Aitken A, Skoulakis EM, Orr HT, Botas J, Zoghbi HY. Chen HK, et al. Cell. 2003 May 16;113(4):457-68. doi: 10.1016/s0092-8674(03)00349-0. Cell. 2003. PMID: 12757707 Free article.

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