Orr HT - Search Results

1

ATAXIN-1 interacts with the repressor Capicua in its native complex to cause SCA1 neuropathology.

Lam YC, Bowman AB, Jafar-Nejad P, Lim J, Richman R, Fryer JD, Hyun ED, Duvick LA, Orr HT, Botas J, Zoghbi HY. Lam YC, et al. Among authors: orr ht. Cell. 2006 Dec 29;127(7):1335-47. doi: 10.1016/j.cell.2006.11.038. Cell. 2006. PMID: 17190598 Free article.

2

Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6p.

Ranum LP, Duvick LA, Rich SS, Schut LJ, Litt M, Orr HT. Ranum LP, et al. Among authors: orr ht. Am J Hum Genet. 1991 Jul;49(1):31-41. Am J Hum Genet. 1991. PMID: 1676561 Free PMC article.

3

A polymorphic DNA probe, p1-10-2, from chromosome 6.

Duvick L, Rich SS, Orr HT. Duvick L, et al. Among authors: orr ht. Nucleic Acids Res. 1990 May 25;18(10):3105. doi: 10.1093/nar/18.10.3105. Nucleic Acids Res. 1990. PMID: 1971928 Free PMC article.

4

Dinucleotide repeat polymorphism at the D6S109 locus.

Ranum LP, Chung MY, Duvick LA, Zoghbi HY, Orr HT. Ranum LP, et al. Among authors: orr ht. Nucleic Acids Res. 1991 Mar 11;19(5):1171. doi: 10.1093/nar/19.5.1171-a. Nucleic Acids Res. 1991. PMID: 2020562 Free PMC article. No abstract available.

5

SCA1 transgenic mice: a model for neurodegeneration caused by an expanded CAG trinucleotide repeat.

Burright EN, Clark HB, Servadio A, Matilla T, Feddersen RM, Yunis WS, Duvick LA, Zoghbi HY, Orr HT. Burright EN, et al. Among authors: orr ht. Cell. 1995 Sep 22;82(6):937-48. doi: 10.1016/0092-8674(95)90273-2. Cell. 1995. PMID: 7553854 Free article.

6

Spinocerebellar ataxia type 1.

Zoghbi HY, Orr HT. Zoghbi HY, et al. Among authors: orr ht. Semin Cell Biol. 1995 Feb;6(1):29-35. doi: 10.1016/1043-4682(95)90012-8. Semin Cell Biol. 1995. PMID: 7620119 Review.

7

Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals.

Servadio A, Koshy B, Armstrong D, Antalffy B, Orr HT, Zoghbi HY. Servadio A, et al. Among authors: orr ht. Nat Genet. 1995 May;10(1):94-8. doi: 10.1038/ng0595-94. Nat Genet. 1995. PMID: 7647801

8

Gametic and somatic tissue-specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1.

Chong SS, McCall AE, Cota J, Subramony SH, Orr HT, Hughes MR, Zoghbi HY. Chong SS, et al. Among authors: orr ht. Nat Genet. 1995 Jul;10(3):344-50. doi: 10.1038/ng0795-344. Nat Genet. 1995. PMID: 7670474

9

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. Among authors: orr ht. Nat Genet. 1994 Aug;7(4):513-20. doi: 10.1038/ng0894-513. Nat Genet. 1994. PMID: 7951322

10

The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locus.

Kwiatkowski TJ Jr, Orr HT, Banfi S, McCall AE, Jodice C, Persichetti F, Novelletto A, LeBorgne-DeMarquoy F, Duvick LA, Frontali M, et al. Kwiatkowski TJ Jr, et al. Among authors: orr ht. Am J Hum Genet. 1993 Aug;53(2):391-400. Am J Hum Genet. 1993. PMID: 8101039 Free PMC article.

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