Duvick LA - Search Results

1

Autosomal dominant spinocerebellar ataxia: locus heterogeneity in a Nebraska kindred.

Ranum LP, Rich SS, Nance MA, Duvick LA, Aita JF, Orr HT, Anton-Johnson S, Schut LJ. Ranum LP, et al. Among authors: duvick la. Neurology. 1992 Feb;42(2):344-7. doi: 10.1212/wnl.42.2.344. Neurology. 1992. PMID: 1736163

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: duvick la. 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. 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: duvick la. 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

Chromosomal organization of the human major histocompatibility complex class I gene family.

Koller BH, Geraghty DE, DeMars R, Duvick L, Rich SS, Orr HT. Koller BH, et al. J Exp Med. 1989 Feb 1;169(2):469-80. doi: 10.1084/jem.169.2.469. J Exp Med. 1989. PMID: 2562983 Free PMC article.

6

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: duvick la. Cell. 1995 Sep 22;82(6):937-48. doi: 10.1016/0092-8674(95)90273-2. Cell. 1995. PMID: 7553854 Free article.

7

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: duvick la. Nat Genet. 1994 Aug;7(4):513-20. doi: 10.1038/ng0894-513. Nat Genet. 1994. PMID: 7951322

8

Molecular and clinical correlations in spinocerebellar ataxia type I: evidence for familial effects on the age at onset.

Ranum LP, Chung MY, Banfi S, Bryer A, Schut LJ, Ramesar R, Duvick LA, McCall A, Subramony SH, Goldfarb L, et al. Ranum LP, et al. Among authors: duvick la. Am J Hum Genet. 1994 Aug;55(2):244-52. Am J Hum Genet. 1994. PMID: 8037204 Free PMC article.

9

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: duvick la. Am J Hum Genet. 1993 Aug;53(2):391-400. Am J Hum Genet. 1993. PMID: 8101039 Free PMC article.

10

Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I.

Chung MY, Ranum LP, Duvick LA, Servadio A, Zoghbi HY, Orr HT. Chung MY, et al. Among authors: duvick la. Nat Genet. 1993 Nov;5(3):254-8. doi: 10.1038/ng1193-254. Nat Genet. 1993. PMID: 8275090

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