Servadio A - Search Results

1

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: servadio a. Nat Genet. 1993 Nov;5(3):254-8. doi: 10.1038/ng1193-254. Nat Genet. 1993. PMID: 8275090

2

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

3

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. Nat Genet. 1995 May;10(1):94-8. doi: 10.1038/ng0595-94. Nat Genet. 1995. PMID: 7647801

4

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

5

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

Orr HT, Chung MY, Banfi S, Kwiatkowski TJ Jr, Servadio A, Beaudet AL, McCall AE, Duvick LA, Ranum LP, Zoghbi HY. Orr HT, et al. Among authors: servadio a. Nat Genet. 1993 Jul;4(3):221-6. doi: 10.1038/ng0793-221. Nat Genet. 1993. PMID: 8358429

6

Ataxin-1 with an expanded glutamine tract alters nuclear matrix-associated structures.

Skinner PJ, Koshy BT, Cummings CJ, Klement IA, Helin K, Servadio A, Zoghbi HY, Orr HT. Skinner PJ, et al. Among authors: servadio a. Nature. 1997 Oct 30;389(6654):971-4. doi: 10.1038/40153. Nature. 1997. PMID: 9353120

7

Cloning and developmental expression analysis of the murine homolog of the spinocerebellar ataxia type 1 gene (Sca1).

Banfi S, Servadio A, Chung M, Capozzoli F, Duvick LA, Elde R, Zoghbi HY, Orr HT. Banfi S, et al. Among authors: servadio a. Hum Mol Genet. 1996 Jan;5(1):33-40. doi: 10.1093/hmg/5.1.33. Hum Mol Genet. 1996. PMID: 8789437

8

Mapping of the Sca1 and pcd genes on mouse chromosome 13 provides evidence that they are different genes.

Servadio A, McCall A, Zoghbi H, Eicher EM. Servadio A, et al. Genomics. 1995 Oct 10;29(3):812-3. doi: 10.1006/geno.1995.9925. Genomics. 1995. PMID: 8575786 No abstract available.

9

Reversibility of symptoms in a conditional mouse model of spinocerebellar ataxia type 3.

Boy J, Schmidt T, Wolburg H, Mack A, Nuber S, Böttcher M, Schmitt I, Holzmann C, Zimmermann F, Servadio A, Riess O. Boy J, et al. Among authors: servadio a. Hum Mol Genet. 2009 Nov 15;18(22):4282-95. doi: 10.1093/hmg/ddp381. Epub 2009 Aug 10. Hum Mol Genet. 2009. PMID: 19666958

10

Phenotypic effects of expanded ataxin-1 polyglutamines with interruptions in vitro.

Calabresi V, Guida S, Servadio A, Jodice C. Calabresi V, et al. Among authors: servadio a. Brain Res Bull. 2001 Oct-Nov 1;56(3-4):337-42. doi: 10.1016/s0361-9230(01)00600-1. Brain Res Bull. 2001. PMID: 11719269

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