152 related articles for article (PubMed ID: 7670474)
21. [Clinico-genetic study of type I spinocerebelllar ataxia].
Svetel M; Culjković B; Sternić N; Dragasević B; Stojković I; Romac S; Kostić VS
Srp Arh Celok Lek; 1999; 127(5-6):157-62. PubMed ID: 10500422
[TBL] [Abstract][Full Text] [Related]
22. Studying human mutations by sperm typing: instability of CAG trinucleotide repeats in the human androgen receptor gene.
Zhang L; Leeflang EP; Yu J; Arnheim N
Nat Genet; 1994 Aug; 7(4):531-5. PubMed ID: 7951325
[TBL] [Abstract][Full Text] [Related]
23. Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features.
Dürr A; Stevanin G; Cancel G; Duyckaerts C; Abbas N; Didierjean O; Chneiweiss H; Benomar A; Lyon-Caen O; Julien J; Serdaru M; Penet C; Agid Y; Brice A
Ann Neurol; 1996 Apr; 39(4):490-9. PubMed ID: 8619527
[TBL] [Abstract][Full Text] [Related]
24. Regional differences of somatic CAG repeat instability do not account for selective neuronal vulnerability in a knock-in mouse model of SCA1.
Watase K; Venken KJ; Sun Y; Orr HT; Zoghbi HY
Hum Mol Genet; 2003 Nov; 12(21):2789-95. PubMed ID: 12952864
[TBL] [Abstract][Full Text] [Related]
25. Analysis of spinocerebellar ataxia type 2 gene and haplotype analysis: (CCG)1-2 polymorphism and contribution to founder effect.
Mizushima K; Watanabe M; Kondo I; Okamoto K; Shizuka M; Abe K; Aoki M; Shoji M
J Med Genet; 1999 Feb; 36(2):112-4. PubMed ID: 10051008
[TBL] [Abstract][Full Text] [Related]
26. Spinocerebellar ataxia type 6: CAG repeat expansion in alpha1A voltage-dependent calcium channel gene and clinical variations in Japanese population.
Ikeuchi T; Takano H; Koide R; Horikawa Y; Honma Y; Onishi Y; Igarashi S; Tanaka H; Nakao N; Sahashi K; Tsukagoshi H; Inoue K; Takahashi H; Tsuji S
Ann Neurol; 1997 Dec; 42(6):879-84. PubMed ID: 9403480
[TBL] [Abstract][Full Text] [Related]
27. Spinocerebellar ataxia type 1.
Zoghbi HY; Orr HT
Semin Cell Biol; 1995 Feb; 6(1):29-35. PubMed ID: 7620119
[TBL] [Abstract][Full Text] [Related]
28. A SCA7 CAG/CTG repeat expansion is stable in Drosophila melanogaster despite modulation of genomic context and gene dosage.
Jackson SM; Whitworth AJ; Greene JC; Libby RT; Baccam SL; Pallanck LJ; La Spada AR
Gene; 2005 Feb; 347(1):35-41. PubMed ID: 15715978
[TBL] [Abstract][Full Text] [Related]
29. Presymptomatic analysis of spinocerebellar ataxia type 1 (SCA1) via the expansion of the SCA1 CAG-repeat in a large pedigree displaying anticipation and parental male bias.
Matilla T; Volpini V; Genís D; Rosell J; Corral J; Dávalos A; Molins A; Estivill X
Hum Mol Genet; 1993 Dec; 2(12):2123-8. PubMed ID: 8111382
[TBL] [Abstract][Full Text] [Related]
30. Spinocerebellar ataxia type 1 (SCA1): phenotype-genotype correlation studies in intermediate alleles.
Zühlke C; Dalski A; Hellenbroich Y; Bubel S; Schwinger E; Bürk K
Eur J Hum Genet; 2002 Mar; 10(3):204-9. PubMed ID: 11973625
[TBL] [Abstract][Full Text] [Related]
31. Analysis of spinocerebellar ataxia type 1 (SCA1)-related CAG trinucleotide expansion in Japan.
Kameya T; Abe K; Aoki M; Sahara M; Tobita M; Konno H; Itoyama Y
Neurology; 1995 Aug; 45(8):1587-94. PubMed ID: 7543989
[TBL] [Abstract][Full Text] [Related]
32. Comparative studies of the CAG repeats in the spinocerebellar ataxia type 1 (SCA1) gene.
Limprasert P; Nouri N; Nopparatana C; Deininger PL; Keats BJ
Am J Med Genet; 1997 Sep; 74(5):488-93. PubMed ID: 9342197
[TBL] [Abstract][Full Text] [Related]
33. CAG repeat analyses in frozen and formalin-fixed tissues following primer extension preamplification for evaluation of mitotic instability of expanded SCA1 alleles.
Zühlke C; Hellenbroich Y; Schaaff F; Gehlken U; Wessel K; Schubert T; Cervos-Navarro J; Pickartz H; Schwinger E
Hum Genet; 1997 Sep; 100(3-4):339-44. PubMed ID: 9272152
[TBL] [Abstract][Full Text] [Related]
34. Spinocerebellar ataxia 1 (SCA1) in the Japanese: analysis of CAG trinucleitide repeat expansion and instability of the repeat for paternal transmission.
Suzuki Y; Sasaki H; Wakisaka A; Takada A; Yoshiki T; Iwabuchi K; Tashiro K; Fukazawa T; Hamada T
Jpn J Hum Genet; 1995 Mar; 40(1):131-43. PubMed ID: 7780164
[TBL] [Abstract][Full Text] [Related]
35. 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
Am J Hum Genet; 1994 Aug; 55(2):244-52. PubMed ID: 8037204
[TBL] [Abstract][Full Text] [Related]
36. Reevaluation of the exact CAG repeat length in hereditary cerebellar ataxias using highly denaturing conditions and long PCR.
Maruyama H; Kawakami H; Nakamura S
Hum Genet; 1996 May; 97(5):591-5. PubMed ID: 8655136
[TBL] [Abstract][Full Text] [Related]
37. Spinocerebellar ataxia type 1 in Russia.
Illarioshkin SN; Slominsky PA; Ovchinnikov IV; Markova ED; Miklina NI; Klyushnikov SA; Shadrina M; Vereshchagin NV; Limborskaya SA; Ivanova-Smolenskaya IA
J Neurol; 1996 Jul; 243(7):506-10. PubMed ID: 8836939
[TBL] [Abstract][Full Text] [Related]
38. [Unstable expansion of CAG repeat and molecular mechanism of neurodegeneration in SCA1].
Sasaki H
Nihon Rinsho; 1999 Apr; 57(4):801-4. PubMed ID: 10222769
[TBL] [Abstract][Full Text] [Related]
39. Expansion, mosaicism and interruption: mechanisms of the CAG repeat mutation in spinocerebellar ataxia type 1.
Kraus-Perrotta C; Lagalwar S
Cerebellum Ataxias; 2016; 3():20. PubMed ID: 27895927
[TBL] [Abstract][Full Text] [Related]
40. Molecular analysis of a de novo mutation for spinocerebellar ataxia type 6 and (CAG)n repeat units in normal elder controls.
Shizuka M; Watanabe M; Ikeda Y; Mizushima K; Okamoto K; Shoji M
J Neurol Sci; 1998 Nov; 161(1):85-7. PubMed ID: 9879686
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]