141 related articles for article (PubMed ID: 21154334)
1. [Mutation analysis of a Chinese family with spinocerebellar ataxia 7].
Yu J; Ma JH; Lei J; Li HT; Zhang XN
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Dec; 27(6):685-7. PubMed ID: 21154334
[TBL] [Abstract][Full Text] [Related]
2. Molecular and clinical study of spinocerebellar ataxia type 7 in Chinese kindreds.
Gu W; Wang Y; Liu X; Zhou B; Zhou Y; Wang G
Arch Neurol; 2000 Oct; 57(10):1513-8. PubMed ID: 11030806
[TBL] [Abstract][Full Text] [Related]
3. Somatic instability of expanded CAG repeats of ATXN7 in Japanese patients with spinocerebellar ataxia type 7.
Katagiri S; Hayashi T; Takeuchi T; Yamada H; Gekka T; Kawabe K; Kurita A; Tsuneoka H
Doc Ophthalmol; 2015 Jun; 130(3):189-95. PubMed ID: 25643591
[TBL] [Abstract][Full Text] [Related]
4. [Studies on the CAG repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese Han].
Wang J; Xu Q; Lei L; Shen L; Jiang H; Li X; Zhou Y; Yi J; Zhou J; Yan X; Pan Q; Xia K; Tang B
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec; 26(6):620-5. PubMed ID: 19953482
[TBL] [Abstract][Full Text] [Related]
5. Analysis of trinucleotide repeats in different SCA loci in spinocerebellar ataxia patients and in normal population of Taiwan.
Tsai HF; Liu CS; Leu TM; Wen FC; Lin SJ; Liu CC; Yang DK; Li C; Hsieh M
Acta Neurol Scand; 2004 May; 109(5):355-60. PubMed ID: 15080863
[TBL] [Abstract][Full Text] [Related]
6. Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds.
Tang B; Liu C; Shen L; Dai H; Pan Q; Jing L; Ouyang S; Xia J
Arch Neurol; 2000 Apr; 57(4):540-4. PubMed ID: 10768629
[TBL] [Abstract][Full Text] [Related]
7. Trinucleotide expansions in the SCA7 gene in a large family with spinocerebellar ataxia and craniocervical dystonia.
Lin Y; Zheng JY; Jin YH; Xie YC; Jin ZB
Neurosci Lett; 2008 Mar; 434(2):230-3. PubMed ID: 18325672
[TBL] [Abstract][Full Text] [Related]
8. Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.
Oda M; Maruyama H; Komure O; Morino H; Terasawa H; Izumi Y; Imamura T; Yasuda M; Ichikawa K; Ogawa M; Matsumoto M; Kawakami H
Arch Neurol; 2004 Feb; 61(2):209-12. PubMed ID: 14967767
[TBL] [Abstract][Full Text] [Related]
9. Identification of the spinocerebellar ataxia type 7 mutation in Taiwan: application of PCR-based Southern blot.
Hsieh M; Lin SJ; Chen JF; Lin HM; Hsiao KM; Li SY; Li C; Tsai CJ
J Neurol; 2000 Aug; 247(8):623-9. PubMed ID: 11041330
[TBL] [Abstract][Full Text] [Related]
10. [Clinical characteristics and molecular biology of hereditary spinocerebellar ataxia type 7: study of 3 Chinese families].
Song XW; Tang BS; Jiang H; Shen L; Yang Q; Liao SS; Li QH; Liang XC; Tang JG
Zhonghua Yi Xue Za Zhi; 2006 Jul; 86(25):1755-8. PubMed ID: 17054842
[TBL] [Abstract][Full Text] [Related]
11. Spinocerebellar ataxia type 7 (SCA7) - correlations between phenotype and genotype in one large Belgian family.
Martin J; Van Regemorter N; Del-Favero J; Löfgren A; Van Broeckhoven C
J Neurol Sci; 1999 Sep; 168(1):37-46. PubMed ID: 10500272
[TBL] [Abstract][Full Text] [Related]
12. [The clinical features and gene mutation analysis in a pedigree of spinocerebellar ataxia type 7].
Yin XZ; Zhang BR; Wu DW; Tian J; Zhang H
Yi Chuan; 2007 Jun; 29(6):688-92. PubMed ID: 17650485
[TBL] [Abstract][Full Text] [Related]
13. Spinocerebellar ataxia 7 (SCA7) in Indian population: predilection of ATXN7-CAG expansion mutation in an ethnic population.
Faruq M; Srivastava AK; Singh S; Gupta R; Dada T; Garg A; Behari M; Mukerji M
Indian J Med Res; 2015 Feb; 141(2):187-98. PubMed ID: 25900954
[TBL] [Abstract][Full Text] [Related]
14. [Gene diagnosis and CAG repeat analysis of spinocerebellar ataxia cases of Guangxi region].
Tan JQ; Wang P; Hu QP; Li SF; Shu W; Ma J; Fang L; Hua R; Ding Y; Yuan ZG
Yi Chuan; 2009 Jun; 31(6):605-10. PubMed ID: 19586860
[TBL] [Abstract][Full Text] [Related]
15. Spinocerebellar ataxia 7 (SCA7).
Lebre AS; Brice A
Cytogenet Genome Res; 2003; 100(1-4):154-63. PubMed ID: 14526176
[TBL] [Abstract][Full Text] [Related]
16. Spinocerebellar ataxia type 1 in China: molecular analysis and genotype-phenotype correlation in 5 families.
Zhou YX; Qiao WH; Gu WH; Xie H; Tang BS; Zhou LS; Yang BX; Takiyama Y; Tsuji S; He HY; Deng CX; Goldfarb LG; Wang GX
Arch Neurol; 2001 May; 58(5):789-94. PubMed ID: 11346374
[TBL] [Abstract][Full Text] [Related]
17. Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.
Brusco A; Gellera C; Cagnoli C; Saluto A; Castucci A; Michielotto C; Fetoni V; Mariotti C; Migone N; Di Donato S; Taroni F
Arch Neurol; 2004 May; 61(5):727-33. PubMed ID: 15148151
[TBL] [Abstract][Full Text] [Related]
18. Post-zygotic de novo trinucleotide repeat expansion at spinocerebellar ataxia type 7 locus: evidence from an Indian family.
Mittal U; Roy S; Jain S; Srivastava AK; Mukerji M
J Hum Genet; 2005; 50(3):155-157. PubMed ID: 15750685
[TBL] [Abstract][Full Text] [Related]
19. [Molecular genetic diagnosis and clinical analysis of spinocerebellar ataxia type 7].
Xie QY; Liang XL; Li XH; Feng YQ
Di Yi Jun Yi Da Xue Xue Bao; 2004 Jan; 24(1):62-5. PubMed ID: 14724100
[TBL] [Abstract][Full Text] [Related]
20. Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansion.
Del-Favero J; Krols L; Michalik A; Theuns J; Löfgren A; Goossens D; Wehnert A; Van den Bossche D; Van Zand K; Backhovens H; van Regenmorter N; Martin JJ; Van Broeckhoven C
Hum Mol Genet; 1998 Feb; 7(2):177-86. PubMed ID: 9425224
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]