148 related articles for article (PubMed ID: 18841561)
1. [Studies on the CTA/CTG trinucleotide repeats of ATXN8OS gene in Chinese Hans].
Wang J; Zhang S; Xu Q; Li X; Song X; Jiang H; Shen L; Yan X; Pan Q; Xia K; Tang B
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):511-4. PubMed ID: 18841561
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. [Polynucleotide repeat expansion of nine spinocerebellar ataxia subtypes and dentatorubral-pallidoluysian atrophy in healthy Chinese Han population].
Wang JL; Wu YQ; Lei LF; Shen L; Jiang H; Zhou YF; Yi JP; Zhou J; Yan XX; Pan Q; Xia K; Tang BS
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Oct; 27(5):501-5. PubMed ID: 20931525
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. SCA8 repeat expansion: large CTA/CTG repeat alleles are more common in ataxic patients, including those with SCA6.
Izumi Y; Maruyama H; Oda M; Morino H; Okada T; Ito H; Sasaki I; Tanaka H; Komure O; Udaka F; Nakamura S; Kawakami H
Am J Hum Genet; 2003 Mar; 72(3):704-9. PubMed ID: 12545428
[TBL] [Abstract][Full Text] [Related]
7. Analysis of CAG repeats in SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci in spinocerebellar ataxia patients and distribution of CAG repeats at the SCA1, SCA2 and SCA6 loci in nine ethnic populations of eastern India.
Basu P; Chattopadhyay B; Gangopadhaya PK; Mukherjee SC; Sinha KK; Das SK; Roychoudhury S; Majumder PP; Bhattacharyya NP
Hum Genet; 2000 Jun; 106(6):597-604. PubMed ID: 10942107
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. Spinocerebellar ataxias in mainland China: an updated genetic analysis among a large cohort of familial and sporadic cases.
Wang J; Shen L; Lei L; Xu Q; Zhou J; Liu Y; Guan W; Pan Q; Xia K; Tang B; Jiang H
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2011 Jun; 36(6):482-9. PubMed ID: 21743138
[TBL] [Abstract][Full Text] [Related]
10. [Frequency analysis of autosomal dominant spinocerebellar ataxias in Han population in the Chinese mainland and clinical and molecular characterization of spinocerebellar ataxia type 6].
Jiang H; Tang B; Xu B; Zhao GH; Shen L; Tang JG; Li QH; Xia K
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):1-4. PubMed ID: 15696468
[TBL] [Abstract][Full Text] [Related]
11. [Molecular genetics and its clinical application in the diagnosis of spinocerebellar ataxias].
Xie QY; Liang XL; Li XH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):71-3. PubMed ID: 15696485
[TBL] [Abstract][Full Text] [Related]
12. Frequency of SCA8, SCA10, SCA12, SCA36, FXTAS and C9orf72 repeat expansions in SCA patients negative for the most common SCA subtypes.
Aydin G; Dekomien G; Hoffjan S; Gerding WM; Epplen JT; Arning L
BMC Neurol; 2018 Jan; 18(1):3. PubMed ID: 29316893
[TBL] [Abstract][Full Text] [Related]
13. Frequency analysis of autosomal dominant spinocerebellar ataxias in mainland Chinese patients and clinical and molecular characterization of spinocerebellar ataxia type 6.
Jiang H; Tang BS; Xu B; Zhao GH; Shen L; Tang JG; Li QH; Xia K
Chin Med J (Engl); 2005 May; 118(10):837-43. PubMed ID: 15989765
[TBL] [Abstract][Full Text] [Related]
14. The occurrence of spinocerebellar ataxias caused by dynamic mutations in Polish patients.
Sułek-Piatkowska A; Zdzienicka E; Raczyńska-Rakowicz M; Krysa W; Rajkiewicz M; Szirkowiec W; Zaremba J
Neurol Neurochir Pol; 2010; 44(3):238-45. PubMed ID: 20625959
[TBL] [Abstract][Full Text] [Related]
15. [Frequency of different subtypes of spinocerebellar ataxia in the Han nationality of Hunan province in China].
Song XW; Tang BS; Jiang H; Shen L; Yang Q; Liao SS; Li QH; Tang JG
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2006 Oct; 31(5):702-5. PubMed ID: 17062934
[TBL] [Abstract][Full Text] [Related]
16. [Copy number variation of trinucleotide repeat in dynamic mutation sites of autosomal dominant cerebellar ataxias related genes].
Chen P; Ma M; Shang H; Su D; Zhang S; Yang Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec; 26(6):626-33. PubMed ID: 19953483
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. SCA8 CTG repeat: en masse contractions in sperm and intergenerational sequence changes may play a role in reduced penetrance.
Moseley ML; Schut LJ; Bird TD; Koob MD; Day JW; Ranum LP
Hum Mol Genet; 2000 Sep; 9(14):2125-30. PubMed ID: 10958651
[TBL] [Abstract][Full Text] [Related]
19. [SCA1, SCA2, MJD/SCA3 (CAG)n mutation detection and analysis in patients with hereditary spinocerebellar ataxia from Chinese families].
Tang B; Wang D; Xia J
Zhonghua Yi Xue Za Zhi; 1997 Nov; 77(11):819-22. PubMed ID: 9772474
[TBL] [Abstract][Full Text] [Related]
20. Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus.
Silveira I; Miranda C; Guimarães L; Moreira MC; Alonso I; Mendonça P; Ferro A; Pinto-Basto J; Coelho J; Ferreirinha F; Poirier J; Parreira E; Vale J; Januário C; Barbot C; Tuna A; Barros J; Koide R; Tsuji S; Holmes SE; Margolis RL; Jardim L; Pandolfo M; Coutinho P; Sequeiros J
Arch Neurol; 2002 Apr; 59(4):623-9. PubMed ID: 11939898
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
