151 related articles for article (PubMed ID: 15223312)
1. Molecular architecture of CAG repeats in human disease related transcripts.
Michlewski G; Krzyzosiak WJ
J Mol Biol; 2004 Jul; 340(4):665-79. PubMed ID: 15223312
[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. [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]
4. [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]
5. Machado-Joseph disease and other rare spinocerebellar ataxias.
Matilla-Dueñas A
Adv Exp Med Biol; 2012; 724():172-88. PubMed ID: 22411243
[TBL] [Abstract][Full Text] [Related]
6. [Analysis and application of SCA1 and SCA3/MJD gene CAG repeats in Han population in Northeastern China].
Jiang M; Jin CL; Lin CK; Qiu GR; Liu ZL; Wang CX; Sun KL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):83-5. PubMed ID: 14767919
[TBL] [Abstract][Full Text] [Related]
7. Diagnosis of five spinocerebellar ataxia disorders by multiplex amplification and capillary electrophoresis.
Dorschner MO; Barden D; Stephens K
J Mol Diagn; 2002 May; 4(2):108-13. PubMed ID: 11986402
[TBL] [Abstract][Full Text] [Related]
8. Absence of spinocerebellar ataxia type 3/Machado-Joseph disease within ataxic patients in the Czech population.
Bauer PO; Zumrova A; Matoska V; Marikova T; Krilova S; Boday A; Singh B; Goetz P
Eur J Neurol; 2005 Nov; 12(11):851-7. PubMed ID: 16241973
[TBL] [Abstract][Full Text] [Related]
9. Searching for mutation in the JPH3, ATN1 and TBP genes in Polish patients suspected of Huntington's disease and without mutation in the IT15 gene.
Sułek-Piatkowska A; Krysa W; Zdzienicka E; Szirkowiec W; Hoffman-Zacharska D; Rajkiewicz M; Fidziańska E; Kowalska G; Zaremba J
Neurol Neurochir Pol; 2008; 42(3):203-9. PubMed ID: 18651325
[TBL] [Abstract][Full Text] [Related]
10. Imperfect CAG repeats form diverse structures in SCA1 transcripts.
Sobczak K; Krzyzosiak WJ
J Biol Chem; 2004 Oct; 279(40):41563-72. PubMed ID: 15292212
[TBL] [Abstract][Full Text] [Related]
11. Polyglutamine (PolyQ) diseases: genetics to treatments.
Fan HC; Ho LI; Chi CS; Chen SJ; Peng GS; Chan TM; Lin SZ; Harn HJ
Cell Transplant; 2014; 23(4-5):441-58. PubMed ID: 24816443
[TBL] [Abstract][Full Text] [Related]
12. [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]
13. Hereditary ataxias.
Evidente VG; Gwinn-Hardy KA; Caviness JN; Gilman S
Mayo Clin Proc; 2000 May; 75(5):475-90. PubMed ID: 10807077
[TBL] [Abstract][Full Text] [Related]
14. Targeting several CAG expansion diseases by a single antisense oligonucleotide.
Evers MM; Pepers BA; van Deutekom JC; Mulders SA; den Dunnen JT; Aartsma-Rus A; van Ommen GJ; van Roon-Mom WM
PLoS One; 2011; 6(9):e24308. PubMed ID: 21909428
[TBL] [Abstract][Full Text] [Related]
15. Difference in disease-free survival curve and regional distribution according to subtype of spinocerebellar ataxia: a study of 1,286 Japanese patients.
Maruyama H; Izumi Y; Morino H; Oda M; Toji H; Nakamura S; Kawakami H
Am J Med Genet; 2002 Jul; 114(5):578-83. PubMed ID: 12116198
[TBL] [Abstract][Full Text] [Related]
16. Genetic testing for spinocerebellar ataxias in patients diagnosed as Parkinson's disease in Bangladesh.
Rahman MS; Sarkar MA; Rahman MF; Paul SK; Nagai SY; Uddin MJ; Toda T
Mymensingh Med J; 2015 Jan; 24(1):44-51. PubMed ID: 25725667
[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. Variation of CAG repeats and two intragenic polymorphisms at SCA3 locus among Machado-Joseph disease/SCA3 patients and diverse normal populations from eastern India.
Chattopadhyay B; Basu P; Gangopadhyay PK; Mukherjee SC; Sinha KK; Chakraborty A; Roy T; Roychoudhury S; Majumder PP; Bhattacharyya NP
Acta Neurol Scand; 2003 Dec; 108(6):407-14. PubMed ID: 14616293
[TBL] [Abstract][Full Text] [Related]
19. [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]
20. RNA structure of trinucleotide repeats associated with human neurological diseases.
Sobczak K; de Mezer M; Michlewski G; Krol J; Krzyzosiak WJ
Nucleic Acids Res; 2003 Oct; 31(19):5469-82. PubMed ID: 14500809
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
