These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

344 related articles for article (PubMed ID: 15167689)

  • 1. No association of the SCA1 (CAG)31 allele with Huntington's disease, myotonic dystrophy type 1 and spinocerebellar ataxia type 3.
    Hellenbroich Y; Kaulich M; Opitz S; Schwinger E; Zühlke C
    Psychiatr Genet; 2004 Jun; 14(2):61-3. PubMed ID: 15167689
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases?
    Savić D; Topisirović I; Keckarević M; Keckarević D; Major T; Culjković B; Stojković O; Rakocević-Stojanović V; Mladenović J; Todorović S; Apostolski S; Romac S
    Psychiatr Genet; 2001 Dec; 11(4):201-5. PubMed ID: 11807410
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 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. 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]  

  • 7. Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study Group.
    Pujana MA; Corral J; Gratacòs M; Combarros O; Berciano J; Genís D; Banchs I; Estivill X; Volpini V
    Hum Genet; 1999 Jun; 104(6):516-22. PubMed ID: 10453742
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Spinocerebellar ataxias types 1, 2 and 3: age adjusted clinical severity of disease at presentation correlates with size of CAG repeat lengths.
    Netravathi M; Pal PK; Purushottam M; Thennarasu K; Mukherjee M; Jain S
    J Neurol Sci; 2009 Feb; 277(1-2):83-6. PubMed ID: 19049837
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [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]  

  • 10. [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]  

  • 11. 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]  

  • 12. Toward cell specificity in SCA1.
    Humbert S; Saudou F
    Neuron; 2002 May; 34(5):669-70. PubMed ID: 12062012
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Patterns of CAG repeat interruptions in SCA1 and SCA2 genes in relation to repeat instability.
    Sobczak K; Krzyzosiak WJ
    Hum Mutat; 2004 Sep; 24(3):236-47. PubMed ID: 15300851
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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]  

  • 15. Molecular analysis of Spinocerebellar ataxias in Koreans: frequencies and reference ranges of SCA1, SCA2, SCA3, SCA6, and SCA7.
    Kim JY; Park SS; Joo SI; Kim JM; Jeon BS
    Mol Cells; 2001 Dec; 12(3):336-41. PubMed ID: 11804332
    [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. SCA1 molecular genetics: a history of a 13 year collaboration against glutamines.
    Orr HT; Zoghbi HY
    Hum Mol Genet; 2001 Oct; 10(20):2307-11. PubMed ID: 11673415
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [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]  

  • 19. Slipped (CTG).(CAG) repeats of the myotonic dystrophy locus: surface probing with anti-DNA antibodies.
    Tam M; Erin Montgomery S; Kekis M; Stollar BD; Price GB; Pearson CE
    J Mol Biol; 2003 Sep; 332(3):585-600. PubMed ID: 12963369
    [TBL] [Abstract][Full Text] [Related]  

  • 20. HD and SCA1: Tales from two 30-year journeys since gene discovery.
    Thompson LM; Orr HT
    Neuron; 2023 Nov; 111(22):3517-3530. PubMed ID: 37863037
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.