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 *

150 related articles for article (PubMed ID: 8751875)

  • 1. Evidence of linkage disequilibrium between schizophrenia and the SCa1 CAG repeat on chromosome 6p23.
    Wang S; Detera-Wadleigh SD; Coon H; Sun CE; Goldin LR; Duffy DL; Byerley WF; Gershon ES; Diehl SR
    Am J Hum Genet; 1996 Sep; 59(3):731-6. PubMed ID: 8751875
    [No Abstract]   [Full Text] [Related]  

  • 2. Possible association between schizophrenia and a CAG repeat polymorphism in the spinocerebellar ataxia type 1 (SCA1) gene on human chromosome 6p23.
    Joo EJ; Lee JH; Cannon TD; Price RA
    Psychiatr Genet; 1999 Mar; 9(1):7-11. PubMed ID: 10335546
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Analysis of the CAG repeats in the SCA1 and B37 genes in schizophrenic and bipolar I disorder patients: tentative association between B37 and schizophrenia.
    Morris-Rosendahl DJ; Burgert E; Uyanik G; Mayerova A; Duval F; Macher JP; Crocq MA
    Am J Med Genet; 1997 May; 74(3):324-30. PubMed ID: 9184318
    [TBL] [Abstract][Full Text] [Related]  

  • 4. No evidence of linkage disequilibrium between a CAG repeat in the SCA1 gene and schizophrenia in Caucasian and Chinese schizophrenic subjects.
    Li T; Breen G; Brown J; Liu X; Murray RM; Shaw DJ; Sham PC; St Clair D; Collier DA
    Psychiatr Genet; 1999 Sep; 9(3):123-7. PubMed ID: 10551541
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Detection of triplet repeat sequences in yeast artificial chromosomes using oligonucleotide probes: application to the SCA1 region in 6p23.
    Nemani M; Bellanné-Chantelot C; Cohen D; Cann HM
    Cytogenet Cell Genet; 1996; 72(1):5-8. PubMed ID: 8565633
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Analysis of amino-acid and nucleotide variants in the spinocerebellar ataxia type 1 (SCA1) gene in schizophrenic patients.
    Pujana MA; Martorell L; Volpini V; Valero J; Labad A; Vilella E; Estivill X
    Hum Genet; 1997 Jun; 99(6):772-5. PubMed ID: 9187671
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. A novel CAG repeat configuration in the SCA1 gene: implications for the molecular diagnostics of spinocerebellar ataxia type 1.
    Quan F; Janas J; Popovich BW
    Hum Mol Genet; 1995 Dec; 4(12):2411-3. PubMed ID: 8634720
    [No Abstract]   [Full Text] [Related]  

  • 11. [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]  

  • 12. 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]  

  • 13. [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]  

  • 14. Cloning and developmental expression analysis of the murine homolog of the spinocerebellar ataxia type 1 gene (Sca1).
    Banfi S; Servadio A; Chung M; Capozzoli F; Duvick LA; Elde R; Zoghbi HY; Orr HT
    Hum Mol Genet; 1996 Jan; 5(1):33-40. PubMed ID: 8789437
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. The status of SCA1, MJD/SCA3, FRDA, DRPLA and MD triplet containing genes in patients with Huntington disease and healthy controls.
    Keckarevic D; Culjkovic B; Savic D; Stojkovic O; Kostic V; Vukosavic S; Romac S
    J Neurogenet; 2000 Dec; 14(4):257-63. PubMed ID: 11342385
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A long CAG repeat in the mouse Sca1 locus replicates SCA1 features and reveals the impact of protein solubility on selective neurodegeneration.
    Watase K; Weeber EJ; Xu B; Antalffy B; Yuva-Paylor L; Hashimoto K; Kano M; Atkinson R; Sun Y; Armstrong DL; Sweatt JD; Orr HT; Paylor R; Zoghbi HY
    Neuron; 2002 Jun; 34(6):905-19. PubMed ID: 12086639
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Comparison of the number of triplets in SCA1, MJD/SCA3, HD, SBMA, DRPLA, MD, FRAXA and FRDA genes in schizophrenic patients and a healthy population.
    Culjković B; Stojković O; Savić D; Zamurović N; Nesić M; Major T; Keckarevi D ; Romac S; Zamurovi B ; Vukosavić S
    Am J Med Genet; 2000 Dec; 96(6):884-7. PubMed ID: 11121205
    [No Abstract]   [Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.