73 related articles for article (PubMed ID: 8565633)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. A YAC contig in 6p23 based on sequence tagged sites.
Nemani M; Cherif D; Chesne H; Pelandakis M; Ougen P; Berger R; Weissenbach J; Le Paslier D; Cohen D; Cann HM
Genomics; 1994 Jul; 22(2):388-96. PubMed ID: 7806226
[TBL] [Abstract][Full Text] [Related]
7. [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]
8. 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]
9. 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]
10. 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]
11. 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]
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. Repeat instability and motor incoordination in mice with a targeted expanded CAG repeat in the Sca1 locus.
Lorenzetti D; Watase K; Xu B; Matzuk MM; Orr HT; Zoghbi HY
Hum Mol Genet; 2000 Mar; 9(5):779-85. PubMed ID: 10749985
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. [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]
16. Progress in pathogenesis studies of spinocerebellar ataxia type 1.
Cummings CJ; Orr HT; Zoghbi HY
Philos Trans R Soc Lond B Biol Sci; 1999 Jun; 354(1386):1079-81. PubMed ID: 10434309
[TBL] [Abstract][Full Text] [Related]
17. Insights into the mutational history and prevalence of SCA1 in the Indian population through anchored polymorphisms.
Mittal U; Sharma S; Chopra R; Dheeraj K; Pal PK; Srivastava AK; Mukerji M
Hum Genet; 2005 Oct; 118(1):107-14. PubMed ID: 16133185
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Detection by hybridization of trinucleotide repeat sequences in yeast artificial chromosomes.
Nemani M; Bellanné-Chantelot C; Cohen D; Cann HM
Biotechniques; 1995 Oct; 19(4):584-7. PubMed ID: 8777051
[No Abstract] [Full Text] [Related]
20. 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]
[Next] [New Search]
