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Items: 1 to 20 of 179

1.
2.

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 31;74(3):324-30.

PMID:
9184318
3.

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.

PMID:
9187671
4.

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. No abstract available.

5.

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 19;74(5):488-93.

PMID:
9342197
6.

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.

PMID:
10551541
7.

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.

PMID:
11807410
8.

Presymptomatic analysis of spinocerebellar ataxia type 1 (SCA1) via the expansion of the SCA1 CAG-repeat in a large pedigree displaying anticipation and parental male bias.

Matilla T, Volpini V, Genís D, Rosell J, Corral J, Dávalos A, Molins A, Estivill X.

Hum Mol Genet. 1993 Dec;2(12):2123-8.

PMID:
8111382
9.

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. Epub 2005 Oct 28.

PMID:
16133185
10.

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.

PMID:
15167689
11.

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 29;354(1386):1079-81. Review.

12.

The unstable trinucleotide repeat story of major psychosis.

Vincent JB, Paterson AD, Strong E, Petronis A, Kennedy JL.

Am J Med Genet. 2000 Spring;97(1):77-97. Review.

PMID:
10813808
13.

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. No abstract available.

PMID:
8634720
14.

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.

PMID:
11346374
15.

Mitotic and meiotic instability of the CAG trinucleotide repeat in spinocerebellar ataxia type 1.

Koefoed P, Hasholt L, Fenger K, Nielsen JE, Eiberg H, Buschard K, Sørensen SA.

Hum Genet. 1998 Nov;103(5):564-9.

PMID:
9860298
16.

The effect of CAT trinucleotide interruptions on the age at onset of spinocerebellar ataxia type 1 (SCA1).

Matsuyama Z, Izumi Y, Kameyama M, Kawakami H, Nakamura S.

J Med Genet. 1999 Jul;36(7):546-8.

17.

Unstable triplet repeat and phenotypic variability of spinocerebellar ataxia type 1.

Goldfarb LG, Vasconcelos O, Platonov FA, Lunkes A, Kipnis V, Kononova S, Chabrashvili T, Vladimirtsev VA, Alexeev VP, Gajdusek DC.

Ann Neurol. 1996 Apr;39(4):500-6.

PMID:
8619528
18.

Association of CAG repeat loci on chromosome 22 with schizophrenia and bipolar disorder.

Saleem Q, Dash D, Gandhi C, Kishore A, Benegal V, Sherrin T, Mukherjee O, Jain S, Brahmachari SK.

Mol Psychiatry. 2001 Nov;6(6):694-700.

19.

Spinocerebellar ataxia type 1 (SCA1): phenotype-genotype correlation studies in intermediate alleles.

Zühlke C, Dalski A, Hellenbroich Y, Bubel S, Schwinger E, Bürk K.

Eur J Hum Genet. 2002 Mar;10(3):204-9.

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