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Journal Abstract Search

138 related items for PubMed ID: 11009068

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  • 4. Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21.
    Antonarakis SE, Blouin JL, Lasseter VK, Gehrig C, Radhakrishna U, Nestadt G, Housman DE, Kazazian HH, Kalman K, Gutman G, Fantino E, Chandy KG, Gargus JJ, Pulver AE.
    Am J Med Genet; 1999 Aug 20; 88(4):348-51. PubMed ID: 10402501
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  • 5. Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15.
    Stöber G, Saar K, Rüschendorf F, Meyer J, Nürnberg G, Jatzke S, Franzek E, Reis A, Lesch KP, Wienker TF, Beckmann H.
    Am J Hum Genet; 2000 Nov 20; 67(5):1201-7. PubMed ID: 11001582
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  • 6. Mapping of hKCa3 to chromosome 1q21 and investigation of linkage of CAG repeat polymorphism to schizophrenia.
    Austin CP, Holder DJ, Ma L, Mixson LA, Caskey CT.
    Mol Psychiatry; 1999 May 20; 4(3):261-6. PubMed ID: 10395216
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  • 8. hKCa3/KCNN3 potassium channel gene: association of longer CAG repeats with schizophrenia in Israeli Ashkenazi Jews, expression in human tissues and localization to chromosome 1q21.
    Dror V, Shamir E, Ghanshani S, Kimhi R, Swartz M, Barak Y, Weizman R, Avivi L, Litmanovitch T, Fantino E, Kalman K, Jones EG, Chandy KG, Gargus JJ, Gutman GA, Navon R.
    Mol Psychiatry; 1999 May 20; 4(3):254-60. PubMed ID: 10395215
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  • 9. No evidence for involvement of KCNN3 (hSKCa3) potassium channel gene in familial and isolated cases of schizophrenia.
    Bonnet-Brilhault F, Laurent C, Campion D, Thibaut F, Lafargue C, Charbonnier F, Deleuze JF, Ménard JF, Jay M, Petit M, Frebourg T, Mallet J.
    Eur J Hum Genet; 1999 May 20; 7(2):247-50. PubMed ID: 10196711
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  • 10. Association of moderate polyglutamine tract expansions in the slow calcium-activated potassium channel type 3 with ataxia.
    Figueroa KP, Chan P, Schöls L, Tanner C, Riess O, Perlman SL, Geschwind DH, Pulst SM.
    Arch Neurol; 2001 Oct 20; 58(10):1649-53. PubMed ID: 11594924
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  • 11. Towards the genetic basis of periodic catatonia: pedigree sample for genome scan I and II.
    Stöber G, Pfuhlmann B, Nürnberg G, Schmidtke A, Reis A, Franzek E, Wienker TF.
    Eur Arch Psychiatry Clin Neurosci; 2001 Oct 20; 251 Suppl 1():I25-30. PubMed ID: 11776268
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  • 14. CAG repeat polymorphisms in KCNN3 (HSKCa3) and PPP2R2B show no association or linkage to schizophrenia.
    Laurent C, Niehaus D, Bauché S, Levinson DF, Soubigou S, Pimstone S, Hayden M, Mbanga I, Emsley R, Deleuze JF, Mallet J.
    Am J Med Genet B Neuropsychiatr Genet; 2003 Jan 01; 116B(1):45-50. PubMed ID: 12497613
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  • 15. Distribution of the B33 CTG repeat polymorphism in a subtype of schizophrenia.
    Bengel D, Balling U, Stöber G, Heils A, Li SH, Ross CA, Jungkunz G, Franzek E, Beckmann H, Riederer P, Lesch KP.
    Eur Arch Psychiatry Clin Neurosci; 1998 Jan 01; 248(2):78-81. PubMed ID: 9684916
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  • 16. CAG-repeat length in exon 1 of KCNN3 does not influence risk for schizophrenia or bipolar disorder: a meta-analysis of association studies.
    Glatt SJ, Faraone SV, Tsuang MT.
    Am J Med Genet B Neuropsychiatr Genet; 2003 Aug 15; 121B(1):14-20. PubMed ID: 12898569
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  • 18. No evidence to support the association of the potassium channel gene hSKCa3 CAG repeat with schizophrenia or bipolar disorder in the Irish population.
    Hawi Z, Mynett-Johnson L, Murphy V, Straub RE, Kendler KS, Walsh D, McKeon P, Gill M.
    Mol Psychiatry; 1999 Sep 15; 4(5):488-91. PubMed ID: 10523823
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