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Journal Abstract Search

118 related items for PubMed ID: 10395215

  • 1. 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; 4(3):254-60. PubMed ID: 10395215
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  • 3. Association study of CAG repeats in the KCNN3 gene in Israeli patients with major psychosis.
    Ritsner M, Amir S, Koronyo-Hamaoui M, Gak E, Ziv H, Halperin T, Kitain L, Navon R.
    Psychiatr Genet; 2003 Sep; 13(3):143-50. PubMed ID: 12960745
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  • 4. The human small conductance calcium-regulated potassium channel gene (hSKCa3) contains two CAG repeats in exon 1, is on chromosome 1q21.3, and shows a possible association with schizophrenia.
    Wittekindt O, Jauch A, Burgert E, Schärer L, Holtgreve-Grez H, Yvert G, Imbert G, Zimmer J, Hoehe MR, Macher JP, Chiaroni P, van Calker D, Crocq MA, Morris-Rosendahl DJ.
    Neurogenetics; 1998 Aug; 1(4):259-65. PubMed ID: 10732800
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  • 7. 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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  • 8. CAG repeat polymorphism within the KCNN3 gene is a significant contributor to susceptibility to anorexia nervosa: a case-control study of female patients and several ethnic groups in the Israeli Jewish population.
    Koronyo-Hamaoui M, Gak E, Stein D, Frisch A, Danziger Y, Leor S, Michaelovsky E, Laufer N, Carel C, Fennig S, Mimouni M, Apter A, Goldman B, Barkai G, Weizman A.
    Am J Med Genet B Neuropsychiatr Genet; 2004 Nov 15; 131B(1):76-80. PubMed ID: 15389773
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  • 10. 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 Nov 15; 7(2):247-50. PubMed ID: 10196711
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  • 11. An association of CAG repeats at the KCNN3 locus with symptom dimensions of schizophrenia.
    Ritsner M, Modai I, Ziv H, Amir S, Halperin T, Weizman A, Navon R.
    Biol Psychiatry; 2002 May 15; 51(10):788-94. PubMed ID: 12007452
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  • 12. 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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  • 17. hKCNN3 which maps to chromosome 1q21 is not the causative gene in periodic catatonia, a familial subtype of schizophrenia.
    Stöber G, Meyer J, Nanda I, Wienker TF, Saar K, Jatzke S, Schmid M, Lesch KP, Beckmann H.
    Eur Arch Psychiatry Clin Neurosci; 2000 Aug 15; 250(4):163-8. PubMed ID: 11009068
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  • 19. Schizophrenia and polymorphic CAG repeats array of calcium-activated potassium channel (KCNN3) gene in Serbian population.
    Ivković M, Ranković V, Tarasjev A, Orolicki S, Damjanović A, Paunović VR, Romac S.
    Int J Neurosci; 2006 Feb 15; 116(2):157-64. PubMed ID: 16393881
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