BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

254 related articles for article (PubMed ID: 16162291)

  • 1. Association analysis of a highly polymorphic CAG Repeat in the human potassium channel gene KCNN3 and migraine susceptibility.
    Curtain R; Sundholm J; Lea R; Ovcaric M; MacMillan J; Griffiths L
    BMC Med Genet; 2005 Sep; 6():32. PubMed ID: 16162291
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 116(2):157-64. PubMed ID: 16393881
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 7(2):247-50. PubMed ID: 10196711
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Association and linkage studies between bipolar affective disorder and the polymorphic CAG/CTG repeat loci ERDA1, SEF2-1B, MAB21L and KCNN3.
    Meira-Lima IV; Zhao J; Sham P; Pereira AC; Krieger JE; Vallada H
    Mol Psychiatry; 2001 Sep; 6(5):565-9. PubMed ID: 11526470
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 88(4):348-51. PubMed ID: 10402501
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic association study of a polymorphic CAG repeats array of calcium-activated potassium channel (KCNN3) gene and schizophrenia among the Chinese population from Taiwan.
    Tsai MT; Shaw CK; Hsiao KJ; Chen CH
    Mol Psychiatry; 1999 May; 4(3):271-3. PubMed ID: 10395218
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association analysis of chromosome 1 migraine candidate genes.
    Fernandez F; Curtain RP; Colson NJ; Ovcaric M; MacMillan J; Griffiths LR
    BMC Med Genet; 2007 Aug; 8():57. PubMed ID: 17727731
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Contribution of syntaxin 1A to the genetic susceptibility to migraine: a case-control association study in the Spanish population.
    Corominas R; Ribasés M; Cuenca-León E; Narberhaus B; Serra SA; del Toro M; Roig M; Fernández-Fernández JM; Macaya A; Cormand B
    Neurosci Lett; 2009 May; 455(2):105-9. PubMed ID: 19368856
    [TBL] [Abstract][Full Text] [Related]  

  • 9. hSKCa3: no association of the polymorphic CAG repeat with bipolar affective disorder and schizophrenia.
    Rohrmeier T; Putzhammer A; Schoeler A; Sartor H; Dallinger P; Nöthen MM; Propping P; Knapp M; Albus M; Borrmann M; Knothe K; Kreiner R; Franzek E; Lichtermann D; Rietschel M; Maier W; Klein HE; Eichhammer P
    Psychiatr Genet; 1999 Dec; 9(4):169-75. PubMed ID: 10697822
    [TBL] [Abstract][Full Text] [Related]  

  • 10. hSKCa3: a candidate gene for schizophrenia?
    Meissner B; Purmann S; Schürmann M; Zühlke C; Lencer R; Arolt V; Müller-Myhsok B; Morris-Rosendahl DJ; Schwinger E
    Psychiatr Genet; 1999 Jun; 9(2):91-6. PubMed ID: 10412188
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A highly polymorphic poly-glutamine stretch in the potassium channel KCNN3 in migraine.
    Mössner R; Weichselbaum A; Marziniak M; Freitag CM; Lesch KP; Sommer C; Meyer J
    Headache; 2005 Feb; 45(2):132-6. PubMed ID: 15705118
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A genetic association study of migraine with dopamine receptor 4, dopamine transporter and dopamine-beta-hydroxylase genes.
    Mochi M; Cevoli S; Cortelli P; Pierangeli G; Soriani S; Scapoli C; Montagna P
    Neurol Sci; 2003 Feb; 23(6):301-5. PubMed ID: 12624717
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 131B(1):76-80. PubMed ID: 15389773
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Transmission disequilibrium analysis of a triplet repeat within the hKCa3 gene using family trios with schizophrenia.
    Li T; Hu X; Chandy KG; Fantino E; Kalman K; Gutman G; Gargus JJ; Freeman B; Murray RM; Dawson E; Liu X; Bruinvels AT; Sham PC; Collier DA
    Biochem Biophys Res Commun; 1998 Oct; 251(2):662-5. PubMed ID: 9792831
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Variants in the human potassium channel gene (KCNN3) are associated with migraine in a high risk genetic isolate.
    Cox HC; Lea RA; Bellis C; Carless M; Dyer T; Blangero J; Griffiths LR
    J Headache Pain; 2011 Dec; 12(6):603-8. PubMed ID: 22030984
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 121B(1):14-20. PubMed ID: 12898569
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spinocerebellar ataxia type 2: polyQ repeat variation in the CACNA1A calcium channel modifies age of onset.
    Pulst SM; Santos N; Wang D; Yang H; Huynh D; Velazquez L; Figueroa KP
    Brain; 2005 Oct; 128(Pt 10):2297-303. PubMed ID: 16000334
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Association between a 19 bp deletion polymorphism at the dopamine beta-hydroxylase (DBH) locus and migraine with aura.
    Fernandez F; Lea RA; Colson NJ; Bellis C; Quinlan S; Griffiths LR
    J Neurol Sci; 2006 Dec; 251(1-2):118-23. PubMed ID: 17095019
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Role of the ACE ID and MTHFR C677T polymorphisms in genetic susceptibility of migraine in a north Indian population.
    Joshi G; Pradhan S; Mittal B
    J Neurol Sci; 2009 Feb; 277(1-2):133-7. PubMed ID: 19081115
    [TBL] [Abstract][Full Text] [Related]  

  • 20. MTHFR T677 homozygosis influences the presence of aura in migraineurs.
    Oterino A; Valle N; Bravo Y; Muñoz P; Sánchez-Velasco P; Ruiz-Alegría C; Castillo J; Leyva-Cobián F; Vadillo A; Pascual J
    Cephalalgia; 2004 Jun; 24(6):491-4. PubMed ID: 15154859
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.