BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

226 related articles for article (PubMed ID: 15955415)

  • 1. Mutation screen of GABRA1, GABRB2 and GABRG2 genes in Japanese patients with absence seizures.
    Ito M; Ohmori I; Nakahori T; Ouchida M; Ohtsuka Y
    Neurosci Lett; 2005 Aug; 383(3):220-4. PubMed ID: 15955415
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations in GABRA1, GABRA5, GABRG2 and GABRD receptor genes are not a major factor in the pathogenesis of familial focal epilepsy preceded by febrile seizures.
    Ma S; Abou-Khalil B; Blair MA; Sutcliffe JS; Haines JL; Hedera P
    Neurosci Lett; 2006 Feb; 394(1):74-8. PubMed ID: 16256272
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association analysis of chromosome 5 GABAA receptor cluster in Japanese schizophrenia patients.
    Ikeda M; Iwata N; Suzuki T; Kitajima T; Yamanouchi Y; Kinoshita Y; Inada T; Ujike H; Ozaki N
    Biol Psychiatry; 2005 Sep; 58(6):440-5. PubMed ID: 15993854
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Familial severe myoclonic epilepsy of infancy: truncation of Nav1.1 and genetic heterogeneity.
    Gennaro E; Veggiotti P; Malacarne M; Madia F; Cecconi M; Cardinali S; Cassetti A; Cecconi I; Bertini E; Bianchi A; Gobbi G; Zara F
    Epileptic Disord; 2003 Mar; 5(1):21-5. PubMed ID: 12773292
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel GABRG2 mutation associated with febrile seizures.
    Audenaert D; Schwartz E; Claeys KG; Claes L; Deprez L; Suls A; Van Dyck T; Lagae L; Van Broeckhoven C; Macdonald RL; De Jonghe P
    Neurology; 2006 Aug; 67(4):687-90. PubMed ID: 16924025
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutational analysis of GABRG2 in a Japanese cohort with childhood epilepsies.
    Shi X; Huang MC; Ishii A; Yoshida S; Okada M; Morita K; Nagafuji H; Yasumoto S; Kaneko S; Kojima T; Hirose S
    J Hum Genet; 2010 Jun; 55(6):375-8. PubMed ID: 20485450
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in the GABRA1 and EFHC1 genes are rare in familial juvenile myoclonic epilepsy.
    Ma S; Blair MA; Abou-Khalil B; Lagrange AH; Gurnett CA; Hedera P
    Epilepsy Res; 2006 Oct; 71(2-3):129-34. PubMed ID: 16839746
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A mutation in the GABA(A) receptor alpha(1)-subunit is associated with absence epilepsy.
    Maljevic S; Krampfl K; Cobilanschi J; Tilgen N; Beyer S; Weber YG; Schlesinger F; Ursu D; Melzer W; Cossette P; Bufler J; Lerche H; Heils A
    Ann Neurol; 2006 Jun; 59(6):983-7. PubMed ID: 16718694
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel α1 and γ2 GABAA receptor subunit mutations in families with idiopathic generalized epilepsy.
    Lachance-Touchette P; Brown P; Meloche C; Kinirons P; Lapointe L; Lacasse H; Lortie A; Carmant L; Bedford F; Bowie D; Cossette P
    Eur J Neurosci; 2011 Jul; 34(2):237-49. PubMed ID: 21714819
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutant GABA(A) receptor subunits in genetic (idiopathic) epilepsy.
    Hirose S
    Prog Brain Res; 2014; 213():55-85. PubMed ID: 25194483
    [TBL] [Abstract][Full Text] [Related]  

  • 11. GABA(A) receptor epilepsy mutations.
    Macdonald RL; Gallagher MJ; Feng HJ; Kang J
    Biochem Pharmacol; 2004 Oct; 68(8):1497-506. PubMed ID: 15451392
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Association of nonsense mutation in GABRG2 with abnormal trafficking of GABAA receptors in severe epilepsy.
    Ishii A; Kanaumi T; Sohda M; Misumi Y; Zhang B; Kakinuma N; Haga Y; Watanabe K; Takeda S; Okada M; Ueno S; Kaneko S; Takashima S; Hirose S
    Epilepsy Res; 2014 Mar; 108(3):420-32. PubMed ID: 24480790
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Association of GABRG2 polymorphisms with idiopathic generalized epilepsy.
    Chou IC; Lee CC; Tsai CH; Tsai Y; Wan L; Hsu YA; Li TC; Tsai FJ
    Pediatr Neurol; 2007 Jan; 36(1):40-4. PubMed ID: 17162195
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association analysis of gamma 2 subunit of gamma- aminobutyric acid type A receptor polymorphisms with febrile seizures.
    Chou IC; Peng CT; Huang CC; Tsai JJ; Tsai FJ; Tsai CH
    Pediatr Res; 2003 Jul; 54(1):26-9. PubMed ID: 12672902
    [TBL] [Abstract][Full Text] [Related]  

  • 15. GABRG2, rs211037 is associated with epilepsy susceptibility, but not with antiepileptic drug resistance and febrile seizures.
    Balan S; Sathyan S; Radha SK; Joseph V; Radhakrishnan K; Banerjee M
    Pharmacogenet Genomics; 2013 Nov; 23(11):605-10. PubMed ID: 24061200
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy.
    Hempelmann A; Cobilanschi J; Heils A; Muhle H; Stephani U; Weber Y; Lerche H; Sander T
    Epilepsy Res; 2007 Apr; 74(1):28-32. PubMed ID: 17215107
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A splice-site mutation in GABRG2 associated with childhood absence epilepsy and febrile convulsions.
    Kananura C; Haug K; Sander T; Runge U; Gu W; Hallmann K; Rebstock J; Heils A; Steinlein OK
    Arch Neurol; 2002 Jul; 59(7):1137-41. PubMed ID: 12117362
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular analysis of the A322D mutation in the GABA receptor alpha-subunit causing juvenile myoclonic epilepsy.
    Krampfl K; Maljevic S; Cossette P; Ziegler E; Rouleau GA; Lerche H; Bufler J
    Eur J Neurosci; 2005 Jul; 22(1):10-20. PubMed ID: 16029191
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic investigation of chromosome 5q GABAA receptor subunit genes in schizophrenia.
    Petryshen TL; Middleton FA; Tahl AR; Rockwell GN; Purcell S; Aldinger KA; Kirby A; Morley CP; McGann L; Gentile KL; Waggoner SG; Medeiros HM; Carvalho C; Macedo A; Albus M; Maier W; Trixler M; Eichhammer P; Schwab SG; Wildenauer DB; Azevedo MH; Pato MT; Pato CN; Daly MJ; Sklar P
    Mol Psychiatry; 2005 Dec; 10(12):1074-88, 1057. PubMed ID: 16172613
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Febrile seizures: traffic slows in the heat.
    Berkovic SF; Petrou S
    Trends Mol Med; 2006 Aug; 12(8):343-4. PubMed ID: 16829199
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.