These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

160 related articles for article (PubMed ID: 12458027)

  • 1. Suggestive evidence for association of two potassium channel genes with different idiopathic generalised epilepsy syndromes.
    Chioza B; Osei-Lah A; Wilkie H; Nashef L; McCormick D; Asherson P; Makoff AJ
    Epilepsy Res; 2002 Dec; 52(2):107-16. PubMed ID: 12458027
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutation analysis of the inwardly rectifying K(+) channels KCNJ6 (GIRK2) and KCNJ3 (GIRK1) in juvenile myoclonic epilepsy.
    Hallmann K; Durner M; Sander T; Steinlein OK
    Am J Med Genet; 2000 Feb; 96(1):8-11. PubMed ID: 10686544
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The voltage gated potassium channel KCNQ2 and idiopathic generalized epilepsy.
    Steinlein OK; Stoodt J; Biervert C; Janz D; Sander T
    Neuroreport; 1999 Apr; 10(6):1163-6. PubMed ID: 10363917
    [TBL] [Abstract][Full Text] [Related]  

  • 4. High-density SNP screen of sodium channel genes by haplotype tagging and DNA pooling for association with idiopathic generalized epilepsy.
    Makoff A; Lai T; Barratt C; Valentin A; Moran N; Asherson P; Nashef L
    Epilepsia; 2010 Apr; 51(4):694-8. PubMed ID: 20041941
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Haplotype and linkage disequilibrium analysis to characterise a region in the calcium channel gene CACNA1A associated with idiopathic generalised epilepsy.
    Chioza B; Osei-Lah A; Nashef L; Suarez-Merino B; Wilkie H; Sham P; Knight J; Asherson P; Makoff AJ
    Eur J Hum Genet; 2002 Dec; 10(12):857-64. PubMed ID: 12461694
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Supportive evidence for an allelic association of the human KCNJ10 potassium channel gene with idiopathic generalized epilepsy.
    Lenzen KP; Heils A; Lorenz S; Hempelmann A; Höfels S; Lohoff FW; Schmitz B; Sander T
    Epilepsy Res; 2005 Feb; 63(2-3):113-8. PubMed ID: 15725393
    [TBL] [Abstract][Full Text] [Related]  

  • 7. No evidence for association between the KCNQ3 gene and susceptibility to idiopathic generalized epilepsy.
    Haug K; Hallmann K; Horvath S; Sander T; Kubisch C; Rau B; Dullinger J; Beyenburg S; Elger CE; Propping P; Heils A
    Epilepsy Res; 2000 Nov; 42(1):57-62. PubMed ID: 10996506
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Association between variation in the human KCNJ10 potassium ion channel gene and seizure susceptibility.
    Buono RJ; Lohoff FW; Sander T; Sperling MR; O'Connor MJ; Dlugos DJ; Ryan SG; Golden GT; Zhao H; Scattergood TM; Berrettini WH; Ferraro TN
    Epilepsy Res; 2004 Feb; 58(2-3):175-83. PubMed ID: 15120748
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Functional expression of two KvLQT1-related potassium channels responsible for an inherited idiopathic epilepsy.
    Yang WP; Levesque PC; Little WA; Conder ML; Ramakrishnan P; Neubauer MG; Blanar MA
    J Biol Chem; 1998 Jul; 273(31):19419-23. PubMed ID: 9677360
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A human pancreatic islet inwardly rectifying potassium channel: cDNA cloning, determination of the genomic structure and genetic variations in Japanese NIDDM patients.
    Tanizawa Y; Matsubara A; Ueda K; Katagiri H; Kuwano A; Ferrer J; Permutt MA; Oka Y
    Diabetologia; 1996 Apr; 39(4):447-52. PubMed ID: 8777994
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Variations in potassium channel genes are associated with distinct trajectories of persistent breast pain after breast cancer surgery.
    Langford DJ; Paul SM; West CM; Dunn LB; Levine JD; Kober KM; Dodd MJ; Miaskowski C; Aouizerat BE
    Pain; 2015 Mar; 156(3):371-380. PubMed ID: 25599232
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Idiopathic epilepsies with a monogenic mode of inheritance.
    Steinlein OK
    Epilepsia; 1999; 40 Suppl 3():9-11. PubMed ID: 10446744
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Neuronal voltage-gated ion channels are genetic modifiers of generalized epilepsy with febrile seizures plus.
    Hawkins NA; Martin MS; Frankel WN; Kearney JA; Escayg A
    Neurobiol Dis; 2011 Mar; 41(3):655-60. PubMed ID: 21156207
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus--and prevalence of variants in patients with epilepsy.
    Escayg A; Heils A; MacDonald BT; Haug K; Sander T; Meisler MH
    Am J Hum Genet; 2001 Apr; 68(4):866-73. PubMed ID: 11254445
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genes and mutations in idiopathic epilepsy.
    Steinlein OK
    Am J Med Genet; 2001; 106(2):139-45. PubMed ID: 11579434
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic association of KCNJ10 rs1130183 with seizure susceptibility and computational analysis of deleterious non-synonymous SNPs of KCNJ10 gene.
    Phani NM; Acharya S; Xavy S; Bhaskaranand N; Bhat MK; Jain A; Rai PS; Satyamoorthy K
    Gene; 2014 Feb; 536(2):247-53. PubMed ID: 24378235
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Structural and mutational analysis of KCNQ2, the major gene locus for benign familial neonatal convulsions.
    Biervert C; Steinlein OK
    Hum Genet; 1999 Mar; 104(3):234-40. PubMed ID: 10323247
    [TBL] [Abstract][Full Text] [Related]  

  • 18. KCNQ2, the first gene found to be mutated in human generalized idiopathic epilepsy.
    Steinlein OK; Jentsch TJ
    Pathol Biol (Paris); 1998 Nov; 46(9):683-4. PubMed ID: 9885816
    [No Abstract]   [Full Text] [Related]  

  • 19. Mitochondrial FAD-glycerophosphate dehydrogenase and G-protein-coupled inwardly rectifying K+ channel: No evidence for linkage in maturity-onset diabetes of the young or NIDDM.
    Warren-Perry MG; Stoffel M; Saker PJ; Zhang Y; Brown LJ; MacDonald MJ; Turner RC
    Diabetes; 1996 May; 45(5):639-41. PubMed ID: 8621016
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Gene defects in idiopathic epilepsy.
    Steinlein OK
    Rev Neurol (Paris); 1999 Jul; 155(6-7):450-3. PubMed ID: 10472657
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.