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Journal Abstract Search

112 related items for PubMed ID: 18059420

  • 1. Polymorphisms in the cardiac sodium channel promoter displaying variant in vitro expression activity.
    Yang P, Koopmann TT, Pfeufer A, Jalilzadeh S, Schulze-Bahr E, Kääb S, Wilde AA, Roden DM, Bezzina CR.
    Eur J Hum Genet; 2008 Mar; 16(3):350-7. PubMed ID: 18059420
    [Abstract] [Full Text] [Related]

  • 2. [Single nucleotide polymorphism in SCN5A and the distribution in Chinese Han ethnic group].
    Xie XD, Wang XX, Chen JZ, Tao M, Shang YP, Guo XG, Zheng LR.
    Sheng Li Xue Bao; 2004 Feb 25; 56(1):36-40. PubMed ID: 14985827
    [Abstract] [Full Text] [Related]

  • 3. A functional SNP in the promoter region of TCOF1 is associated with reduced gene expression and YY1 DNA-protein interaction.
    Masotti C, Armelin-Correa LM, Splendore A, Lin CJ, Barbosa A, Sogayar MC, Passos-Bueno MR.
    Gene; 2005 Oct 10; 359():44-52. PubMed ID: 16102917
    [Abstract] [Full Text] [Related]

  • 4. Cloning and initial characterization of the human cardiac sodium channel (SCN5A) promoter.
    Yang P, Kupershmidt S, Roden DM.
    Cardiovasc Res; 2004 Jan 01; 61(1):56-65. PubMed ID: 14732202
    [Abstract] [Full Text] [Related]

  • 5. Genetic polymorphisms and haplotypes of the human cardiac sodium channel alpha subunit gene (SCN5A) in Japanese and their association with arrhythmia.
    Maekawa K, Saito Y, Ozawa S, Adachi-Akahane S, Kawamoto M, Komamura K, Shimizu W, Ueno K, Kamakura S, Kamatani N, Kitakaze M, Sawada J.
    Ann Hum Genet; 2005 Jul 01; 69(Pt 4):413-28. PubMed ID: 15996170
    [Abstract] [Full Text] [Related]

  • 6. Common sodium channel promoter haplotype in asian subjects underlies variability in cardiac conduction.
    Bezzina CR, Shimizu W, Yang P, Koopmann TT, Tanck MW, Miyamoto Y, Kamakura S, Roden DM, Wilde AA.
    Circulation; 2006 Jan 24; 113(3):338-44. PubMed ID: 16415376
    [Abstract] [Full Text] [Related]

  • 7. Characterization of the cardiac KCNE1 gene promoter.
    Mustapha Z, Pang L, Nattel S.
    Cardiovasc Res; 2007 Jan 01; 73(1):82-91. PubMed ID: 17141204
    [Abstract] [Full Text] [Related]

  • 8. Novel single nucleotide polymorphisms in the specific protein 1 binding site of the bovine PRNP promoter in Japanese Black cattle: impairment of its promoter activity.
    Nakamura I, Xue G, Sakudo A, Saeki K, Matsumoto Y, Ikuta K, Onodera T.
    Intervirology; 2007 Jan 01; 50(3):190-6. PubMed ID: 17283444
    [Abstract] [Full Text] [Related]

  • 9. Genetic variants of chemokine receptor CCR7 in patients with systemic lupus erythematosus, Sjogren's syndrome and systemic sclerosis.
    Kahlmann D, Davalos-Misslitz AC, Ohl L, Stanke F, Witte T, Förster R.
    BMC Genet; 2007 Jun 22; 8():33. PubMed ID: 17587445
    [Abstract] [Full Text] [Related]

  • 10. Genomic organization of the human SCN5A gene encoding the cardiac sodium channel.
    Wang Q, Li Z, Shen J, Keating MT.
    Genomics; 1996 May 15; 34(1):9-16. PubMed ID: 8661019
    [Abstract] [Full Text] [Related]

  • 11. Genomic variations and transcriptional regulation of the human mu-opioid receptor gene.
    Bayerer B, Stamer U, Hoeft A, Stüber F.
    Eur J Pain; 2007 May 15; 11(4):421-7. PubMed ID: 16843022
    [Abstract] [Full Text] [Related]

  • 12. Cardiac sodium channel overlap syndromes: different faces of SCN5A mutations.
    Remme CA, Wilde AA, Bezzina CR.
    Trends Cardiovasc Med; 2008 Apr 15; 18(3):78-87. PubMed ID: 18436145
    [Abstract] [Full Text] [Related]

  • 13. Variants in the SCN5A Promoter Associated With Various Arrhythmia Phenotypes.
    Yagihara N, Watanabe H, Barnett P, Duboscq-Bidot L, Thomas AC, Yang P, Ohno S, Hasegawa K, Kuwano R, Chatel S, Redon R, Schott JJ, Probst V, Koopmann TT, Bezzina CR, Wilde AA, Nakano Y, Aiba T, Miyamoto Y, Kamakura S, Darbar D, Donahue BS, Shigemizu D, Tanaka T, Tsunoda T, Suda M, Sato A, Minamino T, Endo N, Shimizu W, Horie M, Roden DM, Makita N.
    J Am Heart Assoc; 2016 Sep 13; 5(9):. PubMed ID: 27625342
    [Abstract] [Full Text] [Related]

  • 14. Novel sodium channel SCN5A mutations in Brugada syndrome patients from Greece.
    Kotta CM, Anastasakis A, Gatzoulis K, Manolis AS, Stefanadis C.
    Int J Cardiol; 2010 Nov 05; 145(1):45-8. PubMed ID: 19406494
    [Abstract] [Full Text] [Related]

  • 15. Genetic variants of the human dipeptide transporter PEPT1.
    Anderle P, Nielsen CU, Pinsonneault J, Krog PL, Brodin B, Sadée W.
    J Pharmacol Exp Ther; 2006 Feb 05; 316(2):636-46. PubMed ID: 16258023
    [Abstract] [Full Text] [Related]

  • 16. Genetic modulation of brugada syndrome by a common polymorphism.
    Lizotte E, Junttila MJ, Dube MP, Hong K, Benito B, DE Zutter M, Henkens S, Sarkozy A, Huikuri HV, Towbin J, Vatta M, Brugada P, Brugada J, Brugada R.
    J Cardiovasc Electrophysiol; 2009 Oct 05; 20(10):1137-41. PubMed ID: 19549036
    [Abstract] [Full Text] [Related]

  • 17. A GABRB3 promoter haplotype associated with childhood absence epilepsy impairs transcriptional activity.
    Urak L, Feucht M, Fathi N, Hornik K, Fuchs K.
    Hum Mol Genet; 2006 Aug 15; 15(16):2533-41. PubMed ID: 16835263
    [Abstract] [Full Text] [Related]

  • 18. Exclusion of multiple candidate genes and large genomic rearrangements in SCN5A in a Dutch Brugada syndrome cohort.
    Koopmann TT, Beekman L, Alders M, Meregalli PG, Mannens MM, Moorman AF, Wilde AA, Bezzina CR.
    Heart Rhythm; 2007 Jun 15; 4(6):752-5. PubMed ID: 17556197
    [Abstract] [Full Text] [Related]

  • 19. Identification of YWHAE, a gene encoding 14-3-3epsilon, as a possible susceptibility gene for schizophrenia.
    Ikeda M, Hikita T, Taya S, Uraguchi-Asaki J, Toyo-oka K, Wynshaw-Boris A, Ujike H, Inada T, Takao K, Miyakawa T, Ozaki N, Kaibuchi K, Iwata N.
    Hum Mol Genet; 2008 Oct 15; 17(20):3212-22. PubMed ID: 18658164
    [Abstract] [Full Text] [Related]

  • 20. Identification of a novel 12-nucleotide insertion polymorphism in the promoter region of ADRA2B: full linkage with the 9-nucleotide deletion in the coding region and influence on transcriptional activity.
    Crassous PA, Blaise R, Marquette A, Snapir A, Scheinin M, Paris H, Schaak S.
    Biochem Pharmacol; 2010 Feb 01; 79(3):407-12. PubMed ID: 19728989
    [Abstract] [Full Text] [Related]

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