BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

75 related articles for article (PubMed ID: 20646426)

  • 21. Polymorphism screening in the cardiac K+ channel gene KCNA5.
    Simard C; Drolet B; Yang P; Kim RB; Roden DM
    Clin Pharmacol Ther; 2005 Mar; 77(3):138-44. PubMed ID: 15735608
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Characterization of human cardiac Kv1.5 inhibition by the novel atrial-selective antiarrhythmic compound AVE1231.
    Ehrlich JR; Ocholla H; Ziemek D; Rütten H; Hohnloser SH; Gögelein H
    J Cardiovasc Pharmacol; 2008 Apr; 51(4):380-7. PubMed ID: 18427281
    [TBL] [Abstract][Full Text] [Related]  

  • 23. GATA4 loss-of-function mutations in familial atrial fibrillation.
    Yang YQ; Wang MY; Zhang XL; Tan HW; Shi HF; Jiang WF; Wang XH; Fang WY; Liu X
    Clin Chim Acta; 2011 Sep; 412(19-20):1825-30. PubMed ID: 21708142
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A novel PITX2c loss-of-function mutation associated with familial atrial fibrillation.
    Wang J; Zhang DF; Sun YM; Yang YQ
    Eur J Med Genet; 2014 Jan; 57(1):25-31. PubMed ID: 24333117
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Remodeling of Kv1.5 channel in right atria from Han Chinese patients with atrial fibrillation.
    Ou XH; Li ML; Liu R; Fan XR; Mao L; Fan XH; Yang Y; Zeng XR
    Med Sci Monit; 2015 Apr; 21():1207-13. PubMed ID: 25918274
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 27. CD2AP mutations are associated with sporadic nephrotic syndrome and focal segmental glomerulosclerosis (FSGS).
    Gigante M; Pontrelli P; Montemurno E; Roca L; Aucella F; Penza R; Caridi G; Ranieri E; Ghiggeri GM; Gesualdo L
    Nephrol Dial Transplant; 2009 Jun; 24(6):1858-64. PubMed ID: 19131354
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Human atrial ion channel and transporter subunit gene-expression remodeling associated with valvular heart disease and atrial fibrillation.
    Gaborit N; Steenman M; Lamirault G; Le Meur N; Le Bouter S; Lande G; Léger J; Charpentier F; Christ T; Dobrev D; Escande D; Nattel S; Demolombe S
    Circulation; 2005 Jul; 112(4):471-81. PubMed ID: 16027256
    [TBL] [Abstract][Full Text] [Related]  

  • 29. T cell signaling abnormalities in systemic lupus erythematosus are associated with increased mutations/polymorphisms and splice variants of T cell receptor zeta chain messenger RNA.
    Nambiar MP; Enyedy EJ; Warke VG; Krishnan S; Dennis G; Wong HK; Kammer GM; Tsokos GC
    Arthritis Rheum; 2001 Jun; 44(6):1336-50. PubMed ID: 11407693
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Potassium channels involved in human sperm volume regulation--quantitative studies at the protein and mRNA levels.
    Yeung CH; Cooper TG
    Mol Reprod Dev; 2008 Apr; 75(4):659-68. PubMed ID: 18157847
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Gene expression profiling of human atrial myocardium with atrial fibrillation by DNA microarray analysis.
    Ohki R; Yamamoto K; Ueno S; Mano H; Misawa Y; Fuse K; Ikeda U; Shimada K
    Int J Cardiol; 2005 Jul; 102(2):233-8. PubMed ID: 15982490
    [TBL] [Abstract][Full Text] [Related]  

  • 32. N34S mutation in the SPINK1 gene is not associated with alternative splicing.
    Masamune A; Kume K; Takagi Y; Kikuta K; Satoh K; Satoh A; Shimosegawa T
    Pancreas; 2007 May; 34(4):423-8. PubMed ID: 17446841
    [TBL] [Abstract][Full Text] [Related]  

  • 33. GATA6 loss-of-function mutation in atrial fibrillation.
    Yang YQ; Li L; Wang J; Zhang XL; Li RG; Xu YJ; Tan HW; Wang XH; Jiang JQ; Fang WY; Liu X
    Eur J Med Genet; 2012 Oct; 55(10):520-6. PubMed ID: 22750565
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Tetramerization domain mutations in KCNA5 affect channel kinetics and cause abnormal trafficking patterns.
    Burg ED; Platoshyn O; Tsigelny IF; Lozano-Ruiz B; Rana BK; Yuan JX
    Am J Physiol Cell Physiol; 2010 Mar; 298(3):C496-509. PubMed ID: 20018952
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation.
    Olesen MS; Jespersen T; Nielsen JB; Liang B; Møller DV; Hedley P; Christiansen M; Varró A; Olesen SP; Haunsø S; Schmitt N; Svendsen JH
    Cardiovasc Res; 2011 Mar; 89(4):786-93. PubMed ID: 21051419
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Atrial fibrillation--a new cardiac channelopathy.
    Otway R; Vandenberg JI; Fatkin D
    Heart Lung Circ; 2007 Oct; 16(5):356-60. PubMed ID: 17768091
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A double-point mutation in the selectivity filter site of the KCNQ1 potassium channel results in a severe phenotype, LQT1, of long QT syndrome.
    Ikrar T; Hanawa H; Watanabe H; Okada S; Aizawa Y; Ramadan MM; Komura S; Yamashita F; Chinushi M; Aizawa Y
    J Cardiovasc Electrophysiol; 2008 May; 19(5):541-9. PubMed ID: 18266681
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Novel mutations in the MEN1 gene in subjects with multiple endocrine neoplasia-1.
    Jap TS; Chiu CY; Won JG; Wu YC; Chen HS
    Clin Endocrinol (Oxf); 2005 Mar; 62(3):336-42. PubMed ID: 15730416
    [TBL] [Abstract][Full Text] [Related]  

  • 39. In silico assessment of genetic variation in KCNA5 reveals multiple mechanisms of human atrial arrhythmogenesis.
    Colman MA; Ni H; Liang B; Schmitt N; Zhang H
    PLoS Comput Biol; 2017 Jun; 13(6):e1005587. PubMed ID: 28622331
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A novel 1297-1304delGCCTGCCA mutation in the exon 10 of the thyroid hormone receptor beta gene causes resistance to thyroid hormone.
    Rivolta CM; Mallea Gil MS; Ballarino C; Ridruejo MC; Miguel CM; Gimenez SB; Bernacchi SS; Targovnik HM
    Mol Diagn; 2004; 8(3):163-9. PubMed ID: 15771554
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.