PubMed for id: 3230

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23778487,23661673,23644027,23525379,22964646,22920929,22849347,22824467,22719862,22576768,22534315,22527936,22179962,21677783,21464046,21285290,21262546,21188375,21165553,21091212,20932824,20725931,20456451,20212279,20137692,20021795,19595143,19546853,19464101,19395679,19371212,19217179,19181906,19073351,19049681,18997347,18547965,18492690,17891520,17891434,17250822,16706928,16555308,16510504,16245335,15226643,15161646,14607454,14500364,12858555,12798584,12414819,12112663,12074273,11944935,11944934,11457872,11076677,10903346,10772952,10587520,10477287,10398271,10068637,9895330,9778505,9560230,8888684,8628271,8575320,7910553,7797561,7690144,24133047,24041700,24036575,23477547,23285148,22307400,22226977,22146296,21828931,21815254,21691712,21561848,21276881,21152044,21110066,20561859,20549724,20486789,20071776,20037164,20022124,19366374,19302747,19253817,18983250,18939937,18854137,18832095,18724007,18689573,18219441,18178777,18084293,17626279,17544441,17498735,17208226,17133411,16730346,16567502,16429276,16267821,15917268,15673394,15649947,15342699,15340050,14597408,12858530,12824294,12754203,12717733,12499378,12141429,11891982,11889119,11783008,11714651,11042197,9834187,9651244,9621435,9584153,9463356,9312027,8900537,8898212,8798155,7665173,24255096,24161929,24123312,24120474,23924634,23751912,23650201,23620086,23444361,23165293,23139287,23022354,22959235,22666732,22052916,22043484,22028467,22011241,21871065,21519287,21127295,20130022,20065166,19948535,19564151,19533775,19359597,19322764,18976153,18624775,18452913,17868091,17635645,17559079,17441204,17308084,17261658,17008600,15109497,14757752,14645532,12858529,12692125,11702785,11431700,11180966,11073884,10948187,10206974,9409664,8900044,23744058,23300892,23299975,23184148,23056209,21930795,21399557,20658695,20522556,20457810,20221402,20207226,20157192,20018673,19403656,19372463,19218456,18784615,18722343,18202317,18079734,18076106,17947796,16854375,16556595,15469976,15226419,15085192,14975726,12775767,12392994,11668679,11477697,24091702,23335360,23303524,10331975,23093675,22826212,9858576,22504313,22306654,9389458,22012595,21898690,21600894,8887666,21454626,8674419,20807224,20606036,20306498,19910576,19517572,19369973,18583338,18579533,17923686,17003108,16982050,16914384,16720880,16719917,16418214,24335256,12738802,12702154,23027426,12397099,22842336,22647876,22431517,22195568,21989917,21757658,11180810,21640717,10864469,10491254,10331979,9857019,20167925,9192865,19479054,19441085,19395641,9043061,18851995,18718462,18591257,18265012,18178574,7904557,17372176,17286298,16807888,16678093,16137232,15958514,14976138,23836893,14741210,14573518,14550786,14516662,22247485,12952939,12845333,21690310,21466801,12223416,12141427,20974940,20110338,10906473,19660448,10656766,10603341,19345202,19166829,19129488,19116164,19097191,10357891,18781631,9676193,17964124,17604724,17258700,16556915,16284121,16174743,23873040,15944191,15797614,15721864,15653675,15653502,23226434,15175244,14978031,22553207,22168922,21628396,21224256,20816796,20724450,12909711,20529560,12781968,12023302,19158954,19035347,18775691,18568026,10733590,10603087,17681136,24186978,9689086,24140541,17108969,17032765,16847256,23832875,16709898,16618415,9096116,16514068,15550380,15542826,22116619,22087235,15143159,21931855,14662776,21466798,19727199,12912923,19101534,19096026,12128222,18661250,18470945,11336496,17950269,24026123,23783515,17069789,16650823,16107252,9501024,15850572,22046433,15743826,15172687,15162503,15070745,20705924,20139090,19531353,12858532,12297045,12223419,23860396,23805247,23707897,23571217,23124967,22814753,17081981,10888889,22215809,22207710,10625552,21896782,21715426,15998812,10079226,15680351,15644436,15621532,9651684,20824138,14766969,19622544,19232521,19208343,18842815,18755178,18285513,12464436,17715064,22771034,17519332,17344228,11892011,22364862,22312437,21989916,11390666,16556596,21623370,16314583,10882515,16223478,21177342,16079152,10364163,9811571,9748262,20062060,9621431,9344671,9171826,9162005,19081079,23418350,23318642,18407257,18347092,18287057,7894168,17869240,17823370,17668378,17526730,17522258,22094017,17336906,17332425,17234970,12194849,17050624,17038485,21447557,21429986,11784028,20941780,16138909,20558824,10926765,10821756,20305823,15621533,10545242,15169892,19631635,19074308,18849322,18718461,18480752,22865640,18400219,18337497,18328475,18045845,21887258,21839733,17360443,17341133,21382375,21304516,12368263,12223404,12122109,20847311,16399798,20487506,23601687,15073151,23375584,19084512,22912798,18467625,22421361,22155005,21466802,21379568,17336905,17332774,20929948,20858476,11923873,23990796,20007915,23494967,19578332,15329346,19091769,18718762,14502571,18448675,17721442,21364285,17289022,16831833,20339120,16380715,12163410,12149478,12117810,23351706,19729519,11854453,7628699,19103803,22573622,22569553,18832393,22075149,21822279,21338598,17584735,16705083,19706423,22158708,11493559,21803036,21511879,21177343,21145505,17460765,20737509,20713518,20347762,9500551,913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Results by year

Year	Number of Results
1993	3
1994	1
1995	4
1996	8
1997	12
1998	15
1999	17
2000	19
2001	17
2002	34
2003	25
2004	29
2005	38
2006	43
2007	58
2008	68
2009	65
2010	70
2011	81
2012	62
2013	52
2014	3
2024	0

665 results

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Page 1

Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation.

Xie WH, Chang C, Xu YJ, Li RG, Qu XK, Fang WY, Liu X, Yang YQ. Xie WH, et al. Clinics (Sao Paulo). 2013 Jun;68(6):777-84. doi: 10.6061/clinics/2013(06)09. Clinics (Sao Paulo). 2013. PMID: 23778487 Free PMC article.

Functional characterization of a novel mutation in NKX2-5 associated with congenital heart disease and adult-onset cardiomyopathy.

Costa MW, Guo G, Wolstein O, Vale M, Castro ML, Wang L, Otway R, Riek P, Cochrane N, Furtado M, Semsarian C, Weintraub RG, Yeoh T, Hayward C, Keogh A, Macdonald P, Feneley M, Graham RM, Seidman JG, Seidman CE, Rosenthal N, Fatkin D, Harvey RP. Costa MW, et al. Circ Cardiovasc Genet. 2013 Jun;6(3):238-47. doi: 10.1161/CIRCGENETICS.113.000057. Epub 2013 May 9. Circ Cardiovasc Genet. 2013. PMID: 23661673 Free PMC article.

Two novel and functional DNA sequence variants within an upstream enhancer of the human NKX2-5 gene in ventricular septal defects.

Huang W, Meng H, Qiao Y, Pang S, Chen D, Yan B. Huang W, et al. Gene. 2013 Jul 25;524(2):152-5. doi: 10.1016/j.gene.2013.04.043. Epub 2013 May 1. Gene. 2013. PMID: 23644027

A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation.

Huang RT, Xue S, Xu YJ, Zhou M, Yang YQ. Huang RT, et al. Int J Mol Med. 2013 May;31(5):1119-26. doi: 10.3892/ijmm.2013.1316. Epub 2013 Mar 22. Int J Mol Med. 2013. PMID: 23525379

R25C mutation in the NKX2.5 gene in Italian patients affected with non-syndromic and syndromic congenital heart disease.

Beffagna G, Cecchetto A, Dal Bianco L, Lorenzon A, Angelini A, Padalino M, Vida V, Bhattacharya S, Stellin G, Rampazzo A, Daliento L. Beffagna G, et al. J Cardiovasc Med (Hagerstown). 2013 Aug;14(8):582-6. doi: 10.2459/JCM.0b013e328356a326. J Cardiovasc Med (Hagerstown). 2013. PMID: 22964646

Wenckebach periodicity at rest that normalizes with tachycardia in a family with a NKX2.5 mutation.

Guntheroth W, Chun L, Patton KK, Matsushita MM, Page RL, Raskind WH. Guntheroth W, et al. Am J Cardiol. 2012 Dec 1;110(11):1646-50. doi: 10.1016/j.amjcard.2012.07.033. Epub 2012 Aug 22. Am J Cardiol. 2012. PMID: 22920929

Crystal structure of the human NKX2.5 homeodomain in complex with DNA target.

Pradhan L, Genis C, Scone P, Weinberg EO, Kasahara H, Nam HJ. Pradhan L, et al. Biochemistry. 2012 Aug 14;51(32):6312-9. doi: 10.1021/bi300849c. Epub 2012 Aug 3. Biochemistry. 2012. PMID: 22849347 Free PMC article.

Genetic analysis of an enhancer of the NKX2-5 gene in ventricular septal defects.

Qin X, Xing Q, Ma L, Meng H, Liu Y, Pang S, Yan B. Qin X, et al. Gene. 2012 Oct 15;508(1):106-9. doi: 10.1016/j.gene.2012.07.019. Epub 2012 Jul 21. Gene. 2012. PMID: 22824467

Cardiac transcription factor Nkx2.5 is downregulated under excessive O-GlcNAcylation condition.

Kim HS, Woo JS, Joo HJ, Moon WK. Kim HS, et al. PLoS One. 2012;7(6):e38053. doi: 10.1371/journal.pone.0038053. Epub 2012 Jun 15. PLoS One. 2012. PMID: 22719862 Free PMC article.

Genetic and functional analysis of the NKX2-5 gene promoter in patients with ventricular septal defects.

Pang S, Shan J, Qiao Y, Ma L, Qin X, Wanyan H, Xing Q, Wu G, Yan B. Pang S, et al. Pediatr Cardiol. 2012 Dec;33(8):1355-61. doi: 10.1007/s00246-012-0346-0. Epub 2012 May 11. Pediatr Cardiol. 2012. PMID: 22576768

665 results

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