-
1
-
-
16544377641
-
Cited2 controls left-right patterning and heart development through a Nodal-Pitx2c pathway
-
DOI 10.1038/ng1446
-
Bamforth, S.D., Bragança, J., Farthing, C.R., Schneider, J.E., Broadbent, C., Michell, A.C., Clarke, K., Neubauer, S., Norris, D., Brown, N.A., Anderson, R.H., and Bhattacharya, S. (2004). Cited2 controls left-right patterning and heart development through a Nodal-Pitx2c pathway. Nat Genet 36, 1189-1196. (Pubitemid 41288968)
-
(2004)
Nature Genetics
, vol.36
, Issue.11
, pp. 1189-1196
-
-
Bamforth, S.D.1
Braganca, J.2
Farthing, C.R.3
Schneider, J.E.4
Broadbent, C.5
Michell, A.C.6
Clarke, K.7
Neubauer, S.8
Norris, D.9
Brown, N.A.10
Anderson, R.H.11
Bhattacharya, S.12
-
2
-
-
77954763028
-
Examining the cardiac NK-2 genes in early heart development
-
Bartlett, H., Veenstra, G.J., and Weeks, D.L. (2010). Examining the cardiac NK-2 genes in early heart development. Pediatr Cardiol 31, 335-341.
-
(2010)
Pediatr Cardiol
, vol.31
, pp. 335-341
-
-
Bartlett, H.1
Veenstra, G.J.2
Weeks, D.L.3
-
3
-
-
0033430230
-
Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways
-
Benson, D.W., Silberbach, G.M., Kavanaugh-McHugh, A., Cottrill, C., Zhang, Y., Riggs, S., Smalls, O., Johnson, M.C., Watson, M.S., Seidman, J.G., Seidman, C.E., Plowden, J., and Kugler, J.D. (1999). Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways. J Clin Invest 104, 1567-1573. (Pubitemid 30002368)
-
(1999)
Journal of Clinical Investigation
, vol.104
, Issue.11
, pp. 1567-1573
-
-
Benson, D.W.1
Silberbach, G.M.2
Kavanaugh-McHugh, A.3
Cottrill, C.4
Zhang, Y.5
Riggs, S.6
Smalls, O.7
Johnson, M.C.8
Watson, M.S.9
Seidman, J.G.10
Seidman, C.E.11
Plowden, J.12
Kugler, J.D.13
-
4
-
-
0029060788
-
Mutations of the connexin43 gap-junction gene in patients with heart malformations and defects of laterality
-
Britz-Cunningham, S., Shah, M., Zuppan, C., and Fletcher, W. (1995). Mutations of the connexin43 gap-junction gene in patients with heart malformations and defects of laterality. N Engl J Med 332, 1323-1329.
-
(1995)
N Engl J Med
, vol.332
, pp. 1323-1329
-
-
Britz-Cunningham, S.1
Shah, M.2
Zuppan, C.3
Fletcher, W.4
-
5
-
-
39749191367
-
The developmental genetics of congenital heart disease
-
DOI 10.1038/nature06801, PII NATURE06801
-
Bruneau, B.G. (2008). The developmental genetics of congenital heart disease. Nature 451, 943-948. (Pubitemid 351301750)
-
(2008)
Nature
, vol.451
, Issue.7181
, pp. 943-948
-
-
Bruneau, B.G.1
-
6
-
-
77952511899
-
From molecular mechanisms of cardiac development to genetic substrate of congenital heart diseases
-
Cecchetto, A., Rampazzo, A., Angelini, A., Bianco, L.D., Padalino, M., Stellin, G., and Daliento, L. (2010). From molecular mechanisms of cardiac development to genetic substrate of congenital heart diseases. Future Cardiol 6, 373-393.
-
(2010)
Future Cardiol
, vol.6
, pp. 373-393
-
-
Cecchetto, A.1
Rampazzo, A.2
Angelini, A.3
Bianco, L.D.4
Padalino, M.5
Stellin, G.6
Daliento, L.7
-
8
-
-
0141571141
-
Pitx2c attenuation results in cardiac defects and abnormalities of intestinal orientation in developing Xenopus laevis
-
DOI 10.1016/S0012-1606(03)00389-0
-
Dagle, J.M., Sabel, J.L., Littig, J.L., Sutherland, L.B., Kolker, S.J., and Weeks, D.L. (2003). Pitx2c attenuation results in cardiac defects and abnormalities of intestinal orientation in developing Xenopus laevis. Dev Biol 262, 268-281. (Pubitemid 37203437)
-
(2003)
Developmental Biology
, vol.262
, Issue.2
, pp. 268-281
-
-
Dagle, J.M.1
Sabel, J.L.2
Littig, J.L.3
Sutherland, L.B.4
Kolker, S.J.5
Weeks, D.L.6
-
9
-
-
79951727550
-
Normal and abnormal development of pulmonary veins: State of the art and correlation with clinical entities
-
Douglas, Y.L., Jongbloed, M.R., Deruiter, M.C., and Gittenberger-de Groot, A.C. (2011). Normal and abnormal development of pulmonary veins: state of the art and correlation with clinical entities. Int J Cardiol 147, 13-24.
-
(2011)
Int J Cardiol
, vol.147
, pp. 13-24
-
-
Douglas, Y.L.1
Jongbloed, M.R.2
Deruiter, M.C.3
Gittenberger-De Groot, A.C.4
-
10
-
-
84874230096
-
Genetics of congenital heart disease: The glass half empty
-
Fahed, A.C., Gelb, B.D., Seidman, J.G., and Seidman, C.E. (2013). Genetics of congenital heart disease: the glass half empty. Circ Res 112, 707-720.
-
(2013)
Circ Res
, vol.112
, pp. 707-720
-
-
Fahed, A.C.1
Gelb, B.D.2
Seidman, J.G.3
Seidman, C.E.4
-
11
-
-
78650329770
-
Characterization of Pitx2c expression in the mouse heart using a reporter transgene
-
Furtado, M.B., Biben, C., Shiratori, H., Hamada, H., and Harvey, R.P. (2001). Characterization of Pitx2c expression in the mouse heart using a reporter transgene. Dev Dyn 240, 195-203.
-
(2001)
Dev Dyn
, vol.240
, pp. 195-203
-
-
Furtado, M.B.1
Biben, C.2
Shiratori, H.3
Hamada, H.4
Harvey, R.P.5
-
12
-
-
0032722672
-
Dosage requirement of Pitx2 for development of multiple organs
-
Gage, P.J., Suh, H., and Camper, S.A. (1999). Dosage requirement of Pitx2 for development of multiple organs. Development 126, 4643-4651.
-
(1999)
Development
, vol.126
, pp. 4643-4651
-
-
Gage, P.J.1
Suh, H.2
Camper, S.A.3
-
13
-
-
42049107565
-
Atrial myocardium derives from the posterior region of the second heart field, which acquires left-right identity as Pitx2c is expressed
-
DOI 10.1242/dev.014563
-
Galli, D., Domińguez, J.N., Zaffran, S., Munk, A., Brown, N.A., and Buckingham, M.E. (2008). Atrial myocardium derives from the posterior region of the second heart field, which acquires left-right identity as Pitx2c is expressed. Development 135, 1157-1167. (Pubitemid 351578144)
-
(2008)
Development
, vol.135
, Issue.6
, pp. 1157-1167
-
-
Galli, D.1
Dominguez, J.N.2
Zaffran, S.3
Munk, A.4
Brown, N.A.5
Buckingham, M.E.6
-
14
-
-
0038266156
-
PITX2 isoform-specific regulation of atrial natriuretic factor expression: Synergism and repression with Nkx2.5
-
DOI 10.1074/jbc.M210163200
-
Ganga, M., Espinoza, H.M., Cox, C.J., Morton, L., Hjalt, T.A., Lee, Y., and Amendt, B.A. (2003). PITX2 isoform-specific regulation of atrial natriuretic factor expression: synergism and repression with Nkx2.5. J Biol Chem 278, 22437-22445. (Pubitemid 36830296)
-
(2003)
Journal of Biological Chemistry
, vol.278
, Issue.25
, pp. 22437-22445
-
-
Ganga, M.1
Espinoza, H.M.2
Cox, C.J.3
Morton, L.4
Hjalt, T.A.5
Lee, Y.6
Amendt, B.A.7
-
15
-
-
0043267988
-
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5
-
DOI 10.1038/nature01827
-
Garg, V., Kathiriya, I.S., Barnes, R., Schluterman, M.K., King, I.N., Butler, C.A., Rothrock, C.R., Eapen, R.S., Hirayama- Yamada, K., Joo, K., Matsuoka, R., Cohen, J.C., and Srivastava, D. (2003). GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5. Nature 424, 443-447. (Pubitemid 36917494)
-
(2003)
Nature
, vol.424
, Issue.6947
, pp. 443-447
-
-
Garg, V.1
Kathiriya, I.S.2
Barnes, R.3
Schluterman, M.K.4
King, I.N.5
Butler, C.A.6
Rothrock, C.R.7
Eapen, R.S.8
Hirayama-Yamada, K.9
Joo, K.10
Matsuoka, R.11
Cohen, J.C.12
Srivastava, D.13
-
16
-
-
84873174654
-
Somatic mutations in the GATA6 gene underlie sporadic tetralogy of Fallot
-
Huang, R.T., Xue, S., Xu, Y.J., and Yang, Y.Q. (2013). Somatic mutations in the GATA6 gene underlie sporadic tetralogy of Fallot. Int J Mol Med 31, 51-58.
-
(2013)
Int J Mol Med
, vol.31
, pp. 51-58
-
-
Huang, R.T.1
Xue, S.2
Xu, Y.J.3
Yang, Y.Q.4
-
17
-
-
84877016166
-
Prevalence and spectrum of ATA5 mutations associated with congenital heart disease
-
Jiang, J.Q., Li, R.G., Wang, J., Liu, X.Y., Xu, Y.J., Fang, W.Y., Chen, X.Z., Zhang, W., Wang, X.Z., and Yang, Y.Q. (2013). Prevalence and spectrum of ATA5 mutations associated with congenital heart disease. Int J Cardiol 165, 570-573.
-
(2013)
Int J Cardiol
, vol.165
, pp. 570-573
-
-
Jiang, J.Q.1
Li, R.G.2
Wang, J.3
Liu, X.Y.4
Xu, Y.J.5
Fang, W.Y.6
Chen, X.Z.7
Zhang, W.8
Wang, X.Z.9
Yang, Y.Q.10
-
18
-
-
79959714035
-
PITX2c is expressed in the adult left atrium, and reducing Pitx2c expression promotes atrial fibrillation inducibility and complex changes in gene expression
-
Kirchhof, P., Kahr, P.C., Kaese, S., Piccini, I., Vokshi, I., Scheld, H.H., Rotering, H., Fortmueller, L., Laakmann, S., Verheule, S., Schotten, U., Fabritz, L., and Brown, N.A. (2011). PITX2c is expressed in the adult left atrium, and reducing Pitx2c expression promotes atrial fibrillation inducibility and complex changes in gene expression. Circ Cardiovasc Genet 4, 123-133.
-
(2011)
Circ Cardiovasc Genet
, vol.4
, pp. 123-133
-
-
Kirchhof, P.1
Kahr, P.C.2
Kaese, S.3
Piccini, I.4
Vokshi, I.5
Scheld, H.H.6
Rotering, H.7
Fortmueller, L.8
Laakmann, S.9
Verheule, S.10
Schotten, U.11
Fabritz, L.12
Brown, N.A.13
-
19
-
-
33750373636
-
Cardiac morphogenetic defects and conduction abnormalities in mice homozygously deficient for connexin40 and heterozygously deficient for connexin45
-
DOI 10.1016/j.yjmcc.2006.07.005, PII S0022282806007176
-
Krüger, O., Maxeiner, S., Kim, J.S., van Rijen, H.V., de Bakker,J.M., Eckardt, D., Tiemann, K., Lewalter, T., Ghanem, A.,Lüderitz, B., and Willecke, K. (2006). Cardiac morphogenetic defects and conduction abnormalities in mice homozygously deficient for connexin40 and heterozygously deficient for connexin45. J Mol Cell Cardiol 41, 787-797. (Pubitemid 44635563)
-
(2006)
Journal of Molecular and Cellular Cardiology
, vol.41
, Issue.5
, pp. 787-797
-
-
Kruger, O.1
Maxeiner, S.2
Kim, J.-S.3
Van Rijen, H.V.M.4
De Bakker, J.M.T.5
Eckardt, D.6
Tiemann, K.7
Lewalter, T.8
Ghanem, A.9
Luderitz, B.10
Willecke, K.11
-
20
-
-
0033575971
-
Pitx2 regulates lung asymmetry, cardiac positioning and pituitary and tooth morphogenesis
-
Lin, C.R., Kioussi, C., O'Connell, S., Briata, P., Szeto, D., Liu, F., Izpisuá-Belmonte, J.C., and Rosenfeld, M.G. (1999). Pitx2 regulates lung asymmetry, cardiac positioning and pituitary and tooth morphogenesis. Nature 401, 279-282.
-
(1999)
Nature
, vol.401
, pp. 279-282
-
-
Lin, C.R.1
Kioussi, C.2
O'Connell, S.3
Briata, P.4
Szeto, D.5
Liu, F.6
Izpisuá-Belmonte, J.C.7
Rosenfeld, M.G.8
-
21
-
-
0034954830
-
Regulation of left-right asymmetry by thresholds of Pitx2c activity
-
Liu, C., Liu, W., Lu, M.F., Brown, N.A., and Martin, J.F. (2001). Regulation of left-right asymmetry by thresholds of Pitx2c activity. Development 128, 2039-2048. (Pubitemid 32605652)
-
(2001)
Development
, vol.128
, Issue.11
, pp. 2039-2048
-
-
Liu, C.1
Liu, W.2
Lu, M.-F.3
Brown, N.A.4
Martin, J.F.5
-
22
-
-
0036849873
-
Pitx2c patterns anterior myocardium and aortic arch vessels and is required for local cell movement into atrioventricular cushions
-
Liu, C., Liu, W., Palie, J., Lu, M.F., Brown, N.A., and Martin, J.F. (2002). Pitx2c patterns anterior myocardium and aortic arch vessels and is required for local cell movement into atrioventricular cushions. Development 129, 5081-5091. (Pubitemid 35355924)
-
(2002)
Development
, vol.129
, Issue.21
, pp. 5081-5091
-
-
Liu, C.1
Liu, W.2
Palie, J.3
Lu, M.F.4
Brown, N.A.5
Martin, J.F.6
-
23
-
-
80054732631
-
Pitx2c modulates cardiac-specific transcription factors networks in differentiating cardiomyocytes from murine embryonic stem cells
-
Lozano-Velasco, E., Chinchilla, A., Martińez-Fernández, S., Hernández-Torres, F., Navarro, F., Lyons, G.E., Franco, D., and Aránega, A.E. (2011). Pitx2c modulates cardiac-specific transcription factors networks in differentiating cardiomyocytes from murine embryonic stem cells. Cells Tissues Organs 194, 349-362.
-
(2011)
Cells Tissues Organs
, vol.194
, pp. 349-362
-
-
Lozano-Velasco, E.1
Chinchilla, A.2
Martińez-Fernández, S.3
Hernández-Torres, F.4
Navarro, F.5
Lyons, G.E.6
Franco, D.7
Aránega, A.E.8
-
24
-
-
84858770543
-
Transcription factor pathways and congenital heart disease
-
McCulley, D.J., and Black, B.L. (2012). Transcription factor pathways and congenital heart disease. Curr Top Dev Biol 100, 253-277.
-
(2012)
Curr Top Dev Biol
, vol.100
, pp. 253-277
-
-
McCulley, D.J.1
Black, B.L.2
-
25
-
-
37349083151
-
Pitx2c and Nkx2-5 are required for the formation and identity of the pulmonary myocardium
-
DOI 10.1161/CIRCRESAHA.107.161182
-
Mommersteeg, M.T., Brown, N.A., Prall, O.W., de Gier-de Vries, C., Harvey, R.P., Moorman, A.F., and Christoffels, V.M. (2007). Pitx2c and Nkx2-5 are required for the formation and identity of the pulmonary myocardium. Circ Res 101, 902-909. (Pubitemid 350287177)
-
(2007)
Circulation Research
, vol.101
, Issue.9
, pp. 902-909
-
-
Mommersteeg, M.T.M.1
Brown, N.A.2
Prall, O.W.J.3
De Gier-De Vries, C.4
Harvey, R.P.5
Moorman, A.F.M.6
Christoffels, V.M.7
-
26
-
-
79960179710
-
Exercise performance and quality of life is more impaired in Eisenmenger syndrome than in complex cyanotic congenital heart disease with pulmonary stenosis
-
Mü ller, J., Hess, J., and Hager, A. (2011). Exercise performance and quality of life is more impaired in Eisenmenger syndrome than in complex cyanotic congenital heart disease with pulmonary stenosis. Int J Cardiol 150, 177-181.
-
(2011)
Int J Cardiol
, vol.150
, pp. 177-181
-
-
Müller, J.1
Hess, J.2
Hager, A.3
-
27
-
-
84855950631
-
Minor symptoms of depression in patients with congenital heart disease have a larger impact on quality of life than limited exercise capacity
-
Mü ller, J., Hess, J., and Hager, A. (2012). Minor symptoms of depression in patients with congenital heart disease have a larger impact on quality of life than limited exercise capacity. Int J Cardiol 154, 265-269.
-
(2012)
Int J Cardiol
, vol.154
, pp. 265-269
-
-
Müller, J.1
Hess, J.2
Hager, A.3
-
28
-
-
84860257801
-
Factors associated with surgery for active endocarditis in congenital heart disease
-
Murakami, T., Niwa, K., Yoshinaga, M., and Nakazawa, M. (2012). Factors associated with surgery for active endocarditis in congenital heart disease. Int J Cardiol 157, 59-62.
-
(2012)
Int J Cardiol
, vol.157
, pp. 59-62
-
-
Murakami, T.1
Niwa, K.2
Yoshinaga, M.3
Nakazawa, M.4
-
29
-
-
33749361499
-
Gene regulatory networks in the evolution and development of the heart
-
DOI 10.1126/science.1132292
-
Olson, E.N. (2006). Gene regulatory networks in the evolution and development of the heart. Science 313, 1922-1927. (Pubitemid 44497993)
-
(2006)
Science
, vol.313
, Issue.5795
, pp. 1922-1927
-
-
Olson, E.N.1
-
30
-
-
84862691754
-
Sudden cardiac death and malignant arrhythmias: The scope of the problem in adult congenital heart patients
-
Perry, J.C. (2012). Sudden cardiac death and malignant arrhythmias: the scope of the problem in adult congenital heart patients. Pediatr Cardiol 33, 484-490.
-
(2012)
Pediatr Cardiol
, vol.33
, pp. 484-490
-
-
Perry, J.C.1
-
31
-
-
3142566471
-
GATA transcription factors in the developing and adult heart
-
DOI 10.1016/j.cardiores.2004.03.025, PII S0008636304001543
-
Pikkarainen, S., Tokola, H., Kerkelä , R., and Ruskoaho, H. (2004). GATA transcription factors in the developing and adult heart. Cardiovasc Res 63, 196-207. (Pubitemid 38900834)
-
(2004)
Cardiovascular Research
, vol.63
, Issue.2
, pp. 196-207
-
-
Pikkarainen, S.1
Tokola, H.2
Kerkela, R.3
Ruskoaho, H.4
-
32
-
-
78049442656
-
NKX2-5: An update on this hypermutable homeodomain protein and its role in human congenital heart disease (CHD)
-
Reamon-Buettner, S.M., and Borlak, J. (2010). NKX2-5: an update on this hypermutable homeodomain protein and its role in human congenital heart disease (CHD). Hum Mutat 31, 1185-1194.
-
(2010)
Hum Mutat
, vol.31
, pp. 1185-1194
-
-
Reamon-Buettner, S.M.1
Borlak, J.2
-
33
-
-
84855353573
-
Heart disease and stroke statistics-2012 update: A report from the American Heart Association
-
American Heart Association Statistics Committee and Stroke Statistics Subcommittee
-
Roger, V.L., Go, A.S., Lloyd-Jones, D.M., Benjamin, E.J., Berry, J.D., Borden, W.B., Bravata, D.M., Dai, S., Ford, E.S., Fox, C.S., Fullerton, H.J., Gillespie, C., Hailpern, S.M., Heit, J.A., Howard, V.J., Kissela, B.M., Kittner, S.J., Lackland, D.T., Lichtman, J.H., Lisabeth, L.D., Makuc, D.M., Marcus, G.M., Marelli, A., Matchar, D.B., Moy, C.S., Mozaffarian, D., Mussolino, M.E., Nichol, G., Paynter, N.P., Soliman, E.Z., Sorlie, P.D., Sotoodehnia, N., Turan, T.N., Virani, S.S., Wong, N.D., Woo, D., Turner, M.B., and American Heart Association Statistics Committee and Stroke Statistics Subcommittee (2012). Heart disease and stroke statistics-2012 update: a report from the American Heart Association. Circulation 125, e2-e220.
-
(2012)
Circulation
, vol.125
-
-
Roger, V.L.1
Go, A.S.2
Lloyd-Jones, D.M.3
Benjamin, E.J.4
Berry, J.D.5
Borden, W.B.6
Bravata, D.M.7
Dai, S.8
Ford, E.S.9
Fox, C.S.10
Fullerton, H.J.11
Gillespie, C.12
Hailpern, S.M.13
Heit, J.A.14
Howard, V.J.15
Kissela, B.M.16
Kittner, S.J.17
Lackland, D.T.18
Lichtman, J.H.19
Lisabeth, L.D.20
Makuc, D.M.21
Marcus, G.M.22
Marelli, A.23
Matchar, D.B.24
Moy, C.S.25
Mozaffarian, D.26
Mussolino, M.E.27
Nichol, G.28
Paynter, N.P.29
Soliman, E.Z.30
Sorlie, P.D.31
Sotoodehnia, N.32
Turan, T.N.33
Virani, S.S.34
Wong, N.D.35
Woo, D.36
Turner, M.B.37
more..
-
34
-
-
0032479573
-
Congenital heart disease caused by mutations in the transcription factor NKX2-5
-
DOI 10.1126/science.281.5373.108
-
Schott, J.J., Benson, D.W., Basson, C.T., Pease, W., Silberbach, G.M., Moak, J.P., Maron, B.J., Seidman, C.E., and Seidman, J.G. (1998). Congenital heart disease caused by mutations in the transcription factor NKX2-5. Science 281, 108-111. (Pubitemid 28354055)
-
(1998)
Science
, vol.281
, Issue.5373
, pp. 108-111
-
-
Schott, J.-J.1
Benson, D.W.2
Basson, C.T.3
Pease, W.4
Silberbach, G.M.5
Moak, J.P.6
Maron, B.J.7
Seidman, C.E.8
Seidman, J.G.9
-
35
-
-
10544233785
-
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome
-
DOI 10.1038/ng1296-392
-
Semina, E.V., Reiter, R., Leysens, N.J., Alward, W.L., Small, K.W., Datson, N.A., Siegel-Bartelt, J., Bierke-Nelson, D., Bitoun, P., Zabel, B.U., Carey, J.C., and Murray, J.C. (1996). Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome. Nat Genet 14, 392-399. (Pubitemid 26414582)
-
(1996)
Nature Genetics
, vol.14
, Issue.4
, pp. 392-399
-
-
Semina, E.V.1
Reiter, R.2
Leysens, N.J.3
Alward, W.L.M.4
Small, K.W.5
Datson, N.A.6
Siegel-Bartelt, J.7
Bierke-Nelson, D.8
Bitoun, P.9
Zabel, B.U.10
Carey, J.C.11
Murray, J.C.12
-
36
-
-
78751620014
-
Brain maturity and brain injury in newborns with cyanotic congenital heart disease
-
Shedeed, S.A., and Elfaytouri, E. (2011). Brain maturity and brain injury in newborns with cyanotic congenital heart disease. Pediatr Cardiol 32, 47-54.
-
(2011)
Pediatr Cardiol
, vol.32
, pp. 47-54
-
-
Shedeed, S.A.1
Elfaytouri, E.2
-
37
-
-
84862701411
-
A contemporary assessment of the risk for sudden cardiac death in patients with congenital heart disease
-
Silka, M.J., and Bar-Cohen, Y. (2012). A contemporary assessment of the risk for sudden cardiac death in patients with congenital heart disease. Pediatr Cardiol 33, 452-460.
-
(2012)
Pediatr Cardiol
, vol.33
, pp. 452-460
-
-
Silka, M.J.1
Bar-Cohen, Y.2
-
38
-
-
70349338915
-
The Pitx2c N-terminal domain is a critical interaction domain required for asymmetric morphogenesis
-
Simard, A., Di Giorgio, L., Amen, M., Westwood, A., Amendt, B.A., and Ryan, A.K. (2009). The Pitx2c N-terminal domain is a critical interaction domain required for asymmetric morphogenesis.Dev Dyn 238, 2459-2470.
-
(2009)
Dev Dyn
, vol.238
, pp. 2459-2470
-
-
Simard, A.1
Di Giorgio, L.2
Amen, M.3
Westwood, A.4
Amendt, B.A.5
Ryan, A.K.6
-
39
-
-
84858257118
-
Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls
-
Soemedi, R., Topf, A., Wilson, I.J., Darlay, R., Rahman, T., Glen, E., Hall, D., Huang, N., Bentham, J., Bhattacharya, S., Cosgrove, C., Brook, J.D., Granados-Riveron, J., Setchfield, K., Bu'lock, F., Thornborough, C., Devriendt, K., Breckpot, J., Hofbeck, M., Lathrop, M., Rauch, A., Blue, G.M., Winlaw, D.S., Hurles, M., Santibanez-Koref, M., Cordell, H.J., Goodship, J.A., and Keavney, B.D. (2012). Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls. Hum Mol Genet 21, 1513-1520.
-
(2012)
Hum Mol Genet
, vol.21
, pp. 1513-1520
-
-
Soemedi, R.1
Topf, A.2
Wilson, I.J.3
Darlay, R.4
Rahman, T.5
Glen, E.6
Hall, D.7
Huang, N.8
Bentham, J.9
Bhattacharya, S.10
Cosgrove, C.11
Brook, J.D.12
Granados-Riveron, J.13
Setchfield, K.14
Bu'lock, F.15
Thornborough, C.16
Devriendt, K.17
Breckpot, J.18
Hofbeck, M.19
Lathrop, M.20
Rauch, A.21
Blue, G.M.22
Winlaw, D.S.23
Hurles, M.24
Santibanez-Koref, M.25
Cordell, H.J.26
Goodship, J.A.27
Keavney, B.D.28
more..
-
40
-
-
84863833810
-
PITX2 is involved in stress response in ultured human trabecular meshwork cells through regulation of SLC13A3
-
Strungaru, M.H., Footz, T., Liu, Y., Berry, F.B., Belleau, P., Semina, E.V., Raymond, V., and Walter, M.A. (2011). PITX2 is involved in stress response in ultured human trabecular meshwork cells through regulation of SLC13A3. Invest Ophthalmol Vis Sci 52, 7625-7633.
-
(2011)
Invest Ophthalmol Vis Sci
, vol.52
, pp. 7625-7633
-
-
Strungaru, M.H.1
Footz, T.2
Liu, Y.3
Berry, F.B.4
Belleau, P.5
Semina, E.V.6
Raymond, V.7
Walter, M.A.8
-
41
-
-
77953696051
-
The emerging burden of hospital admissions of adults with congenital heart disease
-
Verheugt, C.L., Uiterwaal, C.S., van der Velde, E.T., Meijboom, F.J., Pieper, P.G., Sieswerda, G.T., Plokker, H.W., Grobbee, D.E., and Mulder, B.J. (2010). The emerging burden of hospital admissions of adults with congenital heart disease. Heart 96, 872-878.
-
(2010)
Heart
, vol.96
, pp. 872-878
-
-
Verheugt, C.L.1
Uiterwaal, C.S.2
Van Der Velde, E.T.3
Meijboom, F.J.4
Pieper, P.G.5
Sieswerda, G.T.6
Plokker, H.W.7
Grobbee, D.E.8
Mulder, B.J.9
-
42
-
-
84868034241
-
Novel GATA6 mutations associated with congenital ventricular septal defect or tetralogy of fallot
-
Wang, J., Luo, X.J., Xin, Y.F., Liu, Y., Liu, Z.M., Wang, Q., Li, R.G., Fang, W.Y., Wang, X.Z., and Yang, Y.Q. (2012). Novel GATA6 mutations associated with congenital ventricular septal defect or tetralogy of fallot. DNA Cell Biol 31, 1610-1617.
-
(2012)
DNA Cell Biol
, vol.31
, pp. 1610-1617
-
-
Wang, J.1
Luo, X.J.2
Xin, Y.F.3
Liu, Y.4
Liu, Z.M.5
Wang, Q.6
Li, R.G.7
Fang, W.Y.8
Wang, X.Z.9
Yang, Y.Q.10
-
43
-
-
84871353547
-
GATA5 loss-of-function mutations underlie tetralogy of fallot
-
Wei, D., Bao, H., Liu, X.Y., Zhou, N., Wang, Q., Li, R.G., Xu, Y.J., and Yang, Y.Q. (2013a). GATA5 loss-of-function mutations underlie tetralogy of fallot. Int J Med Sci 10, 34-42.
-
(2013)
Int J Med Sci
, vol.10
, pp. 34-42
-
-
Wei, D.1
Bao, H.2
Liu, X.Y.3
Zhou, N.4
Wang, Q.5
Li, R.G.6
Xu, Y.J.7
Yang, Y.Q.8
-
44
-
-
84879503436
-
GATA5 loss-of-function mutation responsible for the congenital ventriculoseptal defect
-
Wei, D., Bao, H., Zhou, N., Zheng, G.F., Liu, X.Y., and Yang, Y.Q. (2013b). GATA5 loss-of-function mutation responsible for the congenital ventriculoseptal defect. Pediatr Cardiol 34, 504-511.
-
(2013)
Pediatr Cardiol
, vol.34
, pp. 504-511
-
-
Wei, D.1
Bao, H.2
Zhou, N.3
Zheng, G.F.4
Liu, X.Y.5
Yang, Y.Q.6
-
45
-
-
84885609859
-
Prevalence and spectrum of PITX2c mutations associated with familial atrial fibrillation
-
[Epub ahead of print]; DOI: 10.1016/j.ijcard.2013.03.141
-
Yang, Y.Q., Xu, Y.J., Li, R.G., Qu, X.K., Fang, W.Y., and Liu, X. (2013). Prevalence and spectrum of PITX2c mutations associated with familial atrial fibrillation. Int J Cardiol [Epub ahead of print]; DOI: 10.1016/j.ijcard.2013. 03.141.
-
Int J Cardiol
, vol.2013
-
-
Yang, Y.Q.1
Xu, Y.J.2
Li, R.G.3
Qu, X.K.4
Fang, W.Y.5
Liu, X.6
-
46
-
-
84879889111
-
Congenital heart disease: Emerging themes linking genetics and development
-
Yuan, S., Zaidi, S., and Brueckner, M. (2013). Congenital heart disease: emerging themes linking genetics and development. Curr Opin Genet Dev 23, 352-359.
-
(2013)
Curr Opin Genet Dev
, vol.23
, pp. 352-359
-
-
Yuan, S.1
Zaidi, S.2
Brueckner, M.3
-
47
-
-
84879001958
-
De novo mutations in histone-modifying genes in congenital heart disease
-
Zaidi, S., Choi, M., Wakimoto, H., Ma, L., Jiang, J., Overton, J.D., Romano-Adesman, A., Bjornson, R.D., Breitbart, R.E., Brown, K.K., Carriero, N.J., Cheung, Y.H., Deanfield, J., DePalma, S., Fakhro, K.A., Glessner, J., Hakonarson, H., Italia, M.J., Kaltman, J.R., Kaski, J., Kim, R., Kline, J.K., Lee, T., Leipzig, J., Lopez, A., Mane, S.M., Mitchell, L.E., Newburger, J.W., Parfenov, M., Pe'er, I., Porter, G., Roberts, A.E., Sachidanandam, R., Sanders, S.J., Seiden, H.S., State, M.W., Subramanian, S., Tikhonova, I.R., Wang, W., Warburton, D., White, P.S., Williams, I.A., Zhao, H., Seidman, J.G., Brueckner, M., Chung, W.K., Gelb, B.D., Goldmuntz, E., Seidman, C.E., and Lifton, R.P. (2013). De novo mutations in histone-modifying genes in congenital heart disease. Nature 498, 220-223.
-
(2013)
Nature
, vol.498
, pp. 220-223
-
-
Zaidi, S.1
Choi, M.2
Wakimoto, H.3
Ma, L.4
Jiang, J.5
Overton, J.D.6
Romano-Adesman, A.7
Bjornson, R.D.8
Breitbart, R.E.9
Brown, K.K.10
Carriero, N.J.11
Cheung, Y.H.12
Deanfield, J.13
DePalma, S.14
Fakhro, K.A.15
Glessner, J.16
Hakonarson, H.17
Italia, M.J.18
Kaltman, J.R.19
Kaski, J.20
Kim, R.21
Kline, J.K.22
Lee, T.23
Leipzig, J.24
Lopez, A.25
Mane, S.M.26
Mitchell, L.E.27
Newburger, J.W.28
Parfenov, M.29
Pe'er, I.30
Porter, G.31
Roberts, A.E.32
Sachidanandam, R.33
Sanders, S.J.34
Seiden, H.S.35
State, M.W.36
Subramanian, S.37
Tikhonova, I.R.38
Wang, W.39
Warburton, D.40
White, P.S.41
Williams, I.A.42
Zhao, H.43
Seidman, J.G.44
Brueckner, M.45
Chung, W.K.46
Gelb, B.D.47
Goldmuntz, E.48
Seidman, C.E.49
Lifton, R.P.50
more..
-
48
-
-
84860539464
-
A novel GATA6 mutation associated with congenital ventricular septal defect
-
Zheng, G.F., Wei, D., Zhao, H., Zhou, N., Yang, Y.Q., and Liu, X.Y. (2012). A novel GATA6 mutation associated with congenital ventricular septal defect. Int J Mol Med 9, 1065-1071.
-
(2012)
Int J Mol Med
, vol.9
, pp. 1065-1071
-
-
Zheng, G.F.1
Wei, D.2
Zhao, H.3
Zhou, N.4
Yang, Y.Q.5
Liu, X.Y.6
-
49
-
-
84883347914
-
A novel PITX2c loss-of-function mutation underlies lone atrial fibrillation
-
Zhou, Y.M., Zheng, P.X., Yang, Y.Q., Ge, Z.M., and Kang, W.Q. (2013). A novel PITX2c loss-of-function mutation underlies lone atrial fibrillation. Int J Mol Med 32, 827-834.
-
(2013)
Int J Mol Med
, vol.32
, pp. 827-834
-
-
Zhou, Y.M.1
Zheng, P.X.2
Yang, Y.Q.3
Ge, Z.M.4
Kang, W.Q.5
|