-
1
-
-
0015029234
-
Congenital heart disease in 56109 births incidence and natural history
-
Mitchell SC, Korones SB, Berendes HW: Congenital heart disease in 56109 births incidence and natural history. Circulation 43, 323-332 (1971).
-
(1971)
Circulation
, vol.43
, pp. 323-332
-
-
Mitchell, S.C.1
Korones, S.B.2
Berendes, H.W.3
-
2
-
-
0038415874
-
Incidence, mortality and natural history
-
Anderson RH, Baker EJ, Macartney FJ et al. Eds. Churchill Livingstone, London, UK, An essential and explicative article on the general view of congenital heart disease
-
Hoffman JIE: Incidence, mortality and natural history. In: Pediatric Cardiology. Anderson RH, Baker EJ, Macartney FJ et al. (Eds). Churchill Livingstone, London, UK 111-139 (2002). An essential and explicative article on the general view of congenital heart disease.
-
(2002)
Pediatric Cardiology.
, pp. 111-139
-
-
Hoffman, J.I.E.1
-
3
-
-
0031018002
-
A role for bone morphogenetic proteins in the induction of cardiac myogenesis
-
Schultheiss TM, Burch JB, Lassar AB: A role for bone morphogenetic proteins in the induction of cardiac myogenesis. Genes Dev. 11, 451-462 (1997).
-
(1997)
Genes Dev.
, vol.11
, pp. 451-462
-
-
Schultheiss, T.M.1
Burch, J.B.2
Lassar, A.B.3
-
4
-
-
0029149656
-
Bone morphogenetic protein-4 is required for mesoderm formation and patterning in the mouse
-
Winnier G, Blessing M, Labosky PA, Hogan BL: Bone morphogenetic protein-4 is required for mesoderm formation and patterning in the mouse. Genes Dev. 9, 2105-2116 (1995).
-
(1995)
Genes Dev.
, vol.9
, pp. 2105-2116
-
-
Winnier, G.1
Blessing, M.2
Labosky, P.A.3
Hogan, B.L.4
-
5
-
-
0029850112
-
Mice deficient for BMP2 are nonviable and have defects in amnion/chorion and cardiac development
-
Zhang H, Bradley A: Mice deficient for BMP2 are nonviable and have defects in amnion/chorion and cardiac development. Development 122, 2977-2986 (1996).
-
(1996)
Development
, vol.122
, pp. 2977-2986
-
-
Zhang, H.1
Bradley, A.2
-
6
-
-
0032850596
-
Bone morphogenetic proteins induce cardiomyocyte differentiation through the mitogen activated protein kinase kinase kinase TAK1 and cardiac transcription factors Csx/Nkx-2.5 and GATA-4
-
Monzen K, Shiojima I, Hiroi Y, Kudoh S, Oka T, Takimoto E: Bone morphogenetic proteins induce cardiomyocyte differentiation through the mitogen activated protein kinase kinase kinase TAK1 and cardiac transcription factors Csx/Nkx-2.5 and GATA-4. Mol. Cell. Biol. 19, 7096-7105 (1999).
-
(1999)
Mol. Cell. Biol.
, vol.19
, pp. 7096-7105
-
-
Monzen, K.1
Shiojima, I.2
Hiroi, Y.3
Kudoh, S.4
Oka, T.5
Takimoto, E.6
-
7
-
-
7244255984
-
SMAD-mediated modulation of YY1 activity regulates the BMP response and cardiac specific expression of a GATA4/5/6-dependent chick Nkx2.5 enhancer
-
Lee KH, Evans S, Ruan TY, Lassar AB: SMAD-mediated modulation of YY1 activity regulates the BMP response and cardiac specific expression of a GATA4/5/6-dependent chick Nkx2.5 enhancer. Development 131, 4709-4723 (2004).
-
(2004)
Development
, vol.131
, pp. 4709-4723
-
-
Lee, K.H.1
Evans, S.2
Ruan, T.Y.3
Lassar, A.B.4
-
8
-
-
0035895925
-
Characterization of homo- and heterodimerization of cardiac Csx/Nkx2.5 homeoprotein
-
Kasahara H, Usheva A, Ueyama T, Aoki H, Horikoshi N, Izumo S:. Characterization of homo- and heterodimerization of cardiac Csx/Nkx2.5 homeoprotein. J. Biol. Chem. 276, 4570-4580 (2001).
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 4570-4580
-
-
Kasahara, H.1
Usheva, A.2
Ueyama, T.3
Aoki, H.4
Horikoshi, N.5
Izumo, S.6
-
9
-
-
0032959891
-
Identification of the in vivo casein kinase II phosphorylation site within the homeodomain of the cardiac tissue specifying homeobox gene product Csx/Nkx2.5
-
Kasahara H, Izumo S: Identification of the in vivo casein kinase II phosphorylation site within the homeodomain of the cardiac tissue specifying homeobox gene product Csx/Nkx2.5. Mol. Cell. Biol. 19, 526-536 (1999).
-
(1999)
Mol. Cell. Biol.
, vol.19
, pp. 526-536
-
-
Kasahara, H.1
Izumo, S.2
-
10
-
-
21344435944
-
Cardiac transcription factor Csx/Nkx2.5: Its role in cardiac development and disease
-
Akazawa H, Komuro I: Cardiac transcription factor Csx/Nkx2.5: its role in cardiac development and disease. Pharmacol. Ther. 107, 252-268 (2005).
-
(2005)
Pharmacol. Ther.
, vol.107
, pp. 252-268
-
-
Akazawa, H.1
Komuro, I.2
-
11
-
-
0037090906
-
Cardiac-specific activity of an Nkx-2.5 enhancer requires an evolutionarily conserved Smad binding site
-
McAnally CJ, Richardson JA, Olson EN: Cardiac-specific activity of an Nkx-2.5 enhancer requires an evolutionarily conserved Smad binding site. Dev. Biol. 244, 257-266 (2002).
-
(2002)
Dev. Biol.
, vol.244
, pp. 257-266
-
-
McAnally, C.J.1
Richardson, J.A.2
Olson, E.N.3
-
12
-
-
0029000929
-
Heart development in Drosophila requires the segment polarity gene wingless
-
Wu X, Golden K, Bodmer R: Heart development in Drosophila requires the segment polarity gene wingless. Dev. Biol. 169, 619-628 (1995).
-
(1995)
Dev. Biol.
, vol.169
, pp. 619-628
-
-
Wu, X.1
Golden, K.2
Bodmer, R.3
-
13
-
-
0030578428
-
The wingless signaling pathway is directly involved in drosophila heart development
-
Park M, Wu X, Golden K, Axelrod JD, Bodmer R: The wingless signaling pathway is directly involved in Drosophila heart development. Dev. Biol. 177, 104-116 (1996).
-
(1996)
Dev. Biol.
, vol.177
, pp. 104-116
-
-
Park, M.1
Wu, X.2
Golden, K.3
Axelrod, J.D.4
Bodmer, R.5
-
14
-
-
0035252543
-
Wnt antagonism initiates cardiogenesis in Xenopus laevis
-
Schneider VA, Mercola M: Wnt antagonism initiates cardiogenesis in Xenopus laevis. Genes Dev. 15, 304-315 (2001).
-
(2001)
Genes Dev.
, vol.15
, pp. 304-315
-
-
Schneider, V.A.1
Mercola, M.2
-
15
-
-
0037043688
-
Wnt-11 activation of a noncanonical Wnt signalling pathway is required for cardiogenesis
-
Pandur P, Lasche M, Eisenberg LM, Kuhl M: Wnt-11 activation of a noncanonical Wnt signalling pathway is required for cardiogenesis. Nature 418, 636-641 (2002).
-
(2002)
Nature
, vol.418
, pp. 636-641
-
-
Pandur, P.1
Lasche, M.2
Eisenberg, L.M.3
Kuhl, M.4
-
16
-
-
75049083319
-
Wnt signaling in heart valve development and osteogenic gene induction
-
Alfieri CM, Cheek J, Chakraborty S, Yutzey KE: Wnt signaling in heart valve development and osteogenic gene induction. Dev. Biol. 338, 127-135 (2010).
-
(2010)
Dev. Biol.
, vol.338
, pp. 127-135
-
-
Alfieri, C.M.1
Cheek, J.2
Chakraborty, S.3
Yutzey, K.E.4
-
17
-
-
0029849087
-
Heartless encodes a fibroblast growth factor receptor (DFR1/DFGF-R2) involved in the directional migration of early mesodermal cells in the Drosophila embryo
-
Gisselbrecht S, Skeath JB, Doe CQ, Michelson AM: Heartless encodes a fibroblast growth factor receptor (DFR1/DFGF-R2) involved in the directional migration of early mesodermal cells in the Drosophila embryo. Genes Dev. 10, 3003-3017 (1996).
-
(1996)
Genes Dev.
, vol.10
, pp. 3003-3017
-
-
Gisselbrecht, S.1
Skeath, J.B.2
Doe, C.Q.3
Michelson, A.M.4
-
18
-
-
0025774136
-
Expression of a dominant negative mutant of the FGF receptor disrupts mesoderm formation in Xenopus embryos
-
Amaya E, Musci TJ, Kirschner MW: Expression of a dominant negative mutant of the FGF receptor disrupts mesoderm formation in Xenopus embryos. Cell 66, 257-270 (1991).
-
(1991)
Cell.
, vol.66
, pp. 257-270
-
-
Amaya, E.1
Musci, T.J.2
Kirschner, M.W.3
-
19
-
-
0027237596
-
Tinman and bagpipe - Two homeobox genes that determine cell fates in the dorsal mesoderm of Drosophila
-
Azpiazu N, Frasch M: Tinman and bagpipe - two homeobox genes that determine cell fates in the dorsal mesoderm of Drosophila. Genes Dev. 7, 1325-1340 (1993).
-
(1993)
Genes Dev.
, vol.7
, pp. 1325-1340
-
-
Azpiazu, N.1
Frasch, M.2
-
20
-
-
0029004396
-
Ectoderm induces muscle specific gene expression in Drosophila embryos
-
Baker R, Schubiger G: Ectoderm induces muscle specific gene expression in Drosophila embryos. Development 121, 1387-1398 (1995).
-
(1995)
Development
, vol.121
, pp. 1387-1398
-
-
Baker, R.1
Schubiger, G.2
-
21
-
-
0033951035
-
Induction and differentiation of the zebrafish heart requires fibroblast growth factor 8 (FGF8/acerebellar)
-
Reifers F, Walsh EC, Leger S, Stainier DY, Brand M: Induction and differentiation of the zebrafish heart requires fibroblast growth factor 8 (FGF8/acerebellar). Development 127, 225-235 (2000).
-
(2000)
Development
, vol.127
, pp. 225-235
-
-
Reifers, F.1
Walsh, E.C.2
Leger, S.3
Stainier, D.Y.4
Brand, M.5
-
22
-
-
0036333532
-
Regulation of avian cardiogenesis by FGF8 signaling
-
Alsan BH, Schultheiss TM: Regulation of avian cardiogenesis by FGF8 signaling. Development 129, 1935-1943 (2002).
-
(2002)
Development
, vol.129
, pp. 1935-1943
-
-
Alsan, B.H.1
Schultheiss, T.M.2
-
23
-
-
0033575364
-
Differences in left-right axis pathways in mouse and chick: Function of FGF8 and SHH
-
Meyers EN, Martin GR: Differences in left-right axis pathways in mouse and chick: function of FGF8 and SHH. Science 285, 403-406 (1999).
-
(1999)
Science
, vol.285
, pp. 403-406
-
-
Meyers, E.N.1
Martin, G.R.2
-
24
-
-
0242270619
-
Early stage-specific inhibitions of cardiomyocyte differentiation and expression of Csx/Nkx-2.5 and GATA-4 by phosphatidylinositol 3-kinase inhibitor LY294002
-
Naito AT, Tominaga A, Oyamada M, Oyamada Y, Shiraishi I, Monzen K: Early stage-specific inhibitions of cardiomyocyte differentiation and expression of Csx/Nkx-2.5 and GATA-4 by phosphatidylinositol 3-kinase inhibitor LY294002. Exp. Cell Res. 291, 56-69 (2003).
-
(2003)
Exp. Cell. Res.
, vol.291
, pp. 56-69
-
-
Naito, A.T.1
Tominaga, A.2
Oyamada, M.3
Oyamada, Y.4
Shiraishi, I.5
Monzen, K.6
-
26
-
-
0027184211
-
Csx: A murine homeobox-containing gene specifically expressed in the developing heart
-
Komuro I, Izumo S: Csx: a murine homeobox-containing gene specifically expressed in the developing heart. Proc. Natl Acad. Sci. USA 90, 8145-8149 (1993).
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 8145-8149
-
-
Komuro, I.1
Izumo, S.2
-
27
-
-
0027383023
-
Nkx-2.5: A novel murine homeobox gene expressed in early heart progenitor cells and their myogenic descendants
-
Lints TJ, Parsons LM, Hartley L, Lyons I, Harvey RP: Nkx-2.5: a novel murine homeobox gene expressed in early heart progenitor cells and their myogenic descendants. Development 119, 419-431 (1993).
-
(1993)
Development
, vol.119
, pp. 419-431
-
-
Lints, T.J.1
Parsons, L.M.2
Hartley, L.3
Lyons, I.4
Harvey, R.P.5
-
28
-
-
0030587603
-
NK2 homeobox genes and heart development
-
Harvey RP: NK2 homeobox genes and heart development. Dev. Biol. 178, 203-216 (1996).
-
(1996)
Dev. Biol.
, vol.178
, pp. 203-216
-
-
Harvey, R.P.1
-
29
-
-
0242636701
-
NKX2.5 mutations in patients with congenital heart disease
-
NKX 2.5 is an important transcription factor essential for cardiac development; its mutation caused congenital heart disease as described in this article
-
McElhinney DB, Geiger E, Blinder J, Benson DW, Goldmuntz E: NKX2.5 mutations in patients with congenital heart disease. J. Am. Coll. Cardiol. 42, 1650-1655 (2003). NKX 2.5 is an important transcription factor essential for cardiac development; its mutation caused congenital heart disease as described in this article.
-
(2003)
J. Am. Coll. Cardiol.
, vol.42
, pp. 1650-1655
-
-
McElhinney, D.B.1
Geiger, E.2
Blinder, J.3
Benson, D.W.4
Goldmuntz, E.5
-
30
-
-
33646149991
-
A tyrosine-rich domain within homeodomain transcription factor Nkx2.5 is an essential element in the early cardiac transcriptional regulatory machinery
-
Ellitt D, Solloway M, Wise N et al.: A tyrosine-rich domain within homeodomain transcription factor Nkx2.5 is an essential element in the early cardiac transcriptional regulatory machinery. Development 133, 1311-1322 (2006).
-
(2006)
Development
, vol.133
, pp. 1311-1322
-
-
Ellitt, D.1
Solloway, M.2
Wise, N.3
-
31
-
-
0032543267
-
Cardiac and extracardiac expression of Csx/Nkx2.5 homeodomain protein
-
Kasahara, H, Bartunkova S, Schinke M, Tanaka M, Izumo S: Cardiac and extracardiac expression of Csx/Nkx2.5 homeodomain protein. Circ. Res. 82, 936-946 (1998).
-
(1998)
Circ. Res.
, vol.82
, pp. 936-946
-
-
Kasahara, H.1
Bartunkova, S.2
Schinke, M.3
Tanaka, M.4
Izumo, S.5
-
32
-
-
0036362978
-
Efficient Cre-mediated deletion in cardiac progenitor cells conferred by a 3'UTR-ires-Cre allele of the homeobox gene Nkx2-5
-
Stanley EG, Biben C, Elefant A, Barnett L, Koentgen F, Robb L: Efficient Cre-mediated deletion in cardiac progenitor cells conferred by a 3'UTR-ires-Cre allele of the homeobox gene Nkx2-5. Int. J. Dev. Biol. 46, 431-439 (2002).
-
(2002)
Int. J. Dev. Biol.
, vol.46
, pp. 431-439
-
-
Stanley, E.G.1
Biben, C.2
Elefant, A.3
Barnett, L.4
Koentgen, F.5
Robb, L.6
-
33
-
-
0035386434
-
Elevated expression of Nkx-2.5 in developing myocardial conduction cells
-
Thomas PS, Kasahara H, Edmonson AM, Izumo S, Yacoub MH, Barton PJ: Elevated expression of Nkx-2.5 in developing myocardial conduction cells. Anat. Rec. 263, 307-313 (2001).
-
(2001)
Anat. Rec.
, vol.263
, pp. 307-313
-
-
Thomas, P.S.1
Kasahara, H.2
Edmonson, A.M.3
Izumo, S.4
Yacoub, M.H.5
Barton, P.J.6
-
34
-
-
0032937224
-
Control of early cardiac-specific transcription of Nkx2-5 by a GATA-dependent enhancer
-
Lien CL, Wu C, Mercer B, Webb R, Richardson JA, Olson EN: Control of early cardiac-specific transcription of Nkx2-5 by a GATA-dependent enhancer. Development 126, 75-84 (1999).
-
(1999)
Development
, vol.126
, pp. 75-84
-
-
Lien, C.L.1
Wu, C.2
Mercer, B.3
Webb, R.4
Richardson, J.A.5
Olson, E.N.6
-
35
-
-
0031647382
-
A GATA-dependent Nkx-2.5 regulatory element activates early cardiac gene expression in transgenic mice
-
Searcy RD, Vincent EB, Liberatore CM, Yutzey KE: A GATA-dependent Nkx-2.5 regulatory element activates early cardiac gene expression in transgenic mice. Development 125, 4461-4470 (1998).
-
(1998)
Development
, vol.125
, pp. 4461-4470
-
-
Searcy, R.D.1
Vincent, E.B.2
Liberatore, C.M.3
Yutzey, K.E.4
-
36
-
-
0033013018
-
Identification of upstream regulatory regions in the heartexpressed homeobox gene Nkx2-5
-
Reecy JM, Li X, Yamada M, DeMayo FJ, Newman CS, Harvey RP: Identification of upstream regulatory regions in the heartexpressed homeobox gene Nkx2-5. Development 126, 839-849 (1999).
-
(1999)
Development
, vol.126
, pp. 839-849
-
-
Reecy, J.M.1
Li, X.2
Yamada, M.3
DeMayo, F.J.4
Newman, C.S.5
Harvey, R.P.6
-
37
-
-
1642402120
-
The cardiac determination factor, Nkx2-5, is activated by mutual cofactors GATA-4 and Smad1/4 via a novel upstream enhancer
-
Brown III CO, Chi X, Garcia-Gras E, Shirai M, Feng XH, Schwartz R J: The cardiac determination factor, Nkx2-5, is activated by mutual cofactors GATA-4 and Smad1/4 via a novel upstream enhancer. J. Biol. Chem. 279, 10659-10669 (2004).
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 10659-10669
-
-
Brown, I.I.I.C.O.1
Chi, X.2
Garcia-Gras, E.3
Shirai, M.4
Feng, X.H.5
Schwartz, R.J.6
-
38
-
-
11144357335
-
Nkx2-5 pathways and congenital heart disease; loss of ventricular myocyte lineage specification leds to progressive cardiomyopathy and complete heart block
-
Pashmforoush M, Lu JT, Chen H: Nkx2-5 pathways and congenital heart disease; loss of ventricular myocyte lineage specification leds to progressive cardiomyopathy and complete heart block. Cell 117, 373-386 (2004).
-
(2004)
Cell.
, vol.117
, pp. 373-386
-
-
Pashmforoush, M.1
Lu, J.T.2
Chen, H.3
-
39
-
-
33847344204
-
An Nkx2.5/Bmp/Smad1 negative feedback loop controls heart progenitor specification e proliferation
-
Prall OW: An Nkx2.5/Bmp/Smad1 negative feedback loop controls heart progenitor specification e proliferation. Cell 128, 947-959 (2007).
-
(2007)
Cell.
, vol.128
, pp. 947-959
-
-
Prall, O.W.1
-
40
-
-
0034671733
-
The zinc finger-containing transcription factors GATA-4, -5 and -6. Ubiquitously expressed regulators of tissue-specific gene expression
-
Molkentin JD: The zinc finger-containing transcription factors GATA-4, -5 and -6. Ubiquitously expressed regulators of tissue-specific gene expression. J. Biol. Chem. 275, 38949-38952 (2000).
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 38949-38952
-
-
Molkentin, J.D.1
-
41
-
-
0030996908
-
Requirement of the transcription factor GATA4 for heart tube formation and ventral morphogenesis
-
Molkentin JD, Lin Q, Duncan SA, Olson EN: Requirement of the transcription factor GATA4 for heart tube formation and ventral morphogenesis. Genes Dev. 11, 1061-1072 (1997).
-
(1997)
Genes Dev.
, vol.11
, pp. 1061-1072
-
-
Molkentin, J.D.1
Lin, Q.2
Duncan, S.A.3
Olson, E.N.4
-
42
-
-
0030916211
-
GATA4 transcription factor is required for ventral morphogenesis and heart tube formation
-
Kuo CT, Morrisey EE, Anandappa R et al.: GATA4 transcription factor is required for ventral morphogenesis and heart tube formation. Genes Dev. 11, 1048-1060 (1997).
-
(1997)
Genes Dev.
, vol.11
, pp. 1048-1060
-
-
Kuo, C.T.1
Morrisey, E.E.2
Anandappa, R.3
-
43
-
-
0032756903
-
Gata5 is required for the development of the heart and endoderm in zebrafish
-
Reiter JF, Alexander J, Rodaway A et al.: Gata5 is required for the development of the heart and endoderm in zebrafish. Genes Dev. 13, 2983-2995 (1999).
-
(1999)
Genes Dev.
, vol.13
, pp. 2983-2995
-
-
Reiter, J.F.1
Alexander, J.2
Rodaway, A.3
-
44
-
-
0032533241
-
GATA6 regulates HNF4 and is required for differentiation of visceral endoderm in the mouse embryo
-
Morrisey EE, Tang Z, Sigrist K et al.: GATA6 regulates HNF4 and is required for differentiation of visceral endoderm in the mouse embryo. Genes Dev. 12, 3579-3590 (1998).
-
(1998)
Genes Dev.
, vol.12
, pp. 3579-3590
-
-
Morrisey, E.E.1
Tang, Z.2
Sigrist, K.3
-
45
-
-
0032590183
-
The transcription factor GATA6 is essential for early extraembryonic development
-
Koutsourakis M, Langeveld A, Patient R, Beddington R, Grosveld F: The transcription factor GATA6 is essential for early extraembryonic development. Development 126, 723-732 (1999).
-
(1999)
Development
, vol.126
, pp. 723-732
-
-
Koutsourakis, M.1
Langeveld, A.2
Patient, R.3
Beddington, R.4
Grosveld, F.5
-
46
-
-
0033398273
-
The zinc finger proteins Pannier and GATA4 function as cardiogenic factors in Drosophila
-
Gajewski K, Fossett N, Molkentin JD, Schulz RA: The zinc finger proteins Pannier and GATA4 function as cardiogenic factors in Drosophila. Development 126, 5679-5688 (1999).
-
(1999)
Development
, vol.126
, pp. 5679-5688
-
-
Gajewski, K.1
Fossett, N.2
Molkentin, J.D.3
Schulz, R.A.4
-
47
-
-
0031647382
-
A GATA-dependent Nkx-2.5 regulatory element activates early cardiac gene expression in transgenic mice
-
Searcy RD, Vincent EB, Liberatore CM, Yutzey KE: A GATA-dependent Nkx-2.5 regulatory element activates early cardiac gene expression in transgenic mice. Development 125, 4461-4470 (1998).
-
(1998)
Development
, vol.125
, pp. 4461-4470
-
-
Searcy, R.D.1
Vincent, E.B.2
Liberatore, C.M.3
Yutzey, K.E.4
-
48
-
-
0032937224
-
Control of early cardiac-specific transcription of Nkx2-5 by a GATA-dependent enhancer
-
Lien CL, Wu C, Mercer B, Webb R, Richardson JA, Olson EN: Control of early cardiac-specific transcription of Nkx2-5 by a GATA-dependent enhancer. Development 126, 75-84 (1999).
-
(1999)
Development
, vol.126
, pp. 75-84
-
-
Lien, C.L.1
Wu, C.2
Mercer, B.3
Webb, R.4
Richardson, J.A.5
Olson, E.N.6
-
49
-
-
0034650305
-
An Nkx-dependent enhancer regulates GATA-6 gene expression during early stages of heart development
-
Davis DL, Wessels A, Burch JB: An Nkx-dependent enhancer regulates GATA-6 gene expression during early stages of heart development. Dev. Biol. 217, 310-322 (2000).
-
(2000)
Dev. Biol.
, vol.217
, pp. 310-322
-
-
Davis, D.L.1
Wessels, A.2
Burch, J.B.3
-
50
-
-
0034650312
-
Direct activation of a GATA6 cardiac enhancer by Nkx2.5: Evidence for a reinforcing regulatory network of Nkx2.5 and GATA transcription factors in the developing heart
-
Molkentin JD, Antos C, Mercer B, Taigen T, Miano JM, Olson EN: Direct activation of a GATA6 cardiac enhancer by Nkx2.5: evidence for a reinforcing regulatory network of Nkx2.5 and GATA transcription factors in the developing heart. Dev. Biol. 217, 301-309 (2000).
-
(2000)
Dev. Biol.
, vol.217
, pp. 301-309
-
-
Molkentin, J.D.1
Antos, C.2
Mercer, B.3
Taigen, T.4
Miano, J.M.5
Olson, E.N.6
-
51
-
-
0043267988
-
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5
-
Garg V, Kathiriya IS, Barnes R et al.: GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5. Nature 424, 443-447 (2003).
-
(2003)
Nature
, vol.424
, pp. 443-447
-
-
Garg, V.1
Kathiriya, I.S.2
Barnes, R.3
-
52
-
-
16544371915
-
A novel GATA4 mutation completely segregated with atrial septal defect in a large Japanese family
-
Okubo A, Miyoshi O, Baba K et al.: A novel GATA4 mutation completely segregated with atrial septal defect in a large Japanese family. J. Med. Genet. 41, E97 (2004).
-
(2004)
J. Med. Genet.
, vol.41
-
-
Okubo, A.1
Miyoshi, O.2
Baba, K.3
-
53
-
-
35048838310
-
Spectrum of heart disease associated with murine and human GATA4 mutation
-
Rajagopal SK, Ma Q, Obler D et al.: Spectrum of heart disease associated with murine and human GATA4 mutation. J. Mol. Cell. Cardiol. 43, 677-685 (2007).
-
(2007)
J. Mol. Cell. Cardiol.
, vol.43
, pp. 677-685
-
-
Rajagopal, S.K.1
Ma, Q.2
Obler, D.3
-
54
-
-
0031033603
-
D-MEF2 is a target for Tinman activation during Drosophila heart development
-
Gajewski K, Kim Y, Lee YM, Olson EN, Schulz RA: D-MEF2 is a target for Tinman activation during Drosophila heart development. EMBO J. 16, 515-522 (1997).
-
(1997)
EMBO J.
, vol.16
, pp. 515-522
-
-
Gajewski, K.1
Kim, Y.2
Lee, Y.M.3
Olson, E.N.4
Schulz, R.A.5
-
55
-
-
4544236360
-
MEF2c is a direct transcriptional target of ISL1 and GATA factors in the anterior heart field during mouse embryonic development
-
Discusses a new topic and new studies about transcription factors
-
Dodou E, Verzi MP, Anderson JP, Xu S-M, Black BL: MEF2c is a direct transcriptional target of ISL1 and GATA factors in the anterior heart field during mouse embryonic development. Development 131, 3931-3942 (2004). Discusses a new topic and new studies about transcription factors.
-
(2004)
Development
, vol.131
, pp. 3931-3942
-
-
Dodou, E.1
Verzi, M.P.2
Anderson, J.P.3
Xu, S.-M.4
Black, B.L.5
-
56
-
-
0028087974
-
D-mef2: A Drosophila mesoderm-specific MADS box-containing gene with a biphasic expression profile during embryogenesis
-
Nguyen HT, Bodmer R, Abmayr SM, McDermott JC, Spoerel NA: D-mef2: a Drosophila mesoderm-specific MADS box-containing gene with a biphasic expression profile during embryogenesis. Proc. Natl Acad. Sci. USA 91, 7520-7524 (1994).
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 7520-7524
-
-
Nguyen, H.T.1
Bodmer, R.2
Abmayr, S.M.3
McDermott, J.C.4
Spoerel, N.A.5
-
57
-
-
0028229168
-
D-MEF2: A MADS box transcription factor expressed in differentiating mesoderm and muscle cell lineages during Drosophila embryogenesis
-
Lilly B, Galewsky S, Firulli AB, Schulz RA, Olson EN: D-MEF2: a MADS box transcription factor expressed in differentiating mesoderm and muscle cell lineages during Drosophila embryogenesis. Proc. Natl Acad. Sci. USA 91, 5662-5666 (1994).
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 5662-5666
-
-
Lilly, B.1
Galewsky, S.2
Firulli, A.B.3
Schulz, R.A.4
Olson, E.N.5
-
58
-
-
0028917564
-
Requirement of MADS domain transcription factor D-MEF2 for muscle formation in
-
Lilly B, Zhao B, Ranganayakulu G, Paterson BM, Schulz RA, Olson EN: Requirement of MADS domain transcription factor D-MEF2 for muscle formation in Drosophila. Science 267, 688-693 (1995).
-
(1995)
Drosophila. Science
, vol.267
, pp. 688-693
-
-
Lilly, B.1
Zhao, B.2
Ranganayakulu, G.3
Paterson, B.M.4
Schulz, R.A.5
Olson, E.N.6
-
59
-
-
0030911475
-
Control of mouse cardiac morphogenesis and myogenesis by transcription factor MEF2C
-
Lin Q, Schwarz J, Bucana C, Olson EN: Control of mouse cardiac morphogenesis and myogenesis by transcription factor MEF2C. Science 276, 1404-1407 (1997).
-
(1997)
Science
, vol.276
, pp. 1404-1407
-
-
Lin, Q.1
Schwarz, J.2
Bucana, C.3
Olson, E.N.4
-
60
-
-
0036851837
-
Mitochondrial deficiency and cardiac sudden death in mice lacking the MEF2A transcription factor
-
Naya FJ, Black BL, Wu H et al.: Mitochondrial deficiency and cardiac sudden death in mice lacking the MEF2A transcription factor. Nat. Med. 8, 1303-1309 (2002).
-
(2002)
Nat. Med.
, vol.8
, pp. 1303-1309
-
-
Naya, F.J.1
Black, B.L.2
Wu, H.3
-
61
-
-
0029895310
-
MEF2B is a potent transactivator expressed in early myogenic lineages
-
Moleketin JD, Firulli AB, Black BL et al.: MEF2B is a potent transactivator expressed in early myogenic lineages. Mol. Cell. Biol. 16, 3814-3824 (1996).
-
(1996)
Mol. Cell. Biol.
, vol.16
, pp. 3814-3824
-
-
Moleketin, J.D.1
Firulli, A.B.2
Black, B.L.3
-
62
-
-
0033805236
-
Cardiac tissue enriched factors serum response factor and GATA-4 are mutual co-regulators
-
Belaguli NS, Sepulveda JL, Nigam V, Charron F, Nemer M, Schwartz RJ: Cardiac tissue enriched factors serum response factor and GATA-4 are mutual co-regulators. Mol. Cell. Biol. 20, 7550-7558 (2000).
-
(2000)
Mol. Cell. Biol.
, vol.20
, pp. 7550-7558
-
-
Belaguli, N.S.1
Sepulveda, J.L.2
Nigam, V.3
Charron, F.4
Nemer, M.5
Schwartz, R.J.6
-
63
-
-
0035967868
-
Activation of cardiac gene expression by myocardin, a transcriptional cofactor for serum response factor
-
Wang D, Chang PS, Wang Z et al.: Activation of cardiac gene expression by myocardin, a transcriptional cofactor for serum response factor. Cell 105, 851-862 (2001).
-
(2001)
Cell.
, vol.105
, pp. 851-862
-
-
Wang, D.1
Chang, P.S.2
Wang, Z.3
-
64
-
-
18644364557
-
Modulation of cardiac growth and development by HOP, an unusual homeodomain protein
-
Shin C, Liu Z, Passier R et al.: Modulation of cardiac growth and development by HOP, an unusual homeodomain protein. Cell 110, 725-735 (2002).
-
(2002)
Cell.
, vol.110
, pp. 725-735
-
-
Shin, C.1
Liu, Z.2
Passier, R.3
-
65
-
-
18644374460
-
Hop is an unusual homeobox gene that modulates cardiac development
-
Chen F, Kook H, Milewski R et al.: Hop is an unusual homeobox gene that modulates cardiac development. Cell 110, 713-723 (2002).
-
(2002)
Cell.
, vol.110
, pp. 713-723
-
-
Chen, F.1
Kook, H.2
Milewski, R.3
-
66
-
-
2942538855
-
Targeted inactivation of serum response factor in the developing heart results in myocardial defects and embryonic lethality
-
Interesting and useful for the comprehension of the topic
-
Parlakian A, Tuil D, Hamard G et al.: Targeted inactivation of serum response factor in the developing heart results in myocardial defects and embryonic lethality Mol. Cell. Biol. 24, 5281-5289 (2004). Interesting and useful for the comprehension of the topic.
-
(2004)
Mol. Cell. Biol.
, vol.24
, pp. 5281-5289
-
-
Parlakian, A.1
Tuil, D.2
Hamard, G.3
-
67
-
-
0032476590
-
SRF is essential for mesoderm formation during mouse embryogenesis
-
Arsenian S, Weinhold B, Oelgeschlager M, Ruther U, Nordheim A: SRF is essential for mesoderm formation during mouse embryogenesis. EMBO J. 17, 6289-6299 (1998).
-
(1998)
EMBO J.
, vol.17
, pp. 6289-6299
-
-
Arsenian, S.1
Weinhold, B.2
Oelgeschlager, M.3
Ruther, U.4
Nordheim, A.5
-
68
-
-
0034331204
-
-/- ES cells display non-cell-autonomous impairment in mesodermal differentiation
-
-/- ES cells display non-cell-autonomous impairment in mesodermal differentiation. EMBO J. 19, 5845-5844 (2000).
-
(2000)
EMBO J.
, vol.19
, pp. 5845-5844
-
-
Weinhold, B.1
Shratt, G.2
Arsenian, S.3
-
69
-
-
0141764868
-
A handful of questions: The molecular biology of the heart and neural crest derivatives (HAND) -subclass of basic helix-loop-helix transcription factors
-
Firulli AB: A handful of questions: the molecular biology of the heart and neural crest derivatives (HAND) -subclass of basic helix-loop-helix transcription factors. Gene 312, 27-40 (2003).
-
(2003)
Gene
, vol.312
, pp. 27-40
-
-
Firulli, A.B.1
-
70
-
-
0030903857
-
Regulation of cardiac mesodermal and neural crest development by the bHLH transcription factor, dHAND
-
DOI 10.1038/ng0697-154
-
Srivastava D, Thomas T, Lin Q, Kirby ML, Brown D, Olson EN: Regulation of cardiac mesodermal and neural crest development by the bHLH transcription factor, dHAND. Nat. Genet. 16, 154-160 (1997). (Pubitemid 27240613)
-
(1997)
Nature Genetics
, vol.16
, Issue.2
, pp. 154-160
-
-
Srivastava, D.1
Thomas, T.2
Kirby, M.L.3
Brown, D.4
Olson, E.N.5
-
71
-
-
0031882143
-
Heart and extra embryonic mesodermal defects in mouse embryos lacking the bHLH transcription factor Hand1
-
Firulli AB, McFadden DG, Lin Q, Srivastava D, Olson EN: Heart and extra embryonic mesodermal defects in mouse embryos lacking the bHLH transcription factor Hand1. Nat. Genet. 18, 266-270 (1998).
-
(1998)
Nat. Genet.
, vol.18
, pp. 266-270
-
-
Firulli, A.B.1
McFadden, D.G.2
Lin, Q.3
Srivastava, D.4
Olson, E.N.5
-
72
-
-
0031882249
-
The Hand1 bHLH transcription factor is essential for placentation and cardiac morphogenesis
-
Riley P, Anson-Cartwright L, Cross JC: The Hand1 bHLH transcription factor is essential for placentation and cardiac morphogenesis. Nat. Genet. 18, 271-275 (1998).
-
(1998)
Nat. Genet.
, vol.18
, pp. 271-275
-
-
Riley, P.1
Anson-Cartwright, L.2
Cross, J.C.3
-
73
-
-
0035891429
-
The combinatorial activities of Nkx2.5 and dHAND are essential for cardiac ventricle formation
-
Yamagishi H, Yamagishi C, Nakagawa O, Harvey RP, Olson EN, Srivastava D: The combinatorial activities of Nkx2.5 and dHAND are essential for cardiac ventricle formation. Dev. Biol. 239, 190-203 (2001).
-
(2001)
Dev. Biol.
, vol.239
, pp. 190-203
-
-
Yamagishi, H.1
Yamagishi, C.2
Nakagawa, O.3
Harvey, R.P.4
Olson, E.N.5
Srivastava, D.6
-
74
-
-
0037025326
-
The transcription factors GATA4 and dHAND physically interact to synergistically activate cardiac gene expression through a p300-dependent mechanism
-
Dai YS, Cserjesi P, Markham BE, Molkentin JD: The transcription factors GATA4 and dHAND physically interact to synergistically activate cardiac gene expression through a p300-dependent mechanism. J. Biol. Chem. 277, 24390-24398 (2002).
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 24390-24398
-
-
Dai, Y.S.1
Cserjesi, P.2
Markham, B.E.3
Molkentin, J.D.4
-
75
-
-
0036773644
-
The basic-helix-loop-helix transcription factor HAND2 directly regulates transcription of the atrial naturetic peptide gene
-
Thattaliyath BD, Firulli BA, Firulli AB: The basic-helix-loop-helix transcription factor HAND2 directly regulates transcription of the atrial naturetic peptide gene. J. Mol. Cell. Cardiol. 34, 1335-1344 (2002).
-
(2002)
J. Mol. Cell. Cardiol.
, vol.34
, pp. 1335-1344
-
-
Thattaliyath, B.D.1
Firulli, B.A.2
Firulli, A.B.3
-
77
-
-
0033168070
-
Chamber-specific cardiac expression of Tbx5 and heart defects in Holt-Oram syndrome
-
Bruneau BG, Logan M, Davis N et al.: Chamber-specific cardiac expression of Tbx5 and heart defects in Holt-Oram syndrome. Dev. Biol. 211, 100-108 (1999).
-
(1999)
Dev. Biol.
, vol.211
, pp. 100-108
-
-
Bruneau, B.G.1
Logan, M.2
Davis, N.3
-
78
-
-
17944378083
-
A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease
-
Bruneau BG, Nemer G, Schmitt JP et al.: A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease. Cell 106, 709-721 (2001).
-
(2001)
Cell.
, vol.106
, pp. 709-721
-
-
Bruneau, B.G.1
Nemer, G.2
Schmitt, J.P.3
-
79
-
-
0034931034
-
Tbx5 associates with Nkx2-5 and synergistically promotes cardiomyocyte differentiation
-
Hiroi Y, Kudoh S, Monzen K et al.: Tbx5 associates with Nkx2-5 and synergistically promotes cardiomyocyte differentiation. Nat. Genet. 28, 276-280 (2001).
-
(2001)
Nat. Genet.
, vol.28
, pp. 276-280
-
-
Hiroi, Y.1
Kudoh, S.2
Monzen, K.3
-
80
-
-
2442624606
-
Differential expression and function of Tbx5 and Tbx20 in cardiac development
-
Plageman TF Jr, Yutzey KE: Differential expression and function of Tbx5 and Tbx20 in cardiac development. J. Biol. Chem. 279, 19026-19034 (2004).
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 19026-19034
-
-
Plageman Jr., T.F.1
Yutzey, K.E.2
-
81
-
-
21644480925
-
Tbx20 is essential for cardiac chamber differentiation and repression of Tbx2
-
Sinh MK, Christoffels VM, Dias JM et al.: Tbx20 is essential for cardiac chamber differentiation and repression of Tbx2. Development 132, 2697-2707 (2005).
-
(2005)
Development
, vol.132
, pp. 2697-2707
-
-
Sinh, M.K.1
Christoffels, V.M.2
Dias, J.M.3
-
82
-
-
69249229628
-
Molecular embryology for an understanding of congenital heart disease
-
Yamagagishi H, Maeda J, Uchida K et al.: Molecular embryology for an understanding of congenital heart disease. Anat. Sci. Int. 84 (3), 88-94 (2009).
-
(2009)
Anat. Sci. Int.
, vol.84
, Issue.3
, pp. 88-94
-
-
Yamagagishi, H.1
Maeda, J.2
Uchida, K.3
-
83
-
-
2342628902
-
The role of Zic genes in neural development
-
Aruga J: The role of Zic genes in neural development. Mol. Cell. Neurosci. 26, 205-221 (2004).
-
(2004)
Mol. Cell. Neurosci.
, vol.26
, pp. 205-221
-
-
Aruga, J.1
-
84
-
-
0034641605
-
The X-linked mouse mutation Bent tail is associated with a deletion of the Zic3 locus
-
Carrel T, Purandar SM, Harrison W et al.: The X-linked mouse mutation Bent tail is associated with a deletion of the Zic3 locus. Hum. Mol. Genet. 9, 1937-1942 (2000).
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1937-1942
-
-
Carrel, T.1
Purandar, S.M.2
Harrison, W.3
-
85
-
-
0036337344
-
A complex syndrome of left-right axis, central nervous system and axial skeleton defects in Zic3 mutant mice
-
Purandare SM, Ware SM, Kwan KM et al.: A complex syndrome of left-right axis, central nervous system and axial skeleton defects in Zic3 mutant mice. Development 129, 2293-2302 (2002).
-
(2002)
Development
, vol.129
, pp. 2293-2302
-
-
Purandare, S.M.1
Ware, S.M.2
Kwan, K.M.3
-
86
-
-
2342628902
-
The role of Zic genes in neural development
-
Aruga J: The role of Zic genes in neural development. Mol. Cell. Neurosci. 26, 205-221 (2004).
-
(2004)
Mol. Cell. Neurosci.
, vol.26
, pp. 205-221
-
-
Aruga, J.1
-
87
-
-
0034641605
-
The X-linked mouse mutation Bent tail is associated with a deletion of the Zic3 locus
-
Carrel T, Purandar SM, Harrison W et al.: The X-linked mouse mutation Bent tail is associated with a deletion of the Zic3 locus. Hum. Mol. Genet. 9, 1937-1942 (2000).
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1937-1942
-
-
Carrel, T.1
Purandar, S.M.2
Harrison, W.3
-
88
-
-
0036337344
-
A complex syndrome of left-right axis, central nervous system and axial skeleton defects in Zic3 mutant mice
-
Purandare SM, Ware SM, Kwan KM et al.: A complex syndrome of left-right axis, central nervous system and axial skeleton defects in Zic3 mutant mice. Development 129, 2293-2302 (2002).
-
(2002)
Development
, vol.129
, pp. 2293-2302
-
-
Purandare, S.M.1
Ware, S.M.2
Kwan, K.M.3
-
89
-
-
33646181360
-
The vertebrate spalt genes in development and disease
-
Sweetman D, Munsterberg A: The vertebrate spalt genes in development and disease. Dev. Biol. 293, 285-293 (2006).
-
(2006)
Dev. Biol.
, vol.293
, pp. 285-293
-
-
Sweetman, D.1
Munsterberg, A.2
-
90
-
-
31744444444
-
Cooperative and antagonistic interactions between Sall4 and Tbx5 pattern the mouse limb and heart
-
Koshiba-Takeuchi K, Takeuchi JK, Arruda EP et al.: Cooperative and antagonistic interactions between Sall4 and Tbx5 pattern the mouse limb and heart. Nat. Genet. 38, 175-183 (2006).
-
(2006)
Nat. Genet.
, vol.38
, pp. 175-183
-
-
Koshiba-Takeuchi, K.1
Takeuchi, J.K.2
Arruda, E.P.3
-
91
-
-
33747730205
-
The murine homolog of SALL4, a causative gene in Okihiro syndrome, is essential for embryonic stem cell proliferation, and cooperates with Sall1 in ano-rectal, heart, brain and kidney development
-
Sakaki-Yumoto M, Kobayashi C, Sato A et al.: The murine homolog of SALL4, a causative gene in Okihiro syndrome, is essential for embryonic stem cell proliferation, and cooperates with Sall1 in ano-rectal, heart, brain and kidney development. Development 133, 3005-3013 (2006).
-
(2006)
Development
, vol.133
, pp. 3005-3013
-
-
Sakaki-Yumoto, M.1
Kobayashi, C.2
Sato, A.3
-
92
-
-
0032736054
-
Molecular cloning and chromosomal localization of the human CITED2 gene encoding p35srj/Mrg1
-
Leung, MK, Jones T, Michels CL, Livingston DM, Bhattacharya S: Molecular cloning and chromosomal localization of the human CITED2 gene encoding p35srj/Mrg1. Genomics 61, 307-313 (1999).
-
(1999)
Genomics
, vol.61
, pp. 307-313
-
-
Leung, M.K.1
Jones, T.2
Michels, C.L.3
Livingston, D.M.4
Bhattacharya, S.5
-
93
-
-
0344089181
-
Expression of Tfap2d, the gene encoding the transcription factor Ap-2 d, during mouse embryogenesis
-
Zhao F, Lufkin T, Gelb BD: Expression of Tfap2d, the gene encoding the transcription factor Ap-2 d, during mouse embryogenesis. Gene Exp. Patterns 3, 213-217 (2003).
-
(2003)
Gene Exp. Patterns
, vol.3
, pp. 213-217
-
-
Zhao, F.1
Lufkin, T.2
Gelb, B.D.3
-
94
-
-
16544377641
-
Cited2 controls left-right patterning and heart development through a Nodal-Pitx2c pathway
-
Bamforth S, Braganca J, Schneider JE et al.: Cited2 controls left-right patterning and heart development through a Nodal-Pitx2c pathway. Nat. Genet. 36, 1189-1195 (2004).
-
(2004)
Nat. Genet.
, vol.36
, pp. 1189-1195
-
-
Bamforth, S.1
Braganca, J.2
Schneider, J.E.3
-
95
-
-
18344389337
-
Cardiac malformations, adrenal agenesis, neural crest defects and exencephaly in mice lacking Cited2, a new Tfap2 co-activator
-
Bamforth SD: Cardiac malformations, adrenal agenesis, neural crest defects and exencephaly in mice lacking Cited2, a new Tfap2 co-activator. Nat. Genet. 29, 469-474 (2001).
-
(2001)
Nat. Genet.
, vol.29
, pp. 469-474
-
-
Bamforth, S.D.1
-
96
-
-
17244379390
-
Cited2 is required both for heart morphogenesis and establishment of the left-right axis in mouse development
-
Weninger WJ, Floro KL, Bennett MB et al.: Cited2 is required both for heart morphogenesis and establishment of the left-right axis in mouse development. Development 132, 1337-1348 (2005).
-
(2005)
Development
, vol.132
, pp. 1337-1348
-
-
Weninger, W.J.1
Floro, K.L.2
Bennett, M.B.3
-
97
-
-
0033575364
-
Difference in left-right axis pathways in mouse and chick: Function of FGF8 and SHH
-
Meyers EN, Martin GR: Difference in left-right axis pathways in mouse and chick: function of FGF8 and SHH. Science 285, 403-406 (1999).
-
(1999)
Science
, vol.285
, pp. 403-406
-
-
Meyers, E.N.1
Martin, G.R.2
-
98
-
-
0036638625
-
Bmp2 is a positive regulator of nodal signaling during left-right axis formation in the chicken embryo
-
Schlange T, Arnold HH, Brand T: Bmp2 is a positive regulator of nodal signaling during left-right axis formation in the chicken embryo. Development 129, 3421-3429 (2002).
-
(2002)
Development
, vol.129
, pp. 3421-3429
-
-
Schlange, T.1
Arnold, H.H.2
Brand, T.3
-
99
-
-
0035808459
-
Nodal signaling uses activin and transforming growth factor-β receptor-regulated Smads
-
Kumar A, Novoselov V, Celeste AJ, Wolfmann NM, Dijke P, Kuehn MR: Nodal signaling uses activin and transforming growth factor-β receptor-regulated Smads. J. Biol. Chem. 276, 656-661 (2001).
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 656-661
-
-
Kumar, A.1
Novoselov, V.2
Celeste, A.J.3
Wolfmann, N.M.4
Dijke, P.5
Kuehn, M.R.6
-
100
-
-
0033387975
-
Mouse Pitx2 deficiency leads to anomalies of the ventral body wall, heart, extra and peri-ocular mesoderm and right pulmonary isomerism
-
Kitamura K, Miura H, Miyagawa-Tomita S et al.: Mouse Pitx2 deficiency leads to anomalies of the ventral body wall, heart, extra and peri-ocular mesoderm and right pulmonary isomerism. Development 126, 5749-5758 (1999).
-
(1999)
Development
, vol.126
, pp. 5749-5758
-
-
Kitamura, K.1
Miura, H.2
Miyagawa-Tomita, S.3
-
101
-
-
33646706385
-
Tbx1 affects asymmetric cardiac morphogenesis by regulating Pitx2 in the secondary heart field
-
Nowotschin S, Liao J, Gage PJ, Epstein JA, Campione M, Morrow BE: Tbx1 affects asymmetric cardiac morphogenesis by regulating Pitx2 in the secondary heart field. Development 133, 1565-1573 (2006).
-
(2006)
Development
, vol.133
, pp. 1565-1573
-
-
Nowotschin, S.1
Liao, J.2
Gage, P.J.3
Epstein, J.A.4
Campione, M.5
Morrow, B.E.6
-
102
-
-
0033514433
-
Molecular cloning of ZFPM2/FOG2: A modulator of transcription factor GATA4 in cardiomyocytes
-
Svensson EC, Tufts RL, Polk CE, Leiden JM: Molecular cloning of ZFPM2/FOG2: a modulator of transcription factor GATA4 in cardiomyocytes. Proc. Natl Acad. Sci. USA 96, 956-961 (1999).
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 956-961
-
-
Svensson, E.C.1
Tufts, R.L.2
Polk, C.E.3
Leiden, J.M.4
-
103
-
-
0033945862
-
A syndrome of tricuspid atresia in mice with a targeted mutation of the gene encoding ZFPM2/FOG2
-
Svensson EC, Huggins GS, Lin H et al.: A syndrome of tricuspid atresia in mice with a targeted mutation of the gene encoding ZFPM2/FOG2. Nat. Genet. 25, 353-356 (2000).
-
(2000)
Nat. Genet.
, vol.25
, pp. 353-356
-
-
Svensson, E.C.1
Huggins, G.S.2
Lin, H.3
-
104
-
-
0034705318
-
ZFPM2/FOG2, a cofactor for GATA transcription factors, is essential for heart morphogenesis and development of coronary vessels from epicardium
-
Tevosian SG, Deconinck AE, Tanaka M et al.: ZFPM2/FOG2, a cofactor for GATA transcription factors, is essential for heart morphogenesis and development of coronary vessels from epicardium. Cell 101, 729-739 (2000).
-
(2000)
Cell.
, vol.101
, pp. 729-739
-
-
Tevosian, S.G.1
Deconinck, A.E.2
Tanaka, M.3
-
105
-
-
0028277885
-
Isolation of the human LIM/homeodomain gene islet-1 and identification of a simple sequence repeat 1
-
Tanizawa Y, Riggs AC, Dagogo-Jack S et al.: Isolation of the human LIM/homeodomain gene islet-1 and identification of a simple sequence repeat polymorphism. Diabetes 43 (7), 935-941 (1994). (Pubitemid 24196428)
-
(1994)
Diabetes
, vol.43
, Issue.7
, pp. 935-941
-
-
Tanizawa, Y.1
Riggs, A.C.2
Dagogo-Jack, S.3
Vaxillaire, M.4
Froguel, P.5
Liu, L.6
Donis-Keller, H.7
Permutt, M.A.8
-
106
-
-
0030051923
-
Requirement for LIM Homeobox gene Isl1 in motor neuron generation reveals a motor neuron-dependent step in interneuron differentiation
-
Pfaff SL, Mendelsohn M, Stewart CL, Edlund T, Jessell TM: Requirement for LIM Homeobox gene Isl1 in motor neuron generation reveals a motor neuron-dependent step in interneuron differentiation. Cell 84, 309-320 (1996).
-
(1996)
Cell.
, vol.84
, pp. 309-320
-
-
Pfaff, S.L.1
Mendelsohn, M.2
Stewart, C.L.3
Edlund, T.4
Jessell, T.M.5
-
107
-
-
0346783332
-
Isl1 identiflies a cardiac progenitor population that proliferates prior to differentiation and contributes a majority of cells to the heart
-
Cai CL, Liang X, Shi Y et al.: Isl1 identiflies a cardiac progenitor population that proliferates prior to differentiation and contributes a majority of cells to the heart. Dev. Cell 5, 877-889 (2003).
-
(2003)
Dev. Cell.
, vol.5
, pp. 877-889
-
-
Cai, C.L.1
Liang, X.2
Shi, Y.3
-
108
-
-
0025280050
-
Insulin gene enhancer binding protein Isl-1 is a member of a novel class of proteins containing both a homeo- and a Cys- His domain
-
Karlsson O, Thor S, Norberg T, Ohlsson H, Edlund T: Insulin gene enhancer binding protein Isl-1 is a member of a novel class of proteins containing both a homeo- and a Cys- His domain. Nature 344, 879-882 (1990).
-
(1990)
Nature
, vol.344
, pp. 879-882
-
-
Karlsson, O.1
Thor, S.2
Norberg, T.3
Ohlsson, H.4
Edlund, T.5
-
109
-
-
0001590320
-
Mechanisms in the pathogenesis of congenital heart disease
-
Pierpont ME, Moller J Eds. Martinus-Nijoff, Boston, MA, USA, Interesting historical article
-
Clark EB: Mechanisms in the pathogenesis of congenital heart disease. In: The Genetics of Cardiovascular Disease. Pierpont ME, Moller J (Eds). Martinus-Nijoff, Boston, MA, USA 3-11 (1986). Interesting historical article.
-
(1986)
The Genetics of Cardiovascular Disease
, pp. 3-11
-
-
Clark, E.B.1
-
110
-
-
0030437101
-
Pathogenetic mechanisms of congenital cardiovascular malformations revisited
-
Clark EB: Pathogenetic mechanisms of congenital cardiovascular malformations revisited. Semin. Perinatol. 20, 465-472 (1996).
-
(1996)
Semin. Perinatol.
, vol.20
, pp. 465-472
-
-
Clark, E.B.1
-
111
-
-
0019741561
-
Congenital rubella syndrome: The late effects and their relation to early lesions
-
Rosenberg HS, Oppenheimer EH, Esterly JR: Congenital rubella syndrome: the late effects and their relation to early lesions. Perspect. Pediatr. Pathol. 6, 183-202 (1981).
-
(1981)
Perspect. Pediatr. Pathol.
, vol.6
, pp. 183-202
-
-
Rosenberg, H.S.1
Oppenheimer, E.H.2
Esterly, J.R.3
-
112
-
-
38049183155
-
Maternal diabetes induces congenital heart defect in mice by altering the expression of genes involved in cardiovascular development
-
Kumar SD, Dheen ST, Tay SS: Maternal diabetes induces congenital heart defect in mice by altering the expression of genes involved in cardiovascular development. Cardiovasc. Diabetol. 6, 34 (2007).
-
(2007)
Cardiovasc. Diabetol.
, vol.6
, pp. 34
-
-
Kumar, S.D.1
Dheen, S.T.2
Tay, S.S.3
-
113
-
-
0025635631
-
Risk factors for cardiovascular malformations in Finland
-
Tikkanen J, Heinonen OP: Risk factors for cardiovascular malformations in Finland. Eur. J. Epidemiol. 6, 348-356 (1990).
-
(1990)
Eur. J. Epidemiol.
, vol.6
, pp. 348-356
-
-
Tikkanen, J.1
Heinonen, O.P.2
-
114
-
-
77952507512
-
Congenital heart disease in patients with Turner's syndrome. Italian study group for Turner syndrome
-
Mazzanti L, Cacciari E: Congenital heart disease in patients with Turner's syndrome. Italian study group for Turner syndrome. Clin. Endocrinol. 54, 69-73 (2001).
-
(2001)
Clin. Endocrinol.
, vol.54
, pp. 69-73
-
-
Mazzanti, L.1
Cacciari, E.2
-
115
-
-
0026583894
-
Down syndrome: Molecular mapping of the congenital heart disease and duodenal stenosis
-
Korenberg JR, Bradley C, Disteche CM: Down syndrome: molecular mapping of the congenital heart disease and duodenal stenosis. Am. J. Hum. Genet. 50, 294-302 (1992).
-
(1992)
Am. J. Hum. Genet.
, vol.50
, pp. 294-302
-
-
Korenberg, J.R.1
Bradley, C.2
Disteche, C.M.3
-
116
-
-
0036889598
-
Chromosome 22q11.2 deletion syndrome: DiGeorge and velocardiofacial syndromes
-
Perez E, Sullivan KE: Chromosome 22q11.2 deletion syndrome: DiGeorge and velocardiofacial syndromes. Curr. Opin. Pediatr. 14, 678-683 (2002).
-
(2002)
Curr. Opin. Pediatr.
, vol.14
, pp. 678-683
-
-
Perez, E.1
Sullivan, K.E.2
-
117
-
-
10744223651
-
Role of TBX1 in human del22q11.2 syndrome
-
Yagi H, Furutani Y, Hamada H: Role of TBX1 in human del22q11.2 syndrome. Lancet 362, 1366-1373 (2003).
-
(2003)
Lancet
, vol.362
, pp. 1366-1373
-
-
Yagi, H.1
Furutani, Y.2
Hamada, H.3
-
118
-
-
0029015848
-
Strong correlation of elastin deletions, detected by FISH, with Williams syndrome: Evaluation of 235 patients
-
Lowery MC, Morris CA, Ewart A: Strong correlation of elastin deletions, detected by FISH, with Williams syndrome: evaluation of 235 patients. Am. J. Hum. Genet. 57, 49-53 (1995).
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 49-53
-
-
Lowery, M.C.1
Morris, C.A.2
Ewart, A.3
-
119
-
-
18344385476
-
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
-
Tartaglia M, Mehler EL, Goldberg R: Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome. Nat. Genet. 29, 465-468 (2001).
-
(2001)
Nat. Genet.
, vol.29
, pp. 465-468
-
-
Tartaglia, M.1
Mehler, E.L.2
Goldberg, R.3
-
120
-
-
0028281469
-
The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome)
-
Basson CT, Cowley GS, Solomon SD: The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome). N. Engl. J. Med. 330, 885-891 (1994).
-
(1994)
N. Engl. J. Med.
, vol.330
, pp. 885-891
-
-
Basson, C.T.1
Cowley, G.S.2
Solomon, S.D.3
-
121
-
-
77952489664
-
Analysis of cardiovascular phenotype and genotype-phenotype correlation in individuals with a JAG1 mutation and/or Alagille syndrome
-
McElhinney DB, Krantz JD, Bason L: Analysis of cardiovascular phenotype and genotype-phenotype correlation in individuals with a JAG1 mutation and/or Alagille syndrome. Nat. Genet. 16, 235-242 (1997).
-
(1997)
Nat. Genet.
, vol.16
, pp. 235-242
-
-
McElhinney, D.B.1
Krantz, J.D.2
Bason, L.3
-
122
-
-
0034022637
-
Mutations in TFAP2B cause Charge syndrome, a familial form of patent ductus arteriosus
-
Satoda M, Pieropont MEM, Diaz GA: Mutations in TFAP2B cause Charge syndrome, a familial form of patent ductus arteriosus. Nat. Genet. 25, 42-46 (2000).
-
(2000)
Nat. Genet.
, vol.25
, pp. 42-46
-
-
Satoda, M.1
Pieropont, M.E.M.2
Diaz, G.A.3
-
123
-
-
4444239112
-
Mutations in a new member of the chromodomain gene family cause Charge syndrome
-
Vissers LE, van Ravenswaaij CM, Admiraal R: Mutations in a new member of the chromodomain gene family cause Charge syndrome. Nat. Genet. 36, 955-957 (2004).
-
(2004)
Nat. Genet.
, vol.36
, pp. 955-957
-
-
Vissers, L.E.1
Van Ravenswaaij, C.M.2
Admiraal, R.3
-
124
-
-
0034104297
-
Mutations in a new gene for the Ellis-van Creveld syndrome and Weyers acrodental dysostosis
-
Ruiz-Perez VL, Ide SE, Strom TM: Mutations in a new gene for the Ellis-van Creveld syndrome and Weyers acrodental dysostosis. Nat. Genet. 24, 283-286 (2000).
-
(2000)
Nat. Genet.
, vol.24
, pp. 283-286
-
-
Ruiz-Perez, V.L.1
Ide, S.E.2
Strom, T.M.3
-
125
-
-
21044433130
-
Failure to detect an 8p22-8p23.1 duplication in patients with Kabuki (Niikawa-Kuroki) syndrome
-
Sanlaville D, Genevieve D, Bernardin C et al.: Failure to detect an 8p22-8p23.1 duplication in patients with Kabuki (Niikawa-Kuroki) syndrome. Eur. J. Hum. Genet. 13, 690-693 (2005).
-
(2005)
Eur. J. Hum. Genet.
, vol.13
, pp. 690-693
-
-
Sanlaville, D.1
Genevieve, D.2
Bernardin, C.3
-
126
-
-
0034089182
-
Duplication of chromosome region 8p23.1-p23.3: A benign variant?
-
Engelen JJ, Moog U, Evers JL: Duplication of chromosome region 8p23.1-p23.3: a benign variant? Am. J. Med. Genet. 91, 18-21 (2000).
-
(2000)
Am. J. Med. Genet.
, vol.91
, pp. 18-21
-
-
Engelen, J.J.1
Moog, U.2
Evers, J.L.3
-
127
-
-
0014334454
-
Multifactorial inheritance hypothesis for the etiology of congenital heart diseases. The genetic-environmental interaction
-
Nora JJ: Multifactorial inheritance hypothesis for the etiology of congenital heart diseases. The genetic-environmental interaction. Circulation 38, 604-617 (1968).
-
(1968)
Circulation
, vol.38
, pp. 604-617
-
-
Nora, J.J.1
-
128
-
-
77956428378
-
Molecolar mechanisms of congenital heart disease
-
DOI:10.1016/j. carpath.2009.06.008, Epub ahead of print
-
Jing-bin H, Ying-long L, Pei-Wu S, Xiao-dong L, Ming D, Xiang-Ming F: Molecolar mechanisms of congenital heart disease. Cardiovasc. Pathol. DOI:10.1016/j. carpath.2009.06.008 (2009) (Epub ahead of print).
-
(2009)
Cardiovasc. Pathol.
-
-
Jing-bin, H.1
Ying-long, L.2
Pei-Wu, S.3
Xiao-dong, L.4
Ming, D.5
Xiang-Ming, F.6
-
129
-
-
39749191367
-
The developmental genetics of congenital heart disease
-
Bruneau G: The developmental genetics of congenital heart disease. Nature 451, 943-948 (2008).
-
(2008)
Nature
, vol.451
, pp. 943-948
-
-
Bruneau, G.1
-
130
-
-
63049126695
-
Genetics and embryological mechanisms of congenital heart diseases
-
Bajolle F, Zaffran S, Bonnet D: Genetics and embryological mechanisms of congenital heart diseases. Arch. Cardiovasc. Dis. 102, 59-63 (2009).
-
(2009)
Arch. Cardiovasc. Dis.
, vol.102
, pp. 59-63
-
-
Bajolle, F.1
Zaffran, S.2
Bonnet, D.3
-
131
-
-
34250305402
-
Genetic basis for congenital heart defects: Current knowledge
-
Pierpont ME, Craig T, Basson D et al.: Genetic basis for congenital heart defects: current knowledge. Circulation 115, 3015-3038 (2007).
-
(2007)
Circulation
, vol.115
, pp. 3015-3038
-
-
Pierpont, M.E.1
Craig, T.2
Basson, D.3
-
132
-
-
33750736365
-
The geneticist's role in adult congenital heart disease
-
Bernier F P, Spaegens R: The geneticist's role in adult congenital heart disease. Cardiol. Clin. 24, 557-569 (2006).
-
(2006)
Cardiol. Clin.
, vol.24
, pp. 557-569
-
-
Bernier, F.P.1
Spaegens, R.2
-
133
-
-
0036696087
-
The genetics of congenital heart disease: A point in the revolution
-
Benson WD: The genetics of congenital heart disease: a point in the revolution. Cardiol. Clin. 20, 385-394 (2002).
-
(2002)
Cardiol. Clin.
, vol.20
, pp. 385-394
-
-
Benson, W.D.1
-
134
-
-
0035830860
-
Principles for the buffe ring of genetics variation
-
Hartman JLT, GarvikB, Hartwell L: Principles for the buffe ring of genetics variation. Science 291, 1001-1004 (2001).
-
(2001)
Science
, vol.291
, pp. 1001-1004
-
-
Hartman, J.L.T.1
Garvik, B.2
Hartwell, L.3
-
135
-
-
41149125478
-
Genetic mechanisms controlling cardiovascular development
-
Bentham J, Bhattacharya S: Genetic mechanisms controlling cardiovascular development Ann. NY Acad. Sci. 1123, 10-19 (2008).
-
(2008)
Ann. NY Acad. Sci.
, vol.1123
, pp. 10-19
-
-
Bentham, J.1
Bhattacharya, S.2
-
136
-
-
33645473405
-
Maternal MTHFR 677C>T is a risk factor for congenital heart defects: Effect modification by periconceptional folate supplementation
-
Van Beynemun IM, Kapusta L, den Heijer M: Maternal MTHFR 677C>T is a risk factor for congenital heart defects: effect modification by periconceptional folate supplementation. Eur. Heart J. 27, 981-987 (2006).
-
(2006)
Eur. Heart J.
, vol.27
, pp. 981-987
-
-
Van Beynemun, I.M.1
Kapusta, L.2
Heijer, M.D.3
-
137
-
-
0043267988
-
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5
-
Garg V, Kathiriya IS, Barnes R et al.: GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5. Nature 424, 443-447 (2003).
-
(2003)
Nature
, vol.424
, pp. 443-447
-
-
Garg, V.1
Kathiriya, I.S.2
Barnes, R.3
-
138
-
-
0031844382
-
The cardiac tissue-restricted homeobox protein Csx/Nkx2.5 physically associates with the zinc finger protein GATA4 and cooperatively activates atrial natriuretic factor gene expression
-
Lee Y, Shioi T, Kasahara H: The cardiac tissue-restricted homeobox protein Csx/Nkx2.5 physically associates with the zinc finger protein GATA4 and cooperatively activates atrial natriuretic factor gene expression. Mol. Cell. Biol. 18, 3120-3129 (1998).
-
(1998)
Mol. Cell. Biol.
, vol.18
, pp. 3120-3129
-
-
Lee, Y.1
Shioi, T.2
Kasahara, H.3
-
139
-
-
0031815073
-
GATA-4 and Nkx-2.5 coactivate Nkx-2 DNA binding targets: Role for regulating early cardiac gene expression
-
Sepulveda JL, Belaguli N, Nigam V, Chen CY, Nemer M, Schwartz RJ: GATA-4 and Nkx-2.5 coactivate Nkx-2 DNA binding targets: role for regulating early cardiac gene expression. Mol. Cell. Biol. 18, 3405-3415 (1998).
-
(1998)
Mol. Cell. Biol.
, vol.18
, pp. 3405-3415
-
-
Sepulveda, J.L.1
Belaguli, N.2
Nigam, V.3
Chen, C.Y.4
Nemer, M.5
Schwartz, R.J.6
-
140
-
-
20144387341
-
Mutation in myosin heavy chain 6 causes atrial septal defect
-
Ching YH, Ghosh TK, Cross SJ et al.: Mutation in myosin heavy chain 6 causes atrial septal defect. Nat. Genet. 37 (4), 423-428 (2005).
-
(2005)
Nat. Genet.
, vol.37
, Issue.4
, pp. 423-428
-
-
Ching, Y.H.1
Ghosh, T.K.2
Cross, S.J.3
-
141
-
-
0043267988
-
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5
-
Garg V, Kathiriya IS, Barnes R et al.: GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5. Nature 424, 443-447 (2003).
-
(2003)
Nature
, vol.424
, pp. 443-447
-
-
Garg, V.1
Kathiriya, I.S.2
Barnes, R.3
-
142
-
-
37849048968
-
α-Cardiac actin mutations produce atrial septal defects
-
Matsson H, Eason J, Bookwalter CS et al.: α-cardiac actin mutations produce atrial septal defects. Hum. Mol. Genet. 17, 256-265 (2008).
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 256-265
-
-
Matsson, H.1
Eason, J.2
Bookwalter, C.S.3
-
143
-
-
0032479573
-
Congenital heart disease caused by mutations in the transcription factor NKX2-5
-
Schott JJ, Benson DW, Basson CT et al.: Congenital heart disease caused by mutations in the transcription factor NKX2-5. Science 281, 108-111 (1998).
-
(1998)
Science
, vol.281
, pp. 108-111
-
-
Schott, J.J.1
Benson, D.W.2
Basson, C.T.3
-
144
-
-
0029027507
-
Assignment of cardiac homeobox gene CSX to human chromosome 5q34
-
Shiojima I, Komuro I, Inazawa J et al.: Assignment of cardiac homeobox gene CSX to human chromosome 5q34. Genomics 27, 204-206 (1995).
-
(1995)
Genomics
, vol.27
, pp. 204-206
-
-
Shiojima, I.1
Komuro, I.2
Inazawa, J.3
-
145
-
-
0037975739
-
Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: Associations with atrial septal defect and hypoplastic left heart syndrome
-
Elliott DA, Kirk EP, Yeoh T et al.: Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome. J. Am. Coll. Cardiol. 41, 2072-2076 (2003).
-
(2003)
J. Am. Coll. Cardiol.
, vol.41
, pp. 2072-2076
-
-
Elliott, D.A.1
Kirk, E.P.2
Yeoh, T.3
-
146
-
-
0242636701
-
NKX2.5 mutations in patients with congenital heart disease
-
McElhinney DB, Geiger E, Blinder J, Benson DW, Goldmuntz E: NKX2.5 mutations in patients with congenital heart disease. J. Am. Coll. Cardiol. 42, 1650-1655 (2003).
-
(2003)
J. Am. Coll. Cardiol.
, vol.42
, pp. 1650-1655
-
-
McElhinney, D.B.1
Geiger, E.2
Blinder, J.3
Benson, D.W.4
Goldmuntz, E.5
-
147
-
-
37849053289
-
Mutations in GATA4, NKX2.5, CRELD1 and BMP4 are infrequently found in patients with congenital cardiac septal defects
-
Posh M, Perrot A, Schmitt K et al.: Mutations in GATA4, NKX2.5, CRELD1 and BMP4 are infrequently found in patients with congenital cardiac septal defects. Am J. Med. Genet. A 146, 251-253 (2008).
-
(2008)
Am. J. Med. Genet. A
, vol.146
, pp. 251-253
-
-
Posh, M.1
Perrot, A.2
Schmitt, K.3
-
148
-
-
0035923555
-
NKX2.5 mutations in patients with tetralogy of Fallot
-
Geiger E, Benson DW: NKX2.5 mutations in patients with tetralogy of Fallot. Circulation 104, 2565-2568 (2001).
-
(2001)
Circulation
, vol.104
, pp. 2565-2568
-
-
Geiger, E.1
Benson, D.W.2
-
149
-
-
65649113219
-
GATA4 and NKX2.5 gene analysis in Chinese Uygur patients with congenital heart defect
-
Zhang W, Li X, Ma Z et al.: GATA4 and NKX2.5 gene analysis in Chinese Uygur patients with congenital heart defect. Chin. Med. J. 122, 416-419 (2009).
-
(2009)
Chin. Med. J.
, vol.122
, pp. 416-419
-
-
Zhang, W.1
Li, X.2
Ma, Z.3
-
150
-
-
4444298928
-
Somatic NKX2.5 mutations as a novel mechanism of disease in complex congenital heart disease
-
Reamon-Buettner SM, Borlac J: Somatic NKX2.5 mutations as a novel mechanism of disease in complex congenital heart disease. J. Med. Genet. 41, 684-690 (2004).
-
(2004)
J. Med. Genet.
, vol.41
, pp. 684-690
-
-
Reamon-Buettner, S.M.1
Borlac, J.2
-
151
-
-
62149117229
-
Investigation of somatic NKX2.5 mutations in congenital heart disease
-
Draus JM, Hauck MA, Goetsch M, Austin EH, Tomita-Mitchell A, Mitchell ME: Investigation of somatic NKX2.5 mutations in congenital heart disease. J. Med. Genet. 46, 115-122 (2009).
-
(2009)
J. Med. Genet.
, vol.46
, pp. 115-122
-
-
Draus, J.M.1
Hauck, M.A.2
Goetsch, M.3
Austin, E.H.4
Tomita-Mitchell, A.5
Mitchell, M.E.6
-
152
-
-
0032975539
-
Familial atrial septal defect and atrioventricular conduction disturbance associated with a point mutation in the cardiac homeobox gene CSX/NKX2-5 in a Japanese patient
-
Hosoda T, Komuro I, Shiojima I et al.: Familial atrial septal defect and atrioventricular conduction disturbance associated with a point mutation in the cardiac homeobox gene CSX/NKX2-5 in a Japanese patient. Jpn Circ. J. 63, 425-426 (2009).
-
(2009)
Jpn. Circ. J.
, vol.63
, pp. 425-426
-
-
Hosoda, T.1
Komuro, I.2
Shiojima, I.3
-
153
-
-
0033912859
-
Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease
-
Kasahara H, Lee B, Schott JJ et al.: Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease. J. Clin. Invest. 106, 299-308 (2000).
-
(2000)
J. Clin. Invest.
, vol.106
, pp. 299-308
-
-
Kasahara, H.1
Lee, B.2
Schott, J.J.3
-
154
-
-
0034634624
-
Functional analyses of three Csx/Nkx-2.5 mutations that cause human congenital heart disease
-
Zhu W, Shiojima I, Hiroi Y et al.: Functional analyses of three Csx/Nkx-2.5 mutations that cause human congenital heart disease. J. Biol. Chem. 275, 35291-35296 (2000).
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 35291-35296
-
-
Zhu, W.1
Shiojima, I.2
Hiroi, Y.3
-
155
-
-
18744395182
-
Dual effects of the homeobox transcription factor Csx/Nkx2-5 on cardiomyocytes
-
Monzen K, Zhu W, Kasai H et al.: Dual effects of the homeobox transcription factor Csx/Nkx2-5 on cardiomyocytes. Biochem. Biophys. Res. Commun. 298, 493-500 (2002).
-
(2002)
Biochem. Biophys. Res. Commun.
, vol.298
, pp. 493-500
-
-
Monzen, K.1
Zhu, W.2
Kasai, H.3
-
156
-
-
0032771725
-
Ventricular non-compaction and distal chromosome 5q deletion
-
Pauli RM, Scheib-Wixted S, Cripe L, Izumo S, Sekhon GS: Ventricular non-compaction and distal chromosome 5q deletion. Am. J. Med. Genet. 85, 419-423 (1999).
-
(1999)
Am. J. Med. Genet.
, vol.85
, pp. 419-423
-
-
Pauli, R.M.1
Scheib-Wixted, S.2
Cripe, L.3
Izumo, S.4
Sekhon, G.S.5
-
157
-
-
0043267988
-
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5
-
Garg V, Kathiriya IS, Barnes R et al.: GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5. Nature 424, 443-447 (2003).
-
(2003)
Nature
, vol.424
, pp. 443-447
-
-
Garg, V.1
Kathiriya, I.S.2
Barnes, R.3
-
158
-
-
35048838310
-
Spectrum of heart disease associated with murine and human GATA4 mutation
-
Rajagopal SK, Ma Q, Obler D et al.: Spectrum of heart disease associated with murine and human GATA4 mutation. J. Mol. Cell. Cardiol. 43, 677-685 (2007).
-
(2007)
J. Mol. Cell. Cardiol.
, vol.43
, pp. 677-685
-
-
Rajagopal, S.K.1
Ma, Q.2
Obler, D.3
-
159
-
-
20944442976
-
Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect
-
Hirayam-Yamada K, Kamisago M, Akimoto K et al.: Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect. Am. J. Med. Genet. A 135, 47-52 (2005).
-
(2005)
Am. J. Med. Genet. A
, vol.135
, pp. 47-52
-
-
Hirayam-Yamada, K.1
Kamisago, M.2
Akimoto, K.3
-
160
-
-
28444447608
-
Spectrum of atrial septal defects associated with mutations of NKX2.5 and GATA4 transcription factors
-
Sarkozy A, Conti E, Neri C et al.: Spectrum of atrial septal defects associated with mutations of NKX2.5 and GATA4 transcription factors. J. Med. Genet. 42, E16 (2005).
-
(2005)
J. Med. Genet.
, vol.42
-
-
Sarkozy, A.1
Conti, E.2
Neri, C.3
-
161
-
-
28444474221
-
CRELD1 and GATA4 gene analysis in patients with nonsyndromic atrioventricular canal defects
-
Sarkozy A, Esposito G, Conti E et al.: CRELD1 and GATA4 gene analysis in patients with nonsyndromic atrioventricular canal defects. Am J. Med. Genet. 139 (3), 236-238 (2005).
-
(2005)
Am. J. Med. Genet.
, vol.139
, Issue.3
, pp. 236-238
-
-
Sarkozy, A.1
Esposito, G.2
Conti, E.3
-
162
-
-
33746608567
-
A novel mutation in the GATA4 gene in patients with tetralogy of Fallot
-
Nemer G, Fadlalah F, Usta J et al.: A novel mutation in the GATA4 gene in patients with tetralogy of Fallot. Hum. Mutat. 27, 293-294 (2006).
-
(2006)
Hum. Mutat.
, vol.27
, pp. 293-294
-
-
Nemer, G.1
Fadlalah, F.2
Usta, J.3
-
163
-
-
33846682721
-
Screening of 99 Danish patients with congenital heart disease for GATA4 mutations
-
Zhang L, Tumer Z, Jacobsen JR, Andersen PS, Tommerup N, Larsen LA: Screening of 99 Danish patients with congenital heart disease for GATA4 mutations. Genet. Test. 10, 277-280 (2006).
-
(2006)
Genet. Test.
, vol.10
, pp. 277-280
-
-
Zhang, L.1
Tumer, Z.2
Jacobsen, J.R.3
Andersen, P.S.4
Tommerup, N.5
Larsen, L.A.6
-
164
-
-
34147136738
-
Screening and biochemical analysis of GATA4 sequence variations identified in patients with congenital heart disease
-
Schluterman MK, Krysiak AE, Kathiriya IS et al.: Screening and biochemical analysis of GATA4 sequence variations identified in patients with congenital heart disease. Am. J. Med. Genet. A 143 A, 817-823 (2007).
-
(2007)
Am. J. Med. Genet. A
, vol.143 A
, pp. 817-823
-
-
Schluterman, M.K.1
Krysiak, A.E.2
Kathiriya, I.S.3
-
165
-
-
37249090635
-
GATA4 sequence variants in patients with congenital heart disease
-
Tomita-Mitchell A, Maslen CL, Morris CD, Garg V, Goldmuntz E: GATA4 sequence variants in patients with congenital heart disease. J. Med. Genet. 44, 779-783 (2007).
-
(2007)
J. Med. Genet.
, vol.44
, pp. 779-783
-
-
Tomita-Mitchell, A.1
Maslen, C.L.2
Morris, C.D.3
Garg, V.4
Goldmuntz, E.5
-
166
-
-
56649112929
-
GATA4 mutations in 486 Chinese patients with congenital heart disease
-
Zhang W, Li X, Shen A, Jiao W, Guan W, Li Z: GATA4 mutations in 486 Chinese patients with congenital heart disease. Eur. J. Med. Genet. 51, 527-535 (2008).
-
(2008)
Eur. J. Med. Genet.
, vol.51
, pp. 527-535
-
-
Zhang, W.1
Li, X.2
Shen, A.3
Jiao, W.4
Guan, W.5
Li, Z.6
-
167
-
-
28444474221
-
CRELD1 and GATA4 gene analysis in patients with nonsyndromic atrioventricular canal defects
-
Sarkozy A, Esposito G, Conti E et al.: CRELD1 and GATA4 gene analysis in patients with nonsyndromic atrioventricular canal defects. Am. J. Med. Genet. 139 (3), 236-238 (2005).
-
(2005)
Am. J. Med. Genet.
, vol.139
, Issue.3
, pp. 236-238
-
-
Sarkozy, A.1
Esposito, G.2
Conti, E.3
-
168
-
-
34547137690
-
Mutations in the 3'-untranslated region of GATA4 as molecular hotspots for congenital heart disease (CHD)
-
Reamon-Buettner SM, Cho SH, Borlak J: Mutations in the 3'-untranslated region of GATA4 as molecular hotspots for congenital heart disease (CHD). Med. Genet. 8, 38 (2007).
-
(2007)
Med. Genet.
, vol.8
, pp. 38
-
-
Reamon-Buettner, S.M.1
Cho, S.H.2
Borlak, J.3
-
169
-
-
69549138482
-
GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling
-
Kodoa K, Nishizawa T, Furutanib M et al.: GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling. Proc. Natl Acad. Sci. USA 106, 33 (2009).
-
(2009)
Proc. Natl. Acad. Sci. USA
, vol.106
, pp. 33
-
-
Kodoa, K.1
Nishizawa, T.2
Furutanib, M.3
-
170
-
-
0027454207
-
Mapping a gene for familial situs abnormalities to human chromosome Xq24-q27.1
-
Casey B, Devoto M, Jones K, Ballabio A: Mapping a gene for familial situs abnormalities to human chromosome Xq24-q27.1. Nat. Genet. 403-407 (2003).
-
(2003)
Nat. Genet.
, vol.403-407
-
-
Casey, B.1
Devoto, M.2
Jones, K.3
Ballabio, A.4
-
171
-
-
77952487744
-
-
Ferencz C, Loffredo CA, Correa-Villasenor A, Wilson PD Eds. Futura Publishing, Armonk, NY, USA
-
Defects of Laterality and Looping. Ferencz C, Loffredo CA, Correa-Villasenor A, Wilson PD (Eds). Futura Publishing, Armonk, NY, USA (2007).
-
(2007)
Defects of Laterality and Looping.
-
-
-
172
-
-
16944364984
-
X-linked situs abnormalities result from mutations in ZIC3
-
Gebbia M, Ferrero GB, Pilia G et al.: X-linked situs abnormalities result from mutations in ZIC3. Nat. Genet. 17, 305-308 (1997).
-
(1997)
Nat. Genet.
, vol.17
, pp. 305-308
-
-
Gebbia, M.1
Ferrero, G.B.2
Pilia, G.3
-
173
-
-
0033822768
-
Xlinked transposition of the great arteries and incomplete penetrance among males with a nonsense mutation in ZIC3
-
Megarbane A, Salem N, Stephan E et al.: Xlinked transposition of the great arteries and incomplete penetrance among males with a nonsense mutation in ZIC3. Eur. J. Hum. Genet. 8, 704-708 (2000).
-
(2000)
Eur. J. Hum. Genet.
, vol.8
, pp. 704-708
-
-
Megarbane, A.1
Salem, N.2
Stephan, E.3
-
174
-
-
16944362226
-
A submicroscopic deletion in Xq26 associated with familial situs ambiguus
-
Ferrero GB, Gebbia M, Pilia G et al.: A submicroscopic deletion in Xq26 associated with familial situs ambiguus. Am. J. Hum. Genet. 61, 395-401 (1997).
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 395-401
-
-
Ferrero, G.B.1
Gebbia, M.2
Pilia, G.3
-
175
-
-
0347003520
-
Identification and functional analysis of ZIC3 mutations in heterotaxy and related congenital heart defects
-
Ware SM, Peng J, Zhu L et al.: Identification and functional analysis of ZIC3 mutations in heterotaxy and related congenital heart defects. Am. J. Hum. Genet. 74, 93-105 (2004).
-
(2004)
Am. J. Hum. Genet.
, vol.74
, pp. 93-105
-
-
Ware, S.M.1
Peng, J.2
Zhu, L.3
-
176
-
-
34248334109
-
Elucidation of penetrance variability of a zic3 mutation in a family with complex heart defects and functional analysis of zic3 mutations in the first zinc finger domain
-
Chhin B, Hatayama M, Bozon D et al.: Elucidation of penetrance variability of a zic3 mutation in a family with complex heart defects and functional analysis of zic3 mutations in the first zinc finger domain Hum. Mutat. 28 (6), 563-570 (2007).
-
(2007)
Hum. Mutat.
, vol.28
, Issue.6
, pp. 563-570
-
-
Chhin, B.1
Hatayama, M.2
Bozon, D.3
-
177
-
-
24344451553
-
SALL4 mutations in Okihiro syndrome (Duane-radial ray syndrome), acro-renal-ocular syndrome, and related disorders
-
Kohlhase J, Chitayat D, Kotzot D et al.: SALL4 mutations in Okihiro syndrome (Duane-radial ray syndrome), acro-renal-ocular syndrome, and related disorders. Hum. Mutat. 26, 176-183 (2005).
-
(2005)
Hum. Mutat.
, vol.26
, pp. 176-183
-
-
Kohlhase, J.1
Chitayat, D.2
Kotzot, D.3
-
178
-
-
0036848353
-
Okihiro syndrome is caused by SALL4 mutations
-
Kohlhase J, Heinrich M, Schubert L et al.: Okihiro syndrome is caused by SALL4 mutations. Hum. Mol. Genet. 11, 2979-2987 (2002).
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 2979-2987
-
-
Kohlhase, J.1
Heinrich, M.2
Schubert, L.3
-
179
-
-
0037488242
-
Mutations at the SALL4 locus on chromosome 20 result in a range of clinically overlapping phenotypes, including Okihiro syndrome, Holt-Oram syndrome, acro-renal-ocular syndrome, and patients previously reported to represent thalidomide embryopathy
-
Kohlhase J, Schubert L, LiebersM et al.: Mutations at the SALL4 locus on chromosome 20 result in a range of clinically overlapping phenotypes, including Okihiro syndrome, Holt-Oram syndrome, acro-renal-ocular syndrome, and patients previously reported to represent thalidomide embryopathy. J. Med. Genet. 40, 473-478 (2003).
-
(2003)
J. Med. Genet.
, vol.40
, pp. 473-478
-
-
Kohlhase, J.1
Schubert, L.2
Liebers, M.3
-
180
-
-
16544392649
-
Novel mutations in the gene SALL4 provide further evidence for acro-renal-ocular and Okihiro syndromes being allelic entities, and extend the phenotypic spectrum
-
Borozdin W, Wright MJ, Hennekam RCM et al.: Novel mutations in the gene SALL4 provide further evidence for acro-renal-ocular and Okihiro syndromes being allelic entities, and extend the phenotypic spectrum. J. Med. Genet. 41, E102 (2004).
-
(2004)
J. Med. Genet.
, vol.41
-
-
Borozdin, W.1
Wright, M.J.2
Hennekam, R.C.M.3
-
181
-
-
78650028859
-
Genetic variation of SAL-Like 4 (SALL4) in ventricular septal defect
-
DOI:10.1016/j.ijcard. 2009.05.067, Epub ahead of print
-
Wang B, Li L, Xie X et al.: Genetic variation of SAL-Like 4 (SALL4) in ventricular septal defect. Int. J. Cardiol. DOI:10.1016/j.ijcard. 2009.05.067 (2009) (Epub ahead of print).
-
(2009)
Int. J. Cardiol.
-
-
Wang, B.1
Li, L.2
Xie, X.3
-
182
-
-
28844459874
-
Identification and functional analysis of CITED2 mutations in patients with congenital heart defects
-
Sperling S, Grimm CH, Dunkel I et al.: Identification and functional analysis of CITED2 mutations in patients with congenital heart defects. Hum. Mutat. 26 (6), 575-582 (2005).
-
(2005)
Hum. Mutat.
, vol.26
, Issue.6
, pp. 575-582
-
-
Sperling, S.1
Grimm, C.H.2
Dunkel, I.3
-
183
-
-
43049105408
-
A loss-of-function mutation in the binding domain of HAND1 predicts hypoplasia of the human hearts
-
Reamon-Buettner SM, Ciribilli Y, Inga A, Borlak J: A loss-of-function mutation in the binding domain of HAND1 predicts hypoplasia of the human hearts. Hum. Mol. Genet. 17, 1397-1405 (2008).
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 1397-1405
-
-
Reamon-Buettner, S.M.1
Ciribilli, Y.2
Inga, A.3
Borlak, J.4
-
184
-
-
70350757745
-
A functional genetic study identiflies HAND1 mutations in septation defects of the human heart
-
Reamon-Buettner SM, Ciribilli Y, Traverso I, Kuhls B, Inga A, Borlak J: A functional genetic study identiflies HAND1 mutations in septation defects of the human heart. Hum. Mol. Genet. 18, 3567-3578 (2009).
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 3567-3578
-
-
Reamon-Buettner, S.M.1
Ciribilli, Y.2
Traverso, I.3
Kuhls, B.4
Inga, A.5
Borlak, J.6
-
185
-
-
50649120144
-
Novel TFPA2B mutation in nonsindromic patent ductus arteriosus
-
Khetyar M, Syrris P, Tinworth L, Abushaban L, Carter N: Novel TFPA2B mutation in nonsindromic patent ductus arteriosus. Genet. Test. 12, 457-459 (2008).
-
(2008)
Genet. Test.
, vol.12
, pp. 457-459
-
-
Khetyar, M.1
Syrris, P.2
Tinworth, L.3
Abushaban, L.4
Carter, N.5
-
186
-
-
26444605527
-
Mutational analysis of the PITX2 coding region revealed no common cause for transposition of the great arteries (dTGA)
-
Muncke N, Niesler B, Roeth R et al.: Mutational analysis of the PITX2 coding region revealed no common cause for transposition of the great arteries (dTGA). BMC Med. Genet. 6, 20 (2005).
-
(2005)
BMC Med. Genet.
, vol.6
, pp. 20
-
-
Muncke, N.1
Niesler, B.2
Roeth, R.3
-
187
-
-
10744226877
-
Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot
-
Pizzuti A, Sarkozy A, Newton AL et al.: Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot. Hum. Mutat. 22, 372-377 (2003).
-
(2003)
Hum. Mutat.
, vol.22
, pp. 372-377
-
-
Pizzuti, A.1
Sarkozy, A.2
Newton, A.L.3
-
188
-
-
12944255784
-
ZFPM2/FOG2 and HEY2 genes analysis in nonsyndromic tricuspid atresia
-
Sarkozy A, Conti E, D'Agostino R et al.: ZFPM2/FOG2 and HEY2 genes analysis in nonsyndromic tricuspid atresia. Am. J. Med. Genet. 133, 68-70 (2005).
-
(2005)
Am. J. Med. Genet.
, vol.133
, pp. 68-70
-
-
Sarkozy, A.1
Conti, E.2
D'Agostino, R.3
-
189
-
-
0035653927
-
Mutation analysis of Tbx1 in non-deleted patients with features of DGS/VCFS or isolated cardiovascular defects
-
Gong W, Gottlieb S, Collins J et al.: Mutation analysis of Tbx1 in non-deleted patients with features of DGS/VCFS or isolated cardiovascular defects. J. Med. Genet. 38, E45 (2001).
-
(2001)
J. Med. Genet.
, vol.38
-
-
Gong, W.1
Gottlieb, S.2
Collins, J.3
-
190
-
-
34247142485
-
TBX1 gene mutation screening in patients with non-syndromic Fallot Tetralogy
-
Cabuk F, Karabulut HG, Tuncali T, Karademir S, Bozdayi M, Tudie;kudie;n A: TBX1 gene mutation screening in patients with non-syndromic Fallot Tetralogy. Turk. J. Pediatr. 49 (1), 61-68 (2007).
-
(2007)
Turk. J. Pediatr.
, vol.49
, Issue.1
, pp. 61-68
-
-
Cabuk, F.1
Karabulut, H.G.2
Tuncali, T.3
Karademir, S.4
Bozdayi, M.5
Tudie6
kudie7
n, A.8
-
191
-
-
77951874996
-
Comprehensive genotype-phenotype analysis in 230 patients with Tetralogy of Fallot
-
DOI: jmg.2009.070391, Epub ahead of print
-
Rauch R, Hofbeck M, Zweier C et al.: Comprehensive genotype-phenotype analysis in 230 patients with Tetralogy of Fallot. J. Med. Genet. DOI: jmg.2009.070391 (2009) (Epub ahead of print).
-
(2009)
J. Med. Genet.
-
-
Rauch, R.1
Hofbeck, M.2
Zweier, C.3
-
192
-
-
7244238119
-
TBX5 mutations in non-Holt-Oram syndrome (HOS) malformed hearts
-
Buettner SM, Borlak J: TBX5 mutations in non-Holt-Oram syndrome (HOS) malformed hearts. Hum. Mutat. 24 (1), 104 (2004).
-
(2004)
Hum. Mutat.
, vol.24
, Issue.1
, pp. 104
-
-
Buettner, S.M.1
Borlak, J.2
-
193
-
-
70449729496
-
The mechanism of TBX5 abnormal expression in simple congenital heart disease
-
Xin N, Qiu GR, Gong LG, Xu XY, Sun KL: The mechanism of TBX5 abnormal expression in simple congenital heart disease. Yi Chuan. 31 (4), 374-380 (2009).
-
(2009)
Yi Chuan.
, vol.31
, Issue.4
, pp. 374-380
-
-
Xin, N.1
Qiu, G.R.2
Gong, L.G.3
Xu, X.Y.4
Sun, K.L.5
-
194
-
-
34547738523
-
Mutations in cardiac T-Box factor gene TBX20 are associated with diverse cardiac pathologies, including defects of septation and valvulogenesis and cardiomyopathy
-
Kirk EP, Sunde M, Costa MW et al.: Mutations in cardiac T-Box factor gene TBX20 are associated with diverse cardiac pathologies, including defects of septation and valvulogenesis and cardiomyopathy. Am. J. Hum. Genet. 81, 280-291 (2007).
-
(2007)
Am. J. Hum. Genet.
, vol.81
, pp. 280-291
-
-
Kirk, E.P.1
Sunde, M.2
Costa, M.W.3
-
195
-
-
56649091211
-
T-box transcription factor TBX20 mutations in Chinese patients with congenital heart disease
-
Liu C, Shen A, Li X, Jiao W, Zhang X, Li Z: T-box transcription factor TBX20 mutations in Chinese patients with congenital heart disease. Eur. J. Med. Genet. 51, 580-587 (2008).
-
(2008)
Eur. J. Med. Genet.
, vol.51
, pp. 580-587
-
-
Liu, C.1
Shen, A.2
Li, X.3
Jiao, W.4
Zhang, X.5
Li, Z.6
-
196
-
-
77951566722
-
A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects
-
DOI: 10.1136/jmg.2009.069997, Epub ahead of print
-
Megarbane O, Dietz R, Stiller B et al.: A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects. J. Med. Genet. DOI: 10.1136/jmg.2009.069997 (2009) (Epub ahead of print).
-
(2009)
J. Med. Genet.
-
-
Megarbane, O.1
Dietz, R.2
Stiller, B.3
-
197
-
-
33646249816
-
Cardiac developmental biology: From flies to humans
-
Shiojima I, Komuro I: Cardiac developmental biology: from flies to humans. Jpn. J. Physiol. 55, 245-254 (2005).
-
(2005)
Jpn. J. Physiol.
, vol.55
, pp. 245-254
-
-
Shiojima, I.1
Komuro, I.2
-
198
-
-
77952467922
-
-
Elsevier
-
Mandel EM, Callis TE, Wang D-Z, Conlon FL: Transcriptional Mechanisms of Congenital Heart Disease 2 (1), Elsevier (2005).
-
(2005)
Transcriptional Mechanisms of Congenital Heart Disease
, vol.2
, Issue.1
-
-
Mandel, E.M.1
Callis, T.E.2
Wang, D.-Z.3
Conlon, F.L.4
|