-
1
-
-
0037134945
-
The incidence of congenital heart disease
-
J.I. Hoffman, and S. Kaplan The incidence of congenital heart disease J. Am. Coll. Cardiol. 39 2002 1890 1900
-
(2002)
J. Am. Coll. Cardiol.
, vol.39
, pp. 1890-1900
-
-
Hoffman, J.I.1
Kaplan, S.2
-
2
-
-
0037069385
-
Finding genetic contributions to sporadic disease: A recessive locus at 12q24 commonly contributes to patent ductus arteriosus
-
A. Mani, S.M. Meraji, R. Houshyar, J. Radhakrishnan, A. Mani, M. Ahangar, T.M. Rezaie, M.A. Taghavinejad, B. Broumand, H. Zhao, and et al. Finding genetic contributions to sporadic disease: a recessive locus at 12q24 commonly contributes to patent ductus arteriosus Proc. Natl. Acad. Sci. USA 99 2002 15054 15059
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 15054-15059
-
-
Mani, A.1
Meraji, S.M.2
Houshyar, R.3
Radhakrishnan, J.4
Mani, A.5
Ahangar, M.6
Rezaie, T.M.7
Taghavinejad, M.A.8
Broumand, B.9
Zhao, H.10
-
3
-
-
0024431232
-
Endothelin is a potent constrictor of the lamb ductus arteriosus
-
F. Coceani, C. Armstrong, and L. Kelsey Endothelin is a potent constrictor of the lamb ductus arteriosus Can. J. Physiol. Pharmacol. 67 1989 902 904
-
(1989)
Can. J. Physiol. Pharmacol.
, vol.67
, pp. 902-904
-
-
Coceani, F.1
Armstrong, C.2
Kelsey, L.3
-
4
-
-
0028020412
-
Control of the ductus arteriosus - A new function for cytochrome P450, endothelin and nitric oxide
-
F. Coceani Control of the ductus arteriosus - a new function for cytochrome P450, endothelin and nitric oxide Biochem. Pharmacol. 48 1994 1315 1318
-
(1994)
Biochem. Pharmacol.
, vol.48
, pp. 1315-1318
-
-
Coceani, F.1
-
5
-
-
0014704774
-
Morphology and structure of the ductus arteriosus (Botallo's) and genesis of the ligamentum arteriosum in man
-
R. Muti [Morphology and structure of the ductus arteriosus (Botallo's) and genesis of the ligamentum arteriosum in man] Biol. Lat. 22 1970 25 40
-
(1970)
Biol. Lat.
, vol.22
, pp. 25-40
-
-
Muti, R.1
-
6
-
-
0016415044
-
Functional architecture of the ligamentum arteriosum in adults
-
O.S. Garcia [Functional architecture of the ligamentum arteriosum in adults] Acta Anat. (Basel) 91 1975 313 320
-
(1975)
Acta Anat. (Basel)
, vol.91
, pp. 313-320
-
-
Garcia, O.S.1
-
7
-
-
0017648898
-
Commentary: Patent ductus arteriosus and the respiratory distress syndrome - A perspective
-
W.M. Gersony Commentary: patent ductus arteriosus and the respiratory distress syndrome - a perspective J. Pediatr. 91 1977 624 625
-
(1977)
J. Pediatr.
, vol.91
, pp. 624-625
-
-
Gersony, W.M.1
-
8
-
-
84905259560
-
Mortality associated with pulmonary hypertension in congenital rubella syndrome
-
M. Toizumi, H. Motomura, H.M. Vo, K. Takahashi, E. Pham, H.A. Nguyen, T.H. Le, M. Hashizume, K. Ariyoshi, D.A. Dang, and et al. Mortality associated with pulmonary hypertension in congenital rubella syndrome Pediatrics 134 2014 e519 e526
-
(2014)
Pediatrics
, vol.134
, pp. e519-e526
-
-
Toizumi, M.1
Motomura, H.2
Vo, H.M.3
Takahashi, K.4
Pham, E.5
Nguyen, H.A.6
Le, T.H.7
Hashizume, M.8
Ariyoshi, K.9
Dang, D.A.10
-
9
-
-
0034022637
-
Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus
-
M. Satoda, F. Zhao, G.A. Diaz, J. Burn, J. Goodship, H.R. Davidson, M.E. Pierpont, and B.D. Gelb Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus Nat. Genet. 25 2000 42 46
-
(2000)
Nat. Genet.
, vol.25
, pp. 42-46
-
-
Satoda, M.1
Zhao, F.2
Diaz, G.A.3
Burn, J.4
Goodship, J.5
Davidson, H.R.6
Pierpont, M.E.7
Gelb, B.D.8
-
10
-
-
20044365972
-
Syndromic patent ductus arteriosus: Evidence for haploinsufficient TFAP2B mutations and identification of a linked sleep disorder
-
A. Mani, J. Radhakrishnan, A. Farhi, K.S. Carew, C.A. Warnes, C. Nelson-Williams, R.W. Day, B. Pober, M.W. State, and R.P. Lifton Syndromic patent ductus arteriosus: evidence for haploinsufficient TFAP2B mutations and identification of a linked sleep disorder Proc. Natl. Acad. Sci. USA 102 2005 2975 2979
-
(2005)
Proc. Natl. Acad. Sci. USA
, vol.102
, pp. 2975-2979
-
-
Mani, A.1
Radhakrishnan, J.2
Farhi, A.3
Carew, K.S.4
Warnes, C.A.5
Nelson-Williams, C.6
Day, R.W.7
Pober, B.8
State, M.W.9
Lifton, R.P.10
-
11
-
-
84900328675
-
A form of the metabolic syndrome associated with mutations in DYRK1B
-
A.R. Keramati, M. Fathzadeh, G.W. Go, R. Singh, M. Choi, S. Faramarzi, S. Mane, M. Kasaei, K. Sarajzadeh-Fard, J. Hwa, and et al. A form of the metabolic syndrome associated with mutations in DYRK1B N. Engl. J. Med. 370 2014 1909 1919
-
(2014)
N. Engl. J. Med.
, vol.370
, pp. 1909-1919
-
-
Keramati, A.R.1
Fathzadeh, M.2
Go, G.W.3
Singh, R.4
Choi, M.5
Faramarzi, S.6
Mane, S.7
Kasaei, M.8
Sarajzadeh-Fard, K.9
Hwa, J.10
-
12
-
-
84940108581
-
Nonalcoholic fatty liver disease induced by noncanonical Wnt and its rescue by Wnt3a
-
S. Wang, K. Song, R. Srivastava, C. Dong, G.W. Go, N. Li, Y. Iwakiri, and A. Mani Nonalcoholic fatty liver disease induced by noncanonical Wnt and its rescue by Wnt3a FASEB J. 29 2015 3436 3445
-
(2015)
FASEB J.
, vol.29
, pp. 3436-3445
-
-
Wang, S.1
Song, K.2
Srivastava, R.3
Dong, C.4
Go, G.W.5
Li, N.6
Iwakiri, Y.7
Mani, A.8
-
13
-
-
27344435774
-
Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles
-
A. Subramanian, P. Tamayo, V.K. Mootha, S. Mukherjee, B.L. Ebert, M.A. Gillette, A. Paulovich, S.L. Pomeroy, T.R. Golub, E.S. Lander, and J.P. Mesirov Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles Proc. Natl. Acad. Sci. USA 102 2005 15545 15550
-
(2005)
Proc. Natl. Acad. Sci. USA
, vol.102
, pp. 15545-15550
-
-
Subramanian, A.1
Tamayo, P.2
Mootha, V.K.3
Mukherjee, S.4
Ebert, B.L.5
Gillette, M.A.6
Paulovich, A.7
Pomeroy, S.L.8
Golub, T.R.9
Lander, E.S.10
Mesirov, J.P.11
-
14
-
-
0038054341
-
PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes
-
V.K. Mootha, C.M. Lindgren, K.F. Eriksson, A. Subramanian, S. Sihag, J. Lehar, P. Puigserver, E. Carlsson, M. Ridderstråle, E. Laurila, and et al. PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes Nat. Genet. 34 2003 267 273
-
(2003)
Nat. Genet.
, vol.34
, pp. 267-273
-
-
Mootha, V.K.1
Lindgren, C.M.2
Eriksson, K.F.3
Subramanian, A.4
Sihag, S.5
Lehar, J.6
Puigserver, P.7
Carlsson, E.8
Ridderstråle, M.9
Laurila, E.10
-
15
-
-
84879001958
-
De novo mutations in histone-modifying genes in congenital heart disease
-
S. Zaidi, M. Choi, H. Wakimoto, L. Ma, J. Jiang, J.D. Overton, A. Romano-Adesman, R.D. Bjornson, R.E. Breitbart, K.K. Brown, and et al. De novo mutations in histone-modifying genes in congenital heart disease Nature 498 2013 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
-
17
-
-
0347955358
-
Histone methyltransferases direct different degrees of methylation to define distinct chromatin domains
-
J.C. Rice, S.D. Briggs, B. Ueberheide, C.M. Barber, J. Shabanowitz, D.F. Hunt, Y. Shinkai, and C.D. Allis Histone methyltransferases direct different degrees of methylation to define distinct chromatin domains Mol. Cell 12 2003 1591 1598
-
(2003)
Mol. Cell
, vol.12
, pp. 1591-1598
-
-
Rice, J.C.1
Briggs, S.D.2
Ueberheide, B.3
Barber, C.M.4
Shabanowitz, J.5
Hunt, D.F.6
Shinkai, Y.7
Allis, C.D.8
-
18
-
-
33645239290
-
PRISM/PRDM6, a transcriptional repressor that promotes the proliferative gene program in smooth muscle cells
-
C.A. Davis, M. Haberland, M.A. Arnold, L.B. Sutherland, O.G. McDonald, J.A. Richardson, G. Childs, S. Harris, G.K. Owens, and E.N. Olson PRISM/PRDM6, a transcriptional repressor that promotes the proliferative gene program in smooth muscle cells Mol. Cell. Biol. 26 2006 2626 2636
-
(2006)
Mol. Cell. Biol.
, vol.26
, pp. 2626-2636
-
-
Davis, C.A.1
Haberland, M.2
Arnold, M.A.3
Sutherland, L.B.4
McDonald, O.G.5
Richardson, J.A.6
Childs, G.7
Harris, S.8
Owens, G.K.9
Olson, E.N.10
-
19
-
-
38849110886
-
Myocardin regulates expression of contractile genes in smooth muscle cells and is required for closure of the ductus arteriosus in mice
-
J. Huang, L. Cheng, J. Li, M. Chen, D. Zhou, M.M. Lu, A. Proweller, J.A. Epstein, and M.S. Parmacek Myocardin regulates expression of contractile genes in smooth muscle cells and is required for closure of the ductus arteriosus in mice J. Clin. Invest. 118 2008 515 525
-
(2008)
J. Clin. Invest.
, vol.118
, pp. 515-525
-
-
Huang, J.1
Cheng, L.2
Li, J.3
Chen, M.4
Zhou, D.5
Lu, M.M.6
Proweller, A.7
Epstein, J.A.8
Parmacek, M.S.9
-
20
-
-
79960915772
-
A heart-hand syndrome gene: Tfap2b plays a critical role in the development and remodeling of mouse ductus arteriosus and limb patterning
-
F. Zhao, A.K. Bosserhoff, R. Buettner, and M. Moser A heart-hand syndrome gene: Tfap2b plays a critical role in the development and remodeling of mouse ductus arteriosus and limb patterning PLoS ONE 6 2011 e22908
-
(2011)
PLoS ONE
, vol.6
, pp. e22908
-
-
Zhao, F.1
Bosserhoff, A.K.2
Buettner, R.3
Moser, M.4
-
21
-
-
36549071997
-
Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections
-
D.C. Guo, H. Pannu, V. Tran-Fadulu, C.L. Papke, R.K. Yu, N. Avidan, S. Bourgeois, A.L. Estrera, H.J. Safi, E. Sparks, and et al. Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections Nat. Genet. 39 2007 1488 1493
-
(2007)
Nat. Genet.
, vol.39
, pp. 1488-1493
-
-
Guo, D.C.1
Pannu, H.2
Tran-Fadulu, V.3
Papke, C.L.4
Yu, R.K.5
Avidan, N.6
Bourgeois, S.7
Estrera, A.L.8
Safi, H.J.9
Sparks, E.10
-
22
-
-
33644627494
-
Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus
-
L. Zhu, R. Vranckx, P. Khau Van Kien, A. Lalande, N. Boisset, F. Mathieu, M. Wegman, L. Glancy, J.M. Gasc, F. Brunotte, and et al. Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus Nat. Genet. 38 2006 343 349
-
(2006)
Nat. Genet.
, vol.38
, pp. 343-349
-
-
Zhu, L.1
Vranckx, R.2
Khau Van Kien, P.3
Lalande, A.4
Boisset, N.5
Mathieu, F.6
Wegman, M.7
Glancy, L.8
Gasc, J.M.9
Brunotte, F.10
|