Congenital diaphragmatic hernia and pulmonary hypoplasia: New insights from developmental biology and genetics

被引:56
作者
Ackerman, Kate G. [1 ]
Pober, Barbara R. [1 ]
机构
[1] Harvard Univ, Sch Med, Cambridge, MA 02138 USA
关键词
MODEL;
D O I
10.1002/ajmg.c.30133
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:105 / 108
页数:4
相关论文
共 23 条
[1]   Fog2 is required for normal diaphragm and lung development in mice and humans [J].
Ackerman, KG ;
Herron, BJ ;
Vargas, SO ;
Huang, HL ;
Tevosian, SG ;
Kochilas, L ;
Rao, C ;
Pober, BR ;
Babiuk, RP ;
Epstein, JA ;
Greer, JJ ;
Beier, DR .
PLOS GENETICS, 2005, 1 (01) :58-65
[2]  
ACKERMAN KG, 2006, IN PRESS AM J RESP C
[3]  
Andersen DH., 1941, AM J DIS CHILD, V62, P888
[4]   Retinoid X receptor a represses GATA-4-mediated transcription via a retinoid-dependent interaction with the cardiac-enriched repressor FOG-2 [J].
Clabby, ML ;
Robinson, TA ;
Quigley, HF ;
Wilson, DB ;
Kelly, DP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (08) :5760-5767
[5]   Outcomes of congenital diaphragmatic hernia: A population-based study in western Australia [J].
Colvin, J ;
Bower, C ;
Dickinson, JE ;
Sokol, J .
PEDIATRICS, 2005, 116 (03) :E356-E363
[6]  
Gray H., 2000, ANATOMY HUMAN BODY, V20th
[7]   Congenital diaphragmatic hernia - A historical review [J].
Irish, MS ;
Holm, BA ;
Glick, PL .
CLINICS IN PERINATOLOGY, 1996, 23 (04) :625-+
[8]   GATA-4: FOG interactions regulate gastric epithelial development in the mouse [J].
Jacobsen, CM ;
Mannisto, S ;
Porter-Tinge, S ;
Genova, E ;
Parviainen, H ;
Heikinheimo, M ;
Adameyko, II ;
Tevosian, SG ;
Wilson, DB .
DEVELOPMENTAL DYNAMICS, 2005, 234 (02) :355-362
[9]   Impaired mesenchymal cell function in Gata4 mutant mice leads to diaphragmatic hernias and primary lung defects [J].
Jay, Patrick Y. ;
Bielinska, Malgorzata ;
Erlich, Jonathan M. ;
Mannisto, Susanna ;
Pu, William T. ;
Heikinheimo, Markku ;
Wilson, David B. .
DEVELOPMENTAL BIOLOGY, 2007, 301 (02) :602-614
[10]   Findings from aCGH in patients with congenital diaphragmatic hernia (CDH): A possible locus for Fryns syndrome [J].
Kantarci, S ;
Casavant, D ;
Prada, C ;
Russell, M ;
Byrne, J ;
Haug, LW ;
Jennings, R ;
Manning, S ;
Boyd, TK ;
Fryns, JP ;
Holmes, LB ;
Donahoe, PK ;
Lee, C ;
Kimonis, V ;
Pober, BR .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2006, 140A (01) :17-23