Congenital diaphragmatic hernias: from genes to mechanisms to therapies.

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Abrogation of TGF-beta signalling in TAGLN expressing cells recapitulates Pentalogy of Cantrell in the mouse.Developmental origin and morphogenesis of the diaphragm, an essential mammalian muscle.

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P2860

Congenital diaphragmatic hernias: from genes to mechanisms to therapies.

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年论文

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2017年论文

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name

Congenital diaphragmatic hernias: from genes to mechanisms to therapies.

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Congenital diaphragmatic hernias: from genes to mechanisms to therapies.

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Congenital diaphragmatic hernias: from genes to mechanisms to therapies.

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P1476

Congenital diaphragmatic hernias: from genes to mechanisms to therapies

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David J McCulley

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Eric Bogenschutz

http://www.w3.org/2001/XMLSchema#string

Julia Wynn

http://www.w3.org/2001/XMLSchema#string

Linshan Shang

http://www.w3.org/2001/XMLSchema#string

Xin Sun

http://www.w3.org/2001/XMLSchema#string

Yufeng Shen

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Creative Commons Attribution

P2860

Novel GATA6 mutations in patients with pancreatic agenesis and congenital heart malformations

Fog2 is required for normal diaphragm and lung development in mice and humans

Mutations in the human delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis

Prenatal interventions for congenital diaphragmatic hernia for improving outcomes

Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation

Characterization of the chromosome 1q41q42.12 region, and the candidate gene DISP1, in patients with CDH

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5

Identification of COUP-TFII orphan nuclear receptor as a retinoic acid-activated receptor

Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome

GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling

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955-970

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scholarly article

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10.1242/DMM.028365

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P478

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W K Chung

Gabrielle Kardon

Kate G Ackerman

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ScienceSource

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2017-08-01T00:00:00Z

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28768736

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hernia

congenital diaphragmatic hernia

birth defect

P932

5560060

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Congenital diaphragmatic hernias: from genes to mechanisms to therapies.

about

P2860

P2860

Congenital diaphragmatic hernias: from genes to mechanisms to therapies.

description

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type

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prefLabel

P1433

P1476

P2093

P275

P2860

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P31

P356

P433

P478

P50

P5008

P577

P698

P921

P932

P356

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P2093

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P2860

P304

P31

P356

P433

P478

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P5008

P577

P698

P921

P932