Maternal somatic mosaicism of FOXF1 mutation causes recurrent alveolar capillary dysplasia with misalignment of pulmonary veins in siblings.

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Interstitial lung disease in newborns.

P2860

Q39212013-F9877498-B598-4DA2-BEED-F4EA8CF3A0A2

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Maternal somatic mosaicism of FOXF1 mutation causes recurrent alveolar capillary dysplasia with misalignment of pulmonary veins in siblings.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年學術文章

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name

Maternal somatic mosaicism of ...... f pulmonary veins in siblings.

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Maternal somatic mosaicism of ...... f pulmonary veins in siblings.

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type

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Maternal somatic mosaicism of ...... f pulmonary veins in siblings.

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Maternal somatic mosaicism of ...... f pulmonary veins in siblings.

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Maternal somatic mosaicism of ...... f pulmonary veins in siblings.

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Maternal somatic mosaicism of ...... f pulmonary veins in siblings.

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P1476

Maternal somatic mosaicism of ...... f pulmonary veins in siblings.

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Fai Man Ivan Lo

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

Ho Ming Luk

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

Kwong Wai Richard Choy

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

Ming For Tony Tong

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

On Kit Wong

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

Tao Tang

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P2860

FREAC-1 contains a cell-type-specific transcriptional activation domain and is expressed in epithelial-mesenchymal interfaces

Differential activation of lung-specific genes by two forkhead proteins, FREAC-1 and FREAC-2

Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations

Forkhead box F1 is essential for migration of mesenchymal cells and directly induces integrin-beta3 expression

Misalignment of lung vessels and alveolar capillary dysplasia: a cause of persistent pulmonary hypertension.

Persistent pulmonary hypertension of the newborn due to alveolar capillary dysplasia.

Expanding the phenotype of alveolar capillary dysplasia (ACD).

Small noncoding differentially methylated copy-number variants, including lncRNA genes, cause a lethal lung developmental disorder.

A familial case of alveolar capillary dysplasia with misalignment of pulmonary veins supports paternal imprinting of FOXF1 in human

Novel FOXF1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domain.

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1942-1944

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scholarly article

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10.1002/AJMG.A.37660

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English

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170

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2016-04-25T00:00:00Z

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27109257

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P921

sibling

Maternal somatic mosaicism of FOXF1 mutation causes recurrent alveolar capillary dysplasia with misalignment of pulmonary veins in siblings.

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P2860

P2860

Maternal somatic mosaicism of FOXF1 mutation causes recurrent alveolar capillary dysplasia with misalignment of pulmonary veins in siblings.

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P1476

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P2860

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P1476

P2093

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P304

P31

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P478

P577

P698

P921