Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations
about
Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studiesIdentification of de novo mutations and rare variants in hypoplastic left heart syndromeVACTERL/VATER AssociationPreparing for the first breath: genetic and cellular mechanisms in lung developmentThe genetic landscape and clinical implications of vertebral anomalies in VACTERL associationMechanisms underlying structural variant formation in genomic disordersInterstitial Lung Disease in Childhood: Clinical and Genetic AspectsAn official American Thoracic Society clinical practice guideline: classification, evaluation, and management of childhood interstitial lung disease in infancyUnique aspects of the developing lung circulation: structural development and regulation of vasomotor toneGpr177 regulates pulmonary vasculature developmentThree-dimensional reconstruction identifies misaligned pulmonary veins as intrapulmonary shunt vessels in alveolar capillary dysplasia.Integrative analysis of DNA methylation and gene expression data identifies EPAS1 as a key regulator of COPD.Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins (ACD/MPV): A Case Series.Antenatal gastrointestinal anomalies in neonates subsequently found to have alveolar capillary dysplasia.Long noncoding RNAs are spatially correlated with transcription factors and regulate lung development.Genome-wide association study for radiographic vertebral fractures: a potential role for the 16q24 BMD locusPathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veinsThe molecular era of surfactant biology.Comparative transcriptome analyses indicate molecular homology of zebrafish swimbladder and mammalian lung.Review of genetic factors in intestinal malrotation.Mutational analysis of NOG in esophageal atresia and tracheoesophageal fistula patients.Genetic basis of congenital cardiovascular malformationsThe OSR1 rs12329305 polymorphism contributes to the development of congenital malformations in cases of stillborn/neonatal deathContribution of rare copy number variants to isolated human malformations.Diseases of pulmonary surfactant homeostasis.On the spot: very local chromosomal rearrangements.Long-term outcomes of adults with features of VACTERL association.FOXF1 mediates mesenchymal stem cell fusion-induced reprogramming of lung cancer cellsEndothelial cell-specific deletion of transcription factor FoxM1 increases urethane-induced lung carcinogenesis.Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL associationRare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture.Multiple faces of FoxM1 transcription factor: lessons from transgenic mouse models.Genome-wide association study of maternal and inherited effects on left-sided cardiac malformationsComparative analyses of lung transcriptomes in patients with alveolar capillary dysplasia with misalignment of pulmonary veins and in foxf1 heterozygous knockout miceDetection of clinically relevant exonic copy-number changes by array CGH.A consensus approach to the classification of pediatric pulmonary hypertensive vascular disease: Report from the PVRI Pediatric Taskforce, Panama 2011.Alveolar capillary dysplasiaMolecular and clinical analyses of 16q24.1 duplications involving FOXF1 identify an evolutionarily unstable large minisatelliteGenetic Basis of Children's Interstitial Lung Disease.PCSK5 mutation in a patient with the VACTERL association.
P2860
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P2860
Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations
description
2009 nî lūn-bûn
@nan
2009 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Genomic and genic deletions of ...... plasia and other malformations
@ast
Genomic and genic deletions of ...... plasia and other malformations
@en
Genomic and genic deletions of ...... plasia and other malformations
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Genomic and genic deletions of ...... plasia and other malformations
@nl
type
label
Genomic and genic deletions of ...... plasia and other malformations
@ast
Genomic and genic deletions of ...... plasia and other malformations
@en
Genomic and genic deletions of ...... plasia and other malformations
@en-gb
Genomic and genic deletions of ...... plasia and other malformations
@nl
prefLabel
Genomic and genic deletions of ...... plasia and other malformations
@ast
Genomic and genic deletions of ...... plasia and other malformations
@en
Genomic and genic deletions of ...... plasia and other malformations
@en-gb
Genomic and genic deletions of ...... plasia and other malformations
@nl
P2093
P2860
P50
P921
P3181
P1476
Genomic and genic deletions of ...... plasia and other malformations
@en
P2093
Andrew G Nicholson
Ankita Patel
Bassem A Bejjani
Charles Shaw-Smith
Claire Langston
Daniel J Driscoll
Diana Rajan
Duncan McRae
Elaine H Zackai
Elena Prigmore
P2860
P304
P3181
P356
10.1016/J.AJHG.2009.05.005
P407
P577
2009-06-01T00:00:00Z