Cardiovascular defects in a mouse model of HOXA1 syndrome.
about
Rediscovering ACE: novel insights into the many roles of the angiotensin-converting enzymeEvolutionary and developmental origins of the cardiac neural crest: building a divided outflow tractInterrogating congenital heart defects with noninvasive fetal echocardiography in a mouse forward genetic screen.Dynamic regulation of Nanog and stem cell-signaling pathways by Hoxa1 during early neuro-ectodermal differentiation of ES cells.The OSR1 rs12329305 polymorphism contributes to the development of congenital malformations in cases of stillborn/neonatal deathTranscription profiles of endothelial cells in the rat ductus arteriosus during a perinatal period.Insufficient versican cleavage and Smad2 phosphorylation results in bicuspid aortic and pulmonary valvesUnderstanding the molecular mechanisms of human microtia via a pig model of HOXA1 syndromeCongenital cardiac anomalies and white matter injuryA roadmap to investigate the genetic basis of bicuspid aortic valve and its complications: insights from the International BAVCon (Bicuspid Aortic Valve Consortium).Topographic patterns of vascular disease: HOX proteins as determining factors?Nkx2-5 mediates differential cardiac differentiation through interaction with Hoxa10.HOXA1 binds RBCK1/HOIL-1 and TRAF2 and modulates the TNF/NF-κB pathway in a transcription-independent manner.Midbrain and hindbrain malformations: advances in clinical diagnosis, imaging, and genetics.Glimpse into Hox and tale regulation of cell differentiation and reprogramming.Tetralogy of Fallot with coarctation of the aorta: a newly recognised developmental and anatomic syndrome.Review of molecular and mechanical interactions in the aortic valve and aorta: implications for the shared pathogenesis of aortic valve disease and aortopathy.Role of Hox genes in stem cell differentiation.Gene regulatory networks in neural cell fate acquisition from genome-wide chromatin association of Geminin and Zic1The canonical Wingless signaling pathway is required but not sufficient for inflow tract formation in the Drosophila melanogaster heart.Developmental vascular remodeling defects and postnatal kidney failure in mice lacking Gpr116 (Adgrf5) and Eltd1 (Adgrl4).Cardiac, mandibular and thymic phenotypical association indicates that cranial neural crest underlies bicuspid aortic valve formation in hamstersGenetic insights into bicuspid aortic valve formation.HOXA1 gene is not potentially related to ventricular septal defect in Chinese children.Proximate cause, anatomical correlates, and obstetrical implication of a supernumerary lumbar vertebra in humans.Hox Genes in Cardiovascular Development and Diseases.Muscle-specific regulation of right ventricular transcriptional responses to chronic hypoxia-induced hypertrophy by the muscle ring finger-1 (MuRF1) ubiquitin ligase in miceBicuspid aortic valve formation: mutation leads to abnormal lineage patterning of neural crest cells and the second heart fieldSingle cell RNA-seq and ATAC-seq analysis of cardiac progenitor cell transition states and lineage settlement
P2860
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P2860
Cardiovascular defects in a mouse model of HOXA1 syndrome.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Cardiovascular defects in a mouse model of HOXA1 syndrome.
@ast
Cardiovascular defects in a mouse model of HOXA1 syndrome.
@en
type
label
Cardiovascular defects in a mouse model of HOXA1 syndrome.
@ast
Cardiovascular defects in a mouse model of HOXA1 syndrome.
@en
prefLabel
Cardiovascular defects in a mouse model of HOXA1 syndrome.
@ast
Cardiovascular defects in a mouse model of HOXA1 syndrome.
@en
P2860
P356
P1476
Cardiovascular defects in a mouse model of HOXA1 syndrome.
@en
P2093
Mario R Capecchi
Nadja Makki
P2860
P356
10.1093/HMG/DDR434
P577
2011-09-22T00:00:00Z