Cyp26 genes a1, b1 and c1 are down-regulated in Tbx1 null mice and inhibition of Cyp26 enzyme function produces a phenocopy of DiGeorge Syndrome in the chick.
about
Of mice and men: molecular genetics of congenital heart diseaseConnecting teratogen-induced congenital heart defects to neural crest cells and their effect on cardiac functionThe neural crest in cardiac congenital anomaliesTbx1 regulates the BMP-Smad1 pathway in a transcription independent manner.Prdm1 functions in the mesoderm of the second heart field, where it interacts genetically with Tbx1, during outflow tract morphogenesis in the mouse embryoHes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndromeTbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectodermThe mammalian doublesex homolog DMRT1 is a transcriptional gatekeeper that controls the mitosis versus meiosis decision in male germ cellsRoles of retinoic acid and Tbx1/10 in pharyngeal segmentation: amphioxus and the ancestral chordate conditionEvolutionary and developmental origins of the cardiac neural crest: building a divided outflow tractIdentification of putative retinoic acid target genes downstream of mesenchymal Tbx1 during inner ear developmentTbx1 controls the morphogenesis of pharyngeal pouch epithelia through mesodermal Wnt11r and Fgf8a.Tbx1 and Brn4 regulate retinoic acid metabolic genes during cochlear morphogenesis.Decreased levels of embryonic retinoic acid synthesis accelerate recovery from arterial growth delay in a mouse model of DiGeorge syndromeA case of 22q11.2 deletion syndrome with Peters anomaly, congenital glaucoma, and heterozygous mutation in CYP1B1Endothelial neuropilin disruption in mice causes DiGeorge syndrome-like malformations via mechanisms distinct to those caused by loss of Tbx1Cyp26 Enzymes Facilitate Second Heart Field Progenitor Addition and Maintenance of Ventricular Integrity.Pharyngeal mesoderm regulatory network controls cardiac and head muscle morphogenesis22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early development.Hard to swallow: Developmental biological insights into pediatric dysphagia.Retinoic acid deficiency alters second heart field formation.Human cytochromes P450 in health and diseaseKnockdown of FABP3 impairs cardiac development in Zebrafish through the retinoic acid signaling pathway.Genetic modifiers of the physical malformations in velo-cardio-facial syndrome/DiGeorge syndrome.Retinoid regulation of the zebrafish cyp26a1 promoter.Transcription factor TBX1 overexpression induces downregulation of proteins involved in retinoic acid metabolism: a comparative proteomic analysis.Understanding the role of Tbx1 as a candidate gene for 22q11.2 deletion syndromeDysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome.Cyp26 enzymes are required to balance the cardiac and vascular lineages within the anterior lateral plate mesoderm.Myocardial lineage development.Mechanisms of T-box gene function in the developing heart.Tbx1, subpulmonary myocardium and conotruncal congenital heart defects.A molecular and genetic outline of cardiac morphogenesis.Morphological and molecular evolution of the ultimobranchial gland of nonmammalian vertebrates, with special reference to the chicken C cells.Biallelic expression of Tbx1 protects the embryo from developmental defects caused by increased receptor tyrosine kinase signaling.Endothelial cells regulate neural crest and second heart field morphogenesis.DiGeorge syndrome, Tbx1, and retinoic acid signaling come full circle.The duplicated rainbow trout (Oncorhynchus mykiss) T-box transcription factors 1, tbx1a and tbx1b, are up-regulated during testicular development.The 22q11 deletion: DiGeorge and velocardiofacial syndromes and the role of TBX1.
P2860
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P2860
Cyp26 genes a1, b1 and c1 are down-regulated in Tbx1 null mice and inhibition of Cyp26 enzyme function produces a phenocopy of DiGeorge Syndrome in the chick.
description
2006 nî lūn-bûn
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2006年の論文
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2006年学术文章
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2006年学术文章
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2006年学术文章
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name
Cyp26 genes a1, b1 and c1 are ...... iGeorge Syndrome in the chick.
@en
Cyp26 genes a1, b1 and c1 are ...... iGeorge Syndrome in the chick.
@nl
type
label
Cyp26 genes a1, b1 and c1 are ...... iGeorge Syndrome in the chick.
@en
Cyp26 genes a1, b1 and c1 are ...... iGeorge Syndrome in the chick.
@nl
prefLabel
Cyp26 genes a1, b1 and c1 are ...... iGeorge Syndrome in the chick.
@en
Cyp26 genes a1, b1 and c1 are ...... iGeorge Syndrome in the chick.
@nl
P2093
P2860
P356
P1476
Cyp26 genes a1, b1 and c1 are ...... iGeorge Syndrome in the chick.
@en
P2093
Andrew C Cook
Antonio Baldini
Catherine Roberts
Sarah Ivins
P2860
P304
P356
10.1093/HMG/DDL416
P577
2006-10-17T00:00:00Z