Progression of calvarial bone development requires Foxc1 regulation of Msx2 and Alx4
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Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotypeAngiogenesis and intramembranous osteogenesisLongitudinal evaluation of an N-ethyl-N-nitrosourea-created murine model with normal pressure hydrocephalusThe role of the forkhead transcription factor, Foxc1, in the development of the mouse lacrimal glandGli3Xt-J/Xt-J mice exhibit lambdoid suture craniosynostosis which results from altered osteoprogenitor proliferation and differentiationMesodermal Tbx1 is required for patterning the proximal mandible in miceSkeletal gene expression in the temporal region of the reptilian embryos: implications for the evolution of reptilian skull morphologyThe transcription factor Foxc1 is necessary for Ihh-Gli2-regulated endochondral ossificationRegulation of FOXC1 stability and transcriptional activity by an epidermal growth factor-activated mitogen-activated protein kinase signaling cascadeModel organisms inform the search for the genes and developmental pathology underlying malformations of the human hindbrain.Auditory hair cell defects as potential cause for sensorineural deafness in Wolf-Hirschhorn syndromeNovel approaches to studying the genetic basis of cerebellar developmentAnomalous development of brain structure and function in spina bifida myelomeningocele.Bent bone dysplasia syndrome reveals nucleolar activity for FGFR2 in ribosomal DNA transcription.The effect of conditional inactivation of beta 1 integrins using twist 2 Cre, Osterix Cre and osteocalcin Cre lines on skeletal phenotypeβ-catenin/cyclin D1 mediated development of suture mesenchyme in calvarial morphogenesis.Initiation of early osteoblast differentiation events through the direct transcriptional regulation of Msx2 by FOXC1GATA4 regulates estrogen receptor-alpha-mediated osteoblast transcription.Interaction between Foxc1 and Fgf8 during mammalian jaw patterning and in the pathogenesis of syngnathia.Midline craniofacial malformations with a lipomatous cephalocele are associated with insufficient closure of the neural tube in the tuft mouse.A 20 bp Duplication in Exon 2 of the Aristaless-Like Homeobox 4 Gene (ALX4) Is the Candidate Causative Mutation for Tibial Hemimelia Syndrome in Galloway CattleMapping of Craniofacial Traits in Outbred Mice Identifies Major Developmental Genes Involved in Shape DeterminationCortical dysplasia and skull defects in mice with a Foxc1 allele reveal the role of meningeal differentiation in regulating cortical development.Small ubiquitin-like modifier (SUMO) modification mediates function of the inhibitory domains of developmental regulators FOXC1 and FOXC2Prevention of premature fusion of calvarial suture in GLI-Kruppel family member 3 (Gli3)-deficient mice by removing one allele of Runt-related transcription factor 2 (Runx2).Foxc1 controls the growth of the murine frontal bone rudiment by direct regulation of a Bmp response threshold of Msx2.Cholesterol metabolism: the main pathway acting downstream of cytochrome P450 oxidoreductase in skeletal development of the limb.RUNX2 mutations in Chinese patients with cleidocranial dysplasia.Concise review: induced pluripotent stem cells and lineage reprogramming: prospects for bone regeneration.FOXC1: an emerging marker and therapeutic target for cancer.The Boston-type craniosynostosis mutation MSX2 (P148H) results in enhanced susceptibility of MSX2 to ubiquitin-dependent degradation.Foxc1 Expression in Early Osteogenic Differentiation Is Regulated by BMP4-SMAD Activity.Identification of Tgf beta1i4 as a downstream target of Foxc1.Loss-of-Function of Gli3 in Mice Causes Abnormal Frontal Bone Morphology and Premature Synostosis of the Interfrontal Suture.A cascade of morphogenic signaling initiated by the meninges controls corpus callosum formation.Difference in apical and basal growth of the frontal bone primordium in Foxc1ch/ch mice.Alx4 and Msx2 play phenotypically similar and additive roles in skull vault differentiation.Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis.Mechanism of skull suture maintenance and interdigitation.Regulation of Calvarial Osteogenesis by Concomitant De-repression of GLI3 and Activation of IHH Targets.
P2860
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P2860
Progression of calvarial bone development requires Foxc1 regulation of Msx2 and Alx4
description
2003 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2003
@ast
im Oktober 2003 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2003/10/01)
@sk
vědecký článek publikovaný v roce 2003
@cs
wetenschappelijk artikel (gepubliceerd op 2003/10/01)
@nl
наукова стаття, опублікована в жовтні 2003
@uk
مقالة علمية (نشرت في أكتوبر 2003)
@ar
name
Progression of calvarial bone development requires Foxc1 regulation of Msx2 and Alx4
@ast
Progression of calvarial bone development requires Foxc1 regulation of Msx2 and Alx4
@en
Progression of calvarial bone development requires Foxc1 regulation of Msx2 and Alx4
@nl
type
label
Progression of calvarial bone development requires Foxc1 regulation of Msx2 and Alx4
@ast
Progression of calvarial bone development requires Foxc1 regulation of Msx2 and Alx4
@en
Progression of calvarial bone development requires Foxc1 regulation of Msx2 and Alx4
@nl
prefLabel
Progression of calvarial bone development requires Foxc1 regulation of Msx2 and Alx4
@ast
Progression of calvarial bone development requires Foxc1 regulation of Msx2 and Alx4
@en
Progression of calvarial bone development requires Foxc1 regulation of Msx2 and Alx4
@nl
P2093
P1476
Progression of calvarial bone development requires Foxc1 regulation of Msx2 and Alx4
@en
P2093
Bjorn R. Olsen
David P. C. Rice
Ritva Rice
P356
10.1016/S0012-1606(03)00355-5
P407
P577
2003-10-01T00:00:00Z