Control of skeletal patterning by ephrinB1-EphB interactions.
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The BMP antagonist follistatin-like 1 is required for skeletal and lung organogenesisSecreted sulfatases Sulf1 and Sulf2 have overlapping yet essential roles in mouse neonatal survivalEphrinB/EphB signaling controls embryonic germ layer separation by contact-induced cell detachmentMutations of the ephrin-B1 gene cause craniofrontonasal syndrome.The origin of EFNB1 mutations in craniofrontonasal syndrome: frequent somatic mosaicism and explanation of the paucity of carrier malesMutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndromeEph/ephrin molecules--a hub for signaling and endocytosisOsteoimmunology: interactions of the bone and immune systemGrowth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studiesGenetic Syndromes Associated with CraniosynostosisEph-ephrin signaling in nervous system developmentA Genetic-Pathophysiological Framework for CraniosynostosisMolecular basis of cleft palates in miceEphrin-B1 forward and reverse signaling are required during mouse developmentSall genes regulate region-specific morphogenesis in the mouse limb by modulating Hox activitiesHoxd13 and Hoxa13 directly control the expression of the EphA7 Ephrin tyrosine kinase receptor in developing limbsDefective craniofacial development and brain function in a mouse model for depletion of intracellular inositol synthesis.A subset of signal transduction pathways is required for hippocampal growth cone collapse induced by ephrin-A5.Inhibition of gap junction communication at ectopic Eph/ephrin boundaries underlies craniofrontonasal syndromeSporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects females.Targeted disruption of nuclear factor erythroid-derived 2-like 1 in osteoblasts reduces bone size and bone formation in mice.The impact of CFNS-causing EFNB1 mutations on ephrin-B1 functionEphrin B1 regulates bone marrow stromal cell differentiation and bone formation by influencing TAZ transactivation via complex formation with NHERF1.EphA4 and EfnB2a maintain rhombomere coherence by independently regulating intercalation of progenitor cells in the zebrafish neural keel.Genetic aspects of human congenital diaphragmatic hernia.Phenotypes of craniofrontonasal syndrome in patients with a pathogenic mutation in EFNB1.Ablation of MEKK4 kinase activity causes neurulation and skeletal patterning defects in the mouse embryo.Ephrin-B1 forward signaling regulates craniofacial morphogenesis by controlling cell proliferation across Eph-ephrin boundaries.EphA3 functions are regulated by collaborating phosphotyrosine residuesCellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes.Mutations and deletions in PCDH19 account for various familial or isolated epilepsies in females.Presenilin-dependent intramembrane cleavage of ephrin-B1.Transgenic overexpression of ephrin b1 in bone cells promotes bone formation and an anabolic response to mechanical loading in mice.Ephrin-B reverse signaling controls septation events at the embryonic midline through separate tyrosine phosphorylation-independent signaling avenuesSemaphorin and Eph receptor signaling guide a series of cell movements for ventral enclosure in C. elegans.Cortical abnormalities and non-spatial learning deficits in a mouse model of CranioFrontoNasal syndrome.Duplication of the EFNB1 gene in familial hypertelorism: imbalance in ephrin-B1 expression and abnormal phenotypes in humans and mice.Embryonic expression of EphA receptor genes in mice supports their candidacy for involvement in cleft lip and palate.Eph receptor function is modulated by heterooligomerization of A and B type Eph receptorsPalatogenesis: morphogenetic and molecular mechanisms of secondary palate development
P2860
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P2860
Control of skeletal patterning by ephrinB1-EphB interactions.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
2003年论文
@zh
2003年论文
@zh-cn
name
Control of skeletal patterning by ephrinB1-EphB interactions.
@en
Control of skeletal patterning by ephrinB1-EphB interactions.
@nl
type
label
Control of skeletal patterning by ephrinB1-EphB interactions.
@en
Control of skeletal patterning by ephrinB1-EphB interactions.
@nl
prefLabel
Control of skeletal patterning by ephrinB1-EphB interactions.
@en
Control of skeletal patterning by ephrinB1-EphB interactions.
@nl
P2093
P1433
P1476
Control of skeletal patterning by ephrinB1-EphB interactions.
@en
P2093
Amelia Compagni
Malcolm Logan
Rüdiger Klein
P304
P356
10.1016/S1534-5807(03)00198-9
P407
P50
P577
2003-08-01T00:00:00Z