A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia.
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Connexins: a myriad of functions extending beyond assembly of gap junction channelsLife cycle of connexins in health and diseaseBidirectional communication between oocytes and follicle cells: ensuring oocyte developmental competenceGap junctions couple astrocytes and oligodendrocytesBiology of Bone Tissue: Structure, Function, and Factors That Influence Bone CellsGap junctions in inherited human disorders of the central nervous system.Gap junctional regulation of signal transduction in bone cellsGap junction connexins in female reproductive organs: implications for women's reproductive healthUltrasound biomicroscopy in small animal research: applications in molecular and preclinical imaging.A nonsense mutation in the first transmembrane domain of connexin 43 underlies autosomal recessive oculodentodigital syndromeInteraction of connexin43 and protein kinase C-delta during FGF2 signalingCaveolin-1 and -2 interact with connexin43 and regulate gap junctional intercellular communication in keratinocytesOsteoblast connexin43 modulates skeletal architecture by regulating both arms of bone remodelingIf the skull fits: magnetic resonance imaging and microcomputed tomography for combined analysis of brain and skull phenotypes in the mousePremature osteoblast clustering by enamel matrix proteins induces osteoblast differentiation through up-regulation of connexin 43 and N-cadherinStructure and functional studies of N-terminal Cx43 mutants linked to oculodentodigital dysplasia.Inhibition of gap junction communication at ectopic Eph/ephrin boundaries underlies craniofrontonasal syndromeBone marrow connexin-43 expression is critical for hematopoietic regeneration after chemotherapy.Cytopenia induction by 5-fluorouracil identifies thrombopoietic mutants in sensitized ENU mutagenesis screensThe conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans.A dominant loss-of-function GJA1 (Cx43) mutant impairs parturition in the mouseDepression of intraocular pressure following inactivation of connexin43 in the nonpigmented epithelium of the ciliary bodyTranscription factor FoxO1 is essential for enamel biomineralization.Connexin mutant embryonic stem cells and human diseasesCharacterization of hTERT-immortalized osteoblast cell lines generated from wild-type and connexin43-null mouse calvaria.Syndromic and non-syndromic disease-linked Cx43 mutations.First mouse model for combined osteogenesis imperfecta and Ehlers-Danlos syndrome.Mutations in cardiovascular connexin genes.Gap junction intercellular communication: a review of a potential platform to modulate craniofacial tissue engineering.Connexin 43 as a signaling platform for increasing the volume and spatial distribution of regenerated tissue.Connexin 43 channels are essential for normal bone structure and osteocyte viabilityUp-regulation of BMP2/4 signaling increases both osteoblast-specific marker expression and bone marrow adipogenesis in Gja1Jrt/+ stromal cell cultures.The transcriptional activity of osterix requires the recruitment of Sp1 to the osteocalcin proximal promoter.Human dermal fibroblasts derived from oculodentodigital dysplasia patients suggest that patients may have wound-healing defectsEvaluating the role of connexin43 in congenital heart disease: Screening for mutations in patients with outflow tract anomalies and the analysis of knock-in mouse modelsConnexin43 phosphorylation in brain, cardiac, endothelial and epithelial tissues.Myogenic bladder defects in mouse models of human oculodentodigital dysplasiaAdvances in the Molecular Genetics of Non-syndromic Syndactyly.Connexin43 deficiency reduces the sensitivity of cortical bone to the effects of muscle paralysisConnexins and pannexins in the skeleton: gap junctions, hemichannels and more
P2860
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P2860
A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh
2005年學術文章
@zh-hant
name
A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia.
@en
A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia.
@nl
type
label
A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia.
@en
A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia.
@nl
prefLabel
A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia.
@en
A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia.
@nl
P2093
P50
P356
P1433
P1476
A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia.
@en
P2093
Ann M Flenniken
Brian J Nieman
Craig Fleming
Crystal Lounsbury
Geoffrey A Wood
Gerald M Kidder
Gregory I L Veitch
Igor Vukobradovic
P304
P356
10.1242/DEV.02011
P407
P50
P577
2005-10-01T00:00:00Z