BMPR-IA signaling is required for the formation of the apical ectodermal ridge and dorsal-ventral patterning of the limb.
about
Lateral motor column axons execute a ternary trajectory choice between limb and body tissuesOrganogenesis relies on SoxC transcription factors for the survival of neural and mesenchymal progenitorsmBtd is required to maintain signaling during murine limb developmentSp8 is crucial for limb outgrowth and neuropore closureBMP receptor signaling is required for postnatal maintenance of articular cartilageIsl1Cre reveals a common Bmp pathway in heart and limb developmentAntagonistic crosstalk of Wnt/beta-catenin/Bmp signaling within the Apical Ectodermal Ridge (AER) regulates interdigit formationGenetic interaction between Wnt/beta-catenin and BMP receptor signaling during formation of the AER and the dorsal-ventral axis in the limbTemporal deletion of Arl13b reveals that a mispatterned neural tube corrects cell fate over timeEctodermal Wnt3/beta-catenin signaling is required for the establishment and maintenance of the apical ectodermal ridgeSp6 and Sp8 transcription factors control AER formation and dorsal-ventral patterning in limb developmentCharacterization of Cells Isolated from Genetic and Trauma-Induced Heterotopic OssificationDelayed myelination in an intrauterine growth retardation model is mediated by oxidative stress upregulating bone morphogenetic protein 4The closely related transcription factors Sox4 and Sox11 function as survival factors during spinal cord developmentBMP receptor IA is required in mammalian neural crest cells for development of the cardiac outflow tract and ventricular myocardiumHand/foot splitting and the 're-evolution' of mesopodial skeletal elements during the evolution and radiation of chameleonsVertebrate limb development: moving from classical morphogen gradients to an integrated 4-dimensional patterning systemBone morphogenetic protein signaling in the developing telencephalon controls formation of the hippocampal dentate gyrus and modifies fear-related behavior.The transcription factors Sox10 and Myrf define an essential regulatory network module in differentiating oligodendrocytes.Identification of genes associated with regenerative success of Xenopus laevis hindlimbs.Evaluation of Salivary Cytokines for Diagnosis of both Trauma-Induced and Genetic Heterotopic Ossification.PAF and EZH2 induce Wnt/β-catenin signaling hyperactivation.AcvR1-mediated BMP signaling in second heart field is required for arterial pole development: implications for myocardial differentiation and regional identity.Endocardial cushion and myocardial defects after cardiac myocyte-specific conditional deletion of the bone morphogenetic protein receptor ALK3Progesterone receptor activates Msx2 expression by downregulating TNAP/Akp2 and activating the Bmp pathway in EpH4 mouse mammary epithelial cells.Analysis of the Hand1 cell lineage reveals novel contributions to cardiovascular, neural crest, extra-embryonic, and lateral mesoderm derivativesBmp2, Bmp4 and Bmp7 are co-required in the mouse AER for normal digit patterning but not limb outgrowth.An evolutionarily conserved enhancer regulates Bmp4 expression in developing incisor and limb bud.Bone morphogenetic proteins regulate enteric gliogenesis by modulating ErbB3 signaling.BMP-mediated functional cooperation between Dlx5;Dlx6 and Msx1;Msx2 during mammalian limb developmentComparative gene expression analysis of genital tubercle development reveals a putative appendicular Wnt7 network for the epidermal differentiationCanonical Wnt signalling requires the BMP pathway to inhibit oligodendrocyte maturation.Wnt/beta-catenin signaling regulates vertebrate limb regenerationElevated in vivo levels of a single transcription factor directly convert satellite glia into oligodendrocyte-like cellsCell polarity: The missing link in skeletal morphogenesis?Cre-mediated recombination can induce apoptosis in vivo by activating the p53 DNA damage-induced pathwayBMP signaling mutant mice exhibit glial cell maturation defects.Transcriptome of pancreas-specific Bmpr1a-deleted islets links to TPH1-5-HT axisBmp indicator mice reveal dynamic regulation of transcriptional response.Sonic hedgehog acts cell-autonomously on muscle precursor cells to generate limb muscle diversity
P2860
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P2860
BMPR-IA signaling is required for the formation of the apical ectodermal ridge and dorsal-ventral patterning of the limb.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh-hant
name
BMPR-IA signaling is required ...... entral patterning of the limb.
@en
BMPR-IA signaling is required ...... entral patterning of the limb.
@nl
type
label
BMPR-IA signaling is required ...... entral patterning of the limb.
@en
BMPR-IA signaling is required ...... entral patterning of the limb.
@nl
prefLabel
BMPR-IA signaling is required ...... entral patterning of the limb.
@en
BMPR-IA signaling is required ...... entral patterning of the limb.
@nl
P2093
P1433
P1476
BMPR-IA signaling is required ...... ventral patterning of the limb
@en
P2093
Behringer RR
Crenshaw EB 3rd
P304
P407
P577
2001-11-01T00:00:00Z