Constitutively active ALK2 receptor mutants require type II receptor cooperation
about
TGF-β/BMP signaling and other molecular events: regulation of osteoblastogenesis and bone formationActivin receptor-like kinases: a diverse family playing an important role in cancerThe genomic landscape of diffuse intrinsic pontine glioma and pediatric non-brainstem high-grade gliomaBMP type II receptors have redundant roles in the regulation of hepatic hepcidin gene expression and iron metabolismStructure-activity relationship of 3,5-diaryl-2-aminopyridine ALK2 inhibitors reveals unaltered binding affinity for fibrodysplasia ossificans progressiva causing mutants.Bone Morphogenetic Protein (BMP) signaling in development and human diseasesAdult-specific systemic over-expression reveals novel in vivo effects of the soluble forms of ActRIIA, ActRIIB and BMPRII.Molecular and cellular mechanisms of heterotopic ossification.Apyrase as a novel therapeutic inhibitor of heterotopic ossificationNeofunction of ACVR1 in fibrodysplasia ossificans progressiva.Unique genetic and epigenetic mechanisms driving paediatric diffuse high-grade glioma.Common mutations in ALK2/ACVR1, a multi-faceted receptor, have roles in distinct pediatric musculoskeletal and neural orphan disorders.Granting immunity to FOP and catching heterotopic ossification in the Act.Recent advances in understanding contextual TGFβ signalingSignaling Receptors for TGF-β Family Members.Mutant activin-like kinase 2 in fibrodysplasia ossificans progressiva are activated via T203 by BMP type II receptorsConserved signaling pathways underlying heterotopic ossification.Application of human induced pluripotent stem cells to model fibrodysplasia ossificans progressiva.Two tissue-resident progenitor lineages drive distinct phenotypes of heterotopic ossification.New Protocol to Optimize iPS Cells for Genome Analysis of Fibrodysplasia Ossificans Progressiva.BmpR1A is a major type 1 BMP receptor for BMP-Smad signaling during skull development.Regulation of continuous but complex expression pattern of Six1 during early sensory development.Variable signaling activity by FOP ACVR1 mutations.Animal models of fibrodysplasia ossificans progressiva.Variant BMP receptor mutations causing fibrodysplasia ossificans progressiva (FOP) in humans show BMP ligand-independent receptor activation in zebrafish.Stem cells and heterotopic ossification: Lessons from animal models.The orphan GPR50 receptor promotes constitutive TGFβ receptor signaling and protects against cancer development.ACVR1R206H receptor mutation causes fibrodysplasia ossificans progressiva by imparting responsiveness to activin A.
P2860
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P2860
Constitutively active ALK2 receptor mutants require type II receptor cooperation
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
Constitutively active ALK2 receptor mutants require type II receptor cooperation
@en
type
label
Constitutively active ALK2 receptor mutants require type II receptor cooperation
@en
prefLabel
Constitutively active ALK2 receptor mutants require type II receptor cooperation
@en
P2093
P2860
P50
P356
P1476
Constitutively active ALK2 receptor mutants require type II receptor cooperation
@en
P2093
Alex N Bullock
Ashley J Vonner
Carol S C Lai
Donna Y Deng
Hideyuki Beppu
Ivan Alfano
Jan Börgermann
Jana Bagarova
Kelli A Armstrong
Petra Knaus
P2860
P304
P356
10.1128/MCB.01595-12
P407
P577
2013-04-09T00:00:00Z