Two major Smad pathways in TGF-beta superfamily signalling. - Test2 - elhamkhani - TriplyDB

Two major Smad pathways in TGF-beta superfamily signalling.

Two major Smad pathways in TGF-beta superfamily signalling.

http://www.wikidata.org/entity/Q35026971

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Impaired terminal differentiation of hippocampal granule neurons and defective contextual memory in PC3/Tis21 knockout mice Astrocytes as a source for extracellular matrix molecules and cytokines Nodal and ALK7 inhibit proliferation and induce apoptosis in human trophoblast cells Interaction with Smad4 is indispensable for suppression of BMP signaling by c-Ski ZNF580, a novel C2H2 zinc-finger transcription factor, interacts with the TGF-β signal molecule Smad2 Arkadia induces degradation of SnoN and c-Ski to enhance transforming growth factor-beta signaling Endogenous TGF-beta signaling suppresses maturation of osteoblastic mesenchymal cells Transforming growth factor-beta1, transforming growth factor-beta2, and transforming growth factor-beta3 enhance ovarian cancer metastatic potential by inducing a Smad3-dependent epithelial-to-mesenchymal transition Smurf2 participates in human trophoblast cell invasion by inhibiting TGF-beta type I receptor The conditioned medium from a stable human GDF3-expressing CHO cell line, induces the differentiation of PC12 cells An Id-like molecule, HHM, is a synexpression group-restricted regulator of TGF-beta signalling BMP-2/4 and BMP-6/7 differentially utilize cell surface receptors to induce osteoblastic differentiation of human bone marrow-derived mesenchymal stem cells Homeoprotein DLX-1 interacts with Smad4 and blocks a signaling pathway from activin A in hematopoietic cells Arkadia amplifies TGF-beta superfamily signalling through degradation of Smad7 BMP-6 inhibits growth of mature human B cells; induction of Smad phosphorylation and upregulation of Id1 Muscle regeneration in dystrophin-deficient mdx mice studied by gene expression profiling Conditional expression of Smad7 in pancreatic beta cells disrupts TGF-beta signaling and induces reversible diabetes mellitus Meeting the meat: delineating the molecular machinery of muscle development The Regulatory Role of Signaling Crosstalk in Hypertrophy of MSCs and Human Articular Chondrocytes MicroRNAs in ovarian function and disorders Osteoarthritis pathogenesis: a review of molecular mechanisms Oligomeric interactions of TGF-β and BMP receptors A silent H-bond can be mutationally activated for high-affinity interaction of BMP-2 and activin type IIB receptor Molecular Mechanism of the Negative Regulation of Smad1/5 Protein by Carboxyl Terminus of Hsc70-interacting Protein (CHIP)Transforming growth factor-beta-mediated signaling via the p38 MAP kinase pathway activates Smad-dependent transcription through SUMO-1 modification of Smad4 A role for Id in the regulation of TGF-beta-induced epithelial-mesenchymal transdifferentiation Negative regulation of transforming growth factor-beta (TGF-beta) signaling by WW domain-containing protein 1 (WWP1)DMH1, a small molecule inhibitor of BMP type i receptors, suppresses growth and invasion of lung cancer Cross-talk between bone morphogenetic protein and transforming growth factor-beta signaling is essential for exendin-4-induced insulin-positive differentiation of AR42J cells Involvement of Ras GTPase-activating protein SH3 domain-binding protein 1 in the epithelial-to-mesenchymal transition-induced metastasis of breast cancer cells via the Smad signaling pathway.Uterine activin receptor-like kinase 5 is crucial for blastocyst implantation and placental development.Local immunomodulation with CD4 and CD8 antibodies, but not cyclosporine A, improves osteogenesis induced by ADhBMP9 gene therapy.Gremlin-2 is a BMP antagonist that is regulated by the circadian clock Genome wide transcriptional analysis of resting and IL2 activated human natural killer cells: gene expression signatures indicative of novel molecular signaling pathways.ChIP-seq defined genome-wide map of TGFβ/SMAD4 targets: implications with clinical outcome of ovarian cancer.A road map toward defining the role of Smad signaling in hematopoietic stem cells.Lrp4 modulates extracellular integration of cell signaling pathways in development.Transcription factors RUNX1 and RUNX3 in the induction and suppressive function of Foxp3+ inducible regulatory T cells Dynamics of chromatin accessibility during TGF-β-induced EMT of Ras-transformed mammary gland epithelial cells.TGF-beta and the Smad signaling pathway support transcriptomic reprogramming during epithelial-mesenchymal cell transition

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P2860

Two major Smad pathways in TGF-beta superfamily signalling.

http://www.wikidata.org/entity/Q35026971

description

2002 nî lūn-bûn

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2002 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2002 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2002年の論文

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2002年学术文章

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2002年学术文章

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2002年学术文章

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2002年学术文章

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2002年学术文章

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2002年學術文章

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name

Two major Smad pathways in TGF-beta superfamily signalling.

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Two major Smad pathways in TGF-beta superfamily signalling.

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type

label

Two major Smad pathways in TGF-beta superfamily signalling.

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Two major Smad pathways in TGF-beta superfamily signalling.

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prefLabel

Two major Smad pathways in TGF-beta superfamily signalling.

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Two major Smad pathways in TGF-beta superfamily signalling.

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Two major Smad pathways in TGF-beta superfamily signalling

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Kohei Miyazono

http://www.w3.org/2001/XMLSchema#string

Masahiko Shinozaki

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Takane Hara

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Toshio Furuya

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P2860

A SMAD ubiquitin ligase targets the BMP pathway and affects embryonic pattern formation

TGF-beta signal transduction

Negative feedback regulation of TGF-beta signaling by the SnoN oncoprotein

OAZ uses distinct DNA- and protein-binding zinc fingers in separate BMP-Smad and Olf signaling pathways

Crystal structure of the BMP-2-BRIA ectodomain complex

Smurf2 is a ubiquitin E3 ligase mediating proteasome-dependent degradation of Smad2 in transforming growth factor-beta signaling

Regulation of Smad degradation and activity by Smurf2, an E3 ubiquitin ligase

Smad proteins function as co-modulators for MEF2 transcriptional regulatory proteins

Inactivation of menin, a Smad3-interacting protein, blocks transforming growth factor type beta signaling

Smurf1 interacts with transforming growth factor-beta type I receptor through Smad7 and induces receptor degradation

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