Wnt coreceptor Lrp5 is a driver of idiopathic pulmonary fibrosis. - Wikidata - awgldk - TriplyDB

Wnt coreceptor Lrp5 is a driver of idiopathic pulmonary fibrosis.

Wnt coreceptor Lrp5 is a driver of idiopathic pulmonary fibrosis.

http://www.wikidata.org/entity/Q34480454

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Vascular Remodelling and Mesenchymal Transition in Systemic Sclerosis Wnts talking with the TGF-β superfamily: WISPers about modulation of osteoarthritis Signaling in Fibrosis: TGF-β, WNT, and YAP/TAZ Converge The cardiomyocyte protein αT-catenin contributes to asthma through regulating pulmonary vein inflammation Matrix metalloproteinases as therapeutic targets for idiopathic pulmonary fibrosis The cardiac protein αT-catenin contributes to chemical-induced asthma Distinct Roles of Wnt/β-Catenin Signaling in the Pathogenesis of Chronic Obstructive Pulmonary Disease and Idiopathic Pulmonary Fibrosis Enolase 1 (ENO1) and protein disulfide-isomerase associated 3 (PDIA3) regulate Wnt/β-catenin-driven trans-differentiation of murine alveolar epithelial cells.Adiponectin inhibits Wnt co-receptor, Lrp6, phosphorylation and β-catenin signaling.Contribution of the anaphylatoxin receptors, C3aR and C5aR, to the pathogenesis of pulmonary fibrosis.Update in Interstitial Lung Disease 2014.Invasive diagnostic techniques in idiopathic interstitial pneumonias.Immune Mechanisms in Pulmonary Fibrosis.SIRT3 deficiency promotes lung fibrosis by augmenting alveolar epithelial cell mitochondrial DNA damage and apoptosis.WNT Signaling in Lung Aging and Disease.Plasma membrane wounding and repair in pulmonary diseases.'WNT-er is coming': WNT signalling in chronic lung diseases.Lrp5/β-Catenin Signaling Controls Lung Macrophage Differentiation and Inhibits Resolution of Fibrosis.Recurrent copy number variants associated with bronchopulmonary dysplasia.Mitigation of sepsis-induced inflammatory responses and organ injury through targeting Wnt/β-catenin signaling.Activation of Wnt/β-catenin signalling is required for TGF-β/Smad2/3 signalling during myofibroblast proliferation.Interactions between TGF-β1, canonical WNT/β-catenin pathway and PPAR γ in radiation-induced fibrosis.The involvement of the laminin-integrin α7β1 signaling pathway in mechanical ventilation-induced pulmonary fibrosis.Thermodynamic Aspects and Reprogramming Cellular Energy Metabolism during the Fibrosis Process.Therapeutic effects of telomerase in mice with pulmonary fibrosis induced by damage to the lungs and short telomeres.FGF9 prevents pleural fibrosis induced by intrapleural adenovirus injection in mice.Monocyte-derived alveolar macrophages drive lung fibrosis and persist in the lung over the life span.Wnt/β-catenin and transforming growth factor-β signaling in pulmonary fibrosis. A case for antagonistic pleiotropy?Impact of Transcriptomics on Our Understanding of Pulmonary Fibrosis.Wenyang Huazhuo Tongluo formula inhibits fibrosis via suppressing Wnt/β-catenin signaling pathway in a Bleomycin-induced systemic sclerosis mouse model.Potential regulatory role of circular RNA in idiopathic pulmonary fibrosis Ubiquitination in Scleroderma Fibrosis and Its Treatment

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P2860

Wnt coreceptor Lrp5 is a driver of idiopathic pulmonary fibrosis.

http://www.wikidata.org/entity/Q34480454

description

2014 nî lūn-bûn

@nan

2014 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հուլիսին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Wnt coreceptor Lrp5 is a driver of idiopathic pulmonary fibrosis.

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Wnt coreceptor Lrp5 is a driver of idiopathic pulmonary fibrosis.

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Wnt coreceptor Lrp5 is a driver of idiopathic pulmonary fibrosis.

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type

label

Wnt coreceptor Lrp5 is a driver of idiopathic pulmonary fibrosis.

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Wnt coreceptor Lrp5 is a driver of idiopathic pulmonary fibrosis.

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Wnt coreceptor Lrp5 is a driver of idiopathic pulmonary fibrosis.

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prefLabel

Wnt coreceptor Lrp5 is a driver of idiopathic pulmonary fibrosis.

@ast

Wnt coreceptor Lrp5 is a driver of idiopathic pulmonary fibrosis.

@en

Wnt coreceptor Lrp5 is a driver of idiopathic pulmonary fibrosis.

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P356

RCCM.201401-0079OC

P1433

American Journal of Respiratory and Critical Care Medicine

P1476

Wnt coreceptor Lrp5 is a driver of idiopathic pulmonary fibrosis.

@en

P2093

Anna P Lam

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

Annette S Flozak

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

G R Scott Budinger

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

Gökhan M Mutlu

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

John Varga

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

Jose D Herazo-Maya

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Joseph A Sennello

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Susan Russell

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

P2860

Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies

Lrp5 functions in bone to regulate bone mass

WNT1-inducible signaling protein-1 mediates pulmonary fibrosis in mice and is upregulated in humans with idiopathic pulmonary fibrosis

Lrp5 controls bone formation by inhibiting serotonin synthesis in the duodenum

An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management

Decreased BMD and limb deformities in mice carrying mutations in both Lrp5 and Lrp6

Interactions between β-catenin and transforming growth factor-β signaling pathways mediate epithelial-mesenchymal transition and are dependent on the transcriptional co-activator cAMP-response element-binding protein (CREB)-binding protein (CBP).

Beta-catenin phosphorylated at serine 45 is spatially uncoupled from beta-catenin phosphorylated in the GSK3 domain: implications for signaling.

Activity of the beta-catenin phosphodestruction complex at cell-cell contacts is enhanced by cadherin-based adhesion

Idiopathic pulmonary fibrosis: aberrant recapitulation of developmental programs?

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185-195

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scholarly article

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10.1164/RCCM.201401-0079OC

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2

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190

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Naftali Kaminski

Ramanuj Dasgupta

Cara J Gottardi

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2014-07-01T00:00:00Z

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24921217

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pulmonary fibrosis

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4226053

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