Human airway surface epithelial regeneration is delayed and abnormal in cystic fibrosis.
about
Airway epithelial repair in health and disease: Orchestrator or simply a player?Airway epithelial homeostasis and planar cell polarity signaling depend on multiciliated cell differentiationPulmonary fibrosis: pathogenesis, etiology and regulationCharacterization of side population cells from human airway epithelium.Reduced GM1 ganglioside in CFTR-deficient human airway cells results in decreased β1-integrin signaling and delayed wound repairAirway basal stem cells: a perspective on their roles in epithelial homeostasis and remodeling.Cystic fibrosis transmembrane conductance regulator is involved in airway epithelial wound repairCFTR interacts with ZO-1 to regulate tight junction assembly and epithelial differentiation through the ZONAB pathway.Bone marrow-derived progenitor cells in end-stage lung disease patients.Physiological impact of abnormal lipoxin A₄ production on cystic fibrosis airway epithelium and therapeutic potential.GRYFUN: a web application for GO term annotation visualization and analysis in protein sets.Quantitative proteomics reveals an altered cystic fibrosis in vitro bronchial epithelial secretomeHallmarks of therapeutic management of the cystic fibrosis functional landscape.Tissue inhibitor of metalloproteinase-1 moderates airway re-epithelialization by regulating matrilysin activityWhat have we learned from mouse models for cystic fibrosis?cAMP-mediated regulation of cholesterol accumulation in cystic fibrosis and Niemann-Pick type C cellsMyeloperoxidase inactivates TIMP-1 by oxidizing its N-terminal cysteine residue: an oxidative mechanism for regulating proteolysis during inflammation.{alpha}7 nicotinic acetylcholine receptor regulates airway epithelium differentiation by controlling basal cell proliferation.Role of CFTR in epithelial physiology.The role of Lipoxin A4 in Cystic Fibrosis Lung Disease.Stem cell therapy for cystic fibrosis: current status and future prospects.Knowledge translation: airway epithelial cell migration and respiratory diseases.A new theory on the pathogenesis of acquired cholesteatoma: Mucosal traction.Dynamically Regulated CFTR Expression and Its Functional Role in Cutaneous Wound Healing.Activation of MMP-9 by human lung epithelial cells in response to the cystic fibrosis-associated pathogen Burkholderia cenocepacia reduced wound healing in vitro.β-arrestin-2 regulation of the cAMP response element binding proteinCystic fibrosis transmembrane conductance regulator trafficking modulates the barrier function of airway epithelial cell monolayers.EGF and K+ channel activity control normal and cystic fibrosis bronchial epithelia repair.Cystic fibrosis airway epithelium remodelling: involvement of inflammation.Fixing stem cells via genome editing: hope for cystic fibrosis?Nasal abnormalities in cystic fibrosis mice independent of infection and inflammation.Regulation of normal and cystic fibrosis airway epithelial repair processes by TNF-α after injury.Airway Epithelium Dysfunction in Cystic Fibrosis and COPD.
P2860
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P2860
Human airway surface epithelial regeneration is delayed and abnormal in cystic fibrosis.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
2007年學術文章
@zh
2007年學術文章
@zh-hant
name
Human airway surface epithelial regeneration is delayed and abnormal in cystic fibrosis.
@en
Human airway surface epithelial regeneration is delayed and abnormal in cystic fibrosis.
@nl
type
label
Human airway surface epithelial regeneration is delayed and abnormal in cystic fibrosis.
@en
Human airway surface epithelial regeneration is delayed and abnormal in cystic fibrosis.
@nl
prefLabel
Human airway surface epithelial regeneration is delayed and abnormal in cystic fibrosis.
@en
Human airway surface epithelial regeneration is delayed and abnormal in cystic fibrosis.
@nl
P2093
P2860
P356
P1476
Human airway surface epithelial regeneration is delayed and abnormal in cystic fibrosis
@en
P2093
P2860
P304
P356
10.1002/PATH.2118
P577
2007-02-01T00:00:00Z