Biogenesis of lamellar bodies, lysosome-related organelles involved in storage and secretion of pulmonary surfactant.
about
Intracellular targeting of peroxiredoxin 6 to lysosomal organelles requires MAPK activity and binding to 14-3-3εABCA5 resides in lysosomes, and ABCA5 knockout mice develop lysosomal disease-like symptomsProcessing of pulmonary surfactant protein B by napsin and cathepsin HMultiple roles for the actin cytoskeleton during regulated exocytosisSurfactant phospholipid metabolismSNAREs in the maturation and function of LROsGenetic disorders of surfactant dysfunctionCharacterization of the Niemann-Pick C pathway in alveolar type II cells and lamellar bodies of the lungAnalysis of the Proteolytic Processing of ABCA3: Identification of Cleavage Site and Involved ProteasesSurfactant lipid synthesis and lamellar body formation in glycogen-laden type II cellsIn vitro generation of human pluripotent stem cell derived lung organoidsRab38 targets to lamellar bodies and normalizes their sizes in lung alveolar type II epithelial cells.Fusion-activated Ca2+ entry via vesicular P2X4 receptors promotes fusion pore opening and exocytotic content release in pneumocytesLipid specificity of surfactant protein B studied by time-of-flight secondary ion mass spectrometry.Vacuolar ATPase regulates surfactant secretion in rat alveolar type II cells by modulating lamellar body calciumImmune reconstitution during Pneumocystis lung infection: disruption of surfactant component expression and function by S-nitrosylation.Exogenous gene transfer of Rab38 small GTPase ameliorates aberrant lung surfactant homeostasis in Ruby rats.Nedd4-2-mediated ubiquitination facilitates processing of surfactant protein-CReserve autophagic capacity in alveolar epithelia provides a replicative niche for influenza A virus.Characterization of taurine as anti-obesity agent in C. elegans.ABCA3 mutations associated with pediatric interstitial lung disease.Functional and trafficking defects in ATP binding cassette A3 mutants associated with respiratory distress syndrome.Probing the in vitro mechanism of action of cationic lipid/DNA lipoplexes at a nanometric scaleThree-dimensional culture and FGF signaling drive differentiation of murine pluripotent cells to distal lung epithelial cells.Pulmonary abnormalities in animal models due to Niemann-Pick type C1 (NPC1) or C2 (NPC2) diseaseCa2+-dependent actin coating of lamellar bodies after exocytotic fusion: a prerequisite for content release or kiss-and-run.A nonaggregating surfactant protein C mutant is misdirected to early endosomes and disrupts phospholipid recycling.LRRK2 protein levels are determined by kinase function and are crucial for kidney and lung homeostasis in mice.Genetic Basis of Children's Interstitial Lung Disease.Function of the Caenorhabditis elegans ABC transporter PGP-2 in the biogenesis of a lysosome-related fat storage organelle.Adaptation and increased susceptibility to infection associated with constitutive expression of misfolded SP-C.The cell biology of Hermansky-Pudlak syndrome: recent advances.Long Term Culture of the A549 Cancer Cell Line Promotes Multilamellar Body Formation and Differentiation towards an Alveolar Type II Pneumocyte Phenotype.Influence of prenatal hypoxia and postnatal hyperoxia on morphologic lung maturation in mice.Regulation of surfactant secretion in alveolar type II cells.Impaired Lysosomal Integral Membrane Protein 2-dependent Peroxiredoxin 6 Delivery to Lamellar Bodies Accounts for Altered Alveolar Phospholipid Content in Adaptor Protein-3-deficient pearl Mice.A mutation in Rab38 small GTPase causes abnormal lung surfactant homeostasis and aberrant alveolar structure in mice.Spectral monitoring of surfactant clearance during alveolar epithelial type II cell differentiationImaging and imagination: understanding the endo-lysosomal systemVariable stretch pattern enhances surfactant secretion in alveolar type II cells in culture.
P2860
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P2860
Biogenesis of lamellar bodies, lysosome-related organelles involved in storage and secretion of pulmonary surfactant.
description
2002 nî lūn-bûn
@nan
2002 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Biogenesis of lamellar bodies, ...... etion of pulmonary surfactant.
@ast
Biogenesis of lamellar bodies, ...... etion of pulmonary surfactant.
@en
Biogenesis of lamellar bodies, ...... etion of pulmonary surfactant.
@nl
type
label
Biogenesis of lamellar bodies, ...... etion of pulmonary surfactant.
@ast
Biogenesis of lamellar bodies, ...... etion of pulmonary surfactant.
@en
Biogenesis of lamellar bodies, ...... etion of pulmonary surfactant.
@nl
prefLabel
Biogenesis of lamellar bodies, ...... etion of pulmonary surfactant.
@ast
Biogenesis of lamellar bodies, ...... etion of pulmonary surfactant.
@en
Biogenesis of lamellar bodies, ...... etion of pulmonary surfactant.
@nl
P2093
P1476
Biogenesis of lamellar bodies, ...... etion of pulmonary surfactant.
@en
P2093
Cheng-Lun Na
Mildred Stahlman
Timothy E Weaver
P304
P356
10.1016/S1084952102000551
P577
2002-08-01T00:00:00Z