Identification of LBM180, a lamellar body limiting membrane protein of alveolar type II cells, as the ABC transporter protein ABCA3
about
Essential regulation of lung surfactant homeostasis by the orphan G protein-coupled receptor GPR116A distinct "side population" of cells with high drug efflux capacity in human tumor cellsPathogenesis of permeability barrier abnormalities in the ichthyoses: inherited disorders of lipid metabolismGenetic interstitial lung diseaseCalcineurin/Nfat signaling is required for perinatal lung maturation and functionUnderstanding Idiopathic Interstitial Pneumonia: A Gene-Based Review of Stressed LungsStructural Features of the ATP-Binding Cassette (ABC) Transporter ABCA3Genetic disorders of surfactant dysfunctionAlveolar surfactant homeostasis and the pathogenesis of pulmonary diseasePulmonary surfactant pathophysiology: current models and open questionsAnalysis of the Proteolytic Processing of ABCA3: Identification of Cleavage Site and Involved ProteasesIdentification and characterization of rodent ABCA1 in isolated type II pneumocytesCD208/dendritic cell-lysosomal associated membrane protein is a marker of normal and transformed type II pneumocytesRab38 targets to lamellar bodies and normalizes their sizes in lung alveolar type II epithelial cells.An ATP-binding cassette transporter is a major glycoprotein of sea urchin sperm membranes.Identification and characterization of p63 (CKAP4/ERGIC-63/CLIMP-63), a surfactant protein A binding protein, on type II pneumocytes.Synonymous ABCA3 variants do not increase risk for neonatal respiratory distress syndrome.Conditional deletion of Abca3 in alveolar type II cells alters surfactant homeostasis in newborn and adult mice.Pathway to lamellar bodies for surfactant protein A.ABCA3 mutations associated with pediatric interstitial lung disease.Genotype-phenotype correlations for infants and children with ABCA3 deficiencyFunctional and trafficking defects in ATP binding cassette A3 mutants associated with respiratory distress syndrome.Characterization and classification of ATP-binding cassette transporter ABCA3 mutants in fatal surfactant deficiency.Novel mutations in the gene encoding ATP binding cassette protein member A3 (ABCA3) resulting in fatal neonatal lung disease.Heterozygosity for ABCA3 mutations modifies the severity of lung disease associated with a surfactant protein C gene (SFTPC) mutation.Respiratory distress syndrome due to a novel homozygous ABCA3 mutation in a term neonate.A novel conserved targeting motif found in ABCA transporters mediates trafficking to early post-Golgi compartments.Respiratory failure in a term infant with cis and trans mutations in ABCA3A nonaggregating surfactant protein C mutant is misdirected to early endosomes and disrupts phospholipid recycling.Exosomal evasion of humoral immunotherapy in aggressive B-cell lymphoma modulated by ATP-binding cassette transporter A3.Surfactant dysfunction.Genetic Basis of Children's Interstitial Lung Disease.Molecular and cellular characteristics of ABCA3 mutations associated with diffuse parenchymal lung diseases in children.Lysophosphatidylcholine Acyltransferase 1 (LPCAT1) Specifically Interacts with Phospholipid Transfer Protein StarD10 to Facilitate Surfactant Phospholipid Trafficking in Alveolar Type II CellsProteomic analysis reveals down-regulation of surfactant protein B in murine type II pneumocytes infected with influenza A virus.High-efficiency type II cell-enhanced green fluorescent protein expression facilitates cellular identification, tracking, and isolation.Lost after translation: insights from pulmonary surfactant for understanding the role of alveolar epithelial dysfunction and cellular quality control in fibrotic lung disease.Long Term Culture of the A549 Cancer Cell Line Promotes Multilamellar Body Formation and Differentiation towards an Alveolar Type II Pneumocyte Phenotype.Annexin A7 and SNAP23 interactions in alveolar type II cells and in vitro: a role for Ca(2+) and PKC.A disorder of surfactant metabolism without identified genetic mutations
P2860
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P2860
Identification of LBM180, a lamellar body limiting membrane protein of alveolar type II cells, as the ABC transporter protein ABCA3
description
2002 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունիսին հրատարակված գիտական հոդված
@hy
article publié dans la revue scientifique Journal of Biological Chemistry
@fr
artículu científicu espublizáu en 2002
@ast
im Juni 2002 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2002/06/21)
@sk
vědecký článek publikovaný v roce 2002
@cs
wetenschappelijk artikel (gepubliceerd op 2002/06/21)
@nl
наукова стаття, опублікована в червні 2002
@uk
name
Identification of LBM180, a la ...... ABC transporter protein ABCA3
@ast
Identification of LBM180, a la ...... ABC transporter protein ABCA3
@en
Identification of LBM180, a la ...... ABC transporter protein ABCA3
@nl
type
label
Identification of LBM180, a la ...... ABC transporter protein ABCA3
@ast
Identification of LBM180, a la ...... ABC transporter protein ABCA3
@en
Identification of LBM180, a la ...... ABC transporter protein ABCA3
@nl
prefLabel
Identification of LBM180, a la ...... ABC transporter protein ABCA3
@ast
Identification of LBM180, a la ...... ABC transporter protein ABCA3
@en
Identification of LBM180, a la ...... ABC transporter protein ABCA3
@nl
P2093
P2860
P921
P3181
P356
P1476
Identification of LBM180, a la ...... ABC transporter protein ABCA3
@en
P2093
Aron B Fisher
Henry Shuman
Joseph M Gray
Kathleen L Notarfrancesco
Linda W Gonzales
Philip L Ballard
Sheldon I Feinstein
Surafel Mulugeta
P2860
P304
22147-22155
P3181
P356
10.1074/JBC.M201812200
P407
P577
2002-04-08T00:00:00Z