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Pulmonary abnormalities due to ABCA1 deficiency in mice.

Pulmonary abnormalities due to ABCA1 deficiency in mice.

http://www.wikidata.org/entity/Q46627963

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High-density Lipoproteins and Apolipoprotein A-I: Potential New Players in the Prevention and Treatment of Lung Disease Surfactant Lipids at the Host-Environment Interface. Metabolic Sensors, Suppressors, and Effectors of Inflammatory Lung Disease Identification of Biomarker and Co-Regulatory Motifs in Lung Adenocarcinoma Based on Differential Interactions Proteomic identification of novel differentiation plasma protein markers in hypobaric hypoxia-induced rat model.Impact of the loss of caveolin-1 on lung mass and cholesterol metabolism in mice with and without the lysosomal cholesterol transporter, Niemann-Pick type C1.Identification of haptoglobin and apolipoprotein A-I as biomarkers for high altitude pulmonary edema.Genetic deletion of apolipoprotein A-I increases airway hyperresponsiveness, inflammation, and collagen deposition in the lung.5A, an apolipoprotein A-I mimetic peptide, attenuates the induction of house dust mite-induced asthma ATP-binding cassette transporter 1 attenuates ovalbumin-induced neutrophilic airway inflammation.D-4F, an apoA-1 mimetic, decreases airway hyperresponsiveness, inflammation, and oxidative stress in a murine model of asthma.Group X secretory phospholipase A2 enhances TLR4 signaling in macrophages The Effect of Statins on Blood Gene Expression in COPD.Activation of the TLR4 signaling pathway and abnormal cholesterol efflux lead to emphysema in ApoE-deficient mice.Apolipoprotein A-I attenuates ovalbumin-induced neutrophilic airway inflammation via a granulocyte colony-stimulating factor-dependent mechanism.Emerging roles for cholesterol and lipoproteins in lung disease.Impaired pulmonary defense against Pseudomonas aeruginosa in VEGF gene inactivated mouse lung.Expression and biological activity of ABCA1 in alveolar epithelial cells.Regulation of surfactant secretion in alveolar type II cells.An insight into the changes in human plasma proteome on adaptation to hypobaric hypoxia Ablation of Liver X receptors α and β leads to spontaneous peripheral squamous cell lung cancer in mice.Elevated MicroRNA-33 in Sarcoidosis and a Carbon Nanotube Model of Chronic Granulomatous Disease.Transcription repressor Bach2 is required for pulmonary surfactant homeostasis and alveolar macrophage function.New roles of HDL in inflammation and hematopoiesis.Ontogenic changes in lung cholesterol metabolism, lipid content, and histology in mice with Niemann-Pick type C disease.Lung vitamin E transport processes are affected by both age and environmental oxidants in mice.Role of HDL, ABCA1, and ABCG1 transporters in cholesterol efflux and immune responses.Examining the role of ABC lipid transporters in pulmonary lipid homeostasis and inflammation.Differential plasma proteome analysis in patients with high-altitude pulmonary edema at the acute and recovery phases.Lipid-lowering drug therapies and chronic obstructive pulmonary disease: lung failure or just heart failure?The development and function of lung-resident macrophages and dendritic cells.Hepatic Steatosis Accompanies Pulmonary Alveolar Proteinosis.Emerging Roles of Apolipoprotein E and Apolipoprotein A-I in the Pathogenesis and Treatment of Lung Disease.Roles of the Mevalonate Pathway and Cholesterol Trafficking in Pulmonary Host Defense.The effect of diet-induced serum hypercholesterolemia on the surfactant system and the development of lung injury.Targeted PPAR{gamma} deficiency in alveolar macrophages disrupts surfactant catabolism High density lipoprotein promoting proliferation and migration of type II alveolar epithelial cells during inflammation state T-cell-restricted T-bet overexpression induces aberrant hematopoiesis of myeloid cells and impairs function of macrophages in the lung.ABCG1 regulates pulmonary surfactant metabolism in mice and men.Apolipoprotein E deficiency and high-fat diet cooperate to trigger lipidosis and inflammation in the lung via the toll-like receptor 4 pathway.Pseudomonas aeruginosa and sPLA2 IB stimulate ABCA1-mediated phospholipid efflux via ERK-activation of PPARalpha-RXR.

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P2860

Pulmonary abnormalities due to ABCA1 deficiency in mice.

http://www.wikidata.org/entity/Q46627963

description

2005 nî lūn-bûn

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2005年の論文

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2005年学术文章

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2005年学术文章

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2005年学术文章

@zh-cn

2005年学术文章

@zh-hans

2005年学术文章

@zh-my

2005年学术文章

@zh-sg

2005年學術文章

@yue

2005年學術文章

@zh-hant

name

Pulmonary abnormalities due to ABCA1 deficiency in mice.

@en

Pulmonary abnormalities due to ABCA1 deficiency in mice.

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type

label

Pulmonary abnormalities due to ABCA1 deficiency in mice.

@en

Pulmonary abnormalities due to ABCA1 deficiency in mice.

@nl

prefLabel

Pulmonary abnormalities due to ABCA1 deficiency in mice.

@en

Pulmonary abnormalities due to ABCA1 deficiency in mice.

@nl

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AJPLUNG.00234.2005

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American Journal of Physiology - Lung Cellular and Molecular Physiology

P1476

Pulmonary abnormalities due to ABCA1 deficiency in mice.

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P2093

George H Rothblat

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Heidi L Collins

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Jian-Qin Tao

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Omar L Francone

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Sandra R Bates

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P2860

Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

The Tangier disease gene product ABC1 controls the cellular apolipoprotein-mediated lipid removal pathway

ATP-binding cassette transporter A7 (ABCA7) binds apolipoprotein A-I and mediates cellular phospholipid but not cholesterol efflux

Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease

Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1

ATP-binding cassette transporter A1 and cholesterol trafficking

Deficiency of ABCA1 impairs apolipoprotein E metabolism in brain

Abnormal phospholipid composition impairs HDL biogenesis and maturation in mice lacking Abca1

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