Ceramide mediates lung fibrosis in cystic fibrosis. - Wikidata - awgldk - TriplyDB

Ceramide mediates lung fibrosis in cystic fibrosis.

Ceramide mediates lung fibrosis in cystic fibrosis.

http://www.wikidata.org/entity/Q39884057

about

Role of Sphingolipids in the Pathobiology of Lung Inflammation Inhibition of acid sphingomyelinase by tricyclic antidepressants and analogons Microbial, host and xenobiotic diversity in the cystic fibrosis sputum metabolome Amitriptyline Usage Exacerbates the Immune Suppression Following Burn Injury Inhibition of acidic sphingomyelinase reduces established hepatic fibrosis in mice Myofibroblast differentiation and enhanced TGF-B signaling in cystic fibrosis lung disease.Characterization of hepatic lipid profiles in a mouse model with nonalcoholic steatohepatitis and subsequent fibrosis Metabolomics of pulmonary exacerbations reveals the personalized nature of cystic fibrosis disease.Membrane signaling induced by high doses of ionizing radiation in the endothelial compartment. Relevance in radiation toxicity.Burn injury influences the T cell homeostasis in a butyrate-acid sphingomyelinase dependent manner.Neutrophil elastase increases airway ceramide levels via upregulation of serine palmitoyltransferase.

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P2860

Ceramide mediates lung fibrosis in cystic fibrosis.

http://www.wikidata.org/entity/Q39884057

description

2013 nî lūn-bûn

@nan

2013年の論文

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

@zh-my

2013年学术文章

@zh-sg

2013年學術文章

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2013年學術文章

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2013年學術文章

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name

Ceramide mediates lung fibrosis in cystic fibrosis.

@en

Ceramide mediates lung fibrosis in cystic fibrosis.

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type

label

Ceramide mediates lung fibrosis in cystic fibrosis.

@en

Ceramide mediates lung fibrosis in cystic fibrosis.

@nl

prefLabel

Ceramide mediates lung fibrosis in cystic fibrosis.

@en

Ceramide mediates lung fibrosis in cystic fibrosis.

@nl

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J.BBRC.2013.03.032

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Biochemical and Biophysical Research Communications

P1476

Ceramide mediates lung fibrosis in cystic fibrosis.

@en

P2093

Alex B Lentsch

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Brian Henry

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

Michael J Edwards

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Regan Ziobro

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P2860

Acid sphingomyelinase deficient mice: a model of types A and B Niemann-Pick disease

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

Cystic fibrosis

Increased airway epithelial Na+ absorption produces cystic fibrosis-like lung disease in mice

Structure and function of the CFTR chloride channel

Identification of the cystic fibrosis gene: genetic analysis

Alveolar inflammation in cystic fibrosis.

Ceramide upregulation causes pulmonary cell apoptosis and emphysema-like disease in mice.

Loss of anion transport without increased sodium absorption characterizes newborn porcine cystic fibrosis airway epithelia.

Identification of new functional inhibitors of acid sphingomyelinase using a structure-property-activity relation model.

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705-709

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10.1016/J.BBRC.2013.03.032

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23523785

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cystic fibrosis

pulmonary fibrosis

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4031452

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