A novel surfactant protein C mutation resulting in aberrant protein processing and altered subcellular localization causes infantile interstitial lung disease.

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A novel surfactant protein C mutation resulting in aberrant protein processing and altered subcellular localization causes infantile interstitial lung disease.

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http://www.wikidata.org/entity/Q47982722

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

@zh-cn

2017年学术文章

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2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

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2017年學術文章

@zh-hant

name

A novel surfactant protein C m ...... ile interstitial lung disease.

@en

A novel surfactant protein C m ...... ile interstitial lung disease.

@nl

type

Item

label

A novel surfactant protein C m ...... ile interstitial lung disease.

@en

A novel surfactant protein C m ...... ile interstitial lung disease.

@nl

prefLabel

A novel surfactant protein C m ...... ile interstitial lung disease.

@en

A novel surfactant protein C m ...... ile interstitial lung disease.

@nl

P1476

A novel surfactant protein C m ...... ile interstitial lung disease.

@en

P2093

Da Hong

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

Huijun Wang

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

Jing Liu

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

Libo Wang

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

Liling Qian

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

Yuanyuan Qi

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

P2860

A surfactant protein C precursor protein BRICHOS domain mutation causes endoplasmic reticulum stress, proteasome dysfunction, and caspase 3 activation

Alveolar surfactant homeostasis and the pathogenesis of pulmonary disease

A non-BRICHOS surfactant protein c mutation disrupts epithelial cell function and intercellular signaling

The surfactant protein C mutation A116D alters cellular processing, stress tolerance, surfactant lipid composition, and immune cell activation.

Mutant surfactant A2 proteins associated with familial pulmonary fibrosis and lung cancer induce TGF-β1 secretion.

Ubiquitin initiates sorting of Golgi and plasma membrane proteins into the vacuolar degradation pathway.

A non-BRICHOS SFTPC mutant (SP-CI73T) linked to interstitial lung disease promotes a late block in macroautophagy disrupting cellular proteostasis and mitophagy

Hydrophobic surfactant proteins in lung function and disease.

Genetic Basis of Children's Interstitial Lung Disease.

4-Phenylbutyric acid treatment rescues trafficking and processing of a mutant surfactant protein-C.

P2888

pr.2017.29

P304

891-897

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P31

scholarly article

P356

10.1038/PR.2017.29

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P407

English

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P478

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

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2017-02-03T00:00:00Z

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P698

28157837

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