Characterization of mitochondrial function in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function.

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Buserelin alleviates chloride transport defect in human cystic fibrosis nasal epithelial cells.Thymosin α1: a single drug with multiple targets in cystic fibrosis.N-acetyl cysteine reverts the proinflammatory state induced by cigarette smoke extract in lung Calu-3 cells.

P2860

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P2860

Characterization of mitochondrial function in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function.

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http://www.wikidata.org/entity/Q38871529

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

@zh-tw

2016年论文

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2016年论文

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2016年论文

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name

Characterization of mitochondr ...... nce regulator (CFTR) function.

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type

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Characterization of mitochondr ...... nce regulator (CFTR) function.

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Characterization of mitochondr ...... nce regulator (CFTR) function.

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P1476

Characterization of mitochondr ...... ance regulator (CFTR) function

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P2093

Antonella Bobba

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Maria Favia

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Stephan Joel Reshkin

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Valeria Casavola

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P2860

Targeted therapies to improve CFTR function in cystic fibrosis

Targeting mitochondrial dysfunction in lung diseases: emphasis on mitophagy

Superoxide flashes in mouse skeletal muscle are produced by discrete arrays of active mitochondria operating coherently

Cystic fibrosis

The expression of the mitochondrial gene MT-ND4 is downregulated in cystic fibrosis

High protonic potential actuates a mechanism of production of reactive oxygen species in mitochondria

Bcl-2 functions in an antioxidant pathway to prevent apoptosis

Disruption of interleukin-1β autocrine signaling rescues complex I activity and improves ROS levels in immortalized epithelial cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function.

Mitochondrial damage in muscle occurs after marked depletion of glutathione and is prevented by giving glutathione monoester

Impaired uptake of glutathione by hepatic mitochondria from chronic ethanol-fed rats. Tracer kinetic studies in vitro and in vivo and susceptibility to oxidant stress

P2888

s10863-016-9663-y

P304

197-210

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scholarly article

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10.1007/S10863-016-9663-Y

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P478

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Anna Atlante

Lorenzo Guerra

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2016-05-05T00:00:00Z

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P6179

1032144275

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27146408

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P921

cystic fibrosis

transmembrane protein

Characterization of mitochondrial function in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function.

about

P2860

P2860

Characterization of mitochondrial function in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function.

description

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type

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P1476

P2093

P2860

P2888

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P356

P433

P478

P50

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P6179

P698

P921