Architecture and functional properties of the CFTR channel pore.

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CFTR gating: Invisible transitions made visible.AJRCCM: 100-Year Anniversary. Progress along the Pathway of Discovery Leading to Treatment and Cure of Cystic Fibrosis.Structural mechanisms of CFTR function and dysfunction.

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P2860

Architecture and functional properties of the CFTR channel pore.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年學術文章

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2016年學術文章

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2016年學術文章

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Architecture and functional properties of the CFTR channel pore.

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Architecture and functional properties of the CFTR channel pore.

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Architecture and functional properties of the CFTR channel pore.

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P1476

Architecture and functional properties of the CFTR channel pore.

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P2860

ABC transporters: the power to change

The ABC protein turned chloride channel whose failure causes cystic fibrosis

Structure and function of TMEM16 proteins (anoctamins)

Glycine receptor mechanism elucidated by electron cryo-microscopy.

Crystal structure of a human GABAA receptor

The Cystic Fibrosis Transmembrane Conductance Regulator (CFTR): THREE-DIMENSIONAL STRUCTURE AND LOCALIZATION OF A CHANNEL GATE

Structural Basis for Heavy Metal Detoxification by an Atm1-Type ABC Exporter

Structure of an antibacterial peptide ATP-binding cassette transporter in a novel outward occluded state

Crystal structure of human glycine receptor-α3 bound to antagonist strychnine

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

P2888

s00018-016-2389-5

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67-83

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scholarly article

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Architecture and functional properties of the CFTR channel pore.

about

P2860

P2860

Architecture and functional properties of the CFTR channel pore.

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