CFTR function and prospects for therapy.

By John R. Riordan. Annual Review of Biochemistry, 2008

640 citations recorded by the source corpus.

Subfields: Genetics, Pulmonary and Respiratory Medicine

View Paper: https://www.semanticscholar.org/paper/f874350b838690b959b39603a7b36992b8eb907b

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In Genetics

1. K. Locher

In Pulmonary and Respiratory Medicine

1. K. Locher

Citations in the corpus

• Mechanistic diversity in ATP-binding cassette (ABC) transporters (2016, background): “The asymmetry of ATPase sites extends beyond the B-family of ABC transporters: The cystic fibrosis transmembrane conductance regulator (ABCC7) also features a degenerate site in addition to the consensus site and it is currently assumed that binding of ATP to the degenerate site of CFTR is essential”