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Cystic Fibrosis Transmembrane Conductance Regulator

A chloride channel that regulates secretion in many exocrine tissues. Abnormalities in the CFTR gene have been shown to cause cystic fibrosis. (Hum Genet 1994;93(4):364-8)

Year introduced: 1996

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Subheadings:

Tree Number(s): D12.776.157.530.100.304.500, D12.776.157.530.400.175.125, D12.776.157.530.450.074.500.500.500.500, D12.776.543.550.450.175.125, D12.776.543.585.100.304.500, D12.776.543.585.400.175.125, D12.776.543.585.450.074.500.500.500.500

MeSH Unique ID: D019005

Registry Number: 126880-72-6

Entry Terms:

  • CFTR Protein
  • Protein, CFTR
  • Chloride channels, ATP-gated CFTR
  • Chloride channels, ATP gated CFTR

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