Search on: CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR 
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Descriptor English:   Cystic Fibrosis Transmembrane Conductance Regulator 
Descriptor Spanish:   Regulador de Conductancia de Transmembrana de Fibrosis Quística 
Descriptor Portuguese:   Regulador de Condutância Transmembrana em Fibrose Cística 
Synonyms English:   Chloride channels, ATP-gated CFTR
Chloride channels, ATP gated CFTR
Protein, CFTR
CFTR Protein  
Tree Number:   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
Definition English:   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) 
History Note English:   96; was CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR (NM) 1989-95 
Allowable Qualifiers English:  
AD administration & dosage AE adverse effects
AG agonists AN analysis
AI antagonists & inhibitors BI biosynthesis
BL blood CF cerebrospinal fluid
CS chemical synthesis CH chemistry
CL classification DF deficiency
DE drug effects EC economics
GE genetics HI history
IM immunology IP isolation & purification
ME metabolism PK pharmacokinetics
PD pharmacology PH physiology
PO poisoning RE radiation effects
SE secretion ST standards
SD supply & distribution TU therapeutic use
TO toxicity UL ultrastructure
UR urine  
Record Number:   32784 
Unique Identifier:   D019005 

Occurrence in VHL:
 

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