Concept information
Terme préférentiel
Mice, Inbred CFTR
Type
-
mesh:Descriptor
Définition
- A strain of mice widely studied as a model for cystic fibrosis. These mice are generated from embryonic stem cells in which the CFTR (cystic fibrosis transmembrane conductance regulator) gene is inactivated by gene targeting. As a result, all mice have one copy of this altered gene in all their tissues. Mice homozygous for the disrupted gene exhibit many features common to young cystic fibrosis patients, including failure to thrive, meconium ileus, and alteration of mucous and serous glands.
Concept générique
Synonyme(s)
- Mice, CFTR
- Mouse, CFTR
- Mouse, Inbred CFTR
Qualificatif(s) autorisé(s)
- abnormalities (Qualifier)
- anatomy & histology (Qualifier)
- blood (Qualifier)
- cerebrospinal fluid (Qualifier)
- classification (Qualifier)
- embryology (Qualifier)
- genetics (Qualifier)
- growth & development (Qualifier)
- immunology (Qualifier)
- injuries (Qualifier)
- metabolism (Qualifier)
- microbiology (Qualifier)
- parasitology (Qualifier)
- physiology (Qualifier)
- psychology (Qualifier)
- surgery (Qualifier)
- urine (Qualifier)
- virology (Qualifier)
Traductions
-
français
-
Souris CFTR
-
Souris de souche CFTR
URI
http://data.loterre.fr/ark:/67375/JVR-MBKGFT6D-M
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