Structured Summary
Abstract
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.
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Synonyms
9 entry terms
- Mice, CFTR
- Mice, Inbred CFTR
- Mouse, CFTR
- Mouse, Inbred CFTR
- CFTR Mice
- CFTR Mice, Inbred
- CFTR Mouse
- CFTR Mouse, Inbred
- Inbred CFTR Mouse
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Aspects Covered
18 allowable subheadings
Indexed with the subheadings abnormalities, anatomy & histology, blood, cerebrospinal fluid, classification, embryology, genetics, growth & development, immunology, injuries, metabolism, microbiology, parasitology, physiology, psychology, surgery, urine, virology.
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Indexing Annotation
NIM with no qualifiers when experimental animal
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History Note
94
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Previous Indexing
- Mice (1992-1993)
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AMA Style
References
- National Library of Medicine. Inbred CFTR Mice. Medical Subject Headings (MeSH). 2026. Unique ID D018181. http://id.nlm.nih.gov/mesh/2026/D018181
- Inbred CFTR Mice. In: Wikidata. https://www.wikidata.org/wiki/Q68806508