 Mice, Inbred CFTR
"Mice, Inbred CFTR" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D018181
|
| MeSH Number(s) |
B01.050.050.157.520.445 B01.050.050.199.520.520.445 B01.050.150.900.649.865.635.505.500.400.445
|
| Concept/Terms |
Mice, Inbred CFTR- Mice, Inbred CFTR
- CFTR Mice, Inbred
- Inbred CFTR Mice
- Mouse, Inbred CFTR
- CFTR Mouse, Inbred
- Inbred CFTR Mouse
- Mice, CFTR
- CFTR Mice
- Mouse, CFTR
- CFTR Mouse
|
Below are MeSH descriptors whose meaning is more general than "Mice, Inbred CFTR".
Below are MeSH descriptors whose meaning is more specific than "Mice, Inbred CFTR".
This graph shows the total number of publications written about "Mice, Inbred CFTR" by people in UAMS Profiles by year, and whether "Mice, Inbred CFTR" was a major or minor topic of these publications.
![]()
To see the data from this visualization as text, click here.
Below are the most recent publications written about "Mice, Inbred CFTR" by people in Profiles over the past ten years.
|
Similar Concepts
![expand description]()
People who have written about this concept.
_
Top Journals
![expand description]()
Top journals in which articles about this concept have been published.
|