Rett syndrome like phenotypes in the R255X Mecp2 mutant mouse are rescued by MECP2 transgene. [electronic resource]
Producer: 20151222Description: 2662-72 p. digitalISSN:- 1460-2083
- Alleles
- Amino Acid Substitution
- Animals
- Behavior, Animal
- Disease Models, Animal
- Fibroblasts -- drug effects
- Gene Expression
- Genetic Association Studies
- Gentamicins -- pharmacology
- Mechanistic Target of Rapamycin Complex 1
- Methyl-CpG-Binding Protein 2 -- genetics
- Mice
- Mice, Transgenic
- Multiprotein Complexes -- metabolism
- Mutation
- Phenotype
- RNA, Messenger -- genetics
- Rett Syndrome -- diagnosis
- Signal Transduction
- TOR Serine-Threonine Kinases -- metabolism
- Transgenes
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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