Fragile X mouse: strain effects of knockout phenotype and evidence suggesting deficient amygdala function
- 13 September 1999
- journal article
- Published by Elsevier in Neuroscience
- Vol. 94 (1) , 185-192
- https://doi.org/10.1016/s0306-4522(99)00285-7
Abstract
No abstract availableKeywords
This publication has 46 references indexed in Scilit:
- Induction of Gut Mucosal Immune Responses: Importance of Genetic Background and Th1/Th2 Cross‐RegulationScandinavian Journal of Immunology, 1998
- Transgenic mouse model for the fragile X syndromeAmerican Journal of Medical Genetics, 1996
- Long-term potentiation in the hippocampus of fragile X knockout miceAmerican Journal of Medical Genetics, 1996
- Association of FMRP with Ribosomal Precursor Particles in the NucleolusBiochemical and Biophysical Research Communications, 1996
- FMRP is associated to the ribosomes via RNAHuman Molecular Genetics, 1996
- The fragile X mental retardation protein is associated with ribosomesNature Genetics, 1996
- Tissue specific expression of FMR–1 provides evidence for a functional role in fragile X syndromeNature Genetics, 1993
- Absence of expression of the FMR-1 gene in fragile X syndromeCell, 1991
- Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromePublished by Elsevier ,1991
- Spatial localization does not require the presence of local cuesLearning and Motivation, 1981