Abstract
Transgenic fragile X knockout mice have been constructed to provide an animal model to study the physiologic function of the fragile X gene (FMR1) and to gain more insight into the clinical phenotype caused by the absence of the fragile X protein. Initial experiments suggested that the knockout mice show macroorchidism and cognitive and behavioral deficits, abnormalities comparable to those of human fragile X patients. In the present study, we have extended our experiments, and conclude that the Fmr1 knockout mouse is a reliable transgenic model to study the fragile X syndrome.
Publication types
-
Comparative Study
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Aging / physiology
-
Animals
-
Fragile X Mental Retardation Protein
-
Fragile X Syndrome / genetics*
-
Fragile X Syndrome / physiopathology*
-
Fragile X Syndrome / psychology
-
Humans
-
Male
-
Maze Learning*
-
Mice
-
Mice, Knockout
-
Mice, Transgenic
-
Nerve Tissue Proteins / genetics*
-
Nerve Tissue Proteins / physiology
-
Organ Size
-
RNA-Binding Proteins*
-
Reference Values
-
Testis / growth & development
Substances
-
FMR1 protein, human
-
Fmr1 protein, mouse
-
Nerve Tissue Proteins
-
RNA-Binding Proteins
-
Fragile X Mental Retardation Protein