rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
2
|
pubmed:dateCreated |
1996-12-13
|
pubmed:abstractText |
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.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0148-7299
|
pubmed:author |
pubmed-author:BakkerC ECE,
pubmed-author:ClinckeGG,
pubmed-author:D'HoogeRR,
pubmed-author:De BoulleKK,
pubmed-author:De DeynP PPP,
pubmed-author:GuanA LAL,
pubmed-author:NagelsGG,
pubmed-author:OostraB ABA,
pubmed-author:ReyniersEE,
pubmed-author:StormKK,
pubmed-author:WillemsP JPJ
|
pubmed:issnType |
Print
|
pubmed:day |
9
|
pubmed:volume |
64
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
241-5
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:8844056-Aging,
pubmed-meshheading:8844056-Animals,
pubmed-meshheading:8844056-Fragile X Mental Retardation Protein,
pubmed-meshheading:8844056-Fragile X Syndrome,
pubmed-meshheading:8844056-Humans,
pubmed-meshheading:8844056-Male,
pubmed-meshheading:8844056-Maze Learning,
pubmed-meshheading:8844056-Mice,
pubmed-meshheading:8844056-Mice, Knockout,
pubmed-meshheading:8844056-Mice, Transgenic,
pubmed-meshheading:8844056-Nerve Tissue Proteins,
pubmed-meshheading:8844056-Organ Size,
pubmed-meshheading:8844056-RNA-Binding Proteins,
pubmed-meshheading:8844056-Reference Values,
pubmed-meshheading:8844056-Testis
|
pubmed:year |
1996
|
pubmed:articleTitle |
Transgenic mouse model for the fragile X syndrome.
|
pubmed:affiliation |
Department of Medical Genetics, University of Antwerp, Belgium.
|
pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
|