Kudo, S <br/><br/>
Functional analyses of MeCP2 mutations associated with Rett syndrome using transient expression systems.  [electronic resource] 

 -  Brain & development  Dec 2001 
 - S165-73 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0387-7604 
<br/><br/><label>Standard No.: </label>10.1016/s0387-7604(01)00345-x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Cell Compartmentation--genetics<br/>Cell Nucleus--genetics<br/>Cells, Cultured<br/>Chromosomal Proteins, Non-Histone<br/>DNA--genetics<br/>DNA-Binding Proteins--genetics<br/>Drosophila--genetics<br/>Female<br/>Fluorescent Antibody Technique<br/>Gene Expression Regulation, Developmental--genetics<br/>Genes, Regulator--genetics<br/>Green Fluorescent Proteins<br/>Heterochromatin--genetics<br/>Humans<br/>Immunoglobulins--genetics<br/>Indicators and Reagents--metabolism<br/>Luminescent Proteins--genetics<br/>Methyl-CpG-Binding Protein 2<br/>Mice<br/>Mutation--genetics<br/>Mutation, Missense--genetics<br/>Promoter Regions, Genetic--genetics<br/>Recombinant Fusion Proteins--genetics<br/>Repressor Proteins--genetics<br/>Rett Syndrome--genetics