Satoh, Jun-ichi <br/><br/>
Microarray analysis identifies a set of CXCR3 and CCR2 ligand chemokines as early IFNbeta-responsive genes in peripheral blood lymphocytes in vitro: an implication for IFNbeta-related adverse effects in multiple sclerosis.  [electronic resource] 

 -  BMC neurology  May 2006 
 - 18 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1471-2377 
<br/><br/><label>Standard No.: </label>10.1186/1471-2377-6-18  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Computer Systems<br/>Genes--drug effects<br/>Genes, Immediate-Early<br/>Humans<br/>Interferon Type I--adverse effects<br/>Interferon-beta--pharmacology<br/>Ligands<br/>Lymphocytes--metabolism<br/>Male<br/>Middle Aged<br/>Monocytes--metabolism<br/>Multiple Sclerosis--drug therapy<br/>Oligonucleotide Array Sequence Analysis<br/>Receptors, CCR2<br/>Receptors, CXCR3<br/>Receptors, Chemokine--blood<br/>Recombinant Proteins<br/>Reverse Transcriptase Polymerase Chain Reaction<br/>Time Factors