| Literature DB >> 15232606 |
Abstract
Circulating platelets are continually replenished by fragmentation of terminally differentiated megakaryocytes. Processes disrupted in inherited thrombocytopenias frequently shed light on normal thrombopoietic mechanisms. An especially rare condition called Paris-Trousseau syndrome (PTS) seems to occur by virtue of hemizygous loss of the FLI1 transcription factor gene. Provocative new data suggest that FLI1 shows monoallelic expression during a brief window in megakaryocyte differentiation, which thus explains the dominant inheritance pattern of PTS despite the presence of one normal FLI1 allele.Entities:
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Year: 2004 PMID: 15232606 PMCID: PMC437976 DOI: 10.1172/JCI22292
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808