In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis. [electronic resource]
Producer: 20020425Description: 1364-72 p. digitalISSN:- 0006-4971
- Blood Platelet Disorders -- genetics
- Chromosomes, Human, Pair 21 -- genetics
- Core Binding Factor Alpha 2 Subunit
- DNA Mutational Analysis
- DNA-Binding Proteins -- genetics
- Family Health
- Female
- Genes, Dominant
- Genetic Linkage
- Genetic Predisposition to Disease
- Haplotypes
- Humans
- Leukemia, Myeloid, Acute -- etiology
- Male
- Pedigree
- Point Mutation -- physiology
- Protein Binding
- Proto-Oncogene Proteins
- Transcription Factor AP-2
- Transcription Factors -- genetics
- Transcriptional Activation -- drug effects
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
There are no comments on this title.
Log in to your account to post a comment.