2013
Whole-exome sequencing identifies a novel somatic mutation in MMP8 associated with a t(1;22)-acute megakaryoblastic leukemia
Kim Y, Schulz VP, Satake N, Gruber TA, Teixeira AM, Halene S, Gallagher PG, Krause DS. Whole-exome sequencing identifies a novel somatic mutation in MMP8 associated with a t(1;22)-acute megakaryoblastic leukemia. Leukemia 2013, 28: 945-948. PMID: 24157583, PMCID: PMC3981934, DOI: 10.1038/leu.2013.314.Peer-Reviewed Original Research
1994
Localization of the human α-fodrin gene (SPTAN1) to 9q33→q34 by fluorescence in situ hybridization
Upender M, Gallagher PG, Moon RT, Ward DC, Forget BG. Localization of the human α-fodrin gene (SPTAN1) to 9q33→q34 by fluorescence in situ hybridization. Cytogenetic And Genome Research 1994, 66: 39-41. PMID: 8275706, DOI: 10.1159/000133660.Peer-Reviewed Original ResearchMeSH KeywordsCarrier ProteinsCell LineChromosome MappingChromosomes, Human, Pair 22Chromosomes, Human, Pair 9Gene LibraryHumansIn Situ Hybridization, FluorescenceLeukemia, Myelogenous, Chronic, BCR-ABL PositiveLymphocyte ActivationLymphocytesMicrofilament ProteinsMultigene FamilySpectrinTranslocation, GeneticTumor Cells, CulturedConceptsSitu hybridizationCell linesTranslocation breakpoint regionChronic myelogenous leukemia cell lineHuman chronic myelogenous leukemia cell lineSpectrin geneMyelogenous leukemia cell lineLeukemia cell linesGenesTranslocation breakpointsChromosomesBreakpoint regionHybridizationLociFluorescencePh1 chromosomeLinesPhiladelphia chromosomeK562BreakpointsLocalizationMembers