2004
Update on the clinical spectrum and genetics of red blood cell membrane disorders.
Gallagher PG. Update on the clinical spectrum and genetics of red blood cell membrane disorders. Current Hematology Reports 2004, 3: 85-91. PMID: 14965483.Peer-Reviewed Original ResearchConceptsStructure/function relationshipsSignificant genetic heterogeneityPrecise genetic defectGenetic lociMolecular biologyRed blood cell membrane disordersSplicing mutationGene deletionNonsense mutationCell membraneFunction relationshipsGenetic heterogeneityGenetic defectsHereditary elliptocytosisMembrane disordersRed blood cell membraneBlood cell membranesHereditary pyropoikilocytosisMutationsBetter understandingErythrocyte membranesMembraneLociGeneticsBiology
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