2001
Dynamic molecular modeling of pathogenic mutations in the spectrin self-association domain
Zhang Z, Weed S, Gallagher P, Morrow J. Dynamic molecular modeling of pathogenic mutations in the spectrin self-association domain. Blood 2001, 98: 1645-1653. PMID: 11535493, DOI: 10.1182/blood.v98.6.1645.Peer-Reviewed Original ResearchConceptsSelf-association domainPoint mutationsHuman sequenceDrosophila alpha-spectrinDynamic molecular modelingHuman erythrocyte spectrinCytoskeletal functionSpecific point mutationsConservative substitutionsPrimary sequenceConformational rearrangementsAlpha-spectrinHelical regionHydrophilic residuesAmino acidsMutationsSpectrinSalt bridgeErythrocyte spectrinStructural consequencesPathogenic mutationsRepeat unitsMolecular modelingSequenceStructural disruption
1999
Exclusion of the stomatin, α‐adducin and β‐adducin loci in a large kindred with dehydrated hereditary stomatocytosis
Innes D, Sinard J, Gilligan D, Snyder L, Gallagher P, Morrow J. Exclusion of the stomatin, α‐adducin and β‐adducin loci in a large kindred with dehydrated hereditary stomatocytosis. American Journal Of Hematology 1999, 60: 72-74. PMID: 9883810, DOI: 10.1002/(sici)1096-8652(199901)60:1<72::aid-ajh13>3.0.co;2-8.Peer-Reviewed Original Research
1986
Abnormal spectrin in hereditary elliptocytosis.
Marchesi S, Knowles W, Morrow J, Bologna M, Marchesi V. Abnormal spectrin in hereditary elliptocytosis. Blood 1986, 67: 141-51. PMID: 3940543, DOI: 10.1182/blood.v67.1.141.bloodjournal671141.Peer-Reviewed Original ResearchMeSH KeywordsAdolescentAdultAnemia, Hemolytic, CongenitalElliptocytosis, HereditaryFemaleHumansMaleMiddle AgedPolymersSpectrinTrypsinConceptsClinical expressionHemolytic anemiaSubset of patientsRare hemolytic anemiaAlpha iAlpha II domainAlpha subunitHereditary pyropoikilocytosisFunctional resultsSpectrin alpha subunitHereditary elliptocytosisHematologic diseasesAnemiaMild elliptocytosisAbnormal spectrinSeverityPresent studyKD peptideExpressionD-peptidesFrequent occurrenceSpectrin self-association
1983
Molecular and functional changes in spectrin from patients with hereditary pyropoikilocytosis.
Knowles W, Morrow J, Speicher D, Zarkowsky H, Mohandas N, Mentzer W, Shohet S, Marchesi V. Molecular and functional changes in spectrin from patients with hereditary pyropoikilocytosis. Journal Of Clinical Investigation 1983, 71: 1867-1877. PMID: 6863544, PMCID: PMC370392, DOI: 10.1172/jci110942.Peer-Reviewed Original ResearchMeSH KeywordsAdultAnemia, Hemolytic, CongenitalErythrocytesFemaleHot TemperatureHumansMacromolecular SubstancesMaleMembrane ProteinsPeptide FragmentsProtein DenaturationSpectrinTrypsin