1997
A Novel, Heritable, Expanding CTG Repeat in an Intron of the SEF2-1 Gene on Chromosome 18q21.1
Breschel T, McInnis M, Margolis R, Sirugo G, Corneliussen B, Simpson S, McMahon F, MacKinnon D, Xu J, Pleasant N, Huo Y, Ashworth R, Grundstrom C, Grundstrom T, Kidd K, DePaulo J, Ross C. A Novel, Heritable, Expanding CTG Repeat in an Intron of the SEF2-1 Gene on Chromosome 18q21.1. Human Molecular Genetics 1997, 6: 1855-1863. PMID: 9302263, DOI: 10.1093/hmg/6.11.1855.Peer-Reviewed Original ResearchMeSH KeywordsAllelesBase SequenceBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsBipolar DisorderBlotting, SouthernCell LineChromosomes, Human, Pair 18Cloning, MolecularDNA-Binding ProteinsFemaleGene FrequencyHelix-Loop-Helix MotifsHumansIntronsMaleMolecular Sequence DataPedigreeSequence AnalysisTCF Transcription FactorsTrans-ActivatorsTranscription Factor 4Transcription Factor 7-Like 2 ProteinTranscription FactorsTrinucleotide RepeatsConceptsCEPH reference pedigreesSouthern blot analysisReference pedigreesUnstable alleleDNA binding proteinTriplet repeat mutationBlot analysisCTG repeatsTranscriptional regulationGenomic digestsHuman chromosomesKb cloneStable allelesCandidate genesAbnormal phenotypeBinding proteinRepeatsRepeat lociBipolar pedigreesGenesChromosome 18q21.1Repeat mutationsSomatic mutationsIntronsAlleles
1989
The β subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies
Wu J, Giuffra L, Goodfellow P, Myers S, Carson N, Anderson L, Hoyle L, Simpson N, Kidd K. The β subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies. Human Genetics 1989, 83: 383-390. PMID: 2572537, DOI: 10.1007/bf00291386.Peer-Reviewed Original ResearchMeSH KeywordsChromosome MappingChromosomes, Human, Pair 1Chromosomes, Human, Pair 10Chromosomes, Human, Pair 17Chromosomes, Human, Pair 21DNADNA ProbesDNA, NeoplasmFemaleGenetic LinkageGenetic MarkersHaplotypesHumansMaleMultiple Endocrine NeoplasiaPolymorphism, Restriction Fragment LengthReceptors, FibronectinReceptors, ImmunologicConceptsRestriction fragment length polymorphismHuman fibronectin receptorCDNA clonesFragment length polymorphismLinkage analysisDNA restriction fragment length polymorphismsMultiple restriction fragment length polymorphismsPolymorphism information content (PIC) valuesFibronectin receptorHighest polymorphism information content valuePartial cDNA cloneInformation content valuesLength polymorphismLinkage studiesPairwise linkage analysisSouthern blot analysisTypes of polymorphismsChromosome 10 markersGenomic clonesPericentromeric regionTransmembrane proteinDNA markersGenetic linkage studiesDNA sequencesSingle locus
1988
D10S20, a previously unmapped RFLP (OS-3), is located on 10q near D10S4
Miki T, Nishisho I, Tateishi H, Chen Y, Kidd J, Wu J, Pravtcheva D, Pakstis A, Takai S, Ruddle F, Kidd K. D10S20, a previously unmapped RFLP (OS-3), is located on 10q near D10S4. Genomics 1988, 3: 78-81. PMID: 2906046, DOI: 10.1016/0888-7543(88)90163-2.Peer-Reviewed Original ResearchConceptsSomatic cell hybrid DNAsCell hybrid DNAsComparative mapping studiesTaqI RFLPMouse genomic DNASouthern blot analysisCM distalHybrid DNAChromosome 10Genomic DNARsaI RFLPGenetic linkageStrong linkage disequilibriumHuman cloneLinkage disequilibriumLong armBlot analysisRFLPMapping studiesLociDNAClonesBanIIDisequilibriumProbeThe Anonymous RFLP Locus D1S2 Is Close to PGMl on Chromosome 1
Kidd K, Kidd J, Castiglione C, Sparkes R, Egeland J, Bakker E. The Anonymous RFLP Locus D1S2 Is Close to PGMl on Chromosome 1. Human Heredity 1988, 38: 22-26. PMID: 2895061, DOI: 10.1159/000153749.Peer-Reviewed Original Research