1995
Assignment of the 5HT7 receptor gene (HTR7) to chromosome 10q and exclusion of genetic linkage with tourette syndrome
Gelernter J, Rao P, Pauls D, Hamblin M, Sibley D, Kidd K. Assignment of the 5HT7 receptor gene (HTR7) to chromosome 10q and exclusion of genetic linkage with tourette syndrome. Genomics 1995, 26: 207-209. PMID: 7601444, DOI: 10.1016/0888-7543(95)80202-w.Peer-Reviewed Original ResearchMeSH KeywordsBlotting, SouthernChromosome MappingChromosomes, Human, Pair 10GenesHumansLod ScorePolymorphism, Restriction Fragment LengthReceptors, SerotoninTourette SyndromeConceptsGenetic linkageSomatic cell hybridsInteresting candidate genesPairwise linkage analysisCell hybridsNovel serotonin receptorCandidate genesChromosome 10Linkage analysisSouthern blotGenesExtended pedigreesLOD scoreReceptor geneLociGenetic polymorphismsHTR7PolymorphismReceptorsLIPED computer programDNALinkageHybridizationNeuropsychiatric disordersPedigree
1993
Genomic and Yeast Artificial Chromosome Long-Range Regular Article Linking Six Loci in 10q11.2 and Spanning the Multiple Endocrine Neoplasia Type 2A (MEN2A) Region
Brooks-Wilson A, Lichter J, Ward D, Kidd K, Goodfellow P. Genomic and Yeast Artificial Chromosome Long-Range Regular Article Linking Six Loci in 10q11.2 and Spanning the Multiple Endocrine Neoplasia Type 2A (MEN2A) Region. Genomics 1993, 17: 611-617. PMID: 7902324, DOI: 10.1006/geno.1993.1380.Peer-Reviewed Original ResearchConceptsRestriction mappingIdentification of genesLong-range restriction mappingContig assemblyPhysical mapTumor-specific alterationsGenomic DNAYAC contigPhysical linkageCandidate intervalDistal lociLociProto-oncogeneD10S102GenesCandidate regionsRET proto-oncogeneFamilial medullary thyroid carcinomaType 2ARETD10S94Multiple endocrine neoplasia type 2AContigsGenomicsHereditary cancerPhysical and Genetic Maps for Chromosome 10
Lichter J, Difilippantonio M, Pakstis A, Goodfellow P, Ward D, Kidd K. Physical and Genetic Maps for Chromosome 10. Genomics 1993, 16: 320-324. PMID: 8314570, DOI: 10.1006/geno.1993.1192.Peer-Reviewed Original ResearchMeSH KeywordsChromosome MappingChromosomes, Human, Pair 10FemaleGenetic LinkageGenetic MarkersHumansIn Situ Hybridization, FluorescenceMaleRecombination, GeneticReference StandardsSex CharacteristicsConceptsChromosome 10Physical mapOrder of lociGenetic mapLinkage mapGenetic distanceFemale mapGenetic linkage studiesMetaphase chromosomesPolymorphic lociNew lociQ armLociFractional lengthCentromeresLinkage studiesFishPhysical distanceRecombinationCentimorgansChromosomesDistance estimatesFemalesMalesFluorescenceA new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus
Lichter J, Wu J, Brooks-Wilson A, Difillipantonio M, Brewster S, Ward D, Goodfellow P, Kidd K. A new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus. Human Genetics 1993, 90: 516-520. PMID: 8094065, DOI: 10.1007/bf00217451.Peer-Reviewed Original ResearchMeSH KeywordsAnimalsBase SequenceChromosome MappingChromosomes, FungalChromosomes, Human, Pair 10Cloning, MolecularCricetinaeDeoxyribonuclease EcoRIDNADNA ProbesFemaleGene FrequencyGene LibraryGenetic LinkageGenetic MarkersGenome, HumanHumansHybrid CellsIn Situ Hybridization, FluorescenceLod ScoreMaleMolecular Sequence DataMultiple Endocrine NeoplasiaPedigreePolymorphism, GeneticPolymorphism, Restriction Fragment LengthSequence Analysis, DNA
1992
A high-resolution meiotic mapping panel for the pericentromeric region of chromosome 10
Lichter J, Wu J, Miller D, Goodfellow P, Kidd K. A high-resolution meiotic mapping panel for the pericentromeric region of chromosome 10. Genomics 1992, 13: 607-612. PMID: 1353475, DOI: 10.1016/0888-7543(92)90131-b.Peer-Reviewed Original ResearchMeSH KeywordsCentromereChromosome MappingChromosomes, Human, Pair 10Crossing Over, GeneticFemaleGenetic LinkageGenetic MarkersHumansMaleMeiosisMultiple Endocrine NeoplasiaPedigreeIsolation and high-resolution mapping of new DNA markers from the pericentromeric region of chromosome 10
Miller D, Dill F, Lichter J, Kidd K, Goodfellow P. Isolation and high-resolution mapping of new DNA markers from the pericentromeric region of chromosome 10. Genomics 1992, 13: 601-606. PMID: 1353474, DOI: 10.1016/0888-7543(92)90130-k.Peer-Reviewed Original ResearchCentromereChromosome MappingChromosomes, Human, Pair 10DNADNA ProbesGenetic MarkersHumansHybrid CellsMultiple Endocrine NeoplasiaLocalization of the gene for MEN 2A.
Lichter J, Difilippantonio M, Wu J, Miller D, Ward D, Goodfellow P, Kidd K. Localization of the gene for MEN 2A. Henry Ford Hospital Medical Journal 1992, 40: 199-204. PMID: 1362405.Peer-Reviewed Original ResearchMeSH KeywordsChromosome MappingChromosomes, Human, Pair 10Cloning, MolecularGenetic LinkageHumansIn Situ HybridizationMultiple Endocrine NeoplasiaPolymerase Chain ReactionPolymorphism, GeneticConceptsGene mapping techniquesYeast artificial chromosomesMapping panelPericentromeric regionArtificial chromosomesGenetic linkage studiesChromosome 10GenesSitu hybridizationLinkage studiesChromosomesMBMultiple endocrine neoplasia type 2A syndromeDNAHybridizationRegionConsistent orderSmall regionLocalizationFluorescenceMarkers
1990
The mutation for medullary thyroid carcinoma with parathyroid tumors (MTC with PTs) is closely linked to the centromeric region of chromosome 10.
Carson N, Wu J, Jackson C, Kidd K, Simpson N. The mutation for medullary thyroid carcinoma with parathyroid tumors (MTC with PTs) is closely linked to the centromeric region of chromosome 10. American Journal Of Human Genetics 1990, 47: 946-51. PMID: 1978560, PMCID: PMC1683917.Peer-Reviewed Original ResearchA refined linkage map for DNA markers around the pericentromeric region of chromosome 10
Wu J, Myers S, Carson N, Kidd J, Anderson L, Castiglione C, Hoyle L, Lichter J, Sukhatme V, Simpson N, Kidd K. A refined linkage map for DNA markers around the pericentromeric region of chromosome 10. Genomics 1990, 8: 461-468. PMID: 1981049, DOI: 10.1016/0888-7543(90)90032-p.Peer-Reviewed Original ResearchA HaeIII polymorphism at the D10S101 locus
Wu J, Kidd K. A HaeIII polymorphism at the D10S101 locus. Nucleic Acids Research 1990, 18: 5577-5577. PMID: 1977118, PMCID: PMC332269, DOI: 10.1093/nar/18.18.5577-a.Peer-Reviewed Original ResearchChromosomes, Human, Pair 10Deoxyribonucleases, Type II Site-SpecificHumansPolymorphism, Restriction Fragment LengthHincll polymorphism at the D10S95 locus
Wu J, Kidd K. Hincll polymorphism at the D10S95 locus. Nucleic Acids Research 1990, 18: 4965-4965. PMID: 1975682, PMCID: PMC332037, DOI: 10.1093/nar/18.16.4965-a.Peer-Reviewed Original ResearchAn EcoRI polymorphism identified by KW6 (D10S97) on chromosome 10
Wu J, Kidd K. An EcoRI polymorphism identified by KW6 (D10S97) on chromosome 10. Nucleic Acids Research 1990, 18: 1316-1316. PMID: 1969624, PMCID: PMC330479, DOI: 10.1093/nar/18.5.1316.Peer-Reviewed Original ResearchBacteriophagesChromosomes, Human, Pair 10Deoxyribonuclease EcoRIHumansPolymorphism, Restriction Fragment LengthHigh frequency Pvull and Pstl polymorphisms identified by KW31 (D10S96) on chromosome 10
Wu J, Kidd K. High frequency Pvull and Pstl polymorphisms identified by KW31 (D10S96) on chromosome 10. Nucleic Acids Research 1990, 18: 1316-1316. PMID: 1969625, PMCID: PMC330480, DOI: 10.1093/nar/18.5.1316-a.Peer-Reviewed Original ResearchBacteriophage lambdaChromosomes, Human, Pair 10Deoxyribonucleases, Type II Site-SpecificHumansPolymorphism, Restriction Fragment LengthThe CEPH consortium primary linkage map of human chromosome 10
White R, Lalouel J, Nakamura Y, Donis-Keller H, Green P, Bowden D, Mathew C, Easton D, Robson E, Morton N, Gusella J, Haines J, Retief A, Kidd K, Murray J, Lathrop G, Cann H. The CEPH consortium primary linkage map of human chromosome 10. Genomics 1990, 6: 393-412. PMID: 1970325, DOI: 10.1016/0888-7543(90)90469-b.Peer-Reviewed Original ResearchExtensive sequence polymorphisms associated with chromosome 10 alpha satellite DNA and its close linkage to markers from the pericentromeric region
Wu J, Kidd K. Extensive sequence polymorphisms associated with chromosome 10 alpha satellite DNA and its close linkage to markers from the pericentromeric region. Human Genetics 1990, 84: 279-282. PMID: 1968036, DOI: 10.1007/bf00200575.Peer-Reviewed Original ResearchMeSH KeywordsChromosomes, Human, Pair 10DNA, SatelliteGenetic MarkersHumansPolymorphism, Restriction Fragment LengthRepetitive Sequences, Nucleic AcidRestriction MappingConceptsAlpha satellite DNAExtensive sequence polymorphismSatellite DNAPericentromeric regionSequence polymorphismsExcellent genetic markerCentromeric regionsDNA markersGenetic markersEnzyme PstILOD scoreClose linkagePositive lod scoresLinkage studiesDNAType 2AIndependent supportPolymorphismCentromeresMorphsMarkersRBP3LociDistance relationshipsEcoRV
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 locusThe mapping of the locus for multiple endocrine neoplasia type 2A by linkage with chromosome 10 markers.
Simpson N, Kidd K. The mapping of the locus for multiple endocrine neoplasia type 2A by linkage with chromosome 10 markers. Hormone And Metabolic Research. Supplement Series 1989, 21: 5-9. PMID: 2572529.Peer-Reviewed Original ResearchMeSH KeywordsChromosome MappingChromosomes, Human, Pair 10Genetic LinkageGenetic MarkersHumansMultiple Endocrine NeoplasiaConceptsDisease locusInterstitial retinol-binding proteinChromosome 10 markersTest of linkageChromosome 10Disease genesDeletion siteChromosome 20Additional family dataBinding proteinLociGenesExclusion of linkageSitu hybridizationD10S5Ultimate identificationRetinol-binding proteinType 2AMultiple endocrine neoplasia type 2AGenomeMarkersFamily dataLinkageProteinHybridizationClosing in on the MEN2A locus.
Simpson N, Kidd K. Closing in on the MEN2A locus. Henry Ford Hospital Medical Journal 1989, 37: 100-5. PMID: 2576936.Peer-Reviewed Original Research
1988
A HindIII polymorphism identified by the human early growth response gene 2 (EGR2) on chromosome 10
Wu J, Loren J, Sukhatme V, Kidd K. A HindIII polymorphism identified by the human early growth response gene 2 (EGR2) on chromosome 10. Nucleic Acids Research 1988, 16: 11855-11855. PMID: 2905450, PMCID: PMC339153, DOI: 10.1093/nar/16.24.11855.Peer-Reviewed Original ResearchA linkage group of five DNA markers on human chromosome 10
Farrer L, Castiglione C, Kidd J, Myers S, Carson N, Simpson N, Kidd K. A linkage group of five DNA markers on human chromosome 10. Genomics 1988, 3: 72-77. PMID: 2906045, DOI: 10.1016/0888-7543(88)90162-0.Peer-Reviewed Original ResearchConceptsLinkage groupsDNA markersChromosome 10Recombination frequencySex-specific recombination frequenciesAccurate genetic mapHuman chromosome 10Three-locus analysisLong armChromosome 10 markersGenetic mapLinkage mapPericentric regionsMarker lociMap intervalPrevious localizationLinkage analysisProximal regionLociLarge pedigreeType 2APedigreeMultiple endocrine neoplasia type 2AD10S5Markers