1999
Global variation of a 40-bp VNTR in the 3′-untranslated region of the dopamine transporter gene (SLC6A3)
Kang A, Palmatier M, Kidd K. Global variation of a 40-bp VNTR in the 3′-untranslated region of the dopamine transporter gene (SLC6A3). Biological Psychiatry 1999, 46: 151-160. PMID: 10418689, DOI: 10.1016/s0006-3223(99)00101-8.Peer-Reviewed Original Research
1995
The Dopamine Transporter Protein Gene (SLC6A3): Primary Linkage Mapping and Linkage Studies in Tourette Syndrome
Gelernter J, Vandenbergh D, Kruger S, Pauls D, Kurlan R, Pakstis A, Kidd K, Uhl G. The Dopamine Transporter Protein Gene (SLC6A3): Primary Linkage Mapping and Linkage Studies in Tourette Syndrome. Genomics 1995, 30: 459-463. PMID: 8825631, DOI: 10.1006/geno.1995.1265.Peer-Reviewed Original ResearchConceptsTourette syndromeDopamine transporterAttention deficit disorderDopaminergic neuronsPresynaptic reuptakeSpecific localizationPsychiatric illnessPsychostimulant drugsChromosome 5pCocaine-induced paranoiaSyndromeDeficit disorderSLC6A3ScoresMajor siteLinkage studiesNegative lod scoresMarkersTransporter protein gene
1993
Assignment of the norepinephrine transporter protein (NET1) locusto chromosome 16
Gelernter J, Kruger S, Pakstis A, Pacholczyk T, Sparkes R, Kidd K, Amara S. Assignment of the norepinephrine transporter protein (NET1) locusto chromosome 16. Genomics 1993, 18: 690-692. PMID: 7905857, DOI: 10.1016/s0888-7543(05)80375-1.Peer-Reviewed Original ResearchMeSH KeywordsCarrier ProteinsChromosome MappingChromosomes, Human, Pair 16Deoxyribonucleases, Type II Site-SpecificDNA, ComplementaryGenetic LinkageGenetic MarkersHumansNorepinephrineNorepinephrine Plasma Membrane Transport ProteinsPolymorphism, Restriction Fragment LengthRestriction MappingSymportersConceptsNorepinephrine transporter proteinSomatic cell hybrid panelCell hybrid panelHybrid panelHP locusCEPH familiesLarge multigenerational familyTransporter proteinsLinkage analysisChromosome 16Provisional assignmentLinkage dataLociMultigenerational familiesGenetic polymorphismsSite of actionPreliminary assignmentNet1FamilyProteinRFLPSitesPolymorphismPCRLocalization
1991
Rearrangement of the retinoic acid receptor gene in acute promyelocytic leukemia.
Chang K, Trujillo J, Ogura T, Castiglione C, Kidd K, Zhao S, Freireich E, Stass S. Rearrangement of the retinoic acid receptor gene in acute promyelocytic leukemia. Leukemia 1991, 5: 200-4. PMID: 1849600.Peer-Reviewed Original ResearchConceptsAcute promyelocytic leukemiaRAR alpha geneAPL patientsPromyelocytic leukemiaAPL patient samplesRetinoic acid receptor alpha geneAcid receptor alpha geneRAR-alpha mRNAReceptor alpha geneRetinoic acid receptor genesAcute leukemiaPatientsLeukemic samplesPatient samplesLeukemiaReceptor geneNorthern blot analysisBlot analysisMRNA
1990
The Na+/H+ antiporter: a “melt” polymorphism allows regional mapping to the short arm of chromosome 1
Dudley C, Giuffra L, Tippett P, Kidd K, Reeders S. The Na+/H+ antiporter: a “melt” polymorphism allows regional mapping to the short arm of chromosome 1. Human Genetics 1990, 86: 79-83. PMID: 1979310, DOI: 10.1007/bf00205179.Peer-Reviewed Original Research