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Subject Areas on Research
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A logistic regression model for measuring gene-longevity associations.
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Age-related changes of the 3'APOB-VNTR genotype pool in ageing cohorts.
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An allele of HRAS1 3'variable number of tandem repeats is a frailty allele: implication for an evolutionarily-conserved pathway involved in longevity.
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Analysis of the D1S80 (pMCT118) VNTR locus polymorphism in a native Kuwaiti population by the polymerase chain reaction.
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Association of a functional tandem repeats in the downstream of human telomerase gene and lung cancer.
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Attention deficit/hyperactivity disorder children with a 7-repeat allele of the dopamine receptor D4 gene have extreme behavior but normal performance on critical neuropsychological tests of attention.
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Autism and the serotonin transporter: the long and short of it.
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Comparison of seven techniques for typing international epidemic strains of Clostridium difficile: restriction endonuclease analysis, pulsed-field gel electrophoresis, PCR-ribotyping, multilocus sequence typing, multilocus variable-number tandem-repeat analysis, amplified fragment length polymorphism, and surface layer protein A gene sequence typing.
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DRD4 VNTR polymorphism is associated with transient fMRI-BOLD responses to smoking cues.
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Destabilization of yeast micro- and minisatellite DNA sequences by mutations affecting a nuclease involved in Okazaki fragment processing (rad27) and DNA polymerase delta (pol3-t).
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Effects of source of DNA on genotyping success rates and allele percentages in the Preschoolers with Attention-Deficit/Hyperactivity Disorder Treatment Study (PATS).
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From genes to mechanisms to therapies: lessons to be learned from neurological disorders.
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Genetic diversity in the Mycobacterium tuberculosis complex based on variable numbers of tandem DNA repeats.
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Genome engineering: a new approach to gene therapy for neuromuscular disorders.
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Genomic sequencing is required for identification of tuberculosis transmission in Hawaii.
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HPA axis function in male caregivers: effect of the monoamine oxidase-A gene promoter (MAOA-uVNTR).
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Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDH.
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Identification and evolution of an IS6110 low-copy-number Mycobacterium tuberculosis cluster.
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Identification of pathogenic yeasts of the imperfect genus Candida by polymerase chain reaction fingerprinting.
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Immunogenetic associations in childhood dermatomyositis.
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Internal migration and transmission dynamics of tuberculosis in Shanghai, China: an epidemiological, spatial, genomic analysis.
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Lipid levels are associated with a regulatory polymorphism of the monoamine oxidase-A gene promoter (MAOA-uVNTR).
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Maximal stimulation of meiotic recombination by a yeast transcription factor requires the transcription activation domain and a DNA-binding domain.
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Mycobacterial interspersed repetitive-unit-variable-number tandem-repeat analysis and Beijing/W family of Mycobacterium tuberculosis.
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Novelty seeking and the dopamine D4 receptor gene (DRD4) revisited in Asians: haplotype characterization and relevance of the 2-repeat allele.
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Phenotypic and genotypic characterization of Mycobacterium africanum isolates from West Africa.
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Polymorphic variation in the dopamine D4 receptor predicts delay discounting as a function of childhood socioeconomic status: evidence for differential susceptibility.
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Rapid identification of laboratory contamination with Mycobacterium tuberculosis using variable number tandem repeat analysis.
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Relationship of genetic variability and depressive symptoms to adverse events after coronary artery bypass graft surgery.
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Replication studies in longevity: puzzling findings in Danish centenarians at the 3'APOB-VNTR locus.
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Role of genotype in the cycle of violence in maltreated children.
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Serotonin transporter polymorphisms and measures of impulsivity, aggression, and sensation seeking among African-American cocaine-dependent individuals.
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The Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American family.
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The genetic architecture of selection at the human dopamine receptor D4 (DRD4) gene locus.
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The insulin gene is transcribed in the human thymus and transcription levels correlated with allelic variation at the INS VNTR-IDDM2 susceptibility locus for type 1 diabetes.
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Variation of human amygdala response during threatening stimuli as a function of 5'HTTLPR genotype and personality style.