What is str dna

Associations between STR autosomal markers and longevity. Age Biscotti, M. Repetitive DNA in eukaryotic genomes. Chromosome Res 23, — Butler, J. Genetics and genomics of core short tandem repeat loci used in human identity testing. Forensic Sci. Castel, A. Repeat instability as the basis for human diseases and as a potential target for therapy. Cell Biol. Chen, H. The mechanism of transactivation regulation due to polymorphic short tandem repeats STRs using IGF1 promoter as a model.

Chiba, M. Tyrosine hydroxylase gene microsatellite polymorphism associated with insulin resistance in depressive disorder. Metabolism 49, — Cole, S. DNA designation bunk? UL Rev. Colloquy , 54— Courts, C. Significant association of TH01 allele 9. De Benedictis, G. Eisenhofer, G. Catecholamine metabolism: a contemporary view with implications for physiology and medicine. Gaikwad, S. Host microsatellite alleles in malaria predisposition? Gemayel, R. Beyond junk-variable tandem repeats as facilitators of rapid evolution of regulatory and coding sequences.

Genes 3, — Gettings, K. A SNP assay for biogeographic ancestry and phenotype prediction in the U. The genomics of schizophrenia: update and implications.

Graves, J. Sex chromosome specialization and degeneration in mammals. Cell , — Graydon, M. Inferring ethnicity using 15 autosomal STR loci—Comparisons among populations of similar and distinctly different physical traits.

Guan, L. Chinese J. Gymrek, M. A genomic view of short tandem repeats. Abundant contribution of short tandem repeats to gene expression variation in humans. Hannan, A. Tandem repeats mediating genetic plasticity in health and disease. Hu, P. Application of causal inference to genomic analysis: advances in methodology. Hui, L. A new design without control population for identification of gastric cancer-related allele combinations based on interaction of genes.

Gene , 32— Jacewicz, R. Are tetranucleotide microsatellites implicated in neuropsychiatric diseases? Will genetic polymorphism of tetranucleotide sequences help in the diagnostics of major psychiatric disorders?

Katsanis, S. Kaye, D. Colloquy Kidd, K. Kimpton, C. Legal Med. Klintschar, M. A functional polymorphism in the tyrosine hydroxylase gene indicates a role of noradrenalinergic signaling in sudden infant death syndrome.

Kruger, A. A neofunctionalized X-linked ampliconic gene family is essential for male fertility and equal sex ratio in mice. Kurumaji, A. An association of the polymorphic repeat of tetranucleotide TCAT in the first intron of the human tyrosine hydroxylase gene with schizophrenia in a Japanese sample. Neural Transm. La Spada, A. Repeat expansion disease: progress and puzzles in disease pathogenesis.

Lahn, B. Functional coherence of the human Y chromosome. Science , — Laird, R. Lander, E. Initial sequencing and analysis of the human genome. Nature , — Li, Y. Microsatellites within genes: structure, function, and evolution. Liou, J. Human chromosome specific DNA markers are useful in prenatal detection of Down syndrome. Lowe, A. Inferring ethnic origin by means of an STR profile. Predictors of schizophrenia—a review.

McEwen, B. Sex, stress and the hippocampus: allostasis, allostatic load and the aging process. Aging 23, — Meiser, J. Complexity of dopamine metabolism. Cell Commun. Meloni, R. A tetranucleotide polymorphic microsatellite, located in the first intron of the tyrosine hydroxylase gene, acts as a transcription regulatory element in vitro. Meraz-Rios, M. BioMed Res. Modai, S.

Molecular risk factors for schizophrenia. Morimoto, K. Delusional disorder: molecular genetic evidence for dopamine psychosis. Neuropsychopharmacology 26, — Ng, J. Monoamine neurotransmitter disorders—clinical advances and future perspectives. Orr, H. Trinucleotide repeat disorders. Peloso, G. Brinkman and A. Carracedo Amsterdam: Elsevier Science Bv , — Persson, M. Tyrosine hydroxylase allelic distribution in suicide attempters.

Psychiatry Res. Search for the influence of the tyrosine hydroxylase TCAT n repeat polymorphism on personality traits. Qi, X. Genetic risk analysis for an individual according to the theory of programmed onset, illustrated by lung and liver cancers. Gene , — Quilez, J. Polymorphic tandem repeats within gene promoters act as modifiers of gene expression and DNA methylation in humans. Nucleic Acids Res. Ramel, C. Mini- and microsatellites.

Health Perspect. Relethford, J. Hemispheric difference in human skin color. Rogowski, M. Loss of heterozygosity in laryngeal cancer.

Sander, T. Possible allelic association of a tyrosine hydroxylase polymorphism with vulnerability to alcohol-withdrawal delirium. Sarkar, S. Whose DNA is it anyway? European court, junk DNA, and the problem with prediction.

Psychiatry Law 38, — Sawaya, S. Microsatellite tandem repeats are abundant in human promoters and are associated with regulatory elements. PLoS One 8:e Schooler, J. Nature Serretti, A. Tyrosine hydroxylase gene associated with depressive symptomatology in mood disorder. Shi, Y. Studer, J. Tyrosine hydroxylase TH01 9.

Sutherland, G. B Neuropsychiatr. Szibor, R. The HumARA genotype is linked to spinal and bulbar muscular dystrophy and some further disease risks and should no longer be used as a DNA marker for forensic purposes. Tautz, D. Simple sequences. Tochigi, M. Combined analysis of association between personality traits and three functional polymorphisms in the tyrosine hydroxylase, monoamine oxidase A, and catechol-O-methyltransferase genes.

Association of TH01 with human longevity revisited. Wang, Z. Wei, J. Possible association of catecholamine turnover with the polymorphic TCAT n repeat in the first intron of the human tyrosine hydroxylase gene.

Life Sci. Wu, Y. Yang, C. Case-control study of allele frequencies of 15 short tandem repeat loci in males with impulsive violent behavior. Shanghai Arch. Psychiatry 25, — Association study between the genetic polymorphism of 15 STR loci and the suicide behavior in Jiangsu province. Association study between the genetic polymorphism of 15 STR loci and the crime of rape.

Rapid prenatal aneuploidy analysis of chromosomes 13, 18, 21, X and Y. Devyser Extend. Rapid aneuploidy analysis of chromosomes 13, 15, 16, 18, 21, 22, X and Y. Devyser Resolution Rapid prenatal aneuploidy analysis of chromosome Devyser Resolution XY. Rapid aneuploidy analysis of chromosomes X and Y. Devyser CFTR Detects 68 CFTR mutations. Detects the 36 most common mutations found in populations of European origin.

Designed for the Italian population. Detects the normal and mutant alleles at 31 loci of the CFTR gene. Related articles Insights. STR markers A short tandem repeat STR or microsatellite is a pattern of two or more nucleotides that are repeated directly adjacent to each other. Related whitepapers. This paper provides straightforward advice for laboratory professionals on how to operate a high-quality QF-PCR service — from basic set up to best practice guidelines.

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