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Nature Genetics, ISSN 1061-4036, 10/2017, Volume 49, Issue 10, pp. 1495 - 1501
Identifying regions of the genome that are depleted of mutations can distinguish potentially deleterious variants. Short tandem repeats (STRs), also known as... 
GENETIC-VARIATION | POPULATION | TRACT | HUMAN-DISEASE | HUMAN GENOMES | SEQUENCES | EXPANSION | GENETICS & HEREDITY | MICROSATELLITES | DIVERSITY | EXPRESSION | Short tandem repeats | Parameter estimation | Microsatellites | Nucleotide sequence | Genes | Genomes | Mutation rates | Heterozygosity | Mathematical analysis | Population | Genetics | Mutation | Bioinformatics | Age | Genotypes | Deoxyribonucleic acid--DNA | Methods | Index Medicus
Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 06/2018, Volume 42, Issue 6, pp. 807 - 812
Inflammatory myofibroblastic tumor (IMT) is a neoplasm of intermediate malignant potential that only rarely involves the gynecologic tract. Several cases of... 
STR | SURGERY | IMT | DIAGNOSIS | short tandem repeat genotyping | uterus | FEMALE GENITAL-TRACT | inflammatory myofibroblastic tumor | DISTINCTION | placenta | PATHOLOGY | Care and treatment | Genotype | Genetic aspects | Microsatellites (Genetics) | Diagnosis | Uterine cancer | Health aspects | Index Medicus
Journal Article
BMC Genomics, ISSN 1471-2164, 12/2016, Volume 17, Issue 1, pp. 991 - 991
Journal Article
Short tandem repeat technology has diverse applications: individual identification, phylogenetic reconstruction and chimerism based post haematopoietic stem cell transplantation graft monitoring, 07/2004
BACKGROUND: Short Tandem Repeat (STR) loci are widely considered to be effective for variety of applications including forensic applications, phylogenetic... 
Medicine | Short Tandem Repeat, Chimerism, Phylogeny, Haematopoietic Stem Cell transplantation, Forensics ms04053
Journal
Cell, ISSN 0092-8674, 09/2018, Volume 175, Issue 1, pp. 224 - 238.e15
More than 25 inherited human disorders are caused by the unstable expansion of repetitive DNA sequences termed short tandem repeats (STRs). A fundamental... 
trinucleotide repeat expansion disorders | subTADs | genome instability | short tandem repeats | fragile X syndrome | 3D genome folding | TADs | topologically associating domains | higher-order chromatin architecture | LINEAGE COMMITMENT | CTG REPEAT | HUMAN GENOME | DNA METHYLATION | GENE | BIOCHEMISTRY & MOLECULAR BIOLOGY | FRAGILE-X-SYNDROME | CTCF | HUNTINGTONS-DISEASE | TRINUCLEOTIDE REPEATS | MYOTONIC-DYSTROPHY | CELL BIOLOGY | Humans | CCCTC-Binding Factor - genetics | Trinucleotide Repeat Expansion - physiology | Chromatin Assembly and Disassembly - genetics | Fragile X Mental Retardation Protein - physiology | Male | Fragile X Mental Retardation Protein - metabolism | CCCTC-Binding Factor - physiology | Disease - etiology | Chromatin - physiology | Adult | Female | Fragile X Syndrome - genetics | Cell Line | Brain - cytology | Disease - genetics | Fragile X Syndrome - metabolism | Microsatellite Repeats - physiology | CpG Islands - physiology | Genome, Human - genetics | Microsatellite Repeats - genetics | DNA - genetics | Brain - pathology | CpG Islands - genetics | Trinucleotide Repeat Expansion - genetics | Fragile X Mental Retardation Protein - genetics | Chromatin - genetics | Chromatin Assembly and Disassembly - physiology | Epigenetic inheritance | Medical colleges | Anopheles | Chromatin | Genomics | Plants | Nucleotide sequencing | DNA sequencing | Index Medicus
Journal Article
Journal of Affective Disorders, ISSN 0165-0327, 05/2019, Volume 251, pp. 86 - 90
The X-linked gene (also known as ) contains the longest STR, (GA)32, identified in a human protein-coding gene 5′UTR (ENST00000373998.5: ZMYM3-207). This STR... 
Bipolar disorder | ZMYM3 | Disease-only | Short tandem repeat | Extreme | PSYCHIATRY | CORE PROMOTER | GENE-EXPRESSION | CLINICAL NEUROLOGY | Allelomorphism | Medicine, Experimental | Medical research | Medical genetics | Natural selection | Index Medicus
Journal Article
Molecular Cell, ISSN 1097-2765, 11/2018, Volume 72, Issue 3, pp. 525 - 540.e13
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 09/2017, Volume 54, Issue 9, pp. 640 - 650
Journal Article