Quantitative effects on gene silencing by allelic variation at a tetranucleotide microsatellite
about
Genome-wide analysis of microsatellite repeats in humans: their abundance and density in specific genomic regionsThe tissue-specific methylation of the human tyrosine hydroxylase gene reveals new regulatory elements in the first exonZENON, a novel POZ Kruppel-like DNA binding protein associated with differentiation and/or survival of late postmitotic neuronsZFP191 is required by oligodendrocytes for CNS myelinationPolymorphisms in genes encoding dopamine signalling pathway and risk of alcohol dependence: a systematic review.A transcript profiling approach reveals the zinc finger transcription factor ZNF191 is a pleiotropic factor.Association of a functional microsatellite within intron 1 of the BMP5 gene with susceptibility to osteoarthritis.Database of exact tandem repeats in the Zebrafish genome.Association of vWA and TPOX polymorphisms with venous thrombosis in Mexican mestizos.Human tyrosine hydroxylase natural allelic variation: influence on autonomic function and hypertension.FUBP3 interacts with FGF9 3' microsatellite and positively regulates FGF9 translationIdentification of a functional nuclear localization signal mediating nuclear import of the zinc finger transcription factor ZNF24Psychopathological aspects of dopaminergic gene polymorphisms in adolescence and young adulthoodAssociation of TH01 with human longevity revisited.CYP2C9 promoter variable number tandem repeat polymorphism regulates mRNA expression in human livers.Transcription and epigenetic profile of the promoter, first exon and first intron of the human tyrosine hydroxylase geneWhy repetitive DNA is essential to genome function.Establishment of transgenic mice carrying gene encoding human zinc finger protein 191.The endogenous zinc finger transcription factor, ZNF24, modulates the angiogenic potential of human microvascular endothelial cells.Transcriptional repression of VEGF by ZNF24: mechanistic studies and vascular consequences in vivo.Overview of the pharmacogenomics of cigarette smoking.A tyrosine hydroxylase-yellow fluorescent protein knock-in reporter system labeling dopaminergic neurons reveals potential regulatory role for the first intron of the rodent tyrosine hydroxylase gene.Selection of embryonic stem cell-derived enhanced green fluorescent protein-positive dopamine neurons using the tyrosine hydroxylase promoter is confounded by reporter gene expression in immature cell populations.No Evidence for Association between Tyrosine Hydroxylase Gene Val81Met Polymorphism and Susceptibility to Tardive Dyskinesia in SchizophreniaComorbidities Among Persons With Incident Psychiatric Condition.Unbiased discovery of interactions at a control locus driving expression of the cancer-specific therapeutic and diagnostic target, mesothelin.SSRD: simple sequence repeats database of the human genome.A novel sampling design to explore gene-longevity associations: the ECHA study.Tyrosine hydroxylase gene regulation in human neuronal progenitor cells does not depend on Nurr1 as in the murine and rat systems.Microsatellites in the genome of the edible mushroom, Volvariella volvacea.Characterization of five evolutionary conserved regions of the human tyrosine hydroxylase (TH) promoter: implications for the engineering of a human TH minimal promoter assembled in a self-inactivating lentiviral vector system.Functional Mechanisms of Microsatellite DNA in Eukaryotic Genomes.Using progenitor strain information to identify quantitative trait nucleotides in outbred mice.ENCODE and its first impractical application.Functional allelic heterogeneity and pleiotropy of a repeat polymorphism in tyrosine hydroxylase: prediction of catecholamines and response to stress in twins.Replication of IGF2-INS-TH*5 haplotype effect on obesity in older men and study of related phenotypes.Refined association mapping for a quantitative trait: weight in the H19-IGF2-INS-TH region.Transgenic mice expressing yellow fluorescent protein under control of the human tyrosine hydroxylase promoter.Zinc finger protein 191 inhibits hepatocellular carcinoma metastasis through discs large 1-mediated yes-associated protein inactivation.Tyrosine hydroxylase TH01 9.3 allele in the occurrence of sudden infant death syndrome in Swiss Caucasians.
P2860
Q24804665-D9F4E75E-1F8A-471B-9132-4B34F0107F15Q28256201-FE0106D5-AFA6-4C7B-ACD0-4A823BEDB756Q28576766-4FB95D20-9C12-4FF6-87AF-3367C0AC766FQ28593364-B127A500-AF5B-4A74-82C7-FA72F883CF23Q30834350-7C2BECD1-4B5C-42CA-BD8B-3E1CF3B5E260Q33451000-72232A6D-BEA3-4316-9609-E63DB26139E5Q33519752-4CA51BFD-FFA5-4493-9E2C-5DC24547D9EFQ33591777-315828E3-005E-4B9A-858D-C15B116A7A86Q34181424-4CFC33E1-9CE1-49D7-9CA0-1F6209B6750EQ34435146-BFC9A730-9E02-42CD-BC64-6001131EAC83Q34946895-86218331-70DE-4530-B2F2-824697ABAC59Q35041541-B5C3CCFD-AE49-4233-B509-A68A83593107Q35097990-A2C93C74-0803-4FE1-819E-B2B7E7210140Q35212711-7AAC0C4B-A5EE-4218-8C54-2C20F47FACA8Q35913092-E0A0386B-7C15-45A1-A90B-E2A2E9682035Q35990191-E5DBC422-1763-4CF7-B880-EB7B5193F89CQ36141901-B34A6247-0685-4591-BA19-D83A165B3BEBQ36474419-2F240C53-B91D-436C-BFC0-EEC1C79054FFQ36525804-98EA4818-3974-42D0-9864-F7569CDC5AB4Q36569678-F0FC1D3E-A98B-4A82-8555-2ABDBA8C36FEQ36708951-2AB784DC-BACB-4207-B752-BBB545E10195Q37029654-2AAC6685-F183-4839-8A0D-D43AB36BDDBAQ37037504-49ED1E71-386E-4660-A075-7D019AFBC8EAQ37484079-6A50C53E-C2B0-4956-8D63-A83617791288Q37519692-8041B979-DF08-4002-A205-C64929D1261AQ39268512-005FC366-CE55-4A7A-8814-81B259218169Q39804711-134A01F0-6AC1-4BEC-9D4A-51168B5ED5E3Q40156052-71F9E5B8-DFFD-4271-A3B5-EB7AD8613283Q40357574-808831E9-9B73-4383-A449-4884A5748250Q41921366-5C0C2288-6C9F-4DC9-9AFB-2E70347B88F9Q42015600-97AE299D-E467-4C94-8F8B-E152B2E804A7Q42096577-69F997BF-E42C-4FB4-B97C-6D778CFC1855Q42251756-E0E3CAC7-EE7F-4ABC-AB12-DFCC81FB09D4Q42767423-D5E19094-42AD-497E-9AFC-DB4A4DB9CAB0Q45059176-85892024-1AFD-4504-8DD6-B08A7DBDF69AQ46776438-F7B64E48-FC10-4009-A465-413BE5FF07AFQ47317295-237B27D7-0B39-4487-9182-9566BADC443AQ48467133-9FF1DB68-3F50-4B24-A563-E9C64090C2CDQ51274501-7FADDEE8-AE59-4853-8E03-5453141642BBQ51713796-FB0EDFEE-2CAA-453F-BD85-5D4A8002B8B8
P2860
Quantitative effects on gene silencing by allelic variation at a tetranucleotide microsatellite
description
2001 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2001
@ast
im August 2001 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
wetenschappelijk artikel (gepubliceerd op 2001/08/15)
@nl
наукова стаття, опублікована в серпні 2001
@uk
مقالة علمية (نشرت في 15-8-2001)
@ar
name
Quantitative effects on gene s ...... tetranucleotide microsatellite
@ast
Quantitative effects on gene s ...... tetranucleotide microsatellite
@en
type
label
Quantitative effects on gene s ...... tetranucleotide microsatellite
@ast
Quantitative effects on gene s ...... tetranucleotide microsatellite
@en
prefLabel
Quantitative effects on gene s ...... tetranucleotide microsatellite
@ast
Quantitative effects on gene s ...... tetranucleotide microsatellite
@en
P2093
P921
P356
P1476
Quantitative effects on gene s ...... tetranucleotide microsatellite
@en
P2093
N. F. Biguet
P304
P356
10.1093/HMG/10.17.1785
P577
2001-08-15T00:00:00Z