Fragile X syndrome unstable element, p(CCG)n, and other simple tandem repeat sequences are binding sites for specific nuclear proteins.
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Purification of nuclear proteins from human HeLa cells that bind specifically to the unstable tandem repeat (CGG)n in the human FMR1 geneNovel repressor of the human FMR1 gene - identification of p56 human (GCC)(n)-binding protein as a Krüppel-like transcription factor ZF5Simple tandem DNA repeats and human genetic diseasePoly: a quantitative analysis tool for simple sequence repeat (SSR) tracts in DNATandem repeat copy-number variation in protein-coding regions of human genes.CGGBP1--an indispensable protein with ubiquitous cytoprotective functionsThe fragile X gene and its functionRepeat polymorphisms within gene regions: phenotypic and evolutionary implicationsDynamic mutations on the move.An n-allele model for progressive amplification in the FMR1 locusRapid protein sequencing by tandem mass spectrometry and cDNA cloning of p20-CGGBP. A novel protein that binds to the unstable triplet repeat 5'-d(CGG)n-3' in the human FMR1 gene.MsDetector: toward a standard computational tool for DNA microsatellites detectionHairpin properties of single-stranded DNA containing a GC-rich triplet repeat: (CTG)15.Single-stranded DNA binding proteins isolated from mouse brain recognize specific trinucleotide repeat sequences in vitro.Identification of conserved and polymorphic STRs for personal genomes.mreps: Efficient and flexible detection of tandem repeats in DNADeletion of all CGG repeats plus flanking sequences in FMR1 does not abolish gene expressionCharacterization of FMR1 promoter elements by in vivo-footprinting analysis.Triplet repeat RNA structure and its role as pathogenic agent and therapeutic targetSelection processes in simple sequence repeats suggest a correlation with their genomic location: insights from a fungal model system.Trinucleotide repeats in human genome and exome.RNA toxicity induced by expanded CAG repeats in Huntington's disease.Stability of a CTG/CAG trinucleotide repeat in yeast is dependent on its orientation in the genomeCompact structures of d(CNG)n oligonucleotides in solution and their possible relevance to fragile X and related human genetic diseasesExploiting the informativity of 'meaningless' simple repetitive DNA from indirect gene diagnosis to multilocus genome scanning.Genomic simple repetitive DNAs are targets for differential binding of nuclear proteins.Differential effects of simple repeating DNA sequences on gene expression from the SV40 early promoter.Screening for fragile X syndrome: information needs for health planners.Evolution of the cryptic FMR1 CGG repeat.Evolutionary dynamics of the FMR1 locus.Flexible DNA: genetically unstable CTG.CAG and CGG.CCG from human hereditary neuromuscular disease genes.
P2860
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P2860
Fragile X syndrome unstable element, p(CCG)n, and other simple tandem repeat sequences are binding sites for specific nuclear proteins.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
1993年论文
@zh
1993年论文
@zh-cn
name
Fragile X syndrome unstable el ...... for specific nuclear proteins.
@en
type
label
Fragile X syndrome unstable el ...... for specific nuclear proteins.
@en
prefLabel
Fragile X syndrome unstable el ...... for specific nuclear proteins.
@en
P2093
P356
P1476
Fragile X syndrome unstable el ...... for specific nuclear proteins.
@en
P2093
P304
P356
10.1093/HMG/2.9.1429
P577
1993-09-01T00:00:00Z