The fragile X syndrome d(CGG)n nucleotide repeats form a stable tetrahelical structure.
about
Purification of nuclear proteins from human HeLa cells that bind specifically to the unstable tandem repeat (CGG)n in the human FMR1 genePrevalence of quadruplexes in the human genome.Comparative genomics and molecular dynamics of DNA repeats in eukaryotesMolecular basis for expression of common and rare fragile sitesFacile FMR1 mRNA structure regulation by interruptions in CGG repeatsFormation and properties of hairpin and tetraplex structures of guanine-rich regulatory sequences of muscle-specific genesLength-dependent energetics of (CTG)n and (CAG)n trinucleotide repeats.The effect of osmolytes and small molecule on Quadruplex-WC duplex equilibrium: a fluorescence resonance energy transfer study.Advances in mechanisms of genetic instability related to hereditary neurological diseases.CGGBP1--an indispensable protein with ubiquitous cytoprotective functionsRepeat-mediated genetic and epigenetic changes at the FMR1 locus in the Fragile X-related disordersStructures of the potassium-saturated, 2:1, and intermediate, 1:1, forms of a quadruplex DNAStructure and possible function of a G-quadruplex in the long terminal repeat of the proviral HIV-1 genomeUps and Downs: Mechanisms of Repeat Instability in the Fragile X-Related DisordersG-quadruplexes: Emerging roles in neurodegenerative diseases and the non-coding transcriptomeThe DEXH protein product of the DHX36 gene is the major source of tetramolecular quadruplex G4-DNA resolving activity in HeLa cell lysatesMolecular basis of genetic instability of triplet repeatsThe fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif.Intramolecular DNA quadruplexes with different arrangements of short and long loopsA core extended naphtalene diimide G-quadruplex ligand potently inhibits herpes simplex virus 1 replicationConserved presence of G-quadruplex forming sequences in the Long Terminal Repeat Promoter of LentivirusesDNA secondary structure at chromosomal fragile sites in human disease.Interaction of human DNA topoisomerase I with G-quartet structures.Exploring possible DNA structures in real-time polymerase kinetics using Pacific Biosciences sequencer dataA comparison of four different conformations adopted by human telomeric G-Quadruplex using Computer Simulations.Tetraplex formation by the progressive myoclonus epilepsy type-1 repeat: implications for instability in the repeat expansion diseases.Noncovalent interaction of G-quadruplex DNA with acridine at low concentration monitored by MALDI-TOF mass spectrometry.Biochemical techniques for the characterization of G-quadruplex structures: EMSA, DMS footprinting, and DNA polymerase stop assay.Interruption of the fragile X syndrome expanded sequence d(CGG)(n) by interspersed d(AGG) trinucleotides diminishes the formation and stability of d(CGG)(n) tetrahelical structuresG-rich oligonucleotides inhibit HIF-1alpha and HIF-2alpha and block tumor growth.Secondary structure formation and DNA instability at fragile site FRA16BIslands of complex DNA are widespread in Drosophila centric heterochromatin.The cellular protein nucleolin preferentially binds long-looped G-quadruplex nucleic acids.G-quadruplex nucleic acids and human diseaseComplementary roles for exonuclease 1 and Flap endonuclease 1 in maintenance of triplet repeatsDNA instability at chromosomal fragile sites in cancerUnfolding of quadruplex structure in the G-rich strand of the minisatellite repeat by the binding protein UP1.Conformational energetics of stable and metastable states formed by DNA triplet repeat oligonucleotides: implications for triplet expansion diseasesOptimal conditions and specific characteristics of Vent exo- DNA polymerase in ligation-mediated polymerase chain reaction protocols.Rapid 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.
P2860
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P2860
The fragile X syndrome d(CGG)n nucleotide repeats form a stable tetrahelical structure.
description
1994 nî lūn-bûn
@nan
1994 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
The fragile X syndrome d(CGG)n nucleotide repeats form a stable tetrahelical structure.
@ast
The fragile X syndrome d(CGG)n nucleotide repeats form a stable tetrahelical structure.
@en
type
label
The fragile X syndrome d(CGG)n nucleotide repeats form a stable tetrahelical structure.
@ast
The fragile X syndrome d(CGG)n nucleotide repeats form a stable tetrahelical structure.
@en
prefLabel
The fragile X syndrome d(CGG)n nucleotide repeats form a stable tetrahelical structure.
@ast
The fragile X syndrome d(CGG)n nucleotide repeats form a stable tetrahelical structure.
@en
P2860
P356
P1476
The fragile X syndrome d(CGG)n nucleotide repeats form a stable tetrahelical structure.
@en
P2860
P304
P356
10.1073/PNAS.91.11.4950
P407
P577
1994-05-01T00:00:00Z