Non-B DNA conformations, genomic rearrangements, and human disease.
about
Genome-wide prediction of G4 DNA as regulatory motifs: role in Escherichia coli global regulationNon-B DB v2.0: a database of predicted non-B DNA-forming motifs and its associated toolsNon-B DB: a database of predicted non-B DNA-forming motifs in mammalian genomesMetastases suppressor NM23-H2 interaction with G-quadruplex DNA within c-MYC promoter nuclease hypersensitive element induces c-MYC expressionPaired-end mapping reveals extensive structural variation in the human genomeIdentification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndromeDNA models of trinucleotide frameshift deletions: the formation of loops and bulges at the primer-template junctionHotspots of homologous recombination in the human genome: not all homologous sequences are equalAdvances in mechanisms of genetic instability related to hereditary neurological diseases.Kinetic resolution of bimolecular hybridization versus intramolecular folding in nucleic acids by surface plasmon resonance: application to G-quadruplex/duplex competition in human c-myc promoter.Formation of the G-quadruplex and i-motif structures in retinoblastoma susceptibility genes (Rb)The biology of DHX9 and its potential as a therapeutic targetNew Perspectives on DNA and RNA Triplexes As Effectors of Biological ActivityChromatin Dynamics in Vivo: A Game of Musical ChairsDNA topology and transcriptionThe hidden side of unstable DNA repeats: Mutagenesis at a distanceStructural Implications of Homopyrimidine Base Pairs in the Parallel-Stranded d(YGA) MotifThe Growing Importance of CNVs: New Insights for Detection and Clinical InterpretationOrigins and functional impact of copy number variation in the human genomeHuman DHX9 helicase unwinds triple-helical DNA structuresAssociations between intronic non-B DNA structures and exon skippingGene conversion causing human inherited disease: evidence for involvement of non-B-DNA-forming sequences and recombination-promoting motifs in DNA breakage and repair.Metagenomic DNA fragments that affect Escherichia coli mutational pathways.Controlled chaos of polymorphic mucins in a metazoan parasite (Schistosoma mansoni) interacting with its invertebrate host (Biomphalaria glabrata).Genome-wide analyses of recombination prone regions predict role of DNA structural motif in recombination.Independent intrachromosomal recombination events underlie the pericentric inversions of chimpanzee and gorilla chromosomes homologous to human chromosome 16.Cellular pathways controlling integron cassette site folding.Non-B DNA structure-induced genetic instability and evolution.Direct and inverted repeats elicit genetic instability by both exploiting and eluding DNA double-strand break repair systems in mycobacteria.Expansion of microsatellites on evolutionary young Y chromosome.Long homopurine*homopyrimidine sequences are characteristic of genes expressed in brain and the pseudoautosomal region.Microhomology-mediated mechanisms underlie non-recurrent disease-causing microdeletions of the FOXL2 gene or its regulatory domain.Non-B DNA-forming sequences and WRN deficiency independently increase the frequency of base substitution in human cells.Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture.Genetic exchange between homeologous sequences in mammalian chromosomes is averted by local homology requirements for initiation and resolution of recombination.Double-strand breaks in the myotonic dystrophy type 1 and the fragile X syndrome triplet repeat sequences induce different types of mutations in DNA flanking sequences in Escherichia coli.On the sequence-directed nature of human gene mutation: the role of genomic architecture and the local DNA sequence environment in mediating gene mutations underlying human inherited disease.A matter of life or death: how microsatellites emerge in and vanish from the human genome.Detection of G-quadruplex DNA using primer extension as a toolDecrease in topoisomerase I is responsible for activation-induced cytidine deaminase (AID)-dependent somatic hypermutation.
P2860
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P2860
Non-B DNA conformations, genomic rearrangements, and human disease.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Non-B DNA conformations, genomic rearrangements, and human disease.
@ast
Non-B DNA conformations, genomic rearrangements, and human disease.
@en
type
label
Non-B DNA conformations, genomic rearrangements, and human disease.
@ast
Non-B DNA conformations, genomic rearrangements, and human disease.
@en
prefLabel
Non-B DNA conformations, genomic rearrangements, and human disease.
@ast
Non-B DNA conformations, genomic rearrangements, and human disease.
@en
P2860
P356
P1476
Non-B DNA conformations, genomic rearrangements, and human disease.
@en
P2093
Robert D Wells
P2860
P304
47411-47414
P356
10.1074/JBC.R400028200
P407
P577
2004-08-23T00:00:00Z