Replication-associated mutational asymmetry in the human genome. - Wikidata - wikimedia - TriplyDB

Replication-associated mutational asymmetry in the human genome.

Replication-associated mutational asymmetry in the human genome.

http://www.wikidata.org/entity/Q39582800

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Peaks cloaked in the mist: the landscape of mammalian replication origins Why coelacanths are not 'living fossils': a review of molecular and morphological data.Replication fork polarity gradients revealed by megabase-sized U-shaped replication timing domains in human cell lines Asymmetry indices for analysis and prediction of replication origins in eukaryotic genomes.Heterogeneous polymerase fidelity and mismatch repair bias genome variation and composition.Human genome replication proceeds through four chromatin states.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.Embryonic stem cell specific "master" replication origins at the heart of the loss of pluripotency A genome-wide analysis of common fragile sites: what features determine chromosomal instability in the human genome?Evidence of selection for an accessible nucleosomal array in human 3D chromatin conformation correlates with replication timing and is conserved in resting cells Subtelomere organization in the genome of the microsporidian Encephalitozoon cuniculi: patterns of repeated sequences and physicochemical signatures.APOBEC-induced mutations in human cancers are strongly enriched on the lagging DNA strand during replication.Replication landscape of the human genome Mutational Strand Asymmetries in Cancer Genomes Reveal Mechanisms of DNA Damage and Repair.The spatiotemporal program of replication in the genome of Lachancea kluyveri Back to the origin: reconsidering replication, transcription, epigenetics, and cell cycle control.DNA replication origins.Replication timing and its emergence from stochastic processes Measures of compositional strand bias related to replication machinery and its applications.Best practices for mapping replication origins in eukaryotic chromosomes.Structural organization of human replication timing domains.Human mismatch repair system balances mutation rates between strands by removing more mismatches from the lagging strand.APOBEC3A/B-induced mutagenesis is responsible for 20% of heritable mutations in the TpCpW context.Linking the DNA strand asymmetry to the spatio-temporal replication program. I. About the role of the replication fork polarity in genome evolution.Polymerase ζ Activity Is Linked to Replication Timing in Humans: Evidence from Mutational Signatures.DNA replication and strand asymmetry in prokaryotic and mitochondrial genomes.DNA mutation motifs in the genes associated with inherited diseases.Multiscale analysis of genome-wide replication timing profiles using a wavelet-based signal-processing algorithm.Meiotic recombination strongly influences GC-content evolution in short regions in the mouse genome.Revealing long-range interconnected hubs in human chromatin interaction data using graph theory.

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P2860

Replication-associated mutational asymmetry in the human genome.

http://www.wikidata.org/entity/Q39582800

description

2011 nî lūn-bûn

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

@zh-tw

2011年论文

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2011年论文

@zh

2011年论文

@zh-cn

name

Replication-associated mutational asymmetry in the human genome.

@en

Replication-associated mutational asymmetry in the human genome.

@nl

type

label

Replication-associated mutational asymmetry in the human genome.

@en

Replication-associated mutational asymmetry in the human genome.

@nl

prefLabel

Replication-associated mutational asymmetry in the human genome.

@en

Replication-associated mutational asymmetry in the human genome.

@nl

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Molecular Biology and Evolution

P1476

Replication-associated mutational asymmetry in the human genome.

@en

P2093

Alain Arneodo

http://www.w3.org/2001/XMLSchema#string

Antoine Baker

http://www.w3.org/2001/XMLSchema#string

Aurélien Rappailles

http://www.w3.org/2001/XMLSchema#string

Benjamin Audit

http://www.w3.org/2001/XMLSchema#string

Chun-Long Chen

http://www.w3.org/2001/XMLSchema#string

Claude Thermes

http://www.w3.org/2001/XMLSchema#string

Guillaume Guilbaud

http://www.w3.org/2001/XMLSchema#string

Lauranne Duquenne

http://www.w3.org/2001/XMLSchema#string

Maxime Huvet

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Olivier Hyrien

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P2860

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

RNA exosome depletion reveals transcription upstream of active human promoters

Mechanism of DNA chain growth. I. Possible discontinuity and unusual secondary structure of newly synthesized chains

DNA mismatch repair

Enredo and Pecan: genome-wide mammalian consistency-based multiple alignment with paralogs

The high fidelity and unique error signature of human DNA polymerase epsilon

Nascent RNA sequencing reveals widespread pausing and divergent initiation at human promoters

Genome-wide nucleotide-level mammalian ancestor reconstruction

Divergent transcription from active promoters

DNA polymerase fidelity: comparing direct competition of right and wrong dNTP substrates with steady state and pre-steady state kinetics

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2327-2337

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10.1093/MOLBEV/MSR056

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8

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28

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2011-03-02T00:00:00Z

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50267300

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21368316

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