Non-B DB v2.0: a database of predicted non-B DNA-forming motifs and its associated tools - Wikidata - awgldk - TriplyDB

Non-B DB v2.0: a database of predicted non-B DNA-forming motifs and its associated tools

Non-B DB v2.0: a database of predicted non-B DNA-forming motifs and its associated tools

http://www.wikidata.org/entity/Q24595019

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Associations between intronic non-B DNA structures and exon skipping FACT is a sensor of DNA torsional stress in eukaryotic cells.Genomic basis of aromatase excess syndrome: recombination- and replication-mediated rearrangements leading to CYP19A1 overexpression Rate of elongation by RNA polymerase II is associated with specific gene features and epigenetic modifications.Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7.Japanese founder duplications/triplications involving BHLHA9 are associated with split-hand/foot malformation with or without long bone deficiency and Gollop-Wolfgang complex Lentivector integration sites in ependymal cells from a model of metachromatic leukodystrophy: non-B DNA as a new factor influencing integration.SVA retrotransposon insertion-associated deletion represents a novel mutational mechanism underlying large genomic copy number changes with non-recurrent breakpoints.Indolo[3,2-c]quinoline G-quadruplex stabilizers: a structural analysis of binding to the human telomeric G-quadruplex.Intragenic duplication in the PKHD1 gene in autosomal recessive polycystic kidney disease.Modeling the integration of bacterial rRNA fragments into the human cancer genome GNG Motifs Can Replace a GGG Stretch during G-Quadruplex Formation in a Context Dependent Manner Intrastrand triplex DNA repeats in bacteria: a source of genomic instability.Sister chromatid telomere fusions, but not NHEJ-mediated inter-chromosomal telomere fusions, occur independently of DNA ligases 3 and 4.Translocation and deletion breakpoints in cancer genomes are associated with potential non-B DNA-forming sequences Loss-of-Function Mutations in ELMO2 Cause Intraosseous Vascular Malformation by Impeding RAC1 Signaling Genome-wide profiling of HPV integration in cervical cancer identifies clustered genomic hot spots and a potential microhomology-mediated integration mechanism.Detection of cis- and trans-acting Factors in DNA Structure-Induced Genetic Instability Using In silico and Cellular Approaches Genomic determinants of somatic copy number alterations across human cancers.Genome-wide analysis of somatic copy number alterations and chromosomal breakages in osteosarcoma.Large deletions involving the regulatory upstream regions of A4GALT give rise to principally novel P1PK-null alleles.The TTSMI database: a catalog of triplex target DNA sites associated with genes and regulatory elements in the human genome.Signature of backward replication slippage at the copy number variation junction.A novel homozygous complex deletion in CFTR caused cystic fibrosis in a Chinese patient.CNGB3 mutation spectrum including copy number variations in 552 achromatopsia patients.Role of chromatin damage and chromatin trapping of FACT in mediating the anticancer cytotoxicity of DNA-binding small molecule drugs.Defining Functional Genic Regions in the Human Genome through Integration of Biochemical, Evolutionary, and Genetic Evidence.Requirement or exclusion of inverted repeat sequences with cruciform-forming potential in Escherichia coli revealed by genome-wide analyses.Disclosing the Hidden Structure and Underlying Mutational Mechanism of a Novel Type of Duplication CNV Responsible for Hereditary Multiple Osteochondromas

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Non-B DB v2.0: a database of predicted non-B DNA-forming motifs and its associated tools

http://www.wikidata.org/entity/Q24595019

description

2013 nî lūn-bûn

@nan

2013 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի հունվարին հրատարակված գիտական հոդված

@hy

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

name

Non-B DB v2.0: a database of predicted non-B DNA-forming motifs and its associated tools

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Non-B DB v2.0: a database of predicted non-B DNA-forming motifs and its associated tools

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Non-B DB v2.0: a database of predicted non-B DNA-forming motifs and its associated tools

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Non-B DB v2.0: a database of predicted non-B DNA-forming motifs and its associated tools

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Non-B DB v2.0: a database of predicted non-B DNA-forming motifs and its associated tools

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Non-B DB v2.0: a database of predicted non-B DNA-forming motifs and its associated tools

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Non-B DB v2.0: a database of predicted non-B DNA-forming motifs and its associated tools

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Non-B DB v2.0: a database of predicted non-B DNA-forming motifs and its associated tools

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Non-B DB v2.0: a database of predicted non-B DNA-forming motifs and its associated tools

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Nucleic Acids Research

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Non-B DB v2.0: a database of predicted non-B DNA-forming motifs and its associated tools

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Brian T Luke

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

Goran N Halusa

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

Jack R Collins

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

Michael A Loss

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

Natalia Volfovsky

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

Nathan J Starner

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

Nuri A Temiz

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

Regina Z Cer

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

Robert M Stephens

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

Uma S Mudunuri

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

P2860

Non-B DB: a database of predicted non-B DNA-forming motifs in mammalian genomes

The crystal structure of the second Z-DNA binding domain of human DAI (ZBP1) in complex with Z-DNA reveals an unusual binding mode to Z-DNA

Circos: an information aesthetic for comparative genomics

A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21).

Targeting MYC Expression through G-Quadruplexes.

Non-B DNA structure-induced genetic instability and evolution.

G4 motifs correlate with promoter-proximal transcriptional pausing in human genes.

Non-B DNA conformations, genomic rearrangements, and human disease.

The constitutional t(11;22): implications for a novel mechanism responsible for gross chromosomal rearrangements.

Searching for non-B DNA-forming motifs using nBMST (non-B DNA motif search tool)

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D94-D100

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scholarly article

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2283731

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10.1093/NAR/GKS955

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Database issue

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41

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Duncan E Donohue

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2012-11-03T00:00:00Z

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232813919

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23125372

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3531222

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