DNA secondary structure at chromosomal fragile sites in human disease. - Wikidata - awgldk - TriplyDB

DNA secondary structure at chromosomal fragile sites in human disease.

DNA secondary structure at chromosomal fragile sites in human disease.

http://www.wikidata.org/entity/Q30300009

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The Causes and Consequences of Topological Stress during DNA Replication Comprehensive Analysis of Genome Rearrangements in Eight Human Malignant Tumor Tissues Short tandem repeats, segmental duplications, gene deletion, and genomic instability in a rapidly diversified immune gene family Sister chromatid telomere fusions, but not NHEJ-mediated inter-chromosomal telomere fusions, occur independently of DNA ligases 3 and 4.Morphometric Analysis of Recognized Genes for Autism Spectrum Disorders and Obesity in Relationship to the Distribution of Protein-Coding Genes on Human Chromosomes Translocation and deletion breakpoints in cancer genomes are associated with potential non-B DNA-forming sequences Effects of Replication and Transcription on DNA Structure-Related Genetic Instability Role of recombination and replication fork restart in repeat instability.Inhibition of colorectal cancer genomic copy number alterations and chromosomal fragile site tumor suppressor FHIT and WWOX deletions by DNA mismatch repair.Charge evolution during the unfolding of a single DNA i-motif.

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P2860

DNA secondary structure at chromosomal fragile sites in human disease.

http://www.wikidata.org/entity/Q30300009

description

2015 nî lūn-bûn

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2015 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի փետրվարին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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name

DNA secondary structure at chromosomal fragile sites in human disease.

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DNA secondary structure at chromosomal fragile sites in human disease.

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DNA secondary structure at chromosomal fragile sites in human disease.

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DNA secondary structure at chromosomal fragile sites in human disease.

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prefLabel

DNA secondary structure at chromosomal fragile sites in human disease.

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DNA secondary structure at chromosomal fragile sites in human disease.

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Current Genomics

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DNA secondary structure at chromosomal fragile sites in human disease.

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Christine E Lehman

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Levi C T Pierce

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Yuh-Hwa Wang

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P2860

Re-evaluation of the carcinogenic significance of hepatitis B virus integration in hepatocarcinogenesis

The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3;8) breakpoint, is abnormal in digestive tract cancers

Mfold web server for nucleic acid folding and hybridization prediction

Chromosomal instability at common fragile sites in Seckel syndrome

Inhibition of topoisomerase I prevents chromosome breakage at common fragile sites

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

Sensing DNA damage through ATRIP recognition of RPA-ssDNA complexes

CGG/CCG repeats exhibit orientation-dependent instability and orientation-independent fragility in Saccharomyces cerevisiae

An ATR- and Cdc7-dependent DNA damage checkpoint that inhibits initiation of DNA replication

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60-70

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scholarly article

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1

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16

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Ryan Griffin Thys

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