Measuring gene-specific nucleotide excision repair in human cells using quantitative amplification of long targets from nanogram quantities of DNA.
about
AP endonuclease deficiency results in extreme sensitivity to thymidine deprivationPCR-Based Analysis of Mitochondrial DNA Copy Number, Mitochondrial DNA Damage, and Nuclear DNA DamageAsbestos induces mitochondrial DNA damage and dysfunction linked to the development of apoptosis.Recruitment of DNA damage checkpoint proteins to damage in transcribed and nontranscribed sequences.Nucleotide excision repair genes are expressed at low levels and are not detectably inducible in Caenorhabditis elegans somatic tissues, but their function is required for normal adult life after UVC exposureAltered gene expression and DNA damage in peripheral blood cells from Friedreich's ataxia patients: cellular model of pathology.Strategies for the evaluation of DNA damage and repair mechanisms in cancer.QPCR: a tool for analysis of mitochondrial and nuclear DNA damage in ecotoxicology.The endogenous retroviral locus ERVWE1 is a bona fide gene involved in hominoid placental physiologyDecline of nucleotide excision repair capacity in aging Caenorhabditis elegansMitochondrial DNA-depleted A549 cells are resistant to bleomycin.Development and validation of a PCR-based assay for the selection of patients more likely to benefit from therapeutic treatment with alkylating drugs.DNA damage in normally and prematurely aged mice.UV disinfection of adenoviruses: molecular indications of DNA damage efficiency.Cells from long-lived mutant mice exhibit enhanced repair of ultraviolet lesions.Tumor cells have decreased ability to metabolize H2O2: Implications for pharmacological ascorbate in cancer therapy.Biological sensors for solar ultraviolet radiation.Quantitative PCR-based measurement of nuclear and mitochondrial DNA damage and repair in mammalian cells.DNA adducts of decarbamoyl mitomycin C efficiently kill cells without wild-type p53 resulting from proteasome-mediated degradation of checkpoint protein 1.Gene-specific nucleotide excision repair is impaired in human cells expressing elevated levels of high mobility group A1 nonhistone proteins.UV-induced DNA damage in human keratinocytes: quantitation and correlation with long-term survival.The long amplicon quantitative PCR for DNA damage assay as a sensitive method of assessing DNA damage in the environmental model, Atlantic killifish (Fundulus heteroclitus).The YggX protein of Salmonella enterica is involved in Fe(II) trafficking and minimizes the DNA damage caused by hydroxyl radicals: residue CYS-7 is essential for YggX function.Simplified qPCR method for detecting excessive mtDNA damage induced by exogenous factors.Association of mitochondrial haplogroup J and mtDNA oxidative damage in two different North Spain elderly populations
P2860
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P2860
Measuring gene-specific nucleotide excision repair in human cells using quantitative amplification of long targets from nanogram quantities of DNA.
description
2000 nî lūn-bûn
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2000 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Measuring gene-specific nucleo ...... om nanogram quantities of DNA.
@ast
Measuring gene-specific nucleo ...... om nanogram quantities of DNA.
@en
type
label
Measuring gene-specific nucleo ...... om nanogram quantities of DNA.
@ast
Measuring gene-specific nucleo ...... om nanogram quantities of DNA.
@en
prefLabel
Measuring gene-specific nucleo ...... om nanogram quantities of DNA.
@ast
Measuring gene-specific nucleo ...... om nanogram quantities of DNA.
@en
P2093
P1433
P1476
Measuring gene-specific nucleo ...... om nanogram quantities of DNA.
@en
P2093
P356
10.1016/S0921-8777(00)00018-5
P407
P577
2000-07-01T00:00:00Z