Novel DNA sequence variants in the hHR21 DNA repair gene in radiosensitive cancer patients
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Genetics and genomics of radiotherapy toxicity: towards predictionRad21-cohesin haploinsufficiency impedes DNA repair and enhances gastrointestinal radiosensitivity in mice.H2AX phosphorylation screen of cells from radiosensitive cancer patients reveals a novel DNA double-strand break repair cellular phenotype.Testicular cancer survivorship: research strategies and recommendations.Alternative transcript initiation and splicing as a response to DNA damage.A bioinformatics filtering strategy for identifying radiation response biomarker candidates.DNA repair genes: alternative transcription and gene expression at the exon level in response to the DNA damaging agent, ionizing radiationFollistatin is induced by ionizing radiation and potentially predictive of radiosensitivity in radiation-induced fibrosis patient derived fibroblasts.Identification of SNPs associated with susceptibility for development of adverse reactions to radiotherapySingle nucleotide polymorphism at rs1982073:T869C of the TGFbeta 1 gene is associated with the risk of radiation pneumonitis in patients with non-small-cell lung cancer treated with definitive radiotherapy.RAD21 mutations cause a human cohesinopathyCan risk of radiotherapy-induced normal tissue complications be predicted from genetic profiles?Cancer pharmacogenomics: role of DNA repair genetic polymorphisms in individualizing cancer therapy.Radiation-hypersensitive cancer patients do not manifest protein expression abnormalities in components of the nonhomologous end-joining (NHEJ) pathway.Single nucleotide polymorphisms, apoptosis, and the development of severe late adverse effects after radiotherapy.In vitro prediction of breast cancer therapy toxicity.Non-homologous end-joining protein expression screen from radiosensitive cancer patients yields a novel DNA double strand break repair phenotype.Characterization of a 3;6 translocation associated with renal cell carcinoma.Lymphoid and fibroblastic cell lineages from radiosensitive cancer patients: molecular analysis of DNA double strand break repair by major non-homologous end-joining sub-pathways.Expression of RAD51, BRCA1 and P53 does not correlate with cellular radiosensitivity of normal human fibroblasts.
P2860
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P2860
Novel DNA sequence variants in the hHR21 DNA repair gene in radiosensitive cancer patients
description
2001 nî lūn-bûn
@nan
2001 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Novel DNA sequence variants in ...... radiosensitive cancer patients
@ast
Novel DNA sequence variants in ...... radiosensitive cancer patients
@en
Novel DNA sequence variants in ...... radiosensitive cancer patients
@nl
type
label
Novel DNA sequence variants in ...... radiosensitive cancer patients
@ast
Novel DNA sequence variants in ...... radiosensitive cancer patients
@en
Novel DNA sequence variants in ...... radiosensitive cancer patients
@nl
prefLabel
Novel DNA sequence variants in ...... radiosensitive cancer patients
@ast
Novel DNA sequence variants in ...... radiosensitive cancer patients
@en
Novel DNA sequence variants in ...... radiosensitive cancer patients
@nl
P2093
P1476
Novel DNA sequence variants in ...... radiosensitive cancer patients
@en
P2093
D M Severin
P304
P356
10.1016/S0360-3016(01)01608-X
P407
P577
2001-08-01T00:00:00Z