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Ataxia telangiectasia: a human mutation with abnormal radiation sensitivity.

作者信息

Taylor A M, Harnden D G, Arlett C F, Harcourt S A, Lehmann A R, Stevens S, Bridges B A

出版信息

Nature. 1975 Dec 4;258(5534):427-9. doi: 10.1038/258427a0.

DOI:10.1038/258427a0

PMID:1196376

Abstract

摘要

相似文献

Ataxia telangiectasia: a human mutation with abnormal radiation sensitivity.

Nature. 1975 Dec 4;258(5534):427-9. doi: 10.1038/258427a0.

Chromosomal radiation sensitivity in ataxia telangiectasia long-term lymphoblastoid cell lines.

Cytogenet Cell Genet. 1981;31(4):203-13. doi: 10.1159/000131650.

Chromosomal radiosensitivity of ataxia telangiectasia cells at different cell cycle stages.

Hum Genet. 1979 Nov 1;52(1):127-32. doi: 10.1007/BF00284606.

Effect of caffeine in G2 on X-ray-induced chromosomal aberrations and mitotic inhibition in ataxia telangiectasia fibroblast and lymphoblastoid cells.

Hum Genet. 1984;67(3):329-35. doi: 10.1007/BF00291363.

Complementation analysis in ataxia telangiectasia: fibroblast-lymphoblastoid cell heterokaryon assay by radiation-induced chromosome aberrations.

Cytogenet Cell Genet. 1993;64(1):9-11. doi: 10.1159/000133549.

Enhanced radiosensitivity of cultured fibroblasts from ataxia telangiectasia heterozygotes manifested by defective colony-forming ability and reduced DNA repair replication after hypoxic gamma-irradiation.

Cancer Res. 1979 Sep;39(9):3725-34.

Suppression of X-ray-induced chromosome aberrations in ataxia telangiectasia cells by introduction of a normal human chromosome 11.

Mutat Res. 1992 Nov;293(1):31-7. doi: 10.1016/0921-8777(92)90005-n.

Ataxia telangiectasia. Evaluation of radiosensitivity in cultured skin fibroblasts as a diagnostic test.

Arch Dis Child. 1978 May;53(5):386-90. doi: 10.1136/adc.53.5.386.

DNA strained breakage repair in ataxia telangiectasia fibroblast-like cells.

Mutat Res. 1975 Dec;33(2-3):357-66. doi: 10.1016/0027-5107(75)90211-0.

Specific chromosome aberrations in ataxia telangiectasia.

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Ataxia telangiectasia: a human mutation with abnormal radiation sensitivity.

作者信息

Taylor A M, Harnden D G, Arlett C F, Harcourt S A, Lehmann A R, Stevens S, Bridges B A

出版信息

Nature. 1975 Dec 4;258(5534):427-9. doi: 10.1038/258427a0.

DOI:10.1038/258427a0

PMID:1196376

Abstract

摘要

相似文献

Ataxia telangiectasia: a human mutation with abnormal radiation sensitivity.

Nature. 1975 Dec 4;258(5534):427-9. doi: 10.1038/258427a0.

Chromosomal radiation sensitivity in ataxia telangiectasia long-term lymphoblastoid cell lines.

Cytogenet Cell Genet. 1981;31(4):203-13. doi: 10.1159/000131650.

Chromosomal radiosensitivity of ataxia telangiectasia cells at different cell cycle stages.

Hum Genet. 1979 Nov 1;52(1):127-32. doi: 10.1007/BF00284606.

Effect of caffeine in G2 on X-ray-induced chromosomal aberrations and mitotic inhibition in ataxia telangiectasia fibroblast and lymphoblastoid cells.

Hum Genet. 1984;67(3):329-35. doi: 10.1007/BF00291363.

Complementation analysis in ataxia telangiectasia: fibroblast-lymphoblastoid cell heterokaryon assay by radiation-induced chromosome aberrations.

Cytogenet Cell Genet. 1993;64(1):9-11. doi: 10.1159/000133549.

Cancer Res. 1979 Sep;39(9):3725-34.

Suppression of X-ray-induced chromosome aberrations in ataxia telangiectasia cells by introduction of a normal human chromosome 11.

Mutat Res. 1992 Nov;293(1):31-7. doi: 10.1016/0921-8777(92)90005-n.

Ataxia telangiectasia. Evaluation of radiosensitivity in cultured skin fibroblasts as a diagnostic test.

Arch Dis Child. 1978 May;53(5):386-90. doi: 10.1136/adc.53.5.386.

DNA strained breakage repair in ataxia telangiectasia fibroblast-like cells.

Mutat Res. 1975 Dec;33(2-3):357-66. doi: 10.1016/0027-5107(75)90211-0.

Specific chromosome aberrations in ataxia telangiectasia.

J Med Genet. 1975 Sep;12(3):251-62. doi: 10.1136/jmg.12.3.251.

引用本文的文献

The cold immunological landscape of ATM-deficient cancers.

J Immunother Cancer. 2025 May 11;13(5):e010548. doi: 10.1136/jitc-2024-010548.

Long-Term Survival Following Chemoradiation in Locoregional Recurrent Germline Mutated Pancreatic Ductal Adenocarcinoma.

Adv Radiat Oncol. 2025 Feb 21;10(4):101742. doi: 10.1016/j.adro.2025.101742. eCollection 2025 Apr.

Towards Personalized Radiotherapy in Pelvic Cancer: Patient-Related Risk Factors for Late Radiation Toxicity.

Curr Oncol. 2025 Jan 17;32(1):47. doi: 10.3390/curroncol32010047.

Genotype-Directed Synthetic Cytotoxicity of ATR Inhibition with Radiotherapy.

Clin Cancer Res. 2024 Dec 16;30(24):5643-5656. doi: 10.1158/1078-0432.CCR-24-0154.

Double-strand DNA break repair: molecular mechanisms and therapeutic targets.

MedComm (2020). 2023 Oct 5;4(5):e388. doi: 10.1002/mco2.388. eCollection 2023 Oct.

ATM Mutations Associate with Distinct Co-Mutational Patterns and Therapeutic Vulnerabilities in NSCLC.

Clin Cancer Res. 2023 Dec 1;29(23):4958-4972. doi: 10.1158/1078-0432.CCR-23-1122.

Ex Vivo Chromosomal Radiosensitivity Testing in Patients with Pathological Germline Variants in Breast Cancer High-Susceptibility Genes and .

Curr Issues Mol Biol. 2023 Aug 10;45(8):6618-6633. doi: 10.3390/cimb45080418.

Radiology's Ionising Radiation Paradox: Weighing the Indispensable Against the Detrimental in Medical Imaging.

Cureus. 2023 Jul 10;15(7):e41623. doi: 10.7759/cureus.41623. eCollection 2023 Jul.

Prospective Newborn Screening for SCID in Germany: A First Analysis by the Pediatric Immunology Working Group (API).

J Clin Immunol. 2023 Jul;43(5):965-978. doi: 10.1007/s10875-023-01450-6. Epub 2023 Feb 27.

Pancreatic cancer derived 3D organoids as a clinical tool to evaluate the treatment response.

Front Oncol. 2023 Jan 12;12:1072774. doi: 10.3389/fonc.2022.1072774. eCollection 2022.