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Homozygous mutation of MTPAP causes cellular radiosensitivity and persistent DNA double-strand breaks.

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Homozygous deficiency of ubiquitin-ligase ring-finger protein RNF168 mimics the radiosensitivity syndrome of ataxia-telangiectasia.

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Functional and computational assessment of missense variants in the ataxia-telangiectasia mutated (ATM) gene: mutations with increased cancer risk.

Human mutation·2008

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Neuromuscular disorders : NMD·2007

ATM gene founder haplotypes and associated mutations in Polish families with ataxia-telangiectasia.

Annals of human genetics·2005

Rezpegaldesleukin treatment of moderate-to-severe atopic dermatitis (REZOLVE-AD): final results from the 16-week induction period of an international, double-blind, placebo-controlled, randomised phase 2b study.

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Risk of transmission of amyloid β pathology via transfused blood products.

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Lancet (London, England)·2026

DAMPs, PAMPs, and Alarmins: From Mechanism to Therapy.

MedComm·2026

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Cureus·2026

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Archives of Razi Institute·2026

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Pakistan journal of pharmaceutical sciences·2026

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Lymphocyte response to P.H.A. in patients with non-lymphoid tumours

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CAND3: A ubiquitously expressed gene immediately adjacent and in opposite transcriptional orientation to the ATM gene at 1lq23.1.

Homozygous mutation of MTPAP causes cellular radiosensitivity and persistent DNA double-strand breaks.

Homozygous deficiency of ubiquitin-ligase ring-finger protein RNF168 mimics the radiosensitivity syndrome of ataxia-telangiectasia.

Functional and computational assessment of missense variants in the ataxia-telangiectasia mutated (ATM) gene: mutations with increased cancer risk.

Ataxia-oculomotor apraxia 2 patients show no increased sensitivity to ionizing radiation.

ATM gene founder haplotypes and associated mutations in Polish families with ataxia-telangiectasia.

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Liver resection after atezolizumab and bevacizumab versus maintenance therapy for locally advanced hepatocellular carcinoma (TALENTOP): a multicentre, open-label, randomised, phase 3 trial.

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Lymphocyte response to P.H.A. in patients with non-lymphoid tumours

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