- A historical reflection on our understanding of radiation-induced DNA double strand break repairin somatic mammalian cells; interfacing the past with the present.
- A novel ATM mutation associated with elevated atypical lymphocyte populations, hyper-IgM, and cutaneous granulomas.
- A tumor suppressive DNA translocase named FANCM.
- Anti-peptide Antibody Responses in Patients with Ataxia-telangiectasia
- Antioxidant Defense, Redox Homeostasis, and Oxidative Damage in Children With Ataxia Telangiectasia and Nijmegen Breakage Syndrome.
- Ataxia-Telangiectasia Mutated is located in cardiac mitochondria and impacts oxidative phosphorylation.
- Ataxia-telangiectasia: A review of clinical features and molecular pathology.
- ATM expression is attenuated by promoter hypermethylation in human ovarian endometriotic stromal cells.
- ATM mutation spectrum in Russian children with ataxia-telangiectasia.
- ATM orchestrates the DNA-damage response to counter toxic non-homologous end-joining at broken replication forks.
- ATM phosphorylation of the actin-binding protein drebrin controls oxidation stress-resistance in mammalian neurons and C. elegans.
- ATM rs189037 (G > A) polymorphism increased the risk of cancer: an updated meta-analysis.
- Atrophy, oxidative switching and ultrastructural defects in skeletal muscle of Ataxia Telangiectasia mouse model.
- Bladder Artery Embolization for Massive Hematuria Treatment in a Patient With Ataxia-Telangiectasia Acute Lymphoblastic Leukemia.
- Chromosome Instability Syndromes.
- Clinical diagnosis and genetic counseling of atypical ataxia‑telangiectasia in a Chinese family.
- Clinicopathological significance of ataxia telangiectasia-mutated (ATM) kinase and ataxia telangiectasia-mutated and Rad3-related (ATR) kinase in MYC overexpressed breast cancers.
- Cutaneous granulomas with primary immunodeficiency in children: a report of 17 new patients and a review of the literature.
- Dermatofibrosarcoma protuberans in a pediatric patient with ataxia telangiectasia syndrome.
- Diagnostic Value of Next Generation Sequencing Ataxia Panel as a Part of Multistep Investigation Approach in Sporadic and Autosomal Recessive Cerebellar Ataxias in Russia (P1.8-013)
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