Background: Ataxia telangiectasia-mutated (ATM) gene downexpression has been reported in sporadic breast carcinomas (BC); however, the prognostic value and mechanisms of ATM deregulation remain unclear.Patients and methods: ATM and miRNAs (miR-26a, miR-26b, miR-203, miR-421, miR-664, miR-576-5p and miR-18a) expression levels were evaluated by quantitative real-time PCR (RT-qPCR) in 52 BC and 3 normal breast samples. ATM protein expression was assessed by immunohistochemistry in 968 BC and 35 adjacent normal breast tissues. ATM copy number alteration was detected by array comparative genomic hybridization (aCGH) in 42 tumours.Results: Low ATM levels were associated with tumour grade. Absence of ATM protein expression was associated with dist...
Background: MCPH1 is a proximal regulator of DNA damage response pathway that is involved in recruit...
Abstract Background Loss of expression of the gene ataxia-telangiectasia mutated (ATM), occurring in...
Deficiencies in the ability of cells to sense and repair damage in individuals with rare genetic ins...
Deficiencies in the ATM gene are the underlying cause for ataxia telangiectasia, a syndrome characte...
<div><p>Deficiencies in the ATM gene are the underlying cause for ataxia telangiectasia, a syndrome ...
Deficiencies in the ATM gene are the underlying cause for ataxia telangiectasia, a syndrome characte...
Incidence of breast cancer is continuously increasing in the Czech Republic. Tumor development is a ...
Molecular alterations of the Ataxia-telangiectasia (AT) gene are frequently detected in breast cance...
The ATM gene is mutated in ataxia-telangiectasia (A-T), a genetic instability syndrome characterized...
We investigated the correlation of ataxia-telangiectasia-mutated (ATM) protein expression with clini...
Introduction: The ataxia-telangiectasia mutated (ATM) gene (MIM ID 208900) encodes a protein kinase ...
The ataxia telangiectasia mutated gene (ATM), candidate for breast cancer susceptibility gene, encod...
PURPOSE: MYC transcription factor has critical roles in cell growth, proliferation, metabolism, diff...
The ATM gene is mutated in ataxia-telangiectasia (AT). Heterozygote female relatives of AT cases hav...
Background: The ATM gene encoding a putative protein kinase is mutated in ataxia-telangiectasia (A-T...
Background: MCPH1 is a proximal regulator of DNA damage response pathway that is involved in recruit...
Abstract Background Loss of expression of the gene ataxia-telangiectasia mutated (ATM), occurring in...
Deficiencies in the ability of cells to sense and repair damage in individuals with rare genetic ins...
Deficiencies in the ATM gene are the underlying cause for ataxia telangiectasia, a syndrome characte...
<div><p>Deficiencies in the ATM gene are the underlying cause for ataxia telangiectasia, a syndrome ...
Deficiencies in the ATM gene are the underlying cause for ataxia telangiectasia, a syndrome characte...
Incidence of breast cancer is continuously increasing in the Czech Republic. Tumor development is a ...
Molecular alterations of the Ataxia-telangiectasia (AT) gene are frequently detected in breast cance...
The ATM gene is mutated in ataxia-telangiectasia (A-T), a genetic instability syndrome characterized...
We investigated the correlation of ataxia-telangiectasia-mutated (ATM) protein expression with clini...
Introduction: The ataxia-telangiectasia mutated (ATM) gene (MIM ID 208900) encodes a protein kinase ...
The ataxia telangiectasia mutated gene (ATM), candidate for breast cancer susceptibility gene, encod...
PURPOSE: MYC transcription factor has critical roles in cell growth, proliferation, metabolism, diff...
The ATM gene is mutated in ataxia-telangiectasia (AT). Heterozygote female relatives of AT cases hav...
Background: The ATM gene encoding a putative protein kinase is mutated in ataxia-telangiectasia (A-T...
Background: MCPH1 is a proximal regulator of DNA damage response pathway that is involved in recruit...
Abstract Background Loss of expression of the gene ataxia-telangiectasia mutated (ATM), occurring in...
Deficiencies in the ability of cells to sense and repair damage in individuals with rare genetic ins...