ATM is a master regulator of the cellular response to DNA damage. The classical mechanism of ATM activation involves its monomerization in response to DNA double-strand breaks, resulting in ATM-dependent phosphorylation of more than a thousand substrates required for cell cycle progression, DNA repair, and apoptosis. Here, new experimental evidence for non-canonical mechanisms of ATM activation in response to stimuli distinct from DNA double-strand breaks is discussed. It includes cytoskeletal changes, chromatin modifications, RNA-DNA hybrids, and DNA single-strand breaks. Noncanonical ATM activation may be important for the pathology of the multisystemic disease Ataxia Telangiectasia
Ataxia-telangiectasia Mutated (ATM), mutated in the human disorder ataxia-telangiectasia, is rapidly...
The ATM (Ataxia-telangiectasia mutated) kinase is one of the major players of the DNA damage respon...
Ataxia Telangiectasia Mutated (ATM) kinase is a central regulator of the DNA damage response and its...
Ataxia telangiectasia is caused by mutations in ATM and represents a paradigm for cancer predisposit...
Mutations in the ATM gene lead to the genetic disorder ataxia-telangiectasia. ATM encodes a protein ...
ATM (ataxia-telangiectasia mutated) kinase is a key factor in DNA damage responses, and mutations in...
The ability of a cell to conserve and maintain its native DNA sequence is fundamental for the surviv...
Ataxia-telangiectasia mutated kinase (ATM) is a DNA damage-inducible protein kinase, which phosphory...
Ataxia-telangiectasia mutated (ATM) kinase is a component of a signalling mechanism that determines ...
Significant progress has been made in recent years in elucidating the molecular controls of cellular...
ATM-dependent cellular response to DNA double strand breaks plays a pivotal role in the maintenance ...
Ataxia telangiectasia (A-T) is a disorder characterized by cerebellar degeneration, immunodeficiency...
The human genetic disorder ataxia telangiectasia (A-T), caused by mutation in the ATM gene, is chara...
The human tumor suppressor gene ataxia telangiectasia mutated (ATM) encodes a 3056 amino-acid protei...
Ataxia-telangiectasia mutated (ATM) kinase, the mutation of which causes the autosomal recessive dis...
Ataxia-telangiectasia Mutated (ATM), mutated in the human disorder ataxia-telangiectasia, is rapidly...
The ATM (Ataxia-telangiectasia mutated) kinase is one of the major players of the DNA damage respon...
Ataxia Telangiectasia Mutated (ATM) kinase is a central regulator of the DNA damage response and its...
Ataxia telangiectasia is caused by mutations in ATM and represents a paradigm for cancer predisposit...
Mutations in the ATM gene lead to the genetic disorder ataxia-telangiectasia. ATM encodes a protein ...
ATM (ataxia-telangiectasia mutated) kinase is a key factor in DNA damage responses, and mutations in...
The ability of a cell to conserve and maintain its native DNA sequence is fundamental for the surviv...
Ataxia-telangiectasia mutated kinase (ATM) is a DNA damage-inducible protein kinase, which phosphory...
Ataxia-telangiectasia mutated (ATM) kinase is a component of a signalling mechanism that determines ...
Significant progress has been made in recent years in elucidating the molecular controls of cellular...
ATM-dependent cellular response to DNA double strand breaks plays a pivotal role in the maintenance ...
Ataxia telangiectasia (A-T) is a disorder characterized by cerebellar degeneration, immunodeficiency...
The human genetic disorder ataxia telangiectasia (A-T), caused by mutation in the ATM gene, is chara...
The human tumor suppressor gene ataxia telangiectasia mutated (ATM) encodes a 3056 amino-acid protei...
Ataxia-telangiectasia mutated (ATM) kinase, the mutation of which causes the autosomal recessive dis...
Ataxia-telangiectasia Mutated (ATM), mutated in the human disorder ataxia-telangiectasia, is rapidly...
The ATM (Ataxia-telangiectasia mutated) kinase is one of the major players of the DNA damage respon...
Ataxia Telangiectasia Mutated (ATM) kinase is a central regulator of the DNA damage response and its...