The abnormal deposition of proteins in and around neurons is a common pathological feature of many neurodegenerative diseases. Among these pathological proteins, the microtubule-associated protein tau forms intraneuronal filaments in a spectrum of neurological disorders. The discovery that dominant mutations in the MAPT gene encoding tau are associated with familial frontotemporal dementia strongly supports abnormal tau protein as directly involved in disease pathogenesis. This and other evidence suggest that tau is a worthwhile target for the prevention or treatment of tau-associated neurodegenerative diseases, collectively called tauopathies. However, it is critical to understand the normal biological roles of tau, the specific molecular ...
Tau is most intensely studied in relation to its executive role in Tauopathies, a family of neurodeg...
Since the discovery of the microtubule-associated protein Tau (MAPT) over 40 years ago, most studies...
AbstractTau becomes characteristically altered both functionally and structurally in several neurode...
The abnormal deposition of proteins in and around neurons is a common pathological feature of many n...
Accumulation and aggregation of the microtubule-associated protein tau are a pathological hallmark o...
Abnormal deposition of misprocessed and aggregated proteins is a common final pathway of most neurod...
Abnormal deposition of misprocessed and aggregated proteins is a common final pathway of most neurod...
Tau is well established as a microtubule-associated protein in neurons. However, under pathological ...
Tau is well established as a microtubule-associated protein in neurons. However, under pathological ...
Tau protein is a microtubule associated protein mainly expressed in neurons. Under pathological cond...
Tau is the most common misfolded protein responsible for human neurodegenerative diseases. The ident...
Tauopathy is a category of neurodegenerative diseases that are caused or associated with pathologica...
Tau protein is a neuronal microtubule-associated protein (MAP), which localizes primarily in the axo...
Amyloid-β peptide (Aβ) and tau protein deposits in the human brain are the pathological ha...
Tau protein is a neuronal microtubule-associated protein (MAP), which localizes primarily in the axo...
Tau is most intensely studied in relation to its executive role in Tauopathies, a family of neurodeg...
Since the discovery of the microtubule-associated protein Tau (MAPT) over 40 years ago, most studies...
AbstractTau becomes characteristically altered both functionally and structurally in several neurode...
The abnormal deposition of proteins in and around neurons is a common pathological feature of many n...
Accumulation and aggregation of the microtubule-associated protein tau are a pathological hallmark o...
Abnormal deposition of misprocessed and aggregated proteins is a common final pathway of most neurod...
Abnormal deposition of misprocessed and aggregated proteins is a common final pathway of most neurod...
Tau is well established as a microtubule-associated protein in neurons. However, under pathological ...
Tau is well established as a microtubule-associated protein in neurons. However, under pathological ...
Tau protein is a microtubule associated protein mainly expressed in neurons. Under pathological cond...
Tau is the most common misfolded protein responsible for human neurodegenerative diseases. The ident...
Tauopathy is a category of neurodegenerative diseases that are caused or associated with pathologica...
Tau protein is a neuronal microtubule-associated protein (MAP), which localizes primarily in the axo...
Amyloid-β peptide (Aβ) and tau protein deposits in the human brain are the pathological ha...
Tau protein is a neuronal microtubule-associated protein (MAP), which localizes primarily in the axo...
Tau is most intensely studied in relation to its executive role in Tauopathies, a family of neurodeg...
Since the discovery of the microtubule-associated protein Tau (MAPT) over 40 years ago, most studies...
AbstractTau becomes characteristically altered both functionally and structurally in several neurode...