Alzheimer’s disease remains a formidable challenge for therapeutic management. In a recent report in Nature Structural and Molecular Biology, Cohen et al. (2015) present intriguing results showing that “designer” molecular chaperones may hold the key to an evolutionarily conserved program for management of toxic oligomer species contributing to brain pathobiology
Accumulation of amyloid-like aggregates is a hallmark of numerous neurodegenerative disorders such a...
Abstract Background The accumulation of amyloid beta (Aβ) peptides in fibrils is prerequisite for Al...
Neurodegenerative diseases ranging from Alzheimer’s disease and polyglutamine diseases to transmissi...
Alzheimer’s disease remains a formidable challenge for therapeutic management. In a recent report in...
AbstractThe most conspicuous feature of many neurodegenerative disorders, including Alzheimer's, Par...
Protein homeostasis or proteostasis involves an intricate balance between the synthesis, folding, lo...
AbstractFor 20years the amyloid cascade hypothesis of Alzheimer disease (AD) has placed the amyloid-...
Neurodegenerative diseases (NDDs) such as Alzheimer’s disease, Parkinson’s disease and Huntington’s ...
© 2020 by the authors.Age-dependent alterations in the proteostasis network are crucial in the progr...
Most proteins need to adopt a three-dimensional structure in order to function properly. Misfolding,...
AbstractAmyloid-β, the protein implicated in Alzheimer’s disease, along with a number of other prote...
The self-association of misfolded or damaged proteins into ordered amyloid-like aggregates character...
Protein aggregation is a hallmark of a wide range of human disorders, including Alzheimer’s disease...
Intracellular amyloid fibrils linked to neurodegenerative disease typically accumulate in an age-rel...
AbstractElevated cerebral levels of amyloid β-protein occur universally in Alzheimer's disease, yet ...
Accumulation of amyloid-like aggregates is a hallmark of numerous neurodegenerative disorders such a...
Abstract Background The accumulation of amyloid beta (Aβ) peptides in fibrils is prerequisite for Al...
Neurodegenerative diseases ranging from Alzheimer’s disease and polyglutamine diseases to transmissi...
Alzheimer’s disease remains a formidable challenge for therapeutic management. In a recent report in...
AbstractThe most conspicuous feature of many neurodegenerative disorders, including Alzheimer's, Par...
Protein homeostasis or proteostasis involves an intricate balance between the synthesis, folding, lo...
AbstractFor 20years the amyloid cascade hypothesis of Alzheimer disease (AD) has placed the amyloid-...
Neurodegenerative diseases (NDDs) such as Alzheimer’s disease, Parkinson’s disease and Huntington’s ...
© 2020 by the authors.Age-dependent alterations in the proteostasis network are crucial in the progr...
Most proteins need to adopt a three-dimensional structure in order to function properly. Misfolding,...
AbstractAmyloid-β, the protein implicated in Alzheimer’s disease, along with a number of other prote...
The self-association of misfolded or damaged proteins into ordered amyloid-like aggregates character...
Protein aggregation is a hallmark of a wide range of human disorders, including Alzheimer’s disease...
Intracellular amyloid fibrils linked to neurodegenerative disease typically accumulate in an age-rel...
AbstractElevated cerebral levels of amyloid β-protein occur universally in Alzheimer's disease, yet ...
Accumulation of amyloid-like aggregates is a hallmark of numerous neurodegenerative disorders such a...
Abstract Background The accumulation of amyloid beta (Aβ) peptides in fibrils is prerequisite for Al...
Neurodegenerative diseases ranging from Alzheimer’s disease and polyglutamine diseases to transmissi...