The Lewy body in Parkinson's disease and related neurodegenerative disorders
K Wakabayashi, K Tanji, S Odagiri, Y Miki, F Mori… - Molecular …, 2013 - Springer
The histopathological hallmark of Parkinson's disease (PD) is the presence of fibrillar
aggregates referred to as Lewy bodies (LBs), in which α-synuclein is a major constituent …
aggregates referred to as Lewy bodies (LBs), in which α-synuclein is a major constituent …
The Lewy body in Parkinson's disease: molecules implicated in the formation and degradation of α‐synuclein aggregates
K Wakabayashi, K Tanji, F Mori, H Takahashi - Neuropathology, 2007 - Wiley Online Library
The histological hallmark of Parkinson's disease (PD) is the presence of fibrillar aggregates
called Lewy bodies (LBs). LB formation has been considered to be a marker for neuronal …
called Lewy bodies (LBs). LB formation has been considered to be a marker for neuronal …
Proteomic differences in amyloid plaques in rapidly progressive and sporadic Alzheimer's disease
Rapidly progressive Alzheimer's disease (rpAD) is a particularly aggressive form of
Alzheimer's disease, with a median survival time of 7–10 months after diagnosis. Why these …
Alzheimer's disease, with a median survival time of 7–10 months after diagnosis. Why these …
Multiple system atrophy: an oligodendroglioneural synucleinopathy
KA Jellinger - Journal of Alzheimer's Disease, 2018 - content.iospress.com
Multiple system atrophy (MSA) is an orphan, fatal, adult-onset neurodegenerative disorder of
uncertain etiology that is clinically characterized by various combinations of parkinsonism …
uncertain etiology that is clinically characterized by various combinations of parkinsonism …
Multiple system atrophy-associated oligodendroglial protein p25α stimulates formation of novel α-synuclein strain with enhanced neurodegenerative potential
Pathology consisting of intracellular aggregates of alpha-Synuclein (α-Syn) spread through
the nervous system in a variety of neurodegenerative disorders including Parkinson's …
the nervous system in a variety of neurodegenerative disorders including Parkinson's …
The neuropathology, pathophysiology and genetics of multiple system atrophy
Z Ahmed, YT Asi, A Sailer, AJ Lees… - Neuropathology and …, 2012 - Wiley Online Library
Z. Ahmed, YT Asi, A. Sailer, AJ Lees, H. Houlden, T. Revesz and JL Holton (2012)
Neuropathology and Applied Neurobiology38, 4–24 The neuropathology, pathophysiology …
Neuropathology and Applied Neurobiology38, 4–24 The neuropathology, pathophysiology …
[책][B] Structure and function of intrinsically disordered proteins
The existence and functioning of intrinsically disordered proteins (IDPs) challenge the
classical structure-function paradigm that equates function with a well-defined 3D structure …
classical structure-function paradigm that equates function with a well-defined 3D structure …
[HTML][HTML] Identification of blood microRNAs associated to Parkinsońs disease
The present study demonstrates that blood samples can be used as a source of miRNA
identification associated to Parkinson's disease (PD). A set of six differentially expressed …
identification associated to Parkinson's disease (PD). A set of six differentially expressed …
Neuropathology of multiple system atrophy: new thoughts about pathogenesis
KA Jellinger - Movement Disorders, 2014 - Wiley Online Library
Multiple system atrophy (MSA) is a fatal adult‐onset neurodegenerative disorder of
uncertain etiology, clinically manifesting with autonomic failure associated with …
uncertain etiology, clinically manifesting with autonomic failure associated with …
A multiregional proteomic survey of the postnatal human brain
Detailed observations of transcriptional, translational and post-translational events in the
human brain are essential to improving our understanding of its development, function and …
human brain are essential to improving our understanding of its development, function and …