Asset Details
MbrlCatalogueTitleDetail
Do you wish to reserve the book?
Amyotrophic lateral sclerosis—a model of corticofugal axonal spread
by
Lee, Virginia M.
, Trojanowski, John Q.
, Brettschneider, Johannes
, Ludolph, Albert C.
, Braak, Heiko
, Tredici, Kelly Del
in
692/699/375/365/1917
/ Amyotrophic lateral sclerosis
/ Amyotrophic Lateral Sclerosis - metabolism
/ Amyotrophic Lateral Sclerosis - pathology
/ Axonal Transport - physiology
/ Axons - physiology
/ Brain mapping
/ Cerebral Cortex - metabolism
/ Cerebral Cortex - pathology
/ Development and progression
/ Disease
/ DNA binding proteins
/ DNA-Binding Proteins - metabolism
/ Genetic aspects
/ Humans
/ Identification and classification
/ Medicine
/ Medicine & Public Health
/ Models, Neurological
/ Neurology
/ Neurons
/ opinion-2
/ Parkinson's disease
/ Pathogenesis
/ Pathology
/ Propagation
/ Proteins
/ Spinal cord
/ Synaptic Transmission - physiology
2013
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
You are currently in the queue to collect this book. You will be notified once it is your turn to collect the book.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Amyotrophic lateral sclerosis—a model of corticofugal axonal spread
by
Lee, Virginia M.
, Trojanowski, John Q.
, Brettschneider, Johannes
, Ludolph, Albert C.
, Braak, Heiko
, Tredici, Kelly Del
in
692/699/375/365/1917
/ Amyotrophic lateral sclerosis
/ Amyotrophic Lateral Sclerosis - metabolism
/ Amyotrophic Lateral Sclerosis - pathology
/ Axonal Transport - physiology
/ Axons - physiology
/ Brain mapping
/ Cerebral Cortex - metabolism
/ Cerebral Cortex - pathology
/ Development and progression
/ Disease
/ DNA binding proteins
/ DNA-Binding Proteins - metabolism
/ Genetic aspects
/ Humans
/ Identification and classification
/ Medicine
/ Medicine & Public Health
/ Models, Neurological
/ Neurology
/ Neurons
/ opinion-2
/ Parkinson's disease
/ Pathogenesis
/ Pathology
/ Propagation
/ Proteins
/ Spinal cord
/ Synaptic Transmission - physiology
2013
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Amyotrophic lateral sclerosis—a model of corticofugal axonal spread
by
Lee, Virginia M.
, Trojanowski, John Q.
, Brettschneider, Johannes
, Ludolph, Albert C.
, Braak, Heiko
, Tredici, Kelly Del
in
692/699/375/365/1917
/ Amyotrophic lateral sclerosis
/ Amyotrophic Lateral Sclerosis - metabolism
/ Amyotrophic Lateral Sclerosis - pathology
/ Axonal Transport - physiology
/ Axons - physiology
/ Brain mapping
/ Cerebral Cortex - metabolism
/ Cerebral Cortex - pathology
/ Development and progression
/ Disease
/ DNA binding proteins
/ DNA-Binding Proteins - metabolism
/ Genetic aspects
/ Humans
/ Identification and classification
/ Medicine
/ Medicine & Public Health
/ Models, Neurological
/ Neurology
/ Neurons
/ opinion-2
/ Parkinson's disease
/ Pathogenesis
/ Pathology
/ Propagation
/ Proteins
/ Spinal cord
/ Synaptic Transmission - physiology
2013
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Amyotrophic lateral sclerosis—a model of corticofugal axonal spread
Journal Article
Amyotrophic lateral sclerosis—a model of corticofugal axonal spread
2013
Request Book From Autostore
and Choose the Collection Method
Overview
Prion-like propagation of pathogenic proteins has been suggested to underlie several neurodegenerative diseases. In this Perspectives article, Braak
et al
. posit that progressive lesions in amyotrophic lateral sclerosis (ALS) spread through cell-to-cell transfer of 43-kDA transactive response DNA-binding protein, mainly through cortical neuronal projections to other brain areas and the spinal cord. This model could have important implications for our understanding of ALS and approach to treatment.
The pathological process underlying amyotrophic lateral sclerosis (ALS) is associated with the formation of cytoplasmic inclusions consisting mainly of phosphorylated 43-kDa transactive response DNA-binding protein (pTDP-43), which plays an essential part in the pathogenesis of ALS. Preliminary evidence indicates that neuronal involvement progresses at different rates, but in a similar sequence, in different patients with ALS. This observation supports the emerging concept of prion-like propagation of abnormal proteins in noninfectious neurodegenerative diseases. Although the distance between involved regions is often considerable, the affected neurons are connected by axonal projections, indicating that physical contacts between nerve cells along axons are important for dissemination of ALS pathology. This article posits that the trajectory of the spreading pattern is consistent with the induction and dissemination of pTDP-43 pathology chiefly from cortical neuronal projections, via axonal transport, through synaptic contacts to the spinal cord and other regions of the brain.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
/ Amyotrophic lateral sclerosis
/ Amyotrophic Lateral Sclerosis - metabolism
/ Amyotrophic Lateral Sclerosis - pathology
/ Axonal Transport - physiology
/ Cerebral Cortex - metabolism
/ Disease
/ DNA-Binding Proteins - metabolism
/ Humans
/ Identification and classification
/ Medicine
/ Neurons
/ Proteins
This website uses cookies to ensure you get the best experience on our website.