[PDF][PDF] Investigating Endoplasmic Reticulum-Mitochondria Signalling in Amyotrophic Lateral Sclerosis

NJ Hartopp - 2020 - kclpure.kcl.ac.uk
Abstract Amyotrophic Lateral Sclerosis (ALS) is a fatal neurodegenerative disease, causing
progressive muscle wasting and eventual paralysis. A number of the cellular functions that …

[PDF][PDF] Stanovení metabolické aktivity CYP1A2 pomocí kofeinu v moči a slinách

S Brejcha - is.muni.cz
V klinické praxi často dochází k nežádoucím účinkům léčiv v důsledku jejich špatného
dávkování. Těmto nežádoucím účinkům se dá předejít odhalením rychlosti jejich …

Method for genetic treatment using the AAV-XBP1s/GFP virus and use thereof in the prevention and treatment of amyotrophic lateral sclerosis

CAH Flores, VSV Paterakis - US Patent 10,512,698, 2019 - Google Patents
US10512698B2 - Method for genetic treatment using the AAV-XBP1s/GFP virus and use
thereof in the prevention and treatment of amyotrophic lateral sclerosis - Google Patents …

Evaluation of Candidate Therapeutic Agents in Neurodegenerative Diseases

Y Shah - 2017 - jscholarship.library.jhu.edu
Protein quality control is essential for cellular homeostasis, and defects in the same result in
various pathological conditions such as neurodegenerative diseases and cancer …

ER stress and the unfolded protein response in neurodegeneration

C Hetz Flores, S Saxena - 2017 - repositorio.uchile.cl
The clinical manifestation of neurodegenerative diseases is initiated by the selective
alteration in the functionality of distinct neuronal populations. The pathology of many …

Proteostasis disturbance in amyotrophic lateral sclerosis

D Medinas Bilches, V Valenzuela Paterakis… - 2017 - repositorio.uchile.cl
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease affecting
motoneurons in the brain and spinal cord leading to paralysis and death. Although the …

The role of the P2X7 receptor in the progression of amyotrophic lateral sclerosis

R Bartlett - 2016 - ro.uow.edu.au
Amyotrophic lateral sclerosis (ALS) is a late‐onset and rapidly progressive
neurodegenerative disease in humans, which is characterised by the degeneration and loss …

[PDF][PDF] Efficacy and effectiveness of drug treatments in amyotrophic lateral sclerosis: A systematic review with meta-analysis

MC Moura, MRCG Novaes, YSSP Zago, EJ Eduardo… - 2016 - researchgate.net
The results of published studies with various neuroprotectors seeking to preserve motor
neuron function and improve survival in amyotrophic lateral sclerosis patients have poor …

Investigation of the unfolded protein response and other stress-related responses in distinct models of neurodegeneration

M Davies - 2016 - eprints.soton.ac.uk
There is no cure for chronic neurodegenerative diseases and disease-modifying therapies
are limited. In order to develop successful disease-modifying therapies the molecules and …

[PDF][PDF] Rol de la respuesta de proteínas mal plegadas (UPR) en la patología mediada por TDP-43 en la esclerosis lateral amiotrófica

LA Bargsted Elgueda - 2016 - repositorio.uchile.cl
Las enfermedades neurodegenerativas más comunes en los seres humanos, tales como la
enfermedad de Alzheimer, la enfermedad de Parkinson, la enfermedad de Huntington, ELA …