[HTML][HTML] Moderate intrinsic phenotypic alterations in C9orf72 ALS/FTD iPSC-microglia despite the presence of C9orf72 pathological features

I Lorenzini, E Alsop, J Levy, LM Gittings… - Frontiers in cellular …, 2023 - frontiersin.org
While motor and cortical neurons are affected in C9orf72 amyotrophic lateral sclerosis and
frontotemporal dementia (ALS/FTD), it remains largely unknown if and how non-neuronal …

[HTML][HTML] Tackling chronic inflammation with withanolide phytochemicals—A withaferin a perspective

E Logie, W Vanden Berghe - Antioxidants, 2020 - mdpi.com
Chronic inflammatory diseases are considered to be one of the biggest threats to human
health. Most prescribed pharmaceutical drugs aiming to treat these diseases are …

[HTML][HTML] Virus-mediated delivery of antibody targeting TAR DNA-binding protein-43 mitigates associated neuropathology

S Pozzi, SS Thammisetty, P Codron… - The Journal of …, 2019 - Am Soc Clin Investig
The cytoplasmic aggregation of TAR DNA-binding protein-43 (TDP-43) is a hallmark of
degenerating neurons in amyotrophic lateral sclerosis (ALS) and subsets of frontotemporal …

The role of the immune system in neurodegenerative disorders: Adaptive or maladaptive?

KR Doty, MV Guillot-Sestier, T Town - Brain research, 2015 - Elsevier
Neurodegenerative diseases share common features, including catastrophic neuronal loss
that leads to cognitive or motor dysfunction. Neuronal injury occurs in an inflammatory milieu …

The N-terminus of TDP-43 promotes its oligomerization and enhances DNA binding affinity

C Chang, TH Wu, CY Wu, M Chiang, EKW Toh… - Biochemical and …, 2012 - Elsevier
TDP-43 is a DNA/RNA-binding protein associated with different neurodegenerative
diseases such as amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration …

[HTML][HTML] Current concepts on genetic aspects of mitochondrial dysfunction in amyotrophic lateral sclerosis

M Jankovic, I Novakovic… - International Journal of …, 2021 - mdpi.com
Amyotrophic Lateral Sclerosis (ALS), neurodegenerative motor neuron disorder is
characterized as multisystem disease with important contribution of genetic factors. The …

[HTML][HTML] Induction of COX-2-PGE2 synthesis by activation of the MAPK/ERK pathway contributes to neuronal death triggered by TDP-43-depleted microglia

Q Xia, Q Hu, H Wang, H Yang, F Gao, H Ren… - Cell death & …, 2015 - nature.com
Neuroinflammation is a striking hallmark of amyotrophic lateral sclerosis (ALS) and other
neurodegenerative disorders. Previous studies have shown the contribution of glial cells …

[HTML][HTML] Mitochondrial dysfunction and decrease in body weight of a transgenic knock-in mouse model for TDP-43

C Stribl, A Samara, D Trümbach, R Peis… - Journal of Biological …, 2014 - ASBMB
The majority of amyotrophic lateral sclerosis (ALS) cases as well as many patients suffering
from frontotemporal lobar dementia (FTLD) with ubiquitinated inclusion bodies show TDP-43 …

[HTML][HTML] Mitigation of ALS pathology by neuron-specific inhibition of nuclear factor kappa B signaling

K Dutta, SS Thammisetty, H Boutej… - Journal of …, 2020 - Soc Neuroscience
To investigate the role of neuronal NF-κB activity in pathogenesis of amyotrophic lateral
sclerosis (ALS), we generated transgenic mice with neuron-specific expression of a super …

FABP7 upregulation induces a neurotoxic phenotype in astrocytes

KM Killoy, BA Harlan, M Pehar, MR Vargas - Glia, 2020 - Wiley Online Library
Fatty acid binding proteins (FABPs) are key regulators of lipid metabolism, energy
homeostasis, and inflammation. They participate in fatty acid metabolism by regulating their …