The role of TBK1 in cancer pathogenesis and anticancer immunity

AP Runde, R Mack, PB SJ, J Zhang - Journal of Experimental & Clinical …, 2022 - Springer
The TANK-binding kinase 1 (TBK1) is a serine/threonine kinase belonging to the non-
canonical inhibitor of nuclear factor-κB (IκB) kinase (IKK) family. TBK1 can be activated by …

Protein interaction networks in neurodegenerative diseases: From physiological function to aggregation

G Calabrese, C Molzahn, T Mayor - Journal of Biological Chemistry, 2022 - ASBMB
The accumulation of protein inclusions is linked to many neurodegenerative diseases that
typically develop in older individuals, due to a combination of genetic and environmental …

[PDF][PDF] Huntington Disease: mechanism of Pathogenesis and recent developments in its therapeutic strategies: a review

O Eje, C Ogbonna, C Onoyima, F Nduka - J Chem Rev, 2023 - researchgate.net
One of the leading causes of death apart from cancer is a neurodegenerative disease.
Huntington's disease (HD) is such that affects the neurons resulting from the programmed …

The multiple roles of autophagy in neural function and diseases

YY Li, ZH Qin, R Sheng - Neuroscience Bulletin, 2024 - Springer
Autophagy involves the sequestration and delivery of cytoplasmic materials to lysosomes,
where proteins, lipids, and organelles are degraded and recycled. According to the way the …

HD and SCA1: Tales from two 30-year journeys since gene discovery

LM Thompson, HT Orr - Neuron, 2023 - cell.com
One of the more transformative findings in human genetics was the discovery that the
expansion of unstable nucleotide repeats underlies a group of inherited neurological …

[HTML][HTML] TBK1 (TANK-binding kinase 1)-mediated regulation of autophagy in health and disease

L Herhaus - Matrix Biology, 2021 - Elsevier
Abstract TANK-binding kinase 1 (TBK1) is a druggable multifunctional kinase that exerts a
broad spectrum of functions in cells. These range from innate immunity, inflammation and …

GRASP55 regulates the unconventional secretion and aggregation of mutant huntingtin

E Ahat, S Bui, J Zhang, F da Veiga Leprevost… - Journal of Biological …, 2022 - ASBMB
Recent studies demonstrated that the Golgi reassembly stacking proteins (GRASPs),
especially GRASP55, regulate Golgi-independent unconventional secretion of certain …

Cryo-electron tomography provides topological insights into mutant huntingtin exon 1 and polyQ aggregates

JG Galaz-Montoya, SH Shahmoradian, K Shen… - Communications …, 2021 - nature.com
Huntington disease (HD) is a neurodegenerative trinucleotide repeat disorder caused by an
expanded poly-glutamine (polyQ) tract in the mutant huntingtin (mHTT) protein. The …

Neuroprotective Effects of σ2R/TMEM97 Receptor Modulators in the Neuronal Model of Huntington's Disease

J Jin, N Arbez, JJ Sahn, Y Lu, KT Linkens… - ACS chemical …, 2022 - ACS Publications
Huntington's disease (HD) is a genetic neurodegenerative disease caused by an expanded
CAG repeat in the Huntingtin (HTT) gene that encodes for an expanded polyglutamine …

[HTML][HTML] Roscovitine, a CDK inhibitor, reduced neuronal toxicity of mHTT by targeting HTT phosphorylation at S1181 and S1201 in Vitro

H Liu, A McCollum, A Krishnaprakash… - International journal of …, 2024 - mdpi.com
Huntington's disease (HD) is an autosomal dominant neurodegenerative disease caused by
a single mutation in the huntingtin gene (HTT). Normal HTT has a CAG trinucleotide repeat …