Results 31 to 40 of about 26,505 (243)

Role of p62/SQSTM1 in liver physiology and pathogenesis [PDF]

open access: yesExperimental Biology and Medicine, 2013
p62/sequestosome-1/A170/ZIP (hereafter referred to as p62) is a scaffold protein that has multiple functions, such as signal transduction, cell proliferation, cell survival, cell death, inflammation, tumourigenesis and oxidative stress response. While p62 is an autophagy substrate and is degraded by autophagy, p62 serves as an autophagy receptor for ...
Sharon, Manley   +2 more
openaire   +2 more sources

Systemic overexpression of SQSTM1/p62 accelerates disease onset in a SOD1H46R-expressing ALS mouse model

open access: yesMolecular Brain, 2018
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease characterized by a selective loss of upper and lower motor neurons. Recent studies have shown that mutations in SQSTM1 are linked to ALS.
Shun Mitsui   +10 more
doaj   +1 more source

ZZ-dependent regulation of p62/SQSTM1 in autophagy [PDF]

open access: yesNature Communications, 2018
AbstractAutophagic receptor p62 is a critical mediator of cell detoxification, stress response, and metabolic programs and is commonly deregulated in human diseases. The diverse functions of p62 arise from its ability to interact with a large set of ligands, such as arginylated (Nt-R) substrates. Here, we describe the structural mechanism for selective
Yi Zhang   +14 more
openaire   +3 more sources

Identification and functional analysis of Joka2, a tobacco member of the family of selective autophagy cargo receptors [PDF]

open access: yes, 2011
Two main mechanisms of protein turnover exist in eukaryotic cells: the ubiquitin-proteasome system and the autophagylysosomal pathway. Autophagy is an emerging important constituent of many physiological and pathological processes, such as response to ...
Sirko, Agnieszka   +17 more
core   +1 more source

Combined Evaluation of MAP1LC3B and SQSTM1 for Biological and Clinical Significance in Ductal Carcinoma of Breast Cancer

open access: yesBiomedicines, 2021
Breast cancer is the leading cause of cancer death in women worldwide. The microtubule-associated protein light chain 3B (MAP1LC3B) and adaptor sequestosome 1 (SQSTM1) are two major markers for autophagy.
Pei-Feng Liu   +7 more
doaj   +1 more source

Selective turnover of p62/A170/SQSTM1 by autophagy [PDF]

open access: yesAutophagy, 2008
Loss of autophagy causes liver injury, cardiomyopathy and neurodegeneration, associated with the formation of ubiquitin-positive inclusion bodies. However, the pathogenic mechanism and molecular machinery involved in inclusion formation are not fully understood. We recently identified a ubiquitin-binding protein, p62/A170/SQSTM1, as a molecule involved
Yoshinobu, Ichimura   +3 more
openaire   +2 more sources

Identification of a Novel Hemizygous SQSTM1 Nonsense Mutation in Atypical Behavioral Variant Frontotemporal Dementia

open access: yesFrontiers in Aging Neuroscience, 2018
Frontotemporal dementia includes a large spectrum of neurodegenerative disorders. SQSTM1, coding for p62 protein, plays a vital role in the pathogenesis of FTD.
Lin Sun   +6 more
doaj   +1 more source

Loss of SQSTM1/p62 Induces Obesity and Exacerbates Alcohol-Induced Liver Injury in Aged MiceSummary

open access: yesCellular and Molecular Gastroenterology and Hepatology, 2023
Background: Alcohol-associated liver disease (ALD) is a worldwide health problem, of which the effective treatment is still lacking. Both detrimental and protective roles of adipose tissue have been implicated in ALD.
Hui Qian   +9 more
doaj   +1 more source

SQSTM1/p62: A Potential Target for Neurodegenerative Disease [PDF]

open access: yesACS Chemical Neuroscience, 2019
Neurodegenerative diseases, characterized by a progressive loss of brain function, affect the lives of millions of individuals worldwide. The complexity of the brain poses a challenge for scientists trying to map the biochemical and physiological pathways to identify areas of pathological errors.
Shifan Ma   +2 more
openaire   +2 more sources

Protocol for stage 2 of the GaP study (genetic testing acceptability for Paget's disease of the bone) : a questionnaire study to investigate whether relatives of people with Paget's disease would accept genetic testing and preventative treatment if they were available [PDF]

open access: yes, 2008
Background: Paget's disease of bone (PDB) disrupts normal bone architecture and causes pain, deformity, deafness, osteoarthritis, and fractures. Genetic factors play a role in PDB and genetic tests are now conducted for research purposes.
Ralston, Stuart H.   +81 more
core   +1 more source

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