Benjamin Wolozin
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Explore the profile of Benjamin Wolozin including associated specialties, affiliations and a list of published articles.
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119
Citations
7157
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Recent Articles
1.
Chakraborty P, de Opakua A, Purslow J, Fromm S, Chatterjee D, Zachrdla M, et al.
Proc Natl Acad Sci U S A
. 2024 Dec;
121(52):e2414176121.
PMID: 39693350
The pathological deposition of proteins is a hallmark of several devastating neurodegenerative diseases. These pathological deposits comprise aggregates of proteins that adopt distinct structures named strains. However, the molecular factors...
2.
Webber C, van de Spek S, Cruz A, Puri S, Zhang C, Aw J, et al.
bioRxiv
. 2024 Nov;
PMID: 39574689
The RNA binding protein TIA1 is known to regulate stress responses. Here we show that TIA1 plays a much broader role in inflammatory cells, being required for the microglial sensome....
3.
Rondon-Ortiz A, Zhang L, Ash P, Basu A, Puri S, van der Spek S, et al.
J Biol Chem
. 2024 Aug;
300(9):107621.
PMID: 39098523
Sequestosome1 (SQSTM1) is an autophagy receptor that mediates the degradation of intracellular cargo, including protein aggregates, through multiple protein interactions. These interactions form the SQSTM1 protein network, and these interactions...
4.
Jiang L, Roberts R, Wong M, Zhang L, Webber C, Libera J, et al.
Front Neurosci
. 2024 Apr;
18:1372297.
PMID: 38572146
Introduction: The study of the pathophysiology study of Alzheimer's disease (AD) has been hampered by lack animal models that recapitulate the major AD pathologies, including extracellular -amyloid (A) deposition, intracellular...
5.
Ortiz A, Zhang L, Ash P, Basu A, Puri S, van der Spek S, et al.
bioRxiv
. 2024 Jan;
PMID: 38168279
Sequestosome1 (SQSTM1) is an autophagy receptor that mediates degradation of intracellular cargo, including protein aggregates, through multiple protein interactions. These interactions form the SQSTM1 protein network, and these interactions are...
6.
Webber C, Murphy C, Rondon-Ortiz A, van der Spek S, Kelly E, Lampl N, et al.
Hum Mol Genet
. 2023 Jul;
32(20):2966-2980.
PMID: 37522762
Aggregation of TAR DNA-binding protein 43 kDa (TDP-43) is thought to drive the pathophysiology of amyotrophic lateral sclerosis and some frontotemporal dementias. TDP-43 is normally a nuclear protein that in...
7.
Park J, Wu Y, Shao W, Gendron T, van der Spek S, Sultanakhmetov G, et al.
Cell Rep
. 2023 Jul;
42(8):112822.
PMID: 37471224
C9orf72 repeat expansions are the most common genetic cause of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). Poly(GR) proteins are toxic to neurons by forming cytoplasmic inclusions that sequester...
8.
Zhao J, Jiang L, Matlock A, Xu Y, Zhu J, Zhu H, et al.
Light Sci Appl
. 2023 Jun;
12(1):147.
PMID: 37322011
Amyloid proteins are associated with a broad spectrum of neurodegenerative diseases. However, it remains a grand challenge to extract molecular structure information from intracellular amyloid proteins in their native cellular...
9.
Jiang L, Roberts R, Wong M, Zhang L, Webber C, Kilci A, et al.
Res Sq
. 2023 Jun;
PMID: 37292629
The study for the pathophysiology study of Alzheimer's disease (AD) has been hampered by lack animal models that recapitulate the major AD pathologies, including extracellular β-amyloid (Aβ) deposition, intracellular aggregation...
10.
Jiang L, Roberts R, Wong M, Zhang L, Webber C, Kilci A, et al.
bioRxiv
. 2023 Apr;
PMID: 37034774
The study for the pathophysiology study of Alzheimer's disease (AD) has been hampered by lack animal models that recapitulate the major AD pathologies, including extracellular β-amyloid (Aβ) deposition, intracellular aggregation...