de Leiris, Nicolas Perret, Pascale Lombardi, Charlotte Gözel, Bülent Chierici, Sabine Millet, Philippe Debiossat, Marlène Bacot, Sandrine Chames, Patrick Lenormand, Jean-Luc
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Soluble oligomeric forms of Tau protein have emerged as crucial players in the propagation of Tau pathology in Alzheimer’s disease (AD). Our objective is to introduce a single-domain antibody (sdAb) named 2C5 as a novel radiotracer for the efficient detection and longitudinal monitoring of oligomeric Tau species in the human brain. Methods The deve...
Lim, Jie Lay Lin, Chin-Jung Huang, Chih-Ching Chang, Lin-Chau
Published in
Colloids and surfaces. B, Biointerfaces
The amyloid cascade and tau hypotheses both hold significant implications for the pathogenesis of Alzheimer's disease (AD). Curcumin shows potential by inhibiting the aggregation of amyloid beta (Aβ) and reducing tau hyperphosphorylation, however, its use is limited due to issues with solubility and bioavailability. Carbon dots, recognized for thei...
Kumar, Mukesh Quittot, Noé Dujardin, Simon Schlaffner, Christoph N Viode, Arthur Wiedmer, Anne Beerepoot, Pieter Chun, Joshua E Glynn, Calina Fernandes, Analiese R
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Published in
Brain : a journal of neurology
Aggregation prone molecules, such as tau, form both historically well characterized fibrillar deposits (neurofibrillary tangles) and recently identified phosphate-buffered saline (PBS) extract species called proteopathic seeds. Both can cause normal endogenous tau to undergo templated misfolding. The relationship of these seeds to the fibrils that ...
Kumar, Mukesh; Quittot, Noe; Dujardin, Simon; Schlaffner, Christoph N.; Viode, Arthur; Wiedmer, Anne; 162741; Beerepoot, Pieter; Chun, Joshua E.; Glynn, Calina; Fernandes, Analiese R.;
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Aggregation prone molecules, such as tau, form both historically well characterized fibrillar deposits (neurofibrillary tangles) and recently identified phosphate-buffered saline (PBS) extract species called proteopathic seeds. Both can cause normal endogenous tau to undergo templated misfolding. The relationship of these seeds to the fibrils that ...
Lasorsa, Alessia Merzougui, Hamida Cantrelle, François-Xavier Sicoli, Giuseppe Dupré, Elian Hanoulle, Xavier Belle, Valérie Smet-Nocca, Caroline Landrieu, Isabelle
Intrinsically disordered proteins (IDPs) are known to adopt many rapidly interconverting structures, making it difficult to pinpoint the specific conformational states that are relevant for their function. Tau is an important IDP, and its conformation is known to be affected by post-translational modifications (PTMs), such as phosphorylation. To in...
Zhong, Haiyang Liu, Hongli Liu, Huanxiang
Published in
Current medicinal chemistry
Tau dysfunction has a close association with many neurodegenerative diseases, which are collectively referred to as tauopathies. Neurofibrillary tangles (NFTs) formed by misfolding and aggregation of tau are the main pathological process of tauopathy. Therefore, uncovering the misfolding and aggregation mechanism of tau protein will help to reveal ...
Fronza, Mariana G Alves, Diego Praticò, Domenico Savegnago, Lucielli
Published in
Ageing research reviews
Alzheimer's Disease (AD) is the most common form of dementia, affecting almost 50 million of people around the world, characterized by a complex and age-related progressive pathology with projections to duplicate its incidence by the end of 2050. AD pathology has two major hallmarks, the amyloid beta (Aβ) peptides accumulation and tau hyperphosphor...
Zuccarello, Elisa Zhang, Hong Acquarone, Erica Pham, Dang Staniszewski, Anna Deng, Shi-Xian Landry, Donald W Arancio, Ottavio Fiorito, Jole
Published in
Bioorganic & medicinal chemistry letters
Phosphodiesterase 5 (PDE5) is a cyclic guanosine monophosphate-degrading enzyme involved in numerous biological pathways. Inhibitors of PDE5 are important therapeutics for the treatment of neurodegenerative diseases, including Alzheimer's disease (AD). We previously reported the first generation of quinoline-based PDE5 inhibitors for the treatment ...
Veiga Pires, Alix
La Maladie d’Alzheimer est une maladie neurodégénérative qui évolue au stade pré-clinique sur plusieurs mois à plusieurs années, précédant le développement des stades prodromique et clinique avec l’apparition de signes de démence. Le chat peut développer une entité apparentée au cours du vieillissement, appelée Syndrome de Dysfonctionnement Cogniti...
Salvador, Cathrin Lytomt Oppebøen, Mari Vassli, Anja Østeby Pfeiffer, Helle Cecilie Viekilde Varhaug, Kristin Nielsen Elgstøen, Katja Benedikte Prestø Yazdani, Mazyar
Published in
Pediatric neurology
Kearns-Sayre syndrome (KSS) is caused by duplications and/or deletions of mitochondrial DNA (mtDNA) and is typically diagnosed based on a classic triad of symptoms with chronic progressive external ophthalmoplegia (CPEO), retinitis pigmentosa, and onset before age 20 years. The present study aimed to diagnose two patients, on suspicion of KSS. One ...