- |||||||||| Journal: Ethyl acetate extract of Gastrodia (Pubmed Central) - Jul 31, 2023
The present research results demonstrated that the protective effect of EEGE on transgenic C. elegans was to reduce A? protein aggregation, improve the in vivo antioxidant level, effectively remove free radicals and to regulate the expression of genes related to IIS pathway, thereby reducing A?-induced toxicity and delaying nematode paralysis.
- |||||||||| Journal: Interrogation of human microglial phagocytosis by CRISPR genome editing. (Pubmed Central) - Jul 28, 2023
CRISPR genome editing by Cas9 RNP electroporation is a robust approach to genetically modify HMC3 for functional studies such as the interrogation of A? and tumor phagocytosis, and is readily adoptable to investigate other aspects of microglial biology.
- |||||||||| Journal: An ankyrin repeat chaperone targets toxic oligomers during amyloidogenesis. (Pubmed Central) - Jul 11, 2023
The substrate-binding domain of cpSRP43, composed primarily of the ARD, is necessary and sufficient to prevent A?42 aggregation and to protect cells against A?42 toxicity. This work provides an example in which an ARD chaperone non-native to mammalian cells harbors anti-amyloidal activity, which may be exploited for bioengineering.
- |||||||||| Sulfanegen, a 3-mercaptopyruvate sulfurtransferase substrate, as a therapeutic option for Alzheimer (Virtual) - Jul 6, 2023 - Abstract #AAIC2023AAIC_7887;
Collectively, our results show that the provision of a 3MST substrate, sulfanegen, exhibits neuroprotective effects, along with restoration of cognitive function in an AD mouse model. This study suggests an important role of 3MST in AD pathophysiology and potential therapeutic utility of sulfanegen as a disease-modifying treatment.
- |||||||||| Palmitoyl transferase zDHHCs: novel targets in Alzheimer's disease (Virtual) - Jul 6, 2023 - Abstract #AAIC2023AAIC_7618;
This is the first preclinical study on the effect of 2BP treatment on AD-related cognitive decline. Our data indicate that aberrant palmitoylation plays a critical role in the onset and progression of AD and unveil the potential druggable role of zDHHC enzymes in dementia-related neurodegenerative disorders.
- |||||||||| The pTau interactome in sporadic Alzheimer's disease across APOE genotypes (Virtual) - Jul 6, 2023 - Abstract #AAIC2023AAIC_7169;
Our proteomic data highlighted an influence of the APOE polymorphism on pTau metabolism. These results will be validated in the human brain using histological and biochemical methods, paving the way to the identification of new therapeutic targets for AD.
- |||||||||| Modeling neuropathology of Alzheimer (In-Person) - Jul 6, 2023 - Abstract #AAIC2023AAIC_6290;
formation reduces tauopathy and neuronal cell death. Our unique patient specific 3D model system provides opportunities to investigate the interplay between AD pathological events and could serve as a platform for screening compounds and developing personalized therapeutics for AD.
- |||||||||| Sulfanegen, a 3-mercaptopyruvate sulfurtransferase substrate, as a therapeutic option for Alzheimer (Virtual) - Jul 6, 2023 - Abstract #AAIC2023AAIC_5821;
Collectively, our results show that the provision of a 3MST substrate, sulfanegen, exhibits neuroprotective effects, along with restoration of cognitive function in an AD mouse model. This study suggests an important role of 3MST in AD pathophysiology and potential therapeutic utility of sulfanegen as a disease-modifying treatment.
- |||||||||| Palmitoyl transferase zDHHCs: novel targets in Alzheimer's disease (Virtual) - Jul 6, 2023 - Abstract #AAIC2023AAIC_5552;
This is the first preclinical study on the effect of 2BP treatment on AD-related cognitive decline. Our data indicate that aberrant palmitoylation plays a critical role in the onset and progression of AD and unveil the potential druggable role of zDHHC enzymes in dementia-related neurodegenerative disorders.
- |||||||||| The pTau interactome in sporadic Alzheimer's disease across APOE genotypes (Virtual) - Jul 6, 2023 - Abstract #AAIC2023AAIC_5103;
Our proteomic data highlighted an influence of the APOE polymorphism on pTau metabolism. These results will be validated in the human brain using histological and biochemical methods, paving the way to the identification of new therapeutic targets for AD.
- |||||||||| Sulfanegen, a 3-mercaptopyruvate sulfurtransferase substrate, as a therapeutic option for Alzheimer (Virtual) - Jul 6, 2023 - Abstract #AAIC2023AAIC_3575;
Collectively, our results show that the provision of a 3MST substrate, sulfanegen, exhibits neuroprotective effects, along with restoration of cognitive function in an AD mouse model. This study suggests an important role of 3MST in AD pathophysiology and potential therapeutic utility of sulfanegen as a disease-modifying treatment.
- |||||||||| Palmitoyl transferase zDHHCs: novel targets in Alzheimer's disease (Virtual) - Jul 6, 2023 - Abstract #AAIC2023AAIC_3306;
This is the first preclinical study on the effect of 2BP treatment on AD-related cognitive decline. Our data indicate that aberrant palmitoylation plays a critical role in the onset and progression of AD and unveil the potential druggable role of zDHHC enzymes in dementia-related neurodegenerative disorders.
- |||||||||| The pTau interactome in sporadic Alzheimer's disease across APOE genotypes (Virtual) - Jul 6, 2023 - Abstract #AAIC2023AAIC_2857;
Our proteomic data highlighted an influence of the APOE polymorphism on pTau metabolism. These results will be validated in the human brain using histological and biochemical methods, paving the way to the identification of new therapeutic targets for AD.
- |||||||||| The role of Alzheimer (In-Person) - Jul 6, 2023 - Abstract #AAIC2023AAIC_1810;
aggregates and will help to better understand how ApoE isoforms affect A? aggregation.
- |||||||||| Sulfanegen, a 3-mercaptopyruvate sulfurtransferase substrate, as a therapeutic option for Alzheimer (Virtual) - Jul 6, 2023 - Abstract #AAIC2023AAIC_1355;
Collectively, our results show that the provision of a 3MST substrate, sulfanegen, exhibits neuroprotective effects, along with restoration of cognitive function in an AD mouse model. This study suggests an important role of 3MST in AD pathophysiology and potential therapeutic utility of sulfanegen as a disease-modifying treatment.
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