Lv21
200 积分 2025-04-16 加入
The Drosophila ZER1 homolog interacts with ref(2)P to regulate autophagy and Keap1-cnc/NFE2L2/Nrf2-mediated oxidative stress
35分钟前
待确认
HMGB1 gene silencing inhibits neuroinflammation via down-regulation of NF-κB signaling in primary hippocampal neurons induced by Aβ25–35
6天前
已完结
Knockdown of HMGB1 inhibits growth and invasion of gastric cancer cells through the NF-κB pathway in vitro and in vivo
6天前
已完结
Atg9 interacts with dTRAF2/TRAF6 to regulate oxidative stress-induced JNK activation and autophagy induction
13天前
已完结
CRISPR-Cas9 Gene Editing Protects from the A53T-SNCA Overexpression-Induced Pathology of Parkinson's Disease In Vivo
1个月前
已完结
Impaired autophagy and APP processing in Alzheimer's disease: The potential role of Beclin 1 interactome
2个月前
已完结
Architectural regulations and Hmg1
3个月前
已完结
Isorhynchophylline, a natural alkaloid, promotes the degradation of alpha-synuclein in neuronal cells via inducing autophagy
3个月前
已完结
Controlled Activation of TRPV1 Channels on Microglia to Boost Their Autophagy for Clearance of Alpha‐Synuclein and Enhance Therapy of Parkinson's Disease
3个月前
已完结
The interplay between α-Synuclein and NLRP3 inflammasome in Parkinson's disease
3个月前
已完结
Safflower oil body nanoparticles deliver hFGF10 to hair follicles and reduce microinflammation to accelerate hair regeneration in androgenetic alopecia
2个月前
已采纳
α‐Synuclein V15A Variant in Familial Parkinson's Disease Exhibits a Weaker Lipid‐Binding Property
2个月前
已采纳
Association of 4qA-Specific Distal D4Z4 Hypomethylation With Disease Severity and Progression in Facioscapulohumeral Muscular Dystrophy
2个月前
已撤回
Glycogen storage disease type 1a in the Ohio Amish
2个月前
已采纳
Structural basis of glycogen branching enzyme deficiency and pharmacologic rescue by rational peptide design
2个月前
已采纳
Gene panel sequencing improves the diagnostic work-up of patients with idiopathic erythrocytosis and identifies new mutations
2个月前
已采纳
DAG1 mutations associated with asymptomatic hyperCKemia and hypoglycosylation of α-dystroglycan
2个月前
已采纳
Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
2个月前
已采纳
A neurodevelopmental disorder caused by mutations in the VPS51 subunit of the GARP and EARP complexes
2个月前
已采纳
The paradox of R-loops: guardians of the genome or drivers of disease?
2个月前
已采纳
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