Naringenin and SMER28 target lysosomal reformation and rescue SPG11 and SPG15 hereditary spastic paraplegia phenotypes.
第一作者:
Chiara,Vantaggiato
第一单位:
Scientific Institute IRCCS E. Medea, Laboratory of Medical Genetics, Via D. L. Monza 20, Bosisio Parini, Lecco 23842, Italy. Electronic address: chiara.vantaggiato@lanostrafamiglia.it.
作者:
医学主题词
动物(Animals);溶酶体(Lysosomes);人类(Humans);黄烷酮类(Flavanones);痉挛性截瘫, 遗传性(Spastic Paraplegia, Hereditary);自噬(Autophagy);表型(Phenotype);疾病模型, 动物(Disease Models, Animal);果蝇属(Drosophila);蛋白质类(Proteins)
DOI
10.1016/j.phrs.2025.107836
PMID
40550407
发布时间
2025-07-25
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Pharmacological research
107836页
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