Lv11
88 积分 2020-06-20 加入
005 Unusual cerebellar stroke mimic with ATP1A3 mutation
5天前
已关闭
ATP1A3 mutation presenting as CAPOS syndrome + dystonia phenotype
19天前
已关闭
ATP1A3-related phenotypes in Chinese children: AHC, CAPOS, and RECA
19天前
已完结
Precision correction of the GJB2 c.235delC mutation by prime editing in vitro
1个月前
已完结
Mechanisms linking cytoplasmic decay of translation-defective mRNA to transcriptional adaptation
6个月前
已完结
Mutation of a Gene Encoding a Protein with Extracellular Matrix Motifs in Usher Syndrome Type IIa
8个月前
已完结
Biotechnological Effects of Advanced Smart‐Bile Acid Cyclodextrin‐Based Nanogels for Ear Delivery and Treatment of Hearing Loss
8个月前
已完结
Functionalized Nanozyme Microcapsules Targeting Deafness Prevention via Mitochondrial Homeostasis Remodeling
8个月前
已完结
Complete Restoration of Hearing Loss and Cochlear Synaptopathy via Minimally Invasive, Single-Dose, and Controllable Middle Ear Delivery of Brain-Derived Neurotrophic Factor–Poly(dl-lactic acid-co-glycolic acid)-Loaded Hydrogel
8个月前
已完结
Injectable polyplex-loaded glycol chitosan thermogel for efficient and safe inner ear gene delivery
8个月前
已完结