Lv11
100 积分 2025-02-12 加入
Re: Identification of a family with van der Hoeve's syndrome harboring a novel COL1A1 mutation and generation of patient-derived iPSC lines and CRISPR/Cas9-corrected isogenic iPSCs
4小时前
求助中
Osteomimix: A Multidimensional Biomimetic Cascade Strategy for Bone Defect Repair
18天前
已完结
Clinical Phenotypic Characterization of the SLC26A4 Mutation in Pendred Syndrome/Nonsyndromic Enlarged Vestibular Aqueduct
2个月前
已完结
Recent advances in molecular studies on cochlear development and regeneration
2个月前
已完结
Casz1 is required for both inner hair cell fate stabilization and outer hair cell survival
2个月前
已完结
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