Lv2
120 积分 2025-10-23 加入
Myosin storage myopathy associated with a heterozygous missense mutation in MYH7
11天前
已完结
Impaired chaperone-mediated autophagy leads to abnormal SORT1 (sortilin 1) turnover and CES1-dependent triglyceride hydrolysis
19天前
已完结
2‐Ethylhexyl Diphenyl Phosphate Inhibited C2C12 Myoblast Differentiation by Regulating ACTC1
24天前
已完结
Distal arthrogryposis and muscle weakness associated with a β-tropomyosin mutation
1个月前
已完结
Arthrogryposis in children: Etiological assessments and preparation of a protocol for etiological investigations
1个月前
已完结
Clinical and Genetic Findings in a Chinese Cohort of Dentatorubral–Pallidoluysian Atrophy Patients
1个月前
已完结
Heterozygous Variants in KDM4B Lead to Global Developmental Delay and Neuroanatomical Defects
1个月前
已完结
Human phenotype caused by biallelic KDM4B frameshift variant
1个月前
已完结
Synergistic Effects of Maternal PM2.5 and Ozone Co-exposure on Gestational Diabetes Mellitus: A Metabolomic Mechanistic Insight
1个月前
已完结
IDF Diabetes Atlas 11th edition 2025: global prevalence and projections for 2050
1个月前
已完结
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