Lv3
400 积分 2023-08-12 加入
Arthrogryposis With CNS Involvement in AFF3-Related KINSSHIP Syndrome: A Detailed Phenotypic Characterization From a Mexican Patient and Review of the Literature
21天前
已完结
Functional characterization of the AFF (AF4/FMR2) family of RNA-binding proteins: insights into the molecular pathology of FRAXE intellectual disability
1个月前
已完结
Molecular evolution of transcription factors AF4/FMR2 family member (AFF) gene family and the role of lamprey AFF3 in cell proliferation
1个月前
已完结
Comparative analysis of clinical phenotypes and genetic characteristics in MEF2C-associated neurodevelopmental disorders
2个月前
已关闭
DEAD/DEAH-box RNA helicases shape the risk of neurodevelopmental disorders
3个月前
已完结
ADAR1 and its implications in cancer development and treatment
3个月前
已完结
Methylated GCC repeat expansion in AFF3 associates with intellectual disability
3个月前
已完结
GABAergic Interneuron Dysfunction in Neurodevelopmental Disorders: A New Role for the Transcription Factor MEF2C in Regulating Parvalbumin Interneuron Survival and Function
3个月前
已完结
Experience-dependent maturation of somatosensory parvalbumin interneurons during social development in prairie voles
3个月前
已完结
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