Lv2
120 积分 2024-03-04 加入
Targeted long-read sequencing allows for rapid identification of pathogenic disease-causing variants in retinoblastoma
1天前
已完结
Bone Marrow Mesenchymal Stem Cells Carrying FANCD2 Mutation Differ from the Other Fanconi Anemia Complementation Groups in Terms of TGF-β1 Production
7天前
已完结
Synthesizing scientific literature with retrieval-augmented language models
2个月前
已完结
Genome-wide epigenetic signatures facilitated the variant classification of the PURA gene and uncovered the pathomechanism of PURA-related neurodevelopmental disorders
2个月前
已完结
Comprehensive cell atlas of the first-trimester developing human brain
3个月前
已完结
Computational methods for allele-specific expression in single cells
3个月前
已完结
Comprehensive cell atlas of the first-trimester developing human brain
3个月前
已完结
Deleterious, protein-altering variants in GSPT2 are putatively associated with an X-linked neurodevelopmental disorder with intellectual disability, language impairment, autism and epilepsy
3个月前
已关闭
Whole-genome sequencing identifies novel genes for autism in Chinese trios
4个月前
已完结
Spatial Lipid Metabolic Remodeling from Placenta to Multiple Suborgans during the Gestational Micro- or Nanoplastics Exposure
4个月前
已完结
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