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300 积分 2025-08-17 加入
Prenatal diagnosis and genetic study of 22q11.2 microduplication in Chinese fetuses: A series of 31 cases and literature review
8小时前
已完结
Difficulty in genetic counseling of de novo 22q11.2 duplication at amniocentesis and prenatal diagnosis of a 2.9-Mb de novo 22q11.1q11.21 microduplication encompassing TBX1 in a pregnancy associated with no apparently phenotypic abnormality at birth in the fetus
8小时前
已关闭
INTEGRIN β1 IS CRITICAL FOR GASTRIN-RELEASING PEPTIDE RECEPTOR-MEDIATED NEUROBLASTOMA CELL MIGRATION AND INVASION
11小时前
已完结
Maternal Plasma DNA Sequencing Reveals the Genome-Wide Genetic and Mutational Profile of the Fetus
9天前
已完结
Considerations for the Use of SH-SY5Y Neuroblastoma Cells in Neurobiology
2个月前
已完结
Sequential Treatment of SH‐SY5Y Cells with Retinoic Acid and Brain‐Derived Neurotrophic Factor Gives Rise to Fully Differentiated, Neurotrophic Factor‐Dependent, Human Neuron‐Like Cells
2个月前
已完结
Sequential Treatment of SH‐SY5Y Cells with Retinoic Acid and Brain‐Derived Neurotrophic Factor Gives Rise to Fully Differentiated, Neurotrophic Factor‐Dependent, Human Neuron‐Like Cells
3个月前
已完结
Modulation of the β-Catenin Signaling Pathway by the Dishevelled-Associated Protein Hipk1
10个月前
已完结
Dual diagnosis in a child with familial SCN8A-related encephalopathy complicated by a 1p13.2 deletion involving NRAS gene
10个月前
已完结
Interstitial deletion of the short arm of chromosome 1 (1p13.1p21.1) in a girl with mental retardation, short stature and colobomata
10个月前
已完结
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