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Generation of an integration-free induced pluripotent stem cell line (LZUSHI001-A) from an epileptic patient with DGKG mutation.

Generation of a gene corrected human isogenic iPSC line (CPGHi001-A-1) from a hearing loss patient with the TMC1 p.M418K mutation using CRISPR/Cas9.

Synergistic effects of a combined treatment of PI3K/mTOR dual inhibitor LY3023414 and carboplatin on human endometrial carcinoma.

CRISPR/Cas9 mediated generation of a iPSC line EHTJUi005-A-1 with homozygous knockout of the SUV39H1 gene.

Generation of an induced pluripotent stem cell line (FDCHI007-A) derived from a patient with Developmental and epileptic encephalopathy Type 31 carrying heterozygous c.545 C>A mutation in DNM1 gene.

ANGPTL3 impacts proteinuria and hyperlipidemia in primary nephrotic syndrom.

Functional analysis of HECA variants identified in congenital heart disease in the Chinese populati

Generation of an induced pluripotent stem cell line (FDCHi008-A) from an infant with chronic intestinal pseudo-obstruction

Biallelic MED16 variants disrupt neural development and lead to an intellectual disability syndrome

A novel mechanism involving USP53-regulated BSEP trafficking underlies low-GGT intrahepatic cholestasis

Sitosterolemia with Orbital Xanthogranulomas

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