Yue Li

发表

Generation of an induced pluripotent stem cell line (SDQLCHi003-a) from a patient with short rib-thoracic dysplasia syndrome type III carrying compound heterozygous mutations in DYNC2H1.

Z. Gai, Yuqiang Lv, Min Gao, 2019, Stem cell research.

Generation of patient-specific pluripotent induced stem cell line SDUBMSI002-A from a patient with X-linked mental retardation syndrome.

Y. Gong, Wenjie Sun, Jian Ma, 2020, Stem cell research.

Recombinant human megakaryocyte growth and development factor (rhumgdf), a ligand for c‐mpl, produces functional human platelets in vitro

M. Hokom, P. Hunt, G. Grampp, 1995, Stem cells.

Chromosomal microarray analysis of 410 Han Chinese patients with autism spectrum disorder or unexplained intellectual disability and developmental delay

S. Scherer, E. Higginbotham, M. Zarrei, 2022, NPJ genomic medicine.

Generation of an induced pluripotent stem cell line (SDQLCHi008-A) from a patient with ASD and DD carrying an 830 kb de novo deletion at chr7q11.22 including the exon 1 of AUTS2 gene.

G. Pan, Z. Gai, Yi Liu, 2019, Stem cell research.

SWI/SNF complex gene variations are associated with a higher tumor mutational burden and a better response to immune checkpoint inhibitor treatment: a pan-cancer analysis of next-generation sequencing data corresponding to 4591 cases

Jiangjun Ma, Xin-hua Yang, Yue Li, 2022, Cancer Cell International.

Human MD2 deficiency-an inborn error of immunity with pleiotropic features.

S. Snapper, H. Uhlig, C. Walz, 2022, The Journal of allergy and clinical immunology.

Generation of an induced pluripotent stem cell line (SDQLCHi009-A) from a patient with 47,XXY and ornithine transcarbamylase deficiency carrying a hemizygote mutation in OTC.

Qi Zhou, Z. Gai, Dong Wang, 2020, Stem cell research.

Generation of an induced pluripotent stem cell line (SDQLCHi044-A) from a patient with autosomal dominant mental retardation type 5 harboring heterozygous mutation in SYNGAP1 gene.

Z. Gai, Yuqiang Lv, Yi Liu, 2022, Stem cell research.

Establishment of a human induced pluripotent stem cell line (SDQLCHi037-A) from a patient with Alagille syndrome carrying heterozygous mutation in JAG1 gene.

Z. Gai, Min Gao, Yi Liu, 2021, Stem cell research.

Phenotype and genotype analyses of Chinese patients with autosomal dominant mental retardation type 5 caused by SYNGAP1 gene mutations

Jian-guo Shi, Z. Gai, Yuqiang Lv, 2022, Frontiers in Genetics.

Single-cell transcriptome analysis reveals the cellular atlas of human intracranial aneurysm and highlights inflammation features associated with aneurysm rupture

Hang Ji, Ruiqi Chen, Anqi Xiao, 2023, bioRxiv.

An induced pluripotent stem cells line (SDQLCHi014-A) derived from urine cells of a patient with ASD and hyperactivity carrying a 303 kb de novo deletion at chr3p26.1 implicating GRM7 gene.

Z. Gai, Yi Liu, Tiancheng Zhou, 2019, Stem cell research.

Establishment of a novel human iPSC line (SDQLCHi032-A) derived from a patient with primary hypertrophic osteoarthropathy caused by HPGD homozygous mutation.

Z. Gai, Yi Liu, Haiyan Zhang, 2021, Stem Cell Research.

Reprogramming of human peripheral blood mononuclear cell (PBMC) from a patient suffering from hearing loss into iPSC line (SDQLCHi035-A) maintaining compound heterozygous variations in GJB2 gene.

Z. Gai, Yuqiang Lv, Yi Liu, 2021, Stem cell research.

COVPRIG robustly predicts the overall survival of IDH wild-type glioblastoma and highlights METTL1+ neural-progenitor-like tumor cell in driving unfavorable outcome

Hang Ji, Shaoshan Hu, Yi Liu, 2023, Journal of Translational Medicine.

Genotypic and phenotypic characteristics of sodium channel-associated epilepsy in Chinese population.

Z. Gai, Kaihui Zhang, Yuqiang Lv, 2024, Journal of human genetics.

Generation and characterization of a human induced pluripotent stem cell line (SDQLCHi052-A) from peripheral blood mononuclear cells derived from a healthy Chinese donor.

Zirui Wan, Haiyan Zhang, Xiaomeng Yang, 2023, Stem cell research.