Biblio

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Journal Article

Zhang J, Wang T, Shi R, Zhao Y, Zhang Y, Zhang C, Xing Q, Zhou T, Shan Y, Yao H, et al. YTHDF1 facilitates PRC1-mediated H2AK119ub in human ES cells. J Cell Physiol. 2023.

Xiao L, Shan Y, Ma L, Dunk C, Yu Y, Wei Y. Tuning FOXD3 expression dose-dependently balances human embryonic stem cells between pluripotency and meso-endoderm fates. Biochim Biophys Acta Mol Cell Res. 2019:118531.

Ma N, Liao B, Zhang H, Wang L, Shan Y, Xue Y, Huang K, Chen S, Zhou X, Chen Y, et al. TALEN-mediated gene correction in integration-free β-thalassemia iPSCs. J Biol Chem. 2013.

Zhang C, Shan Y, Lin H, Zhang Y, Xing Q, Zhu J, Zhou T, Lin A, Chen Q, Wang J, et al. HBO1 determines SMAD action in pluripotency and mesendoderm specification. Nucleic Acids Res. 2024.

Shan Y, Ma L, Zhang C, Zhang Y, Zhang J, Xiao L, Wei Y, Yu Y. Generation of two RNF2 homozygous knockout human embryonic stem cell lines by CRISPR/Cas9 system. Stem Cell Res. 2020;47:101885.

Zhang J, Zhou T, Shan Y, Pan G. Generation of RYBP FLAG-HA knock-in human embryonic stem cell line through CRISPR/Cas9-mediated homologous recombination. Stem Cell Res. 2022;62:102803.

Zhang D, Zhou M, Zhang Y, Shan Y, Pan G. Generation of an RNF1-deficient human pluripotent stem cell line using CRISPR/Cas9 technology. Stem Cell Res. 2022;62:102809.

Zhu Y, Zhang Z, Fan N, Huang K, Li H, Gu J, Zhang Q, Ouyang Z, Zhang T, Tang J, et al. Generating functional cells through enhanced interspecies chimerism with human pluripotent stem cells. Stem Cell Reports. 2022.

Xue Y, Cai X, Wang L, Liao B, Zhang H, Shan Y, Chen Q, Zhou T, Li X, Hou J, et al. Generating a Non-Integrating Human Induced Pluripotent Stem Cell Bank from Urine-Derived Cells. PLoS One. 2013;8(8):e70573.

Zhang C, Wei Y, Zhang Y, Zhang J, Xing Q, Zhou M, Shan Y. Establishment of a CRISPR/Cas9-mediated ANP32A homozygous knockout human embryonic stem cell line. Stem Cell Res. 2021;52:102234.

Zhao Y, Wang T, Zhang Y, Shi L, Zhang C, Zhang J, Yao J, Chen Q, Zhong X, Wei Y, et al. Coordination of EZH2 and SOX2 specifies human neural fate decision. Cell Regen. 2021;10(1):30.

Xu P, Chen Z, Ma J, Shan Y, Wang Y, Xie B, Zheng D, Guo F, Song X, Gao G, et al. Biallelic CLCN2 mutations cause retinal degeneration by impairing retinal pigment epithelium phagocytosis and chloride channel function. Hum Genet. 2023.

Gu J, Zhu Y, Lin H, Huang Y, Zhang Y, Xing Q, Kang B, Zhang Z, Wang M, Zhou T, et al. Autophagy is essential for human myelopoiesis. Stem Cell Reports. 2023.