Biblio

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Journal Article

Zhang, Y., Li, W., Du, J., Cao, W., Lu, G., and Tan, Y. (2014). [Analysis of a novel mutation of AR gene in a patient featuring mild androgen insensitivity syndrome].Zhonghua Yi Xue Yi Chuan Xue Za Zhi31, 219-22.

Wang, H., Meng, L., Li, W., Du, J., Tan, Y., Gong, F., Lu, G., Lin, G., and Zhang, Q. (2019). Combinations of exonic deletions and rare mutations lead to misdiagnosis of propionic acidemia.Clin Chim Acta.

Dong, R., Du, J., Wang, L., Wang, J., Ding, G., Wang, S., and Fan, Z. (2014). Comparison of Long Noncoding RNA and mRNA Expression Profiles in Mesenchymal Stem Cells Derived from Human Periodontal Ligament and Bone Marrow.Biomed Res Int2014, 317853.

Cao, Y., Wang, L., Yang, H., Lin, X., Li, G., Han, N., Du, J., and Fan, Z. (2018). Epiregulin promotes the migration and chemotaxis ability of adipose-derived mesenchymal stem cells via mitogen-activated protein kinase signaling pathways.J Cell Biochem.

Liu, M., Li, Y., Liu, A., Li, R., Su, Y., Du, J., Li, C., and Zhu, A.Jian (2016). The exon junction complex regulates the splicing of cell polarity gene dlg1 to control Wingless signaling in development.Elife5.

Liu, J.-S., Du, J., Cheng, X., Zhang, X.-Z., Li, Y., and Chen, X.-L. (2019). Exosomal miR-451 from human umbilical cord mesenchymal stem cells attenuates burn-induced acute lung injury.J Chin Med Assoc82, 895-901.

Du, J., Wu, Y., Ai, Z., Shi, X., Chen, L., and Guo, Z. (2014). Mechanism of SB431542 in inhibiting mouse embryonic stem cell differentiation.Cell Signal.

Dai, C., Zeng, S., Tan, Z., Yang, X., Du, J., Lu, G., and Wang, J. (2019). Neurodevelopmental Disorder with Progressive Microcephaly, Spasticity, and Brain Anomalies in China Caused by Novel Mutations of PLAA.Clin Genet.

Wang, J., Kong, G., Liu, Y., Du, J., Chang, Y.-I., Tey, S.Ruow, Zhang, X., Ranheim, E.A., Saba-El-Leil, M.K., Meloche, S., et al. (2013). NrasG12D/+ promotes leukemogenesis by aberrantly regulating hematopoietic stem cell functions.Blood.

Li, W., Chen, Q., Zhang, Q., Li, X., and Du, J. (2016). [Paramyotonia congenita caused by a novel mutation of SCN4A gene in a Chinese family].Zhonghua Yi Xue Yi Chuan Xue Za Zhi33, 131-134.

Wang, T., Xia, C., Dong, Y., Chen, X., Wang, J., and Du, J. (2018). Trim27 confers myeloid hematopoiesis competitiveness by up-regulating myeloid master genes.J Leukoc Biol.

Wu, H., Wu, Y., Ai, Z., Yang, L., Gao, Y., Du, J., Guo, Z., and Zhang, Y. (2013). Vitamin C enhances nanog expression via activation of the JAK/STAT signaling pathway.Stem Cells.

Zhang, Y.-X., Li, H.-Y., Bin He, W.-, Tu, C., Du, J., Li, W., Lu, G.-X., Lin, G., Yang, Y., and Tan, Y.-Q. (2018). XRCC2 mutation causes premature ovarian insufficiency as well as non-obstructive azoospermia in humans.Clin Genet.

Dai, C., Chen, Y., Hu, L., Du, J., Gong, F., Dai, J., Zhang, S., Wang, M., Chen, J., Guo, J., et al. (2019). ZP1 mutations are associated with empty follicle syndrome: evidence for the existence of an intact oocyte and a zona pellucida in follicles up to the early antral stage. A case report.Hum Reprod.