Biblio

Author Title [ Type(Asc)] Year
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Journal Article
Dai C, Chen Y, Hu L, Du J, Gong F, Dai J, Zhang S, Wang M, Chen J, Guo J, et al. 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. 2019.
Zhang Y-X, Li H-Y, Bin He W-, Tu C, Du J, Li W, Lu G-X, Lin G, Yang Y, Tan Y-Q. XRCC2 mutation causes premature ovarian insufficiency as well as non-obstructive azoospermia in humans. Clin Genet. 2018.
Wu H, Wu Y, Ai Z, Yang L, Gao Y, Du J, Guo Z, Zhang Y. Vitamin C enhances nanog expression via activation of the JAK/STAT signaling pathway. Stem Cells. 2013.
Wang T, Xia C, Dong Y, Chen X, Wang J, Du J. Trim27 confers myeloid hematopoiesis competitiveness by up-regulating myeloid master genes. J Leukoc Biol. 2018.
Zhang Q, Wu B, Weng Q, Hu F, Lin Y, Xia C, Peng H, Wang Y, Liu X, Liu L, et al. Regeneration of immunocompetent B lymphopoiesis from pluripotent stem cells guided by transcription factors. Cell Mol Immunol. 2021.
Li W, Chen Q, Zhang Q, Li X, Du J. [Paramyotonia congenita caused by a novel mutation of SCN4A gene in a Chinese family]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016;33(2):131-134.
Wang J, Kong G, Liu Y, Du J, Chang Y-I, Tey SRuow, Zhang X, Ranheim EA, Saba-El-Leil MK, Meloche S, et al. NrasG12D/+ promotes leukemogenesis by aberrantly regulating hematopoietic stem cell functions. Blood. 2013.
Dai C, Zeng S, Tan Z, Yang X, Du J, Lu G, Wang J. Neurodevelopmental Disorder with Progressive Microcephaly, Spasticity, and Brain Anomalies in China Caused by Novel Mutations of PLAA. Clin Genet. 2019.
Hassan G, Afify SM, Du J, Nawara HM, Sheta M, Monzur S, Zahra MH, Quora HAAbu, Mansour H, El-Ghlban S, et al. MEK1/2 is a bottleneck that induces cancer stem cells to activate the PI3K/AKT pathway. Biochem Biophys Res Commun. 2021;583:49-55.
Du J, Wu Y, Ai Z, Shi X, Chen L, Guo Z. Mechanism of SB431542 in inhibiting mouse embryonic stem cell differentiation. Cell Signal. 2014.
Xu Y, Yuan D, Fan Z, Wang S, Du J. Identification and profiles of microRNAs in different development stages of miniature pig secondary palate. Genomics. 2021.
Wang X, Ma Z, Wu Y, Chen J, Peng X, Wang Y, Fan M, Du J. Expression pattern of Ptch2 in mouse embryonic maxillofacial development. Acta Histochem. 2021;124(1):151835.
Liu J-S, Du J, Cheng X, Zhang X-Z, Li Y, Chen X-L. Exosomal miR-451 from human umbilical cord mesenchymal stem cells attenuates burn-induced acute lung injury. J Chin Med Assoc. 2019;82(12):895-901.
Liu M, Li Y, Liu A, Li R, Su Y, Du J, Li C, Zhu AJian. The exon junction complex regulates the splicing of cell polarity gene dlg1 to control Wingless signaling in development. Elife. 2016;5.
Cao Y, Wang L, Yang H, Lin X, Li G, Han N, Du J, Fan Z. Epiregulin promotes the migration and chemotaxis ability of adipose-derived mesenchymal stem cells via mitogen-activated protein kinase signaling pathways. J Cell Biochem. 2018.
Dong R, Du J, Wang L, Wang J, Ding G, Wang S, Fan Z. Comparison of Long Noncoding RNA and mRNA Expression Profiles in Mesenchymal Stem Cells Derived from Human Periodontal Ligament and Bone Marrow. Biomed Res Int. 2014;2014:317853.
Wang H, Meng L, Li W, Du J, Tan Y, Gong F, Lu G, Lin G, Zhang Q. Combinations of exonic deletions and rare mutations lead to misdiagnosis of propionic acidemia. Clin Chim Acta. 2019.
Hassan G, Du J, Afify SM, Seno A, Seno M. Cancer stem cell generation by silenced MAPK enhancing PI3K/AKT signaling. Med Hypotheses. 2020;141:109742.
Qian J-J, Hu X, Wang Y, Zhang Y, Du J, Yang M, Tong H, Bin Qian W-, Wei J, Yu W, et al. CAG regimen for refractory or relapsed adult T-cell acute lymphoblastic leukemia: A retrospective, multicenter, cohort study. Cancer Med. 2020.
Tan C, Meng L, Lv M, He X, Sha Y, Tang D, Tan Y, Hu T, He W, Tu C, et al. Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice. Am J Hum Genet. 2021.
Zhang Y, Li W, Du J, Cao W, Lu G, Tan Y. [Analysis of a novel mutation of AR gene in a patient featuring mild androgen insensitivity syndrome]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014;31(2):219-22.
Luo S, He W, Liao Y, Tang W, Li X, Hu L, Du J, Zhang Q, Tan Y, Lin G, et al. [Analysis and prenatal diagnosis of FMR1 gene mutations among patients with unexplained mental retardation]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021;38(5):439-445.