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AAV-Mediated Gene Replacement Therapy Restores Viability of BCD Patient iPSC Derived RPE Cells and Vision of Cyp4v3 Knockout Mice. Hum Mol Genet. 2022..
[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.
[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..
Autologous hematopoietic stem cell transplantation activity for lymphoma and multiple myeloma in China. Bone Marrow Transplant. 2022.
CAG regimen for refractory or relapsed adult T-cell acute lymphoblastic leukemia: A retrospective, multicenter, cohort study. Cancer Med. 2020.
Cancer stem cell generation by silenced MAPK enhancing PI3K/AKT signaling. Med Hypotheses. 2020;141:109742..
Combinations of exonic deletions and rare mutations lead to misdiagnosis of propionic acidemia. Clin Chim Acta. 2019..
Comparative analysis of mouse embryonic palatal mesenchymal cells isolated by two primary culture methods. Tissue Cell. 2022;76:101783..
Epiregulin promotes the migration and chemotaxis ability of adipose-derived mesenchymal stem cells via mitogen-activated protein kinase signaling pathways. J Cell Biochem. 2018..
The exon junction complex regulates the splicing of cell polarity gene dlg1 to control Wingless signaling in development. Elife. 2016;5..
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..
Expression pattern of Ptch2 in mouse embryonic maxillofacial development. Acta Histochem. 2021;124(1):151835..
MEK1/2 is a bottleneck that induces cancer stem cells to activate the PI3K/AKT pathway. Biochem Biophys Res Commun. 2021;583:49-55.
Neurodevelopmental Disorder with Progressive Microcephaly, Spasticity, and Brain Anomalies in China Caused by Novel Mutations of PLAA. Clin Genet. 2019..
Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype. Clin Genet. 2022.
[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..
Up-regulation of Dsg2 confered stem cells with malignancy through wnt/β-catenin signaling pathway. Exp Cell Res. 2022:113416.