Biblio

Author Title [ Type(Asc)] Year
Filters: Author is Du, Juan  [Clear All Filters]
Journal Article
Hu X, Wang W, Luo K, Dai J, Zhang Y, Wan Z, He W, Zhang S, Yang L, Tan Q, et al. Extended application of PGT-M strategies for small pathogenic CNVs. J Assist Reprod Genet. 2024.
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.
Huang H, Du J. Editorial: Congenital craniofacial deformities: genetic and clinical aspects. Front Oral Health. 2023;4:1298447.
Du J, Liu X, Wong CWing Yan, Wong KKak Yuen, Yuan Z. Direct cellular reprogramming and transdifferentiation of fibroblasts on wound healing-Fantasy or reality?. Chronic Dis Transl Med. 2023;9(3):191-199.
Yi S, Wang W, Su L, Meng L, Li Y, Tan C, Liu Q, Zhang H, Fan L, Lu G, et al. Deleterious variants in X-linked RHOXF1 cause male infertility with oligo- and azoospermia. Mol Hum Reprod. 2024.
Sun J, Zhang H, Liu D, Liu W, Du J, Wen D, Li L, Zhang A, Jiang J, Zeng L. CTGF promotes the repair and regeneration of alveoli after acute lung injury by promoting the proliferation of subpopulation of AEC2s. Respir Res. 2023;24(1):227.
Zhou Y-W, Ren Y, Lu M-M, Xu L-L, Cheng W-X, Zhang M-M, Ding L-P, Chen D, Gao J-G, Du J, et al. Crohn's disease as the intestinal manifestation of pan-lymphatic dysfunction: An exploratory proposal based on basic and clinical data. World J Gastroenterol. 2024;30(1):34-49.
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 X, Peng X, Chen J, Wang Y, Zhao X, Li T, Du J. Comparative analysis of mouse embryonic palatal mesenchymal cells isolated by two primary culture methods. Tissue Cell. 2022;76:101783.
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.
Cheng D, Lu C-F, Gong F, Du J, Yuan S, Luo K-L, Tan Y-Q, Lu G-X, Lin G. A case report of a normal fertile woman with 46,XX/46,XY somatic chimerism reveals a critical role for germ cells in sex determination. Hum Reprod. 2024.
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.
Wang W, Su L, Meng L, He J, Tan C, Yi D, Cheng D, Zhang H, Lu G, Du J, et al. Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia. Hum Reprod. 2023.
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.
Liu W, Ji J, Zou D, Cao Y, Xu Y, Zhou J, Gao S, Wang F, Chen W, Du J, et al. Autologous hematopoietic stem cell transplantation activity for lymphoma and multiple myeloma in China. Bone Marrow Transplant. 2022.
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.
Jia R, Meng X, Chen S, Zhang F, Du J, Liu X, Yang L. AAV-Mediated Gene Replacement Therapy Restores Viability of BCD Patient iPSC Derived RPE Cells and Vision of Cyp4v3 Knockout Mice. Hum Mol Genet. 2022.

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