Biblio

Author Title [ Type(Asc)] Year
Filters: Author is Deng, Chunhua  [Clear All Filters]
Journal Article
Chen Z, Liu M, Hu J-H, Gao Y, Deng C, Jiang MHua. Substance P restores spermatogenesis in busulfan-treated mice: A new strategy for male infertility therapy. Biomed Pharmacother. 2020;133:110868.
Chi A, Yang B, Dai H, Li X, Mo J, Gao Y, Chen Z, Feng X, Ma M, Li Y, et al. Stem Leydig cells support macrophage immunological homeostasis through mitochondrial transfer in mice. Nat Commun. 2024;15(1):2120.
Xia K, Wang F, Tan Z, Zhang S, Lai X, Ou W, Yang C, Chen H, Peng H, Luo P, et al. Precise Correction of Lhcgr Mutation in Stem Leydig Cells by Prime Editing Rescues Hereditary Primary Hypogonadism in Mice. Adv Sci (Weinh). 2023:e2300993.
Xie Y, Lv L, Yao J, Zhang C, Chen H, Chen W, Liang X, Sun X, Deng C, Liu G. Phosphorylated mixed lineage kinase domain-like protein in human seminal plasma: A potential novel biomarker of spermatogenic function. Andrologia. 2019:e13310.
Liu G, Wu R, Yang B, Deng C, Lu X, Walker SJ, Ma PX, Mou S, Atala A, Zhang Y. Human Urine-Derived Stem Cell Differentiation to Endothelial Cells with Barrier Function and Nitric Oxide Production. Stem Cells Transl Med. 2018.
Xia K, Ma Y, Feng X, Deng R, Ke Q, Xiang APeng, Deng C. Endosialin defines human stem Leydig cells with regenerative potential. Hum Reprod. 2020.
Xia K, Yu J, Liu G, Chen H, Ge R, Deng C. Editorial: Aging and male hypogonadism. Front Endocrinol (Lausanne). 2023;14:1207907.
Liu G, Sun X, Bian J, Wu R, Guan X, Ouyang B, Huang Y, Xiao H, Luo D, Atala A, et al. Correction of diabetic erectile dysfunction with adipose derived stem cells modified with the vascular endothelial growth factor gene in a rodent diabetic model. PLoS One. 2013;8(8):e72790.
Luo P, Feng X, Deng R, Wang F, Zhang Y, Li X, Zhang M, Wan Z, Xiang APeng, Xia K, et al. An autofluorescence-based isolation of Leydig cells for testosterone deficiency treatment. Mol Cell Endocrinol. 2021:111389.
Xia K, Wang F, Lai X, Dong L, Luo P, Zhang S, Yang C, Chen H, Ma Y, Huang W, et al. AAV-mediated gene therapy produces fertile offspring in the Lhcgr-deficient mouse model of Leydig cell failure. Cell Rep Med. 2022:100792.