المؤلفون: Zhou J, Yao Z, Zheng Z, Yang J, Wang R, Fu S, Pan X, Liu Z, Wu K

المصدر: OncoTargets and Therapy, Vol Volume 13, Pp 9701-9719 (2020)

مصطلحات موضوعية: g-mdscs, exosomes, mirna-143-3p, itm2b, proliferation, lung cancer, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

Relation: https://www.dovepress.com/g-mdscs-derived-exosomal-mirna-143-3p-promotes-proliferation-via-targe-peer-reviewed-article-OTT; https://doaj.org/toc/1178-6930; https://doaj.org/article/9f2b4a62fb1946ae8103c56eda9e8d65

الاتاحة: https://doaj.org/article/9f2b4a62fb1946ae8103c56eda9e8d65

المؤلفون: Ya‑Jing Fu, Yong‑Jun Jiang, Si-Yao Li, Zining Zhang, Hong Shang

المصدر: Journal of Translational Medicine
Journal of Translational Medicine, Vol 18, Iss 1, Pp 1-11 (2020)

مصطلحات موضوعية: 0301 basic medicine, Microarray, T cell, lcsh:Medicine, HIV Infections, Biology, CD8-Positive T-Lymphocytes, CD8+ T cells, General Biochemistry, Genetics and Molecular Biology, Transcriptome, 03 medical and health sciences, Resolvers, 0302 clinical medicine, Long-term non-progressors, microRNA, medicine, Cytotoxic T cell, Humans, Gene, miRNA-143-3p, Coinfection, Research, Gene Expression Profiling, lcsh:R, virus diseases, HIV, General Medicine, Hepatitis C, TLR2, Meta-analysis, 030104 developmental biology, medicine.anatomical_structure, 030220 oncology & carcinogenesis, Immunology, HCV, CD8

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f865ebed0daf4f9092c60666b4cbcf13
http://europepmc.org/articles/PMC7038596