Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 3 (of 3 Records) |
Query Trace: Engraftment Syndrome[original query] |
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Engraftment syndrome, but not acute GVHD, younger age, CYP3A5 or MDR1 polymorphisms, increases tacrolimus clearance in pediatric hematopoietic SCT. Bone marrow transplantation 2011 Jan 46 (1): 90-7. Yanagisawa R, Katsuyama Y, Shigemura T, Saito S, Tanaka M, Nakazawa Y, Sakashita K, Shiohara M, Koike |
The influence of methotrexate-related transporter and metabolizing enzyme gene polymorphisms on peri-engraftment syndrome and graft-versus-host disease after haplo-hematopoietic stem cell transplantation in pediatric patients with malignant hematological diseases. Frontiers in immunology 2023 9 14 1229266. Qi Ji, Yongping Zhang, Yixin Hu, Lixia Liu, Shanbo Cao, Li Gao, Bohan Li, Yuanyuan Tian, Lingjun Kong, Shuiyan Wu, Jing Ling, Peifang Xiao, Jun Lu, Jie Li, Yanhua Yao, Jiayue Qin, Shaoyan |
Post-transplant complications revealed by mycophenolate mofetil related transporters and metabolic enzymes gene polymorphisms in pediatric patients with hematological disorders. BMC cancer 2024 12 24 (1): 1516. Qi Ji, Yixin Hu, Minyuan Liu, Lixia Liu, Jiajia Zheng, Zhizhuo Du, Li Gao, Peifang Xiao, Jing Ling, Liyan Fan, Xinni Bian, Feng Lou, Shanbo Cao, Jie Li, Yuanyuan Tian, Jun Lu, Jiayue Qin, Shaoyan |
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