Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Jun-dan Xie"'
Autor:
Qian Wang, Ling Zhang, Ming-qing Zhu, Zhao Zeng, Bao-zhi Fang, Jun-dan Xie, Jin-lan Pan, Chun-xiao Wu, Ni Wu, Ri Zhang, Su-ning Chen, Hai-ping Dai
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
To define the fusion genes in T/myeloid mixed-phenotype acute leukemia (T/M MPAL), we performed transcriptome sequencing of diagnostic bone marrow samples from 20 adult patients. Our analysis identified a second instance of a recurrent MED14-HOXA9 ch
Externí odkaz:
https://doaj.org/article/2746ba3f19554019ba6c321fe56bf540
Autor:
Qian Wang, Hai-ping Dai, Dan-dan Liu, Jun-dan Xie, Hong Yao, Zi-xuan Ding, Ting-ting Tao, Su-ning Chen, Ri Zhang
Publikováno v:
Leukemia Research Reports, Vol 14, Iss , Pp 100229- (2020)
Myelodysplastic/myeloproliferative neoplasm, unclassifiable (MDS/MPN-U) is a rare but heterogeneous subtype of MDS/MPN, with no specific genetic alterations and standard treatments. ASXL1, SRSF2, TET2, JAK2 and NRAS are commonly mutated in MDS/MPN-U.
Externí odkaz:
https://doaj.org/article/d7abbc2e37684b93a53f5b9ad05c2e74
Autor:
Wen-Juan, Wang, Jun-Dan, Xie, Hong, Yao, Zi-Xuan, Ding, Ai-Rui, Jiang, Liang, Ma, Hong-Jie, Shen, Su-Ning, Chen
Publikováno v:
Clinical Genetics. 103:67-78
Hereditary spherocytosis (HS) is the most common type of hereditary erythrocyte membrane disease and has varied phenotypic features and genetic patterns. We herein performed a retrospective study of 94 patients with HS and aimed to investigate the ge
Autor:
Guo-Fa, Xu, Li-Min, Liu, Man, Wang, Zhi-Bo, Zhang, Jun-Dan, Xie, Hui-Ying, Qiu, Su-Ning, Chen
Publikováno v:
Leukemia & Lymphoma. 63:2652-2662
Philadelphia chromosome-like acute lymphoblastic leukemia (Ph-like ALL) is a high-risk subtype of ALL. We retrospectively studied 70 cases with Ph-like ALL and here present the largest study of CAR-T cell treatment and haplo-HSCT for this leukemia. M
Autor:
Qian Wang, Wen‐zhi Cai, Qin‐rong Wang, Ming‐qing Zhu, Ling‐zhi Yan, Yan Yu, Xie‐bing Bao, Hong‐jie Shen, Hong Yao, Jun‐dan Xie, Tong‐tong Zhang, Ling Zhang, Xiao‐yu Xu, Zhe Shan, Hong Liu, Jian‐nong Cen, Dan‐dan Liu, Jin‐lan Pan, Da‐ru Lu, Jia Chen, Yang Xu, Ri Zhang, Ying Wang, Sheng‐li Xue, Miao Miao, Yue Han, Xiao‐wen Tang, Hui‐ying Qiu, Ai‐ning Sun, Jin‐yan Huang, Hai‐ping Dai, De‐pei Wu, Su‐ning Chen
Publikováno v:
American journal of hematologyREFERENCES. 98(1)
Mixed phenotype acute leukemia (MPAL) is a subtype of leukemia in which lymphoid and myeloid markers are co-expressed. Knowledge regarding the genetic features of MPAL is lacking due to its rarity and heterogeneity. Here, we applied an integrated gen
Autor:
Qian, Wang, Ling, Zhang, Ming-Qing, Zhu, Zhao, Zeng, Bao-Zhi, Fang, Jun-Dan, Xie, Jin-Lan, Pan, Chun-Xiao, Wu, Ni, Wu, Ri, Zhang, Su-Ning, Chen, Hai-Ping, Dai
Publikováno v:
Frontiers in Oncology
To define the fusion genes in T/myeloid mixed-phenotype acute leukemia (T/M MPAL), we performed transcriptome sequencing of diagnostic bone marrow samples from 20 adult patients. Our analysis identified a second instance of a recurrent MED14-HOXA9 ch
Publikováno v:
Zhongguo shi yan xue ye xue za zhi. 26(6)
To investigate the feasibility of sensitive and quantitative detection of MYD88 gene L265P mutation in lymphoma patients by using ARMS-PCR combined with capillary electrophoresis.ARMS-PCR amplified MYD88 gene was analyzed by capillary electrophoresis
Autor:
Wen-Juan, Wang, Jun-Dan, Xie, Qian, Wang, Ting-Ting, Tao, Hong, Yao, Li-Jun, Wen, You-Ning, Zhou, Su-Ning, Chen
Publikováno v:
Zhongguo shi yan xue ye xue za zhi. 23(6)
To investigate the genotype distribution of hemoglobinopathy in Chinese Jiangsu population.A total of 4115 samples were screened for hemaglobinopathy by using MCV combined with erythrocyte fragility tests and HPLC. Thalassemia genotypes were identifi
Autor:
Hai-Ping, Dai, Qian, Wang, Li-Li, Wu, Na-Na, Ping, Chun-Xiao, Wu, Jun-Dan, Xie, Jin-Lan, Pan, Yong-Quan, Xue, De-Pei, Wu, Su-Ning, Chen
Publikováno v:
Zhongguo shi yan xue ye xue za zhi. 20(5)
This study was aimed to investigate the occurrence and clinical significance of the SET-NUP214 fusion gene in patients with T-cell acute lymphoblastic leukemia (T-ALL), analyse clinical and biological characteristics in this disease. RT-PCR was used