Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Kun-yin Qiu"'
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-7 (2024)
Abstract Purpose The current study aims to investigate the significance of N6-methyladenosine (m6A) methylationrelated genes in the clinical prognosis of childhood relapsed B-cell acute lymphoblastic leukemia (B-ALLL) patient. Methods Transcriptome d
Externí odkaz:
https://doaj.org/article/126062dd837c4b2e863b9363f8678000
Publikováno v:
BMC Cancer, Vol 23, Iss 1, Pp 1-13 (2023)
Abstract Purpose To explore the outcome and prognostic factors between inv(16) and t(8;21) disrupt core binding factor (CBF) in acute myeloid leukemia (AML). Methods The clinical characteristic, probability of achieving complete remission (CR), overa
Externí odkaz:
https://doaj.org/article/bf1c9252028842ca9314938850774aff
Autor:
Kun-yin Qiu, Dun-hua Zhou, Xiong-yu Liao, Ke Huang, Yang Li, Hong-gui Xu, Wen-jun Weng, Lu-hong Xu, Jian-pei Fang
Publikováno v:
BMC Cancer, Vol 22, Iss 1, Pp 1-13 (2022)
Abstract Purpose To evaluate the prognostic factors and outcome for acute lymphoblastic leukemia (ALL) in children with MLL rearrangement (MLL-r). Methods A total of 124 pediatric patients who were diagnosed with ALL were classified into two groups b
Externí odkaz:
https://doaj.org/article/05242078cda84627a5242240d75eeb76
Autor:
Kun-yin Qiu, Shu-yi Guo, Yang-hui Zeng, Xiong-yu Liao, Shao-fen Lin, Jian-pei Fang, Dun-hua Zhou
Publikováno v:
Hematology, Vol 27, Iss 1, Pp 874-880 (2022)
Purpose Our aim is to analyze the clinical characteristics and prognostic factors of Epstein-Barr (EB) virus-associated hemophagocytic lymphohistiocytosis (EBV-HLH) in children. Methods Children with newly diagnosed HLH were retrospectively analyzed.
Externí odkaz:
https://doaj.org/article/5547a07e08ae4381a5266a8a5b18af1d
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-12 (2022)
Activating FLT3 mutations are the most common mutations in AML. Here, the authors explore the relationship between the FLT3/ITD allelic ratio and prognosis in pediatric AML patients and identify an optimal threshold to stratify patients.
Externí odkaz:
https://doaj.org/article/0daa3487045a467d94b7c5d3a7e050ab
Autor:
Kun-yin Qiu, Xiong-yu Liao, Zhan-wen He, Ruo-hao Wu, Yang Li, Lu-hong Xu, Dun-hua Zhou, Jian-pei Fang
Publikováno v:
BMC Cancer, Vol 21, Iss 1, Pp 1-10 (2021)
Abstract Background This study was aimed to evaluate the value of DNA index(DI) among pediatric acute lymphoblastic leukemia (ALL) treated on Children’s Oncology Group (COG) protocols between 2000 and 2015. Methods Retrospective study were analysis
Externí odkaz:
https://doaj.org/article/bf7a3be71af847b18a9bac98b7deeeb4
Autor:
Dian-Dian Liu, Wei-Cong Hong, Kun-Yin Qiu, Xin-Yu Li, Yong Liu, Li-Wen Zhu, Wei-Xin Lai, Han- Chen, Hua-Qing Yang, Lu-Hong Xu, Jian-Pei Fang
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
Chimeric antigen receptor T (CAR-T) cell therapy is an effective treatment for relapsed and refractory acute lymphoblastic leukemia (R/R ALL). However, autologous CAR-T cells derived from patients with B-ALL often show poor amplification ability, exh
Externí odkaz:
https://doaj.org/article/5791ccd389974e9a910a2a56642c6946
Autor:
Kun-yin Qiu, Hong-gui Xu, Xue-qun Luo, Hui-rong Mai, Ning Liao, Li-hua Yang, Min-cui Zheng, Wu-qing Wan, Xue-dong Wu, Ri-yang Liu, Qi-wen Chen, Hui-qin Chen, Xiao-fei Sun, Hua Jiang, Xing-jiang Long, Guo-hua Chen, Xin-yu Li, Chang-gang Li, Li-bin Huang, Ya-yun Ling, Dan-na Lin, Chuan Wen, Wen-yong Kuang, Xiao-qin Feng, Zhong-lv Ye, Bei-yan Wu, Xiang-lin He, Qiao-ru Li, Li-na Wang, Xian-ling Kong, Lu-hong Xu, Chi-kong Li, Jian-pei Fang
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
PurposeTo analyzed the outcome of ETV6/RUNX1-positive pediatric acute B lymphoblastic leukemia (B-ALL) with the aim of identifying prognostic value.MethodA total of 2,530 pediatric patients who were diagnosed with B-ALL were classified into two group
Externí odkaz:
https://doaj.org/article/348375087ff341a19f0e6f40c3406e09
Publikováno v:
Journal of International Medical Research, Vol 49 (2021)
De novo germline variants of the casein kinase 2α subunit (CK2α) gene ( CSNK2A1 ) have been reported in individuals with the congenital neuropsychiatric disorder Okur–Chung neurodevelopmental syndrome (OCNS). Here, we report on two unrelated chil
Externí odkaz:
https://doaj.org/article/f88f1a7d5a624acc974914abcf871e46
Autor:
Ruo-hao Wu, Dong-fang Li, Wen-ting Tang, Kun-yin Qiu, Yu Li, Xiong-yu Liao, Dan-xia Tang, Li-jun Qin, Bing-qing Deng, Xiang-yang Luo
Publikováno v:
Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-7 (2018)
Abstract Background Atrial septal defect often become more severe when encountered in genetic syndromes. Congenital disorder of glycosylation type 1a is an inherited metabolic disorder associated with mutations in PMM2 gene and can affect almost all
Externí odkaz:
https://doaj.org/article/0a1cc4f0e02346c8862b6af5821bffcf