Upregulation of CD22 by Chidamide promotes CAR T cells functionality

por Yang, Xin, Yu, Qiuxia, Xu, Hao, Zhou, Jianfeng
Publicado 2021

Abnormal Expression of Dysferlin in Blood Monocytes Supports Primary Dysferlinopathy in Patients Confirmed by Genetic Analyses

por Zhang, Huili, Li, Yaqin, Cheng, Qiusheng, Chen, Xi, Yu, Qiuxia, Li, Ze
Publicado 2021

Primary Testicular and Cutaneous Philadelphia Chromosome Positive B-Cell Lymphoblastic Lymphoma: A Rare Case and Review

por Yu, Qiuxia, Wang, Gaoxiang, Wang, Jue, Zhang, Wei, Meng, Li, Cao, Yang
Publicado 2022

MicroRNA Let-7i Regulates Innate TLR4 Pathways in Peripheral Blood Mononuclear Cells of Patients with Ankylosing Spondylitis

por Lu, Liangjie, Fang, Haiming, Gu, Mengchao, Wang, Huihan, Yu, Qiuxia, Chen, Aqiong, Gan, Kai-feng
Publicado 2023

Case report: Germline RECQL mutation potentially involved in hereditary predisposition to acute leukemia

por Yuan, Wei, Shang, Zhen, Shen, Kefeng, Yu, Qiuxia, Lv, Qiuxia, Cao, Yang, Wang, Jue, Yang, Yi
Publicado 2023

Primary gastrointestinal stromal tumor of the prostate: A case report and literature review

por LIU, SULAI, YU, QIUXIA, HAN, WEIQING, QI, LIN, ZU, XIONGBING, ZENG, FUHUA, XIE, YU, LIU, JINGSHI
Publicado 2014

Analysis of Mutation Spectra of 28 Pathogenic Genes Associated With Congenital Hypothyroidism in the Chinese Han Population

por Huang, Miao, Lu, Xiyan, Dong, Guoqing, Li, Jianxu, Chen, Chengcong, Yu, Qiuxia, Li, Mingzhu, Su, Yueyue
Publicado 2021

Anti-Hyperuricemic and Nephroprotective Effects of Dihydroberberine in Potassium Oxonate- and Hypoxanthine-Induced Hyperuricemic Mice

por Xu, Lieqiang, Lin, Guoshu, Yu, Qiuxia, Li, Qiaoping, Mai, Liting, Cheng, Juanjuan, Xie, Jianhui, Liu, Yuhong, Su, Ziren, Li, Yucui
Publicado 2021

Integrating network pharmacology and experimental validation to clarify the anti-hyperuricemia mechanism of cortex phellodendri in mice

por Xu, Lieqiang, Cheng, Juanjuan, Lu, Jieyi, Lin, Guoshu, Yu, Qiuxia, Li, Yucui, Chen, Jiannan, Xie, Jianhui, Su, Ziren, Zhou, Qi
Publicado 2022

Prenatal Diagnosis of Chromosome 16p11.2 Microdeletion

por Wang, You, Zhou, Hang, Fu, Fang, Cheng, Ken, Yu, Qiuxia, Huang, Ruibin, Lei, Tingying, Yang, Xin, Li, Dongzhi, Liao, Can
Publicado 2022

Case Report: Two Novel L1CAM Mutations in Two Unrelated Chinese Families With X-Linked Hydrocephalus

por Zhou, Hang, Yu, Qiuxia, Li, Yingsi, Fu, Fang, Li, Ru, Chen, Guilan, Wang, Dan, Lu, Yan, Yang, Xin, Li, Dongzhi, Liao, Can
Publicado 2022

Mutations in immunodeficiency-related genes may increase the risk of infection after CAR-T-cell therapy: a report of two cases

por Wang, Di, He, Li, Li, Chunhui, Xu, Menglei, Yu, Qiuxia, Almeida, Varlene Daniela Fernandes, Que, Yimei, Xu, Yanjie, Xiao, Yi, Li, Chunrui
Publicado 2023

The discovery of berberine erythrocyte-hemoglobin self-assembly delivery system: a neglected carrier underlying its pharmacokinetics

por Yu, Qiuxia, Li, Minhua, Chen, Hanbin, Xu, Lieqiang, Cheng, Juanjuan, Lin, Guoshu, Liu, Yuhong, Su, Ziren, Yang, Xiaobo, Li, Yucui, Chen, Jiannan, Xie, Jianhui
Publicado 2022

Anti-Inflammatory Activation of Phellodendri Chinensis Cortex is Mediated by Berberine Erythrocytes Self-Assembly Targeted Delivery System

por Li, Minhua, Qin, Zehui, Yu, Qiuxia, Huang, Ziwei, Cheng, Juanjuan, Zhong, Linjiang, Liu, Yuhong, Xie, Jianhui, Li, Yucui, Chen, Jiannan, Zhan, Ruoting, Su, Ziren
Publicado 2022

Genetic Analysis and Sonography Characteristics in Fetus with SHOX Haploinsufficiency

por Li, Lushan, Fu, Fang, Li, Ru, Jing, Xiangyi, Yu, Qiuxia, Zhou, Hang, Wang, You, Yang, Xin, Pan, Min, Han, Jin, Zhen, Li, Li, Dongzhi, Liao, Can
Publicado 2023

Prenatal Diagnosis and Outcomes in Fetuses with Hemivertebra

por Zhou, Hang, Wang, You, Huang, Ruibin, Fu, Fang, Li, Ru, Cheng, Ken, Wang, Dan, Yu, Qiuxia, Zhang, Yongling, Jing, Xiangyi, Lei, Tingying, Han, Jin, Yang, Xin, Li, Dongzhi, Liao, Can
Publicado 2022

Genetic diagnosis of fetal microcephaly at a single tertiary center in China

por Wang, You, Fu, Fang, Lei, Tingying, Zhen, Li, Deng, Qiong, Zhou, Hang, Ma, Chunling, Cheng, Ken, Huang, Ruibin, Li, Ru, Yu, Qiuxia, Li, Lushan, Han, Jin, Yang, Xin, Li, Dongzhi, Liao, Can
Publicado 2023

Exome sequencing improves genetic diagnosis of congenital orofacial clefts

por Yan, Shujuan, Fu, Fang, Li, Ru, Yu, Qiuxia, Li, Fucheng, Zhou, Hang, Wang, You, Huang, Ruibin, Ma, Chunling, Guo, Fei, Wang, Dan, Yang, Xin, Han, Jin, Lei, Tingyin, Li, Dongzhi, Liao, Can
Publicado 2023

Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencing

por Fu, Fang, Li, Ru, Dang, Xiao, Yu, Qiuxia, Xu, Ke, Gu, Weiyue, Wang, Dan, Yang, Xin, Pan, Min, Zhen, Li, Zhang, Yongling, Li, Fatao, Jing, Xiangyi, Li, Fucheng, Li, Dongzhi, Liao, Can
Publicado 2022

A novel two-step administration of XPO-1 inhibitor may enhance the effect of anti-BCMA CAR-T in relapsed/refractory extramedullary multiple myeloma

por Wang, Di, Fu, Haiying, Que, Yimei, Ruan, Haitao, Xu, Menglei, Long, Xiaolu, Yu, Qiuxia, Li, Chunhui, Li, Zhe, Cai, Songbai, Chen, Wei, Sun, Cong, Hu, Guang, Wang, Shuai, He, Donggou, Mei, Jianming, Wang, Wen, Li, Chunrui
Publicado 2023