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Scientific Reports|January 11, 2022
The differential effects of tumor burdens on predicting the net benefits of ssCART-19 cell treatment on r/r B-ALL patientsMinghao Li, Sheng-Li Xue, Xiaowen Tang, et al.
Gene|March 8, 2007
Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutationXiaowen Tang, Li Yang, Yi Zhu, et al.
Frontiers in Oncology|June 11, 2021
A Prospective Investigation of Bispecific CD19/22 CAR T Cell Therapy in Patients With Relapsed or Refractory B Cell Non-Hodgkin LymphomaYing Zhang, Jiaqi Li, Xiaoyan Lou, et al.
Mitochondrion|October 13, 2009
Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutationJianxin Lu, Yaping Qian, Zhiyuan Li, et al.
Blood|January 31, 2016
The ubiquitin ligase HERC4 mediates c-Maf ubiquitination and delays the growth of multiple myeloma xenografts in nude miceZubin Zhang, Jiefei Tong, Xiaowen Tang, et al.
Frontiers in Immunology|March 19, 2026
Quantitative evaluation of T-cell repertoire restoration following hematopoietic stem cell transplantation in patients with and without graft versus host diseaseXin Zhang, Pengyi Song, Longhai Tang, et al.
Blood Cancer Journal|April 24, 2023
Which one is better for refractory/relapsed acute B-cell lymphoblastic leukemia: Single-target (CD19) or dual-target (tandem or sequential CD19/CD22) CAR T-cell therapy?Sining Liu, Xinyue Zhang, Haiping Dai, et al.
Leukemia & Lymphoma|March 13, 2024
Comparison of valganciclovir <i>versus</i> foscarnet for the treatment of cytomegalovirus viremia in adult acute leukemia patients after allogeneic hematopoietic cell transplantationJinjin Zhu, Mimi Xu, Yuhua Ru, et al.
Biochemical and Biophysical Research Communications|July 31, 2007
Mitochondrial tRNASer(UCN) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing lossLongjin Jin, Aifen Yang, Yi Zhu, et al.
Gene|August 19, 2007
Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigreesJianfu Chen, Li Yang, Aifen Yang, et al.
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