Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Wei-Jun Jiang"'
Autor:
Chang-Tze Ricky Yu, Yu-Ting Amber Liao, Chi-Yin Nina Chiang, Jo-Mei Maureen Chen, Hsin-Yu Bella Pan, Chia-Yun Pan, Wei-Jun Jiang, Jia-Rung Tsai, Tsung-Ying Yang, Chieh-Lin Jerry Teng
Publikováno v:
Journal of Translational Medicine, Vol 22, Iss 1, Pp 1-16 (2024)
Abstract Background Bortezomib is a standard treatment for multiple myeloma (MM), working by the accumulation of toxic misfolded proteins in cancer cells. However, a significant clinical challenge arises from the development of resistance to bortezom
Externí odkaz:
https://doaj.org/article/4806aba446d64437bc25baae10746681
Publikováno v:
Nuclear Science and Techniques. 33
Publikováno v:
Communications in Statistics - Theory and Methods. 50:2900-2917
In this paper, we consider the weighted composite quantile regression for the linear model when the data are right censored and the censoring indicators are missing at random. The adaptive penalize...
Autor:
Tao, Luo, Hui-Jie, Zhi, Qiu-Yue, Wu, Wei-Wei, Li, Pei-Ran, Zhu, Wei-Jun, Jiang, Guo-Guo, Zhao, Fan, Wang, Xin-Yi, Xia, Qin, Yao
Publikováno v:
Zhonghua nan ke xue = National journal of andrology. 26(7)
To investigate the mutation of the DPY19L2 gene in patients with globozoospermia.We collected the clinical data and peripheral blood from 2 patients with globozoospermia and screened for mutation of the DPY19L2 gene by PCR amplification and DNA seque
Autor:
Fan, Wang, Lei, Wang, Qiu-Yue, Wu, Pei-Ran, Zhu, Wei-Jun, Jiang, Guo-Guo, Zhao, Xin-Yi, Xia, Xiao-Feng, Xu
Publikováno v:
Zhonghua nan ke xue = National journal of andrology. 26(9)
To investigate the relationship between microRNA-34b/c single nucleotide polymorphism (SNP) rs4938723 and the risk of male infertility.This case-control study included 553 males aged 19-40 (29.42 ± 5.09) years with idiopathic infertility, 153 with
Autor:
Hai-Hong, Liu, Jun, Zhao, Jin, Xu, Pei-Ran, Zhu, Mao-Mao, Yu, Wei-Jun, Jiang, Jing, Zhang, Wei-Wei, Li, Qiu-Yue, Wu, Zheng-Rong, Li, Xin-Yi, Xia
Publikováno v:
Zhonghua nan ke xue = National journal of andrology. 24(8)
To investigate the correlation between the single nucleotide polymorphism (SNP) rs662 of the paraoxonase 1 gene (PON1) and the risk of male infertility.This case-control study included 403 male idiopathic infertility patients aged 29.00 ± 4.48 years
Autor:
Meng-Xia, Ni, Hui-Jie, Zhi, Shuai-Mei, Liu, Pei-Ran, Zhu, Jing, Zhang, Qiu-Yue, Wu, Wei-Jun, Jiang, Mao-Mao, Yu, Wei-Wei, Li, Jin, Cao, Hao-Qin, Xu, Xin-Yi, Xia, Xiao-Feng, Xu, Liang, Shi
Publikováno v:
Zhonghua nan ke xue = National journal of andrology. 23(2)
To investigate the correlation of the single nucleotide polymorphism (SNP) rs1042522 of the tumor protein p53 (TP53) gene with the risk of male infertility.This casecontrol study included 380 male patients with idiopathic infertility and 398 norma
Autor:
Pei-Ran, Zhu, Qiu-Yue, Wu, Mao-Mao, Yu, Ming-Chao, Zhang, Meng-Xia, Ni, Shuai-Mei, Liu, Wei-Jun, Jiang, Jing, Zhang, Wei-Wei, Li, Jin, Cao, Yi, Li, Xin-Yi, Xia, Xiao-Yu, Yang, Hao-Qin, Xu
Publikováno v:
Zhonghua nan ke xue = National journal of andrology. 23(2)
To investigate the correlation of the single nucleotide polymorphism (SNP) rs4880 of the superoxide dismutase 2 (SOD2) gene with the risk of male infertility.This casecontrol study included 519 male patients with idiopathic infertility (aged 19-
Autor:
Shuai-Mei, Liu, Meng-Xia, Ni, Ming-Chao, Zhang, Pei-Ran, Zhu, Qiu-Yu, Wu, Wei-Jun, Jiang, Jing, Zhang, Wei-Wei, Li, Xin-Yi, Xia
Publikováno v:
Journal of genetics. 96(6)
Dyschromatosis symmetrica hereditaria (DSH) is a rare autosomal dominant pigmentary genodermatosis, which is characterized by a mixture of hyperpigmented and hypopigmented macules on the dorsal of the hands and feet, and on the face presented like fr
Autor:
Hai Li, Lei Shen, Jing Hua, Xiong Ma, Shan Shan Huang, Shen Li, Wei Jun Jiang, De Kai Qiu, Qi Xia Wang, Xiao Xiao, Haiyan Zhang, Qi Miao
Publikováno v:
Journal of Digestive Diseases. 14:175-180
Objective This study aimed to define the clinical features of Chinese patients with autoantibody-negative autoimmune hepatitis (AIH) and to refine the diagnosis and management of these atypical patients in a single Chinese center. Methods A retrospec