Zobrazeno 1 - 10
of 88
pro vyhledávání: '"Weihua Lan"'
Autor:
Shuo Wang, Xuzhi Yan, Weihua Lan, Yapeng Wang, Ze Wang, Dali Tong, Yao Zhang, Qiang Ran, Haoyang Li, Junhao Jin, Haiyang Xiao, Jing Xu, Qian Yan, Dianzheng Zhang, Qiang Ma, Hualiang Xiao, Jun Qin, Luofu Wang, Jun Jiang, Qiuli Liu
Publikováno v:
Cancer Medicine, Vol 13, Iss 21, Pp n/a-n/a (2024)
ABSTRACT Purpose Upper tract urothelial carcinoma (UTUC) and urothelial carcinoma of the bladder (UCB) share histomorphological and therapeutic features but distinct epidemiologic and clinicopathologic characteristics. We examined alterations of chro
Externí odkaz:
https://doaj.org/article/201eedb184814545a6b753b70c4efd00
Autor:
Bo Wang, Xiaoxing Liu, Huan Xu, Shu Shang, Danfeng Yan, Jie Deng, Yanfeng Li, Weihua Lan, Dali Tong
Publikováno v:
American Journal of Men's Health, Vol 18 (2024)
Varicoceles are a common cause of male infertility, affecting up to 35% of men undergoing fertility evaluations. This study aims to investigate the potential influence of altitude and residence time on the occurrence of varicoceles, as well as on spe
Externí odkaz:
https://doaj.org/article/eafa0add7676469dbb02821d2995b318
Autor:
Weihua, Lan1 (AUTHOR), Xinfeng, Li1 (AUTHOR) xiaohengcupb@163.com, Jian, Liang1 (AUTHOR), Ting, Xiong1 (AUTHOR), Ziyan, Ni1 (AUTHOR)
Publikováno v:
Chemistry & Technology of Fuels & Oils. May2024, Vol. 60 Issue 2, p410-419. 10p.
Autor:
Peng Tang, Jun Zhang, Song Peng, Xuzhi Yan, Yapeng Wang, Shuo Wang, Yao Zhang, Gaolei Liu, Jing Xu, Yiqiang Huang, Dianzheng Zhang, Qiuli Liu, Jun Jiang, Weihua Lan
Publikováno v:
BMC Endocrine Disorders, Vol 23, Iss 1, Pp 1-8 (2023)
Abstract Background Primary bilateral macronodular adrenocortical hyperplasia (PBMAH) is a highly heterogeneous disease with divergent manifestations ranging from asymptomatic subclinical Cushing syndrome (CS) to overt Cushing syndrome with severe co
Externí odkaz:
https://doaj.org/article/f50e7ec39a69401bba70819483bfb705
Publikováno v:
Cancer Innovation, Vol 1, Iss 1, Pp 114-118 (2022)
Abstract The TMPRSS2‐ERG fusion gene has frequently been found in prostate cancer and is associated with malignancy. Identifying novel fusions will help to stratify patients and establish patient‐tailored therapies. A 78‐year‐old man presente
Externí odkaz:
https://doaj.org/article/ff648cc394274f4e95cceaffef157765
Autor:
Peng Tang, Jun Zhang, Song Peng, Yapeng Wang, Haoyang Li, Ze Wang, Yao Zhang, Yiqiang Huang, Jing Xu, Dianzheng Zhang, Qiuli Liu, Luofu Wang, Weihua Lan, Jun Jiang
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
Introduction21-hydroxylase deficiency (21OHD) is the most common cause of congenital adrenal hyperplasia (CAH). However, patients with 21OHD manifest various phenotypes due to a wide-spectrum residual enzyme activity of different CYP21A2 mutations.Me
Externí odkaz:
https://doaj.org/article/7dab075b12754d15bafcb6372f8d6230
Autor:
Qiubo Xie, Tang Tang, Jian Pang, Jing Xu, Xingxia Yang, Linang Wang, Yiqiang Huang, Zhuowei Huang, Gaolei Liu, Dali Tong, Yao Zhang, Luofu Wang, Dianzheng Zhang, Weihua Lan, Qiuli Liu, Jun Jiang
Publikováno v:
Frontiers in Oncology, Vol 10 (2020)
Epithelial-to-mesenchymal transition (EMT) is one of the important underlying molecular mechanisms for most types of cancers including bladder cancer. The precise underlying molecular mechanism in EMT-mediated bladder cancer progression is far from c
Externí odkaz:
https://doaj.org/article/f1f35d9051be42cdba52289df2acd859
Autor:
Yiqiang Huang, Lin-ang Wang, Qiubo Xie, Jian Pang, Luofu Wang, Yuting Yi, Jun Zhang, Yao Zhang, Rongrong Chen, Weihua Lan, Dianzheng Zhang, Jun Jiang
Publikováno v:
Endocrine Connections, Vol 7, Iss 12, Pp 1217-1225 (2018)
Pheochromocytoma and paragangliomas (PCC/PGL) are neuroendocrine tumors that arise from chromaffin cells of the adrenal medulla and sympathetic/parasympathetic ganglia, respectively. Of clinical relevance regarding diagnosis is the highly variable pr
Externí odkaz:
https://doaj.org/article/6a74e0627424493f996a01c4457fb8d6
Autor:
Qiuli Liu, Lin-ang Wang, Jian Su, Dali Tong, Weihua Lan, Luofu Wang, Gaolei Liu, Jun Zhang, Victor Wei Zhang, Dianzheng Zhang, Rongrong Chen, Qingyi Zhu, Jun Jiang
Publikováno v:
Endocrine Connections, Vol 7, Iss 11, Pp 1136-1141 (2018)
Congenital adrenal hyperplasia (CAH) is one of the most prevalent, and potentially severe, genetic inborn errors of steroid synthesis directly affecting metabolism. Most patients are diagnosed and treated at an early age. There have been very limited
Externí odkaz:
https://doaj.org/article/02a1a4ff5c26454da4d8407b9e11189c
Autor:
Qiuli Liu, Gang Yuan, Dali Tong, Gaolei Liu, Yuting Yi, Jun Zhang, Yao Zhang, Lin-ang Wang, Luofu Wang, Dianzheng Zhang, Rongrong Chen, Yanfang Guan, Xin Yi, Weihua Lan, Jun Jiang
Publikováno v:
Endocrine Connections, Vol 7, Iss 7, Pp 870-878 (2018)
Context: Von Hippel–Lindau (VHL) disease manifests as a variety of benign and malignant neoplasms. Previous studies of VHL disease have documented several genotype–phenotype correlations; however, many such correlations are still unknown. Increas
Externí odkaz:
https://doaj.org/article/8009051e69934b0c95a6eac26aa6fa48