Zhi-Long Dong
Lanzhou University
GeneInternal medicineOncologyRandomized controlled trialIntensive care medicineSystematic reviewPathologicalN6-MethyladenosineCochrane LibraryMale infertilityOligospermiaRehabilitationDiseaseErectile dysfunctionGemcitabineBladder cancerTeratospermiaRNA methylationShock wave therapyMolecular levelEpigeneticsIncidence (epidemiology)BioinformaticsStatistical significanceRNAMedicineBiologyMethyltransferaseIntensity (physics)DNA-binding proteinMeta-analysis
4Publications
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3Citations
Publications 4
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#1Rongxin Li (Lanzhou University)H-Index: 1
#2Ye Li (Lanzhou University)H-Index: 1
Last. Zhi-Long Dong (Lanzhou University)H-Index: 3
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BACKGROUND Mitomycin (MMC) has been frequently used as the compound for intravesical treatment. The relatively new pyrimidine analog gemcitabine (GEM) has exhibited anticancer effect on various solid cancers, such as the advanced bladder cancer. In this study, the GEM and MMC in treating non-muscle invasive bladder cancer (NMIBC) cases was compared through systemic review. METHODS In accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement, the el...
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#1Cheng CH-Index: 1
#2Zhi-Long Dong (Lanzhou University)H-Index: 3
Last. Zhiping Wang (Lanzhou University)H-Index: 22
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The prevalence of erectile dysfunction (ED) is increasing, especially among men over 40 years old, and is positively correlated with age. It is predicted that there will be as many as 300 million ED patients around the world by the year 2025. Recent years has witnessed deeper insights into the pathophysiological mechanisms of ED and significant breakthroughs in its treatment. However, few achievements have been made in the studies of its pathological change at the molecular level and the measure...
#1Ke Gao (Lanzhou University)H-Index: 1
#2Zhi-Qiang WangH-Index: 1
Last. Wen-Sheng ShanH-Index: 1
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: 目前研究发现与精子发生相关的基因约2 300个,其表达在调控精子的发生过程中起着重要的作用。近年来,少、弱、畸精症的相关遗传基因成为研究的热点,相关研究试图从分子水平上探讨少、弱、畸精症发生的机制,并取得了一些成果,一些基因如GSTM1、DNMT3L和CYP1A1可能与少精症的发生有关;一些基因如CATSPER1、 CRISP2、SEPT4、TCTE3、TEKT4和DNAH1可能与弱精症的发生有关;一些基因如DPY19L2、AURKC,可能与畸精症的发生有关。这些相关的基因研究为少、弱、畸精症的发病机制提供了可能的分子基础,同时也为探索新的诊治技术提供了新的思路。本文就少、弱、畸精症的部分相关遗传基因的最新研究进展作一综述。.
1 Citations