日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

CircPRDM5 inhibits the proliferation, migration, invasion, and glucose metabolism of gastric cancer cells by reducing GCNT4 expression in a miR-485-3p-dependent manner

CircPRDM5通过miR-485-3p依赖的方式降低GCNT4的表达,从而抑制胃癌细胞的增殖、迁移、侵袭和葡萄糖代谢。

Zhang-Zhang Lan,Feng-Hua Sun,Chuan Chen,Li Niu,Jing-Dong Shi,Wen-Yong Zhang

The Association of Novel Single-Nucleotide Variants in the Collagen Matrix-Encoding Gene PRDM5 with Aortic Aneurysmal Disease

胶原基质编码基因PRDM5中新型单核苷酸变异与主动脉瘤疾病的关联

Moore, Peyton; Wolf, Adam; Sathyamoorthy, Mohanakrishnan

Homozygous Val6Gly Variation in PRDM5 Gene Causing Brittle Cornea Syndrome: A New Turkish Case

PRDM5基因Val6Gly纯合变异导致脆性角膜综合征:一例新的土耳其病例

Sanrı, Aslıhan; Demir, Selma; Gurkan, Hakan

Low expression of PRDM5 predicts poor prognosis of esophageal squamous cell carcinoma

PRDM5低表达预示食管鳞状细胞癌预后不良

Guo, Jing; Yang, Qiuxing; Wei, Sheng; Shao, Jingjing; Zhao, Tianye; Guo, Liyuan; Liu, Jia; Chen, Jia; Wang, Gaoren

Downregulation of promoter methylation gene PRDM5 contributes to the development of tumor proliferation and predicts poor prognosis in gastric cancer

PRDM5基因启动子甲基化下调促进肿瘤增殖,并预示胃癌预后不良。

Teng, Jing-Jing; Zhao, Wen-Jing; Zhang, Xun-Lei; Zhao, Da-Kun; Qiu, Xin-Yue; Chen, Xu-Dong; Yang, Lei

The SAGA core module is critical during Drosophila oogenesis and is broadly recruited to promoters

SAGA 核心模块在果蝇卵子发生过程中至关重要,并被广泛招募到启动子

Jelly H M Soffers, Sergio G-M Alcantara, Xuanying Li, Wanqing Shao, Christopher W Seidel, Hua Li, Julia Zeitlinger, Susan M Abmayr, Jerry L Workman

Case report of a PRDM5 linked brittle cornea syndrome type 2 in association with a novel SLC6A5 mutation

一例与新型SLC6A5突变相关的PRDM5连锁脆性角膜综合征2型病例报告

Selina, Agnes; John, Deepa; Loganathan, Lakshmi; Madhuri, Vrisha

LncRNA DGCR5 suppresses neuronal apoptosis to improve acute spinal cord injury through targeting PRDM5

lncRNA DGCR5通过靶向PRDM5抑制神经元凋亡,从而改善急性脊髓损伤。

Zhang, Huafeng; Wang, Wengang; Li, Ning; Li, Peng; Liu, Ming; Pan, Junwei; Wang, Dan; Li, Junwei; Xiong, Yuanyuan; Xia, Lei

Whole exome sequencing identifies a heterozygous missense variant in the PRDM5 gene in a family with Axenfeld-Rieger syndrome

全外显子组测序在一个患有Axenfeld-Rieger综合征的家族中发现了PRDM5基因的杂合错义变异。

Micheal, Shazia; Siddiqui, Sorath Noorani; Zafar, Saemah Nuzhat; Venselaar, Hanka; Qamar, Raheel; Khan, Muhammad Imran; den Hollander, Anneke I

Genome-based discovery of a novel membrane-bound 1,6-dihydroxyphenazine prenyltransferase from a marine actinomycete

基于基因组的海洋放线菌中新型膜结合 1,6-二羟基吩嗪异戊烯基转移酶的发现

Philipp Zeyhle, Judith S Bauer, Jörn Kalinowski, Kazuo Shin-ya, Harald Gross, Lutz Heide