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期刊名:Cell and bioscience

缩写:CELL BIOSCI

ISSN:N/A

e-ISSN:2045-3701

IF/分区:6.5/Q1

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共收录本刊相关文章索引1842条
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Xiangxiang Song,Yun Zhong,Nasha Yu et al. Xiangxiang Song et al.
Background: Diffuse large B-cell lymphoma (DLBCL) is an aggressive subtype of non-Hodgkin lymphoma. Fatty acid synthase (FASN) is a key lipogenic enzyme implicated in tumor progression, but its regulation in DLBCL is poor...
Huiyu Hao,Yuanhao Li,Xiaoyu Li et al. Huiyu Hao et al.
Sevoflurane, a widely used volatile anesthetic, has raised concerns regarding its potential developmental toxicity, particularly due to its extensive application in non-obstetric surgeries and fetal intervention procedures during pregnancy....
Li Zhao,Rongjun Xie,Li Li et al. Li Zhao et al.
The progression of colorectal cancer (CRC) is closely associated with aberrant epigenetic regulation. As a key regulator of m5C modification, the role and mechanism of Aly/REF export factor (ALYREF) in CRC remain unclear. This study aims to...
Emeric M Louis,Nga Luu,Laurent M Sachs et al. Emeric M Louis et al.
Epigenetic modifications of histones play key roles in transcriptional regulation by diverse transcription factors. One such modification is the methylation of histone H3 at lysine 79 (H3K79). The methyltransferase DOT1L is the only known, ...
Gai-Gai Liu,Li-Yan Shuang,Qian Zhang et al. Gai-Gai Liu et al.
Hypoxic-ischemic encephalopathy (HIE) represents the leading cause of acute neonatal mortality and chronic neurological disorders. The impact of HIE on neonatal immune system development and the underlying mechanisms remain unclear. In this...
Haibo Li,Ying Jiang,Lusi Zhang et al. Haibo Li et al.
Neuronal intranuclear inclusion disease (NIID) patients frequently exhibit ocular abnormalities, yet the pathogenic mechanisms remain unclear. Using a transgenic mouse model ubiquitously expressing NOTCH2NLC with 98GGC repeats, we revealed ...