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期刊名:Cell

缩写:CELL

ISSN:0092-8674

e-ISSN:1097-4172

IF/分区:42.5/Q1

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共收录本刊相关文章索引9728
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
N Bishara Marzook,Ok-Ryul Song,Lotta Baumgärtel et al. N Bishara Marzook et al.
Cryptosporidium is a leading cause of diarrheal disease, yet little is known regarding the infection cell biology of this intracellular intestinal parasite. To this end, we implemented an arrayed genome-wide CRISPR-Cas9 knockout screen to m...
Hyoung-Soo Cho,Ji-Sun Yoo,Xinyang Song et al. Hyoung-Soo Cho et al.
Commensals are constantly shaping the host's immunological landscape. Lipopolysaccharides found in gram-negative microbes have a terminal lipid A in their outer membrane. Here, we report that structural variations in symbiotic lipid A lead ...
Erica Wolin,Jimmy K Guo,Mario R Blanco et al. Erica Wolin et al.
RNA-binding proteins (RBPs) regulate all stages of the mRNA life cycle, yet current methods generally map RNA targets of RBPs one protein at a time. To overcome this limitation, we developed SPIDR (split-and-pool identification of RBP targe...
Qiaoling Zhu,Feng Yin,Jiachen Qin et al. Qiaoling Zhu et al.
Protein C receptor+ (Procr+) cells were identified as stem or progenitor cells in multiple adult tissues. However, whether mechanical stimuli fine-tune their activation and differentiation remain unknown. Here, we found rare Procr+ cells in...
Daniela C Soto,José M Uribe-Salazar,Gulhan Kaya et al. Daniela C Soto et al.
Duplicated genes expanded in the human lineage likely contributed to brain evolution, yet challenges exist in their discovery due to sequence-assembly errors. We used a complete telomere-to-telomere genome sequence to identify 213 human-spe...
Doris Kaltenecker,Søren Fisker Schmidt,Peter Weber et al. Doris Kaltenecker et al.
In cancer cachexia, the presence of a tumor triggers systemic metabolic disruption that leads to involuntary body weight loss and accelerated mortality in affected patients. Here, we conducted transcriptomic and epigenomic profiling of the ...
Alexander A Sousa,Markus Terrey,Holt A Sakai et al. Alexander A Sousa et al.
Alternating hemiplegia of childhood (AHC) is a neurodevelopmental disorder with no disease-modifying treatment. Mutations in ATP1A3, encoding an Na+/K+ ATPase subunit, cause 70% of AHC cases. Here, we present prime editing (PE) and base edi...
Yaqiao Li,Carlota Pereda Serras,Jessica Blumenfeld et al. Yaqiao Li et al.
Alzheimer's disease (AD) is a multifactorial neurodegenerative disorder characterized by heterogeneous molecular changes across diverse cell types, posing significant challenges for treatment development. To address this, we introduced a ce...