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期刊名:Nar genomics and bioinformatics

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e-ISSN:2631-9268

IF/分区:3.0/Q2

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共收录本刊相关文章索引974
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
Maria Bilen,Yubing Liu,Imane Chakroun et al. Maria Bilen et al.
Mitochondrial dysfunction and fragmentation are observed in various circumstances, such as neurodegeneration and aging. Studies have shown that altered mitochondrial function activates the integrated stress response (ISR), with ATF4 serving...
Hirotaka Matsumoto,Jing Hong Hirotaka Matsumoto
Protozoan parasites cause major infectious diseases and pose persistent global health challenges, particularly the emergence of drug-resistant strains. Tandem repeats and other repetitive architectures are widespread in proteomes and have b...
Kushani Shah,Eleni Anastasakou,Leinal Sejour et al. Kushani Shah et al.
SLNCR is a long non-coding RNA (lncRNA) that promotes melanoma formation. Previously, we have shown that SLNCR regulates gene expression via its interactions with different transcription factors. Here we show that SLNCR is associated with s...
Amy Z M Stephen,Arian Raje,Heather H Sestili et al. Amy Z M Stephen et al.
Differences in enhancer activity between species can help drive phenotypic diversity, yet enhancers often have conserved functions despite rapid sequence evolution, posing a challenge for quantifying their functional differences between spe...
Luca Schlegel,Fabio Gómez Cano,Alexandre P Marand et al. Luca Schlegel et al.
Scalable proxies for 3D genome contacts-such as single-cell co-accessibility and deep learning predictions-have emerged as powerful alternatives to chromatin capture-based methods, but predictions systematically overestimate long-range inte...
Dimitri Desvillechabrol,Rania Ouazahrou,Juliana Pipoli da Fonseca et al. Dimitri Desvillechabrol et al.
Genome assembly from long-read sequencing data has become a standard approach for resolving complex genomic regions and producing high-contiguity assemblies. However, the diversity of available assemblers, their varying performance across s...
Guillaume Kellermann,Olivier Croce,Baharia Mograbi et al. Guillaume Kellermann et al.
Shared epitopes pose safety and efficacy issues for T-cell immunotherapy. To characterize the extent of this problem, we performed a computational analysis establishing a complete atlas of shared identical sequences across the human and mur...
Xavier Farré,Mireia Gasco,Natalia Blay et al. Xavier Farré et al.
Phenome-wide association studies (PheWAS) using polygenic risk scores (PRS) offer a powerful framework for exploring the shared genetic architecture of complex traits across diverse phenotypic domains. However, no standardized, portable pip...
Rita Martins-Silva,Alexandre Kaizeler,Nuno L Barbosa-Morais Rita Martins-Silva
Many biological processes, including cellular senescence, manifest as diverse phenotypes across cell types and conditions. Lacking definitive markers, researchers often rely on the expression of sets of genes to identify these complex state...