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Max Bone,Gareth J Inman Max Bone
Transcriptional start and end variance, a less-explored aspect of lncRNA biology, is a critical determinant of isoform diversity in human RNA. While alternative splicing (AS) has been extensively studied as a mechanism of isoform generation...
Valentina A Grushina,Ivan S Yevshin,Oleg A Gusev et al. Valentina A Grushina et al.
Promoter shifting, characterized by alterations in Transcription Start Site (TSS) coordinates, is a well-documented phenomenon. The impact and statistical significance of promoter shifting can be assessed through analysis of Cap Analysis of...
Pavel Merkulov,Anastasiia Latypova,Kirill Tiurin et al. Pavel Merkulov et al.
In some cases, ONSEN insertions provided alternative transcription start or termination sites, generating novel transcript isoforms. Genome-wide methylation analysis revealed that new ONSEN copies were efficiently and precisely targeted by DNA methylation.
Benpeng Miao,Xinlong Luo,Amina Ademovic et al. Benpeng Miao et al.
Our results demonstrated that TE-derived alternative transcription initiation significantly enhances the variety of translated protein products, e.g., changes in the N-terminal peptide length of WNT2B caused by TE-derived transcription result in isoform-specific subcellular localization.
Kevin Vo,Sharmin Shila,Yashica Sharma et al. Kevin Vo et al.
This complex phenomenon arises from various mechanisms, such as using alternative transcription start sites and alternative post-transcriptional processing events.
Mayank Murali,Jamie Saquing,Senbao Lu et al. Mayank Murali et al.
Using Biosurfer, we analyzed the differences in 35,082 pairs of GENCODE annotated protein isoforms, finding a majority (70%) of variable N-termini are due to the alternative transcription start sites, while only 9% arise from 5' UTR alternative splicing (AS).
Christina Akirtava,Gemma E May,C Joel McManus Christina Akirtava
In addition, our work quantitated the effects of alternative transcription start site usage on gene expression in yeast. Thus, our study provides new quantitative insights into the roles of TL cis-acting sequences in regulating gene expression.
Rilu Feng,Roman Liebe,Hong-Lei Weng Rilu Feng
hepatic transcription factors, such as hepatic nuclear factor 4 alpha (HNF4α) and CCAAT-enhancer binding protein α (C/EBPα), which ensure normal liver function; (2) When the expression of both HNF4α and C/EBPα in hepatocytes are disrupted by severe inflammation, retinoic acid receptor (RAR) is the alternative...transcription factor that compensates for their absence; (3) When massive hepatic necrosis occurs, a similar transcription network including FOXA2 and HNF4α, is activated as a "rescue network" in LPCs to maintain vital liver functions when hepatocytes fail, and thus ensures survival.
Xinlu Li,XiaoJing Dong,Wen Zhang et al. Xinlu Li et al.
Integrated scRNA-seq and transcriptomic analyses have revealed novel insights into DR pathogenesis, including alternative transcription start site events, fluctuations in cell populations, altered gene expression profiles, and critical signaling pathways within retinal cells.
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