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Effective extraction of polyribosomes from astrocytes enables future discoveries on translation regulation
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作者 orna elroy-stein 《Neural Regeneration Research》 SCIE CAS 2025年第4期1083-1084,共2页
Translation regulation is an important layer of gene expression:Generation of genome-wide expression datasets at multi-omics levels in spatial,temporal,and cell-type resolution is essential for deciphering brain compl... Translation regulation is an important layer of gene expression:Generation of genome-wide expression datasets at multi-omics levels in spatial,temporal,and cell-type resolution is essential for deciphering brain complexity.Regulation of gene expression is a highly dynamic process aiming at the production of precise levels of gene products to guarantee optimal cellular function,in response to physiological cues.Speedy advances in next-generation sequencing enabled the understanding of epigenomic and transcriptomic dynamic landscapes of different brain regions along development,aging,and disease progression.However,the correlation of the“transcriptome”with protein levels is poor because numerous mRNAs are subjected to manipulation of their translation efficiency,to warrant a favorable result under certain conditions.Hence,it is widely accepted that regulation at the translation level is a vital layer of gene expression.Quantification of actively translated mRNA populations(i.e.,“translatome”)is a more reliable predictor of the“proteome”(Wang et al.,2020). 展开更多
关键词 TRANSLATION enable LANDSCAPE
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Mitochondrial malfunction in vanishing white matter disease: a disease of the cytosolic translation machinery 被引量:1
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作者 orna elroy-stein 《Neural Regeneration Research》 SCIE CAS CSCD 2017年第10期1610-1612,共3页
Vanishing white matter (VWM) disease - a disease of the cytosolic translation machinery: VWM is a recessive genet- ic neurodegenerative disease caused by mutations in any of the five genes encoding the subunits of ... Vanishing white matter (VWM) disease - a disease of the cytosolic translation machinery: VWM is a recessive genet- ic neurodegenerative disease caused by mutations in any of the five genes encoding the subunits of translation initiation factor 2B (eIF2B) (Leegwater et al., 2001; OMIM 306896). 展开更多
关键词 Mitochondrial malfunction in vanishing white matter disease:a disease of the cytosolic translation machinery ETC
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