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Effective extraction of polyribosomes from astrocytes enables future discoveries on translation regulation

从星形胶质细胞中高效提取多核糖体，有助于未来在翻译调控方面取得突破性进展。

期刊:Neural Regeneration Research

影响因子:6.7

doi:10.4103/NRR.NRR-D-24-00204

The translational landscape of reactive astrocytes reveals the impact of eIF2B-mediated dysregulation in VWM disease

反应性星形胶质细胞的转化图谱揭示了eIF2B介导的失调对VWM疾病的影响

期刊:

影响因子:

doi:10.1093/narmme/ugaf009

Mandelboum, Shir; Lev-Ari, Liat; Atzmon, Andrea; Herrero, Melisa; Brezner, Naama; Benhalevy, Daniel; Elroy-Stein, Orna

Correction: Nonsense mutation suppression is enhanced by targeting different stages of the protein synthesis process

更正：通过靶向蛋白质合成过程的不同阶段，可以增强对无义突变的抑制。

期刊:PLoS Biology

影响因子:7.2

doi:10.1371/journal.pbio.3002524

Wittenstein, Amnon; Caspi, Michal; Rippin, Ido; Elroy-Stein, Orna; Eldar-Finkelman, Hagit; Thoms, Sven; Rosin-Arbesfeld, Rina

发表日期：2024

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Recurrent functional misinterpretation of RNA-seq data caused by sample-specific gene length bias

样本特异性基因长度偏差导致RNA-seq数据出现反复的功能性误读

期刊:PLoS Biology

影响因子:7.2

doi:10.1371/journal.pbio.3000481

Mandelboum, Shir; Manber, Zohar; Elroy-Stein, Orna; Elkon, Ran

发表日期：2019

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PUNCH-P for global translatome profiling: Methodology, insights and comparison to other techniques

PUNCH-P 用于全球翻译组分析：方法、见解及与其他技术的比较

期刊:

影响因子:

doi:10.4161/trla.27516

Aviner, Ranen; Geiger, Tamar; Elroy-Stein, Orna

发表日期：2013

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Poor cerebral inflammatory response in eIF2B knock-in mice: implications for the aetiology of vanishing white matter disease.

eIF2B 敲入小鼠脑部炎症反应不良：对消失性白质疾病病因学的启示

期刊:PLoS One

影响因子:2.6

doi:10.1371/journal.pone.0046715

Cabilly Yuval, Barbi Mali, Geva Michal, Marom Liraz, Chetrit David, Ehrlich Marcelo, Elroy-Stein Orna

Quantitative single cell monitoring of protein synthesis at subcellular resolution using fluorescently labeled tRNA.

利用荧光标记的tRNA对蛋白质合成进行亚细胞分辨率的单细胞定量监测

期刊:Nucleic Acids Research

影响因子:13.1

doi:10.1093/nar/gkr601

Barhoom Sima, Kaur Jaskiran, Cooperman Barry S, Smorodinsky Nechama I, Smilansky Zeev, Ehrlich Marcelo, Elroy-Stein Orna

细胞生物学

发表日期：2011

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Mitotic modulation of translation elongation factor 1 leads to hindered tRNA delivery to ribosomes

有丝分裂过程中翻译延伸因子1的调控导致tRNA向核糖体的递送受阻

期刊:Journal of Biological Chemistry

影响因子:3.9

doi:10.1074/jbc.M111.255810

Sivan, Gilad; Aviner, Ranen; Elroy-Stein, Orna

信号转导

发表日期：2011

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A point mutation in translation initiation factor eIF2B leads to function--and time-specific changes in brain gene expression.

翻译起始因子 eIF2B 的点突变导致大脑基因表达的功能和时间特异性变化

期刊:PLoS One

影响因子:2.6

doi:10.1371/journal.pone.0026992

Marom Liraz, Ulitsky Igor, Cabilly Yuval, Shamir Ron, Elroy-Stein Orna

神经科学

发表日期：2011

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Repurposed hnRNPC binds mature mRNAs and safeguards the mitotic transcriptome

重新利用的hnRNPC结合成熟的mRNA并保护有丝分裂转录组。

Effective extraction of polyribosomes from astrocytes enables future discoveries on translation regulation

从星形胶质细胞中高效提取多核糖体，有助于未来在翻译调控方面取得突破性进展。

The translational landscape of reactive astrocytes reveals the impact of eIF2B-mediated dysregulation in VWM disease

反应性星形胶质细胞的转化图谱揭示了eIF2B介导的失调对VWM疾病的影响

Correction: Nonsense mutation suppression is enhanced by targeting different stages of the protein synthesis process

更正：通过靶向蛋白质合成过程的不同阶段，可以增强对无义突变的抑制。

Recurrent functional misinterpretation of RNA-seq data caused by sample-specific gene length bias

样本特异性基因长度偏差导致RNA-seq数据出现反复的功能性误读

PUNCH-P for global translatome profiling: Methodology, insights and comparison to other techniques

PUNCH-P 用于全球翻译组分析：方法、见解及与其他技术的比较

Poor cerebral inflammatory response in eIF2B knock-in mice: implications for the aetiology of vanishing white matter disease.

eIF2B 敲入小鼠脑部炎症反应不良：对消失性白质疾病病因学的启示

Quantitative single cell monitoring of protein synthesis at subcellular resolution using fluorescently labeled tRNA.

利用荧光标记的tRNA对蛋白质合成进行亚细胞分辨率的单细胞定量监测

Mitotic modulation of translation elongation factor 1 leads to hindered tRNA delivery to ribosomes

有丝分裂过程中翻译延伸因子1的调控导致tRNA向核糖体的递送受阻

A point mutation in translation initiation factor eIF2B leads to function--and time-specific changes in brain gene expression.

翻译起始因子 eIF2B 的点突变导致大脑基因表达的功能和时间特异性变化