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標(biāo)題: Titlebook: RNA Metabolism in Neurodegenerative Diseases; Rita Sattler,Christopher J. Donnelly Book 2018 Springer International Publishing AG, part of [打印本頁(yè)]

作者: 宣告無(wú)效    時(shí)間: 2025-3-21 19:15
書目名稱RNA Metabolism in Neurodegenerative Diseases影響因子(影響力)




書目名稱RNA Metabolism in Neurodegenerative Diseases影響因子(影響力)學(xué)科排名




書目名稱RNA Metabolism in Neurodegenerative Diseases網(wǎng)絡(luò)公開(kāi)度




書目名稱RNA Metabolism in Neurodegenerative Diseases網(wǎng)絡(luò)公開(kāi)度學(xué)科排名




書目名稱RNA Metabolism in Neurodegenerative Diseases被引頻次




書目名稱RNA Metabolism in Neurodegenerative Diseases被引頻次學(xué)科排名




書目名稱RNA Metabolism in Neurodegenerative Diseases年度引用




書目名稱RNA Metabolism in Neurodegenerative Diseases年度引用學(xué)科排名




書目名稱RNA Metabolism in Neurodegenerative Diseases讀者反饋




書目名稱RNA Metabolism in Neurodegenerative Diseases讀者反饋學(xué)科排名





作者: 憤憤不平    時(shí)間: 2025-3-21 21:16

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Ashley Boehringer,Robert Bowserconductivity. In these studies, one grapples with the usual problems governing accuracy in small molecules: the completeness of the one- and many-electron basis sets. In addition, the appropriateness of the background potential and the convergence of the results as a function of cluster size must be
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978-3-030-07832-4Springer International Publishing AG, part of Springer Nature 2018
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Rita Sattler,Christopher J. DonnellyLooks at major neurodegenerative diseases affected by RNA toxicity.Explores multiple disease mechanisms triggered by RNA metabolism.Taken together, the chapters provide insight on potential therapeuti
作者: 捕鯨魚叉    時(shí)間: 2025-3-24 21:49

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作者: Tremor    時(shí)間: 2025-3-25 15:23
RNA Nucleocytoplasmic Transport Defects in Neurodegenerative Diseases,s into the cytoplasm. This is accomplished by a variety of transport complexes that contain either a member of the exportin family of proteins and translocation fueled by GTP hydrolysis or in the case of mRNA by complexes containing the export protein NXF1. Recent evidence indicates that RNA transpo
作者: Ingredient    時(shí)間: 2025-3-25 19:49

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作者: 仔細(xì)閱讀    時(shí)間: 2025-3-26 02:00

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Senataxin, A Novel Helicase at the Interface of RNA Transcriptome Regulation and Neurobiology: Fromave established the importance of SETX for neural function, as recessive mutations in the . gene cause Ataxia with Oculomotor Apraxia type 2 (AOA2) (OMIM: 606002), which is the third most common form of recessive ataxia, after Friedreich’s ataxia and Ataxia-Telangiectasia. In addition, rare, dominan
作者: callous    時(shí)間: 2025-3-26 19:29
Lost in Translation: Evidence for Protein Synthesis Deficits in ALS/FTD and Related Neurodegeneratiit. Although the complexity provides robust regulation of proteostasis, it also offers several opportunities for translational dysregulation, as has been observed in many neurodegenerative disorders. Defective mRNA localization, mRNA sequatration, inhibited ribogenesis, mutant tRNA synthetases, and
作者: 大都市    時(shí)間: 2025-3-27 01:02
Mechanism of Splicing Regulation of Spinal Muscular Atrophy Genes, have been implicated in the regulation of . exon 7 splicing. There is evidence to support that multiple exons of . are alternatively spliced during oxidative stress, which is associated with a growing number of pathological conditions. Here, we provide the most up to date account of the mechanism of splicing regulation of the . genes.
作者: indicate    時(shí)間: 2025-3-27 04:15
RNA Nucleocytoplasmic Transport Defects in Neurodegenerative Diseases,ation and aggregation of the nucleoporins that make up the nuclear pore; alterations in the Ran gradient and the proteins that control it which impacts exportin based nuclear export; and alterations of proteins that are required for the export of mRNA leading nuclear accumulation of mRNA.
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作者: 600    時(shí)間: 2025-3-27 17:05

作者: immunity    時(shí)間: 2025-3-27 18:11
Stress Granules and ALS: A Case of Causation or Correlation?, summarize current understanding of stress granules, focusing on assembly and clearance. We also assess the evidence linking alterations in stress granule formation and dynamics to ALS protein aggregates and disease pathology.
作者: CRAB    時(shí)間: 2025-3-27 22:39

作者: foreign    時(shí)間: 2025-3-28 04:19

作者: 向宇宙    時(shí)間: 2025-3-28 09:19
RNP Assembly Defects in Spinal Muscular Atrophy, important role in an extensive and diverse set of cellular processes that regulate neuronal growth, differentiation, and the maturation and plasticity of synapses. This review discusses the role of SMN in RNP assembly and localization, focusing on molecular defects that affect mRNA processing and may contribute to SMA pathology.
作者: 維持    時(shí)間: 2025-3-28 14:12

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作者: 世俗    時(shí)間: 2025-3-28 20:18
Senataxin, A Novel Helicase at the Interface of RNA Transcriptome Regulation and Neurobiology: From pathology uncovered in familial ALS. Like other RNA processing proteins linked to ALS, the basis for SETX gain-of-function motor neuron toxicity remains ill-defined. Studies of yeast Sen1p and mammalian SETX protein have revealed a range of important RNA regulatory functions, including resolution o
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作者: confederacy    時(shí)間: 2025-3-29 06:51

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Mark T. W. Ebbert,Rebecca J. Lank,Veronique V. Belzileters for models which can be extended to larger clusters have also been the focus of SCF/CI and DFT studies. This bootstrap approach is pragmatic, but unsettling. There is always the worry that in mapping the results onto a simpler model, one throws out the baby with the bathwater. In the current c




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