A disease-causing point mutation in human mitochondrial tRNAMet results in tRNA misfolding leading to defects in translational initiation and elongation.
about
A Cytidine Deaminase Edits C to U in Transfer RNAs in ArchaeaAnalysis of the functional consequences of lethal mutations in mitochondrial translational elongation factorsNative tertiary structure and nucleoside modifications suppress tRNA's intrinsic ability to activate the innate immune sensor PKR.Mechanism of protein biosynthesis in mammalian mitochondria.The human mitochondrial tRNAMet: structure/function relationship of a unique modification in the decoding of unconventional codons.A deafness-associated tRNAAsp mutation alters the m1G37 modification, aminoacylation and stability of tRNAAsp and mitochondrial function.RNA modification enzyme TruB is a tRNA chaperone.Emerging roles of tRNA in adaptive translation, signalling dynamics and disease.Inhibiting translation elongation can aid genome duplication in Escherichia coli.tRNA Modifications: Impact on Structure and Thermal Adaptation.Altered mitochondrial function and genome frequency post exposure to γ-radiation and bystander factors.Structure and Dynamics of tRNA Containing Core Substitutions
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P2860
A disease-causing point mutation in human mitochondrial tRNAMet results in tRNA misfolding leading to defects in translational initiation and elongation.
description
2008 nî lūn-bûn
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2008年の論文
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2008年論文
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2008年論文
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2008年論文
@zh-hk
2008年論文
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2008年論文
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2008年论文
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2008年论文
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2008年论文
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name
A disease-causing point mutati ...... nal initiation and elongation.
@en
type
label
A disease-causing point mutati ...... nal initiation and elongation.
@en
prefLabel
A disease-causing point mutati ...... nal initiation and elongation.
@en
P2093
P2860
P356
P1476
A disease-causing point mutati ...... nal initiation and elongation.
@en
P2093
Christie N Jones
Christopher I Jones
Linda L Spremulli
Paul F Agris
William D Graham
P2860
P304
34445-34456
P356
10.1074/JBC.M806992200
P407
P577
2008-10-03T00:00:00Z