4.8 Article

A deafness-associated tRNA mutation caused pleiotropic effects on the m1G37 modification, processing, stability and aminoacylation of tRNAIIe and mitochondrial translation

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Review Neurosciences

Pathology and mechanisms of cochlear aging

Elizabeth M. Keithley

JOURNAL OF NEUROSCIENCE RESEARCH (2020)

Article Cell Biology

Mitochondrial tRNA mutations in 887 Chinese subjects with hearing loss

Jing Zheng et al.

MITOCHONDRION (2020)

Article Biochemistry & Molecular Biology

Complex I mutations synergize to worsen the phenotypic expression of Leber's hereditary optic neuropathy

Yanchun Ji et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2020)

Article Medicine, Research & Experimental

PRICKLE3 linked to ATPase biogenesis manifested Leber's hereditary optic neuropathy

Jialing Yu et al.

JOURNAL OF CLINICAL INVESTIGATION (2020)

Article Multidisciplinary Sciences

Complete chemical structures of human mitochondrial tRNAs

Takeo Suzuki et al.

NATURE COMMUNICATIONS (2020)

Article Biochemistry & Molecular Biology

Matching tRNA modifications in humans to their known and predicted enzymes

Valerie de Crecy-Lagard et al.

NUCLEIC ACIDS RESEARCH (2019)

Article Multidisciplinary Sciences

Differential expression of human tRNA genes drives the abundance of tRNA-derived fragments

Adrian Gabriel Torres et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2019)

Article Biochemistry & Molecular Biology

Cytosine-5 RNA methylation links protein synthesis to cell metabolism

Nikoletta A. Gkatza et al.

PLOS BIOLOGY (2019)

Article Biochemistry & Molecular Biology

A coronary artery disease-associated tRNAThr mutation altered mitochondrial function, apoptosis and angiogenesis

Zidong Jia et al.

NUCLEIC ACIDS RESEARCH (2019)

Article Biochemistry & Molecular Biology

MODOMICS: a database of RNA modification pathways. 2017 update

Pietro Boccaletto et al.

NUCLEIC ACIDS RESEARCH (2018)

Article Biochemistry & Molecular Biology

Metabolic and chemical regulation of tRNA modification associated with taurine deficiency and human disease

Kana Asano et al.

NUCLEIC ACIDS RESEARCH (2018)

Article Multidisciplinary Sciences

CO2-sensitive tRNA modification associated with human mitochondrial disease

Huan Lin et al.

NATURE COMMUNICATIONS (2018)

Review Biochemistry & Molecular Biology

The mitochondrial epitranscriptome: the roles of RNA modifications in mitochondrial translation and human disease

Markus T. Bohnsack et al.

CELLULAR AND MOLECULAR LIFE SCIENCES (2018)

Review Biochemistry & Molecular Biology

The modified base isopentenyladenosine and its derivatives in tRNA

Ulrich Schweizer et al.

RNA BIOLOGY (2017)

Review Cell Biology

Cleaning House: Selective Autophagy of Organelles

Allyson L. Anding et al.

DEVELOPMENTAL CELL (2017)

Review Biochemistry & Molecular Biology

Trm5 and TrmD: Two Enzymes from Distinct Origins Catalyze the Identical tRNA Modification, m1G37

Sakurako Goto-Ito et al.

BIOMOLECULES (2017)

Article Multidisciplinary Sciences

Deficient methylation and formylation of mt- tRNAMet wobble cytosine in a patient carrying mutations in NSUN3

Lindsey Van Haute et al.

NATURE COMMUNICATIONS (2016)

Review Biochemistry & Molecular Biology

Mitochondrial degradation and energy metabolism

Su Melser et al.

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2015)

Article Biochemistry & Molecular Biology

Oxidative stress in inherited mitochondrial diseases

Genki Hayashi et al.

FREE RADICAL BIOLOGY AND MEDICINE (2015)

Article Biochemistry & Molecular Biology

A deafness-associated tRNAHis mutation alters the mitochondrial function, ROS production and membrane potential

Shasha Gong et al.

NUCLEIC ACIDS RESEARCH (2014)

Review Genetics & Heredity

Transfer RNA and human disease

Jamie A. Abbott et al.

FRONTIERS IN GENETICS (2014)

Review Genetics & Heredity

Methylated nucleosides in tRNA and tRNA methyltransferases

Hiroyuki Hori

FRONTIERS IN GENETICS (2014)

Article Biochemistry & Molecular Biology

A cyclic form of N6-threonylcarbamoyladenosine as a widely distributed tRNA hypermodification

Kenjyo Miyauchi et al.

NATURE CHEMICAL BIOLOGY (2013)

Article Genetics & Heredity

Mutations of the Mitochondrial-tRNA Modifier MTO1 Cause Hypertrophic Cardiomyopathy and Lactic Acidosis

Daniele Ghezzi et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2012)

Review Genetics & Heredity

Biosynthesis and Function of Posttranscriptional Modifications of Transfer RNAs

Basma El Yacoubi et al.

ANNUAL REVIEW OF GENETICS, VOL 46 (2012)

Article Biochemistry & Molecular Biology

Mitochondrial Stress Engages E2F1 Apoptotic Signaling to Cause Deafness

Nuno Raimundo et al.

Article Genetics & Heredity

Novel mitochondrial DNA mutations responsible for maternally inherited nonsyndromic hearing loss

Nicolas Gutierrez Cortes et al.

HUMAN MUTATION (2012)

Review Biochemistry & Molecular Biology

Physiological Roles of Mitochondrial Reactive Oxygen Species

Laura A. Sena et al.

MOLECULAR CELL (2012)

Review Genetics & Heredity

Human Mitochondrial tRNAs: Biogenesis, Function, Structural Aspects, and Diseases

Tsutomu Suzuki et al.

ANNUAL REVIEW OF GENETICS, VOL 45 (2011)

Article Biochemistry & Molecular Biology

Assessing bioenergetic function in response to oxidative stress by metabolic profiling

Brian P. Dranka et al.

FREE RADICAL BIOLOGY AND MEDICINE (2011)

Review Cell Biology

Mechanisms of mitophagy

Richard J. Youle et al.

NATURE REVIEWS MOLECULAR CELL BIOLOGY (2011)

Article Biochemistry & Molecular Biology

Nucleotide modifications and tRNA anticodon-mRNA codon interactions on the ribosome

Olof Allner et al.

Review Cell Biology

tRNA biology charges to the front

Eric M. Phizicky et al.

GENES & DEVELOPMENT (2010)

Article Genetics & Heredity

Acute Infantile Liver Failure Due to Mutations in the TRMU Gene

Avraham Zeharia et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2009)

Editorial Material Cell Biology

A novel link between autophagy and the ubiquitin-proteasome system

Viktor I. Korolchuk et al.

AUTOPHAGY (2009)

Article Biochemistry & Molecular Biology

Maternally inherited hypertension is associated with the mitochondrial tRNAIle A4295G mutation in a Chinese family

Zongbin Li et al.

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2008)

Article Biochemistry & Molecular Biology

Mistranslation-induced protein misfolding as a dominant constraint on coding-sequence evolution

D. Allan Drummond et al.

Article Biochemistry & Molecular Biology

Eukaryotic wobble uridine modifications promote a functionally redundant decoding system

Marcus J. O. Johansson et al.

MOLECULAR AND CELLULAR BIOLOGY (2008)

Article Biochemistry & Molecular Biology

Crystal Structure of archaeal tRNA(m1G37)methyltransferase aTrm5

Sakurako Goto-Ito et al.

PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS (2008)

Article Biochemistry & Molecular Biology

An assembled complex IV maintains the stability and activity of complex I in mammalian mitochondria

Youfen Li et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2007)

Article Genetics & Heredity

Tissue-specific differences in human transfer RNA expression

Kimberly A. Dittmar et al.

PLOS GENETICS (2006)

Review Chemistry, Multidisciplinary

The Amber biomolecular simulation programs

DA Case et al.

JOURNAL OF COMPUTATIONAL CHEMISTRY (2005)

Article Multidisciplinary Sciences

Specific correlation between the wobble modification deficiency in mutant tRNAs and the clinical features of a human mitochondrial disease

Y Kirino et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)

Article Biochemistry & Molecular Biology

Reduction of mitochondrial tRNA Leu(UUR) aminoacylation by some MELAS-associated mutations

R Hao et al.

FEBS LETTERS (2004)

Article Biochemistry & Molecular Biology

The role of modifications in codon discrimination by tRNALys UUU

FV Murphy et al.

NATURE STRUCTURAL & MOLECULAR BIOLOGY (2004)

Article Chemistry, Multidisciplinary

UCSF chimera - A visualization system for exploratory research and analysis

EF Pettersen et al.

JOURNAL OF COMPUTATIONAL CHEMISTRY (2004)