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。Ribosome stalling induced by mutation of a CNS-specific tRNA causes neurodegeneration
Ryuta Ishimura et al.
SCIENCE (2014)
Defective i6A37 Modification of Mitochondrial and Cytosolic tRNAs Results from Pathogenic Mutations in TRIT1 and Its Substrate tRNA
John W. Yarham et al.
PLOS GENETICS (2014)
Mutation in ADAT3, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus
Anas M. Alazami et al.
JOURNAL OF MEDICAL GENETICS (2013)
Lack of tRNA Modification Isopentenyl-A37 Alters mRNA Decoding and Causes Metabolic Deficiencies in Fission Yeast
Tek N. Lamichhane et al.
MOLECULAR AND CELLULAR BIOLOGY (2013)
MODOMICS: a database of RNA modification pathways-2013 update
Magdalena A. Machnicka et al.
NUCLEIC ACIDS RESEARCH (2013)
tRNAHis 5-methylcytidine levels increase in response to several growth arrest conditions in Saccharomyces cerevisiae
Melanie A. Preston et al.
RNA (2013)
Modification of tRNAUUULys by Elongator Is Essential for Efficient Translation of Stress mRNAs
Jorge Fernandez-Vazquez et al.
PLOS GENETICS (2013)
Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability
Muzammil Ahmad Khan et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2012)
Mutations in NSUN2 Cause Autosomal-Recessive Intellectual Disability
Lia Abbasi-Moheb et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2012)
The Revised Classification of Eukaryotes
Sina M. Adl et al.
JOURNAL OF EUKARYOTIC MICROBIOLOGY (2012)
Whole exome sequencing identifies a splicing mutation in NSUN2 as a cause of a Dubowitz-like syndrome
Fernando Jose Martinez et al.
JOURNAL OF MEDICAL GENETICS (2012)
A Genetic Investigation of the KEOPS Complex in Halophilic Archaea
Adit Naor et al.
PLOS ONE (2012)
Yeast Trm7 interacts with distinct proteins for critical modifications of the tRNAPhe anticodon loop
Michael P. Guy et al.
RNA (2012)
Reprogramming of tRNA modifications controls the oxidative stress response by codon-biased translation of proteins
Clement T. Y. Chan et al.
NATURE COMMUNICATIONS (2012)
The highly conserved KEOPS/EKC complex is essential for a universal tRNA modification, t6A
Madhusudhan Srinivasan et al.
EMBO JOURNAL (2011)
A role for the universal Kae1/Qri7/YgjD (COG0533) family in tRNA modification
Basma El Yacoubi et al.
EMBO JOURNAL (2011)
Two novel WD40 domain-containing proteins, Ere1 and Ere2, function in the retromer-mediated endosomal recycling pathway
Yufeng Shi et al.
MOLECULAR BIOLOGY OF THE CELL (2011)
Deep sequencing reveals 50 novel genes for recessive cognitive disorders
Hossein Najmabadi et al.
NATURE (2011)
Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3
Zi-Jiang Chen et al.
NATURE GENETICS (2011)
Unexpected Accumulation of ncm5U and ncm5s2U in a trm9 Mutant Suggests an Additional Step in the Synthesis of mcm5U and mcm5s2U
Changchun Chen et al.
PLOS ONE (2011)
2′-O-methylation of the wobble residue of elongator pre-tRNAMet in Haloferax volcanii is guided by a box C/D RNA containing unique features
Archi Joardar et al.
RNA BIOLOGY (2011)
Elongator Complex Influences Telomeric Gene Silencing and DNA Damage Response by Its Role in Wobble Uridine tRNA Modification
Changchun Chen et al.
PLOS GENETICS (2011)
Do all modifications benefit all tRNAs?
Eric M. Phizicky et al.
FEBS LETTERS (2010)
Mammalian ALKBH8 Possesses tRNA Methyltransferase Activity Required for the Biogenesis of Multiple Wobble Uridine Modifications Implicated in Translational Decoding
Lene Songe-Moller et al.
MOLECULAR AND CELLULAR BIOLOGY (2010)
Human AlkB Homolog ABH8 Is a tRNA Methyltransferase Required for Wobble Uridine Modification and DNA Damage Survival
Dragony Fu et al.
MOLECULAR AND CELLULAR BIOLOGY (2010)
A role for the elongator complex in zygotic paternal genome demethylation
Yuki Okada et al.
NATURE (2010)
Analysis of a genome-wide set of gene deletions in the fission yeast Schizosaccharomyces pombe
Dong-Uk Kim et al.
NATURE BIOTECHNOLOGY (2010)
Armadillo-repeat protein functions: questions for little creatures
Rita Tewari et al.
TRENDS IN CELL BIOLOGY (2010)
A Quantitative Systems Approach Reveals Dynamic Control of tRNA Modifications during Cellular Stress
Clement T. Y. Chan et al.
PLOS GENETICS (2010)
Elongator Controls the Migration and Differentiation of Cortical Neurons through Acetylation of α-Tubulin
Catherine Creppe et al.
CELL (2009)
A loss-of-function mutation in the FTSJ1 gene causes nonsyndromic X-linked mental retardation in a Japanese family
Kyoko Takano et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2008)
Degradation of several hypomodified mature tRNA species in Saccharomyces cerevisiae is mediated by Met22 and the 5′-3′ exonucleases Rat1 and Xrn1
Irina Chernyakov et al.
GENES & DEVELOPMENT (2008)
Chromatin-associated genes protect the yeast genome from Ty1 insertional mutagenesis
Katherine M. Nyswaner et al.
GENETICS (2008)
Eukaryotic wobble uridine modifications promote a functionally redundant decoding system
Marcus J. O. Johansson et al.
MOLECULAR AND CELLULAR BIOLOGY (2008)
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
Eleftheria Zeggini et al.
NATURE GENETICS (2008)
Mitochondrial Dysfunction Increases Oxidative Stress and Decreases Chronological Life Span in Fission Yeast
Alice Zuin et al.
PLOS ONE (2008)
Trm9-catalyzed tRNA modifications link translation to the DNA damage response
Ulrike Begley et al.
MOLECULAR CELL (2007)
Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region
Guy Froyen et al.
HUMAN GENETICS (2007)
Structural and evolutionary bioinformatics of the SPOUT superfamily of methyltransferases
Karolina L. Tkaczuk et al.
BMC BIOINFORMATICS (2007)
tRNA's wobble decoding of the genome: 40 years of modification
Paul F. Agris et al.
JOURNAL OF MOLECULAR BIOLOGY (2007)
Elevated levels of two tRNA species bypass the requirement for elongator complex in transcription and exocytosis
Anders Esberg et al.
MOLECULAR CELL (2006)
Biosynthesis of wybutosine, a hyper-modified nucleoside in eukaryotic phenylalanine tRNA
Akiko Noma et al.
EMBO JOURNAL (2006)
Rapid tRNA decay can result from lack of nonessential modifications
A Alexandrov et al.
MOLECULAR CELL (2006)
New genes with roles in the C-elegans embryo revealed using RNAi of ovary-enriched ORFeome clones
AG Fernandez et al.
GENOME RESEARCH (2005)
A splice site mutation in the methyltransferase gene FTSJ1 in Xp11.23 is associated with non-syndromic mental retardation in a large Belgian family (MRX9)
J Ramser et al.
JOURNAL OF MEDICAL GENETICS (2004)
Mutations in the FTSJ1 gene coding for a novel S-adenosylmethionine- binding protein cause nonsyndromic X-linked mental retardation
K Freude et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Nuclear surveillance and degradation of hypomodified initiator tRNAMet in S-cerevisiae
S Kadaba et al.
GENES & DEVELOPMENT (2004)
Novel methyltransferase for modified uridine residues at the wobble position of tRNA
HR Kalhor et al.
MOLECULAR AND CELLULAR BIOLOGY (2003)
Identification of a gene rearranged by 2p21 aberrations in thyroid adenomas
V Rippe et al.
ONCOGENE (2003)
Identification of the yeast gene encoding the tRNA m1G methyltransferase responsible for modification at position 9
JE Jackman et al.
RNA (2003)
The origin and evolution of model organisms
SB Hedges
NATURE REVIEWS GENETICS (2002)
tadA, an essential tRNA-specific adenosine deaminase from Escherichia coli
J Wolf et al.
EMBO JOURNAL (2002)
Trm7p catalyses the formation of two 2′-O-methylriboses in yeast tRNA anticodon loop
L Pintard et al.
EMBO JOURNAL (2002)
Improvement of reading frame maintenance is a common function for several tRNA modifications
J Urbonavicius et al.
EMBO JOURNAL (2001)
Familial dysautonomia is caused by mutations of the IKAP gene
SL Anderson et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
The human tRNA(m22G26)dimethyltransferase:: functional expression and characterization of a cloned hTRM1 gene
JM Liu et al.
NUCLEIC ACIDS RESEARCH (2000)