标题
Matching tRNA modifications in humans to their known and predicted enzymes
作者
关键词
-
出版物
NUCLEIC ACIDS RESEARCH
Volume 47, Issue 5, Pages 2143-2159
出版商
Oxford University Press (OUP)
发表日期
2019-01-11
DOI
10.1093/nar/gkz011
参考文献
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。- Pseudouridylation of tRNA-Derived Fragments Steers Translational Control in Stem Cells
- (2018) Nicola Guzzi et al. CELL
- Speech and language delay in a patient with WDR4 mutations
- (2018) Xiang Chen et al. European Journal of Medical Genetics
- Elongator subunit 3 (ELP3) modifies ALS through tRNA modification
- (2018) Andre Bento-Abreu et al. HUMAN MOLECULAR GENETICS
- Roles of Mitochondrial 17β-Hydroxysteroid Dehydrogenase Type 10 in Alzheimer’s Disease
- (2018) Xue-Ying He et al. JOURNAL OF ALZHEIMERS DISEASE
- The Uba4 domain interplay is mediated via a thioester that is critical for tRNA thiolation through Urm1 thiocarboxylation
- (2018) Martin Termathe et al. NUCLEIC ACIDS RESEARCH
- Metabolic and chemical regulation of tRNA modification associated with taurine deficiency and human disease
- (2018) Kana Asano et al. NUCLEIC ACIDS RESEARCH
- CO2-sensitive tRNA modification associated with human mitochondrial disease
- (2018) Huan Lin et al. Nature Communications
- RNA cytosine methylation and methyltransferases mediate chromatin organization and 5-azacytidine response and resistance in leukaemia
- (2018) Jason X. Cheng et al. Nature Communications
- Alcohol intake interacts with CDKAL1 ,HHEX and OAS3 genetic variants, associated with insulin secretion, to increase the risk of type 2 diabetes in Korean adults
- (2018) Sunmin Park et al. ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH
- Mutations in WDR4 as a new cause of Galloway-Mowat syndrome
- (2018) Daniela A. Braun et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- A familial case of Galloway-Mowat syndrome due to a novel TP53RK mutation: a case report
- (2018) Hye Sun Hyun et al. BMC Medical Genetics
- Queuosine‐modified tRNAs confer nutritional control of protein translation
- (2018) Francesca Tuorto et al. EMBO JOURNAL
- Codon-specific translation reprogramming promotes resistance to targeted therapy
- (2018) Francesca Rapino et al. NATURE
- Pancreatic β-cell tRNA hypomethylation and fragmentation link TRMT10A deficiency with diabetes
- (2018) Cristina Cosentino et al. NUCLEIC ACIDS RESEARCH
- Nephrological and urological complications of homozygous c.974G>A (p.Arg325Gln) OSGEP mutations
- (2018) Peter Zhan Tao Wang et al. PEDIATRIC NEPHROLOGY
- Prenatal diagnosis of a 3.2-Mb 2p16.1-p15 duplication associated with familial intellectual disability
- (2018) Chih-Ping Chen et al. Taiwanese Journal of Obstetrics & Gynecology
- Body mass index modulates the association between CDKAL1 rs10946398 variant and type 2 diabetes among Taiwanese women
- (2018) Oswald Ndi Nfor et al. Scientific Reports
- Multiple short-chain dehydrogenases/reductases are regulated in pathological cardiac hypertrophy
- (2018) Elise Roussel et al. FEBS Open Bio
- Mutations in the tRNA methyltransferase 1 gene TRMT1 cause congenital microcephaly, isolated inferior vermian hypoplasia and cystic leukomalacia in addition to intellectual disability
- (2018) Kathrin Blaesius et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- AlkAniline-Seq: Profiling of m7 G and m3 C RNA Modifications at Single Nucleotide Resolution
- (2018) Virginie Marchand et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- A null variant in PUS3 confirms its involvement in intellectual disability and further delineates the associated neurodevelopmental disease
- (2018) Hanadi A. Abdelrahman et al. CLINICAL GENETICS
- Impact of tRNA Modifications and tRNA-Modifying Enzymes on Proteostasis and Human Disease
- (2018) Marisa Pereira et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- Recent topics: the diagnosis, molecular genesis, and treatment of mitochondrial diseases
- (2018) Kei Murayama et al. JOURNAL OF HUMAN GENETICS
- tRNA N6-adenosine threonylcarbamoyltransferase defect due to KAE1/TCS3 (OSGEP) mutation manifest by neurodegeneration and renal tubulopathy
- (2017) Simon Edvardson et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Structural asymmetry in the eukaryotic Elongator complex
- (2017) Maria I. Dauden et al. FEBS LETTERS
- The human tRNA-modifying protein, TRIT1, forms amyloid fibers in vitro
- (2017) T.J. Waller et al. GENE
- Matchmaking facilitates the diagnosis of an autosomal-recessive mitochondrial disease caused by biallelic mutation of the tRNA isopentenyltransferase (TRIT1 ) gene
- (2017) Kristin D. Kernohan et al. HUMAN MUTATION
- A hypertension-associated mitochondrial DNA mutation introduces an m1G37 modification into tRNAMet, altering its structure and function
- (2017) Mi Zhou et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Three distinct 3-methylcytidine (m 3 C) methyltransferases modify tRNA and mRNA in mice and humans
- (2017) Luang Xu et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- The Pseudouridine Synthase RPUSD4 Is an Essential Component of Mitochondrial RNA Granules
- (2017) Sofia Zaganelli et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- A ROR1–HER3–lncRNA signalling axis modulates the Hippo–YAP pathway to regulate bone metastasis
- (2017) Chunlai Li et al. NATURE CELL BIOLOGY
- Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly
- (2017) Daniela A Braun et al. NATURE GENETICS
- The emerging complexity of the tRNA world: mammalian tRNAs beyond protein synthesis
- (2017) Paul Schimmel NATURE REVIEWS MOLECULAR CELL BIOLOGY
- Cdk5rap1-mediated 2-methylthio-N6-isopentenyladenosine modification is absent from nuclear-derived RNA species
- (2017) Md. Fakruddin et al. NUCLEIC ACIDS RESEARCH
- ALKBH1 is an RNA dioxygenase responsible for cytoplasmic and mitochondrial tRNA modifications
- (2017) Layla Kawarada et al. NUCLEIC ACIDS RESEARCH
- MODOMICS: a database of RNA modification pathways. 2017 update
- (2017) Pietro Boccaletto et al. NUCLEIC ACIDS RESEARCH
- tRNA-derived small RNAs target transposable element transcripts
- (2017) German Martinez et al. NUCLEIC ACIDS RESEARCH
- Frameshift Mutations in Repeat Sequences of ANK3, HACD4, TCP10L, TP53BP1, MFN1, LCMT2, RNMT, TRMT6, METTL8 and METTL16 Genes in Colon Cancers
- (2017) Su Yeon Yeon et al. PATHOLOGY & ONCOLOGY RESEARCH
- Wobble uridine modifications–a reason to live, a reason to die?!
- (2017) Raffael Schaffrath et al. RNA Biology
- The RNA modification landscape in human disease
- (2017) Nicky Jonkhout et al. RNA
- Reciprocal amplification of caspase-3 activity by nuclear export of a putative human RNA-modifying protein, PUS10 during TRAIL-induced apoptosis
- (2017) Sujata Jana et al. Cell Death & Disease
- Characterizing Expression and Processing of Precursor and Mature Human tRNAs by Hydro-tRNAseq and PAR-CLIP
- (2017) Tasos Gogakos et al. Cell Reports
- Lost in Translation: Defects in Transfer RNA Modifications and Neurological Disorders
- (2017) Andrea Bednářová et al. Frontiers in Molecular Neuroscience
- Cdkal1, a type 2 diabetes susceptibility gene, regulates mitochondrial function in adipose tissue
- (2017) Colin J. Palmer et al. Molecular Metabolism
- Physical Interactions and Expression Quantitative Traits Loci Identify Regulatory Connections for Obesity and Type 2 Diabetes Associated SNPs
- (2017) Tayaza Fadason et al. Frontiers in Genetics
- Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies
- (2016) Metodi D. Metodiev et al. AMERICAN JOURNAL OF HUMAN GENETICS
- The syndrome dysmorphic facies, renal agenesis, ambiguous genitalia, microcephaly, polydactyly and lissencephaly (DREAM-PL): Report of two additional patients
- (2016) Ranad Shaheen et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- ADAT3-related intellectual disability: Further delineation of the phenotype
- (2016) Ayman W. El-Hattab et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Posttranscriptional methylation of transfer and ribosomal RNA in stress response pathways, cell differentiation, and cancer
- (2016) Martyna C. Popis et al. CURRENT OPINION IN ONCOLOGY
- tRNA methyltransferase homologue geneTRMT10Amutation in young adult-onset diabetes with intellectual disability, microcephaly and epilepsy
- (2016) T. W. Yew et al. DIABETIC MEDICINE
- NSUN3 and ABH1 modify the wobble position of mt‐tRNAMetto expand codon recognition in mitochondrial translation
- (2016) Sara Haag et al. EMBO JOURNAL
- A pseudouridine synthase module is essential for mitochondrial protein synthesis and cell viability
- (2016) Hana Antonicka et al. EMBO REPORTS
- A homozygous truncating mutation in PUS3 expands the role of tRNA modification in normal cognition
- (2016) Ranad Shaheen et al. HUMAN GENETICS
- Elp3 links tRNA modification to IRES-dependent translation of LEF1 to sustain metastasis in breast cancer
- (2016) Sylvain Delaunay et al. JOURNAL OF EXPERIMENTAL MEDICINE
- A mutation in the THG1L gene in a family with cerebellar ataxia and developmental delay
- (2016) Simon Edvardson et al. NEUROGENETICS
- An integrated, structure- and energy-based view of the genetic code
- (2016) Henri Grosjean et al. NUCLEIC ACIDS RESEARCH
- Ribosome biogenesis factor Tsr3 is the aminocarboxypropyl transferase responsible for 18S rRNA hypermodification in yeast and humans
- (2016) Britta Meyer et al. NUCLEIC ACIDS RESEARCH
- The BioGRID interaction database: 2017 update
- (2016) Andrew Chatr-aryamontri et al. NUCLEIC ACIDS RESEARCH
- RNA modification enzyme TruB is a tRNA chaperone
- (2016) Laura Carole Keffer-Wilkes et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- tRNA base methylation identification and quantification via high-throughput sequencing
- (2016) Wesley C. Clark et al. RNA
- Small RNA Modifications: Integral to Function and Disease
- (2016) Xudong Zhang et al. TRENDS IN MOLECULAR MEDICINE
- Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
- (2016) Fergus J. Couch et al. Nature Communications
- Deficient methylation and formylation of mt-tRNAMet wobble cytosine in a patient carrying mutations in NSUN3
- (2016) Lindsey Van Haute et al. Nature Communications
- Identification of breast cancer candidate genes using gene co-expression and protein-protein interaction information
- (2016) Zhenyu Yue et al. Oncotarget
- Overexpression of NSUN2 by DNA hypomethylation is associated with metastatic progression in human breast cancer
- (2016) Jie Yi et al. Oncotarget
- Deposition of 5-Methylcytosine on Enhancer RNAs Enables the Coactivator Function of PGC-1α
- (2016) Francesca Aguilo et al. Cell Reports
- Going global: the new era of mapping modifications in RNA
- (2016) Patrick A. Limbach et al. Wiley Interdisciplinary Reviews-RNA
- TRMT5 Mutations Cause a Defect in Post-transcriptional Modification of Mitochondrial tRNA Associated with Multiple Respiratory-Chain Deficiencies
- (2015) Christopher A. Powell et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Homozygous deletion ofTRMT10Aas part of a contiguous gene deletion in a syndrome of failure to thrive, delayed puberty, intellectual disability and diabetes mellitus
- (2015) Amnon Zung et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Genetic variation affects congenital heart defect susceptibility in offspring exposed to maternal tobacco use
- (2015) Xinyu Tang et al. BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY
- Endogenous tRNA-Derived Fragments Suppress Breast Cancer Progression via YBX1 Displacement
- (2015) Hani Goodarzi et al. CELL
- Cdk5rap1-Mediated 2-Methylthio Modification of Mitochondrial tRNAs Governs Protein Translation and Contributes to Myopathy in Mice and Humans
- (2015) Fan-Yan Wei et al. Cell Metabolism
- Accelerating matchmaking of novel dysmorphology syndromes through clinical and genomic characterization of a large cohort
- (2015) Ranad Shaheen et al. GENETICS IN MEDICINE
- Microdeletions ofELP4Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation
- (2015) Laura Addis et al. HUMAN MUTATION
- Defects in tRNA Anticodon Loop 2′-O-Methylation Are Implicated in Nonsyndromic X-Linked Intellectual Disability due to Mutations inFTSJ1
- (2015) Michael P. Guy et al. HUMAN MUTATION
- Elp3 drives Wnt-dependent tumor initiation and regeneration in the intestine
- (2015) Aurélie Ladang et al. JOURNAL OF EXPERIMENTAL MEDICINE
- A Novel Single-Nucleotide Deletion (c.1020delA) in NSUN2 Causes Intellectual Disability in an Emirati Child
- (2015) Makanko Komara et al. JOURNAL OF MOLECULAR NEUROSCIENCE
- Targeted exploration and analysis of large cross-platform human transcriptomic compendia
- (2015) Qian Zhu et al. NATURE METHODS
- Efficient and quantitative high-throughput tRNA sequencing
- (2015) Guanqun Zheng et al. NATURE METHODS
- ARM-seq: AlkB-facilitated RNA methylation sequencing reveals a complex landscape of modified tRNA fragments
- (2015) Aaron E Cozen et al. NATURE METHODS
- Alzheimer's disease is associated with altered expression of genes involved in immune response and mitochondrial processes in astrocytes
- (2015) Shobana Sekar et al. NEUROBIOLOGY OF AGING
- GtRNAdb 2.0: an expanded database of transfer RNA genes identified in complete and draft genomes
- (2015) Patricia P. Chan et al. NUCLEIC ACIDS RESEARCH
- Structural and functional insights into tRNA binding and adenosine N1-methylation by an archaeal Trm10 homologue
- (2015) Bart Van Laer et al. NUCLEIC ACIDS RESEARCH
- MitoCarta2.0: an updated inventory of mammalian mitochondrial proteins
- (2015) Sarah E. Calvo et al. NUCLEIC ACIDS RESEARCH
- Database resources of the National Center for Biotechnology Information
- (2015) NUCLEIC ACIDS RESEARCH
- TRM6/61 connects PKCα with translational control through tRNAiMet stabilization: impact on tumorigenesis
- (2015) F Macari et al. ONCOGENE
- A common variant in the CLDN7/ELP5 locus predicts adiponectin change with lifestyle intervention and improved fitness in obese individuals with diabetes
- (2015) L. Maria Belalcazar et al. PHYSIOLOGICAL GENOMICS
- Rectifier of aberrant mRNA splicing recovers tRNA modification in familial dysautonomia
- (2015) Mayumi Yoshida et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The Queuine Micronutrient: Charting a Course from Microbe to Man
- (2015) Claire Fergus et al. Nutrients
- Genetic variation affects congenital heart defect susceptibility in offspring exposed to maternal tobacco use
- (2015) Xinyu Tang et al. BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY
- The Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri Families
- (2015) Behzad Davarniya et al. PLoS One
- Concurrent Mutations in ATM and Genes Associated with Common γ Chain Signaling in Peripheral T Cell Lymphoma
- (2015) Haley M. Simpson et al. PLoS One
- Pseudouridine: Still mysterious, but never a fake (uridine)!
- (2015) Felix Spenkuch et al. RNA Biology
- Diversity of the biosynthesis pathway for threonylcarbamoyladenosine (t6A), a universal modification of tRNA
- (2015) Patrick C Thiaville et al. RNA Biology
- Convergent evolution of AUA decoding in bacteria and archaea
- (2015) Tsutomu Suzuki et al. RNA Biology
- Modify or die? - RNA modification defects in metazoans
- (2015) L Peter Sarin et al. RNA Biology
- Plant, Animal, and Fungal Micronutrient Queuosine Is Salvaged by Members of the DUF2419 Protein Family
- (2014) Rémi Zallot et al. ACS Chemical Biology
- Mutations in GTPBP3 Cause a Mitochondrial Translation Defect Associated with Hypertrophic Cardiomyopathy, Lactic Acidosis, and Encephalopathy
- (2014) Robert Kopajtich et al. AMERICAN JOURNAL OF HUMAN GENETICS
- GSK-3 -Regulated N-Acetyltransferase 10 Is Involved in Colorectal Cancer Invasion
- (2014) H. Zhang et al. CLINICAL CANCER RESEARCH
- Cross Kingdom Functional Conservation of the Core Universally Conserved Threonylcarbamoyladenosine tRNA Synthesis Enzymes
- (2014) Patrick C. Thiaville et al. EUKARYOTIC CELL
- The ROS-sensitive microRNA-9/9* controls the expression of mitochondrial tRNA-modifying enzymes and is involved in the molecular mechanism of MELAS syndrome
- (2014) Salvador Meseguer et al. HUMAN MOLECULAR GENETICS
- Use of Whole-Exome Sequencing to Determine the Genetic Basis of Multiple Mitochondrial Respiratory Chain Complex Deficiencies
- (2014) Robert W. Taylor et al. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- Long-term prospective clinical follow-up afterBRCA1/2presymptomatic testing:BRCA2risks higher than in adjusted retrospective studies
- (2014) D Gareth Evans et al. JOURNAL OF MEDICAL GENETICS
- TRMT10A dysfunction is associated with abnormalities in glucose homeostasis, short stature and microcephaly
- (2014) David Gillis et al. JOURNAL OF MEDICAL GENETICS
- The diphthamide modification pathway fromSaccharomyces cerevisiae- revisited
- (2014) Raffael Schaffrath et al. MOLECULAR MICROBIOLOGY
- A draft map of the human proteome
- (2014) Min-Sik Kim et al. NATURE
- An integrated genomics approach identifies drivers of proliferation in luminal-subtype human breast cancer
- (2014) Michael L Gatza et al. NATURE GENETICS
- Discovery of the β-barrel–type RNA methyltransferase responsible forN6-methylation ofN6-threonylcarbamoyladenosine in tRNAs
- (2014) Satoshi Kimura et al. NUCLEIC ACIDS RESEARCH
- Genenames.org: the HGNC resources in 2015
- (2014) Kristian A. Gray et al. NUCLEIC ACIDS RESEARCH
- The flavoprotein Mcap0476 (RlmFO) catalyzes m5U1939 modification inMycoplasma capricolum23S rRNA
- (2014) Carole Lartigue et al. NUCLEIC ACIDS RESEARCH
- A complete landscape of post-transcriptional modifications in mammalian mitochondrial tRNAs
- (2014) T. Suzuki et al. NUCLEIC ACIDS RESEARCH
- UniProt: a hub for protein information
- (2014) NUCLEIC ACIDS RESEARCH
- Ribosome stalling induced by mutation of a CNS-specific tRNA causes neurodegeneration
- (2014) R. Ishimura et al. SCIENCE
- Role of tRNA modifications in human diseases
- (2014) Adrian Gabriel Torres et al. TRENDS IN MOLECULAR MEDICINE
- Nuclear-encoded mitochondrial MTO1 and MRPL41 are regulated in an opposite epigenetic mode based on estrogen receptor status in breast cancer
- (2013) Tae Woo Kim et al. BMC CANCER
- Association of polymorphisms and haplotype in the region of TRIT1, MYCL1 and MFSD2A with the risk and clinicopathological features of gastric cancer in a southeast Chinese population
- (2013) S. Chen et al. CARCINOGENESIS
- Whole exome sequencing unravels disease-causing genes in consanguineous families in Qatar
- (2013) S. Fahiminiya et al. CLINICAL GENETICS
- Mutation inADAT3, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus
- (2013) Anas M Alazami et al. JOURNAL OF MEDICAL GENETICS
- PhylomeDB v4: zooming into the plurality of evolutionary histories of a genome
- (2013) Jaime Huerta-Cepas et al. NUCLEIC ACIDS RESEARCH
- Mod5 protein binds to tRNA gene complexes and affects local transcriptional silencing
- (2013) M. Pratt-Hyatt et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Role of forefinger and thumb loops in production of 54 and 55 in tRNAs by archaeal Pus10
- (2013) A. Joardar et al. RNA
- Loss of a Conserved tRNA Anticodon Modification Perturbs Cellular Signaling
- (2013) Boris Zinshteyn et al. PLoS Genetics
- tRNA Methyltransferase Homolog Gene TRMT10A Mutation in Young Onset Diabetes and Primary Microcephaly in Humans
- (2013) Mariana Igoillo-Esteve et al. PLoS Genetics
- Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability
- (2012) Muzammil Ahmad Khan et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Mutations of the Mitochondrial-tRNA Modifier MTO1 Cause Hypertrophic Cardiomyopathy and Lactic Acidosis
- (2012) Daniele Ghezzi et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability
- (2012) Lia Abbasi-Moheb et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Biosynthesis and Function of Posttranscriptional Modifications of Transfer RNAs
- (2012) Basma El Yacoubi et al. Annual Review of Genetics
- Risk-Association of DNA Methyltransferases Polymorphisms with Gastric Cancer in the Southern Chinese Population
- (2012) Xue-Xi Yang et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- Dual Role of the Molybdenum Cofactor Biosynthesis Protein MOCS3 in tRNA Thiolation and Molybdenum Cofactor Biosynthesis in Humans
- (2012) Mita Mullick Chowdhury et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- DERP6 (ELP5) and C3ORF75 (ELP6) Regulate Tumorigenicity and Migration of Melanoma Cells as Subunits of Elongator
- (2012) Pierre Close et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Identification of a functional variant in theKIF5A-CYP27B1-METTL1-FAM119Blocus associated with multiple sclerosis
- (2012) Antonio Alcina et al. JOURNAL OF MEDICAL GENETICS
- Whole exome sequencing identifies a splicing mutation inNSUN2as a cause of a Dubowitz-like syndrome
- (2012) Fernando Jose Martinez et al. JOURNAL OF MEDICAL GENETICS
- Associations between maternal genotypes and metabolites implicated in congenital heart defects
- (2012) Shimul Chowdhury et al. MOLECULAR GENETICS AND METABOLISM
- Crystal structures of the tRNA:m 2 G6 methyltransferase Trm14/TrmN from two domains of life
- (2012) Marcus Fislage et al. NUCLEIC ACIDS RESEARCH
- The human tRNA m5C methyltransferase Misu is multisite-specific
- (2012) Sylvie Auxilien et al. RNA Biology
- Genetic Variation Predicting Cisplatin Cytotoxicity Associated with Overall Survival in Lung Cancer Patients Receiving Platinum-Based Chemotherapy
- (2011) X.-L. Tan et al. CLINICAL CANCER RESEARCH
- Frequent Increased Gene Copy Number and High Protein Expression of tRNA (Cytosine-5-)-Methyltransferase (NSUN2) in Human Cancers
- (2011) Mayumi Okamoto et al. DNA AND CELL BIOLOGY
- Transfer RNA Methytransferases and Their Corresponding Modifications in Budding Yeast and Humans: Activities, Predications, and Potential Roles in Human Health
- (2011) William L. Towns et al. DNA AND CELL BIOLOGY
- Q8IYL2 is a candidate gene for the familial epilepsy syndrome of Partial Epilepsy with Pericentral Spikes (PEPS)
- (2011) Guy D. Leschziner et al. EPILEPSY RESEARCH
- Expression levels of the microRNA maturing microprocessor complex component DGCR8 and the RNA-induced silencing complex (RISC) components argonaute-1, argonaute-2, PACT, TARBP1, and TARBP2 in epithelial skin cancer
- (2011) Michael Sand et al. MOLECULAR CARCINOGENESIS
- Deep sequencing reveals 50 novel genes for recessive cognitive disorders
- (2011) Hossein Najmabadi et al. NATURE
- Unexpected Accumulation of ncm5U and ncm5s2U in a trm9 Mutant Suggests an Additional Step in the Synthesis of mcm5U and mcm5s2U
- (2011) Changchun Chen et al. PLoS One
- RNA methylation by Radical SAM enzymes RlmN and Cfr proceeds via methylene transfer and hydride shift
- (2011) F. Yan et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- A Meta-Analysis of Genome-Wide Association Scans Identifies IL18RAP, PTPN2, TAGAP, and PUS10 As Shared Risk Loci for Crohn's Disease and Celiac Disease
- (2011) Eleonora A. M. Festen et al. PLoS Genetics
- The AlkB Domain of Mammalian ABH8 Catalyzes Hydroxylation of 5-Methoxycarbonylmethyluridine at the Wobble Position of tRNA
- (2010) Ye Fu et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- The expression of TRMT2A, a novel cell cycle regulated protein, identifies a subset of breast cancer patients with HER2 over-expression that are at an increased risk of recurrence
- (2010) David G Hicks et al. BMC CANCER
- Defining the RNA polymerase III transcriptome: Genome-wide localization of the RNA polymerase III transcription machinery in human cells
- (2010) D. Canella et al. GENOME RESEARCH
- Acute liver failure with subsequent cirrhosis as the primary manifestation of TRMU mutations
- (2010) Ulrike Schara et al. JOURNAL OF INHERITED METABOLIC DISEASE
- Mammalian ALKBH8 Possesses tRNA Methyltransferase Activity Required for the Biogenesis of Multiple Wobble Uridine Modifications Implicated in Translational Decoding
- (2010) L. Songe-Moller et al. MOLECULAR AND CELLULAR BIOLOGY
- Human AlkB Homolog ABH8 Is a tRNA Methyltransferase Required for Wobble Uridine Modification and DNA Damage Survival
- (2010) D. Fu et al. MOLECULAR AND CELLULAR BIOLOGY
- Pol II and its associated epigenetic marks are present at Pol III–transcribed noncoding RNA genes
- (2010) Artem Barski et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- Structural basis for the methylation of G1405 in 16S rRNA by aminoglycoside resistance methyltransferase Sgm from an antibiotic producer: a diversity of active sites in m 7 G methyltransferases
- (2010) Nilofer Husain et al. NUCLEIC ACIDS RESEARCH
- Genomic Aberrations in Lung Adenocarcinoma in Never Smokers
- (2010) Bastien Job et al. PLoS One
- Characterization of the human tRNA-guanine transglycosylase: Confirmation of the heterodimeric subunit structure
- (2010) Y. C. Chen et al. RNA
- Acute Infantile Liver Failure Due to Mutations in the TRMU Gene
- (2009) Avraham Zeharia et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Genomic gain of 5p15 leads to over-expression of Misu (NSUN2) in breast cancer
- (2009) Michaela Frye et al. CANCER LETTERS
- Queuosine Formation in Eukaryotic tRNA Occurs via a Mitochondria-localized Heteromeric Transglycosylase
- (2009) Coilin Boland et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Ubiquitin-related modifier Urm1 acts as a sulphur carrier in thiolation of eukaryotic transfer RNA
- (2009) Sebastian Leidel et al. NATURE
- tRNA over-expression in breast cancer and functional consequences
- (2009) Mariana Pavon-Eternod et al. NUCLEIC ACIDS RESEARCH
- Structural basis of AdoMet-dependent aminocarboxypropyl transfer reaction catalyzed by tRNA-wybutosine synthesizing enzyme, TYW2
- (2009) M. Umitsu et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- RNA Sequence and Two-dimensional Structure Features Required for Efficient Substrate Modification by theSaccharomyces cerevisiaeRNA:Ψ-Synthase Pus7p
- (2008) Alan Urban et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- IHG-1 Amplifies TGF- 1 Signaling and Is Increased in Renal Fibrosis
- (2008) M. Murphy et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Eukaryotic Wobble Uridine Modifications Promote a Functionally Redundant Decoding System
- (2008) M. J. O. Johansson et al. MOLECULAR AND CELLULAR BIOLOGY
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now