scholarly article | Q13442814 |
P50 | author | Yubin Xie | Q55143479 |
P2093 | author name string | Li Chen | |
Zhixiang Zuo | |||
Jian Ren | |||
Ya Zhang | |||
Shuai Jiang | |||
Yuli Zhao | |||
Yanyan Miao | |||
Zhihao He | |||
Yueyuan Zheng | |||
P2860 | cites work | Model-based analysis of ChIP-Seq (MACS) | Q21183902 |
Genome-wide QTL mapping for three traits related to teat number in a White Duroc x Erhualian pig resource population | Q21261513 | ||
ALKBH5 is a mammalian RNA demethylase that impacts RNA metabolism and mouse fertility | Q24304362 | ||
A METTL3-METTL14 complex mediates mammalian nuclear RNA N6-adenosine methylation | Q24311871 | ||
Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes | Q24534193 | ||
The NHGRI GWAS Catalog, a curated resource of SNP-trait associations | Q24568334 | ||
The NCBI dbGaP database of genotypes and phenotypes | Q24569609 | ||
Comprehensive analysis of mRNA methylation reveals enrichment in 3' UTRs and near stop codons | Q24598126 | ||
iRNA-Methyl: Identifying N(6)-methyladenosine sites using pseudo nucleotide composition. | Q50567651 | ||
FTO Plays an Oncogenic Role in Acute Myeloid Leukemia as a N6-Methyladenosine RNA Demethylase. | Q51236778 | ||
Synonymous Mutations Frequently Act as Driver Mutations in Human Cancers | Q55554493 | ||
Evidence for Purifying Selection Against Synonymous Mutations in Mammalian Exonic Splicing Enhancers | Q59303878 | ||
An open access database of genome-wide association results | Q95780251 | ||
SRAMP: prediction of mammalian N6-methyladenosine (m6A) sites based on sequence-derived features | Q36958992 | ||
Mistranslation-induced protein misfolding as a dominant constraint on coding-sequence evolution. | Q37227320 | ||
Loss-of-function mutation in the dioxygenase-encoding FTO gene causes severe growth retardation and multiple malformations | Q37253402 | ||
Identification of deleterious mutations within three human genomes | Q37363175 | ||
Hypoxia-inducible factors regulate pluripotency factor expression by ZNF217- and ALKBH5-mediated modulation of RNA methylation in breast cancer cells | Q37662078 | ||
Understanding the contribution of synonymous mutations to human disease | Q37924093 | ||
Gene expression regulation mediated through reversible m⁶A RNA methylation | Q38198852 | ||
A novel, de novo mutation in the PRKAG2 gene: infantile-onset phenotype and the signaling pathway involved. | Q38760684 | ||
Mutation of N-linked glycosylation in EpCAM affected cell adhesion in breast cancer cells | Q38896224 | ||
Role of post-transcriptional regulation of mRNA stability in renal pathophysiology: focus on chronic kidney disease | Q39010143 | ||
m(6)A RNA methylation is regulated by microRNAs and promotes reprogramming to pluripotency | Q39038754 | ||
Dynamic RNA Modifications in Gene Expression Regulation | Q39378718 | ||
MutPred Splice: machine learning-based prediction of exonic variants that disrupt splicing | Q40621425 | ||
Using combined evidence from replicates to evaluate ChIP-seq peaks. | Q40957850 | ||
pRNAm-PC: Predicting N(6)-methyladenosine sites in RNA sequences via physical-chemical properties | Q40989473 | ||
What, where, and when: the importance of post-transcriptional regulation in the brain | Q41813462 | ||
piRNABank: a web resource on classified and clustered Piwi-interacting RNAs | Q42150407 | ||
Predicting the functional, molecular, and phenotypic consequences of amino acid substitutions using hidden Markov models | Q42288039 | ||
A missense mutation in the transmembrane domain of CESA4 affects protein abundance in the plasma membrane and results in abnormal cell wall biosynthesis in rice | Q44216135 | ||
MIMP: predicting the impact of mutations on kinase-substrate phosphorylation. | Q45954450 | ||
Nucleotide-specific recognition of iron-responsive elements by iron regulatory protein 1. | Q46782145 | ||
m6AVar: a database of functional variants involved in m6A modification | Q47159279 | ||
The RNA modification landscape in human disease | Q50266881 | ||
Identification of a pathogenic FTO mutation by next-generation sequencing in a newborn with growth retardation and developmental delay | Q50351896 | ||
SILVA: a comprehensive online resource for quality checked and aligned ribosomal RNA sequence data compatible with ARB | Q24685829 | ||
Evidence for selection on synonymous mutations affecting stability of mRNA secondary structure in mammals | Q24814018 | ||
Recent advances in dynamic m6A RNA modification | Q26744188 | ||
A method and server for predicting damaging missense mutations | Q27860835 | ||
5' UTR m(6)A Promotes Cap-Independent Translation | Q28114851 | ||
Nuclear m(6)A Reader YTHDC1 Regulates mRNA Splicing | Q28114974 | ||
A majority of m6A residues are in the last exons, allowing the potential for 3' UTR regulation | Q28267771 | ||
Mutations of phosphorylation sites in lamin A that prevent nuclear lamina disassembly in mitosis | Q28286361 | ||
N6-methyladenosine modification destabilizes developmental regulators in embryonic stem cells | Q28585513 | ||
RNA-methylation-dependent RNA processing controls the speed of the circadian clock | Q28591141 | ||
ClinVar: public archive of interpretations of clinically relevant variants | Q28603051 | ||
miRBase: annotating high confidence microRNAs using deep sequencing data | Q28660701 | ||
Mutation of A677 in histone methyltransferase EZH2 in human B-cell lymphoma promotes hypertrimethylation of histone H3 on lysine 27 (H3K27) | Q29147438 | ||
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data | Q29547161 | ||
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm | Q29547194 | ||
The genetic association database | Q29617244 | ||
The role of the linker between the SH2 domain and catalytic domain in the regulation and function of Src. | Q30176292 | ||
starBase v2.0: decoding miRNA-ceRNA, miRNA-ncRNA and protein-RNA interaction networks from large-scale CLIP-Seq data | Q30705717 | ||
BioCircos.js: an interactive Circos JavaScript library for biological data visualization on web applications. | Q31040612 | ||
A novel algorithm for calling mRNA m6A peaks by modeling biological variances in MeRIP-seq data | Q31108439 | ||
PhosSNP for systematic analysis of genetic polymorphisms that influence protein phosphorylation | Q33517577 | ||
Associations between an obesity related genetic variant (FTO rs9939609) and prostate cancer risk | Q33728225 | ||
The genetics of obesity: FTO leads the way. | Q34005975 | ||
Hypoxia induces the breast cancer stem cell phenotype by HIF-dependent and ALKBH5-mediated m⁶A-demethylation of NANOG mRNA. | Q34519307 | ||
CLIPdb: a CLIP-seq database for protein-RNA interactions | Q35079291 | ||
High-resolution N(6) -methyladenosine (m(6) A) map using photo-crosslinking-assisted m(6) A sequencing | Q35413587 | ||
Structure and thermodynamics of N6-methyladenosine in RNA: a spring-loaded base modification | Q35511241 | ||
Single-nucleotide-resolution mapping of m6A and m6Am throughout the transcriptome | Q35804751 | ||
How do RNA folding algorithms work? | Q35940963 | ||
miR-212/132 expression and functions: within and beyond the neuronal compartment | Q36008128 | ||
SIFT web server: predicting effects of amino acid substitutions on proteins | Q36088562 | ||
DASHR: database of small human noncoding RNAs | Q36434778 | ||
GtRNAdb 2.0: an expanded database of transfer RNA genes identified in complete and draft genomes | Q36434994 | ||
METTL13 is downregulated in bladder carcinoma and suppresses cell proliferation, migration and invasion | Q36499467 | ||
Preventing E-cadherin aberrant N-glycosylation at Asn-554 improves its critical function in gastric cancer | Q36868502 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 5 | |
P577 | publication date | 2018-05-01 | |
P1433 | published in | GigaScience | Q19969338 |
P1476 | title | m6ASNP: a tool for annotating genetic variants by m6A function. | |
P478 | volume | 7 |
Q97521123 | Bioinformatics approaches for deciphering the epitranscriptome: Recent progress and emerging topics |
Q64079753 | DRUM: Inference of Disease-Associated mA RNA Methylation Sites From a Multi-Layer Heterogeneous Network |
Q91826392 | Genome-wide enrichment of m6A-associated single-nucleotide polymorphisms in the lipid loci |
Q61451737 | Global analysis of N6-methyladenosine functions and its disease association using deep learning and network-based methods |
Q91881019 | N6-methyladenosine regulatory machinery in plants: composition, function and evolution |
Q90115119 | Predict Epitranscriptome Targets and Regulatory Functions of N 6-Methyladenosine (m6A) Writers and Erasers |
Q98177281 | Prediction of RNA Methylation Status From Gene Expression Data Using Classification and Regression Methods |
Q64076452 | RNAMethyPro: a biologically conserved signature of N6-methyladenosine regulators for predicting survival at pan-cancer level |
Q90404858 | m6A Modification in Coding and Non-coding RNAs: Roles and Therapeutic Implications in Cancer |
Q99630274 | m6A RNA modification modulates PI3K/Akt/mTOR signal pathway in Gastrointestinal Cancer |
Q98771745 | m6A Reader: Epitranscriptome Target Prediction and Functional Characterization of N 6-Methyladenosine (m6A) Readers |
Search more.