BioGPS and MyGene.info: organizing online, gene-centric information
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P1343
The ubiquilin gene family: evolutionary patterns and functional insightsGenome-wide association study identifies novel loci associated with diisocyanate-induced occupational asthmaTMTC1 and TMTC2 are novel endoplasmic reticulum tetratricopeptide repeat-containing adapter proteins involved in calcium homeostasisStructural basis for different phosphoinositide specificities of the PX domains of sorting nexins regulating G-protein signalingPeroxisome proliferator-activated receptor γ coactivator 1 (PGC-1)- and estrogen-related receptor (ERR)-induced regulator in muscle 1 (Perm1) is a tissue-specific regulator of oxidative capacity in skeletal muscle cellsAdvances in understanding - genetic basis of intellectual disabilityLysine deacetylase (KDAC) regulatory pathways: an alternative approach to selective modulationInducible, dose-adjustable and time-restricted reconstitution of STAT1 deficiency in vivoTBC1D24 genotype-phenotype correlation: Epilepsies and other neurologic features.Glycine and Folate Ameliorate Models of Congenital Sideroblastic AnemiaHigh-performance web services for querying gene and variant annotationThyroid malignant neoplasm-associated biomarkers as targets for oncolytic virotherapyPhosphoSitePlus, 2014: mutations, PTMs and recalibrationsA splice donor mutation in NAA10 results in the dysregulation of the retinoic acid signalling pathway and causes Lenz microphthalmia syndromeFunctional characterization of enzymes catalyzing ceramide phosphoethanolamine biosynthesis in miceStructural basis of a unique interferon-β signaling axis mediated via the receptor IFNAR1Deciphering the Developmental Dynamics of the Mouse Liver TranscriptomeAn Interferon Regulated MicroRNA Provides Broad Cell-Intrinsic Antiviral Immunity through Multihit Host-Directed Targeting of the Sterol PathwayTranslational bioinformatics in the era of real-time biomedical, health care and wellness data streamsMouse Genome Database (MGD)-2017: community knowledge resource for the laboratory mouseMutation of the ER retention receptor KDELR1 leads to cell-intrinsic lymphopenia and a failure to control chronic viral infectionFAM46 proteins are novel eukaryotic non-canonical poly(A) polymerasesEvolutionary signatures amongst disease genes permit novel methods for gene prioritization and construction of informative gene-based networksPGBD5: a neural-specific intron-containing piggyBac transposase domesticated over 500 million years ago and conserved from cephalochordates to humansA theoretical study on predicted protein targets of apple polyphenols and possible mechanisms of chemoprevention in colorectal cancerBioGPS: building your own mash-up of gene annotations and expression profiles.Identification and characterization of long non-coding RNAs related to mouse embryonic brain development from available transcriptomic data.Expanded CCUG repeat RNA expression in Drosophila heart and muscle trigger Myotonic Dystrophy type 1-like phenotypes and activate autophagocytosis genes.GeneAnalytics: An Integrative Gene Set Analysis Tool for Next Generation Sequencing, RNAseq and Microarray Data.Data sources for in vivo molecular profiling of human phenotypes."Upstream Analysis": An Integrated Promoter-Pathway Analysis Approach to Causal Interpretation of Microarray Data.Nlrp9b inflammasome restricts rotavirus infection in intestinal epithelial cells.IQRray, a new method for Affymetrix microarray quality control, and the homologous organ conservation score, a new benchmark method for quality control metrics.Proteomic mapping of cytosol-facing outer mitochondrial and ER membranes in living human cells by proximity biotinylationMulti-omics approaches to disease.In SilicoModel-driven Assessment of the Effects of Brain-derived Neurotrophic Factor Deficiency on Glutamate and Gamma-Aminobutyric Acid: Implications for Understanding Schizophrenia Pathophysiology.Modeling complex patterns of differential DNA methylation that associate with gene expression changes.Chemistry-based molecular signature underlying the atypia of clozapine.Let-7 represses Nr6a1 and a mid-gestation developmental program in adult fibroblasts.The genetic basis of DOORS syndrome: an exome-sequencing study
P2860
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P2860
BioGPS and MyGene.info: organizing online, gene-centric information
description
2013 nî lūn-bûn
@nan
2013 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
BioGPS and MyGene.info: organizing online, gene-centric information
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BioGPS and MyGene.info: organizing online, gene-centric information
@en
BioGPS and MyGene.info: organizing online, gene-centric information
@nl
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label
BioGPS and MyGene.info: organizing online, gene-centric information
@ast
BioGPS and MyGene.info: organizing online, gene-centric information
@en
BioGPS and MyGene.info: organizing online, gene-centric information
@nl
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BioGPS and MyGene.info: organizing online, gene-centric information
@ast
BioGPS and MyGene.info: organizing online, gene-centric information
@en
BioGPS and MyGene.info: organizing online, gene-centric information
@nl
P2860
P3181
P356
P1476
BioGPS and MyGene.info: organizing online, gene-centric information
@en
P2093
Chunlei Wu
Ian Macleod
P2860
P304
P3181
P356
10.1093/NAR/GKS1114
P407
P433
Database issue
P50
P577
2013-01-01T00:00:00Z