about
Initial sequencing and analysis of the human genomeIntegrated genetic and epigenetic analysis identifies haplotype-specific methylation in the FTO type 2 diabetes and obesity susceptibility locusPromiscuity of enhancer, coding and non-coding transcription functions in ultraconserved elementsWhole-Genome Shotgun Assembly and Analysis of the Genome of Fugu rubripesGenome-wide signatures of convergent evolution in echolocating mammalsA novel function for FOXP3 in humans: intrinsic regulation of conventional T cellsThe kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypesMutation of SALL2 causes recessive ocular coloboma in humans and miceARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomaliesThe Ensembl genome database projectThe IKMC web portal: a central point of entry to data and resources from the International Knockout Mouse ConsortiumThe Bioperl toolkit: Perl modules for the life sciencesHistone Modifications in a Mouse Model of Early Adversities and Panic Disorder: Role for Asic1 and Neurodevelopmental Genes.The transcriptional landscape of the mammalian genomeThe BioMart community portal: an innovative alternative to large, centralized data repositoriesPhylogenomic analyses elucidate the evolutionary relationships of batsTprg, a gene predominantly expressed in skin, is a direct target of the transcription factor p63Large-scale open bioinformatics data resources.Mixed lineage kinase 3 gene mutations in mismatch repair deficient gastrointestinal tumours.PRGdb: a bioinformatics platform for plant resistance gene analysis.Biopipe: a flexible framework for protocol-based bioinformatics analysis.Identification of common carp innate immune genes with whole-genome sequencing and RNA-Seq data.Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.Lentiviral hematopoietic stem cell gene therapy benefits metachromatic leukodystrophy.Characterisation and validation of insertions and deletions in 173 patient exomesThe TATA-binding protein regulates maternal mRNA degradation and differential zygotic transcription in zebrafish.Comparative methylome analysis of benign and malignant peripheral nerve sheath tumors.A strong anti-inflammatory signature revealed by liver transcription profiling of Tmprss6-/- mice.Genome-wide methylation and gene expression changes in newborn rats following maternal protein restriction and reversal by folic acidDissecting the signaling pathways associated with the oncogenic activity of MLK3 P252H mutationGenome wide identification of aberrant alternative splicing events in myotonic dystrophy type 2.Impact of MS genetic loci on familial aggregation, clinical phenotype, and disease prediction.Genome-wide mapping of Myc binding and gene regulation in serum-stimulated fibroblasts.Comparative analysis of the testis and ovary transcriptomes in zebrafish by combining experimental and computational toolsSocial Epigenetics and Equality of Opportunity.Germline CDH1 deletions in hereditary diffuse gastric cancer familiesDynamic regulation of the transcription initiation landscape at single nucleotide resolution during vertebrate embryogenesisAsthma in seniors: Part 1. Evidence for underdiagnosis, undertreatment, and increasing morbidity and mortality.Targeted transgene integration overcomes variability of position effects in zebrafish.Integrated genomic analysis identifies recurrent mutations and evolution patterns driving the initiation and progression of follicular lymphoma.
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description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Elia Stupka
@ast
Elia Stupka
@en
Elia Stupka
@es
Elia Stupka
@fr
Elia Stupka
@nl
Elia Stupka
@sl
type
label
Elia Stupka
@ast
Elia Stupka
@en
Elia Stupka
@es
Elia Stupka
@fr
Elia Stupka
@nl
Elia Stupka
@sl
prefLabel
Elia Stupka
@ast
Elia Stupka
@en
Elia Stupka
@es
Elia Stupka
@fr
Elia Stupka
@nl
Elia Stupka
@sl
P106
P21
P2456
P31
P496
0000-0003-3154-4011