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Eiríkur Steingrímsson - Prófessor

Eiríkur Steingrímsson

–

Heilbrigðisvísindasvið

Eiríkur Steingrímsson

Prófessor

Aðsetur
Sturlugata 8
Sími
5254270
Tölvupóstur
eirikurs [hjá] hi.is

Starfseining
Læknadeild, Lífefnafræði

Ferilskrá
Eiríkur Steingrímsson - ferilskrá
ORCID vefsíða
https://orcid.org/0000-0001-5826-7486
Rannsóknagátt – Eiríkur Steingrímsson

Show Útgefið efni

2025

Antagonistic roles for MITF and TFE3 in melanoma plasticityCell Reports

2024

ATG7(2) Interacts With Metabolic Proteins and Regulates Central Energy MetabolismTraffic
Differentiation status determines the effects of IFNγ on the expression of PD-L1 and immunomodulatory genes in melanomaCell Communication and Signaling
Mitf regulates gene expression networks implicated in B cell homeostasis, germinal center responses, and toleranceFrontiers in Immunology
Novel mechanisms of MITF regulation identified in a mouse suppressor screenEMBO Reports
Reduction in the olfactory ability in aging Mitf mutant mice without evidence of neurodegenerationFrontiers in Aging
The Nobel prize in medicine - microRNA and gene regulationLaeknabladid

2023

Acetylation reprograms MITF target selectivity and residence timeNature Communications

2022

Germline variants of ATG7 in familial cholangiocarcinoma alter autophagy and p62Scientific Reports
Hedgehog signalling in bone and osteoarthritisFEBS Journal
TFAP2 paralogs facilitate chromatin access for MITF at pigmentation and cell proliferation genesPLoS Genetics

2021

BRN2 is a non-canonical melanoma tumor-suppressorNature Communications
Cell-type-specific meQTLs extend melanoma GWAS annotation beyond eQTLs and inform melanocyte gene-regulatory mechanismsAmerican Journal of Human Genetics
Diffuse idiopathic skeletal hyperostosis in elderly Icelanders and its association with the metabolic syndromeScandinavian Journal of Rheumatology
Epigenetic regulation during melanocyte development and homeostasisExperimental Dermatology
Mitf reprograms the extracellular matrix and focal adhesion in melanomaeLife
User guide to MiT-TFE isoforms and post-translational modificationsPigment Cell and Melanoma Research

2020

Mechanism of conditional partner selectivity in MITF/TFE family transcription factors with a conserved coiled coil stammer motifNucleic Acids Research
Melanoma risk and melanocyte biologyActa Dermato-Venereologica
MITF and TFEB cross-regulation in melanoma cellsPLoS ONE
Mitf Links Neuronal Activity and Long-Term Homeostatic Intrinsic PlasticityeNeuro
Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1Clinical Genetics
Tuning Transcription Factor Availability through Acetylation-Mediated Genomic RedistributionMolecular Cell

2019

Distribution of mast cells within the mouse heart and its dependency on MitfMolecular Immunology
MITF has a central role in regulating starvation-induced autophagy in melanomaScientific Reports
Proton pump inhibitor use and risk of breast cancer, prostate cancer, and malignant melanomaPharmacoepidemiology and Drug Safety
Subcellular localization and stability of MITF are modulated by the bHLH-Zip domainPigment Cell and Melanoma Research
The microphthalmia-associated transcription factor (Mitf) gene and its role in regulating eye functionScientific Reports
Zebrafish MITF-low melanoma subtype models reveal transcriptional subclusters and MITF-independent residual diseaseCancer Research

2018

A short isoform of ATG7 fails to lipidate LC3/GABARAPScientific Reports
BRAF/MAPK and GSK3 signaling converges to control MITF nuclear exportProceedings of the National Academy of Sciences
Erratum toScientific Reports
Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritisNature Genetics
Proton-pump inhibitors among adultsTherapeutic Advances in Gastroenterology

2017

An eye on microphthalmiaPigment cell & melanoma research
Dægurklukkan og Nóbelsverðlaunin í lífeðlis-og læknisfræði 2017Laeknabladid
Genomic regions controlling shape variation in the first upper molar of the house mouseeLife
KIT^D816V induces SRC-mediated tyrosine phosphorylation of MITF and altered transcription program in melanomaMolecular Cancer Research

2015

Altered E-cadherin levels and distribution in melanocytes precede clinical manifestations of vitiligoJournal of Investigative Dermatology
Meningeal melanocytes in the mouseFrontiers in Neuroanatomy
Mitf is a master regulator of the v-ATPase, forming a control module for cellular homeostasis with v-ATPase and TORC1Journal of Cell Science
MITF regulation - more hints from WntPigment Cell and Melanoma Research
Tilfelli mánaðarins.Læknablaðið

2014

Selection, p53, and pigmentation.Pigment cell & melanoma research
Sun-induced frecklingPigment Cell and Melanoma Research

2013

Differential activity of c-KIT splice forms is controlled by extracellular peptide insert lengthCellular Signalling
Expression and Functional Role of Sprouty-2 in Breast MorphogenesisPLoS ONE
Lífvísindasetur Háskóla ÍslandsLaeknabladid
MITF mutations associated with pigment deficiency syndromes and melanoma have different effects on protein functionHuman Molecular Genetics
Nonsense mutation in the LGR4 gene is associated with several human diseases and other traitsNature
XA polymorphism in IRF4 affects human pigmentation through a tyrosinase-dependent MITF/TFAP2A pathwayCell

2012

Restricted leucine zipper dimerization and specificity of DNA recognition of the melanocyte master regulator MITFGenes and Development

2011

C-KIT signaling depends on microphthalmia-associated transcription factor for effects on cell proliferationPLoS ONE

2010

A detailed genome-wide reconstruction of mouse metabolism based on human Recon 1BMC Systems Biology
Interpretation of complex phenotypesPigment Cell and Melanoma Research
miR-148 regulates Mitf in melanoma cellsPLoS ONE

2009

Design and analysis of microarray experiments for pharmacogenomics
Litfrumur og sortuæxliLaeknabladid
The role of MITF phosphorylation sites during coat color and eye development in mice analyzed by bacterial artificial chromosome transgene rescueGenetics

2008

All for one, one for allPigment Cell and Melanoma Research
An unstable targeted allele of the mouse Mitf gene with a high somatic and germline reversion rateGenetics
Novel MITF targets identified using a two-step DNA microarray strategyPigment Cell and Melanoma Research

2007

Evolutionary sequence comparison of the Mitf gene reveals novel conserved domainsPigment Cell Research
Statistically designing microarrays and microarray experiments to enhance sensitivity and specificityBriefings in Bioinformatics

2006

A population-based study on the familial aggregation of cutaneous malignant melanoma in IcelandEuropean Journal of Cancer
Familial risk of colon and rectal cancer in IcelandInternational Journal of Cancer
Mouse coat color mutationsDevelopmental Dynamics
The effective size of the Icelandic population and the prospects for LD mappingEuropean Journal of Human Genetics
The microphthalmia-associated transcription factor Mitf interacts with β-catenin to determine target gene expressionMolecular and Cellular Biology
Umritunarþættir og stofnfrumur litfrumna.

2005

Melanocyte stem cell maintenance and hair grayingCell
Transcription factor Tfec contributes to the IL-4-inducible expression of a small group of genes in mouse macrophages including the granulocyte colony-stimulating factor receptorJournal of Immunology

2004

BRCA2, but not BRCA1, mutations account for familial ovarian cancer in IcelandEuropean Journal of Cancer
Electroretinographic and histologic assessment of retinal function in Microphthalmia mutant miceExperimental Eye Research
Melanocytes and the Microphthalmia transcription factor networkAnnual Review of Genetics
The basic helix-loop-helix leucine zipper transcription factor Mitf is conserved in Drosophila and functions in eye developmentGenetics
The Icelandic Cancer Project - A population-wide approach to studying cancerNature Reviews Cancer
The novel mouse microphthalmia mutations Mitf^mi-enu5 and Mitf^mi-bcc2 produce dominant negative Mitf proteinsGenomics

2003

Eiginleikar stofnfrumnaLæknablaðið
Interallelic complementation at the mouse Mitf locusGenetics

2002

Mitf and Tfe3, two members of the Mitf-Tfe family of bHLH-Zip transcription factors, have important but functionally redundant roles in osteoclast developmentProceedings of the National Academy of Sciences of the United States of America

2001

MODY in Iceland is associated with mutations in HNF-1α and a novel mutation in NeuroD1Diabetologia

2000

CorrigendumEMBO Journal
Genomic, transcriptional and mutational analysis of the mouse microphthalmia locusGenetics

1999

Mga, a dual-specificity transcription factor that interacts with Max and contains a T-domain DNA-binding motifEMBO Journal
The murine Bin1 gene functions early in myogenesis and defines a new region of synteny between mouse chromosome 18 and human chromosome 2Genomics

1998

Mitfmi-enu122 is a missense mutation in the HLH dimerization domain.Mammalian genome : official journal of the International Mammalian Genome Society
The bHLH-Zip transcription factor Tfeb is essential for placental vascularizationDevelopment

1997

Cloning and characterization of two vertebrate homologs of the Drosophila eyes absent geneGenome Research
NEUROD2 and NEUROD3 genes map to human chromosomes 17q12 and 5q23-q31 and mouse chromosomes 11 and 13, respectivelyGenomics

1996

Mad3 and Mad4The EMBO journal
The NEUROD gene maps to human chromosome 2q32 and mouse chromosome 2Genomics
The semidominant Mi^b mutation identifies a role for the HLH domain in DNA binding in addition to its role in protein dimerizationEMBO Journal

1995

Hxt encodes a basic helix-loop-helix transcription factor that regulates trophoblast cell developmentDevelopment
Mad3 and Mad4EMBO Journal
Meso1, a basic-helix-loop-helix protein involved in mammalian presomitic mesoderm developmentProceedings of the National Academy of Sciences of the United States of America
Mild osteopetrosis in the microphthalmia-oak ridge mouseAmerican Journal of Pathology
Murine chromosomal location of five bHLH-Zip transcription factor genesGenomics
Posterior stripe expression of hunchback is driven from two promoters by a common enhancer elementDevelopment

1994

Genomic organization, alternative polyadenylation, and chromosomal localization of grg, a mouse gene related to the groucho transcript of the drosophila enhancer of split complexGenomics
Mapping of two genes encoding members of a distinct subfamily of MAX interacting proteinsOncogene
microphthalmia, A critical factor in melanocyte development, defines a discrete transcription factor familyGenes and Development
Molecular basis of mouse microphthalmia (mi) mutations helps explain their developmental and phenotypic consequencesNature Genetics

1993

Characterization of downstream elements in a Raf-1 pathwayProceedings of the National Academy of Sciences of the United States of America
Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper proteinCell

1992

Bicoid and the terminal system activate Tailless expression in the early Drosophila embryoDevelopment

1991

Dual role of the Drosophila pattern gene tailless in embryonic terminiScience

1990

The Drosophila gene tailless is expressed at the embryonic termini and is a member of the steroid receptor superfamilyCell

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