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Jón Þór Bergþórsson - Dósent

Jón Þór Bergþórsson

–

Heilbrigðisvísindasvið

Jón Þór Bergþórsson

Dósent

Aðsetur
LSH - Hringbraut
Tölvupóstur
jthb1 [hjá] hi.is

Starfseining
Læknadeild, Geisla- og lífeindafræði

ORCID vefsíða
https://orcid.org/0000-0002-0560-2639
Rannsóknagátt – Jón Þór Bergþórsson

Útgefið efni

2024

Unlocking protein-based biomarker potential for graft-versus-host disease following allogenic hematopoietic stem cell transplantsFrontiers in Immunology

2023

Pathology and Molecular Biology of MelanomaCurrent Issues in Molecular Biology
Flow Cytometry of CD5-Positive Hairy Cell LeukemiaMolecular Diagnosis and Therapy
Design and preclinical testing of an anti-CD41 CAR T cell for the treatment of acute megakaryoblastic leukaemiaJournal of Cellular and Molecular Medicine
RNA sequencing suggests that non-coding RNAs play a role in the development of acquired haemophiliaJournal of Cellular and Molecular Medicine
Pitfalls in patenting academic CAR-T cells therapyExpert Opinion on Therapeutic Patents

2020

Melflufen, a peptide‐conjugated alkylator, is an efficient anti‐neo‐plastic drug in breast cancer cell linesCancer Medicine
The BLIMP1—EZH2 nexus in a non-Hodgkin lymphomaOncogene
Transforming growth factor β‐mediated micromechanics modulates disease progression in primary myelofibrosisJournal of Cellular and Molecular Medicine
Expression of ncRNAs on the DLK1-DIO3 Locus Is Associated With Basal and Mesenchymal Phenotype in Breast Epithelial Progenitor CellsFrontiers in Cell and Developmental Biology
The BLIMP1—EZH2 nexus in a non-Hodgkin lymphomaOncogene

2016

Epithelial Plasticity During Human Breast Morphogenesis and Cancer ProgressionJournal of Mammary Gland Biology and Neoplasia

2015

MicroRNA-200c-141 and δNp63 are required for breast epithelial differentiation and branching morphogenesisDevelopmental Biology

2014

Functional role of the microrna-200 family in breast morphogenesis and NeoplasiaGenes
DeltaNp63 has a role in maintaining epithelial integrity in airway epitheliumPLoS ONE

2013

Endothelial-rich microenvironment supports growth and branching morphogenesis of prostate epithelial cellsProstate

2009

Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populationsNature Genetics

2008

A variant associated with nicotine dependence, lung cancer and peripheral arterial diseaseNature
Common variants on chromosome 5p12 confer susceptibility to estrogen receptor-positive breast cancerNature Genetics
Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traitsNature Genetics
Sequence variant on 8q24 confers susceptibility to urinary bladder cancerNature Genetics

2007

Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24Nature Genetics
Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancerNature Genetics
Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetesNature Genetics

2006

A genome-wide study of allelic imbalance in human testicular germ cell tumors using microsatellite markersCancer Genetics and Cytogenetics
Testicular germ cell tumours in IcelandAPMIS
The BARD1 Cys557Ser variant and breast cancer risk in IcelandPLoS Medicine
A common variant associated with prostate cancer in European and African populationsNature Genetics

2003

A population-based analysis of increased incidence and improved survival of testicular cancer patients in IcelandScandinavian Journal of Urology and Nephrology

2002

Mutation analysis of the CHK2 gene in breast carcinoma and other cancersBreast Cancer Research
High frequency of LOH, MSI and abnormal expression of FHIT in gastric cancerEuropean Journal of Cancer
A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer developmentHuman Genetics

2001

BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young ageJournal of Medical Genetics
Functional analysis of BRCA1 C-terminal missense mutations identified in breast and ovarian cancer familiesHuman Molecular Genetics
Stökkbreytingagreining á CHK2 geni í brjóstakrabbameini

2000

Áhrif erfðaóstöðugleika á æxlisvöxt - Stökkbreytingar í genum sem innihalda stuttar endurteknar raðir í æxlisgerðum tengdum HNPCC
Analysis of HPC1, HPCX, and PCaP in Icelandic hereditary prostate cancerHuman Genetics
Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locusProceedings of the National Academy of Sciences of the United States of America
The effect of mismatch repair deficiency on tumourigenesis; microsatellite instability affecting genes containing short repeated sequences.International Journal of Oncology

1999

Replication error in colorectal carcinomaAnticancer Research

1998

Identification of a novel splicesite mutation of the BRCAL gene in two breast cancer familiesHuman Mutation
Chromosome imbalance at the 3p14 region in human breast tumoursEuropean Journal of Cancer
Deletions at the BRCA2 locus associate with breast tumor progression and patient survival.European Journal of Cancer
A population study of mutations and LOH at breast cancer gene loci in tumours from sister pairsJournal of Medical Genetics

1996

High prevalence of the 999del5 mutation in icelandic breast and ovarian cancer patientsCancer Research
Frequent occurrence of BRCA2 linkage in Icelandic breast cancer families and segregation of a common BRCA2 haplotypeAmerican Journal of Human Genetics

1995

Different Tumor Types from BRCA2 Carriers Show Wild-Type Chromosome Deletions on 13q12-q13Cancer Research
Loss of heterozygosity on chromosome 9 in human breast cancerInternational Journal of Cancer
Linkage analysis and allelic imbalance in human breast cancer kindreds using microsatellite markers from the short arm of chromosome 3Human Genetics
Mapping of chromosome 3 alterations in human breast cancer using microsatellite PCR markersInternational Journal of Oncology
Identification of a breast tumor with microsatellite instability in a potential carrier of the hereditary non‐polyposis colon cancer traitClinical Genetics

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