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Sigurður Ingvarsson - Professor

Sigurður Ingvarsson

–

School of Health Sciences

Sigurður Ingvarsson

Professor

Professor and director

Phone
5855123 8943235
Email
siguring [at] hi.is

Unit
Faculty of Medicine
Website
https://keldur.is/is

Published works

2025

Tilraunastöð Háskóla Íslands í meinafræði að Keldum - Ársskýrsla 2024

2023

How visible is “Icelandic Agricultural Sciences” in international bibliographic databases?

2021

Hversu sýnilegt er "Icelandic Agricultural Sciences" í alþjóðlegum vefsetrum?

2020

Hif umritunarþáttur og Nóbelsverðlaunin í Líf- og Læknisfræði árið 2019 - Best þekkta sameindaferlið sem tekur þátt í súrefnisjafnvægi

2019

Tilraunastöð Háskóla Íslands í meinafræði að Keldum. Árbók Háskóla Íslands 2019
Opponent of the doctoral dissertation of Remina Dilixiati
Hif umritunarþáttur og Nóbelsverðlaunin í líf- og læknisfræði árið 2019
Hif umritunarþáttur og Nóbelsverðlaunin í líf- og læknisfræði árið 2019

2018

Vísindadagur á Keldum á sjötíu ára starfsafmæli
Tilraunastöð Háskóla Íslands í meinafræði að Keldum
Keldur - Leiðandi stofnun í rannsóknum á dýrasjúkdómum
Keldur - Leiðandi stofnun í rannsóknum á dýrasjúkdómum
Smitandi æxlisfrumur í ljósi þróunar
Hvað hefur vísindamaðurinn Sigurður Ingvarsson rannsakað?Vísindavefurinn

2017

Opponent of the doctoral dissertation of Sigurdís Haraldsdóttir
3rd World Congress on Cancer and Prevention Methods3rd World Congress on Cancer and Prevention Methods
Genomic, proteomic and clinicopathological events in carriers of the Icelandic BRCA2 999del5 founder mutation
Tilraunastöð Háskóla Íslands í meinafræði að Keldum. Árbók Háskóla Íslands 2017

2016

Tilraunastöð Háskóla Íslands í meinafræði að Keldum - greinargerð í Árbók HÍ
Epigenetic control of MLH1 expression by promoter variant and methylation spreading from Alu repeats
Vísindadagur á Keldum 2016
The 18th Nordic Congress in Human GeneticsThe 18th Nordic Congress in Human Genetics
Vísindadagur á Keldum 2016Vísindadagur á Keldum 2016

2015

MicroRNA451 bælir æxlisvöxt með því að minnka tjáningu IL6R gens
Tilraunastöð Háskóla Íslands í meinafræði að Keldum. Árbók Háskóla Íslands 2015, pp. 301-303.
DNA viðgerðir og Nóbelsverðlaunin í efnafræði árið 2015

2014

Úttekt á sýnileika vísindatímaritsins „Icelandic Agricultural Sciences“ í alþjóðlegum vefsetrum
Virkni Hif-umritunarþáttar er stýrt með prótein-niðurbroti
42nd Annual Meeting of the Scandinavian Society for Immunology42nd Annual Meeting of the Scandinavian Society for Immunology
Greining á ritverkum Keldna 2004-2013
The IL6R Expression is Downregulated by miR-451 in Tumour ProgressionScandinavian Journal of Immunology
THE GENETIC LANDSCAPE OF FAMILIAL BREAST CANCER IN ICELANDAnticancer Research
MicroRNA-451 suppresses tumor cell growth by down-regulating IL6R gene expressionCancer Epidemiology
Tilraunastöð Háskóla Íslands í meinafræði að Keldum. Árbók Háskóla Íslands 2014, pp. 447-448
Vísindadagur á Keldum 2014
Nord Forsk meeting on ”Chromatin, Transcription and Cancer” Nord Forsk meeting on ”Chromatin, Transcription and
Cancer”
Vísindadagur á Keldum 2014Vísindadagur á Keldum 2014
Ninth International Conference of Anticancer ResearchNinth International Conference of Anticancer Research
EditorialIcelandic Agricultural Sciences
The genetic landscape of familial breast cancer in IcelandAnticancer Research

2013

Tilraunastöð Háskóla Íslands í meinafræði að Keldum. Árbók Háskóla Íslands 2013, pp. 375-377.
EditorialIcelandic Agricultural Sciences
In memoriam Bjorn Sigurdsson born 100 years agoIcelandic Agricultural Sciences
Anders Jahre-verðlaunin veitt fyrir rannsóknir á sykursýkiLæknablaðið
Hlutverk Limd1 í stjórnunarferli Hif1 umritunarþáttar

2012

Brautryðjandi í sykursýkisrannsóknum fær Jahre-verðlauninLæknablaðið
Vísindadagur á Keldum 2012
Rannsóknir og þjónusta á Keldum í þágu dýraheilbrigðisBændablaðið
Hif, lykilumritunarþáttur í efnaskiptum og æðamyndun
Opponent of the doctoral dissertation of Valgarður Sigurðsson
Nordforsk network ”Chromatin, Transcription and cancer”. Second annual meetingNordforsk network ”Chromatin, Transcription and cancer”. Second annual meeting
Hif, lykilumritunarþáttur í efnaskiptum og æðamyndun
Meinafræði að Keldum í minningu Guðmundar Georgssonar
The LIMD1 protein bridges an association between the prolyl hydroxylases and VHL to repress HIF-1 activityNature Cell Biology
Tilraunastöð Háskóla Íslands í meinafræði að Keldum. Árbók Háskóla Íslands 2012, pp. 402-404
Demethylation of the region around exon 2 of MLH1 gene in gastrointestinal cancerAnticancer Research
Universal RNA editing in a human liver at the fetal stageOpen Journal of Genetics
Greining á ISI-ritverkum Tilraunastöðvar Háskóla Íslands í meinafræði að Keldum frá árunum 2002-2011

2011

Metýlun stjórnraðar og tjáning Lactoferrins í lungnaæxlum.Læknablaðið
Quantitative analysis of miRNa expression in seven human foetal and adult organsPLoS ONE
Metýlun stjórnraðar og tjáning Lactoferrins í lungnaæxlumLæknablaðið
Stökkbreytingar sem leiða til æxlisvaxtar: Náttúrulegt val?
Spreading of alu methylation to the promoter of the mlh1 gene in gastrointestinal cancerPLoS ONE
Veiting heiðursdoktorsnafnbótar við Læknadeild Háskóla Íslands: Margrét GuðnadóttirVeiting heiðursdoktorsnafnbótar við Læknadeild Háskóla Íslands: Margrét Guðnadóttir
Lactoferrin prótein tjáning er minnkuð í lungnaæxlum
Metýlun stjórnraðar og tjáning Lactoferrins í lungnaæxlum.
Ávarp - Lofsvert Lagnaverk 2009Fréttabréf Lagnafélags Íslands
Tilraunastöð Háskóla Íslands í meinafræði að Keldum. Árbók Háskóla Íslands 2011, pp. 408-410
Anders Jahre-verðlauninLaeknabladid

2010

Development, growth and function of lymphatic vessels in healthy and diseased tissue
Tilraunastöð Háskóla Íslands í meinafræði að Keldum - Ársskýrsla 2010
The MLH1 -93 promoter variant influences gene expressionCancer Epidemiology
Þroski, vöxtur og starfsemi vessaæða í heilbrigðum og sjúkum vef
Tjáning á LIMD1 og HIF1-alpha próteinum í nýrnaæxlum
Opponent of the doctoral dissertation of Benedikta S. Hafliðadóttir
Tilraunastöð Háskóla Íslands í meinafræði að Keldum. Árbók Háskóla Íslands 2010, pp. 294-295
Quantitative analysis of miRNA expression in several developmental stages of human liversHepatology Research

2009

Identification of miRNAs in a liver of a human fetus by a modified methodPLoS ONE
Nóbelsverðlaunin í lífeðlis- og læknisfræði 2009: Litningaendar og lífhvatinn telómeraseRAUST - Tímarit um raunvísindi og stærðfræði
Nóbelsverðlaunin í líf- og læknisfræði 2009: Litningaendar og telómerasi
Hvernig litningaendar eru varðir af litningaendum og lífhvatinn telómerasi
Tilraunastöð Háskóla Íslands í meinafræði að Keldum. Árbók Háskóla Íslands 2009, pp. 284-285
Tilraunastöð Háskóla Íslands í meinafræði að Keldum - Ársskýrsla 2009
Lactoferrin prótein tjáning er minnkuð í lungnaæxlum
The Nobel Prize in Physiology or Medicine 2009; How chromosomes are protected by telomeres and the enzyme telomerase.
Lactoferrin prótein tjáning er minnkuð í lungnaæxlumLæknablaðið
Rannsóknastofa HÍ í meinafræði með málþing til heiðurs Valgarði Egilssyni prófessorRannsóknastofa HÍ í meinafræði með málþing til heiðurs Valgarði Egilssyni prófessor
The sixty year anniversary of the Institute for Experimental Pathology, University of Iceland at Keldur PrefaceIcelandic Agricultural Sciences

2008

In vitro analysis of expression vectors for DNA vaccination of horses: The effect of a Kozak sequenceActa Veterinaria Scandinavica
CELLULAR BIOLOGY OF BREAST CANCER, FOCUSING ON GENOMIC AND CLINICOPATHOLOGICAL EVENTS IN CARRIERS OF A BRCA2 FOUNDER MUTATIONAnticancer Research
In vitro analysis of expression vectors for DNA vaccination of horsesActa Veterinaria Scandinavica
Minnkuð lactotransferrin tjáning í lungnaæxlum
Ársskýrsla Tilraunatöðvar Háskóla Íslands í meinafræði að Keldum - 2008
Population approach in breast cancer research based on integration of genetic, clinicopathological and genealogical cluesThe Open Cancer Journal
Genomic instability in breast cancer
Tilraunastöð Háskóla Íslands í meinafræði að Keldum. Árbók Háskóla Íslands 2008, pp. 262-263
60 ára starfsafmæli Tilraunastöðvar Háskóla Íslands í meinafræði að KeldumBændablaðið
The 1st international conference on drug design and discoveryThe 1st international conference on drug design and discovery
Frontiers in Breast Cancer Research
Opponent of the doctoral dissertation of Sigríður Klara Böðvarsdóttir
Icelandic Agricultural Sciences: Alþjóðlegt tímarit á ensku fyrir vísindagreinar í lífvísindumFræðaþing Landbúnaðarins
THE EIGHTH INTERNATIONAL CONFERENCE OF ANTICANCER RESEARCHTHE EIGHTH INTERNATIONAL CONFERENCE OF ANTICANCER RESEARCH

2007

Opponent of the doctoral dissertation of Alexander Schepsky
Duplicated sequence motif in the long terminal repeat of maedi-visna viras extends cell tropism and is associated with neurovirulenceJournal of Virology
In vitro analysis of expression vectors for DNA vaccination in horses
A29T fjölbreytileiki í LTF er algengur í lungnaæxlum
Ársskýrsla 2007 - Tilraunastöð Háskóla Íslands í meinafræði að Keldum
Tilraunastöð Háskóla Íslands í meinafræði að Keldum
Veggspjald - A29T fjölbreytileiki í Lactotransferrin (LTF) geni er algengur í lungnaæxlum
Stökkbreytingaleit í LIMD1 og LTF genum á 3p21.3 í æxlum

2006

Sameindalíffræði RNA inngrips
Hvað er RNA-inngrip?Vísindavefurinn
Nóbelsverðlaun í lífeðlis- eða læknisfræði 2006 – RNA íhlutun
Leit að stökkbreytingum í LIMD1 og LTF genum á CER1 svæði á mannalitningi 3p21.3 í 10 mismunandi æxlisgerðum
Ársskýrsla 2006 - Tilraunastöð Háskóla Íslands í meinafræði að Keldum
Opponent of the doctoral dissertation of Jón Hallsteinn Hallsson
Nóbelsverðlaun í lífeðlis- eða læknisfræði 2006 – RNA íhlutun
Leit að stökkbreytingum í LIMD1 og LTF genum á CER1 svæði á mannalitningi 3p21.3 í 10 mismunandi
Tilraunastöð Háskóla Íslands í meinafræði að Keldum
Erfðagreyping og sjúkdómsmynd
Erfðagreyping og sjúkdómsmynd
Genomic instability and breast cancer progressionCancer Genomics and Proteomics

2005

Uniparental disomy of chromosome 11 in a patient with Beckwith-Wiedemann syndrome. First reported case in IcelandLæknablaðið
Deletions at the chromosome 3 common eliminated region 1 on 3p21.3 in human breast tumorsBreast Cancer Research
Tvístæða litnings nr. 11 frá föður hjá sjúklingi með Beckwith-Wiedemann heilkenni. Fyrsta greining á Íslandi--Sjúkratilfelli.Læknabladid
Ráðstefna um príon og hæggengar veirurRáðstefna um príon og hæggengar veirur
2005 World DNA & Genome Day2005 World DNA & Genome Day
Tilraunastöð Háskóla Íslands í meinafræði að Keldum - Ársskýrsla 2005
Ralt er æxlisbæliprótein sem hefur áhrif á lyfjanæmi
Tilraunastöð Háskóla Íslands í meinafræði að Keldum. Árbók Háskóla Íslands 2005, pp. 228-228
Loss of RALT/MIG-6 expression in ERBB2-amplified breast carcinomas enhances ErbB-2 oncogenic potency and favors resistance to HerceptinOncogene
Tumor suppressor genes on human chromosome 3 and cancer pathogenesisCancer Genomics and Proteomics
Tumour suppressor genes at chromosome 3 and cancer pathogenesis
Breytingar á litningi 3 og framvinda æxlisvaxtar í nagdýrum og mönnum

2004

ALTERATIONS AT CHROMOSOME 3 AND CANCER PATHOGENESISAnticancer Research
Tilraunastöð Háskóla Íslands í meinafræði að Keldum - Ársskýrsla 2004
Nóbelsverðlaunin í efnafræði 2004 – Ubiquitin miðlað próteinniðurbrotRAUST - Tímarit um raunvísindi og stærðfræði
Ósamfelldar úrfellingar á C3CER1 litningasvæði eru algengar í æxlum frá tíu mismunandi vefjum
The Seventh International Conference of Anticancer Research The Seventh International Conference of Anticancer Research
Genetics of breast cancerDrugs of Today
Nóbelsverðlaunin í efnafræði 2004 – Ubiquitin miðlað próteinniðurbrotRAUST - Tímarit um raunvísindi og stærðfræði
Interstitial deletions including chromosome 3 common eliminated region 1 (C3CER1) prevail in human solid tumors from 10 different tissuesGenes Chromosomes and Cancer
Tilraunastöð Háskóla Íslands í meinafræði að Keldum. Árbók Háskóla Íslands 2004, pp. 203-204

2003

Tap á arfblendni innan C3CER1 svæðis á litningi 3p21.3 í æxlum frá tíu mismunandi líffærum
Rannsóknir á E-cadherini, beta-catenini og FHIT í magakrabbameinum
Molecular Genetics of Breast CancerInternational Journal of Human Genetics
The 24th Congress of the International Association for Breast Cancer Research.The 24th Congress of the International Association for Breast Cancer Research.
Germline mutations in DNA repair and cell cycle checkpoint genes: consequential somatic gene alterations and genome instabilityBreast Cancer Research
Tilraunastöð Háskóla Íslands í meinafræði að Keldum. Árbók Háskóla Íslands 2003, pp. 177-179
Vorþing á Keldum 2003Vorþing á Keldum 2003

2002

Pattern of FHIT LOH in different solid human tumors; association with survival in colorectal cancer patientsCancer Epidemiology Biomarkers & Prevention
Tilraunastöð Háskóla Íslands í meinafræði að Keldum. Árbók Háskóla Íslands 2002, pp. 160-161
High frequency of LOH, MSI and abnormal expression of FHIT in gastric cancerEuropean Journal of Cancer
Alterations of E-cadherin, beta-Catenin and FHIT in Gastric Cancer.European Journal of Cancer
Mutation analysis of the CHK2 gene in breast carcinoma and other cancersBreast Cancer Research
Epidemiology — laboratoryEuropean journal of cancer (Oxford, England : 1990)
Loss of heterozygosity at the FHIT gene in different solid human tumours and its association with survival in colorectal cancer patientsAnticancer Research

2001

The European Cancer ConferenceThe European Cancer Conference
Similar regions of human chromosome 3 are eliminated from or retained in human/human and human/mouse microcell hybrids during tumor growth in severe combined immunodeficient (SCID) miceProceedings of the National Academy of Sciences of the United States of America
Alterations of the FHIT gene in breast cancer: Association with tumour progression and patient survival.Cancer Detection and Prevention
92nd Annual Meeting of the American Association for Cancer Research92nd Annual Meeting of the American Association for Cancer Research
Tilraunastöð Háskóla Íslands í meinafræði að Keldum. Árbók Háskóla Íslands 2001, pp. 158-159
Stökkbreytingagreining á CHK2 geni í brjóstakrabbameini
Alterations of the FHIT gene in breast cancerCancer Detection and Prevention
Seminars in Cancer Biology (Fræðitímarit)
FHIT alterations in breast cancerSeminars in Cancer Biology
Alterations of E-cadherin and β-catenin in gastric cancerBMC Cancer
Breast cancerSeminars in Cancer Biology

2000

Molecular biology of breast cancer.Oncology Reports
Altered expression of E-cadherin in breast cancer: patterns, mechanisms and clinical significanceEuropean Journal of Cancer
Sómatískar erfðaefnisbreytingar í ættlægum og sporadískum brjóstaæxlum
Áhrif erfðaóstöðugleika á æxlisvöxt - Stökkbreytingar í genum sem innihalda stuttar endurteknar raðir í æxlisgerðum tengdum HNPCC
The Second International Symposium on the Molecular Biology of Breast CancerThe Second International Symposium on the Molecular Biology of Breast Cancer
Analysis of chromosome alterations and the E-cadherin and FHIT genes in lobular breast cancer.Breast Cancer Research
Analysis of the fragile histidine triad (FHIT) gene in lobular breast cancerEuropean Journal of Cancer
Alteration of the FHIT gene in breast cancer: association with tumour progression and patient survival
XIV Nordiske Kongres i RetsmedicinXIV Nordiske Kongres i Retsmedicin
5th International Symposium on Biotechnology in Preventive Oncology5th International Symposium on Biotechnology in Preventive Oncology
The effect of mismatch repair deficiency on tumourigenesis; microsatellite instability affecting genes containing short repeated sequences.International Journal of Oncology
Leit að próteinum sem bindast afurð æxlisbæligensins FHIT með Yeast-two-hybrid aðferð
Chromosome 8p alterations in sporadic and BRCA2 999de15 linked breast cancerJournal of Medical Genetics
Altered expression of E-cadherin in breast cancer: patterns, mechanisms and clinical significanceEuropean Journal of Cancer
Genetic defects in lobular breast cancer
Population studies and validation of paternity determinations by six microsatellite lociJournal of Forensic Sciences

1999

Replication error in colorectal carcinomaAnticancer Research
Tap á arfblendni litningasvæðis 3p14.2 og lækkuð tjáning á Fhit í brjóstaæxlum frá einstaklingum sem bera BRCA2 999del5 kímlínubreytingu
Somatic alterations of chromosome 8p in sporadic and BRCA2 999del5 linked breast cancerAmerican Journal of Human Genetics
Chromosome alterations and E-cadherin gene mutations in human lobular breast cancerBritish Journal of Cancer
Tap á arfblendni litningasvæðis 3p14.2 og lækkuð tjáning á Fhit í brjóstaæxlum frá einstaklingum sem bera BRCA2 999del5 kímlínubreytinguLæknablaðið
Molecular genetics of breast cancer progressionSeminars in Cancer Biology
Reduced Fhit expression in sporadic and BRCA2-linked breast carcinomasCancer Research
The Brca1 and Brca2 proteins and tumor pathogenesisAnticancer Research
Replication error in human breast cancerOncology Reports
Úrfellingar á litningi 8p í brjóstakrabbameini
The American Society of Human Genetics 49th annual meetingThe American Society of Human Genetics 49th annual meeting
Loss of heterozygosity at chromosome 1p in different solid human tumoursBritish Journal of Cancer

1998

High frequency of LOH at chromosome 18q in human breast cancerAnticancer Research
High incidence of loss of heterozygosity in breast tumors from carriers of the BRCA2 999del5 mutationCancer Research
Chromosome imbalance at the 3p14 region in human breast tumoursEuropean Journal of Cancer
Identification of a novel splicesite mutation of the BRCAL gene in two breast cancer familiesHuman Mutation
Breytingar í erfðaefni brjóstaæxla frá einstaklingum sem bera 999del5 kímlínubreytingu í BRCA2 geni.
High incidence of loss of heterozygosity at chromosome 17p13 in breast tumours from BRCA2 mutation carriersOncogene
The Sixth International Conference of Anticancer ResearchThe Sixth International Conference of Anticancer Research
Mapping loss of heterozygosity at chromosome 13qEuropean Journal of Cancer
Óstöðugleiki í erfðamengi ristilkrabbameinsæxla
Deletions at chromosome 18q harbouring the DCC and SMAD genes in human breast cancer: Association with clinicopathology and deletions at other chromosome regions.
Erfðaefnisbreytingar í ættgengu ristilkrabbameini.
Samanburður á erfðaefnisbrenglunum BRCA2 æxla og sporadiskra æxla á litningum 9, 11, 13, 17 og 20
Tap á erfðaefni á litningi 1p í tíu gerðum krabbameina hjá mönnum.

1997

Ristilkrabbamein og erfðir
Loss of heterozygosity at chromosome 7q in human breast cancerAnticancer Research
Molecular genetics of cancer: Second Joint Conference of the American Association for Cancer Research and the European Association for Cancer Research.Molecular genetics of cancer: Second Joint Conference of the American Association for Cancer Research and the European Association for Cancer Research.
Tap á arfblendni á litningi 1p í mannabrjóstakrabbameini. Samband við háan S-fasa, verri lífslíkur og úrfellingar á öðrum litningum
Meeting report; Molecular Genetics of Cancer. Second joint conference of the American Association for Cancer Reserach and the European Association for Cancer Research. 9-13 Sept. 1997, Oxford University, UKCurrent Drugs ID weekly highlights
Distinct somatic genetic changes associated with tumor progression in carriers of BRCA1 and BRCA2 germ-line mutationsCancer Research
Samanburður á úrfellingatíðni á styttra armi litnings 3 í mismunandi krabbameinsgerðum
Sameindalíffræði nefkokskrabbameina
Distinct somatic genetic changes associated with tumor progression in carriers of BRCA1 and BRCA2 germ-line mutationsProceedings of the american society for cancer research
Tíðni BRCA1 og BRCA2 stökkbreytinga í brjóstaæxlum íslenskra kvennaLæknablaðið
Tap á erfðaefni litningasvæðis 13q12-14 í brjótstaæxlum. Fylgni við verri horfur sjúklinga.
Tíðni BRCA1 og BRCA2 stökkbreytinga í brjóstaæxlum íslenskra kvenna.

1996

Erfðaefnistap á litningasvæði BRCA2 gensins í brjóstaæxlum. Fylgni við verri horfur sjúklinga
Tap á arfblendni á litningi 1p í brjóstakrabbameini og samband þess við klínískar breytur og úrfellingar á öðrum litningum
Frequent occurrence of BRCA2 linkage in Icelandic breast cancer families and segregation of a common BRCA2 haplotypeAmerican Journal of Human Genetics
High prevalence of the 999del5 mutation in icelandic breast and ovarian cancer patientsCancer Research
5th Workshop of the Nordic Genome Initiative5th Workshop of the Nordic Genome Initiative
Kortlagning úrfellinga og leit að æxlisbæligenum á litningi 16q í brjóstakrabbameini
Report of the fourth international workshop on human chromosome 16 mapping 1995 - Held on 12-14 November 1995 at the University of Leiden, The NetherlandsCytogenetics and Cell Genetics
Deletion mapping of chromosome 16 in human breast cancer; Putative location of tumor suppressor gene(s)Cytogenetics and Cell Genetics
Loss of heterozygosity on chromosome arm 3p in nasopharyngeal carcinomaGenes Chromosomes and Cancer
Samantekt úrfellinga á 9 litningasvæðum í brjóstakrabbameinssýnum
BRCA2 genið í íslenskum brjóstakrabbameinsfjölskyldum, mögulegur sameiginlegur uppruni stökkbreytingar og fjölbreytileiki í æxlisgerðum
Leit að stökkbreytingum í hMSH2 og hMLH1 genum í íslenskum ristilkrabbameinssjúklingum
“Elimination test”: Solid tumor progression model based on the non-random changes of human chromosomes 3 in monochromosomal microcell hybrid.Cancer Genetics and Cytogenetics
Loss of heterozygosity at chromosome 1p in human breast cancerInternational Journal of Oncology

1995

The Fourth International Workshop on Human Chromosome 16 Mapping 1995The Fourth International Workshop on Human Chromosome 16 Mapping 1995
Mapping of chromosome 3 alterations in human breast cancer using microsatellite PCR markersInternational Journal of Oncology
Kortlagning úrfellinga á lengri armi litnings 6 í brjóstakrabbameinsæxlum
Magnanir og úrfellingar á litningi 11 í brjóstakrabbameini
Kortlagning breytinga á litningi 3 og 16 í brjóstakrabbameini
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
Identification of a breast tumor with microsatellite instability in a potential carrier of the hereditary non‐polyposis colon cancer traitClinical Genetics
Different Tumor Types from BRCA2 Carriers Show Wild-Type Chromosome Deletions on 13q12-q13Cancer Research
High frequency of allelic imbalance at chromosome region 16q22‐23 in human breast cancerInternational Journal of Cancer
Loss of heterozygosity at chromosome 6q correlates with tumor progression and patient survivalInternational Journal of Oncology
Loss of heterozygosity at chromosome 11 in breast cancerBritish Journal of Cancer
Óstöðugleiki í stuttum endurteknum röðum í ristil- og brjóstaæxlum frá krabbameinsfjölskyldum

1994

Norrænn PCR-lyklabanki til rannsókna á erfðamengi mannsinsLæknablaðið
Leit að æxlisbæligeni með samanburði á tjáðum genum í krabbameinsfrumum með mismunandi arfgerð og vaxtarhraðaIcelandic Medical Journal
The v‐erbA Oncoprotein of the AEV Transforming Retrovirus Binds to the Promoter Region of the Erythroid‐specific Band 3 GeneAnnals of the New York Academy of Sciences

1993

Urinary system tumours in a familyEuropean Journal of Cancer
22nd FEBS Meeting22nd FEBS Meeting
XXVI Nordic Congress of DermatologyXXVI Nordic Congress of Dermatology
Slow Infections of the Central Nervous System: The Legacy of Dr. Bjorn Sigurdsson (Annals of the New York Academy of Sciences) Slow Infections of the Central Nervous System: The Legacy of Dr. Bjorn Sigurdsson (Annals of the New York Academy of Sciences)

1992

Úrfellingar og hugsanlegar kímlínubreytingar á litningi 3 í brjóstakrabbameini.
XXIII Nordic Congress in Clinical ChemistryXXIII Nordic Congress in Clinical Chemistry
Rannsóknir á erfðamengi mannsins – Norrænt HUGO verkefniLæknablaðið
Genetics and Molecular Biology of Breast CancerGenetics and Molecular Biology of Breast Cancer
ErbA æxlisgen og stjórnun á genatjáningu
Rannsóknir á erfðamengi mannsins – Norrænt HUGO verkefniIcelandic Medical Journal
Second Nordic Genome WorkshopSecond Nordic Genome Workshop

1991

XIV Congress of the Scandinavian Association of GeneticsXIV Congress of the Scandinavian Association of Genetics
First Nordic Genome WorkshopFirst Nordic Genome Workshop
The most frequently lost allelic site in human renal cell carcinoma D3f15s2 on the short arm of chromosome 3 has homologous sequences on rat chromosome 8Cytogenetic and Genome Research
Chromosomal assignment of five cancer-associated rat genesOncogene
Chromosomal assignment of retinoic acid receptor (RAR) genes in the human, mouse, and rat genomesGenomics

1990

Recombinant plasmid expressing the entire coding region of the Bmyc putative protein.Journal of clinical & laboratory immunology
Differences in C‐myc and pvt‐1 amplification in sewa sarcoma sublines selected for adherent or non‐adherent growthInternational Journal of Cancer
A gene near the D3F15S2 site on 3p is expressed in normal human kidney but not or only at a severely reduced level in 11 of 15 primary renal cell carcinomas (RCC)Oncogene
The myc gene family proteins and their role in transformation and differentiationSeminars in Cancer Biology

1989

Nucleotide sequence of the rat Bmyc geneOncogene
The Molecular Basis of Cell Growth RegulationThe Molecular Basis of Cell Growth Regulation
Myc family of genes; structure, expression and activation in tumor pathogenesis
Myc family of genes; structure, expression and activation in tumor pathogenesis
Fifth Annual Meeting on OncogenesFifth Annual Meeting on Oncogenes

1988

Elevated expression of c-myc and N-myc produces distinct changes in nuclear fine structure and chromatin organizationOncogene
Drosophila homolog of the murine Int-1 protooncogeneProceedings of the National Academy of Sciences of the United States of America
Amplification of c-myc and pvt-1 homologous sequences in acute nonlymphatic leukemiaLeukemia Research
Chromosome localization and expression pattern of Lmyc and Bmyc in murine embryonal carcinoma cellsOncogene
Consistent chromosome 3p deletion and loss of heterozygosity in renal cell carcinomaProceedings of the National Academy of Sciences of the United States of America
Oncogenes and Growth ControlOncogenes and Growth Control
Rat c-raf oncogene is located on chromosome 4 and may be activated by sequences from chromosome 13Somatic Cell and Molecular Genetics
Structure and expression of B-myc, a new member of the myc gene familyMolecular and Cellular Biology

1987

Mapping of Lmyc and Nmyc to rat chromosomes 5 and 6Somatic Cell and Molecular Genetics
Specific polypeptide differences in normal versus malignant human breast tissues by two-dimensional electrophoresisBreast Cancer Research and Treatment
The rat misl/pvi-/locus is syntenic with myc on chromosome 7Cytogenetic and Genome Research
Elevated c-myc expression facilitates the replication of SV40 DNA in human lymphoma cells
Similarities and differences in the regulation of N-myc and c-myc genes in murine embryonal carcinoma cellsExperimental Cell Research
THE RAT MIS1/PVT-1 LOCUS IS SYNTENIC WITH MYC ON CHROMOSOME-7Cytogenetics and Cell Genetics
Chromosome abberation and oncogene activation in two histologically related human and rat B-cell tumorsViral Carcinogenesis

1986

c-myc activation in spontaneous rat immunocytomas containing a 6;7 chromosomal translocation.Current Topics in Microbiology and Immunology
Catabolite repressive effects of 5-thio-D-glucose on Saccharomyces cerevisiae.Journal of General Microbiology
Sjúklingur með krabbamein í blöðruhálskirtli og hægfara eitlafrumuhvítblæði: Fækkun eitilfrumna í blóði eftir estrógen-meðferðLæknablaðið
Multiple chromosomal rearrangements in a spontaneously arising t(6;7) rat immunocytoma juxtapose c-myc and immunoglobulin heavy chain sequencesProceedings of the National Academy of Sciences of the United States of America
C-Myc activation in spontaneous immunocytomas containing a 6;7 chromosomal translocation. Alfred Benzon Symposium 24, Copenhagen June 15-19, 1986, Ed. Kjeldgaard NO, Forchhammer J. Munksgaard, p. 38.

1985

Sixteenth Annual General Meeting of the Scandinavian Society for ImmunologySixteenth Annual General Meeting of the Scandinavian Society for Immunology
Gene localization on sorted chromosomesProceedings of the National Academy of Sciences of the United States of America
CLONING AND CHARACTERIZATION OF THE DNA-SEQUENCE TRANSPOSED TO THE ONCOGENE C-MYC IN RAT IMMUNOCYTOMAS WITH T(6-7) CHROMOSOMAL TRANSLOCATIONScandinavian Journal of Immunology

1984

Mælingar á Estrógen- og Prógesterón-viðtökum í BrjóstakrabbameinumLæknablaðið
Isoenzyme pattern and subcellular localization of hexokinases in human breast cancer and nonpathological breast tissueInternational Journal of Cancer

Keywords for Specialisation:

Molecular biology