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Best matches for Nexø BA[au]:

[Endogenous retroviruses are associated with autoimmune diseases]. Nexø BA et al. Ugeskr Laeger. (2016)

Two endogenous retroviral loci appear to contribute to Multiple Sclerosis. Nexø BA et al. BMC Neurol. (2016)

New basal cell carcinoma susceptibility loci. Stacey SN et al. Nat Commun. (2015)

Search results

Items: 1 to 50 of 84

1.

A new theory on autoimmunity with reference to multiple sclerosis.

Nexø BA.

Immunol Res. 2018 Jun;66(3):336-339. doi: 10.1007/s12026-018-9003-x.

PMID:
29882036
2.

Genetically determined high activity of IL-12 and IL-18 in ulcerative colitis and TLR5 in Crohns disease were associated with non-response to anti-TNF therapy.

Bank S, Andersen PS, Burisch J, Pedersen N, Roug S, Galsgaard J, Turino SY, Brodersen JB, Rashid S, Rasmussen BK, Avlund S, Olesen TB, Hoffmann HJ, Nexø BA, Sode J, Vogel U, Andersen V.

Pharmacogenomics J. 2018 Jan;18(1):87-97. doi: 10.1038/tpj.2016.84. Epub 2017 Jan 31.

PMID:
28139755
3.

[Endogenous retroviruses are associated with autoimmune diseases].

Nexø BA, Jensen SB, Hansen B, Laska MJ.

Ugeskr Laeger. 2016 Jun 13;178(24). pii: V12150980. Review. Danish.

PMID:
27292833
4.

Two endogenous retroviral loci appear to contribute to Multiple Sclerosis.

Nexø BA, Jensen SB, Nissen KK, Hansen B, Laska MJ.

BMC Neurol. 2016 Apr 30;16:57. doi: 10.1186/s12883-016-0580-9. Review.

5.

Synergy of two human endogenous retroviruses in multiple myeloma.

Schmidt KL, Vangsted AJ, Hansen B, Vogel UB, Hermansen NE, Jensen SB, Laska MJ, Nexø BA.

Leuk Res. 2015 Oct;39(10):1125-8. doi: 10.1016/j.leukres.2015.06.014. Epub 2015 Jun 24.

PMID:
26231931
6.

Are human endogenous retroviruses triggers of autoimmune diseases? Unveiling associations of three diseases and viral loci.

Nexø BA, Villesen P, Nissen KK, Lindegaard HM, Rossing P, Petersen T, Tarnow L, Hansen B, Lorenzen T, Hørslev-Petersen K, Jensen SB, Bahrami S, Lajer M, Schmidt KL, Parving HH, Junker P, Laska MJ.

Immunol Res. 2016 Feb;64(1):55-63. doi: 10.1007/s12026-015-8671-z.

7.

New basal cell carcinoma susceptibility loci.

Stacey SN, Helgason H, Gudjonsson SA, Thorleifsson G, Zink F, Sigurdsson A, Kehr B, Gudmundsson J, Sulem P, Sigurgeirsson B, Benediktsdottir KR, Thorisdottir K, Ragnarsson R, Fuentelsaz V, Corredera C, Gilaberte Y, Grasa M, Planelles D, Sanmartin O, Rudnai P, Gurzau E, Koppova K, Nexø BA, Tjønneland A, Overvad K, Jonasson JG, Tryggvadottir L, Johannsdottir H, Kristinsdottir AM, Stefansson H, Masson G, Magnusson OT, Halldorsson BV, Kong A, Rafnar T, Thorsteinsdottir U, Vogel U, Kumar R, Nagore E, Mayordomo JI, Gudbjartsson DF, Olafsson JH, Stefansson K.

Nat Commun. 2015 Apr 9;6:6825. doi: 10.1038/ncomms7825.

8.

Effectiveness of anti-tumour necrosis factor-α therapy in Danish patients with inflammatory bowel diseases.

Bank S, Andersen PS, Burisch J, Pedersen N, Roug S, Galsgaard J, Turino SY, Brodersen JB, Rashid S, Avlund S, Olesen TB, Green A, Hoffmann HJ, Thomsen MK, Thomsen VØ, Nexø BA, Vogel U, Andersen V.

Dan Med J. 2015 Mar;62(3). pii: A4994.

PMID:
25748864
9.

Common variants in CYP2R1 and GC genes are both determinants of serum 25-hydroxyvitamin D concentrations after UVB irradiation and after consumption of vitamin D₃-fortified bread and milk during winter in Denmark.

Nissen J, Vogel U, Ravn-Haren G, Andersen EW, Madsen KH, Nexø BA, Andersen R, Mejborn H, Bjerrum PJ, Rasmussen LB, Wulf HC.

Am J Clin Nutr. 2015 Jan;101(1):218-27. doi: 10.3945/ajcn.114.092148. Epub 2014 Nov 5.

PMID:
25527766
10.

A non-synonymous single-nucleotide polymorphism in the gene encoding Toll-like Receptor 3 (TLR3) is associated with sero-negative rheumatoid arthritis (RA) in a Danish population.

Laska MJ, Hansen B, Troldborg A, Lorenzen T, Stengaard-Pedersen K, Junker P, Nexø BA, Lindegaard HM.

BMC Res Notes. 2014 Oct 10;7:716. doi: 10.1186/1756-0500-7-716.

11.

Real-life use of vitamin D3-fortified bread and milk during a winter season: the effects of CYP2R1 and GC genes on 25-hydroxyvitamin D concentrations in Danish families, the VitmaD study.

Nissen J, Vogel U, Ravn-Haren G, Andersen EW, Nexø BA, Andersen R, Mejborn H, Madsen KH, Rasmussen LB.

Genes Nutr. 2014 Jul;9(4):413. doi: 10.1007/s12263-014-0413-7. Epub 2014 Jun 17.

12.

Associations between functional polymorphisms in the NFκB signaling pathway and response to anti-TNF treatment in Danish patients with inflammatory bowel disease.

Bank S, Andersen PS, Burisch J, Pedersen N, Roug S, Galsgaard J, Turino SY, Brodersen JB, Rashid S, Rasmussen BK, Avlund S, Olesen TB, Hoffmann HJ, Thomsen MK, Thomsen VØ, Frydenberg M, Nexø BA, Sode J, Vogel U, Andersen V.

Pharmacogenomics J. 2014 Dec;14(6):526-34. doi: 10.1038/tpj.2014.19. Epub 2014 Apr 29.

PMID:
24776844
13.

Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma.

Stacey SN, Sulem P, Gudbjartsson DF, Jonasdottir A, Thorleifsson G, Gudjonsson SA, Masson G, Gudmundsson J, Sigurgeirsson B, Benediktsdottir KR, Thorisdottir K, Ragnarsson R, Fuentelsaz V, Corredera C, Grasa M, Planelles D, Sanmartin O, Rudnai P, Gurzau E, Koppova K, Hemminki K, Nexø BA, Tjønneland A, Overvad K, Johannsdottir H, Helgadottir HT, Thorsteinsdottir U, Kong A, Vogel U, Kumar R, Nagore E, Mayordomo JI, Rafnar T, Olafsson JH, Stefansson K.

Hum Mol Genet. 2014 Jun 1;23(11):3045-53. doi: 10.1093/hmg/ddt671. Epub 2014 Jan 8.

14.

Restriction genes for retroviruses influence the risk of multiple sclerosis.

Nexø BA, Hansen B, Nissen KK, Gundestrup L, Terkelsen T, Villesen P, Bahrami S, Petersen T, Pedersen FS, Laska MJ.

PLoS One. 2013 Sep 16;8(9):e74063. doi: 10.1371/journal.pone.0074063. eCollection 2013.

15.

Polymorphisms within Toll-like receptors are associated with systemic lupus erythematosus in a cohort of Danish females.

Laska MJ, Troldborg A, Hansen B, Stengaard-Pedersen K, Junker P, Nexø BA, Voss A.

Rheumatology (Oxford). 2014 Jan;53(1):48-55. doi: 10.1093/rheumatology/ket316. Epub 2013 Sep 24.

PMID:
24064706
16.

Endogenous retroviruses and multiple sclerosis-new pieces to the puzzle.

Nissen KK, Laska MJ, Hansen B, Terkelsen T, Villesen P, Bahrami S, Petersen T, Pedersen FS, Nexø BA.

BMC Neurol. 2013 Aug 28;13:111. doi: 10.1186/1471-2377-13-111. Review.

17.

High-quality and -quantity DNA extraction from frozen archival blood clots for genotyping of single-nucleotide polymorphisms.

Bank S, Nexø BA, Andersen V, Vogel U, Andersen PS.

Genet Test Mol Biomarkers. 2013 Jun;17(6):501-3. doi: 10.1089/gtmb.2012.0429. Epub 2013 Apr 10.

PMID:
23574531
18.

(Some) cellular mechanisms influencing the transcription of human endogenous retrovirus, HERV-Fc1.

Laska MJ, Nissen KK, Nexø BA.

PLoS One. 2013;8(1):e53895. doi: 10.1371/journal.pone.0053895. Epub 2013 Jan 28.

19.

Treatment of HIV and risk of multiple sclerosis.

Nexø BA, Pedersen L, Sørensen HT, Koch-Henriksen N.

Epidemiology. 2013 Mar;24(2):331-2. doi: 10.1097/EDE.0b013e318281e48a. No abstract available.

PMID:
23377093
20.

No additional copies of HERV-Fc1 in the germ line of multiple sclerosis patients.

Nissen KK, Laska MJ, Hansen B, Pedersen FS, Nexø BA.

Virol J. 2012 Sep 8;9:188.

21.

Expression of HERV-Fc1, a human endogenous retrovirus, is increased in patients with active multiple sclerosis.

Laska MJ, Brudek T, Nissen KK, Christensen T, Møller-Larsen A, Petersen T, Nexø BA.

J Virol. 2012 Apr;86(7):3713-22. doi: 10.1128/JVI.06723-11. Epub 2012 Jan 25.

22.

Genetic association of multiple sclerosis with the marker rs391745 near the endogenous retroviral locus HERV-Fc1: analysis of disease subtypes.

Hansen B, Oturai AB, Harbo HF, Celius EG, Nissen KK, Laska MJ, Søndergaard HB, Petersen T, Nexø BA.

PLoS One. 2011;6(10):e26438. doi: 10.1371/journal.pone.0026438. Epub 2011 Oct 25.

23.

A germline variant in the TP53 polyadenylation signal confers cancer susceptibility.

Stacey SN, Sulem P, Jonasdottir A, Masson G, Gudmundsson J, Gudbjartsson DF, Magnusson OT, Gudjonsson SA, Sigurgeirsson B, Thorisdottir K, Ragnarsson R, Benediktsdottir KR, Nexø BA, Tjønneland A, Overvad K, Rudnai P, Gurzau E, Koppova K, Hemminki K, Corredera C, Fuentelsaz V, Grasa P, Navarrete S, Fuertes F, García-Prats MD, Sanambrosio E, Panadero A, De Juan A, Garcia A, Rivera F, Planelles D, Soriano V, Requena C, Aben KK, van Rossum MM, Cremers RG, van Oort IM, van Spronsen DJ, Schalken JA, Peters WH, Helfand BT, Donovan JL, Hamdy FC, Badescu D, Codreanu O, Jinga M, Csiki IE, Constantinescu V, Badea P, Mates IN, Dinu DE, Constantin A, Mates D, Kristjansdottir S, Agnarsson BA, Jonsson E, Barkardottir RB, Einarsson GV, Sigurdsson F, Moller PH, Stefansson T, Valdimarsson T, Johannsson OT, Sigurdsson H, Jonsson T, Jonasson JG, Tryggvadottir L, Rice T, Hansen HM, Xiao Y, Lachance DH, O Neill BP, Kosel ML, Decker PA, Thorleifsson G, Johannsdottir H, Helgadottir HT, Sigurdsson A, Steinthorsdottir V, Lindblom A; Swedish Low-risk Colorectal Cancer Study Group, Sandler RS, Keku TO, Banasik K, Jørgensen T, Witte DR, Hansen T, Pedersen O, Jinga V, Neal DE, Catalona WJ, Wrensch M, Wiencke J, Jenkins RB, Nagore E, Vogel U, Kiemeney LA, Kumar R, Mayordomo JI, Olafsson JH, Kong A, Thorsteinsdottir U, Rafnar T, Stefansson K.

Nat Genet. 2011 Sep 25;43(11):1098-103. doi: 10.1038/ng.926.

24.

Single nucleotide polymorphisms in the promoter region of the IL1B gene influence outcome in multiple myeloma patients treated with high-dose chemotherapy independently of relapse treatment with thalidomide and bortezomib.

Vangsted AJ, Klausen TW, Abildgaard N, Andersen NF, Gimsing P, Gregersen H, Nexø BA, Vogel U.

Ann Hematol. 2011 Oct;90(10):1173-81. doi: 10.1007/s00277-011-1194-3. Epub 2011 Feb 24.

PMID:
21347685
25.

The etiology of multiple sclerosis: genetic evidence for the involvement of the human endogenous retrovirus HERV-Fc1.

Nexø BA, Christensen T, Frederiksen J, Møller-Larsen A, Oturai AB, Villesen P, Hansen B, Nissen KK, Laska MJ, Petersen TS, Bonnesen S, Hedemand A, Wu T, Wang X, Zhang X, Brudek T, Maric R, Søndergaard HB, Sellebjerg F, Brusgaard K, Kjeldbjerg AL, Rasmussen HB, Nielsen AL, Nyegaard M, Petersen T, Børglum AD, Pedersen FS.

PLoS One. 2011 Feb 2;6(2):e16652. doi: 10.1371/journal.pone.0016652.

26.

The importance of a sub-region on chromosome 19q13.3 for prognosis of multiple myeloma patients after high-dose treatment and stem cell support: a linkage disequilibrium mapping in RAI and CD3EAP.

Vangsted AJ, Klausen TW, Gimsing P, Abildgaard N, Andersen NF, Gregersen H, Nexø BA, Vogel UB.

Ann Hematol. 2011 Jun;90(6):675-84. doi: 10.1007/s00277-010-1105-z. Epub 2010 Nov 3.

PMID:
21046104
27.

p53 and PPP1R13L (alias iASPP or RAI) form a feedback loop to regulate genotoxic stress responses.

Laska MJ, Vogel UB, Jensen UB, Nexø BA.

Biochim Biophys Acta. 2010 Dec;1800(12):1231-40. doi: 10.1016/j.bbagen.2010.09.002. Epub 2010 Sep 15.

PMID:
20840860
28.

Association of a single nucleotide polymorphic variation in the human chromosome 19q13.3 with drug responses in the NCI60 cell lines.

Nissen KK, Vogel U, Nexø BA.

Anticancer Drugs. 2009 Mar;20(3):174-8. doi: 10.1097/CAD.0b013e3283229ae3.

PMID:
19396015
29.

Enforced expression of PPP1R13L increases tumorigenesis and invasion through p53-dependent and p53-independent mechanisms.

Laska MJ, Lowe SW, Zender L, Hearn S, Vogel U, Jensen UB, Bric A, Nexø BA.

Mol Carcinog. 2009 Sep;48(9):832-42. doi: 10.1002/mc.20528.

30.

Haplotype frequencies in a sub-region of chromosome 19q13.3, related to risk and prognosis of cancer, differ dramatically between ethnic groups.

Schierup MH, Mailund T, Li H, Wang J, Tjønneland A, Vogel U, Bolund L, Nexø BA.

BMC Med Genet. 2009 Mar 3;10:20. doi: 10.1186/1471-2350-10-20.

31.

Linkage disequilibrium mapping of a breast cancer susceptibility locus near RAI/PPP1R13L/iASPP.

Nexø BA, Vogel U, Olsen A, Nyegaard M, Bukowy Z, Rockenbauer E, Zhang X, Koca C, Mains M, Hansen B, Hedemand A, Kjeldgaard A, Laska MJ, Raaschou-Nielsen O, Cold S, Overvad K, Tjønneland A, Bolund L, Børglum AD.

BMC Med Genet. 2008 Jun 27;9:56. doi: 10.1186/1471-2350-9-56.

32.

Polymorphisms in genes involved in the inflammatory response and interaction with NSAID use or smoking in relation to lung cancer risk in a prospective study.

Vogel U, Christensen J, Wallin H, Friis S, Nexø BA, Raaschou-Nielsen O, Overvad K, Tjønneland A.

Mutat Res. 2008 Mar 1;639(1-2):89-100. doi: 10.1016/j.mrfmmm.2007.11.004. Epub 2007 Nov 26.

PMID:
18164040
33.

Expression of the RAI gene is conducive to apoptosis: studies of induction and interference.

Laska MJ, Strandbygård D, Kjeldgaard A, Mains M, Corydon TJ, Memon AA, Sørensen BS, Vogel U, Jensen UB, Nexø BA.

Exp Cell Res. 2007 Jul 15;313(12):2611-21. Epub 2007 May 22.

PMID:
17570360
34.

Prospective study of interaction between alcohol, NSAID use and polymorphisms in genes involved in the inflammatory response in relation to risk of colorectal cancer.

Vogel U, Christensen J, Dybdahl M, Friis S, Hansen RD, Wallin H, Nexø BA, Raaschou-Nielsen O, Andersen PS, Overvad K, Tjønneland A.

Mutat Res. 2007 Nov 1;624(1-2):88-100. Epub 2007 Apr 27.

PMID:
17544013
35.

Polymorphisms in COX-2, NSAID use and risk of basal cell carcinoma in a prospective study of Danes.

Vogel U, Christensen J, Wallin H, Friis S, Nexø BA, Tjønneland A.

Mutat Res. 2007 Apr 1;617(1-2):138-46. Epub 2007 Jan 20.

PMID:
17307204
36.

Polymorphisms in the genes ERCC2, XRCC3 and CD3EAP influence treatment outcome in multiple myeloma patients undergoing autologous bone marrow transplantation.

Vangsted A, Gimsing P, Klausen TW, Nexø BA, Wallin H, Andersen P, Hokland P, Lillevang ST, Vogel U.

Int J Cancer. 2007 Mar 1;120(5):1036-45.

37.

Peroxisome proliferator-activated [corrected] receptor-gamma2 [corrected] Pro12Ala, interaction with alcohol intake and NSAID use, in relation to risk of breast cancer in a prospective study of Danes.

Vogel U, Christensen J, Nexø BA, Wallin H, Friis S, Tjønneland A.

Carcinogenesis. 2007 Feb;28(2):427-34. Epub 2006 Sep 6. Erratum in: Carcinogenesis. 2007 Sep;28(9):2062.

PMID:
16959787
38.

Increased mRNA expression levels of ERCC1, OGG1 and RAI in colorectal adenomas and carcinomas.

Saebø M, Skjelbred CF, Nexø BA, Wallin H, Hansteen IL, Vogel U, Kure EH.

BMC Cancer. 2006 Aug 16;6:208.

39.

Effects of polymorphisms in ERCC1, ASE-1 and RAI on the risk of colorectal carcinomas and adenomas: a case control study.

Skjelbred CF, Saebø M, Nexø BA, Wallin H, Hansteen IL, Vogel U, Kure EH.

BMC Cancer. 2006 Jul 3;6:175.

40.

Gene-environment interactions between smoking and a haplotype of RAI, ASE-1 and ERCC1 polymorphisms among women in relation to risk of lung cancer in a population-based study.

Vogel U, Sørensen M, Hansen RD, Tjønneland A, Overvad K, Wallin H, Nexø BA, Raaschou-Nielsen O.

Cancer Lett. 2007 Mar 8;247(1):159-65. Epub 2006 May 11.

PMID:
16690207
41.

Polymorphisms of the XRCC1, XRCC3 and XPD genes and risk of colorectal adenoma and carcinoma, in a Norwegian cohort: a case control study.

Skjelbred CF, Saebø M, Wallin H, Nexø BA, Hagen PC, Lothe IM, Aase S, Johnson E, Hansteen IL, Vogel U, Kure EH.

BMC Cancer. 2006 Mar 16;6:67.

42.

Associations between GPX1 Pro198Leu polymorphism, erythrocyte GPX activity, alcohol consumption and breast cancer risk in a prospective cohort study.

Ravn-Haren G, Olsen A, Tjønneland A, Dragsted LO, Nexø BA, Wallin H, Overvad K, Raaschou-Nielsen O, Vogel U.

Carcinogenesis. 2006 Apr;27(4):820-5. Epub 2005 Nov 14.

PMID:
16287877
43.

ERCC1, XPD and RAI mRNA levels in lymphocytes are not associated with lung cancer risk in a prospective study of Danes.

Vogel U, Nexø BA, Tjønneland A, Wallin H, Hertel O, Raaschou-Nielsen O.

Mutat Res. 2006 Jan 29;593(1-2):88-96. Epub 2005 Jul 28.

PMID:
16054657
44.

GPX Pro198Leu and OGG1 Ser326Cys polymorphisms and risk of development of colorectal adenomas and colorectal cancer.

Hansen R, Saebø M, Skjelbred CF, Nexø BA, Hagen PC, Bock G, Bowitz Lothe IM, Johnson E, Aase S, Hansteen IL, Vogel U, Kure EH.

Cancer Lett. 2005 Nov 8;229(1):85-91.

PMID:
15946795
45.

Effect of polymorphisms in XPD, RAI, ASE-1 and ERCC1 on the risk of basal cell carcinoma among Caucasians after age 50.

Vogel U, Olsen A, Wallin H, Overvad K, Tjønneland A, Nexø BA.

Cancer Detect Prev. 2005;29(3):209-14. Epub 2005 Apr 22.

PMID:
15936590
46.

Polymorphisms in RAI and in genes of nucleotide and base excision repair are not associated with risk of testicular cancer.

Laska MJ, Nexø BA, Vistisen K, Poulsen HE, Loft S, Vogel U.

Cancer Lett. 2005 Jul 28;225(2):245-51.

PMID:
15885892
47.

Combinations of polymorphisms in XPD, XPC and XPA in relation to risk of lung cancer.

Vogel U, Overvad K, Wallin H, Tjønneland A, Nexø BA, Raaschou-Nielsen O.

Cancer Lett. 2005 May 10;222(1):67-74.

PMID:
15837542
48.

SNP genotyping using microsphere-linked PNA and flow cytometric detection.

Rockenbauer E, Petersen K, Vogel U, Bolund L, Kølvraa S, Nielsen KV, Nexø BA.

Cytometry A. 2005 Apr;64(2):80-6.

49.

No association between base excision repair gene polymorphisms and risk of lung cancer.

Vogel U, Nexø BA, Wallin H, Overvad K, Tjønneland A, Raaschou-Nielsen O.

Biochem Genet. 2004 Dec;42(11-12):453-60.

PMID:
15587988
50.

No association between OGG1 Ser326Cys and risk of basal cell carcinoma.

Vogel U, Olsen A, Wallin H, Overvad K, Tjønneland A, Nexø BA.

Cancer Epidemiol Biomarkers Prev. 2004 Oct;13(10):1680-1. No abstract available.

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