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Literature citations Results

Citation
The T cell regulator gene SH2D2A contributes to the genetic susceptibility of multiple sclerosis.

Dai K.Z., Harbo H.F., Celius E.G., Oturai A., Sorensen P.S., Ryder L.P., Datta P., Svejgaard A., Hillert J., Fredrikson S. et al.

Genes Immun. 2:263-268(2001) · Mapped (4)

The influence of mannose binding lectin polymorphisms on disease outcome in early polyarthritis. TIRA Group.

Jacobsen S., Madsen H.O., Klarlund M., Jensen T., Skjodt H., Jensen K.E., Svejgaard A., Garred P.

J. Rheumatol. 28:935-942(2001) · Mapped (3)

Protein phosphatase 2A (PP2A) regulates interleukin-4-mediated STAT6 signaling.

Woetmann A., Brockdorff J., Lovato P., Nielsen M., Leick V., Rieneck K., Svejgaard A., Geisler C., Odum N.

J. Biol. Chem. 278:2787-2791(2003) · Mapped (23)

Oligonucleotide fishing for STAT6: cross-talk between IL-4 and chemokines.

Eriksen K.W., Nielsen M., Kaltoft K., Svejgaard A., Nissen M.H., Ropke C., Odum N.

Exp. Clin. Immunogenet. 18:233-241(2001) · Mapped (20)

Nomenclature for factors of the HLA system, 2010.

Marsh S.G., Albert E.D., Bodmer W.F., Bontrop R.E., Dupont B., Erlich H.A., Fernandez-Vina M., Geraghty D.E., Holdsworth R., Hurley C.K. et al.

Tissue Antigens 75:291-455(2010) · UniProtKB (3)

No linkage or association of the nitric oxide synthase genes to multiple sclerosis.

Modin H., Dai Y., Masterman T., Svejgaard A., Sorensen P.S., Oturai A., Ryder L.P., Spurkland A., Vartdal F., Laaksonen M. et al.

J. Neuroimmunol. 119:95-100(2001) · Mapped (14)

Mice lacking all conventional MHC class II genes.

Madsen L., Labrecque N., Engberg J., Dierich A., Svejgaard A., Benoist C., Mathis D., Fugger L.

Proc. Natl. Acad. Sci. U.S.A. 96:10338-10343(1999) · Mapped (72)

Mannose-binding lectin variant alleles and HLA-DR4 alleles are associated with giant cell arteritis.

Jacobsen S., Baslund B., Madsen H.O., Tvede N., Svejgaard A., Garred P.

J. Rheumatol. 29:2148-2153(2002) · Mapped (1,747)

Mannose-binding lectin polymorphisms and susceptibility to infection in systemic lupus erythematosus.

Garred P., Madsen H.O., Halberg P., Petersen J., Kronborg G., Svejgaard A., Andersen V., Jacobsen S.

Arthritis Rheum. 42:2145-2152(1999) · Mapped (3)

Limited protective effect of the CCR5Delta32/CCR5Delta32 genotype on human immunodeficiency virus infection incidence in a cohort of patients with hemophilia and selection for genotypic X4 virus.

Iversen A.K., Christiansen C.B., Attermann J., Eugen-Olsen J., Schulman S., Berntorp E., Ingerslev J., Fugger L., Scheibel E., Tengborn L. et al.

J. Infect. Dis. 187:215-225(2003) · UniProtKB (9) · Mapped (100)

IL-6 gene polymorphism in rheumatoid arthritis, pauciarticular juvenile rheumatoid arthritis, systemic lupus erythematosus, and in healthy Danes.

Fugger L., Morling N., Bendtzen K., Ryder L., Andersen V., Heilman C., Karup Pedersen F., Friis J., Halbert P., Svejgaard A.

J. Immunogenet. 16:461-465(1989) · Mapped (8)

Identification of new sensitive biomarkers for the in vivo response to interferon-beta treatment in multiple sclerosis using DNA-array evaluation.

Sellebjerg F., Krakauer M., Hesse D., Ryder L.P., Alsing I., Jensen P.E., Koch-Henriksen N., Svejgaard A., Soelberg Sorensen P.

Eur. J. Neurol. 16:1291-1298(2009) · Mapped (8)

Genetic polymorphisms in the genes encoding human interleukin-7 receptor-alpha: prognostic significance in allogeneic stem cell transplantation.

Shamim Z., Ryder L.P., Heilmann C., Madsen H., Lauersen H., Andersen P.K., Svejgaard A., Jacobsen N., Muller K.

Bone Marrow Transplant. 37:485-491(2006) · Mapped (4)

Genes in the HLA class I region may contribute to the HLA class II-associated genetic susceptibility to multiple sclerosis.

Harbo H.F., Lie B.A., Sawcer S., Celius E.G., Dai K.Z., Oturai A., Hillert J., Lorentzen A.R., Laaksonen M., Myhr K.M. et al.

Tissue Antigens 63:237-247(2004) · Mapped (11,069)

Disease severity in Danish multiple sclerosis patients evaluated by MRI and three genetic markers (HLA-DRB1*1501, CCR5 deletion mutation, apolipoprotein E).

Schreiber K., Otura A.B., Ryder L.P., Madsen H.O., Jorgensen O.S., Svejgaard A., Sorensen P.S.

Mult. Scler. 8:295-298(2002) · Mapped (1,856)

Different molecular events result in low protein levels of mannan-binding lectin in populations from South-East Africa and South America.

Madsen H.O., Satz M.L., Hogh B., Svejgaard A., Garred P.

J. Immunol. 161:3169-3175(1998) · UniProtKB (1)

CXC chemokine receptor 3 expression on CD34(+) hematopoietic progenitors from human cord blood induced by granulocyte-macrophage colony-stimulating factor: chemotaxis and adhesion induced by its ligands, interferon gamma-inducible protein 10 and monokine induced by interferon gamma.

Jinquan T., Quan S., Jacobi H.H., Jing C., Millner A., Jensen B., Madsen H.O., Ryder L.P., Svejgaard A., Malling H.J. et al.

Blood 96:1230-1238(2000)

Crystal structure of HLA-DQ0602 that protects against type 1 diabetes and confers strong susceptibility to narcolepsy.

Siebold C., Hansen B.E., Wyer J.R., Harlos K., Esnouf R.E., Svejgaard A., Bell J.I., Strominger J.L., Jones E.Y., Fugger L.

Proc. Natl. Acad. Sci. U.S.A. 101:1999-2004(2004) · UniProtKB (4) · Mapped (1,466)

Constitutive STAT3 activation in intestinal T cells from patients with Crohn's disease.

Lovato P., Brender C., Agnholt J., Kelsen J., Kaltoft K., Svejgaard A., Eriksen K.W., Woetmann A., Odum N.

J. Biol. Chem. 278:16777-16781(2003) · Mapped (16)

C1q deficiency in an Inuit family: identification of a new class of C1q disease-causing mutations.

Marquart H.V., Schejbel L., Sjoholm A., Martensson U., Nielsen S., Koch A., Svejgaard A., Garred P.

Clin. Immunol. 124:33-40(2007) · Mapped (3)

Association between genetic polymorphisms in the human interleukin-7 receptor alpha-chain and inhalation allergy.

Shamim Z., Muller K., Svejgaard A., Poulsen L.K., Bodtger U., Ryder L.P.

Int. J. Immunogenet. 34:149-151(2007) · Mapped (4)

A humanized model for multiple sclerosis using HLA-DR2 and a human T-cell receptor.

Madsen L.S., Andersson E.C., Jansson L., krogsgaard M., Andersen C.B., Engberg J., Strominger J.L., Svejgaard A., Hjorth J.P., Holmdahl R. et al.

Nat. Genet. 23:343-347(1999) · Mapped (4)

A functional and structural basis for TCR cross-reactivity in multiple sclerosis.

Lang H.L.E., Jacobsen H., Ikemizu S., Andersson C., Harlos K., Madsen L., Hjorth P., Sondergaard L., Svejgaard A., Wucherpfennig K. et al.

Nat. Immunol. 3:940-943(2002) · UniProtKB (3)

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