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L Truedsson

Showing results (111-120 of 125) with videos related to

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Human Immunology|January 1, 1988
The distribution of human C4 DNA variants in relation to major histocompatibility complex alleles and extended haplotypesA S Whitehead, L Truedsson, P M Schneider, et al.
Clinical and Experimental Immunology|November 11, 1999
Properdin deficiency in a large Swiss family: identification of a stop codon in the properdin gene, and association of meningococcal disease with lack of the IgG2 allotype marker G2m(n)P J Späth, A G Sjöholm, G N Fredrikson, et al.
Molecular Immunology|March 4, 2000
Properdin deficiency: molecular basis and disease associationC A Fijen, R van den Bogaard, M Schipper, et al.
Genes and Immunity|December 19, 2008
Additive effects of the major risk alleles of IRF5 and STAT4 in primary Sjögren's syndromeG Nordmark, G Kristjansdottir, E Theander, et al.
Experimental and Clinical Immunogenetics|March 11, 1999
Reference typing report for complement receptor 1 (CR1)J M Moulds, M Brai, J Cohen, et al.
Journal of Autoimmunity|March 24, 2000
A susceptibility locus for human systemic lupus erythematosus (hSLE1) on chromosome 2qA K Lindqvist, K Steinsson, B Johanneson, et al.
Genes and Immunity|February 24, 2001
Association analysis with microsatellite and SNP markers does not support the involvement of BCL-2 in systemic lupus erythematosus in Mexican and Swedish patients and their familiesC Johansson, C Castillejo-López, B Johanneson, et al.
Genes and Immunity|January 6, 2012
Genetic association of miRNA-146a with systemic lupus erythematosus in Europeans through decreased expression of the geneS E Löfgren, J Frostegård, L Truedsson, et al.
Genes and Immunity|March 29, 2013
Contribution of IKBKE and IFIH1 gene variants to SLE susceptibilityC Wang, A Ahlford, N Laxman, et al.
The Journal of Rheumatology|October 21, 1999
Genetic analysis of the contribution of IL10 to systemic lupus erythematosusM E Alarcón-Riquelme, A K Lindqvist, I Jonasson, et al.
Pageof 13

Showing results (111-120 of 125) with videos related to

Sort By:
Pageof 13
Human Immunology|January 1, 1988
The distribution of human C4 DNA variants in relation to major histocompatibility complex alleles and extended haplotypesA S Whitehead, L Truedsson, P M Schneider, et al.
Clinical and Experimental Immunology|November 11, 1999
Properdin deficiency in a large Swiss family: identification of a stop codon in the properdin gene, and association of meningococcal disease with lack of the IgG2 allotype marker G2m(n)P J Späth, A G Sjöholm, G N Fredrikson, et al.
Molecular Immunology|March 4, 2000
Properdin deficiency: molecular basis and disease associationC A Fijen, R van den Bogaard, M Schipper, et al.
Genes and Immunity|December 19, 2008
Additive effects of the major risk alleles of IRF5 and STAT4 in primary Sjögren's syndromeG Nordmark, G Kristjansdottir, E Theander, et al.
Experimental and Clinical Immunogenetics|March 11, 1999
Reference typing report for complement receptor 1 (CR1)J M Moulds, M Brai, J Cohen, et al.
Journal of Autoimmunity|March 24, 2000
A susceptibility locus for human systemic lupus erythematosus (hSLE1) on chromosome 2qA K Lindqvist, K Steinsson, B Johanneson, et al.
Genes and Immunity|February 24, 2001
Association analysis with microsatellite and SNP markers does not support the involvement of BCL-2 in systemic lupus erythematosus in Mexican and Swedish patients and their familiesC Johansson, C Castillejo-López, B Johanneson, et al.
Genes and Immunity|January 6, 2012
Genetic association of miRNA-146a with systemic lupus erythematosus in Europeans through decreased expression of the geneS E Löfgren, J Frostegård, L Truedsson, et al.
Genes and Immunity|March 29, 2013
Contribution of IKBKE and IFIH1 gene variants to SLE susceptibilityC Wang, A Ahlford, N Laxman, et al.
The Journal of Rheumatology|October 21, 1999
Genetic analysis of the contribution of IL10 to systemic lupus erythematosusM E Alarcón-Riquelme, A K Lindqvist, I Jonasson, et al.
Pageof 13