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C Rittner

Showing results (141-150 of 162) with videos related to

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European Journal of Pediatrics|December 1, 1989
Possible association of sudden infant death with partial complement C4 deficiency revealed by post-mortem DNA typing of HLA class II and III genesP M Schneider, C Wendler, T Riepert, et al.
Immunogenetics|January 1, 1988
Antigenic determinants expressed by human C4 allotypes; a study of 325 families provides evidence for the structural antigenic modelC M Giles, B Uring-Lambert, J Goetz, et al.
Physical Review Letters|November 24, 2011
Metastability in spin-polarized Fermi gasesY A Liao, M Revelle, T Paprotta, et al.
Human Genetics|July 12, 1978
Evidence for subtypic determinants in the HLA-DW3 clusterD Niese, H Grosse-Wilde, B Dupont, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 15, 1997
The human complement C9 gene: identification of two mutations causing deficiency and revision of the gene structureK Witzel-Schlömp, P J Späth, M J Hobart, et al.
Complement and Inflammation|January 1, 1990
C4 nomenclature statement (1990)G Mauff, C A Alper, R Dawkins, et al.
Annals of the Rheumatic Diseases|March 13, 1998
No primary association between LMP2 polymorphisms and extraspinal manifestations in spondyloarthropathiesT Höhler, T Schäper, P M Schneider, et al.
The Journal of Clinical Investigation|September 1, 1986
Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variantsP M Schneider, M C Carroll, C A Alper, et al.
Immunogenetics|June 20, 1998
Heterogeneity in the genetic basis of human complement C9 deficiencyK Witzel-Schlömp, M J Hobart, B A Fernie, et al.
Transplantation Proceedings|March 1, 1977
B-cell-specific alloantigens in recombinant familiesE D Albert, S Scholz, B Kuntz, et al.
Pageof 17

Showing results (141-150 of 162) with videos related to

Sort By:
Pageof 17
European Journal of Pediatrics|December 1, 1989
Possible association of sudden infant death with partial complement C4 deficiency revealed by post-mortem DNA typing of HLA class II and III genesP M Schneider, C Wendler, T Riepert, et al.
Immunogenetics|January 1, 1988
Antigenic determinants expressed by human C4 allotypes; a study of 325 families provides evidence for the structural antigenic modelC M Giles, B Uring-Lambert, J Goetz, et al.
Physical Review Letters|November 24, 2011
Metastability in spin-polarized Fermi gasesY A Liao, M Revelle, T Paprotta, et al.
Human Genetics|July 12, 1978
Evidence for subtypic determinants in the HLA-DW3 clusterD Niese, H Grosse-Wilde, B Dupont, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 15, 1997
The human complement C9 gene: identification of two mutations causing deficiency and revision of the gene structureK Witzel-Schlömp, P J Späth, M J Hobart, et al.
Complement and Inflammation|January 1, 1990
C4 nomenclature statement (1990)G Mauff, C A Alper, R Dawkins, et al.
Annals of the Rheumatic Diseases|March 13, 1998
No primary association between LMP2 polymorphisms and extraspinal manifestations in spondyloarthropathiesT Höhler, T Schäper, P M Schneider, et al.
The Journal of Clinical Investigation|September 1, 1986
Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variantsP M Schneider, M C Carroll, C A Alper, et al.
Immunogenetics|June 20, 1998
Heterogeneity in the genetic basis of human complement C9 deficiencyK Witzel-Schlömp, M J Hobart, B A Fernie, et al.
Transplantation Proceedings|March 1, 1977
B-cell-specific alloantigens in recombinant familiesE D Albert, S Scholz, B Kuntz, et al.
Pageof 17