Class III POU genes of zebrafish are predominantly expressed in the central nervous system.

Por Spaniol, P, Bornmann, C, Hauptmann, G, Gerster, T
Publicado em 1996

Acquired C1 inhibitor deficiency in a case of lymphosarcoma of the spleen. Reversal of complement abnormalities after splenectomy.

Por Hauptmann, G, Petitjean, F, Lang, J M, Oberling, F
Publicado em 1979

Genetic deficiency of C4, C2 or C1q and lupus syndromes. Association with anti-Ro (SS-A) antibodies.

Por Meyer, O, Hauptmann, G, Tappeiner, G, Ochs, H D, Mascart-Lemone, F
Publicado em 1985

Formation of soluble immune complexes by complement in sera of patients with various hypocomplementemic states. Difference between inhibition of immune precipitation and solubiliza...

Por Schifferli, J A, Steiger, G, Hauptmann, G, Spaeth, P J, Sjöholm, A G
Publicado em 1985

Difference in the biological properties of the two forms of the fourth component of human complement (C4).

Por Schifferli, J A, Steiger, G, Paccaud, J P, Sjöholm, A G, Hauptmann, G
Publicado em 1986

Familial properdin deficiency associated with chronic discoid lupus erythematosus.

Por Holme, E R, Veitch, J, Johnston, A, Hauptmann, G, Uring-Lambert, B, Seywright, M, Docherty, V, Morley, W N, Whaley, K
Publicado em 1989

Rearrangements and point mutations of P450c21 genes are distinguished by five restriction endonuclease haplotypes identified by a new probing strategy in 57 families with congenita...

Por Morel, Y, André, J, Uring-Lambert, B, Hauptmann, G, Bétuel, H, Tossi, M, Forest, M G, David, M, Bertrand, J, Miller, W L
Publicado em 1989

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 G...

Por Späth, P J, Sjöholm, A G, Nordin Fredrikson, G, Misiano, G, Scherz, R, Schaad, U B, Uhring-Lambert, B, Hauptmann, G, Westberg, J, Uhlén, M, Wadelius, C, Truedsson, L
Publicado em 1999