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Inherited complement C3 deficiency: A defect in C3 secretion
European Journal of Immunology, 1994AbstractThe molecular basis of inherited complement C3 deficiency in a 20‐year‐old newly diagnosed male patient was studied. Using an enzyme‐linked immunosorbent assay, the patient's C3 serum level was found to be approximately 7 μg/ml, which is less than 1 % of normal.
Y, Katz +4 more
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C3-Like Activity in C3-Deficient Dog Serum
Complement, 1987A complete absence of the third component of complement has been demonstrated in a colony of Brittany spaniels. The deficiency is inherited in an autosomal recessive fashion and is clinically characterized by an increased susceptibility to infection and renal disease.
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Inhibitor of Human C3 Associated with Preparations of C3 Dissociated from C3-Zymosan Complex
The Journal of Immunology, 1969Abstract Incubation of human serum with zymosan at 37°C, followed by removal of the zymosan residue by centrifugation, resulted in C3-zymosan complex. The C3-zymosan complex could be dissociated and C3 recovered in the eluate. Preparations of dissociated C3 did not contain the hemolytically active component of complement, C1 esterase, or
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C3−C3′ and C6−C6′ Oxidative Couplings of Carbazoles
Chemistry – A European Journal, 2018Abstract9‐Substituted carbazoles are widely used units in materials science, and their oxidative reactions have been utilized for the synthesis and characterization of polymers. Though the oxidative mechanism of carbazoles has been known for a few decades, structural definition has remained difficult, because their polymers are generally insoluble with
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