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Human Heredity|January 1, 1992
Type II hereditary angio-oedema associated with two mutations in one allele of the C1-inhibitor gene around the reactive-site coding regionZ Siddique, A R McPhaden, K WhaleyHuman Heredity|March 1, 1995
Characterisation of nucleotide sequence variants and disease-specific mutations involving the 3' end of the C1-inhibitor gene in hereditary angio-oedemaZ Siddique, A R McPhaden, K WhaleyThe Journal of Clinical Investigation|June 1, 1976
C3b inactivator in the rheumatic diseases. Measurement by radial immunodiffusion and by inhibition of formation of properdin pathway C3 convertaseK Whaley, P H Schur, S RuddyHuman Genetics|September 1, 1993
C1-inhibitor gene nucleotide insertion causes type II hereditary angio-oedemaZ Siddique, A R McPhaden, K WhaleyImmunology|February 1, 1983
Serum-treated antigen-antibody complexes inhibit the production of C2 and factor B by mononuclear phagocytesK Whaley, D Lappin, A O HamiltonBiochimica Et Biophysica Acta|May 30, 1997
The sequence of a cDNA encoding functional murine C1-inhibitor proteinJ A Russell, K Whaley, S HeaphyMolecular Medicine (Cambridge, Mass.)|April 16, 1998
Mechanism of action of anti-C1-inhibitor autoantibodies: prevention of the formation of stable C1s-C1-inh complexesS He, R B Sim, K WhaleyHepatology (Baltimore, Md.)|June 1, 1989
Localization of adrenergic and neuropeptide tyrosine-containing nerves in the mammalian liverA D Burt, D Tiniakos, R N MacSween, et al.Immunology|June 1, 1997
Differential expression of CD32 isoforms following alloactivation of human T cellsG P Sandilands, S A MacPherson, E R Burnett, et al.Pageof 161