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K Whaley

Showing results (91-100 of 198) with videos related to

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Human Heredity|May 1, 1993
A point mutation in the C1-inhibitor gene causes type I hereditary angiooedemaZ Siddique, A R McPhaden, J E Fothergill, et al.
Current Medical Research and Opinion|January 1, 1986
Comparative study of endralazine and hydralazine for the treatment of hypertension uncontrolled by a beta-blocker and diureticB I Chazan, D A Duff, A McCallum, et al.
Postgraduate Medical Journal|March 1, 1991
Disseminated gonococcal infection associated with deficiency of the second component of complementP H McWhinney, P Langhorne, W C Love, et al.
Human Genetics|December 1, 1991
An RNA splice site mutation in the C1-inhibitor gene causes type I hereditary angio-oedemaZ Siddique, A R McPhaden, D F Lappin, et al.
Australian and New Zealand Journal of Medicine|August 1, 1986
Inhibition of complement-mediated solubilisation of antigen-antibody complexes by serum factor(s) in patients with various connective tissue diseasesJ Webb, A Zoma, S Cobb, et al.
Immunology|July 1, 1984
IgM-RF prevents complement-mediated inhibition of immune precipitationW S Mitchell, J K Naama, J Veitch, et al.
Journal of Clinical & Laboratory Immunology|February 1, 1984
Complement levels in serum and bile in patients with extra-hepatic biliary tract obstructionL Morrison, S Blamey, J Veitch, et al.
Clinical and Experimental Immunology|February 1, 1986
Circulating immune complexes associated with decreased complement-mediated inhibition of immune precipitation in sera from patients with bacterial endocarditisM A Kerr, E Wilton, J K Naama, et al.
Rheumatology International|January 1, 1994
Expression of the components and regulatory proteins of the classical pathway of complement in normal and diseased synoviumP Gulati, D Guc, C Lemercier, et al.
Clinical and Experimental Immunology|October 1, 1989
Complement biosynthesis in human synovial tissueG J Moffat, D Lappin, G D Birnie, et al.
Pageof 20

Showing results (91-100 of 198) with videos related to

Sort By:
Pageof 20
Human Heredity|May 1, 1993
A point mutation in the C1-inhibitor gene causes type I hereditary angiooedemaZ Siddique, A R McPhaden, J E Fothergill, et al.
Current Medical Research and Opinion|January 1, 1986
Comparative study of endralazine and hydralazine for the treatment of hypertension uncontrolled by a beta-blocker and diureticB I Chazan, D A Duff, A McCallum, et al.
Postgraduate Medical Journal|March 1, 1991
Disseminated gonococcal infection associated with deficiency of the second component of complementP H McWhinney, P Langhorne, W C Love, et al.
Human Genetics|December 1, 1991
An RNA splice site mutation in the C1-inhibitor gene causes type I hereditary angio-oedemaZ Siddique, A R McPhaden, D F Lappin, et al.
Australian and New Zealand Journal of Medicine|August 1, 1986
Inhibition of complement-mediated solubilisation of antigen-antibody complexes by serum factor(s) in patients with various connective tissue diseasesJ Webb, A Zoma, S Cobb, et al.
Immunology|July 1, 1984
IgM-RF prevents complement-mediated inhibition of immune precipitationW S Mitchell, J K Naama, J Veitch, et al.
Journal of Clinical & Laboratory Immunology|February 1, 1984
Complement levels in serum and bile in patients with extra-hepatic biliary tract obstructionL Morrison, S Blamey, J Veitch, et al.
Clinical and Experimental Immunology|February 1, 1986
Circulating immune complexes associated with decreased complement-mediated inhibition of immune precipitation in sera from patients with bacterial endocarditisM A Kerr, E Wilton, J K Naama, et al.
Rheumatology International|January 1, 1994
Expression of the components and regulatory proteins of the classical pathway of complement in normal and diseased synoviumP Gulati, D Guc, C Lemercier, et al.
Clinical and Experimental Immunology|October 1, 1989
Complement biosynthesis in human synovial tissueG J Moffat, D Lappin, G D Birnie, et al.
Pageof 20