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H R Colten

Showing results (151-160 of 200) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|February 1, 1985
Expression of the alpha 1-proteinase inhibitor gene in human monocytes and macrophagesD H Perlmutter, F S Cole, P Kilbridge, et al.
The Journal of Biological Chemistry|April 17, 1999
Disruption of disulfide bonds is responsible for impaired secretion in human complement factor H deficiencyB Z Schmidt, N L Fowler, T Hidvegi, et al.
Science (New York, N.Y.)|May 16, 1986
Regulation of class III major histocompatibility complex gene products by interleukin-1D H Perlmutter, G Goldberger, C A Dinarello, et al.
Clinical Immunology and Immunopathology|March 1, 1981
Biosynthesis of complement by human monocytesD W Beatty, A E Davis, F S Cole, et al.
Science (New York, N.Y.)|July 1, 1983
Isolation of human C-reactive protein complementary DNA and localization of the gene to chromosome 1A S Whitehead, G A Bruns, A F Markham, et al.
The Journal of Allergy and Clinical Immunology|January 1, 1977
Hypersensitivity to pancreatic extracts in parents of patients with cystic fibrosisF J Twarog, S F Weinstein, K T Khaw, et al.
The Journal of Clinical Investigation|January 1, 1976
Homozygous human C3 deficiency. The role of C3 in antibody production, C-1s-induced vasopermeability, and cobra venom-induced passive hemolysisC A Alper, H R Colten, J S Gear, et al.
Journal of Immunology (Baltimore, Md. : 1950)|September 1, 1980
Control of complement synthesis and secretion in bronchoalveolar and peritoneal macrophagesF S Cole, W J Matthews, J T Marino, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 27, 1999
Deficiency of human complement protein C4 due to identical frameshift mutations in the C4A and C4B genesM L Lokki, A Circolo, P Ahokas, et al.
The New England Journal of Medicine|March 25, 1982
Deficiency of a granulocyte-membrane glycoprotein (gp150) in a boy with recurrent bacterial infectionsM A Arnaout, J Pitt, H J Cohen, et al.
Pageof 20

Showing results (151-160 of 200) with videos related to

Sort By:
Pageof 20
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1985
Expression of the alpha 1-proteinase inhibitor gene in human monocytes and macrophagesD H Perlmutter, F S Cole, P Kilbridge, et al.
The Journal of Biological Chemistry|April 17, 1999
Disruption of disulfide bonds is responsible for impaired secretion in human complement factor H deficiencyB Z Schmidt, N L Fowler, T Hidvegi, et al.
Science (New York, N.Y.)|May 16, 1986
Regulation of class III major histocompatibility complex gene products by interleukin-1D H Perlmutter, G Goldberger, C A Dinarello, et al.
Clinical Immunology and Immunopathology|March 1, 1981
Biosynthesis of complement by human monocytesD W Beatty, A E Davis, F S Cole, et al.
Science (New York, N.Y.)|July 1, 1983
Isolation of human C-reactive protein complementary DNA and localization of the gene to chromosome 1A S Whitehead, G A Bruns, A F Markham, et al.
The Journal of Allergy and Clinical Immunology|January 1, 1977
Hypersensitivity to pancreatic extracts in parents of patients with cystic fibrosisF J Twarog, S F Weinstein, K T Khaw, et al.
The Journal of Clinical Investigation|January 1, 1976
Homozygous human C3 deficiency. The role of C3 in antibody production, C-1s-induced vasopermeability, and cobra venom-induced passive hemolysisC A Alper, H R Colten, J S Gear, et al.
Journal of Immunology (Baltimore, Md. : 1950)|September 1, 1980
Control of complement synthesis and secretion in bronchoalveolar and peritoneal macrophagesF S Cole, W J Matthews, J T Marino, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 27, 1999
Deficiency of human complement protein C4 due to identical frameshift mutations in the C4A and C4B genesM L Lokki, A Circolo, P Ahokas, et al.
The New England Journal of Medicine|March 25, 1982
Deficiency of a granulocyte-membrane glycoprotein (gp150) in a boy with recurrent bacterial infectionsM A Arnaout, J Pitt, H J Cohen, et al.
Pageof 20