M C Carroll|C A Alper - JoVE Visualize

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Investigative Ophthalmology & Visual Science|May 14, 1998

A small molecular weight factor in aqueous humor acts on C1q to prevent antibody-dependent complement activationW R Goslings, A P Prodeus, J W Streilein, et al.

The Journal of Experimental Medicine|April 1, 1996

Antibody response to a T-dependent antigen requires B cell expression of complement receptorsD A Croix, J M Ahearn, A M Rosengard, et al.

The Journal of Experimental Medicine|April 1, 1988

Organization of the genes encoding complement receptors type 1 and 2, decay-accelerating factor, and C4-binding protein in the RCA locus on human chromosome 1M C Carroll, E M Alicot, P J Katzman, et al.

Biorxiv : the Preprint Server for Biology|July 3, 2023

Invasion of spontaneous germinal centers by naive B cells is rapid and persistentT van den Broek, K Oleinika, S Rahmayanti, et al.

Kidney International|September 30, 2000

Complement is activated in kidney by endotoxin but does not cause the ensuing acute renal failureP N Cunningham, V M Holers, J J Alexander, et al.

Journal of Immunology (Baltimore, Md. : 1950)|May 1, 1992

A single arginine to tryptophan interchange at beta-chain residue 458 of human complement component C4 accounts for the defect in classical pathway C5 convertase activity of allotype C4A6. Implications for the location of a C5 binding site in C4R O Ebanks, A S Jaikaran, M C Carroll, et al.

Human Immunology|January 23, 1998

Relationship between protein complotypes and DNA variant haplotypes: complotype-RFLP constellations (CRC)S Simon, L Truedsson, D Marcus-Bagley, et al.

Genes and Immunity|April 11, 2001

Hepatitis B surface antigen- and tetanus toxoid-specific clonal expansion of CD4+ cells in vitro determined by TCRBV CDR3 length and nucleotide sequenceG P Uko, P A Fraser, Z L Awdeh, et al.

The Journal of Clinical Endocrinology and Metabolism|December 1, 1993

Association of HLA-DQB1*0201 with stiff-man syndromeA Pugliese, M Solimena, Z L Awdeh, et al.

Human Immunology|October 31, 1998

Characterization of non-expressed C4 genes in a case of complete C4 deficiency: identification of a novel point mutation leading to a premature stop codonG N Fredrikson, B Gullstrand, P M Schneider, et al.

Pageof 26

Showing results (191-200 of 251) with videos related to

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Pageof 26

Investigative Ophthalmology & Visual Science|May 14, 1998

A small molecular weight factor in aqueous humor acts on C1q to prevent antibody-dependent complement activationW R Goslings, A P Prodeus, J W Streilein, et al.

The Journal of Experimental Medicine|April 1, 1996

Antibody response to a T-dependent antigen requires B cell expression of complement receptorsD A Croix, J M Ahearn, A M Rosengard, et al.

The Journal of Experimental Medicine|April 1, 1988

Organization of the genes encoding complement receptors type 1 and 2, decay-accelerating factor, and C4-binding protein in the RCA locus on human chromosome 1M C Carroll, E M Alicot, P J Katzman, et al.

Biorxiv : the Preprint Server for Biology|July 3, 2023

Invasion of spontaneous germinal centers by naive B cells is rapid and persistentT van den Broek, K Oleinika, S Rahmayanti, et al.

Kidney International|September 30, 2000

Complement is activated in kidney by endotoxin but does not cause the ensuing acute renal failureP N Cunningham, V M Holers, J J Alexander, et al.

Journal of Immunology (Baltimore, Md. : 1950)|May 1, 1992

A single arginine to tryptophan interchange at beta-chain residue 458 of human complement component C4 accounts for the defect in classical pathway C5 convertase activity of allotype C4A6. Implications for the location of a C5 binding site in C4R O Ebanks, A S Jaikaran, M C Carroll, et al.

Human Immunology|January 23, 1998

Relationship between protein complotypes and DNA variant haplotypes: complotype-RFLP constellations (CRC)S Simon, L Truedsson, D Marcus-Bagley, et al.

Genes and Immunity|April 11, 2001

Hepatitis B surface antigen- and tetanus toxoid-specific clonal expansion of CD4+ cells in vitro determined by TCRBV CDR3 length and nucleotide sequenceG P Uko, P A Fraser, Z L Awdeh, et al.

The Journal of Clinical Endocrinology and Metabolism|December 1, 1993

Association of HLA-DQB1*0201 with stiff-man syndromeA Pugliese, M Solimena, Z L Awdeh, et al.

Human Immunology|October 31, 1998

Characterization of non-expressed C4 genes in a case of complete C4 deficiency: identification of a novel point mutation leading to a premature stop codonG N Fredrikson, B Gullstrand, P M Schneider, et al.

Pageof 26