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Showing results (261-270 of 310) with videos related to

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Clinical Immunology and Immunopathology|November 1, 1977
Homozygous C3 deficiency: detection of C3 by radioimmunoassayA E Davis, J S Davis, A R Rabson, 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.
Journal of Clinical Immunology|April 18, 2002
HLA-Cw7 zygosity affects the size of a subset of CD158b+ natural killer cellsZaheed Husain, Edward Levitan, Charles E Larsen, 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.
Tissue Antigens|November 5, 1998
HLA-Cw alleles associated with HLA extended haplotypes and C2 deficiencyO P Clavijo, J C Delgado, Z L Awdeh, et al.
The Journal of Clinical Investigation|December 1, 1991
A restriction fragment of the C2 gene is a unique marker for C2 deficiency and the uncommon C2 allele C2*B (a marker for type 1 diabetes)S Simon, Z Awdeh, R D Campbell, et al.
The Journal of Clinical Investigation|June 1, 1994
Two subsets of HLA-DQA1 alleles mark phenotypic variation in levels of insulin autoantibodies in first degree relatives at risk for insulin-dependent diabetesA Pugliese, T Bugawan, R Moromisato, et al.
The New England Journal of Medicine|May 29, 1975
Biosynthetic defect in monocytes from human beings with genetic deficiency of the second component of complementL P Einstein, C A Alper, K J Bloch, et al.
Diabetes|June 1, 1995
HLA-DQB1*0602 is associated with dominant protection from diabetes even among islet cell antibody-positive first-degree relatives of patients with IDDMA Pugliese, R Gianani, R Moromisato, et al.
Pageof 31

Showing results (261-270 of 310) with videos related to

Sort By:
Pageof 31
Clinical Immunology and Immunopathology|November 1, 1977
Homozygous C3 deficiency: detection of C3 by radioimmunoassayA E Davis, J S Davis, A R Rabson, 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.
Journal of Clinical Immunology|April 18, 2002
HLA-Cw7 zygosity affects the size of a subset of CD158b+ natural killer cellsZaheed Husain, Edward Levitan, Charles E Larsen, 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.
Tissue Antigens|November 5, 1998
HLA-Cw alleles associated with HLA extended haplotypes and C2 deficiencyO P Clavijo, J C Delgado, Z L Awdeh, et al.
The Journal of Clinical Investigation|December 1, 1991
A restriction fragment of the C2 gene is a unique marker for C2 deficiency and the uncommon C2 allele C2*B (a marker for type 1 diabetes)S Simon, Z Awdeh, R D Campbell, et al.
The Journal of Clinical Investigation|June 1, 1994
Two subsets of HLA-DQA1 alleles mark phenotypic variation in levels of insulin autoantibodies in first degree relatives at risk for insulin-dependent diabetesA Pugliese, T Bugawan, R Moromisato, et al.
The New England Journal of Medicine|May 29, 1975
Biosynthetic defect in monocytes from human beings with genetic deficiency of the second component of complementL P Einstein, C A Alper, K J Bloch, et al.
Diabetes|June 1, 1995
HLA-DQB1*0602 is associated with dominant protection from diabetes even among islet cell antibody-positive first-degree relatives of patients with IDDMA Pugliese, R Gianani, R Moromisato, et al.
Pageof 31