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Experimental and Clinical Immunogenetics
|
January 1, 1985
Possible human analogs of the murine T/t complex
C A Alper, Z L Awdeh, D D Raum, et al.
Vox Sanguinis
|
January 1, 1983
Serum complement 'supergenes' of the major histocompatibility complex in man (complotypes)
C A Alper, D Raum, S Karp, et al.
Immunogenetics
|
March 1, 1981
The location of C2, C4, and BF relative to HLA-B and HLA-D
D D Raum, Z L Awdeh, D Glass, et al.
Tissue Antigens
|
October 3, 2001
Polymorphism of the human retinoid X receptor beta and linkage disequilibrium with HLA-DPB1
R Rajsbaum, D Fici, P A Fraser, et al.
Journal of Autoimmunity
|
October 1, 1994
The paternally inherited insulin gene B allele (1,428 FokI site) confers protection from insulin-dependent diabetes in families
A Pugliese, Z L Awdeh, C A Alper, et al.
Transplantation Proceedings
|
December 1, 1995
The INS B allele (1,428 Fok I) is associated with reduced IDDM incidence in autoantibody-positive first degree relatives despite the presence of autoantibodies and high-risk HLA alleles
A Pugliese, Z L Awdeh, C A Alper, et al.
Biochemical Genetics
|
July 1, 1974
Analysis of human erythrocyte glucose 6-phosphate dehydrogenase isozymes by isoelectric focusing in polyacrylamide gel
V M Der Kaloustian, S H Idriss-Daouk, R T Hallal, et al.
Human Immunology
|
February 1, 1988
Two variants of DRw52, DR3, and DQw2 specificities distinguish two different DR3-bearing extended haplotypes
J D Dasgupta, V Relias, Z L Awdeh, et al.
Tissue Antigens
|
September 1, 1995
Predictability of alloreactivity among unrelated individuals: role for HLA-DPB1
Z L Awdeh, C A Alper, D A Fici, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
November 15, 1993
Characterization of type I complement C2 deficiency MHC haplotypes. Strong conservation of the complotype/HLA-B-region and absence of disease association due to linked class II genes
L Truedsson, C A Alper, Z L Awdeh, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 53) with videos related to
Sort By:
Page
of 6
Experimental and Clinical Immunogenetics
|
January 1, 1985
Possible human analogs of the murine T/t complex
C A Alper, Z L Awdeh, D D Raum, et al.
Vox Sanguinis
|
January 1, 1983
Serum complement 'supergenes' of the major histocompatibility complex in man (complotypes)
C A Alper, D Raum, S Karp, et al.
Immunogenetics
|
March 1, 1981
The location of C2, C4, and BF relative to HLA-B and HLA-D
D D Raum, Z L Awdeh, D Glass, et al.
Tissue Antigens
|
October 3, 2001
Polymorphism of the human retinoid X receptor beta and linkage disequilibrium with HLA-DPB1
R Rajsbaum, D Fici, P A Fraser, et al.
Journal of Autoimmunity
|
October 1, 1994
The paternally inherited insulin gene B allele (1,428 FokI site) confers protection from insulin-dependent diabetes in families
A Pugliese, Z L Awdeh, C A Alper, et al.
Transplantation Proceedings
|
December 1, 1995
The INS B allele (1,428 Fok I) is associated with reduced IDDM incidence in autoantibody-positive first degree relatives despite the presence of autoantibodies and high-risk HLA alleles
A Pugliese, Z L Awdeh, C A Alper, et al.
Biochemical Genetics
|
July 1, 1974
Analysis of human erythrocyte glucose 6-phosphate dehydrogenase isozymes by isoelectric focusing in polyacrylamide gel
V M Der Kaloustian, S H Idriss-Daouk, R T Hallal, et al.
Human Immunology
|
February 1, 1988
Two variants of DRw52, DR3, and DQw2 specificities distinguish two different DR3-bearing extended haplotypes
J D Dasgupta, V Relias, Z L Awdeh, et al.
Tissue Antigens
|
September 1, 1995
Predictability of alloreactivity among unrelated individuals: role for HLA-DPB1
Z L Awdeh, C A Alper, D A Fici, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
November 15, 1993
Characterization of type I complement C2 deficiency MHC haplotypes. Strong conservation of the complotype/HLA-B-region and absence of disease association due to linked class II genes
L Truedsson, C A Alper, Z L Awdeh, et al.
Page
of 6