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Nucleic Acids Research
|
March 25, 1991
Regulatory factor-X binding to mutant HLA-DRA promoter sequences
S L Hasegawa, J H Sloan, W Reith, et al.
Human Immunology
|
August 1, 1990
DR-restricted T-cell reactivities associated with the Dw19 specificity can be directed against the products of either locus DRB3 (DRw52c) or locus DRB1
D Zeliszewski, J M Tiercy, I Dorval, et al.
The EMBO Journal
|
March 3, 1997
RFXAP, a novel subunit of the RFX DNA binding complex is mutated in MHC class II deficiency
B Durand, P Sperisen, P Emery, et al.
Molecular and Cellular Biology
|
May 18, 1999
Dimeric RFX proteins contribute to the activity and lineage specificity of the interleukin-5 receptor alpha promoter through activation and repression domains
A Iwama, J Pan, P Zhang, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 1, 1989
Cloning of the major histocompatibility complex class II promoter binding protein affected in a hereditary defect in class II gene regulation
W Reith, E Barras, S Satola, et al.
Nucleic Acids Research
|
June 20, 1998
DNA binding properties of a chemically synthesized DNA binding domain of hRFX1
F Cornille, P Emery, W Schüler, et al.
Molecular and Cellular Biology
|
October 1, 1993
RFX1 is identical to enhancer factor C and functions as a transactivator of the hepatitis B virus enhancer
C A Siegrist, B Durand, P Emery, et al.
British Journal of Haematology
|
October 1, 1993
Replacement of HLA class II serology by the HLA-DR microtitre plate oligotyping assay: a one-year experience in unrelated bone marrow donor selection
J M Tiercy, E Roosnek, D Speiser, et al.
Genes & Development
|
May 1, 1995
A novel DNA-binding regulatory factor is mutated in primary MHC class II deficiency (bare lymphocyte syndrome)
V Steimle, B Durand, E Barras, et al.
The New England Journal of Medicine
|
September 11, 1997
Mutation of RFXAP, a regulator of MHC class II genes, in primary MHC class II deficiency
J Villard, B Lisowska-Grospierre, P van den Elsen, et al.
Page
of 17
Search research articles
Search
Showing results (101-110 of 164) with videos related to
Sort By:
Page
of 17
Nucleic Acids Research
|
March 25, 1991
Regulatory factor-X binding to mutant HLA-DRA promoter sequences
S L Hasegawa, J H Sloan, W Reith, et al.
Human Immunology
|
August 1, 1990
DR-restricted T-cell reactivities associated with the Dw19 specificity can be directed against the products of either locus DRB3 (DRw52c) or locus DRB1
D Zeliszewski, J M Tiercy, I Dorval, et al.
The EMBO Journal
|
March 3, 1997
RFXAP, a novel subunit of the RFX DNA binding complex is mutated in MHC class II deficiency
B Durand, P Sperisen, P Emery, et al.
Molecular and Cellular Biology
|
May 18, 1999
Dimeric RFX proteins contribute to the activity and lineage specificity of the interleukin-5 receptor alpha promoter through activation and repression domains
A Iwama, J Pan, P Zhang, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 1, 1989
Cloning of the major histocompatibility complex class II promoter binding protein affected in a hereditary defect in class II gene regulation
W Reith, E Barras, S Satola, et al.
Nucleic Acids Research
|
June 20, 1998
DNA binding properties of a chemically synthesized DNA binding domain of hRFX1
F Cornille, P Emery, W Schüler, et al.
Molecular and Cellular Biology
|
October 1, 1993
RFX1 is identical to enhancer factor C and functions as a transactivator of the hepatitis B virus enhancer
C A Siegrist, B Durand, P Emery, et al.
British Journal of Haematology
|
October 1, 1993
Replacement of HLA class II serology by the HLA-DR microtitre plate oligotyping assay: a one-year experience in unrelated bone marrow donor selection
J M Tiercy, E Roosnek, D Speiser, et al.
Genes & Development
|
May 1, 1995
A novel DNA-binding regulatory factor is mutated in primary MHC class II deficiency (bare lymphocyte syndrome)
V Steimle, B Durand, E Barras, et al.
The New England Journal of Medicine
|
September 11, 1997
Mutation of RFXAP, a regulator of MHC class II genes, in primary MHC class II deficiency
J Villard, B Lisowska-Grospierre, P van den Elsen, et al.
Page
of 17