Search

Haplotypes
 
Advanced search
Browse by...
Refine your research by the most used items
Deposit
Highlights
More informations
Show items per page
Elements: 73
Page 1 on 4
 TitleAuthors / EditorsDate
add to browser selection
 Autoimmune T lymphocytes in myasthenia gravis : determination of target epitopes using T lines and recombinant products of the mouse nicotinic acetylcholine receptor gene Melms, A.; Chrestel, S.; Schalke, B.C.; Wekerle, H.; ... Barkas, T. 1989
add to browser selection
 Interethnic genetic differentiation : GM polymorphism in Eastern Senegal Blanc, Madeleine; Sanchez-Mazas, Alicia; Hubert Van Blyenburgh, Ninian; Sevin, André; ... Langaney, André 1990
add to browser selection
 A worldwide population study of the Ag-system haplotypes, a genetic polymorphism of human low-density lipoprotein Breguet, Georges; Bütler, R.; Bütler-Brunner, E.; Sanchez-Mazas, Alicia 1990
add to browser selection
 Oligonucleotide typing reveals association of type I psoriasis with the HLA-DRB1*0701/2, -DQA1*0201, -DQB1*0303 extended haplotype Schmitt-Egenolf, M.; Boehncke, Wolf-Henning; Stander, M.; Eiermann, T. H.; Sterry, Wolfram 1993
add to browser selection
 Induction of diabetes is influenced by the infectious virus and local expression of MHC class I and tumor necrosis factor-alpha Ohashi, P. S.; Oehen, S.; Aichele, P.; Pircher, H.; ... Zinkernagel, R. M. 1993
add to browser selection
 H-2D haplotype-linked expression and involvement of TNF-alpha in Th2 cell-mediated tissue inflammation Mueller, Kai Michael; Lisby, Steen; Arrighi, Jean-François; Grau, Georges; ... Hauser, Conrad 1994
add to browser selection
 A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3 Sertie, A. L.; Quimby, M.; Moreira, E. S.; Murray, J.; ... Passos-Bueno, M. R. 1996
add to browser selection
 Molecular characterization of HLA-C incompatibilities in HLA-ABDR-matched unrelated bone marrow donor-recipient pairs. Sequence of two new Cw alleles (Cw*02023 and Cw*0707) and recognition by cytotoxic T lymphocytes Grundschober, C; Rufer, Nathalie; Sanchez-Mazas, Alicia; Madrigal, A; ... Tiercy, Jean-Marie 1997
add to browser selection
 HLA class II DRB1, DQA1 and DQB1 polymorphisms in the Polish population from Wielkopolska Jungerman, M; Sanchez-Mazas, Alicia; Fichna, P; Ivanova, R; ... Djoulah, S 1997
add to browser selection
 Positional cloning of the APECED gene Nagamine, K.; Peterson, P.; Scott, Hamish Steele; Kudoh, J.; ... Shimizu, N. 1997
add to browser selection
 Common mutations in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients of different origins Scott, Hamish Steele; Heino, M.; Peterson, P.; Mittaz, L.; ... Antonarakis, Stylianos 1998
add to browser selection
 PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy Guicheney, P; Vignier, N; Zhang, X; He, Y; ... Tryggvason, K 1998
add to browser selection
 A common mutation in Sardinian autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients Rosatelli, M. C.; Meloni, A.; Devoto, M.; Cao, A.; ... Antonarakis, Stylianos 1998
add to browser selection
 Control of separate pathogenic autoantibody responses marks MHC gene contributions to murine lupus Vyse, T. J.; Halterman, R. K.; Rozzo, S. J.; Izui, Shozo; Kotzin, B. L. 1999
add to browser selection
 Y-chromosome specific YCAII, DYS19 and YAP polymorphisms in human populations: a comparative study Quintana-Murci, L.; Semino, O.; Poloni, Estella S.; Liu, A.; ... Santachiara-Benerecetti, A S. 1999
add to browser selection
 Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiency Neerman Arbez, Marguerite; Johnson, K. M.; Morris, Michael Andréw; McVey, J. H.; ... Tuddenham, E. G. 1999
add to browser selection
 Protection of murine lupus by the Ead transgene is MHC haplotype-dependent Ibnou-Zekri, Nabila; Iwamoto, Masahiro; Gershwin, M. E.; Izui, Shozo 2000
add to browser selection
 Founder effect for a 26-bp deletion in the RFXANK gene in North African major histocompatibility complex class II-deficient patients belonging to complementation group B Wiszniewski, W.; Fondaneche, M. C.; Lambert, N.; Masternak, Krzysztof; ... Lisowska-Grospierre, B. 2000
add to browser selection
 Genetic differentiation of Yemeni people according to rhesus and Gm polymorphisms Chaabani, H.; Sanchez-Mazas, Alicia; Sallami, S. F. 2000
add to browser selection
 A linkage disequilibrium map of the MHC region based on the analysis of 14 loci haplotypes in 50 French families Sanchez-Mazas, Alicia; Djoulah, S.; Busson, M.; Le Monnier de Gouville, I.; ... Hors, J. 2000
<< previous | 1 | 2 | 3 | 4 |