| Title | Authors / Editors | Date |
unige:85389 |
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 |
unige:14330 |
Interethnic genetic differentiation : GM polymorphism in Eastern Senegal |
Blanc, Madeleine; Sanchez-Mazas, Alicia; Hubert Van Blyenburgh, Ninian; Sevin, André; ... Langaney, André |
1990 |
unige:14331 |
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 |
unige:29833 |
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 |
unige:8944 |
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 |
unige:107291 |
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 |
unige:9032 |
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 |
unige:16902 |
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 |
unige:17064 |
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 |
unige:8918 |
Positional cloning of the APECED gene |
Nagamine, K.; Peterson, P.; Scott, Hamish Steele; Kudoh, J.; ... Shimizu, N. |
1997 |
unige:74595 |
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 |
unige:9001 |
A common mutation in Sardinian autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients |
Rosatelli, M. C.; Meloni, A.; Devoto, M.; Cao, A.; ... Antonarakis, Stylianos |
1998 |
unige:9028 |
Common mutations in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients of different origins |
Scott, Hamish Steele; Heino, M.; Peterson, P.; Mittaz, L.; ... Antonarakis, Stylianos |
1998 |
unige:8935 |
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 |
unige:11627 |
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 |
unige:13238 |
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 |
unige:11089 |
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 |
unige:2012 |
Genetic differentiation of Yemeni people according to rhesus and Gm polymorphisms |
Chaabani, H.; Sanchez-Mazas, Alicia; Sallami, S. F. |
2000 |
unige:8639 |
Refined localization of autosomal recessive nonsyndromic deafness DFNB10 locus using 34 novel microsatellite markers, genomic structure, and exclusion of six known genes in the region |
Berry, A.; Scott, Hamish Steele; Kudoh, J.; Talior, I.; ... Bonne-Tamir, B. |
2000 |
unige:8930 |
Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia |
Neerman Arbez, Marguerite; De Moerloose, Philippe; Bridel, C.; Honsberger, A.; ... Morris, Michael Andréw |
2000 |