| Title | Authors / Editors | Date |
unige:44186 |
Loss of heterozygosity for the short arm of chromosome 11 (11p15) in human milk epithelial cells immortalized by microinjection of SV40 DNA. |
Garcia, Irène; Brandt, D; Weintraub, J; Zhou, W G; Aapro, M |
1991 |
unige:14357 |
HLA-DR polymorphism in a Senegalese Mandenka population : DNA oligotyping and population genetics of DRB1 specificities |
Tiercy, Jean-Marie; Sanchez-Mazas, Alicia; Excoffier, Laurent Georges Louis; Shi-Isaac, Xiaowen; ... Langaney, André |
1992 |
unige:9164 |
Report of the Fourth International Workshop on Human Chromosome 21 |
Delabar, J. M.; Creau, N.; Sinet, P. M.; Ritter, O.; ... Patterson, D. |
1993 |
unige:104579 |
Loss of heterozygosity at the RB locus correlates with loss of RB protein in primary malignant neuro-endocrine lung carcinomas |
Gouyer, V; Gazzeri, S; Brambilla, E; Bolon, Isabelle; ... Brambilla, C |
1994 |
unige:8614 |
Factor VIII gene inversions in severe hemophilia A: results of an international consortium study |
Antonarakis, Stylianos |
1995 |
unige:11431 |
Constitutive expression of bcl-2 in B cells causes a lethal form of lupuslike autoimmune disease after induction of neonatal tolerance to H-2b alloantigens |
Lopez-Hoyos, Marcos; Carrio, R.; Merino, Ramon; Buelta, Luis; ... Merino, Jesus |
1996 |
unige:85021 |
Chromatin insulator elements block the silencing of a target gene by the Drosophila polycomb response element (PRE) but allow trans interactions between PREs on different chromosomes |
Sigrist, Christian; Pirrotta, Vincenzo |
1997 |
unige:7436 |
Genetic polymorphism of CCR5 gene and HIV disease: the heterozygous (CCR5/delta ccr5) genotype is neither essential nor sufficient for protection against disease progression. Swiss HIV Cohort |
Morawetz, R. A.; Rizzardi, G. P.; Glauser, Dominique; Rutschmann, Olivier Thierry; ... Pantaleo, G. |
1997 |
unige:74566 |
Different missense mutations in histidine-108 of lysosomal acid lipase cause cholesteryl ester storage disease in unrelated compound heterozygous and hemizygous individuals |
Ries, S; Büchler, C; Schindler, G; Aslanidis, C; ... Schmitz, G |
1998 |
unige:8891 |
Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity |
Mehenni, H.; Gehrig, Corinne; Nezu, J.; Oku, A.; ... Antonarakis, Stylianos |
1998 |
unige:7580 |
Electron currents generated by the human phagocyte NADPH oxidase |
Schrenzel, Jacques; Serrander, Lena; Banfi, Botond; Nusse, Olivier; ... Krause, Karl-Heinz |
1998 |
unige:10914 |
MHC-linked control of murine SLE |
Ibnou-Zekri, Nabila; Vyse, T. J.; Rozzo, S. J.; Iwamoto, Masahiro; ... Izui, Shozo |
1999 |
unige:73868 |
beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the gene encoding the basic helix-loop-helix transcription factor neurogenic differentiation 4 (NEUROD4) in Japanese patients with MODY. |
Horikawa, Yohko; Horikawa, Yukio; Cox, Nancy J.; Iwasaki, Naoko; ... Bell, Graeme I. |
2000 |
unige:9883 |
Isolation of Su(var)3-7 mutations by homologous recombination in Drosophila melanogaster |
Seum, Carole; Pauli, Daniel; Delattre, Marion; Jaquet, Yannis; ... Spierer, Pierre |
2002 |
unige:9079 |
Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion |
Vu, Dung; Bolton-Maggs, P. H.; Parr, J. R.; Morris, Michael Andréw; ... Neerman Arbez, Marguerite |
2003 |
unige:8759 |
Specific BACE1 genotypes provide additional risk for late-onset Alzheimer disease in APOE epsilon 4 carriers |
Gold, Gabriel; Blouin, Jean-Louis; Herrmann, François; Michon, Agnès; ... Antonarakis, Stylianos |
2003 |
unige:8828 |
Dominant negative pathogenesis by mutant proinsulin in the Akita diabetic mouse |
Izumi, Tetsuro; Yokota-Hashimoto, Hiromi; Zhao, Shengli; Wang, Jie; ... Takeuchi, Toshiyuki |
2003 |
unige:136230 |
Adenosine diphosphate-induced platelet aggregation is associated with P2Y12 gene sequence variations in healthy subjects |
Fontana, Pierre; Dupont, Annabelle; Gandrille, Sophie; Bachelot-Loza, Christilla; ... Gaussem, Pascale |
2003 |
unige:114083 |
APOE and modulation of Alzheimer's and frontotemporal dementia |
Boccardi, Marina; Sabattoli, F; Testa, C; Beltramello, A; ... Frisoni, Giovanni |
2004 |
unige:9080 |
Hypofibrinogenaemia caused by a novel FGG missense mutation (W253C) in the gamma chain globular domain impairing fibrinogen secretion |
Vu, Dung; De Moerloose, Philippe; Batorova, A.; Lazur, J.; ... Neerman Arbez, Marguerite |
2005 |