| Title | Authors / Editors | Date |
unige:19111 |
A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in function |
Spinazzi, Marco; Cazzola, Silvia; Bortolozzi, Mario; Baracca, Alessandra; ... Vergani, Lodovica |
2008 |
unige:8999 |
A novel frameshift mutation in FGA accounting for congenital afibrinogenemia predicted to encode an aberrant peptide terminating 158 amino acids downstream |
Robert-Ebadi, Helia; De Moerloose, Philippe; El Khorassani, M.; El Khattab, M.; Neerman Arbez, Marguerite |
2009 |
unige:30079 |
A SAGA-independent function of SPT3 mediates transcriptional deregulation in a mutant of the Ccr4-not complex in Saccharomyces cerevisiae |
James, Nicole; Landrieux, Emilie; Collart, Martine |
2007 |
unige:139732 |
A Sendai virus vector leading to the efficient expression of mutant M proteins interfering with virus particle budding |
Mottet-Osman, Geneviève; Muehlemann, Andréas Samuel; Tapparel, Caroline; Hoffmann, Frédéric Olivier; Roux, Laurent |
1996 |
unige:17518 |
A truncation in the 14 kDa protein of the signal recognition particle leads to tertiary structure changes in the RNA and abolishes the elongation arrest activity of the particle |
Thomas, Yves; Bui, Nazarena; Strub, Katharina |
1997 |
unige:8846 |
Altered spacing of promoter elements due to the dodecamer repeat expansion contributes to reduced expression of the cystatin B gene in EPM1 |
Lalioti, M. D.; Scott, Hamish Steele; Antonarakis, Stylianos |
1999 |
unige:25536 |
Analyses of the functional regions of DEAD-box RNA "helicases" with deletion and chimera constructs tested in vivo and in vitro |
Banroques, Josette; Cordin, Olivier; Doere, Monique; Linder, Patrick; Tanner, N Kyle |
2011 |
unige:135903 |
Analysis of Deletions and Thermosensitive Mutations in Rous Sarcoma Virus gag Protein p10 |
Dupraz, Philippe Victor Leon; Spahr, Pierre-François |
1993 |
unige:862 |
CFTR in a lipid raft-TNFR1 complex modulates gap junctional intercellular communication and IL-8 secretion |
Dudez, Tecla; Borot, Florence; Huang, Song; Kwak, Brenda; ... Chanson, Marc |
2008 |
unige:143934 |
Clinical and biological features of PTPN2-deleted adult and pediatric T-cell acute lymphoblastic leukemia |
Alcantara, Marion; Simonin, Mathieu; Lhermitte, Ludovic; Touzart, Aurore; ... Asnafi, Vahid |
2019 |
unige:21040 |
Combined pancreatic islet-lung transplantation: a novel approach to the treatment of end-stage cystic fibrosis |
Kessler, L.; Bakopoulou, S.; Kessler, R.; Massard, G.; ... Berney, Thierry |
2010 |
unige:17546 |
Conservation of functional domains involved in RNA binding and protein-protein interactions in human and Saccharomyces cerevisiae pre-mRNA splicing factor SF1 |
Rain, J C; Rafi, Zahra; Rhani, Zakaria; Legrain, P; Kraemer, Angela |
1998 |
unige:20737 |
Control of the Staphylococcus aureus toxic shock tst promoter by the global regulator SarA |
Andrey, Diego Olivier; Renzoni, Adriana Maria; Monod, Antoinette; Lew, Daniel Pablo; ... Kelley, William |
2010 |
unige:13226 |
Coordination of Hpr1 and ubiquitin binding by the UBA domain of the mRNA export factor Mex67 |
Hobeika, Maria; Brockmann, Christoph; Iglesias, Nahid; Gwizdek, Carole; ... Dargemont, Catherine |
2007 |
unige:9166 |
Disease-causing 7.4 kb cis-regulatory deletion disrupting conserved non-coding sequences and their interaction with the FOXL2 promotor: implications for mutation screening |
D'Haene, B.; Attanasio, Catia; Beysen, Diane; Dostie, Josee; ... De Baere, Elfride |
2009 |
unige:11445 |
Dysregulated expression of the Cd22 gene as a result of a short interspersed nucleotide element insertion in Cd22a lupus-prone mice |
Mary, Charles; Laporte, Catherine; Parzy, Daniel; Santiago-Raber, Marie-Laure; ... Reininger, Luc |
2000 |
unige:17547 |
Essential domains of the PRP21 splicing factor are implicated in the binding to PRP9 and PRP11 proteins and are conserved through evolution |
Rain, J C; Tartakoff, A M; Kraemer, Angela; Legrain, P |
1996 |
unige:7529 |
Fibrinogen and fibronectin binding cooperate for valve infection and invasion in Staphylococcus aureus experimental endocarditis |
Que, Y. A.; Haefliger, J. A.; Piroth, Lionel; Francois, Patrice; ... Moreillon, Philippe |
2005 |
unige:8922 |
Fibrinogen gene mutations accounting for congenital afibrinogenemia |
Neerman Arbez, Marguerite |
2001 |
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 |