Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Bernard Conrad"'
Publikováno v:
PLoS ONE, Vol 18, Iss 3, p e0281661 (2023)
All life forms on earth ultimately descended from a primordial population dubbed the last universal common ancestor or LUCA via Darwinian evolution. Extant living systems share two salient functional features, a metabolism extracting and transforming
Externí odkaz:
https://doaj.org/article/a6a9eb1571bc4ff488303ba792a07d8c
Autocatalytic networks likely played a central role in the shift from inanimate systems to protocells. Using an established hyperparasite framework, we model the emergence of antiparasite immunity using the Lotka Volterra equations. It builds on auto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24040b70caa5ec6b4d380b241c100967
https://doi.org/10.1101/2023.05.25.542273
https://doi.org/10.1101/2023.05.25.542273
Autor:
Bernard Conrad, Christian De Geyter, Gideon Sartorius, Olav Lapaire, Rebecca Moffat, Anna Raggi
Publikováno v:
Swiss Medical Forum ‒ Schweizerisches Medizin-Forum.
Der Trend, immer spater im Leben Mutter zu werden, nimmt stetig zu. Je spater der Kinderwunsch jedoch beginnt, desto eher wird er nicht in Erfullung gehen.
Autor:
Olav Lapaire, Christian De Geyter, Bernard Conrad, Rebecca Moffat, Anna Raggi, Gideon Sartorius
Publikováno v:
Forum Médical Suisse ‒ Swiss Medical Forum.
La tendance a devenir mere de plus en plus tard ne cesse d’augmenter. Mais plus le desir d’enfant debute tardivement, plus il aura tendance a ne pas se concretiser.
Autor:
Brigitte T. Huber, Bernard Conrad, Samuel Marguerat, Thierry Pelet, Natalie Sutkowski, Françoise Meylan, Catherine Ucla, Yves Stauffer
Publikováno v:
Immunity. 15(4):591-601
We earlier proposed that a human endogenous retroviral (HERV) superantigen (SAg) IDDMK(1,2)22 may cause type I diabetes by activating autoreactive T cells. Viral infections and induction of interferon-alpha (IFN-alpha) are tightly associated with the
Autor:
Bernard Conrad, Denis F. Hochstrasser, Walter Reith, Bernard Mach, Krzysztof Masternak, Garry L. Corthals, Jean-Charles Sanchez, Madeleine Zufferey, Emmanuèle Barras, Ruedi Aebersold
Publikováno v:
Nature Genetics, Vol. 20, No 3 (1998) pp. 273-277
Major histocompatibility class II (MHC-II) molecules are transmembrane proteins that have a central role in development and control of the immune system. They are encoded by a multigene family and their expression is tightly regulated. MHC-II deficie
Autor:
Bernard Conrad, Isabelle Bouchardy, Jacqueline Schoumans, Armand Bottani, Annick Toutain, Bruno Pardo
Publikováno v:
American Journal of Medical Genetics Part A. :903-905
Kabuki syndrome (KS, OMIM 147920), also known as Kabuki make-up syndrome or Niikawa–Kuroki syndrome, is a multiple congenital anomaly/mental retardation syndrome of hitherto unknown cause [Wessels et al., 2002; Matsumoto and Niikawa, 2003]. The pre
Autor:
Rosanna Arcari, Bernard Conrad, Jürg Böni, Richard Nicolas Weissmahr, Jörg Schüpbach, Bernard Mach
Publikováno v:
Cell. 90:303-313
Microbial superantigens (SAGs) have been implicated in the pathogenesis of human autoimmune diseases. Preferential expansion of the Vβ7 T cell receptor positive T cell subset in patients suffering from acute-onset type I diabetes has indicated the p
Autor:
Edel A. O'Toole, Mariann Tihanyi, Celia Moss, Malcolm H.A. Rustin, Chris Bennett, Philip Bland, Catherine M T Chronnell, Daniel Poon, László Gárdos, Ishwar C. Verma, Daniela Nitoiu, John I. Harper, Saleem M. Taibjee, Nigel Burrows, David P. Kelsell, Diana C. Blaydon, Bernard Conrad, David Bourn, Andrea Császár, Vincent Plagnol, Claire A. Scott
Publikováno v:
The Journal of investigative dermatology. 133(2)
cated that MBTPS2 is mainly expressed in the upper granular layer in normal skin, as previously shown (Aten et al., 2010); however, in OS skin, MBTPS2 was expressed throughout the epidermis (Figure 2c). There was no apparent difference in MBTPS2 loca
Autor:
Cécile, Martel, Michelle, Mollin, Sylvain, Beaumel, Jean Paul, Brion, Charles, Coutton, Véronique, Satre, Gaëlle, Vieville, Mary, Callanan, Christine, Lefebvre, Alexandra, Salmon, Anne, Pagnier, Dominique, Plantaz, Cécile, Bost-Bru, Laurence, Eitenschenck, Isabelle, Durieu, Daniel, Floret, Claire, Galambrun, Hervé, Chambost, Gérard, Michel, Jean-Louis, Stephan, Olivier, Hermine, Stéphane, Blanche, Nathalie, Blot, Hervé, Rubié, Guillaume, Pouessel, Stephanie, Drillon-Haus, Bernard, Conrad, Klara M, Posfay-Barbe, Zuzana, Havlicekova, Tamara, Voskresenky-Baricic, Kelecic, Jadranka, Maria Cristina, Arriazu, Luis Alberto, Garcia, Lamia, Sfaihi, Lamia Sfaihi Ben, Mansour, Pierre, Bordigoni, Marie José, Stasia
Publikováno v:
Journal of Clinical Immunology, Vol. 32, No 5 (2012) pp. 942-58
Journal of Clinical Immunology
Journal of Clinical Immunology, Springer Verlag, 2012, 32 (5), pp.942-58. ⟨10.1007/s10875-012-9698-8⟩
Journal of Clinical Immunology, Springer Verlag, 2012, 32 (5), pp.942-58. 〈10.1007/s10875-012-9698-8〉
Journal of Clinical Immunology
Journal of Clinical Immunology, Springer Verlag, 2012, 32 (5), pp.942-58. ⟨10.1007/s10875-012-9698-8⟩
Journal of Clinical Immunology, Springer Verlag, 2012, 32 (5), pp.942-58. 〈10.1007/s10875-012-9698-8〉
International audience; Chronic granulomatous disease is an inherited disorder in which phagocytes lack a functional NADPH oxidase and cannot produce superoxide anions. The most common form is caused by mutations in CYBB encoding gp91phox. We investi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7af4c7f99fc92140fce0715edcc28be6
https://archive-ouverte.unige.ch/unige:31691
https://archive-ouverte.unige.ch/unige:31691