Zobrazeno 1 - 10
of 117
pro vyhledávání: '"Chapgier, Ariane"'
Autor:
Zhang, Shen-Ying, Jouanguy, Emmanuelle, Ugolini, Sophie, Smahi, Asma, Elain, Gaëlle, Romero, Pedro, Segal, David, Sancho-Shimizu, Vanessa, Lorenzo, Lazaro, Puel, Anne, Picard, Capucine, Chapgier, Ariane, Plancoulaine, Sabine, Titeux, Matthias, Cognet, Céline, von Bernuth, Horst, Ku, Cheng-Lung, Casrouge, Armanda, Zhang, Xin-Xin, Barreiro, Luis, Leonard, Joshua, Hamilton, Claire, Lebon, Pierre, Héron, Bénédicte, Vallée, Louis, Quintana-Murci, Lluis, Hovnanian, Alain, Rozenberd, Flore, Vivier, Eric, Geissmann, Frédéric, Tardieu, Marc, Abel, Laurent, Casanova, Jean-Laurent
Publikováno v:
Science, 2007 Sep . 317(5844), 1522-1527.
Externí odkaz:
https://www.jstor.org/stable/20037798
Autor:
Bustamante, Jacinta, Aksu, Guzide, Vogt, Guillaume, de Beaucoudrey, Ludovic, Genel, Ferah, Chapgier, Ariane, Filipe-Santos, Orchidée, Feinberg, Jacqueline, Emile, Jean-François, Kutukculer, Necil, Casanova, Jean-Laurent
Publikováno v:
In The Journal of Allergy and Clinical Immunology 2007 120(1):32-38
Autor:
Chapgier, Ariane1, Boisson-Dupuis, Stéphanie1, Jouanguy, Emmanuelle1,2, Vogt, Guillaume1, Feinberg, Jacqueline1, Prochnicka-Chalufour, Ada3, Casrouge, Armanda1, Kun Yang1,2, Soudais, Claire1, Fieschi, Claire1,4, Santos, Orchidée Filipe1, Bustamante, Jacinta1, Picard, Capucine1,5, de Beaucoudrey, Ludovic1, Emile, Jean-François6, Arkwright, Peter D.7, Schreiber, Robert D.8, Rolinck-Werninghaus, Claudia9, Rösen-Wolff, Angela10, Magdorf, Klaus9
Publikováno v:
PLoS Genetics. Aug2006, Vol. 3 Issue 2, pe131-1206. 14p. 6 Diagrams, 2 Charts, 3 Graphs.
Autor:
Tsolia, Maria N.1 matsolia@ath.forthnet.gr, Chapgier, Ariane2, Taprantzi, Polyxeni1, Servitzoglou, Marina1, Tassios, Ioannis1, Spyridis, Nikolaos1, Papageorgiou, Fotini1, Santos, Orchidée Filipe2, Casanova, Jean-Laurent2, Spyridis, Panayotis1, Santos, Orchidée Filipe (AUTHOR)
Publikováno v:
European Journal of Pediatrics. Jul2006, Vol. 165 Issue 7, p458-461. 4p. 1 Color Photograph, 1 Graph.
Autor:
Vogt, Guillaume1, Chapgier, Ariane1, Yang, Kun1,2, Chuzhanova, Nadia3,4, Feinberg, Jacqueline1, Fieschi, Claire1,5, Boisson-Dupuis, Stéphanie1, Alcais, Alexandre1, Filipe-Santos, Orchidée1, Bustamante, Jacinta1, de Beaucoudrey, Ludovic1, Al-Mohsen, Ibrahim6, Al-Hajjar, Sami6, Al-Ghonaium, Abdulaziz6, Adimi, Parisa7, Mirsaeidi, Mehdi7, Khalilzadeh, Soheila7, Rosenzweig, Sergio8, de la Calle Martin, Oscar9, Bauer, Thomas R.10
Publikováno v:
Nature Genetics. Jul2005, Vol. 37 Issue 7, p692-700. 9p.
Akademický článek
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Autor:
Dilg, Daniel, Saleh, Rasha Noureldin M., Phelps, Sarah Elizabeth Lee, Rose, Yoann, Dupays, Laurent, Murphy, Cian, Mohun, Timothy, Anderson, Robert H., Scambler, Peter J., Chapgier, Ariane L. A.
Publikováno v:
PLoS ONE, Vol 11, Iss 8, p e0161096 (2016)
PLoS ONE
PLoS ONE
Chromatin remodelling is essential for cardiac development. Interestingly, the role of histone chaperones has not been investigated in this regard. HIRA is a member of the HUCA (HIRA/UBN1/CABIN1/ASF1a) complex that deposits the variant histone H3.3 o
Autor:
Waters, Aoife M, Asfahani, Rowan, Carroll, Paula, Bicknell, Louise, Lescai, Francesco, Bright, Alison, Chanudet, Estelle, Brooks, Anthony, Christou-Savina, Sonja, Osman, Guled, Walsh, Patrick, Bacchelli, Chiara, Chapgier, Ariane, Vernay, Bertrand, Bader, David M, Deshpande, Charu, O' Sullivan, Mary, Ocaka, Louise, Stanescu, Horia, Stewart, Helen S, Hildebrandt, Friedhelm, Otto, Edgar, Johnson, Colin A, Szymanska, Katarzyna, Katsanis, Nicholas, Davis, Erica, Kleta, Robert, Hubank, Mike, Doxsey, Stephen, Jackson, Andrew, Stupka, Elia, Winey, Mark, Beales, Philip L
Publikováno v:
Waters, A M, Asfahani, R, Carroll, P, Bicknell, L, Lescai, F, Bright, A, Chanudet, E, Brooks, A, Christou-Savina, S, Osman, G, Walsh, P, Bacchelli, C, Chapgier, A, Vernay, B, Bader, D M, Deshpande, C, O' Sullivan, M, Ocaka, L, Stanescu, H, Stewart, H S, Hildebrandt, F, Otto, E, Johnson, C A, Szymanska, K, Katsanis, N, Davis, E, Kleta, R, Hubank, M, Doxsey, S, Jackson, A, Stupka, E, Winey, M & Beales, P L 2015, ' The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes ', Journal of Medical Genetics, vol. 52, no. 3, pp. 147-156 . https://doi.org/10.1136/jmedgenet-2014-102691
Journal of Medical Genetics
Journal of medical genetics, vol 52, iss 3
Journal of Medical Genetics
Journal of medical genetics, vol 52, iss 3
Background Mutations in microtubule-regulating genes are associated with disorders of neuronal migration and microcephaly. Regulation of centriole length has been shown to underlie the pathogenesis of certain ciliopathy phenotypes. Using a next-gener
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::42bbce5f5890f1eda143030a18aafeaf
https://hdl.handle.net/20.500.11820/8fa39511-4772-4703-938c-b1563ce410d8
https://hdl.handle.net/20.500.11820/8fa39511-4772-4703-938c-b1563ce410d8
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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We describe the case of a 2-year-old boy with disseminated infection by a rapidly growing, poorly pathogenic mycobacterial species that belonged to the Mycobacterium fortuitum-Mycobacterium peregrinum complex. He had a severe course characterized by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::c7b544034771a9050b6983f4e4333d0d
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3099897
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3099897