Zobrazeno 1 - 10
of 193
pro vyhledávání: '"G, Plessis"'
Publikováno v:
Advances in Medical Sciences. 57:314-321
Purpose Loss-of-function mutations in FGFR1 have been identified in approximately 10% of the Kallmann syndrome (KS) patients. Previous reports have focused mainly on olfactory, reproductive, and some other features such as cleft lip/palate and dental
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39e4bd0eab473f6bb2e76b9be81bf92c
https://doi.org/10.2478/v10039-012-0036-4
https://doi.org/10.2478/v10039-012-0036-4
Autor:
C. Charrin, Anne Hagemeijer, Carole Barin, M J Mozzicconacci, Barbara Cauwelier, Christine Lefebvre, Bruno Verhasselt, Isabelle Luquet, M.J. Gregoire, Philippe Jonveaux, Hélène Cavé, Barbara De Moerloose, Christine Terré, Kim De Keersmaecker, Anne De Paepe, G Plessis, F Sigaux, Nicole Dastugue, Bruce Poppe, Michel Lessard, B Laurence, Laurent Mauvieux, Hélène Antoine-Poirel, Marina Lafage-Pochitaloff, Francine Mugneret, Emmanuelle Clappier, J van den Akker, J Soulier, C Graux, Yves Benoit, Jan Cools, Carine Gervais, Franki Speleman, Pascale Cornillet-Lefebvre, Marie-Pierre Pages, C Chalas, Dominique Leroux, N. Van Roy, Christine Perot, Pierre Heimann, Roland Berger
Publikováno v:
Leukemia
Leukemia, Nature Publishing Group: Open Access Hybrid Model Option B, 2007, 21 (1), pp.121-8. ⟨10.1038/sj.leu.2404410⟩
Leukemia, 2007, 21 (1), pp.121-8. ⟨10.1038/sj.leu.2404410⟩
Leukemia, Nature Publishing Group: Open Access Hybrid Model Option B, 2007, 21 (1), pp.121-8. <10.1038/sj.leu.2404410>
Leukemia, Nature Publishing Group: Open Access Hybrid Model Option B, 2007, 21 (1), pp.121-8. ⟨10.1038/sj.leu.2404410⟩
Leukemia, 2007, 21 (1), pp.121-8. ⟨10.1038/sj.leu.2404410⟩
Leukemia, Nature Publishing Group: Open Access Hybrid Model Option B, 2007, 21 (1), pp.121-8. <10.1038/sj.leu.2404410>
International audience; Recently, we and others described a new chromosomal rearrangement, that is, inv(7)(p15q34) and t(7;7)(p15;q34) involving the T-cell receptor beta (TCRbeta) (7q34) and the HOXA gene locus (7p15) in 5% of T-cell acute lymphoblas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be0e2a8fa5b81d3b8f190bc9464a5df5
https://doi.org/10.1038/sj.leu.2404410
https://doi.org/10.1038/sj.leu.2404410
Publikováno v:
Computer Methods in Applied Mechanics and Engineering. 189:863-873
The problem of structures' sensitivities to uncertain boundary conditions is presented in this paper and the effect of uncertain prescribed displacements on the static response of structures is discussed. The imprecise or uncertain prescribed displac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5feca1306132b02c3027a65791be5b16
https://doi.org/10.1016/s0045-7825(99)00401-6
https://doi.org/10.1016/s0045-7825(99)00401-6
Publikováno v:
Journal of Sound and Vibration. 233:797-812
In order to identify modal parameters with uncertain experimental data, a non-deterministic identification method based on fuzzy formalism is proposed. The aim is to provide a degree of confidence in the modal parameters identified.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac35867f94e37531ceb39dcdc4a92ba0
https://doi.org/10.1006/jsvi.1999.2851
https://doi.org/10.1006/jsvi.1999.2851
Autor:
E. Erdei, N. Souleyreau-Therville, Lluis Quintana-Murci, Marc Fellous, Ken McElreavey, G. Arvis, D. Delafontaine, Sandrine Barbaux, J.-P. Dadoune, Csilla Krausz, E. Jeandidier, Jean Pierre Siffroi, Attila Tar, J. M. Antoine, Thomas Bourgeron, Hassan Rouba, G. Plessis, J. P. Taar
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 84:3606-3612
Microdeletions of the long arm of the human Y chromosome are associated with spermatogenic failure and have been used to define three regions of Yq (AZFa, AZFb, and AZFc) that are recurrently deleted in infertile males. In a blind study we screened 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::481eb0ce53a29e3744a35b2a1eb96b15
https://doi.org/10.1210/jcem.84.10.6040
https://doi.org/10.1210/jcem.84.10.6040
Publikováno v:
Engineering Computations. 16:572-583
This paper presents a new framework to predict a structure’s effective properties and sensitivities to multiple simultaneous uncertain endogenous parameters. The methodology is based on the use of fuzzy sets and this paper extends the fuzzy set the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9207c2792d558a6521cdc41b4119ccf9
https://doi.org/10.1108/02644409910277933
https://doi.org/10.1108/02644409910277933
Autor:
S Gilgenkrantz, J.C Lambert, M.F. Croquette, C Moutou, B. Delobel, J.L Lanoe, C. Stoll, G Plessis, J.-C. Bouix, Jean-Louis Mandel, V Biancalana, Mireille Cossée, G Malpuech, M Pechevis
Publikováno v:
Archives de Pédiatrie. 4:227-236
Resume Le retard mental avec chromosome X fragile est la cause la plus frequente de retard mental hereditaire. L'identification de la mutation instable responsable a permis la mise au point d'un test moleculaire entierement fiable tant pour le diagno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3382cba2688a47e8f0eb808bf1c577bb
https://doi.org/10.1016/s0929-693x(97)87235-1
https://doi.org/10.1016/s0929-693x(97)87235-1
Akademický článek
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Autor:
Jian-Min Chen, C. Le Gall, Claude Férec, Odile Raguenes, J. Chipponi, Nadia Chuzhanova, C. Le Maréchal, G. Plessis
Publikováno v:
Scopus-Elsevier
Mutations in the serine protease inhibitor Kazal type 1 gene (SPINK1) encoding pancreatic secretory trypsin inhibitor (PSTI) have recently been found to be associated with chronic pancreatitis. Nevertheless, knowledge of severe mutations is particula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e94234364cef911a7903419913429e2
https://pubmed.ncbi.nlm.nih.gov/14722925
https://pubmed.ncbi.nlm.nih.gov/14722925
Conference
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