Zobrazeno 1 - 10
of 538
pro vyhledávání: '"J. Andrieux"'
Publikováno v:
Geofísica Internacional, Vol 25, Iss 1, Pp 207-231 (1986)
La zona sísmica del sur de México se puede dividir en cuatro regiones de características diferentes, aun cuando la actividad se considera como el resultado de la interacción de las placas Pacífico, Norteamericana, cocos, Caribe y Rivera. En este
Externí odkaz:
https://doaj.org/article/348d3e3a9b5b40448dfd105c3092ba2f
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
J. Andrieux, Dmitri V. Louzguine-Luzgin, Louis Hennet, Kengo Nishio, Rodion V. Belosludov, Konstantinos Georgarakis, T. Morishita
Publikováno v:
Intermetallics
Intermetallics, Elsevier, 2020, 122, pp.106795. ⟨10.1016/j.intermet.2020.106795⟩
Intermetallics, Elsevier, 2020, 122, pp.106795. ⟨10.1016/j.intermet.2020.106795⟩
International audience; Structural changes in the Zr55Cu30Ni5Al10 liquid alloy on cooling from above the equilibrium liquidus temperature are studied by synchrotron radiation X-ray diffraction and compared with the results of first-principles molecul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e245a58d383ef829335df494d02f65f
https://dspace.lib.cranfield.ac.uk/handle/1826/15488
https://dspace.lib.cranfield.ac.uk/handle/1826/15488
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
A-C, Thuresson, G, Van Buggenhout, F, Sheth, M, Kamate, J, Andrieux, J, Clayton Smith, C, Soussi Zander
Publikováno v:
Clinical genetics. 91(1)
Duplications at 2q24.3 encompassing the voltage-gated sodium channel gene cluster are associated with early onset epilepsy. All cases described in the literature have presented in addition with different degrees of intellectual disability, and have i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d6290ede81a6b6c0f97e276f50cafbd9
https://pubmed.ncbi.nlm.nih.gov/27153334
https://pubmed.ncbi.nlm.nih.gov/27153334
Autor:
J. Andrieux
Publikováno v:
Pathologie Biologie. 56:368-374
Cytogenetics allows detection of genomic anomalies between 10 and 15 Mb (classical cytogenetics) and between 3 and 5 Mb (high-resolution cytogenetics). These pangenomic techniques are associated with more accurate analyses, single probe interstitial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89a161827f8722cc0864d9c36670d636
https://doi.org/10.1016/j.patbio.2008.04.011
https://doi.org/10.1016/j.patbio.2008.04.011
Autor:
C. Roche-Lestienne, J. Andrieux
Publikováno v:
Pathologie Biologie. 55:49-55
Myelofibrosis with myeloid metaplasia (MMM) is a rare myeloproliferative disorder (MPD) characterized by clonal proliferation of hematopoietic progenitors. 40-50% of karyotypes on blood (or more rarely on bone marrow) revealed at least one abnormalit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f14ca603b97d14faecd7694d8f60cf71
https://doi.org/10.1016/j.patbio.2006.04.010
https://doi.org/10.1016/j.patbio.2006.04.010
Autor:
Virginie Scotet, C Roge, I. Frachon, Claude Férec, Christophe Leroyer, Marie-Pierre Audrézet, J Andrieux
Publikováno v:
Clinical Genetics. 62:60-67
Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene are associated with different related disorders such as congenital bilateral absence of the vas deferens, chronic idiopathic pancreatitis, or disseminated bronchiectasis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::657854a2d92af24b83ad6fdb4c7e029d
https://doi.org/10.1034/j.1399-0004.2002.620108.x
https://doi.org/10.1034/j.1399-0004.2002.620108.x
Publikováno v:
Annales d'Endocrinologie. 78:232
Une alteration du gene TCF2, codant pour HNF1β, entraine un diabete MODY 5 (ou un syndrome RCAD), d’expressivite variable. Une deletion plus large de l’emplacement comportant TCF2 conduit au syndrome 17q12. L’objectif etait de comparer les pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0cade70a478705e73801eb0768e442e
https://doi.org/10.1016/j.ando.2017.07.063
https://doi.org/10.1016/j.ando.2017.07.063
Autor:
F, Petit, A-S, Jourdain, J, Andrieux, G, Baujat, C, Baumann, C, Beneteau, A, David, L, Faivre, D, Gaillard, B, Gilbert-Dussardier, P-S, Jouk, C, Le Caignec, P, Loget, L, Pasquier, N, Porchet, M, Holder-Espinasse, S, Manouvrier-Hanu, F, Escande
Publikováno v:
Clinical genetics. 85(5)
Split hand/foot malformation (SHFM) with long-bone deficiency (SHFLD, MIM#119100) is a rare condition characterized by SHFM associated with long-bone malformation usually involving the tibia. Previous published data reported several unrelated patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2b289490f49fe0d73667efc0c9550f68
https://pubmed.ncbi.nlm.nih.gov/23790188
https://pubmed.ncbi.nlm.nih.gov/23790188