Subglacial hydrological control on flow of an Antarctic Peninsula palaeo-ice stream

Autor: R. D. Larter, K. A. Hogan, C.-D. Hillenbrand, J. A. Smith, C. L. Batchelor, M. Cartigny, A. J. Tate, J. D. Kirkham, Z. A. Roseby, G. Kuhn, A. G. C. Graham, J. A. Dowdeswell

Publikováno v: The Cryosphere, Vol 13, Pp 1583-1596 (2019)

Basal hydrological systems play an important role in controlling the dynamic behaviour of ice streams. Data showing their morphology and relationship to geological substrates beneath modern ice streams are, however, sparse and difficult to collect. W

Externí odkaz: https://doaj.org/article/10084b80a80949f88c4c230be2de7609

Author response for 'Therapeutic indications and metabolic effects of metreleptin in patients with lipodystrophy syndromes: Real‐life experience from a national reference network'

Autor: null H. Mosbah, null MC. Vantyghem, null E. Nobécourt, null F. Andreelli, null F. Archambeaud, null E. Bismuth, null C. Briet, null M. Cartigny, null B. Chevalier, null B. Donadille, null A. Daguenel, null M. Fichet, null JF. Gautier, null S. Janmaat, null I. Jéru, null C. Legagneur, null L. Leguier, null J. Maitre, null E. Mongeois, null C. Poitou, null E. Renard, null Y. Reznik, null A. Spiteri, null F. Travert, null B. Vergès, null J. Zammouri, null C. Vigouroux, null C. Vatier

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8ad88c05624f69d75a8159810b0c846d
https://doi.org/10.1111/dom.14726/v2/response1

X chromosome gene dosage as a determinant of congenital malformations and of age-related comorbidity risk in patients with Turner syndrome, from childhood to early adulthood

Autor: Elodie Fiot, Delphine Zénaty, Priscilla Boizeau, Jérémie Haignere, Sophie Dos Santos, Juliane Léger, J C Carel, S Cabrol, P Chanson, S Christin-Maitre, C Courtillot, B Donadille, J Dulon, M Houang, M Nedelcu, I Netchine, M Polak, S Salenave, D Samara-Boustani, D Simon, P Touraine, M Viaud, H Bony, K Braun, R Desailloud, A M Bertrand, B Mignot, F Schillo, P Barat, V Kerlan, C Metz, E Sonnet, Y Reznik, V Ribault, H Carla, I Tauveron, C Bensignor, F Huet, B Verges, O Chabre, C Dupuis, A Spiteri, M Cartigny, C Stuckens, J Weill, A Lienhardt, C Naud-Saudreau, F Borson-Chazot, A Brac de la Perriere, M Pugeat, T Brue, R Reynaud, G Simonin, F Paris, C Sultan, B Leheup, G Weryha, S Baron, B Charbonnel, S Dubourdieu, E Baechler, P Fenichel, K Wagner, F Compain, H Crosnier, C Personnier, B Delemer, A C Hecart, P F Souchon, M De Kerdanet, F Galland, S Nivot-Adamiak, M Castanet, C Lecointre, O Richard, N Jeandidier, S Soskin, P Lecomte, M Pepin-Donat, P Pierre

Publikováno v: European Journal of Endocrinology
European Journal of Endocrinology, 2019, 180 (6), pp.397-406. ⟨10.1530/EJE-18-0878⟩
European Journal of Endocrinology, BioScientifica, 2019, 180 (6), pp.397-406. ⟨10.1530/EJE-18-0878⟩

ObjectiveTurner Syndrome is associated with several phenotypic conditions associated with a higher risk of subsequent comorbidity. We aimed to evaluate the prevalence of congenital malformations and the occurrence of age-related comorbid conditions a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90141f9c76344ac051168fc9f8ff886a
https://doi.org/10.1530/eje-18-0878

Peer Review #1 of 'Deep-sea water displacement from a turbidity current induced by the Super Typhoon Hagibis (v0.2)'

Autor: M Cartigny

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::feb179accb227e26304db2bf0d11b34f
https://doi.org/10.7287/peerj.10429v0.2/reviews/1

SF1 and spleen development: new heterozygous mutation, literature review and consequences for NR5A1- mutated patient's management

Autor: C, Colson, E, Aubry, M, Cartigny, A-A, Rémy, H, Franquet, X, Leroy, G, Kéchid, C, Lefèvre, R, Besson, M, Cools, A F, Spinoit, C, Sultan, S, Manouvrier, P, Philibert, J, Ghoumid

Publikováno v: Clinical Genetics
Clinical Genetics, Wiley, 2017, 92 (1), pp.99-103. ⟨10.1111/cge.12957⟩
Clinical Genetics, 2017, 92 (1), pp.99-103. ⟨10.1111/cge.12957⟩

International audience; Steroidogenic factor 1 (encoded by SF1/NR5A1) is a transcription factor with multiple target genes involved in the development and function of multiple steroidogenic and non-steroidogenic tissues. NR5A1 mutations lead to sever

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::d0f9667a69107c1ce2e71dddd71204a7
https://hal.archives-ouvertes.fr/hal-01793127