Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Sophie, Moog"'
Autor:
Antoine de Zélicourt, Abdallah Fayssoil, Mbarka Dakouane‐Giudicelli, Isley De Jesus, Ahmed Karoui, Faouzi Zarrouki, Florence Lefebvre, Arnaud Mansart, Jean‐Marie Launay, Jerome Piquereau, Mariana G Tarragó, Marcel Bonay, Anne Forand, Sophie Moog, France Piétri‐Rouxel, Elise Brisebard, Claudia C S Chini, Sonu Kashyap, Matthew J Fogarty, Gary C Sieck, Mathias Mericskay, Eduardo N Chini, Ana Maria Gomez, José‐Manuel Cancela, Sabine de la Porte
Publikováno v:
EMBO Molecular Medicine, Vol 14, Iss 5, Pp 1-23 (2022)
Abstract Duchenne muscular dystrophy (DMD) is characterized by progressive muscle degeneration. Two important deleterious features are a Ca2+ dysregulation linked to Ca2+ influxes associated with ryanodine receptor hyperactivation, and a muscular nic
Externí odkaz:
https://doaj.org/article/ff8aa5831114408f802cc62d7a45fce4
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b10a8e3f2409976fbed8cdc0e067116
https://doi.org/10.1530/endoabs.90.p390
https://doi.org/10.1530/endoabs.90.p390
Autor:
Puga Francisca Marques, Ghuzlan Abir Al, Dana M. Hartl, Mohamed-Amine Bani, Sophie Moog, Fabiana Pani, Ingrid Breuskin, Joanne Guerlain, Matthieu Faron, Desiree Denadreis, Eric Baudin, Julien Hadoux, Livia Lamartina
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1da3fbdbc2cf8ba63e02afcaae398fcc
https://doi.org/10.1530/endoabs.90.p651
https://doi.org/10.1530/endoabs.90.p651
Autor:
Matthieu Faron, Livia Lamartina, Segolene Hescot, Sophie Moog, Frederic Deschamps, Charles Roux, Rosella Libe, Jerome Durand-Labrunie, Abir Al Ghuzlan, Julien Hadoux, Eric Baudin
Publikováno v:
Endocrine. 77:419-424
Adrenocortical carcinoma (ACC) is a very rare and aggressive malignant disease. Therefore, overall survival (OS) has long been considered as the best endpoint. Yet, a unique endpoint is not optimal to take into account the heterogeneity in tumor prof
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18e2acb6449debbf5ec079604d424022
https://doi.org/10.1007/s12020-022-03128-2
https://doi.org/10.1007/s12020-022-03128-2
Autor:
Sophie Moog, Betty Salgues, Yasmine Braik-Djellas, Thomas Viel, Daniel Balvay, Gwennhael Autret, Estelle Robidel, Anne-Paule Gimenez-Roqueplo, Bertrand Tavitian, Charlotte Lussey-Lepoutre, Judith Favier
Publikováno v:
Endocrine-Related Cancer
Endocrine-Related Cancer, 2022, 29 (6), pp.375-388. ⟨10.1530/ERC-22-0030⟩
Endocrine-Related Cancer, 2022, 29 (6), pp.375-388. ⟨10.1530/ERC-22-0030⟩
Therapies for metastatic SDHB-dependent pheochromocytoma and paraganglioma (PPGL) are limited and poorly efficient. New targeted therapies and identification of early non-invasive biomarkers of response are thus urgently needed for these patients. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d582c8aef21ccd33c6c8f1d36d5141e
https://doi.org/10.1530/erc-22-0030
https://doi.org/10.1530/erc-22-0030
Autor:
Sophie Moog, Judith Favier
Publikováno v:
médecine/sciences
médecine/sciences, EDP Sciences, 2022, 38 (3), pp.255-262. ⟨10.1051/medsci/2022024⟩
médecine/sciences, EDP Sciences, 2022, 38 (3), pp.255-262. ⟨10.1051/medsci/2022024⟩
International audience; La succinate déshydrogénase (SDH) est une enzyme mitochondriale qui participe au cycle de Krebs et à la chaîne respiratoire. Quand elles sont à l’origine de cancers, les mutations des gènes codant les différentes sous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7e54733a0bdfa9c0ed1d528174c2943
https://doi.org/10.1051/medsci/2022024
https://doi.org/10.1051/medsci/2022024
Autor:
Judith Favier, Daniel A. Tennant, Eric Letouzé, Anne-Paule Gimenez-Roqueplo, Fatima Mechta-Grigoriou, Raphaël Rodriguez, Jennie Roberts, Lisa Vettore, Alpesh Thakker, Paule Bénit, Charlotte Lussey-Lepoutre, Cynthia L. Andoniadou, Theodora J. Stewart, Katarina Kluckova, Alexander P. Morrell, Sebastian Müller, Géraldine Gentric, Aurélie Morin, Sophie Moog, Judith Goncalves
Supplementary Figure 1 - Supplementary Figure 2 - Supplementary Figure 3 - Supplementary Figure 4 - Supplementary Figure 5 - Supplementary Figure 6 - Supplementary Table 1 - Supplementary Table 2 - Supplementary Table 3 - Supplementary Table 4 - Supp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14fa5c66a17bcd42509bb7c99b59f814
https://doi.org/10.1158/0008-5472.22428819
https://doi.org/10.1158/0008-5472.22428819
Autor:
Judith Favier, Daniel A. Tennant, Eric Letouzé, Anne-Paule Gimenez-Roqueplo, Fatima Mechta-Grigoriou, Raphaël Rodriguez, Jennie Roberts, Lisa Vettore, Alpesh Thakker, Paule Bénit, Charlotte Lussey-Lepoutre, Cynthia L. Andoniadou, Theodora J. Stewart, Katarina Kluckova, Alexander P. Morrell, Sebastian Müller, Géraldine Gentric, Aurélie Morin, Sophie Moog, Judith Goncalves
Succinate dehydrogenase is a key enzyme in the tricarboxylic acid cycle and the electron transport chain. All four subunits of succinate dehydrogenase are tumor suppressor genes predisposing to paraganglioma, but only mutations in the SDHB subunit ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8344fed531abd70c4e2067dd3f8dac8
https://doi.org/10.1158/0008-5472.c.6513153.v1
https://doi.org/10.1158/0008-5472.c.6513153.v1
Autor:
Judith Favier, Daniel A. Tennant, Eric Letouzé, Anne-Paule Gimenez-Roqueplo, Fatima Mechta-Grigoriou, Raphaël Rodriguez, Jennie Roberts, Lisa Vettore, Alpesh Thakker, Paule Bénit, Charlotte Lussey-Lepoutre, Cynthia L. Andoniadou, Theodora J. Stewart, Katarina Kluckova, Alexander P. Morrell, Sebastian Müller, Géraldine Gentric, Aurélie Morin, Sophie Moog, Judith Goncalves
Supplementary Table 2 Related to Figure 2. Differentially methylated gene-based features in Sdhb-/- versus Sdhd-/- imCCs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78b04c08f42c8e0660b2c6f91c099c84
https://doi.org/10.1158/0008-5472.22428816.v1
https://doi.org/10.1158/0008-5472.22428816.v1
Autor:
Daniel J. Owens, Martina Fischer, Saline Jabre, Sophie Moog, Kamel Mamchaoui, Gillian Butler-Browne, Catherine Coirault
Publikováno v:
Cells, Vol 9, Iss 4, p 816 (2020)
Mutations in the LMNA gene, encoding the nuclear envelope A-type lamins, are responsible for muscular dystrophies, the most severe form being the LMNA-related congenital muscular dystrophy (L-CMD), with severe defects in myonucleus integrity. We prev
Externí odkaz:
https://doaj.org/article/cacc582cb6754e9ba0763b4b233ac557