Zobrazeno 1 - 3
of 3
pro vyhledávání: '"MESH: Genetic Predisposition to Disease / genetics"'
Autor:
Cristina Beltrami, Owen J. L. Rackham, Costanza Emanueli, Nithya Devapragash, Wei-Ping Yu, Xi-Ming Sun, Stuart A. Cook, Norbert Hubner, Francesco Pesce, Ee Ling Heng, Elisabeth Tan, Aida Moreno-Moral, Enrique Lara-Pezzi, Gianni D Angelini, Enrico Petretto, Huimei Chen, Paul J.R. Barton, Nathan Harmston, Michal Pravenec, Sebastian Schafer, Maxime Rotival, Nicole Tee, Massimilano Mancini, Leanne E. Felkin, Leonardo Bottolo, Prashant K. Srivastava, Kirill Shkura
Publikováno v:
Nature Communications
Nature Communications, 2019, 10 (1), pp.3616. ⟨10.1038/s41467-019-11551-9⟩
Nature Communications, Vol 10, Iss 1, Pp 1-19 (2019)
Chen, H, Moreno-Moral, A, Pesce, F, Devapragash, N, Mancini, M, Heng, E L, Rotival, M, Srivastava, P K, Harmston, N, Shkura, K, Rackham, O J L, Yu, W P, Sun, X M, Tee, N G Z, Tan, E L S, Barton, P J R, Felkin, L E, Lara-Pezzi, E, Angelini, G, Beltrami, C, Pravenec, M, Schafer, S, Bottolo, L, Hubner, N, Emanueli, C, Cook, S A & Petretto, E 2019, ' WWP2 regulates pathological cardiac fibrosis by modulating SMAD2 signalling ', Nature Communications, vol. 10, 3616 . https://doi.org/10.1038/s41467-019-11551-9
Nature Communications, Nature Publishing Group, 2019, 10 (1), pp.3616. ⟨10.1038/s41467-019-11551-9⟩
Repisalud
Instituto de Salud Carlos III (ISCIII)
Nature Communications, 2019, 10 (1), pp.3616. ⟨10.1038/s41467-019-11551-9⟩
Nature Communications, Vol 10, Iss 1, Pp 1-19 (2019)
Chen, H, Moreno-Moral, A, Pesce, F, Devapragash, N, Mancini, M, Heng, E L, Rotival, M, Srivastava, P K, Harmston, N, Shkura, K, Rackham, O J L, Yu, W P, Sun, X M, Tee, N G Z, Tan, E L S, Barton, P J R, Felkin, L E, Lara-Pezzi, E, Angelini, G, Beltrami, C, Pravenec, M, Schafer, S, Bottolo, L, Hubner, N, Emanueli, C, Cook, S A & Petretto, E 2019, ' WWP2 regulates pathological cardiac fibrosis by modulating SMAD2 signalling ', Nature Communications, vol. 10, 3616 . https://doi.org/10.1038/s41467-019-11551-9
Nature Communications, Nature Publishing Group, 2019, 10 (1), pp.3616. ⟨10.1038/s41467-019-11551-9⟩
Repisalud
Instituto de Salud Carlos III (ISCIII)
Cardiac fibrosis is a final common pathology in inherited and acquired heart diseases that causes cardiac electrical and pump failure. Here, we use systems genetics to identify a pro-fibrotic gene network in the diseased heart and show that this netw
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b9a8eae768aaa77cac0482318b75243
https://doi.org/10.1038/s41467-019-11551-9
https://doi.org/10.1038/s41467-019-11551-9
Autor:
M. Benazzouz, Aziz Benjouad, Abdellah Akil, Rajaa Afifi, Sayeh Ezzikouri, Pascal Pineau, Abdellah Essaid El Feydi, Soumaya Benjelloun, Ama Gassama Diagne, Anne Dejean
Publikováno v:
Cancer Epidemiology
Cancer Epidemiology, 2012, 36 (5), pp.e300-e305. ⟨10.1016/j.canep.2012.05.011⟩
Cancer Epidemiology, Elsevier, 2012, 36 (5), pp.e300-e305. ⟨10.1016/j.canep.2012.05.011⟩
Cancer Epidemiology, 2012, 36 (5), pp.e300-e305. ⟨10.1016/j.canep.2012.05.011⟩
Cancer Epidemiology, Elsevier, 2012, 36 (5), pp.e300-e305. ⟨10.1016/j.canep.2012.05.011⟩
Background and aims : Hepatocellular carcinoma (HCC) is a common cause of death by cancer worldwide. In Morocco, HCC is characterized by few mutations and a mild chromosome instability suggesting that epigenetic changes may represent the driving forc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a1a22fd93c751047ddc0d7af3d618b1
https://pubmed.ncbi.nlm.nih.gov/22709982
https://pubmed.ncbi.nlm.nih.gov/22709982
Autor:
Latifa El Kihal, Rajae Afifi, Mohammed Hassar, Pascal Pineau, M. Benazzouz, Sayeh Ezzikouri, Abdellah Essaid El Feydi, Abdelaziz Chafik, Soumaya Benjelloun
Publikováno v:
Archives of Medical Research
Archives of Medical Research, Elsevier, 2008, 39 (2), pp.236-241. ⟨10.1016/j.arcmed.2007.09.006⟩
Archives of Medical Research, 2008, 39 (2), pp.236-241. ⟨10.1016/j.arcmed.2007.09.006⟩
Archives of Medical Research, Elsevier, 2008, 39 (2), pp.236-241. ⟨10.1016/j.arcmed.2007.09.006⟩
Archives of Medical Research, 2008, 39 (2), pp.236-241. ⟨10.1016/j.arcmed.2007.09.006⟩
International audience; Background: Hereditary hemochromatosis and SERPINA1 mutation were reported to affect liver functions. Our objective was to estimate the prevalence of HFE and SERPINA1 (formerly known as alpha1-antitrypsin, AAT) mutations and a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5658b90e28110c32f640b50cd367309c
https://hal-pasteur.archives-ouvertes.fr/pasteur-02870414
https://hal-pasteur.archives-ouvertes.fr/pasteur-02870414
