Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Laia Morató"'
Autor:
Laia, Morató, Simone, Astori, Ioannis, Zalachoras, Joao, Rodrigues, Sriparna, Ghosal, Wei, Huang, Isabelle, Guillot de Suduiraut, Jocelyn, Grosse, Olivia, Zanoletti, Lei, Cao, Johan, Auwerx, Carmen, Sandi
Publikováno v:
Science advances. 8(9)
Obesity is frequently associated with impairments in the social domain, and stress at puberty can lead to long-lasting changes in visceral fat deposition and in social behaviors. However, whether stress-induced changes in adipose tissue can affect fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f44145e457554623d6a744beda39f5f7
https://pubmed.ncbi.nlm.nih.gov/35235362
https://pubmed.ncbi.nlm.nih.gov/35235362
Autor:
Elisabeth B. Binder, Tracy L. Bale, Tallie Z. Baram, David André Barrière, Jessica L. Bolton, Mallory E. Bowers, Dennis S. Charney, Alon Chen, Matthew Cranshaw, John F. Cryan, E. Ron de Kloet, Jan M. Deussing, Olivia Engmann, C. Neill Epperson, Edward Ganz, Jakob Hartmann, Marloes J.A.G. Henckens, James P. Herman, Matthew N. Hill, S.B. Hill, Brian M. Iacoviello, Orna Issler, Thérèse M. Jay, Marian Joëls, C.D. King, Stafford L. Lightman, Ekaterina Likhtik, Zachary S. Lorsch, David M. Lyons, Ricardo Magalhães, Isabelle M. Mansuy, Bruce S. McEwen, Sébastien Mériaux, Laia Morató, Kathleen E. Morrison, Iris Müller, Charles B. Nemeroff, Eric J. Nestler, Olivia F. O'Leary, Lilia Papst, Sachin Patel, Rony Paz, K.J. Ressler, Gal Richter-Levin, Mariana Rodrigues, Carmen Sandi, R. Angela Sarabdjitsingh, Alan F. Schatzberg, Mathias V. Schmidt, A.V. Seligowski, Annabel K. Short, Nuno Sousa, Francesca Spiga, Oliver Stork, Shariful A. Syed, Kuldeep Tripathi, Christiaan H. Vinkers, A.P. Wingo, Rachel Yehuda
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d3a1ba362412a9efdeaf9ef2fa098d2
https://doi.org/10.1016/b978-0-12-813983-7.01002-8
https://doi.org/10.1016/b978-0-12-813983-7.01002-8
Autor:
Laia Morató, Carmen Sandi
Stress is a major risk factor for the development of stress-related disorders, such as depression and posttraumatic stress disorder. However, there is a considerable heterogeneity in the susceptibility to develop these disorders following stress expo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a8c93fbadeb394bee08ddfb88171580e
https://doi.org/10.1016/b978-0-12-813983-7.00009-4
https://doi.org/10.1016/b978-0-12-813983-7.00009-4
Autor:
Alba Naudí, Reinald Pamplona, Laia Morató, Stéphane Fourcade, Noel Y. Calingasan, Montserrat Ruiz, Mariona Jové, Cristina Guilera, Aurora Pujol, Jordi Boada, Manuel Portero-Otin, Manuel Serrano, Jorge Galino, M. F. Beal, Isidro Ferrer
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
instname
Oxidative stress and mitochondrial failure are prominent factors in the axonal degeneration process. In this study, we demonstrate that sirtuin 1 (SIRT1), a key regulator of the mitochondrial function, is impaired in the axonopathy and peroxisomal di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab40e58983d59794f597e9f21171f494
https://doi.org/10.1038/cdd.2015.20
https://doi.org/10.1038/cdd.2015.20
Autor:
Odile Boespflug-Tanguy, Marie-Noëlle Bonnet-Dupeyron, Mélina Bégou, Johan Auwerx, Jone López-Erauskin, Aurora Pujol, Nathalie Launay, Céline Guéret-Gonthier, Catherine Vaurs-Barrière, Pablo Ranea-Robles, Patrizia Bianchi, Stéphane Fourcade, Bérengère Petit, Laia Morató, Montserrat Ruiz, Cristina Guilera
Publikováno v:
Brain Pathology
Brain Pathology, 2017, ⟨10.1111/bpa.12571⟩
Brain Pathology, Wiley, 2017, ⟨10.1111/bpa.12571⟩
Dipòsit Digital de la UB
Universidad de Barcelona
Brain Pathology, Wiley, 2017, 〈10.1111/bpa.12571〉
Brain Pathology, 2017, ⟨10.1111/bpa.12571⟩
Brain Pathology, Wiley, 2017, ⟨10.1111/bpa.12571⟩
Dipòsit Digital de la UB
Universidad de Barcelona
Brain Pathology, Wiley, 2017, 〈10.1111/bpa.12571〉
Pelizaeus‐Merzbacher disease (PMD) is a fatal hypomyelinating disorder characterized by early impairment of motor development, nystagmus, choreoathetotic movements, ataxia and progressive spasticity. PMD is caused by variations in the proteolipid p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21be927e5d376dd6689ba3c95b010238
https://hal.uca.fr/hal-01662573
https://hal.uca.fr/hal-01662573
Autor:
Montserrat Ruiz, Patrick Aubourg, Laia Morató, Reinald Pamplona, Manuel Portero-Otin, Aurora Pujol, Jorge Galino, Magali Dumont, Noel Y. Calingasan, Elena Galea, Anatoly A. Starkov, Juan José Martínez, Stéphane Fourcade, Alba Naudí, M. Flint Beal, Isidre Ferrer
Publikováno v:
Brain; Vol 136
Brain
Recercat. Dipósit de la Recerca de Catalunya
instname
Brain
Recercat. Dipósit de la Recerca de Catalunya
instname
X-linked adrenoleukodystrophy is a neurometabolic disorder caused by inactivation of the peroxisomal ABCD1 transporter of very long-chain fatty acids. In mice, ABCD1 loss causes late onset axonal degeneration in the spinal cord in association with lo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::289a1c5f32fcb6d6b5bd8cb2630c2751
https://doi.org/10.1093/brain/awt143
https://doi.org/10.1093/brain/awt143
Autor:
Juliet Reid, Lluís Espinosa, Ted Cook, Elena Galea, Alistair McLaren, Ekaterina V. Ilieva, Aurora Pujol, Stéphane Fourcade, Fiona Kelly, Stewart Bates, Agatha Schlüter, Eva López, Jorge Galino, Laia Morató, Patrick Aubourg, Muriel Asheuer
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics; Vol 21
Human Molecular Genetics; Vol 21
X-linked adrenoleukodystrophy (X-ALD) is an inherited disorder characterized by axonopathy and demyelination in the central nervous system and adrenal insufficiency. Main X-ALD phenotypes are: (i) an adult adrenomyeloneuropathy (AMN) with axonopathy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94571f1749054f371c84a6fd0455f479
Autor:
Laia Morató, Wei Li, Jef Verbeek, Carlo Viscomi, Keir J. Menzies, Kristina Schoonjans, Massimo Zeviani, Aurora Pujol, Silvie Timmers, Evan G. Williams, Laurent Mouchiroud, Ralph Imhof, Hongbo Zhang, Anthony A. Sauve, Young Suk Jo, Barbara van Loon, Carolina E. Hagberg, Norman Moullan, Carles Cantó, Patrick Schrauwen, Eija Pirinen, Johan Auwerx
Publikováno v:
Cell Metabolism, 19(6), 1034-1041
Cell Metabolism
Cell Metabolism, 19, 1034-41
Cell Metabolism, 19(6), 1034-1041. Cell Press
Cell metabolism
Cell Metabolism 19 (2014) 6
Cell Metabolism, 19, 6, pp. 1034-41
Cell Metabolism
Cell Metabolism, 19, 1034-41
Cell Metabolism, 19(6), 1034-1041. Cell Press
Cell metabolism
Cell Metabolism 19 (2014) 6
Cell Metabolism, 19, 6, pp. 1034-41
Item does not contain fulltext We previously demonstrated that the deletion of the poly(ADP-ribose)polymerase (Parp)-1 gene in mice enhances oxidative metabolism, thereby protecting against diet-induced obesity. However, the therapeutic use of PARP i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3cc9ef160e5b9e3a462f083f521664a
https://research.wur.nl/en/publications/pharmacological-inhibition-of-polyadp-ribose-polymerases-improves
https://research.wur.nl/en/publications/pharmacological-inhibition-of-polyadp-ribose-polymerases-improves
Autor:
Graziella Uziel, Enrico Bertini, Laia Morató, Montse Ruiz, Anna Ardissone, Daniela Verrigni, Aurora Pujol, Isidre Ferrer
Defects of mitochondrial respiration and function had been proposed as a major culprit in the most common neurodegenerative diseases, including prototypic diseases of central nervous system (CNS) white matter such as multiple sclerosis. The importanc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dda136b23bf48eb80a4495fb0c95a50
http://hdl.handle.net/10281/205473
http://hdl.handle.net/10281/205473
Autor:
Mara Dierssen, Paloma Martinez-Redondo, Tatiana Ruiz-Cortés, Aurora Pujol, Montserrat Ruiz, Janani Parameswaran, Isidre Ferrer, Alejandro Vaquero, Mariona Jové, Stéphane Fourcade, Alba Naudí, Reinald Pamplona, Francesc Villarroya, M. Portero-Otin, Laia Morató
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
Repositorio Abierto de la UdL
Universitad de Lleida
Dipòsit Digital de la UB
Universidad de Barcelona
Aging Cell
instname
Repositorio Abierto de la UdL
Universitad de Lleida
Dipòsit Digital de la UB
Universidad de Barcelona
Aging Cell
Sirtuin 2 (SIRT2) is a member of a family of NAD+-dependent histone deacetylases (HDAC) that play diverse roles in cellular metabolism and especially for aging process. SIRT2 is located in the nucleus, cytoplasm, and mitochondria, is highly expressed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c587d72fdd2f4a0916f4e197b43c195
http://hdl.handle.net/2445/127260
http://hdl.handle.net/2445/127260