Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Beatriz Fernández Domínguez"'
Autor:
Luis G. Sarmiento, Thomas Roger, Jérôme Giovinazzo, B. Alex Brown, Bertram Blank, Dirk Rudolph, Anu Kankainen, Héctor Alvarez-Pol, Alex Arokia Raj, Pauline Ascher, Michael Block, Manuel Caamaño-Fresco, Lucia Caceres, Laetitia Canete, Daniel M. Cox, Tommi Eronen, Claes Fahlander, Beatriz Fernández-Domínguez, Ulrika Forsberg, Juan Lois-Fuentes, Mathias Gerbaux, Jürgen Gerl, Pavel Golubev, Stéphane Grévy, Gwen F. Grinyer, Tobias Habermann, Jani Hakala, Ari Jokinen, Omar Kamalou, Ivan Kojouharov, Veli S. Kolhinen, Jukka Koponen, Nikolaus Kurz, Nataša Lalović, Christian Lorenz, Benoit Mauss, Alice Mentana, Iain D. Moore, Aurora Ortega Moral, Julien Pancin, Philippos Papadakis, Jérôme Pibernat, Julien Piot, Ilkka Pohjalainen, Juuso Reinikainen, Sami Rinta-Antila, Henning Schaffner, Olivier Sorlin, Christelle Stodel, Jean-Charles Thomas, Maud Versteegen, Annika Voss
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-7 (2023)
Abstract The observation of a weak proton-emission branch in the decay of the 3174-keV 53mCo isomeric state marked the discovery of proton radioactivity in atomic nuclei in 1970. Here we show, based on the partial half-lives and the decay energies of
Externí odkaz:
https://doaj.org/article/a30b90ff59e44785aa0cabad771cb095
Autor:
Beatriz Castejón-Vega, Alejandro Rubio, Antonio J. Pérez-Pulido, José L. Quiles, Jon D. Lane, Beatriz Fernández-Domínguez, María Begoña Cachón-González, Carmen Martín-Ruiz, Alberto Sanz, Timothy M. Cox, Elísabet Alcocer-Gómez, Mario D. Cordero
Publikováno v:
Cells, Vol 10, Iss 11, p 3122 (2021)
Aims: Tay–Sachs and Sandhoff diseases (GM2 gangliosidosis) are autosomal recessive disorders of lysosomal function that cause progressive neurodegeneration in infants and young children. Impaired hydrolysis catalysed by β-hexosaminidase A (HexA) l
Externí odkaz:
https://doaj.org/article/f52039e69fcc4dfe90d6e42e02924715
Autor:
Simone Amaducci, Nicola Colonna, Luigi Cosentino, Sergio Cristallo, Paolo Finocchiaro, Milan Krtička, Cristian Massimi, Mario Mastromarco, Annamaria Mazzone, Alberto Mengoni, Stanislav Valenta, Oliver Aberle, Victor Alcayne, Józef Andrzejewski, Laurent Audouin, Victor Babiano-Suarez, Michael Bacak, Massimo Barbagallo, Samuel Bennett, Eric Berthoumieux, Jon Billowes, Damir Bosnar, Adam Brown, Maurizio Busso, Manuel Caamaño, Luis Caballero-Ontanaya, Francisco Calviño, Marco Calviani, Daniel Cano-Ott, Adria Casanovas, Francesco Cerutti, Enrico Chiaveri, Guillem Cortés, Miguel Cortés-Giraldo, Lucia-Anna Damone, Paul-John Davies, Maria Diakaki, Mirco Dietz, Cesar Domingo-Pardo, Rugard Dressler, Quentin Ducasse, Emmeric Dupont, Ignacio Durán, Zinovia Eleme, Beatriz Fernández-Domínguez, Alfredo Ferrari, Valter Furman, Kathrin Göbel, Ruchi Garg, Aleksandra Gawlik, Simone Gilardoni, Isabel Gonçalves, Enrique González-Romero, Carlos Guerrero, Frank Gunsing, Hideo Harada, Stephan Heinitz, Jan Heyse, David Jenkins, Arnd Junghans, Franz Käppeler, Yacine Kadi, Atsushi Kimura, Ingrid Knapova, Michael Kokkoris, Yuri Kopatch, Deniz Kurtulgil, Ion Ladarescu, Claudia Lederer-Woods, Helmut Leeb, Jorge Lerendegui-Marco, Sarah-Jane Lonsdale, Daniela Macina, Alice Manna, Trinitario Martínez, Alessandro Masi, Pierfrancesco Mastinu, Emilio-Andrea Maugeri, Emilio Mendoza, Veatriki Michalopoulou, Paolo Milazzo, Federica Mingrone, Javier Moreno-Soto, Agatino Musumarra, Alexandru Negret, Francisco Ogállar, Andreea Oprea, Nikolas Patronis, Andreas Pavlik, Jarosław Perkowski, Luciano Piersanti, Cristina Petrone, Elisa Pirovano, Ignacio Porras, Javier Praena, José-Manuel Quesada, Diego Ramos-Doval, Thomas Rauscher, René Reifarth, Dimitri Rochman, Carlo Rubbia, Marta Sabaté-Gilarte, Alok Saxena, Peter Schillebeeckx, Dorothea Schumann, Adhitya Sekhar, Gavin Smith, Nikolay Sosnin, Peter Sprung, Athanasios Stamatopoulos, Giuseppe Tagliente, José Tain, Ariel Tarifeño-Saldivia, Laurent Tassan-Got, Benedikt Thomas, Pablo Torres-Sánchez, Andrea Tsinganis, Jiri Ulrich, Sebastian Urlass, Gianni Vannini, Vincenzo Variale, Pedro Vaz, Alberto Ventura, Diego Vescovi, Vasilis Vlachoudis, Rosa Vlastou, Anton Wallner, PhilipJohn Woods, Tobias Wright, Petar Žugec
Publikováno v:
Universe, Vol 7, Iss 6, p 200 (2021)
An accurate measurement of the 140Ce(n,γ) energy-dependent cross-section was performed at the n_TOF facility at CERN. This cross-section is of great importance because it represents a bottleneck for the s-process nucleosynthesis and determines to a
Externí odkaz:
https://doaj.org/article/d92c7f7895cc49cdb531e918172250d2
Autor:
Mario D. Cordero, José L. Quiles, Maria Begoña Cachón-González, Alberto Sanz, Alejandro Rubio, Pedro Bullón, Carmen Martin-Ruiz, Jon D. Lane, Beatriz Castejón-Vega, Antonio J. Pérez-Pulido, Beatriz Fernández Domínguez, Timothy M. Cox, Débora Lendines-Cordero, Elísabet Alcocer-Gómez
Tay-Sachs and Sandhoff diseases (GM2 gangliosidosis) are autosomal recessive disorders of lysosomal function that cause fatal and progressive neurodegeneration in infants and young children. Impaired hydrolysis catalysed by β-hexosaminidase A (HexA)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::687aabc13355f77b5beabb03f30417b0
https://doi.org/10.1101/2021.05.28.446132
https://doi.org/10.1101/2021.05.28.446132
Autor:
Alejandro Rubio, José L. Quiles, Antonio J. Pérez-Pulido, Beatriz Fernández-Domínguez, Beatriz Castejón-Vega, Elísabet Alcocer-Gómez, Jon D. Lane, Carmen Martin-Ruiz, Maria Begoña Cachón-González, Alberto Sanz, Mario D. Cordero, Timothy M. Cox
Publikováno v:
Cells
Volume 10
Issue 11
Digital.CSIC. Repositorio Institucional del CSIC
instname
Digibug. Repositorio Institucional de la Universidad de Granada
Castejon Vega, B, Rubio, A, Perez-Pulido, A, Quiles, J, Lane, J D, Fernandez-Dominguez, B, Cachon-Gonzales, M, Martin-Ruiz, C, Sanz, A, Cox, T, Alcocer-Gomez, E & Cordero, M 2021, ' L-Arginine Ameliorates Defective Autophagy in GM2 Gangliosidoses by mTOR Modulation ', Cells, vol. 10, no. 11, 3122 . https://doi.org/10.3390/cells10113122
Cells, Vol 10, Iss 3122, p 3122 (2021)
Volume 10
Issue 11
Digital.CSIC. Repositorio Institucional del CSIC
instname
Digibug. Repositorio Institucional de la Universidad de Granada
Castejon Vega, B, Rubio, A, Perez-Pulido, A, Quiles, J, Lane, J D, Fernandez-Dominguez, B, Cachon-Gonzales, M, Martin-Ruiz, C, Sanz, A, Cox, T, Alcocer-Gomez, E & Cordero, M 2021, ' L-Arginine Ameliorates Defective Autophagy in GM2 Gangliosidoses by mTOR Modulation ', Cells, vol. 10, no. 11, 3122 . https://doi.org/10.3390/cells10113122
Cells, Vol 10, Iss 3122, p 3122 (2021)
Aims: Tay–Sachs and Sandhoff diseases (GM2 gangliosidosis) are autosomal recessive disorders of lysosomal function that cause progressive neurodegeneration in infants and young children. Impaired hydrolysis catalysed by β-hexosaminidase A (HexA) l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23aa2a1f3f1a3fa6642540dc57aa082c
http://hdl.handle.net/10481/71460
http://hdl.handle.net/10481/71460