Zobrazeno 1 - 10
of 164
pro vyhledávání: '"Marta Luna"'
Autor:
Emma Puighermanal, Marta Luna-Sánchez, Alejandro Gella, Gunter van der Walt, Andrea Urpi, María Royo, Paula Tena-Morraja, Isabella Appiah, Maria Helena de Donato, Fabien Menardy, Patrizia Bianchi, Anna Esteve-Codina, Laura Rodríguez-Pascau, Cristina Vergara, Mercè Gómez-Pallarès, Giovanni Marsicano, Luigi Bellocchio, Marc Martinell, Elisenda Sanz, Sandra Jurado, Francesc Xavier Soriano, Pilar Pizcueta, Albert Quintana
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-21 (2024)
Abstract Mutations in mitochondrial energy-producing genes lead to a heterogeneous group of untreatable disorders known as primary mitochondrial diseases (MD). Leigh syndrome (LS) is the most common pediatric MD and is characterized by progressive ne
Externí odkaz:
https://doaj.org/article/622861ac6cc14a5babd24370dd72d435
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 17, Iss , Pp 1071-1078 (2020)
Leigh syndrome, or infantile necrotizing subacute encephalopathy (OMIM #256000), is one of the most common manifestations of mitochondrial dysfunction, due to mutations in more than 75 genes, with mutations in respiratory complex I subunits being the
Externí odkaz:
https://doaj.org/article/8df2cebf8cc74595af229759906059a8
Autor:
Alexia Suárez-Cabrera, Dolly Viviana Fiallo-Suárez, Ruth Stuckey, Marta Luna Uroz-de la Iglesia, Yanira Florido, Angelina Lemes-Castellano, Miguel Ángel Perera-Álvarez, Hugo Luzardo-Henríquez, Haridian de la Nuez, Paula Fernández-Caldas, Silvia de la Iglesia, María Teresa Gómez-Casares, Cristina Bilbao-Sieyro
Publikováno v:
Diagnostics, Vol 12, Iss 8, p 1802 (2022)
Chronic lymphocytic leukemia (CLL) has a variable clinical evolution, with some patients living treatment-free for decades while others require therapy shortly after diagnosis. In a consecutive series of 217 CLL patients, molecular biomarkers with pr
Externí odkaz:
https://doaj.org/article/b2da8c5392ed45e3971b3b379f7afb1e
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 16, p 8523 (2021)
Symbiosis between the mitochondrion and the ancestor of the eukaryotic cell allowed cellular complexity and supported life. Mitochondria have specialized in many key functions ensuring cell homeostasis and survival. Thus, proper communication between
Externí odkaz:
https://doaj.org/article/05bae7e012ef45fc87f02d020d38daa4
Autor:
Marta Luna‐Sánchez, Agustín Hidalgo‐Gutiérrez, Tatjana M Hildebrandt, Julio Chaves‐Serrano, Eliana Barriocanal‐Casado, Ángela Santos‐Fandila, Miguel Romero, Ramy KA Sayed, Juan Duarte, Holger Prokisch, Markus Schuelke, Felix Distelmaier, Germaine Escames, Darío Acuña‐Castroviejo, Luis C López
Publikováno v:
EMBO Molecular Medicine, Vol 9, Iss 1, Pp 78-95 (2016)
Abstract Coenzyme Q (CoQ) is a key component of the mitochondrial respiratory chain, but it also has several other functions in the cellular metabolism. One of them is to function as an electron carrier in the reaction catalyzed by sulfide:quinone ox
Externí odkaz:
https://doaj.org/article/cfc05c1d2c8d4810a7dc5eb296a00eff
Autor:
Marta Luna‐Sánchez, Elena Díaz‐Casado, Emanuele Barca, Miguel Ángel Tejada, Ángeles Montilla‐García, Enrique Javier Cobos, Germaine Escames, Dario Acuña‐Castroviejo, Catarina M Quinzii, Luis Carlos López
Publikováno v:
EMBO Molecular Medicine, Vol 7, Iss 5, Pp 670-687 (2015)
Abstract Primary coenzyme Q10 (CoQ10) deficiency is due to mutations in genes involved in CoQ biosynthesis. The disease has been associated with five major phenotypes, but a genotype–phenotype correlation is unclear. Here, we compare two mouse mode
Externí odkaz:
https://doaj.org/article/f4d8987aef6d405389fe3b02b95dd32d
Autor:
Catarina M. Quinzii, Marta Luna-Sanchez, Marcello Ziosi, Agustin Hidalgo-Gutierrez, Giulio Kleiner, Luis C. Lopez
Publikováno v:
Frontiers in Physiology, Vol 8 (2017)
Coenzyme Q (CoQ) is a lipid present in all cell membranes. One of the multiple metabolic functions of CoQ is to transport electrons in the reaction catalyzed by sulfide:quinone oxidoreductase (SQOR), the first enzyme of the oxidation pathway of sulfi
Externí odkaz:
https://doaj.org/article/6fd703c29f6043fd868edd7faeb0406a
Akademický článek
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Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 8523, p 8523 (2021)
International Journal of Molecular Sciences, Vol 22, Iss 8523, p 8523 (2021)
Funding: This work was supported by a Juan de la Cierva grant (IJC2018-036938-I). A.Q. received funds from the European Research Council (Starting grant NEUROMITO, ERC-2014-StG-638106), MINECO Proyectos I + D de Excelencia (SAF2014-57981P; SAF2017-88
Autor:
Marta Luna
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
Redined, Red de Información Educativa
Ministerio de Educación, Cultura y Deporte (MECD)
Recercat: Dipósit de la Recerca de Catalunya
Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Educar; 2000: Núm.: 26 Educación y desarrollo de competencias; p. 75-87
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Educar, Vol 26 (2000)
instname
Redined, Red de Información Educativa
Ministerio de Educación, Cultura y Deporte (MECD)
Recercat: Dipósit de la Recerca de Catalunya
Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Educar; 2000: Núm.: 26 Educación y desarrollo de competencias; p. 75-87
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Educar, Vol 26 (2000)
Diem que algú domina una llengua que l'entén, la parla, la llegeix i l'escriu. El llenguatge és experiència. La riquesa d'interaccions és la que facilita les adquisicions lingüístiques. La intervenció de l'adult, pare, mare, ensenyant, acompa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::7b07e9e9c3b30a326bc1a3ae01e1b0c9
http://hdl.handle.net/2072/379103
http://hdl.handle.net/2072/379103