Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Arantza Sanz"'
Autor:
Sofia Lachiondo-Ortega, Claudia M. Rejano-Gordillo, Jorge Simon, Fernando Lopitz-Otsoa, Teresa C. Delgado, Krystyna Mazan-Mamczarz, Naroa Goikoetxea-Usandizaga, L. Estefanía Zapata-Pavas, Ana García-del Río, Pietro Guerra, Patricia Peña-Sanfélix, Natalia Hermán-Sánchez, Ruba Al-Abdulla, Carmen Fernandez-Rodríguez, Mikel Azkargorta, Alejandro Velázquez-Cruz, Joris Guyon, César Martín, Juan Diego Zalamea, Leire Egia-Mendikute, Arantza Sanz-Parra, Marina Serrano-Maciá, Irene González-Recio, Monika Gonzalez-Lopez, Luis Alfonso Martínez-Cruz, Patrizia Pontisso, Ana M. Aransay, Rosa Barrio, James D. Sutherland, Nicola G.A. Abrescia, Félix Elortza, Amaia Lujambio, Jesus M. Banales, Raúl M. Luque, Manuel D. Gahete, Asís Palazón, Matias A. Avila, Jose J. G. Marin, Supriyo De, Thomas Daubon, Antonio Díaz-Quintana, Irene Díaz-Moreno, Myriam Gorospe, Manuel S. Rodríguez, María Luz Martínez-Chantar
Publikováno v:
Cell Reports, Vol 43, Iss 3, Pp 113924- (2024)
Summary: The posttranslational modification of proteins critically influences many biological processes and is a key mechanism that regulates the function of the RNA-binding protein Hu antigen R (HuR), a hub in liver cancer. Here, we show that HuR is
Externí odkaz:
https://doaj.org/article/ac05448b67bf43d08eefd6737eb5e995
Autor:
Chiara Bruzzone, Rubén Gil-Redondo, Marisa Seco, Rocío Barragán, Laura de la Cruz, Claire Cannet, Hartmut Schäfer, Fang Fang, Tammo Diercks, Maider Bizkarguenaga, Beatriz González-Valle, Ana Laín, Arantza Sanz-Parra, Oscar Coltell, Ander López de Letona, Manfred Spraul, Shelly C. Lu, Elisabetta Buguianesi, Nieves Embade, Quentin M. Anstee, Dolores Corella, José M. Mato, Oscar Millet
Publikováno v:
Cardiovascular Diabetology, Vol 20, Iss 1, Pp 1-13 (2021)
Abstract Background Metabolic syndrome (MetS) is a multimorbid long-term condition without consensual medical definition and a diagnostic based on compatible symptomatology. Here we have investigated the molecular signature of MetS in urine. Methods
Externí odkaz:
https://doaj.org/article/fdd2825fb92b43c38b52b9294746026e
Publikováno v:
International Journal of Advanced Robotic Systems, Vol 2, Iss 2 (2008)
This paper presents a robust control scheme for flexible link robotic manipulators, which is based on considering the flexible mechanical structure as a system with slow (rigid) and fast (flexible) modes that can be controlled separately. The rigid d
Externí odkaz:
https://doaj.org/article/ac7450ee5c21404ba2db6ac8e1a25fbf
Publikováno v:
International Journal of Advanced Robotic Systems, Vol 2 (2005)
This paper presents a robust control scheme for flexible link robotic manipulators, which is based on considering the flexible mechanical structure as a system with slow (rigid) and fast (flexible) modes that can be controlled separately. The rigid d
Externí odkaz:
https://doaj.org/article/6cfc25a99af947389cd720ad72c14537
Autor:
Sofia Lachiondo-Ortega, Miren Bravo, Irene González-Recio, María J. González Rellán, Jorge Simón Espinosa, Naroa Goikoetxea, Petar Petrov, Rubén Rodríguez Agudo, Arantza Sanz-Parra, Begoña Rodriguez Iruretagoyena, Teresa Cardoso Delgado, Dan A. Dixon, Myriam Gorospe, Ruben Nogueiras, María Luz Martínez-Chantar
Publikováno v:
Journal of Hepatology. 77:S84-S85
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e9188c1a60260d849fe944ddfed6824
https://doi.org/10.1016/s0168-8278(22)00562-1
https://doi.org/10.1016/s0168-8278(22)00562-1
Autor:
Antonio Fontanellas, Rafael Enríquez de Salamanca, Arantza Sanz-Parra, Oscar Millet, Ana Sampedro, Naroa Serna, Fernando J. Corrales, Pedro Berraondo, Irantzu Serrano-Mendioroz
Publikováno v:
Human Molecular Genetics. 27:3688-3696
A first-in-human gene therapy trial using a recombinant adeno-associated viral (rAAV) vector for acute intermittent porphyria (AIP) reveals that higher doses would be required to reach therapeutic levels of the porphobilinogen deaminase (PBGD) transg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38510d102e43dc5ce61fa769a7d0cfca
https://doi.org/10.1093/hmg/ddy283
https://doi.org/10.1093/hmg/ddy283
Autor:
Chiara Bruzzone, Rubén Gil-Redondo, Laura delaCruz-Villar, Arantza Sanz-Parra, Dolores Corella, Nieves Embade, José M. Mato, Oscar Millet
Publikováno v:
Journal of Hepatology. 73:S288-S289
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abb536c66b14bc408c4d789f315d64b5
https://doi.org/10.1016/s0168-8278(20)31083-7
https://doi.org/10.1016/s0168-8278(20)31083-7
Autor:
José M. Mato, Ganeko Bernardo-Seisdedos, Oscar Millet, Luca Unione, Jon Gil-Martínez, Arantza Sanz-Parra, David Fernández-Ramos, Iratxe Macías, Ana Laín, Fernando Lopitz-Otsoa
Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 4
International Journal of Molecular Sciences, Vol 22, Iss 1789, p 1789 (2021)
Volume 22
Issue 4
International Journal of Molecular Sciences, Vol 22, Iss 1789, p 1789 (2021)
Fumarylacetoacetate hydrolase (FAH) is the fifth enzyme in the tyrosine catabolism pathway. A deficiency in human FAH leads to hereditary tyrosinemia type I (HT1), an autosomal recessive disorder that results in the accumulation of toxic metabolites
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f13ee09c1e3c2ce1850fa1c9d52a270d
https://doi.org/10.3390/ijms22041789
https://doi.org/10.3390/ijms22041789
Autor:
Joaquín Castilla, Pedro Urquiza, Jean-Marc Blouin, Fredj Ben Bdira, Virginia Gutiérrez-de-Juan, Iratxe Macías, Oscar Millet, Ana Laín, Arantza Sanz-Parra, Juan Anguita, José M. Mato, Ganeko Bernardo-Seisdedos, Gabriel Ortega, Jorge Moreno, Juan M. Falcón-Pérez, Julen Oyarzabal, Itxaso San Juan, Juan Rodríguez-Cuesta, Emmanuel Richard, Emilio Díez, Sandra García, Paula Pluta, Rosario González-Muñiz, Pierre Dubus, Hubert de Verneuil, Hasier Eraña, Esperanza Gonzalez
Publikováno v:
Science Translational Medicine. 10
Congenital erythropoietic porphyria is a rare autosomal recessive disease produced by deficient activity of uroporphyrinogen III synthase, the fourth enzyme in the heme biosynthetic pathway. The disease impacts many organs, can be life-threatening an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86b1675f349d66423cc53902653bb287
https://doi.org/10.1126/scitranslmed.aat7467
https://doi.org/10.1126/scitranslmed.aat7467
Autor:
Cécile Ged, Ganeko Bernardo-Seisdedos, Pedro Urquiza, Emmanuel Richard, Arantza Sanz-Parra, Jean-Marc Blouin, Magalie Lalanne, Julie Esteve, Hubert de Verneuil, Oscar Millet, Emma Sasso
Publikováno v:
Human molecular genetics. 26(8)
Congenital erythropoietic porphyria (CEP) is an inborn error of heme biosynthesis characterized by uroporphyrinogen III synthase (UROS) deficiency resulting in deleterious porphyrin accumulation in blood cells responsible for hemolytic anemia and cut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::843c2cc30733e97506c745b0734101da
https://pubmed.ncbi.nlm.nih.gov/28334762
https://pubmed.ncbi.nlm.nih.gov/28334762