Browsing "Genètica, Microbiologia i Estadística" by Title
Showing results 1 to 20 of 1915
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| Issue Date | Title | Author(s) |
|---|---|---|
| 6-Jul-2010 | 10 anys del genoma | Bueno i Torrens, David, 1965- |
| 13-Dec-2020 | 10 coses que encara no sabem del cervell | Bueno i Torrens, David, 1965- |
| 18-Mar-2017 | 151 gens per poder regenerar una pota sencera | Bueno i Torrens, David, 1965- |
| 20-Apr-2022 | 17th Spanish Society for Developmental Biology Meeting: New Trends in Developmental Biology | Araújo, Sofia J.; Barrio, Rosa |
| 2019 | 3' untranslated regions: regulation at the end of the road | El Mouali, Youssef; Balsalobre Parra, Carlos |
| 16-Nov-2022 | 3D spatial organization and improved antibiotic treatment of a Pseudomonas aeruginosaStaphylococcus aureus wound biofilm by nanoparticle enzyme delivery | Rubio-Canalejas, Alba; Baelo, Aida; Herbera, Sara; Blanco-Cabra, Núria; Vukomanovic, Marija; Torrents Serra, Eduard |
| 7-Feb-2024 | 45S5/PEEK Coatings by Cold Gas Spray with In Vitro Bioactivity Degradation and Cellular Proliferation | Garrido Domínguez, Beatriz; Albaladejo-Fuentes, Vicente; Dosta Parras, Sergi; Garcia Giralt, Natàlia; García Cano, Irene |
| 23-Nov-2023 | 45S5/PEEK Coatings by Cold Gas Spray with In Vitro Bioactivity, Degradation, and Cellular Proliferation | Garrido Fernández, Blas; Albaladejo-Fuentes, Vicente; Dosta Parras, Sergi; Garcia Giralt, Natàlia; García Cano, Irene |
| 9-Mar-2018 | 4Cin: A computational pipeline for 3D genome modeling and virtual Hi-C analyses from 4C dataGómez-Skarmeta | Irastorza-Azcarate, Ibai; Acemel, Rafael D.; Tena, Juan J.; Maeso, Ignacio; Gómez-Skarmeta, José Luis; Devos, Damien P. |
| Nov-2018 | 5 principios de la neuroeducación que la familia debería saber y poner en práctica | Bueno i Torrens, David, 1965-; Forés i Miravalles, Anna |
| 9-Jul-2013 | A Broad Genomic Survey Reveals Multiple Origins and Frequent Losses in the Evolution of Respiratory Hemerythrins and Hemocyanins | Martín Durán, José M.; Mendoza Soler, Alexandre de; Sebé Pedrós, Arnau; Ruiz Trillo, Iñaki; Hejnol, Andreas |
| 18-Sep-2014 | A broad spectrum of genomic changes in Latinamerican patients with EXT1/EXT2-CDG | Delgado, M. A.; Martinez-Domenech, G.; Sarrión Pérez-Caballero, Patricia; Urreizti, Roser; Zecchini, L.; Robledo, H. H.; Segura, F.; Dodelson de Kremer, Raquel; Balcells Comas, Susana; Grinberg Vaisman, Daniel Raúl; Asteggiano, Carla |
| 4-Oct-2017 | A C-terminally truncated form of β-catenin acts as a novel regulator of Wnt/β-catenin signaling in planarians | Su, Hanxia; Sureda Gómez, Miquel; Rabaneda Lombarte, Neus; Gelabert, Maria; Xie, Jianlei; Wu, Wei; Adell i Creixell, Teresa |
| 17-Jul-2023 | A causal effects of gut microbiota in the development of migraine | Cormand Rifà, Bru; Cuenca León, Ester; International Headache Genetics Consortium; He, Qiang; Wang, Wenjing; Xiong, Yang; Tao, Chuanyuan; Ma, Lu; Ma, Junpeng; You, Chao |
| 6-Jul-2013 | A Common 56-kilobase deletion in a primate-specific segmental duplication creates a novel Butyrophilin-Like protein | Aigner, Johanna; Villatoro, Sergi; Rabionet Janssen, Raquel; Roquer, Jaume; Jiménez Conde, Jordi; Martí Puig, Eulàlia; Estivill, Xavier, 1955- |
| 18-Jun-2018 | A conserved role for Syntaxin-1 in pre- and post-commissural midline axonal guidance in fly, chick, and mouse | Ros i Torres, Oriol; Barrecheguren Manero, Pablo José; Cotrufo, Tiziana; Schaettin, Martina; Roselló Busquets, Cristina; Vílchez Acosta, Alba del Valle; Hernaiz Llorens, Marc; Martínez Mármol, Ramón; Ulloa Darquea, Fausto Alexander; Stoeckli, Esther T.; Araújo, Sofia J.; Soriano García, Eduardo |
| 2018 | A conserved Shh cis-regulatory module highlights a common developmental origin of unpaired and paired fins | Letelier, Joaquín; De La Calle-Mustienes, Elisa; Pieretti, Joyce; Naranjo, Silvia; Maeso, Ignacio; Nakamura, Tetsuya; Pascual-Anaya, Juan; Shubin, Neil H; Igor, Schneider; Martinez-Morales, Juan Ramón; Gómez-Skarmeta, José Luis |
| 11-Feb-2020 | A contemporary picture of enterococcal endocarditis | Pericàs, Juan M.; Llopis Pérez, Jaime; Muñoz, Patricia; Gálvez Acebal, Juan; Kestler, Martha; Valerio, Maricela; Hernández-Meneses, Marta; Goneaga, Miguel A.; Cobo Belaustegui, Manuel; Montejo, Miguel; Ojeda Burgos, Guillermo; Sousa Regueiro, M. Dolores; Alarcón, Aristides de; Ramos Martínez, Antonio; Miró Meda, José M.; GAMES Investigators |
| 12-Jan-2018 | A de novo FOXP1 truncating mutation in a patient originally diagnosed as C Syndrome | Urreizti, Roser; Damanti, Sarah; Esteve, Carla; Franco Valls, Héctor; Castilla Vallmanya, Laura; Tonda, Raul; Cormand Rifà, Bru; Vilageliu i Arqués, Lluïsa; Opitz, John M.; Neri, Giovanni; Grinberg Vaisman, Daniel Raúl; Balcells Comas, Susana |
| 10-Mar-2017 | A de novo nonsense mutation in MAGEL2 in a patient initially diagnosed as Opitz-C: Similarities between Schaaf-Yang and Opitz-C syndromes | Urreizti, Roser; Cueto Gonzalez, Anna Maria; Franco Valls, Héctor; Mort Farre, Sílvia; Roca Ayats, Neus; Ponomarenko, Julia; Cozzuto, Luca; Company, Carlos; Bosio, Mattia; Ossowski, Stephan; Montfort Roca, Magda; Hecht, Jochen; Tizzano Ferrari, Eduardo; Cormand Rifà, Bru; Vilageliu i Arqués, Lluïsa; Opitz, John M.; Neri, Giovanni; Grinberg Vaisman, Daniel Raúl; Balcells Comas, Susana |