Browsing by Author Lapunzina, Pablo
Showing results 5 to 10 of 10
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| Issue Date | Title | Author(s) |
|---|---|---|
| 17-Apr-2019 | Genetic analyses of aplastic anemia and idiopathic pulmonary fibrosis patients with short telomeres, possible implication of DNA-repair genes | Arias Salgado, Elena G.; Galvez, Eva M.; Planas Cerezales, Lurdes; Pintado Berninches, Laura; Vallespin, Elena; Martínez, Pilar; Carrillo, Jaime; Iarriccio, Laura; Ruiz Llobet, Anna; Catalá, Albert; Badell Serra, Isabel; González Granado, Luis Ignacio; Martín Nalda, Andrea; Martínez Gallo, Mónica; Galera Miñarro, Ana; Rodríguez Vigil, Carmen; Bastos Oreiro, Mariana; Perez de Nanclares, Guiomar; Leiro Fernández, Virginia; Uria, Maria Luz; Diaz Heredia, Cristina; Valenzuela, Claudia; Martín, Sara; López Muñiz, Belén; Lapunzina, Pablo; Sevilla, Julian; Molina Molina, María; Perona, Rosario; Sastre, Lenadro |
| 1-Apr-2014 | Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment | Court, Franck; Tayama, Chiharu; Romanelli, Valeria; Martín Trujillo, Alex; Iglesias Platas, Isabel; Okamura, Kohji; Sugahara, Naoko; Simón, Carlos; Moore, Harry; Harness, Julie V.; Keirstead, Hans; Sanchez-Mut, Jose Vicente; Kaneki, Eisuke; Lapunzina, Pablo; Soejima, Hidenobu; Wake, Norio; Esteller, Manel; Ogata, Tsutomu; Hata, Kenichiro; Nakabayashi, Kazuhiko; Monk, David |
| 26-Feb-2013 | Mutations in the EXT1 and EXT2 genes in Spanish patients with multiple osteochondromas | Sarrión Pérez-Caballero, Patricia; Sangorrin, A.; Urreizti, Roser; Delgado, A.; Artuch Iriberri, Rafael; Martorell, L.; Armstrong i Morón, Judith; Antón López, Jordi; Torner Rubies, Ferran; Vilaseca, M. A.; Nevado, J.; Lapunzina, Pablo; Asteggiano, Carla; Balcells Comas, Susana; Grinberg Vaisman, Daniel Raúl |
| 28-May-2022 | Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith–Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances | Pignata, Laura; Cecere, Francesco; Verma, Ankit; Hay Mele, Bruno; Monticelli, Maria; Acurzio, Basilia; Giaccari, Carlo; Sparago, Angela; Hernandez Mora, Jose Ramon; Monteagudo Sánchez, Ana; Esteller, Manel; Pereda, Arrate; Tenorio Castano, Jair; Palumbo, Orazio; Carella, Massimo; Prontera, Paolo; Piscopo, Carmelo; Accadia, Maria; Lapunzina, Pablo; Cubellis, Maria Vittoria; Perez de Nanclares, Guiomar; Monk, David; Riccio, Andrea; Cerrato, Flavia |
| 1-Mar-2021 | Shorter androgen receptor polyQ alleles protect against life-threatening COVID-19 disease in European males | Baldassarri, Margherita; Picchiotti, Nicola; Fava, Francesca; Fallerini, Chiara; Benetti, Elisa; Daga, Sergio; Valentino, Floriana; Doddato, Gabriella; Furini, Simone; Giliberti, Annarita; Tita, Rossella; Amitrano, Sara; Bruttini, Mirella; Croci, Susanna; Meloni, Ilaria; Pinto, Anna Maria; Iuso, Nicola; Gabbi, Chiara; Sciarra, Francesca; Venneri, Mary Anna; Gori, Marco; Sanarico, Maurizio; Crawley, Francis P.; Pagotto, Uberto; Fanelli, Flaminia; Mezzullo, Marco; Dominguez Garrido, Elena; Planas Serra, Laura; Schlüter, Agatha; Colobran, Roger; Soler Palacín, Pere; Lapunzina, Pablo; Tenorio, Jair; Pujol Onofre, Aurora; Castagna, Maria Grazia; Marcelli, Marco; Isidori, Andrea M.; Renieri, Alessandra; Frullanti, Elisa; Mari, Francesca; Spanish Covid HGE, GENCOVID Multicenter Study |
| 14-Oct-2020 | The role of ZFP57 and additional KRAB-Zinc Finger proteins in the maintenance of human imprinted methylation and multi-locus imprinting disturbances | Monteagudo Sánchez, Ana; Hernandez Mora, Jose Ramon; Simón, Carlos; Burton, Adam; Tenorio, Jair; Lapunzina, Pablo; Clark, Stephen; Esteller, Manel; Kelsey, Gavin; López-Siguero, Juan Pedro; Perez de Nanclares, Guiomar; Torres Padilla, Maria Elena |