Browsing by Author Perez de Nanclares, Guiomar
Showing results 1 to 6 of 6
| Issue Date | Title | Author(s) |
|---|---|---|
| 26-Feb-2019 | Differences in expression rather than methylation at placenta-specific imprinted loci is associated with intrauterine growth restriction | Monteagudo Sánchez, Ana; Sánchez Delgado, Marta; Hernandez Mora, Jose Ramon; Tubío Santamaría, Nuria; Gratacós Solsona, Eduard; Esteller, Manel; López de Heredia, Miguel; Nunes Martínez, Virginia; Choux, Cecile; Fauque, Patricia; Perez de Nanclares, Guiomar; Anton, Lauren; Elovitz, Michal A.; Iglesias Platas, Isabel; Monk, David |
| 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 |
| 26-Jan-2016 | Genome-wide DNA methylation analysis of pseudohypoparathyroidism patients with GNAS imprinting defects | Rochtus, Anne; Martín Trujillo, Alex; Izzi, Benedetta; Elli, Francesca; Garin, Intza; Linglart, Agnès; Mantovani, Giovanna; Perez de Nanclares, Guiomar; Thiele, Suzanne; Decallonne, Brigitte; Van Geet, Chris; Monk, Dave Nicholas; Freson, Kathleen |
| 14-Nov-2015 | Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci | Eggermann, Thomas; Perez de Nanclares, Guiomar; Maher, Eamonn R.; Temple, I. Karen; Tümer, Zeynep; Monk, Dave Nicholas; Mackay, Deborah J. G.; Grønskov, Karen; Riccio, Andrea; Linglart, Agnès; Netchine, Irène |
| 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 |
| 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 |