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Absence of Maternal Methylation in Biparental Hydatidiform Moles from Women with NLRP7 Maternal-Effect Mutations Reveals Widespread Placenta-Specific Imprinting.
Sanchez-Delgado M, Martin-Trujillo A, Tayama C, Vidal E, Esteller M, Iglesias-Platas I, Deo N, Barney O, Maclean K, Hata K, Nakabayashi K, Fisher R, Monk D. Sanchez-Delgado M, et al. PLoS Genet. 2015 Nov 6;11(11):e1005644. doi: 10.1371/journal.pgen.1005644. eCollection 2015 Nov. PLoS Genet. 2015. PMID: 26544189 Free PMC article.
Human Oocyte-Derived Methylation Differences Persist in the Placenta Revealing Widespread Transient Imprinting.
Sanchez-Delgado M, Court F, Vidal E, Medrano J, Monteagudo-Sánchez A, Martin-Trujillo A, Tayama C, Iglesias-Platas I, Kondova I, Bontrop R, Poo-Llanillo ME, Marques-Bonet T, Nakabayashi K, Simón C, Monk D. Sanchez-Delgado M, et al. PLoS Genet. 2016 Nov 11;12(11):e1006427. doi: 10.1371/journal.pgen.1006427. eCollection 2016 Nov. PLoS Genet. 2016. PMID: 27835649 Free PMC article.
Preimplantation genetic testing for a chr14q32 microdeletion in a family with Kagami-Ogata syndrome and Temple syndrome.
Sabria-Back J, Monteagudo-Sánchez A, Sánchez-Delgado M, Ferguson-Smith AC, Gómez O, Pertierra Cartada A, Tenorio J, Nevado J, Lapunzina P, Pereda Aguirre A, Giménez Sevilla C, Toro Toro E, Perez de Nanclares G, Monk D. Sabria-Back J, et al. Among authors: sanchez delgado m. J Med Genet. 2022 Mar;59(3):253-261. doi: 10.1136/jmedgenet-2020-107433. Epub 2021 Feb 12. J Med Genet. 2022. PMID: 33579810
Characterization of parent-of-origin methylation using the Illumina Infinium MethylationEPIC array platform.
Hernandez Mora JR, Tayama C, Sánchez-Delgado M, Monteagudo-Sánchez A, Hata K, Ogata T, Medrano J, Poo-Llanillo ME, Simón C, Moran S, Esteller M, Tenorio J, Lapunzina P, Kagami M, Monk D, Nakabayashi K. Hernandez Mora JR, et al. Among authors: sanchez delgado m. Epigenomics. 2018 Jul;10(7):941-954. doi: 10.2217/epi-2017-0172. Epub 2018 Jul 2. Epigenomics. 2018. PMID: 29962238
26 results