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Page 1
Vertical transmission of maternal DNA through extracellular vesicles associates with altered embryo bioenergetics during the periconception period.
Bolumar D, Moncayo-Arlandi J, Gonzalez-Fernandez J, Ochando A, Moreno I, Monteagudo-Sanchez A, Marin C, Diez A, Fabra P, Checa MA, Espinos JJ, Gardner DK, Simon C, Vilella F. Bolumar D, et al. Among authors: monteagudo sanchez a. Elife. 2023 Dec 27;12:RP88008. doi: 10.7554/eLife.88008. Elife. 2023. PMID: 38149847 Free PMC article.
Conservation and divergence of canonical and non-canonical imprinting in murids.
Richard Albert J, Kobayashi T, Inoue A, Monteagudo-Sánchez A, Kumamoto S, Takashima T, Miura A, Oikawa M, Miura F, Takada S, Hirabayashi M, Korthauer K, Kurimoto K, Greenberg MVC, Lorincz M, Kobayashi H. Richard Albert J, et al. Among authors: monteagudo sanchez a. Genome Biol. 2023 Mar 14;24(1):48. doi: 10.1186/s13059-023-02869-1. Genome Biol. 2023. PMID: 36918927 Free PMC article.
Single-cell multi-omic analysis profiles defective genome activation and epigenetic reprogramming associated with human pre-implantation embryo arrest.
Hernandez Mora JR, Buhigas C, Clark S, Del Gallego Bonilla R, Daskeviciute D, Monteagudo-Sánchez A, Poo-Llanillo ME, Medrano JV, Simón C, Meseguer M, Kelsey G, Monk D. Hernandez Mora JR, et al. Among authors: monteagudo sanchez a. Cell Rep. 2023 Feb 28;42(2):112100. doi: 10.1016/j.celrep.2023.112100. Epub 2023 Feb 9. Cell Rep. 2023. PMID: 36763500 Free article.
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 L, Cecere F, Verma A, Hay Mele B, Monticelli M, Acurzio B, Giaccari C, Sparago A, Hernandez Mora JR, Monteagudo-Sánchez A, Esteller M, Pereda A, Tenorio-Castano J, Palumbo O, Carella M, Prontera P, Piscopo C, Accadia M, Lapunzina P, Cubellis MV, de Nanclares GP, Monk D, Riccio A, Cerrato F. Pignata L, et al. Among authors: monteagudo sanchez a. Clin Epigenetics. 2022 May 28;14(1):71. doi: 10.1186/s13148-022-01292-w. Clin Epigenetics. 2022. PMID: 35643636 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: monteagudo sanchez a. 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
The role of ZFP57 and additional KRAB-zinc finger proteins in the maintenance of human imprinted methylation and multi-locus imprinting disturbances.
Monteagudo-Sánchez A, Hernandez Mora JR, Simon C, Burton A, Tenorio J, Lapunzina P, Clark S, Esteller M, Kelsey G, López-Siguero JP, de Nanclares GP, Torres-Padilla ME, Monk D. Monteagudo-Sánchez A, et al. Nucleic Acids Res. 2020 Nov 18;48(20):11394-11407. doi: 10.1093/nar/gkaa837. Nucleic Acids Res. 2020. PMID: 33053156 Free PMC article.
Differences in expression rather than methylation at placenta-specific imprinted loci is associated with intrauterine growth restriction.
Monteagudo-Sánchez A, Sánchez-Delgado M, Mora JRH, Santamaría NT, Gratacós E, Esteller M, de Heredia ML, Nunes V, Choux C, Fauque P, de Nanclares GP, Anton L, Elovitz MA, Iglesias-Platas I, Monk D. Monteagudo-Sánchez A, et al. Clin Epigenetics. 2019 Feb 26;11(1):35. doi: 10.1186/s13148-019-0630-4. Clin Epigenetics. 2019. PMID: 30808399 Free PMC article.
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: monteagudo sanchez a. Epigenomics. 2018 Jul;10(7):941-954. doi: 10.2217/epi-2017-0172. Epub 2018 Jul 2. Epigenomics. 2018. PMID: 29962238
PM20D1 is a quantitative trait locus associated with Alzheimer's disease.
Sanchez-Mut JV, Heyn H, Silva BA, Dixsaut L, Garcia-Esparcia P, Vidal E, Sayols S, Glauser L, Monteagudo-Sánchez A, Perez-Tur J, Ferrer I, Monk D, Schneider B, Esteller M, Gräff J. Sanchez-Mut JV, et al. Among authors: monteagudo sanchez a. Nat Med. 2018 May;24(5):598-603. doi: 10.1038/s41591-018-0013-y. Epub 2018 May 7. Nat Med. 2018. PMID: 29736028 Free article.
14 results