Zobrazeno 1 - 10 of 280 pro vyhledávání: '"epigenome and environment interact"'
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Akademický článek
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Genomic imprinting disorders: lessons on how genome, epigenome and environment interact
Autor: Andrea Riccio, Thomas Eggermann, Eamonn R. Maher, Deborah J G Mackay, Dave Nicholas Monk
Publikováno v: Nature reviews. Genetics (Online) 20 (2019): 235–248. doi:10.1038/s41576-018-0092-0
info:cnr-pdr/source/autori:Monk D.; Mackay D.J.G.; Eggermann T.; Maher E.R.; Riccio A./titolo:Genomic imprinting disorders: lessons on how genome, epigenome and environment interact/doi:10.1038%2Fs41576-018-0092-0/rivista:Nature reviews. Genetics (Online)/anno:2019/pagina_da:235/pagina_a:248/intervallo_pagine:235–248/volume:20
Dipòsit Digital de la UB
Universidad de Barcelona
Genomic imprinting, the monoallelic and parent-of-origin-dependent expression of a subset of genes, is required for normal development. Its disruption leads to human disease involving isolated or multi-locus epigenetic changes that can be traced back
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50fbddadd60a5fb5d8a862639e9f3520
https://doi.org/10.1038/s41576-018-0092-0
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3
Akademický článek
Comprehensive molecular and clinical findings in 29 patients with multi-locus imprinting disturbance.
Autor: Urakawa, Tatsuki1,2 (AUTHOR), Soejima, Hidenobu3 (AUTHOR), Yamoto, Kaori4 (AUTHOR), Hara-Isono, Kaori1 (AUTHOR), Nakamura, Akie1 (AUTHOR), Kawashima, Sayaka1 (AUTHOR), Narusawa, Hiromune1 (AUTHOR), Kosaki, Rika5 (AUTHOR), Nishimura, Yutaka6 (AUTHOR), Yamazawa, Kazuki7 (AUTHOR), Hattori, Tetsuo8 (AUTHOR), Muramatsu, Yukako9 (AUTHOR), Inoue, Takanobu1,10 (AUTHOR), Matsubara, Keiko1,11 (AUTHOR), Fukami, Maki1 (AUTHOR), Saitoh, Shinji12 (AUTHOR), Ogata, Tsutomu4,13 (AUTHOR), Kagami, Masayo1 (AUTHOR) kagami-ms@ncchd.go.jp
Publikováno v: Clinical Epigenetics. 10/5/2024, Vol. 16 Issue 1, p1-18. 18p.
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4
Akademický článek
Deciphering DNA Methylation in Gestational Diabetes Mellitus: Epigenetic Regulation and Potential Clinical Applications.
Autor: Li, Nan1 (AUTHOR), Liu, Huan-Yu2,3 (AUTHOR), Liu, Song-Mei1,3 (AUTHOR) smliu@whu.edu.cn
Publikováno v: International Journal of Molecular Sciences. Sep2024, Vol. 25 Issue 17, p9361. 21p.
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5
Akademický článek
A case of an Angelman-syndrome caused by an intragenic duplication of UBE3A uncovered by adaptive nanopore sequencing.
Autor: Holthöfer, Laura1 (AUTHOR), Diederich, Stefan1 (AUTHOR), Haug, Verena2 (AUTHOR), Lehmann, Lioba1 (AUTHOR), Hewel, Charlotte1 (AUTHOR), Paul, Norbert W.3 (AUTHOR), Schweiger, Susann1 (AUTHOR), Gerber, Susanne1 (AUTHOR), Linke, Matthias1 (AUTHOR) matthias.linke@unimedizin-mainz.de
Publikováno v: Clinical Epigenetics. 8/2/2024, Vol. 16 Issue 1, p1-8. 8p.
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Akademický článek
Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis.
Autor: Mackay, Deborah J. G.1 (AUTHOR) djgm@soton.ac.uk, Gazdagh, Gabriella1,2 (AUTHOR), Monk, David3 (AUTHOR), Brioude, Frederic4 (AUTHOR), Giabicani, Eloise4 (AUTHOR), Krzyzewska, Izabela M.5 (AUTHOR), Kalish, Jennifer M.6,7 (AUTHOR), Maas, Saskia M.5 (AUTHOR), Kagami, Masayo8 (AUTHOR), Beygo, Jasmin9 (AUTHOR), Kahre, Tiina10,11 (AUTHOR), Tenorio-Castano, Jair12,13 (AUTHOR), Ambrozaitytė, Laima14 (AUTHOR), Burnytė, Birutė14 (AUTHOR), Cerrato, Flavia15 (AUTHOR), Davies, Justin H.1,16 (AUTHOR), Ferrero, Giovanni Battista17 (AUTHOR), Fjodorova, Olga10 (AUTHOR), Manero-Azua, Africa18 (AUTHOR), Pereda, Arrate18 (AUTHOR)
Publikováno v: Clinical Epigenetics. 8/1/2024, Vol. 16 Issue 1, p1-19. 19p.
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Akademický článek
Imprinted DNA methylation of the H19 ICR is established and maintained in vivo in the absence of Kaiso.
Autor: Matsuzaki, Hitomi1 (AUTHOR) matsuzaki@tara.tsukuba.ac.jp, Kimura, Minami2 (AUTHOR), Morihashi, Mizuki2 (AUTHOR), Tanimoto, Keiji1 (AUTHOR)
Publikováno v: Epigenetics & Chromatin. 6/5/2024, Vol. 17 Issue 1, p1-16. 16p.
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8
Akademický článek
Allelic reprogramming of chromatin states in human early embryos.
Autor: Yuan, Shenli1,2,3,4 (AUTHOR), Gao, Lei2 (AUTHOR) gaol@big.ac.cn, Tao, Wenrong1,5 (AUTHOR), Zhan, Jianhong2,3 (AUTHOR), Lu, Gang4 (AUTHOR), Zhang, Jingye1,5 (AUTHOR), Zhang, Chuanxin1,5 (AUTHOR), Yi, Lizhi2 (AUTHOR), Liu, Zhenbo2 (AUTHOR), Hou, Zhenzhen1,5 (AUTHOR), Dai, Min3 (AUTHOR), Zhao, Han1,5 (AUTHOR), Chen, Zi-Jiang1,5,6 (AUTHOR) chenzijiang@hotmail.com, Liu, Jiang2,3,7 (AUTHOR) liuj@big.ac.cn, Wu, Keliang1,5 (AUTHOR) wukeliang_527@163.com
Publikováno v: National Science Review. Mar2024, Vol. 11 Issue 3, p1-14. 14p.
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9
Akademický článek
ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming.
Autor: Verma, Ankit1,2 (AUTHOR) ankitverma9079@gmail.com, Poondi Krishnan, Varsha2 (AUTHOR) vincenzo.lullo@igb.cnr.it, Cecere, Francesco1 (AUTHOR) francesco.cecere@unicampania.it, D'Angelo, Emilia1 (AUTHOR) emilia.dangelo@unicampania.it, Lullo, Vincenzo2 (AUTHOR) maria.strazzullo@igb.cnr.it, Strazzullo, Maria2 (AUTHOR), Selig, Sara3,4 (AUTHOR) seligs@technion.ac.il, Angelini, Claudia5 (AUTHOR) claudia.angelini@cnr.it, Matarazzo, Maria R.2 (AUTHOR) maria.matarazzo@igb.cnr.it, Riccio, Andrea1,2 (AUTHOR) maria.matarazzo@igb.cnr.it
Publikováno v: Biomolecules (2218-273X). Dec2023, Vol. 13 Issue 12, p1717. 18p.
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