受强制性开放获取政策约束的文章 - Francesco Cecere了解详情
可在其他位置公开访问的文章：10 篇
The number of the CTCF binding sites of the H19/IGF2:IG-DMR correlates with DNA methylation and expression imprinting in a humanized mouse model
A Freschi, R Del Prete, L Pignata, F Cecere, F Manfrevola, M Mattia, ...
Human Molecular Genetics 30 (16), 1509-1520, 2021
强制性开放获取政策： US National Institutes of Health, Fondazione Telethon, Italy, Government of …
Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith–Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi …
L Pignata, F Cecere, A Verma, B Hay Mele, M Monticelli, B Acurzio, ...
Clinical Epigenetics 14 (1), 1-15, 2022
强制性开放获取政策： European Commission, Government of Spain, Government of Italy, AIRC …
Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs
B Acurzio, A Verma, A Polito, C Giaccari, F Cecere, S Fioriniello, ...
Scientific Reports 11 (1), 13802, 2021
强制性开放获取政策： Fondazione Telethon, Italy, European Commission, Government of Italy, AIRC …
A maternal-effect Padi6 variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos
C Giaccari, F Cecere, L Argenziano, A Pagano, A Galvao, D Acampora, ...
Genes & Development 38 (3-4), 131-150, 2024
强制性开放获取政策： UK Biotechnology and Biological Sciences Research Council, UK Medical …
Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism?
L Pignata, F Cecere, F Acquaviva, E D’Angelo, D Cioffi, V Pellino, ...
Frontiers in Cell and Developmental Biology 11, 1237629, 2023
强制性开放获取政策： AIRC Foundation for Cancer Research in Italy
Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver–Russell Syndrome …
F Passaretti, L Pignata, G Vitiello, V Alesi, G D’Elia, F Cecere, ...
Genes 13 (10), 1875, 2022
强制性开放获取政策： Government of Italy, AIRC Foundation for Cancer Research in Italy
Co-Occurrence of Beckwith–Wiedemann Syndrome and Early-Onset Colorectal Cancer
F Cecere, L Pignata, B Hay Mele, A Saadat, E D’Angelo, O Palumbo, ...
Cancers 15 (7), 1944, 2023
强制性开放获取政策： Government of Italy, AIRC Foundation for Cancer Research in Italy
The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complex
B Acurzio, F Cecere, C Giaccari, A Verma, R Russo, M Valletta, ...
Epigenetics & Chromatin 15 (1), 1-13, 2022
强制性开放获取政策： Government of Italy, AIRC Foundation for Cancer Research in Italy
ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming
A Verma, V Poondi Krishnan, F Cecere, E D’Angelo, V Lullo, M Strazzullo, ...
Biomolecules 13 (12), 1717, 2023
强制性开放获取政策： European Commission, AIRC Foundation for Cancer Research in Italy
A maternal-effect Padi6 variant results in abnormal nuclear localization of DNMT1 and failure of epigenetic reprogramming and zygotic genome activation in mouse embryos
C Giaccari, F Cecere, L Argenziano, A Galvao, D Acampora, G Rossi, ...
bioRxiv, 2023.10. 09.561545, 2023
强制性开放获取政策： UK Biotechnology and Biological Sciences Research Council, UK Medical …
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