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Flavia Cerrato

Showing results (31-40 of 50) with videos related to

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American Journal of Hematology|January 16, 2026
Adult-Onset β-Thalassemia Major as Acquired Imprinting DisorderEmilia D'Angelo, Giorgia Mandrile, Nicolò Tesio, et al.
Clinical Epigenetics|September 15, 2020
Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbanceMaria Vittoria Cubellis, Laura Pignata, Ankit Verma, et al.
Cancers|April 13, 2023
Co-Occurrence of Beckwith-Wiedemann Syndrome and Early-Onset Colorectal CancerFrancesco Cecere, Laura Pignata, Bruno Hay Mele, et al.
Nucleic Acids Research|October 21, 2015
ZFP57 recognizes multiple and closely spaced sequence motif variants to maintain repressive epigenetic marks in mouse embryonic stem cellsZahra Anvar, Marco Cammisa, Vincenzo Riso, et al.
Epigenetics & Chromatin|July 24, 2025
Identification of genetic and non-genetic modifiers of genomic imprinting through screening of imprinted DMR methylation in humansFrancesco Cecere, Raissa Relator, Michael Levy, et al.
Clinical Epigenetics|November 23, 2025
Hypomethylation of the MEG8:Int2-DMR in patients with pathogenic PLAG1 variants suggests new role of the chr14q32 imprinting cluster in Silver-Russell syndromeEmilia D'Angelo, Laura Pignata, Francesco Cecere, et al.
Plos Genetics|February 23, 2018
Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in miceAndrea Freschi, Stella K Hur, Federica Maria Valente, et al.
Genes & Development|March 7, 2024
A maternal-effect <i>Padi6</i> variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryosCarlo Giaccari, Francesco Cecere, Lucia Argenziano, et al.
Human Molecular Genetics|September 17, 2011
The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome casesNicoletta Chiesa, Agostina De Crescenzo, Kankadeb Mishra, et al.
Human Molecular Genetics|February 5, 2008
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumourFlavia Cerrato, Angela Sparago, Gaetano Verde, et al.
Pageof 5

Showing results (31-40 of 50) with videos related to

Sort By:
Pageof 5
American Journal of Hematology|January 16, 2026
Adult-Onset β-Thalassemia Major as Acquired Imprinting DisorderEmilia D'Angelo, Giorgia Mandrile, Nicolò Tesio, et al.
Clinical Epigenetics|September 15, 2020
Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbanceMaria Vittoria Cubellis, Laura Pignata, Ankit Verma, et al.
Cancers|April 13, 2023
Co-Occurrence of Beckwith-Wiedemann Syndrome and Early-Onset Colorectal CancerFrancesco Cecere, Laura Pignata, Bruno Hay Mele, et al.
Nucleic Acids Research|October 21, 2015
ZFP57 recognizes multiple and closely spaced sequence motif variants to maintain repressive epigenetic marks in mouse embryonic stem cellsZahra Anvar, Marco Cammisa, Vincenzo Riso, et al.
Epigenetics & Chromatin|July 24, 2025
Identification of genetic and non-genetic modifiers of genomic imprinting through screening of imprinted DMR methylation in humansFrancesco Cecere, Raissa Relator, Michael Levy, et al.
Clinical Epigenetics|November 23, 2025
Hypomethylation of the MEG8:Int2-DMR in patients with pathogenic PLAG1 variants suggests new role of the chr14q32 imprinting cluster in Silver-Russell syndromeEmilia D'Angelo, Laura Pignata, Francesco Cecere, et al.
Plos Genetics|February 23, 2018
Tissue-specific and mosaic imprinting defects underlie opposite congenital growth disorders in miceAndrea Freschi, Stella K Hur, Federica Maria Valente, et al.
Genes & Development|March 7, 2024
A maternal-effect <i>Padi6</i> variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryosCarlo Giaccari, Francesco Cecere, Lucia Argenziano, et al.
Human Molecular Genetics|September 17, 2011
The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome casesNicoletta Chiesa, Agostina De Crescenzo, Kankadeb Mishra, et al.
Human Molecular Genetics|February 5, 2008
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumourFlavia Cerrato, Angela Sparago, Gaetano Verde, et al.
Pageof 5