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Angela Sparago

Showing results (21-30 of 41) with videos related to

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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.
Genome Medicine|December 19, 2019
A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisationHannah Demond, Zahra Anvar, Bahia Namavar Jahromi, et al.
Human Molecular Genetics|December 13, 2006
Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumourAngela Sparago, Silvia Russo, Flavia Cerrato, 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|June 4, 2016
ZFP57 maintains the parent-of-origin-specific expression of the imprinted genes and differentially affects non-imprinted targets in mouse embryonic stem cellsVincenzo Riso, Marco Cammisa, Harpreet Kukreja, 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.
Journal of Medical Genetics|September 17, 2020
Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidyNayeralsadat Fatemi, Najmeh Salehi, Laura Pignata, 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.
Cancers|December 17, 2024
Molecular and Clinical Features of Adrenocortical Tumors in Beckwith-Wiedemann SpectrumDiana Carli, Federico Rondot, Maria Luca, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
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.
Genome Medicine|December 19, 2019
A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisationHannah Demond, Zahra Anvar, Bahia Namavar Jahromi, et al.
Human Molecular Genetics|December 13, 2006
Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumourAngela Sparago, Silvia Russo, Flavia Cerrato, 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|June 4, 2016
ZFP57 maintains the parent-of-origin-specific expression of the imprinted genes and differentially affects non-imprinted targets in mouse embryonic stem cellsVincenzo Riso, Marco Cammisa, Harpreet Kukreja, 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.
Journal of Medical Genetics|September 17, 2020
Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidyNayeralsadat Fatemi, Najmeh Salehi, Laura Pignata, 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.
Cancers|December 17, 2024
Molecular and Clinical Features of Adrenocortical Tumors in Beckwith-Wiedemann SpectrumDiana Carli, Federico Rondot, Maria Luca, et al.
Pageof 5