Francesco Cecere

发表

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

M. Bartolomei, G. Cobellis, A. Riccio, 2021, Human molecular genetics.

The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complex

A. Chambery, C. Angelini, A. Verma, 2022, Epigenetics & chromatin.

ZBTB2 protein is a new partner of the Nucleosome Remodeling and Deacetylase (NuRD) complex.

A. Chambery, C. Angelini, R. Russo, 2020, International journal of biological macromolecules.

Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver–Russell Syndrome Spectrum

A. Iolascon, A. Novelli, A. Riccio, 2022, Genes.

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

M. Esteller, P. Lapunzina, A. Verma, 2022, Clinical epigenetics.

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

M. Esteller, P. Lapunzina, B. H. Mele, 2022, Clinical Epigenetics.

Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs

C. Angelini, A. Verma, A. Fico, 2021, Scientific Reports.

Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism?

M. Carella, O. Palumbo, A. Riccio, 2023, Frontiers in cell and developmental biology.

Co-Occurrence of Beckwith–Wiedemann Syndrome and Early-Onset Colorectal Cancer

G. Scarano, C. Angelini, M. Carella, 2023, Cancers.

A maternal-effect Padi6 variant results in abnormal nuclear localization of DNMT1 and failure of epigenetic reprogramming and zygotic genome activation in mouse embryos

G. Kelsey, B. H. Mele, M. Cubellis, 2023, bioRxiv.

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

G. Kelsey, M. Cubellis, B. Hay Mele, 2024, Genes & development.

ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming

M. R. Matarazzo, Francesco Cecere, Ankit Verma, 2023, Biomolecules.

A novel iPSC-based model of ICF syndrome subtype 2 recapitulates the molecular phenotype of ZBTB24 deficiency

G. Giardino, C. Pignata, M. R. Matarazzo, 2024, bioRxiv.