11 series
Export
<<<Page of 1 >>>
Accession Title Series type(s) Organism(s) Samples GDS Supplementary Contact Release date
Remove filtersFilter Remove filterFrancesco Cecere
GSE195873
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
18 Francesco Cecere Jun 02, 2022
GSE205041
The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complex (ChIP-Seq)
6 Francesco Cecere Aug 16, 2022
GSE205042
The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complex (RRBS)
1 Francesco Cecere Aug 16, 2022
GSE205043
The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complex
7 Francesco Cecere Aug 16, 2022
GSE224222
Co-occurrence of Beckwith–Wiedemann Syndrome and colorectal cancer in a young woman
11 Francesco Cecere Apr 01, 2023
GSE237676
Co-occurrence of Beckwith-Wiedemann syndrome and Pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism?
5 Francesco Cecere Aug 01, 2023
GSE245423
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 [scRNA-seq]
96 Francesco Cecere Oct 18, 2023
GSE245424
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 [scBS-seq]
96 Francesco Cecere Oct 18, 2023
GSE245425
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 [WGS]
1 Francesco Cecere Oct 18, 2023
GSE245426
A maternal-effect Padi6 variant causes nuclear and cytoplasmic abnormalities in oocytes as well 2 as failure of epigenetic reprogramming and zygotic genome activation in embryos
193 Francesco Cecere Oct 18, 2023
GSE262957
Generation of a novel iPSC-based model to explore the molecular and functional phenotype of a rare genetic immunodeficiency, the ICF syndrome type 2.
5 Francesco Cecere May 31, 2024