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Flavia Cerrato

Showing results (11-20 of 50) with videos related to

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European Journal of Medical Genetics|May 17, 2011
A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndromeAgostina De Crescenzo, Filomena Coppola, Pietro Falco, et al.
Italian Journal of Pediatrics|September 25, 2023
Beckwith-Wiedemann syndrome and twinning: case report and brief review of literaturePierandrea Elefante, Beatrice Spedicati, Flavio Faletra, et al.
Genes|April 30, 2021
Mosaic Segmental and Whole-Chromosome Upd(11)mat in Silver-Russell SyndromeLaura Pignata, Angela Sparago, Orazio Palumbo, et al.
Journal of Medical Genetics|December 18, 2012
Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restrictionAgostina De Crescenzo, Angela Sparago, Flavia Cerrato, et al.
Epigenetics & Chromatin|April 17, 2026
Loss of maternal PADI6 disrupts DNA methylation and genomic imprinting maintenance in late preimplantation mouse embryosCarlo Giaccari, Francesco Cecere, Angela Pagano, et al.
Pediatrics|June 22, 2017
Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann SyndromeAlessandro Mussa, Cristina Molinatto, Flavia Cerrato, et al.
Human Molecular Genetics|January 11, 2005
The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 clusterFlavia Cerrato, Angela Sparago, Ines Di Matteo, et al.
Cancers|November 21, 2020
Both Epimutations and Chromosome Aberrations Affect Multiple Imprinted Loci in Aggressive Wilms TumorsLaura Pignata, Orazio Palumbo, Flavia Cerrato, et al.
Human Molecular Genetics|June 16, 2021
The number of the CTCF binding sites of the H19/IGF2:IG-DMR correlates with DNA methylation and expression imprinting in a humanized mouse modelAndrea Freschi, Rosita Del Prete, Laura Pignata, et al.
BMC Medical Genetics|May 7, 2015
A novel large deletion of the ICR1 region including H19 and putative enhancer elementsHelen Fryssira, Stella Amenta, Deniz Kanber, et al.
Pageof 5

Showing results (11-20 of 50) with videos related to

Sort By:
Pageof 5
European Journal of Medical Genetics|May 17, 2011
A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndromeAgostina De Crescenzo, Filomena Coppola, Pietro Falco, et al.
Italian Journal of Pediatrics|September 25, 2023
Beckwith-Wiedemann syndrome and twinning: case report and brief review of literaturePierandrea Elefante, Beatrice Spedicati, Flavio Faletra, et al.
Genes|April 30, 2021
Mosaic Segmental and Whole-Chromosome Upd(11)mat in Silver-Russell SyndromeLaura Pignata, Angela Sparago, Orazio Palumbo, et al.
Journal of Medical Genetics|December 18, 2012
Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restrictionAgostina De Crescenzo, Angela Sparago, Flavia Cerrato, et al.
Epigenetics & Chromatin|April 17, 2026
Loss of maternal PADI6 disrupts DNA methylation and genomic imprinting maintenance in late preimplantation mouse embryosCarlo Giaccari, Francesco Cecere, Angela Pagano, et al.
Pediatrics|June 22, 2017
Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann SyndromeAlessandro Mussa, Cristina Molinatto, Flavia Cerrato, et al.
Human Molecular Genetics|January 11, 2005
The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 clusterFlavia Cerrato, Angela Sparago, Ines Di Matteo, et al.
Cancers|November 21, 2020
Both Epimutations and Chromosome Aberrations Affect Multiple Imprinted Loci in Aggressive Wilms TumorsLaura Pignata, Orazio Palumbo, Flavia Cerrato, et al.
Human Molecular Genetics|June 16, 2021
The number of the CTCF binding sites of the H19/IGF2:IG-DMR correlates with DNA methylation and expression imprinting in a humanized mouse modelAndrea Freschi, Rosita Del Prete, Laura Pignata, et al.
BMC Medical Genetics|May 7, 2015
A novel large deletion of the ICR1 region including H19 and putative enhancer elementsHelen Fryssira, Stella Amenta, Deniz Kanber, et al.
Pageof 5