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Flavia Cerrato

Showing results (21-30 of 50) with videos related to

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Scientific Reports|July 6, 2021
Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCsBasilia Acurzio, Ankit Verma, Alessia Polito, et al.
Genes|October 27, 2022
Different Mechanisms Cause Hypomethylation of Both <i>H19</i> and <i>KCNQ1OT1</i> Imprinted Differentially Methylated Regions in Two Cases of Silver-Russell Syndrome SpectrumFrancesco Passaretti, Laura Pignata, Giuseppina Vitiello, et al.
Journal of Human Genetics|March 27, 2015
A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotypeAgostina De Crescenzo, Valentina Citro, Andrea Freschi, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 14, 2016
Humanized H19/Igf2 locus reveals diverged imprinting mechanism between mouse and human and reflects Silver-Russell syndrome phenotypesStella K Hur, Andrea Freschi, Folami Ideraabdullah, et al.
Endocrine Development|March 19, 2009
Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumorAndrea Riccio, Angela Sparago, Gaetano Verde, et al.
Plos One|March 28, 2008
Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancerAdele Murrell, Yoko Ito, Gaetano Verde, et al.
Clinical Epigenetics|June 18, 2016
Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypesSusanne Eriksen Boonen, Andrea Freschi, Rikke Christensen, et al.
Frontiers in Cell and Developmental Biology|August 28, 2023
Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism?Laura Pignata, Francesco Cecere, Fabio Acquaviva, 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.
Cancer Genetics and Cytogenetics|September 13, 2008
High frequency of loss of heterozygosity at 11p15 and IGF2 overexpression are not related to clinical outcome in childhood adrenocortical tumors positive for the R337H TP53 mutationRoberto Rosati, Flavia Cerrato, Mabrouka Doghman, et al.
Pageof 5

Showing results (21-30 of 50) with videos related to

Sort By:
Pageof 5
Scientific Reports|July 6, 2021
Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCsBasilia Acurzio, Ankit Verma, Alessia Polito, et al.
Genes|October 27, 2022
Different Mechanisms Cause Hypomethylation of Both <i>H19</i> and <i>KCNQ1OT1</i> Imprinted Differentially Methylated Regions in Two Cases of Silver-Russell Syndrome SpectrumFrancesco Passaretti, Laura Pignata, Giuseppina Vitiello, et al.
Journal of Human Genetics|March 27, 2015
A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotypeAgostina De Crescenzo, Valentina Citro, Andrea Freschi, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 14, 2016
Humanized H19/Igf2 locus reveals diverged imprinting mechanism between mouse and human and reflects Silver-Russell syndrome phenotypesStella K Hur, Andrea Freschi, Folami Ideraabdullah, et al.
Endocrine Development|March 19, 2009
Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumorAndrea Riccio, Angela Sparago, Gaetano Verde, et al.
Plos One|March 28, 2008
Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancerAdele Murrell, Yoko Ito, Gaetano Verde, et al.
Clinical Epigenetics|June 18, 2016
Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypesSusanne Eriksen Boonen, Andrea Freschi, Rikke Christensen, et al.
Frontiers in Cell and Developmental Biology|August 28, 2023
Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism?Laura Pignata, Francesco Cecere, Fabio Acquaviva, 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.
Cancer Genetics and Cytogenetics|September 13, 2008
High frequency of loss of heterozygosity at 11p15 and IGF2 overexpression are not related to clinical outcome in childhood adrenocortical tumors positive for the R337H TP53 mutationRoberto Rosati, Flavia Cerrato, Mabrouka Doghman, et al.
Pageof 5