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Flavia Cerrato

Showing results (1-10 of 50) with videos related to

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Clinical Epigenetics|February 28, 2018
Is ZFP57 binding to <i>H19/IGF2</i>:IG-DMR affected in Silver-Russell syndrome?Angela Sparago, Flavia Cerrato, Andrea Riccio
European Journal of Human Genetics : EJHG|October 17, 2013
Looking for CDKN1C enhancersFlavia Cerrato, Agostina De Crescenzo, Andrea Riccio
Cancer Letters|May 20, 2019
Origins of DNA methylation defects in Wilms tumorsZahra Anvar, Basilia Acurzio, Josep Roma, et al.
European Journal of Human Genetics : EJHG|January 24, 2008
MS-MLPA is a specific and sensitive technique for detecting all chromosome 11p15.5 imprinting defects of BWS and SRS in a single-tube experimentManuela Priolo, Angela Sparago, Corrado Mammì, et al.
Nature Genetics|August 18, 2004
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndromeAngela Sparago, Flavia Cerrato, Maria Vernucci, et al.
Psychological Reports|March 7, 2014
Effects of prolonged wakefulness: the role of PERIOD3 genotypes and personality traitsGiuseppe Barbato, Antonio Costanzo, Ciro Della Monica, et al.
Human Molecular Genetics|December 19, 2003
Developmentally regulated functions of the H19 differentially methylated domainMaria Vernucci, Flavia Cerrato, Paolo V Pedone, et al.
Human Genetics|July 24, 2002
The 5' end of the KCNQ1OT1 gene is hypomethylated in the Beckwith-Wiedemann syndromeFlavia Cerrato, Maria Vernucci, Paolo V Pedone, et al.
Human Molecular Genetics|October 9, 2003
Paternal imprints can be established on the maternal Igf2-H19 locus without altering replication timing of DNAFlavia Cerrato, Wendy Dean, Karen Davies, et al.
Genes|June 2, 2021
Variable Expressivity of the Beckwith-Wiedemann Syndrome in Four Pedigrees Segregating Loss-of-Function Variants of <i>CDKN1C</i>Angela Sparago, Flavia Cerrato, Laura Pignata, et al.
Pageof 5

Showing results (1-10 of 50) with videos related to

Sort By:
Pageof 5
Clinical Epigenetics|February 28, 2018
Is ZFP57 binding to <i>H19/IGF2</i>:IG-DMR affected in Silver-Russell syndrome?Angela Sparago, Flavia Cerrato, Andrea Riccio
European Journal of Human Genetics : EJHG|October 17, 2013
Looking for CDKN1C enhancersFlavia Cerrato, Agostina De Crescenzo, Andrea Riccio
Cancer Letters|May 20, 2019
Origins of DNA methylation defects in Wilms tumorsZahra Anvar, Basilia Acurzio, Josep Roma, et al.
European Journal of Human Genetics : EJHG|January 24, 2008
MS-MLPA is a specific and sensitive technique for detecting all chromosome 11p15.5 imprinting defects of BWS and SRS in a single-tube experimentManuela Priolo, Angela Sparago, Corrado Mammì, et al.
Nature Genetics|August 18, 2004
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndromeAngela Sparago, Flavia Cerrato, Maria Vernucci, et al.
Psychological Reports|March 7, 2014
Effects of prolonged wakefulness: the role of PERIOD3 genotypes and personality traitsGiuseppe Barbato, Antonio Costanzo, Ciro Della Monica, et al.
Human Molecular Genetics|December 19, 2003
Developmentally regulated functions of the H19 differentially methylated domainMaria Vernucci, Flavia Cerrato, Paolo V Pedone, et al.
Human Genetics|July 24, 2002
The 5' end of the KCNQ1OT1 gene is hypomethylated in the Beckwith-Wiedemann syndromeFlavia Cerrato, Maria Vernucci, Paolo V Pedone, et al.
Human Molecular Genetics|October 9, 2003
Paternal imprints can be established on the maternal Igf2-H19 locus without altering replication timing of DNAFlavia Cerrato, Wendy Dean, Karen Davies, et al.
Genes|June 2, 2021
Variable Expressivity of the Beckwith-Wiedemann Syndrome in Four Pedigrees Segregating Loss-of-Function Variants of <i>CDKN1C</i>Angela Sparago, Flavia Cerrato, Laura Pignata, et al.
Pageof 5