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Angela Sparago

Showing results (11-20 of 41) with videos related to

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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.
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.
FEBS Letters|March 19, 2013
Genetic and epigenetic mutations affect the DNA binding capability of human ZFP57 in transient neonatal diabetes type 1Ilaria Baglivo, Sabrina Esposito, Lucia De Cesare, 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.
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.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|December 24, 2009
Silver-Russell syndrome and Beckwith-Wiedemann syndrome phenotypes associated with 11p duplication in a single familyLaura Cardarelli, Angela Sparago, Agostina De Crescenzo, 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.
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.
Epigenetics & Chromatin|March 27, 2014
The PEG13-DMR and brain-specific enhancers dictate imprinted expression within the 8q24 intellectual disability risk locusFranck Court, Cristina Camprubi, Cristina Vicente Garcia, 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.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
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.
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.
FEBS Letters|March 19, 2013
Genetic and epigenetic mutations affect the DNA binding capability of human ZFP57 in transient neonatal diabetes type 1Ilaria Baglivo, Sabrina Esposito, Lucia De Cesare, 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.
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.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|December 24, 2009
Silver-Russell syndrome and Beckwith-Wiedemann syndrome phenotypes associated with 11p duplication in a single familyLaura Cardarelli, Angela Sparago, Agostina De Crescenzo, 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.
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.
Epigenetics & Chromatin|March 27, 2014
The PEG13-DMR and brain-specific enhancers dictate imprinted expression within the 8q24 intellectual disability risk locusFranck Court, Cristina Camprubi, Cristina Vicente Garcia, 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.
Pageof 5