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Valentina Casa

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

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Frontiers in Genetics|October 13, 2012
A repetitive elements perspective in Polycomb epigeneticsValentina Casa, Davide Gabellini
RNA Biology|October 11, 2012
A novel molecular mechanism in human genetic disease: a DNA repeat-derived lncRNADaphne S Cabianca, Valentina Casa, Davide Gabellini
Human Molecular Genetics|January 2, 2017
Polycomb repressive complex 1 provides a molecular explanation for repeat copy number dependency in FSHD muscular dystrophyValentina Casa, Valeria Runfola, Stefano Micheloni, et al.
Plos One|July 7, 2011
Recognition of 5-hydroxymethylcytosine by the Uhrf1 SRA domainCarina Frauer, Thomas Hoffmann, Sebastian Bultmann, et al.
Cell|May 1, 2012
A long ncRNA links copy number variation to a polycomb/trithorax epigenetic switch in FSHD muscular dystrophyDaphne S Cabianca, Valentina Casa, Beatrice Bodega, et al.
Genome Research|April 8, 2020
Redundant and specific roles of cohesin STAG subunits in chromatin looping and transcriptional controlValentina Casa, Macarena Moronta Gines, Eduardo Gade Gusmao, et al.
Plos Genetics|December 21, 2017
Regulation of the cohesin-loading factor NIPBL: Role of the lncRNA NIPBL-AS1 and identification of a distal enhancer elementJessica Zuin, Valentina Casa, Jelena Pozojevic, et al.
Iscience|January 6, 2026
STAG2-truncating variants reveal a mosaic STAG2 inactivation pattern and compensatory mechanisms involving cohesin complex remodelingMacarena Moronta Gines, Marja W Wessels, Valentina Casa, et al.
Cell Reports|May 21, 2020
MAU2 and NIPBL Variants Impair the Heterodimerization of the Cohesin Loader Subunits and Cause Cornelia de Lange SyndromeIlaria Parenti, Farah Diab, Sara Ruiz Gil, et al.
Brain : a Journal of Neurology|July 24, 2019
Cohesin complex-associated holoprosencephalyPaul Kruszka, Seth I Berger, Valentina Casa, et al.
Pageof 1

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

Sort By:
Pageof 1
Frontiers in Genetics|October 13, 2012
A repetitive elements perspective in Polycomb epigeneticsValentina Casa, Davide Gabellini
RNA Biology|October 11, 2012
A novel molecular mechanism in human genetic disease: a DNA repeat-derived lncRNADaphne S Cabianca, Valentina Casa, Davide Gabellini
Human Molecular Genetics|January 2, 2017
Polycomb repressive complex 1 provides a molecular explanation for repeat copy number dependency in FSHD muscular dystrophyValentina Casa, Valeria Runfola, Stefano Micheloni, et al.
Plos One|July 7, 2011
Recognition of 5-hydroxymethylcytosine by the Uhrf1 SRA domainCarina Frauer, Thomas Hoffmann, Sebastian Bultmann, et al.
Cell|May 1, 2012
A long ncRNA links copy number variation to a polycomb/trithorax epigenetic switch in FSHD muscular dystrophyDaphne S Cabianca, Valentina Casa, Beatrice Bodega, et al.
Genome Research|April 8, 2020
Redundant and specific roles of cohesin STAG subunits in chromatin looping and transcriptional controlValentina Casa, Macarena Moronta Gines, Eduardo Gade Gusmao, et al.
Plos Genetics|December 21, 2017
Regulation of the cohesin-loading factor NIPBL: Role of the lncRNA NIPBL-AS1 and identification of a distal enhancer elementJessica Zuin, Valentina Casa, Jelena Pozojevic, et al.
Iscience|January 6, 2026
STAG2-truncating variants reveal a mosaic STAG2 inactivation pattern and compensatory mechanisms involving cohesin complex remodelingMacarena Moronta Gines, Marja W Wessels, Valentina Casa, et al.
Cell Reports|May 21, 2020
MAU2 and NIPBL Variants Impair the Heterodimerization of the Cohesin Loader Subunits and Cause Cornelia de Lange SyndromeIlaria Parenti, Farah Diab, Sara Ruiz Gil, et al.
Brain : a Journal of Neurology|July 24, 2019
Cohesin complex-associated holoprosencephalyPaul Kruszka, Seth I Berger, Valentina Casa, et al.
Pageof 1