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Davide Gabellini

Showing results (21-30 of 44) with videos related to

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Plos One|December 30, 2014
DNA methylation analysis of the macrosatellite repeat associated with FSHD muscular dystrophy at single nucleotide levelClaudia Huichalaf, Stefano Micheloni, Giulia Ferri, et al.
Cells|December 24, 2021
DUX4 Role in Normal Physiology and in FSHD Muscular DystrophyEmanuele Mocciaro, Valeria Runfola, Paola Ghezzi, et al.
Science Advances|September 15, 2023
DUX4-r exerts a neomorphic activity that depends on GTF2I in acute lymphoblastic leukemiaDaniele Campolungo, Mara Salomé, Beatrice Biferali, et al.
Cell Reports|September 13, 2023
MATR3 is an endogenous inhibitor of DUX4 in FSHD muscular dystrophyValeria Runfola, Roberto Giambruno, Claudia Caronni, et al.
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.
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.
Journal of Cell Science|March 26, 2013
Overexpression of facioscapulohumeral muscular dystrophy region gene 1 causes primary defects in myogenic stem cellsAlexandros Xynos, Maria Victoria Neguembor, Roberta Caccia, et al.
Nature Communications|November 30, 2018
The Trithorax protein Ash1L promotes myoblast fusion by activating Cdon expressionIlaria Castiglioni, Roberta Caccia, Jose Manuel Garcia-Manteiga, et al.
Plos Genetics|January 10, 2013
Rbfox1 downregulation and altered calpain 3 splicing by FRG1 in a mouse model of Facioscapulohumeral muscular dystrophy (FSHD)Mariaelena Pistoni, Lily Shiue, Melissa S Cline, et al.
The EMBO Journal|July 11, 2003
Early mitotic degradation of the homeoprotein HOXC10 is potentially linked to cell cycle progressionDavide Gabellini, Ivan N Colaluca, Hartmut C Vodermaier, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
Plos One|December 30, 2014
DNA methylation analysis of the macrosatellite repeat associated with FSHD muscular dystrophy at single nucleotide levelClaudia Huichalaf, Stefano Micheloni, Giulia Ferri, et al.
Cells|December 24, 2021
DUX4 Role in Normal Physiology and in FSHD Muscular DystrophyEmanuele Mocciaro, Valeria Runfola, Paola Ghezzi, et al.
Science Advances|September 15, 2023
DUX4-r exerts a neomorphic activity that depends on GTF2I in acute lymphoblastic leukemiaDaniele Campolungo, Mara Salomé, Beatrice Biferali, et al.
Cell Reports|September 13, 2023
MATR3 is an endogenous inhibitor of DUX4 in FSHD muscular dystrophyValeria Runfola, Roberto Giambruno, Claudia Caronni, et al.
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.
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.
Journal of Cell Science|March 26, 2013
Overexpression of facioscapulohumeral muscular dystrophy region gene 1 causes primary defects in myogenic stem cellsAlexandros Xynos, Maria Victoria Neguembor, Roberta Caccia, et al.
Nature Communications|November 30, 2018
The Trithorax protein Ash1L promotes myoblast fusion by activating Cdon expressionIlaria Castiglioni, Roberta Caccia, Jose Manuel Garcia-Manteiga, et al.
Plos Genetics|January 10, 2013
Rbfox1 downregulation and altered calpain 3 splicing by FRG1 in a mouse model of Facioscapulohumeral muscular dystrophy (FSHD)Mariaelena Pistoni, Lily Shiue, Melissa S Cline, et al.
The EMBO Journal|July 11, 2003
Early mitotic degradation of the homeoprotein HOXC10 is potentially linked to cell cycle progressionDavide Gabellini, Ivan N Colaluca, Hartmut C Vodermaier, et al.
Pageof 5