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Cell
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May 1, 2012
A long ncRNA links copy number variation to a polycomb/trithorax epigenetic switch in FSHD muscular dystrophy
Daphne S Cabianca, Valentina Casa, Beatrice Bodega, et al.
Cancer Biology & Therapy
|
January 16, 2007
Forced expression of RDH10 gene retards growth of HepG2 cells
Elena Rossi, Paola Picozzi, Beatrice Bodega, et al.
International Journal of Molecular Sciences
|
February 11, 2023
Transposable Elements Co-Option in Genome Evolution and Gene Regulation
Erica Gasparotto, Filippo Vittorio Burattin, Valeria Di Gioia, et al.
Plos One
|
June 23, 2011
Expression profiling of FSHD-1 and FSHD-2 cells during myogenic differentiation evidences common and distinctive gene dysregulation patterns
Stefania Cheli, Stephanie François, Beatrice Bodega, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
March 30, 2022
Evolution Increases Primates Brain Complexity Extending RbFOX1 Splicing Activity to LSD1 Modulation
Chiara Forastieri, Maria Italia, Emanuela Toffolo, et al.
Nature Cell Biology
|
August 11, 2015
Genome-wide association between YAP/TAZ/TEAD and AP-1 at enhancers drives oncogenic growth
Francesca Zanconato, Mattia Forcato, Giusy Battilana, et al.
Cell Reports. Medicine
|
September 11, 2024
Early-onset cancers: Biological bases and clinical implications
Gianluca Mauri, Giorgio Patelli, Andrea Sartore-Bianchi, et al.
Scientific Reports
|
May 20, 2020
Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients
Davide Rovina, Marta La Vecchia, Alice Cortesi, et al.
Genome Research
|
May 18, 2019
4q-D4Z4 chromatin architecture regulates the transcription of muscle atrophic genes in facioscapulohumeral muscular dystrophy
Alice Cortesi, Matthieu Pesant, Shruti Sinha, et al.
Scientific Reports
|
December 2, 2025
Neurodevelopmental outcome at 5 to 6 years of age of an early intervention program in preterm infants
Camilla Fontana, Livia Provitera, Chiara Bonfanti, et al.
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of 4
Search research articles
Search
Showing results (11-20 of 37) with videos related to
Sort By:
Page
of 4
Cell
|
May 1, 2012
A long ncRNA links copy number variation to a polycomb/trithorax epigenetic switch in FSHD muscular dystrophy
Daphne S Cabianca, Valentina Casa, Beatrice Bodega, et al.
Cancer Biology & Therapy
|
January 16, 2007
Forced expression of RDH10 gene retards growth of HepG2 cells
Elena Rossi, Paola Picozzi, Beatrice Bodega, et al.
International Journal of Molecular Sciences
|
February 11, 2023
Transposable Elements Co-Option in Genome Evolution and Gene Regulation
Erica Gasparotto, Filippo Vittorio Burattin, Valeria Di Gioia, et al.
Plos One
|
June 23, 2011
Expression profiling of FSHD-1 and FSHD-2 cells during myogenic differentiation evidences common and distinctive gene dysregulation patterns
Stefania Cheli, Stephanie François, Beatrice Bodega, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
March 30, 2022
Evolution Increases Primates Brain Complexity Extending RbFOX1 Splicing Activity to LSD1 Modulation
Chiara Forastieri, Maria Italia, Emanuela Toffolo, et al.
Nature Cell Biology
|
August 11, 2015
Genome-wide association between YAP/TAZ/TEAD and AP-1 at enhancers drives oncogenic growth
Francesca Zanconato, Mattia Forcato, Giusy Battilana, et al.
Cell Reports. Medicine
|
September 11, 2024
Early-onset cancers: Biological bases and clinical implications
Gianluca Mauri, Giorgio Patelli, Andrea Sartore-Bianchi, et al.
Scientific Reports
|
May 20, 2020
Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients
Davide Rovina, Marta La Vecchia, Alice Cortesi, et al.
Genome Research
|
May 18, 2019
4q-D4Z4 chromatin architecture regulates the transcription of muscle atrophic genes in facioscapulohumeral muscular dystrophy
Alice Cortesi, Matthieu Pesant, Shruti Sinha, et al.
Scientific Reports
|
December 2, 2025
Neurodevelopmental outcome at 5 to 6 years of age of an early intervention program in preterm infants
Camilla Fontana, Livia Provitera, Chiara Bonfanti, et al.
Page
of 4