• 1249 Citations
  • 18 h-Index
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Fingerprint Dive into the research topics where Davide Gabellini is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 1 Similar Profiles
Facioscapulohumeral Muscular Dystrophy Medicine & Life Sciences
Muscular Dystrophies Medicine & Life Sciences
Epigenomics Medicine & Life Sciences
Long Noncoding RNA Medicine & Life Sciences
Muscles Medicine & Life Sciences
Genes Medicine & Life Sciences
Inborn Genetic Diseases Medicine & Life Sciences
Alternative Splicing Medicine & Life Sciences

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Research Output 2000 2019

  • 1249 Citations
  • 18 h-Index
  • 31 Article
  • 1 Chapter
1 Citation (Scopus)

The Suv420h histone methyltransferases regulate PPAR-γ and energy expenditure in response to environmental stimuli

Pedrotti, S., Caccia, R., Neguembor, M. V., Garcia-Manteiga, J. M., Ferri, G., De Palma, C., Canu, T., Giovarelli, M., Marra, P., Fiocchi, A., Molineris, I., Raso, M., Sanvito, F., Doglioni, C., Esposito, A., Clementi, E. & Gabellini, D., Jan 1 2019, In : Science Advances. 5, 4, eaav1472.

Research output: Contribution to journalArticle

Open Access
adipose tissues

Amino acid deprivation triggers a novel GCN2-independent response leading to the transcriptional reactivation of non-native DNA sequences

De Vito, A., Lazzaro, M., Palmisano, I., Cittaro, D., Riba, M., Lazarevic, D., Bannai, M., Gabellini, D. & Schiaffino, MV., 2018, In : PLoS One. 13, 7, e0200783.

Research output: Contribution to journalArticle

Essential Amino Acids
DNA sequences

Diversification of the muscle proteome through alternative splicing

Nakka, K., Ghigna, C., Gabellini, D. & Dilworth, FJ., 2018, In : Skeletal Muscle. 8, 1, 8.

Research output: Contribution to journalArticle

Alternative Splicing
Protein Isoforms

The Trithorax protein Ash1L promotes myoblast fusion by activating Cdon expression

Castiglioni, I., Caccia, R., Garcia-Manteiga, JM., Ferri, G., Caretti, G., Molineris, I., Nishioka, K. & Gabellini, D., 2018, In : Nature Communications. 9, 5026.

Research output: Contribution to journalArticle

Fusion reactions

Polycomb repressive complex 1 provides a molecular explanation for repeat copy number dependency in FSHD muscular dystrophy

Casà, V., Runfola, V., Micheloni, S., Aziz, A., Dilworth, FJ. & Gabellini, D., 2017, In : Human Molecular Genetics. 26, 4, p. 753-767 15 p.

Research output: Contribution to journalArticle

Polycomb Repressive Complex 1
Facioscapulohumeral Muscular Dystrophy
Muscular Dystrophies