Gabellini D - Search Results

1

WDR5 is required for DUX4 expression and its pathological effects in FSHD muscular dystrophy.

Mocciaro E, Giambruno R, Micheloni S, Cernilogar FM, Andolfo A, Consonni C, Pannese M, Ferri G, Runfola V, Schotta G, Gabellini D. Mocciaro E, et al. Among authors: gabellini d. Nucleic Acids Res. 2023 Jun 9;51(10):5144-5161. doi: 10.1093/nar/gkad230. Nucleic Acids Res. 2023. PMID: 37021550 Free PMC article.

2

FSHD muscular dystrophy region gene 1 binds Suv4-20h1 histone methyltransferase and impairs myogenesis.

Neguembor MV, Xynos A, Onorati MC, Caccia R, Bortolanza S, Godio C, Pistoni M, Corona DF, Schotta G, Gabellini D. Neguembor MV, et al. Among authors: gabellini d. J Mol Cell Biol. 2013 Oct;5(5):294-307. doi: 10.1093/jmcb/mjt018. Epub 2013 May 29. J Mol Cell Biol. 2013. PMID: 23720823

3

Direct interplay between two candidate genes in FSHD muscular dystrophy.

Ferri G, Huichalaf CH, Caccia R, Gabellini D. Ferri G, et al. Among authors: gabellini d. Hum Mol Genet. 2015 Mar 1;24(5):1256-66. doi: 10.1093/hmg/ddu536. Epub 2014 Oct 17. Hum Mol Genet. 2015. PMID: 25326393 Free PMC article.

4

DNA methylation analysis of the macrosatellite repeat associated with FSHD muscular dystrophy at single nucleotide level.

Huichalaf C, Micheloni S, Ferri G, Caccia R, Gabellini D. Huichalaf C, et al. Among authors: gabellini d. PLoS One. 2014 Dec 29;9(12):e115278. doi: 10.1371/journal.pone.0115278. eCollection 2014. PLoS One. 2014. PMID: 25545674 Free PMC article.

5

Rbfox proteins regulate tissue-specific alternative splicing of Mef2D required for muscle differentiation.

Runfola V, Sebastian S, Dilworth FJ, Gabellini D. Runfola V, et al. Among authors: gabellini d. J Cell Sci. 2015 Feb 15;128(4):631-7. doi: 10.1242/jcs.161059. Epub 2015 Jan 20. J Cell Sci. 2015. PMID: 25609712 Free PMC article.

6

A Human Pluripotent Stem Cell Model of Facioscapulohumeral Muscular Dystrophy-Affected Skeletal Muscles.

Caron L, Kher D, Lee KL, McKernan R, Dumevska B, Hidalgo A, Li J, Yang H, Main H, Ferri G, Petek LM, Poellinger L, Miller DG, Gabellini D, Schmidt U. Caron L, et al. Among authors: gabellini d. Stem Cells Transl Med. 2016 Sep;5(9):1145-61. doi: 10.5966/sctm.2015-0224. Epub 2016 May 23. Stem Cells Transl Med. 2016. PMID: 27217344 Free PMC article.

7

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

Casa V, Runfola V, Micheloni S, Aziz A, Dilworth FJ, Gabellini D. Casa V, et al. Among authors: gabellini d. Hum Mol Genet. 2017 Feb 15;26(4):753-767. doi: 10.1093/hmg/ddw426. Hum Mol Genet. 2017. PMID: 28040729 Free PMC article.

8

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. Castiglioni I, et al. Among authors: gabellini d. Nat Commun. 2018 Nov 28;9(1):5026. doi: 10.1038/s41467-018-07313-8. Nat Commun. 2018. PMID: 30487570 Free PMC article.

9

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

Pedrotti S, Caccia R, Neguembor MV, Garcia-Manteiga JM, 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. Pedrotti S, et al. Among authors: gabellini d. Sci Adv. 2019 Apr 17;5(4):eaav1472. doi: 10.1126/sciadv.aav1472. eCollection 2019 Apr. Sci Adv. 2019. PMID: 31001581 Free PMC article.

10

DUX4 Role in Normal Physiology and in FSHD Muscular Dystrophy.

Mocciaro E, Runfola V, Ghezzi P, Pannese M, Gabellini D. Mocciaro E, et al. Among authors: gabellini d. Cells. 2021 Nov 26;10(12):3322. doi: 10.3390/cells10123322. Cells. 2021. PMID: 34943834 Free PMC article. Review.

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