Gabellini D - Search Results

1

Transcriptional derepression as a cause of genetic diseases.

Gabellini D, Tupler R, Green MR. Gabellini D, et al. Curr Opin Genet Dev. 2003 Jun;13(3):239-45. doi: 10.1016/s0959-437x(03)00050-9. Curr Opin Genet Dev. 2003. PMID: 12787785 Review.

2

When enough is enough: genetic diseases associated with transcriptional derepression.

Gabellini D, Green MR, Tupler R. Gabellini D, et al. Curr Opin Genet Dev. 2004 Jun;14(3):301-7. doi: 10.1016/j.gde.2004.04.010. Curr Opin Genet Dev. 2004. PMID: 15172674 Review.

3

Molecular basis of facioscapulohumeral muscular dystrophy.

Tupler R, Gabellini D. Tupler R, et al. Among authors: gabellini d. Cell Mol Life Sci. 2004 Mar;61(5):557-566. doi: 10.1007/s00018-003-3285-3. Cell Mol Life Sci. 2004. PMID: 15004695 Review.

4

Inappropriate gene activation in FSHD: a repressor complex binds a chromosomal repeat deleted in dystrophic muscle.

Gabellini D, Green MR, Tupler R. Gabellini D, et al. Cell. 2002 Aug 9;110(3):339-48. doi: 10.1016/s0092-8674(02)00826-7. Cell. 2002. PMID: 12176321 Free article.

5

Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1.

Gabellini D, D'Antona G, Moggio M, Prelle A, Zecca C, Adami R, Angeletti B, Ciscato P, Pellegrino MA, Bottinelli R, Green MR, Tupler R. Gabellini D, et al. Among authors: d antona g. Nature. 2006 Feb 23;439(7079):973-7. doi: 10.1038/nature04422. Epub 2005 Dec 11. Nature. 2006. PMID: 16341202

6

The cell biology of disease: FSHD: copy number variations on the theme of muscular dystrophy.

Cabianca DS, Gabellini D. Cabianca DS, et al. Among authors: gabellini d. J Cell Biol. 2010 Dec 13;191(6):1049-60. doi: 10.1083/jcb.201007028. J Cell Biol. 2010. PMID: 21149563 Free PMC article. Review.

7

A long ncRNA links copy number variation to a polycomb/trithorax epigenetic switch in FSHD muscular dystrophy.

Cabianca DS, Casa V, Bodega B, Xynos A, Ginelli E, Tanaka Y, Gabellini D. Cabianca DS, et al. Among authors: gabellini d. Cell. 2012 May 11;149(4):819-31. doi: 10.1016/j.cell.2012.03.035. Epub 2012 Apr 26. Cell. 2012. PMID: 22541069 Free PMC article.

8

Meeting report: the 2021 FSHD International Research Congress.

Jagannathan S, de Greef JC, Hayward LJ, Yokomori K, Gabellini D, Mul K, Sacconi S, Arjomand J, Kinoshita J, Harper SQ. Jagannathan S, et al. Among authors: gabellini d. Skelet Muscle. 2022 Jan 17;12(1):1. doi: 10.1186/s13395-022-00287-8. Skelet Muscle. 2022. PMID: 35039091 Free PMC article. Review.

9

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.

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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