Similar articles for PMID: 16243356

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1

Trim32 is a ubiquitin ligase mutated in limb girdle muscular dystrophy type 2H that binds to skeletal muscle myosin and ubiquitinates actin.

Kudryashova E, Kudryashov D, Kramerova I, Spencer MJ. Kudryashova E, et al. J Mol Biol. 2005 Nov 25;354(2):413-24. doi: 10.1016/j.jmb.2005.09.068. Epub 2005 Oct 10. J Mol Biol. 2005. PMID: 16243356

2

Analysis of the Zn-Binding Domains of TRIM32, the E3 Ubiquitin Ligase Mutated in Limb Girdle Muscular Dystrophy 2H.

Lazzari E, El-Halawany MS, De March M, Valentino F, Cantatore F, Migliore C, Onesti S, Meroni G. Lazzari E, et al. Cells. 2019 Mar 16;8(3):254. doi: 10.3390/cells8030254. Cells. 2019. PMID: 30884854 Free PMC article.

3

Mutations that impair interaction properties of TRIM32 associated with limb-girdle muscular dystrophy 2H.

Saccone V, Palmieri M, Passamano L, Piluso G, Meroni G, Politano L, Nigro V. Saccone V, et al. Hum Mutat. 2008 Feb;29(2):240-7. doi: 10.1002/humu.20633. Hum Mutat. 2008. PMID: 17994549

4

TRIM32 is an E3 ubiquitin ligase for dysbindin.

Locke M, Tinsley CL, Benson MA, Blake DJ. Locke M, et al. Hum Mol Genet. 2009 Jul 1;18(13):2344-58. doi: 10.1093/hmg/ddp167. Epub 2009 Apr 6. Hum Mol Genet. 2009. PMID: 19349376 Free PMC article.

5

Deficiency of the E3 ubiquitin ligase TRIM32 in mice leads to a myopathy with a neurogenic component.

Kudryashova E, Wu J, Havton LA, Spencer MJ. Kudryashova E, et al. Hum Mol Genet. 2009 Apr 1;18(7):1353-67. doi: 10.1093/hmg/ddp036. Epub 2009 Jan 19. Hum Mol Genet. 2009. PMID: 19155210 Free PMC article.

6

Limb-girdle muscular dystrophy 2H and the role of TRIM32.

Shieh PB, Kudryashova E, Spencer MJ. Shieh PB, et al. Handb Clin Neurol. 2011;101:125-33. doi: 10.1016/B978-0-08-045031-5.00009-8. Handb Clin Neurol. 2011. PMID: 21496629 Review.

7

Novel TRIM32 mutation in sarcotubular myopathy.

Panicucci C, Traverso M, Baratto S, Romeo C, Iacomino M, Gemelli C, Tagliafico A, Broda P, Zara F, Bruno C, Minetti C, Fiorillo C. Panicucci C, et al. Acta Myol. 2019 Mar 1;38(1):8-12. eCollection 2019 Mar. Acta Myol. 2019. PMID: 31309175 Free PMC article.

8

Commonality of TRIM32 mutation in causing sarcotubular myopathy and LGMD2H.

Schoser BG, Frosk P, Engel AG, Klutzny U, Lochmüller H, Wrogemann K. Schoser BG, et al. Ann Neurol. 2005 Apr;57(4):591-5. doi: 10.1002/ana.20441. Ann Neurol. 2005. PMID: 15786463

9

The interaction of Piasy with Trim32, an E3-ubiquitin ligase mutated in limb-girdle muscular dystrophy type 2H, promotes Piasy degradation and regulates UVB-induced keratinocyte apoptosis through NFkappaB.

Albor A, El-Hizawi S, Horn EJ, Laederich M, Frosk P, Wrogemann K, Kulesz-Martin M. Albor A, et al. J Biol Chem. 2006 Sep 1;281(35):25850-66. doi: 10.1074/jbc.M601655200. Epub 2006 Jun 30. J Biol Chem. 2006. PMID: 16816390 Free article.

10

TRIM32 ubiquitin E3 ligase, one enzyme for several pathologies: From muscular dystrophy to tumours.

Lazzari E, Meroni G. Lazzari E, et al. Int J Biochem Cell Biol. 2016 Oct;79:469-477. doi: 10.1016/j.biocel.2016.07.023. Epub 2016 Jul 22. Int J Biochem Cell Biol. 2016. PMID: 27458054 Review.

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