Merla G - Search Results

1

A New Split Hand/Foot Malformation with Long Bone Deficiency Familial Case.

Fusco C, Nittis P, Alfaiz AA, Pellico MT, Augello B, Malerba N, Zelante L, Reymond A, Merla G. Fusco C, et al. Among authors: merla g. J Pediatr Genet. 2017 Jun;6(2):98-102. doi: 10.1055/s-0036-1588029. Epub 2016 Aug 31. J Pediatr Genet. 2017. PMID: 28496997 Free PMC article.

2

Mlx, a new Max-like bHLHZip family member: the center stage of a novel transcription factors regulatory pathway?

Meroni G, Cairo S, Merla G, Messali S, Brent R, Ballabio A, Reymond A. Meroni G, et al. Among authors: merla g. Oncogene. 2000 Jul 6;19(29):3266-77. doi: 10.1038/sj.onc.1203634. Oncogene. 2000. PMID: 10918583

3

WBSCR14, a gene mapping to the Williams--Beuren syndrome deleted region, is a new member of the Mlx transcription factor network.

Cairo S, Merla G, Urbinati F, Ballabio A, Reymond A. Cairo S, et al. Among authors: merla g. Hum Mol Genet. 2001 Mar 15;10(6):617-27. doi: 10.1093/hmg/10.6.617. Hum Mol Genet. 2001. PMID: 11230181

4

Identification of additional transcripts in the Williams-Beuren syndrome critical region.

Merla G, Ucla C, Guipponi M, Reymond A. Merla G, et al. Hum Genet. 2002 May;110(5):429-38. doi: 10.1007/s00439-002-0710-x. Epub 2002 Mar 28. Hum Genet. 2002. PMID: 12073013

5

The subcellular localization of the ChoRE-binding protein, encoded by the Williams-Beuren syndrome critical region gene 14, is regulated by 14-3-3.

Merla G, Howald C, Antonarakis SE, Reymond A. Merla G, et al. Hum Mol Genet. 2004 Jul 15;13(14):1505-14. doi: 10.1093/hmg/ddh163. Epub 2004 May 26. Hum Mol Genet. 2004. PMID: 15163635

6

Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genes.

Merla G, Howald C, Henrichsen CN, Lyle R, Wyss C, Zabot MT, Antonarakis SE, Reymond A. Merla G, et al. Am J Hum Genet. 2006 Aug;79(2):332-41. doi: 10.1086/506371. Epub 2006 Jun 23. Am J Hum Genet. 2006. PMID: 16826523 Free PMC article.

7

An 11-bp duplication in the promoter region of the VHL gene in a patient with cerebellar hemangioblastoma and renal oncocytoma.

Muscarella LA, Barbano R, Augello B, Formica V, Micale L, Zelante L, D'Agruma L, Merla G. Muscarella LA, et al. Among authors: merla g. J Hum Genet. 2007;52(6):485-491. doi: 10.1007/s10038-007-0138-1. Epub 2007 Apr 17. J Hum Genet. 2007. PMID: 17437055

8

Side effects of genome structural changes.

Reymond A, Henrichsen CN, Harewood L, Merla G. Reymond A, et al. Among authors: merla g. Curr Opin Genet Dev. 2007 Oct;17(5):381-6. doi: 10.1016/j.gde.2007.08.009. Epub 2007 Oct 24. Curr Opin Genet Dev. 2007. PMID: 17913489 Review.

9

Williams-Beuren syndrome TRIM50 encodes an E3 ubiquitin ligase.

Micale L, Fusco C, Augello B, Napolitano LM, Dermitzakis ET, Meroni G, Merla G, Reymond A. Micale L, et al. Among authors: merla g. Eur J Hum Genet. 2008 Sep;16(9):1038-49. doi: 10.1038/ejhg.2008.68. Epub 2008 Apr 9. Eur J Hum Genet. 2008. PMID: 18398435 Free PMC article.

10

Promoter methylation correlates with reduced NDRG2 expression in advanced colon tumour.

Piepoli A, Cotugno R, Merla G, Gentile A, Augello B, Quitadamo M, Merla A, Panza A, Carella M, Maglietta R, D'Addabbo A, Ancona N, Fusilli S, Perri F, Andriulli A. Piepoli A, et al. Among authors: merla a, merla g. BMC Med Genomics. 2009 Mar 3;2:11. doi: 10.1186/1755-8794-2-11. BMC Med Genomics. 2009. PMID: 19257893 Free PMC article.

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