Merla G - Search Results

1

Amplification and overexpression of PRUNE in human sarcomas and breast carcinomas-a possible mechanism for altering the nm23-H1 activity.

Forus A, D'Angelo A, Henriksen J, Merla G, Maelandsmo GM, Flørenes VA, Olivieri S, Bjerkehagen B, Meza-Zepeda LA, del Vecchio Blanco F, Müller C, Sanvito F, Kononen J, Nesland JM, Fodstad Ø, Reymond A, Kallioniemi OP, Arrigoni G, Ballabio A, Myklebost O, Zollo M. Forus A, et al. Among authors: merla g. Oncogene. 2001 Oct 18;20(47):6881-90. doi: 10.1038/sj.onc.1204874. Oncogene. 2001. PMID: 11687967

2

Evidence for interaction between human PRUNE and nm23-H1 NDPKinase.

Reymond A, Volorio S, Merla G, Al-Maghtheh M, Zuffardi O, Bulfone A, Ballabio A, Zollo M. Reymond A, et al. Among authors: merla g. Oncogene. 1999 Dec 2;18(51):7244-52. doi: 10.1038/sj.onc.1203140. Oncogene. 1999. PMID: 10602478

3

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

4

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

5

The tripartite motif family identifies cell compartments.

Reymond A, Meroni G, Fantozzi A, Merla G, Cairo S, Luzi L, Riganelli D, Zanaria E, Messali S, Cainarca S, Guffanti A, Minucci S, Pelicci PG, Ballabio A. Reymond A, et al. Among authors: merla g. EMBO J. 2001 May 1;20(9):2140-51. doi: 10.1093/emboj/20.9.2140. EMBO J. 2001. PMID: 11331580 Free PMC article.

6

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

7

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

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

Using transcription modules to identify expression clusters perturbed in Williams-Beuren syndrome.

Henrichsen CN, Csárdi G, Zabot MT, Fusco C, Bergmann S, Merla G, Reymond A. Henrichsen CN, et al. Among authors: merla g. PLoS Comput Biol. 2011 Jan 20;7(1):e1001054. doi: 10.1371/journal.pcbi.1001054. PLoS Comput Biol. 2011. PMID: 21304579 Free PMC article.

10

The tripartite motif: structure and function.

Micale L, Chaignat E, Fusco C, Reymond A, Merla G. Micale L, et al. Among authors: merla g. Adv Exp Med Biol. 2012;770:11-25. Adv Exp Med Biol. 2012. PMID: 23630997 Review.

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