Merla G - Search Results

1

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

2

Circadian Genes Expression Patterns in Disorders Due to Enzyme Deficiencies in the Heme Biosynthetic Pathway.

Savino M, Guida CC, Nardella M, Murgo E, Augello B, Merla G, De Cosmo S, Savino AF, Tarquini R, Cei F, Aucella F, Mazzoccoli G. Savino M, et al. Among authors: merla g. Biomedicines. 2022 Dec 9;10(12):3198. doi: 10.3390/biomedicines10123198. Biomedicines. 2022. PMID: 36551954 Free PMC article.

3

The ubiquitin ligase TRIM32 promotes the autophagic response to Mycobacterium tuberculosis infection in macrophages.

Romagnoli A, Di Rienzo M, Petruccioli E, Fusco C, Palucci I, Micale L, Mazza T, Delogu G, Merla G, Goletti D, Piacentini M, Fimia GM. Romagnoli A, et al. Among authors: merla g. Cell Death Dis. 2023 Aug 5;14(8):505. doi: 10.1038/s41419-023-06026-1. Cell Death Dis. 2023. PMID: 37543647 Free PMC article.

4

FOXI3 pathogenic variants cause one form of craniofacial microsomia.

Mao K, Borel C, Ansar M, Jolly A, Makrythanasis P, Froehlich C, Iwaszkiewicz J, Wang B, Xu X, Li Q, Blanc X, Zhu H, Chen Q, Jin F, Ankamreddy H, Singh S, Zhang H, Wang X, Chen P, Ranza E, Paracha SA, Shah SF, Guida V, Piceci-Sparascio F, Melis D, Dallapiccola B, Digilio MC, Novelli A, Magliozzi M, Fadda MT, Streff H, Machol K, Lewis RA, Zoete V, Squeo GM, Prontera P, Mancano G, Gori G, Mariani M, Selicorni A, Psoni S, Fryssira H, Douzgou S, Marlin S, Biskup S, De Luca A, Merla G, Zhao S, Cox TC, Groves AK, Lupski JR, Zhang Q, Zhang YB, Antonarakis SE. Mao K, et al. Among authors: merla g. Nat Commun. 2023 Apr 11;14(1):2026. doi: 10.1038/s41467-023-37703-6. Nat Commun. 2023. PMID: 37041148 Free PMC article.

5

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

6

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

7

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.

8

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

9

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

10

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

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