Meroni G - Search Results

1

The combination of transcriptomics and informatics identifies pathways targeted by miR-204 during neurogenesis and axon guidance.

Conte I, Merella S, Garcia-Manteiga JM, Migliore C, Lazarevic D, Carrella S, Marco-Ferreres R, Avellino R, Davidson NP, Emmett W, Sanges R, Bockett N, Van Heel D, Meroni G, Bovolenta P, Stupka E, Banfi S. Conte I, et al. Among authors: meroni g. Nucleic Acids Res. 2014 Jul;42(12):7793-806. doi: 10.1093/nar/gku498. Epub 2014 Jun 3. Nucleic Acids Res. 2014. PMID: 24895435 Free PMC article.

2

Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations.

Migliore C, Athanasakis E, Dahoun S, Wonkam A, Lees M, Calabrese O, Connell F, Lynch SA, Izzi C, Pompilii E, Thakur S, van Maarle M, Wilson LC, Meroni G. Migliore C, et al. Among authors: meroni g. Eur J Med Genet. 2013 Aug;56(8):404-10. doi: 10.1016/j.ejmg.2013.05.009. Epub 2013 Jun 19. Eur J Med Genet. 2013. PMID: 23791568

3

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. Among authors: meroni g. Cells. 2019 Mar 16;8(3):254. doi: 10.3390/cells8030254. Cells. 2019. PMID: 30884854 Free PMC article.

4

SPECC1L Mutations Are Not Common in Sporadic Cases of Opitz G/BBB Syndrome.

Migliore C, Vendramin A, McKee S, Prontera P, Faravelli F, Sachdev R, Dias P, Mascaro M, Licastro D, Meroni G. Migliore C, et al. Among authors: meroni g. Genes (Basel). 2022 Jan 28;13(2):252. doi: 10.3390/genes13020252. Genes (Basel). 2022. PMID: 35205294 Free PMC article.

5

Zinc-finger-based transcriptional repression of rhodopsin in a model of dominant retinitis pigmentosa.

Mussolino C, Sanges D, Marrocco E, Bonetti C, Di Vicino U, Marigo V, Auricchio A, Meroni G, Surace EM. Mussolino C, et al. Among authors: meroni g. EMBO Mol Med. 2011 Mar;3(3):118-28. doi: 10.1002/emmm.201000119. Epub 2011 Jan 26. EMBO Mol Med. 2011. PMID: 21268285 Free PMC article.

6

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: meroni 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.

7

Molecular and biochemical characterisation of a novel sulphatase gene: Arylsulfatase G (ARSG).

Ferrante P, Messali S, Meroni G, Ballabio A. Ferrante P, et al. Among authors: meroni g. Eur J Hum Genet. 2002 Dec;10(12):813-8. doi: 10.1038/sj.ejhg.5200887. Eur J Hum Genet. 2002. PMID: 12461688

8

PML interacts with Myc, and Myc target gene expression is altered in PML-null fibroblasts.

Cairo S, De Falco F, Pizzo M, Salomoni P, Pandolfi PP, Meroni G. Cairo S, et al. Among authors: meroni g. Oncogene. 2005 Mar 24;24(13):2195-203. doi: 10.1038/sj.onc.1208338. Oncogene. 2005. PMID: 15735755

9

Mig12, a novel Opitz syndrome gene product partner, is expressed in the embryonic ventral midline and co-operates with Mid1 to bundle and stabilize microtubules.

Berti C, Fontanella B, Ferrentino R, Meroni G. Berti C, et al. Among authors: meroni g. BMC Cell Biol. 2004 Feb 29;5:9. doi: 10.1186/1471-2121-5-9. BMC Cell Biol. 2004. PMID: 15070402 Free PMC article.

10

MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during development.

Buchner G, Montini E, Andolfi G, Quaderi N, Cainarca S, Messali S, Bassi MT, Ballabio A, Meroni G, Franco B. Buchner G, et al. Among authors: meroni g. Hum Mol Genet. 1999 Aug;8(8):1397-407. doi: 10.1093/hmg/8.8.1397. Hum Mol Genet. 1999. PMID: 10400986

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