Napolitano LM - Search Results

1

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: napolitano lm. 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.

2

TRIM family: Pleiotropy and diversification through homomultimer and heteromultimer formation.

Napolitano LM, Meroni G. Napolitano LM, et al. IUBMB Life. 2012 Jan;64(1):64-71. doi: 10.1002/iub.580. Epub 2011 Nov 30. IUBMB Life. 2012. PMID: 22131136 Free article. Review.

3

The E3 ubiquitin ligase MID1/TRIM18 promotes atypical ubiquitination of the BRCA2-associated factor 35, BRAF35.

Zanchetta ME, Napolitano LMR, Maddalo D, Meroni G. Zanchetta ME, et al. Biochim Biophys Acta Mol Cell Res. 2017 Oct;1864(10):1844-1854. doi: 10.1016/j.bbamcr.2017.07.014. Epub 2017 Jul 29. Biochim Biophys Acta Mol Cell Res. 2017. PMID: 28760657 Free article.

4

Functional interactions between ubiquitin E2 enzymes and TRIM proteins.

Napolitano LM, Jaffray EG, Hay RT, Meroni G. Napolitano LM, et al. Biochem J. 2011 Mar 1;434(2):309-19. doi: 10.1042/BJ20101487. Biochem J. 2011. PMID: 21143188

5

Lack of Mid1, the mouse ortholog of the Opitz syndrome gene, causes abnormal development of the anterior cerebellar vermis.

Lancioni A, Pizzo M, Fontanella B, Ferrentino R, Napolitano LM, De Leonibus E, Meroni G. Lancioni A, et al. Among authors: napolitano lm. J Neurosci. 2010 Feb 24;30(8):2880-7. doi: 10.1523/JNEUROSCI.4196-09.2010. J Neurosci. 2010. PMID: 20181585 Free PMC article.

6

TRIM27 negatively regulates NOD2 by ubiquitination and proteasomal degradation.

Zurek B, Schoultz I, Neerincx A, Napolitano LM, Birkner K, Bennek E, Sellge G, Lerm M, Meroni G, Söderholm JD, Kufer TA. Zurek B, et al. Among authors: napolitano lm. PLoS One. 2012;7(7):e41255. doi: 10.1371/journal.pone.0041255. Epub 2012 Jul 19. PLoS One. 2012. PMID: 22829933 Free PMC article.

7

Two further patients with Warsaw breakage syndrome. Is a mild phenotype possible?

Bottega R, Napolitano LMR, Carbone A, Cappelli E, Corsolini F, Onesti S, Savoia A, Gasparini P, Faletra F. Bottega R, et al. Mol Genet Genomic Med. 2019 May;7(5):e639. doi: 10.1002/mgg3.639. Epub 2019 Mar 28. Mol Genet Genomic Med. 2019. PMID: 30924321 Free PMC article.

8

Combining FRET and optical tweezers to study RhoGTPases spatio-temporal dynamics upon local stimulation.

Iseppon F, Napolitano LM, Torre V, Cojoc D. Iseppon F, et al. Among authors: napolitano lm. J Biol Methods. 2017 Mar 7;4(1):e65. doi: 10.14440/jbm.2017.159. eCollection 2017. J Biol Methods. 2017. PMID: 31453225 Free PMC article.

9

Genomic integrity and mitochondrial metabolism defects in Warsaw syndrome cells: a comparison with Fanconi anemia.

Bottega R, Ravera S, Napolitano LMR, Chiappetta V, Zini N, Crescenzi B, Arniani S, Faleschini M, Cortone G, Faletra F, Medagli B, Sirchia F, Moretti M, de Lange J, Cappelli E, Mecucci C, Onesti S, Pisani FM, Savoia A. Bottega R, et al. J Cell Physiol. 2021 Aug;236(8):5664-5675. doi: 10.1002/jcp.30265. Epub 2021 Jan 11. J Cell Physiol. 2021. PMID: 33432587 Free article.

10

Molecular and Cellular Functions of the Warsaw Breakage Syndrome DNA Helicase DDX11.

Pisani FM, Napolitano E, Napolitano LMR, Onesti S. Pisani FM, et al. Genes (Basel). 2018 Nov 21;9(11):564. doi: 10.3390/genes9110564. Genes (Basel). 2018. PMID: 30469382 Free PMC article. Review.

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