Romeo G - Search Results

1

The netrin-1 receptors UNC5H are putative tumor suppressors controlling cell death commitment.

Thiebault K, Mazelin L, Pays L, Llambi F, Joly MO, Scoazec JY, Saurin JC, Romeo G, Mehlen P. Thiebault K, et al. Among authors: romeo g. Proc Natl Acad Sci U S A. 2003 Apr 1;100(7):4173-8. doi: 10.1073/pnas.0738063100. Epub 2003 Mar 24. Proc Natl Acad Sci U S A. 2003. PMID: 12655055 Free PMC article.

2

Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma.

Gasparre G, Hervouet E, de Laplanche E, Demont J, Pennisi LF, Colombel M, Mège-Lechevallier F, Scoazec JY, Bonora E, Smeets R, Smeitink J, Lazar V, Lespinasse J, Giraud S, Godinot C, Romeo G, Simonnet H. Gasparre G, et al. Among authors: romeo g. Hum Mol Genet. 2008 Apr 1;17(7):986-95. doi: 10.1093/hmg/ddm371. Epub 2007 Dec 21. Hum Mol Genet. 2008. PMID: 18156159

3

Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors.

Gasparre G, Porcelli AM, Bonora E, Pennisi LF, Toller M, Iommarini L, Ghelli A, Moretti M, Betts CM, Martinelli GN, Ceroni AR, Curcio F, Carelli V, Rugolo M, Tallini G, Romeo G. Gasparre G, et al. Among authors: romeo g. Proc Natl Acad Sci U S A. 2007 May 22;104(21):9001-6. doi: 10.1073/pnas.0703056104. Epub 2007 May 15. Proc Natl Acad Sci U S A. 2007. PMID: 17517629 Free PMC article.

4

Genome-wide search for loss of heterozygosity in Burkitt lymphoma cell lines.

Sobol H, Benziane A, Kerangueven F, Yin L, Noguchi T, Pauly S, Eisinger F, Longy M, Romeo G, Lenoir G, Birnbaum D. Sobol H, et al. Among authors: romeo g. Genes Chromosomes Cancer. 2002 Feb;33(2):217-24. doi: 10.1002/gcc.10022. Genes Chromosomes Cancer. 2002. PMID: 11793449

5

A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman.

Palombo F, Al-Wardy N, Ruscone GA, Oppo M, Kindi MN, Angius A, Al Lamki K, Girotto G, Giangregorio T, Benelli M, Magi A, Seri M, Gasparini P, Cucca F, Sazzini M, Al Khabori M, Pippucci T, Romeo G. Palombo F, et al. Among authors: romeo g. J Hum Genet. 2017 Feb;62(2):259-264. doi: 10.1038/jhg.2016.120. Epub 2016 Oct 13. J Hum Genet. 2017. PMID: 27734841

6

Heterogeneity of mRNA expression in Italian fucosidosis patients.

Guazzi S, Persici P, Gatti R, Durand P, O'Brien JS, Romeo G. Guazzi S, et al. Among authors: romeo g. Hum Genet. 1989 Apr;82(1):63-6. doi: 10.1007/BF00288274. Hum Genet. 1989. PMID: 2565868

7

Genotype-phenotype correlation and germline mosaicism in DMD/BMD patients with deletions of the dystrophin gene.

Covone AE, Lerone M, Romeo G. Covone AE, et al. Among authors: romeo g. Hum Genet. 1991 Jul;87(3):353-60. doi: 10.1007/BF00200919. Hum Genet. 1991. PMID: 1864612

8

Impairment of capping in lymphoblastoid cell lines of Duchenne patients indicates an intrinsic cellular defect.

Baricordi OR, Sensi A, Balboni A, Romeo G, Rocchi M, Melchiorri L, Gandini E. Baricordi OR, et al. Among authors: romeo g. Hum Genet. 1989 Oct;83(3):217-9. doi: 10.1007/BF00285158. Hum Genet. 1989. PMID: 2793164

9

Interstitial deletion of the endothelin-B receptor gene in the spotting lethal (sl) rat.

Ceccherini I, Zhang AL, Matera I, Yang G, Devoto M, Romeo G, Cass DT. Ceccherini I, et al. Among authors: romeo g. Hum Mol Genet. 1995 Nov;4(11):2089-96. doi: 10.1093/hmg/4.11.2089. Hum Mol Genet. 1995. PMID: 8589685

10

Estimating the allele frequency of autosomal recessive disorders through mutational records and consanguinity: the Homozygosity Index (HI).

Gialluisi A, Pippucci T, Anikster Y, Ozbek U, Medlej-Hashim M, Mégarbané A, Romeo G. Gialluisi A, et al. Among authors: romeo g. Ann Hum Genet. 2012 Mar;76(2):159-67. doi: 10.1111/j.1469-1809.2011.00693.x. Epub 2011 Dec 21. Ann Hum Genet. 2012. PMID: 22188137

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