Merello E - Search Results

1

Hypoxia transcriptionally induces macrophage-inflammatory protein-3alpha/CCL-20 in primary human mononuclear phagocytes through nuclear factor (NF)-kappaB.

Battaglia F, Delfino S, Merello E, Puppo M, Piva R, Varesio L, Bosco MC. Battaglia F, et al. Among authors: merello e. J Leukoc Biol. 2008 Mar;83(3):648-62. doi: 10.1189/jlb.0607349. Epub 2007 Dec 18. J Leukoc Biol. 2008. PMID: 18089854

2

Induction of macrophage glutamine: fructose-6-phosphate amidotransferase expression by hypoxia and by picolinic acid.

Manzari B, Kudlow JE, Fardin P, Merello E, Ottaviano C, Puppo M, Eva A, Varesio L. Manzari B, et al. Among authors: merello e. Int J Immunopathol Pharmacol. 2007 Jan-Mar;20(1):47-58. doi: 10.1177/039463200702000106. Int J Immunopathol Pharmacol. 2007. PMID: 17346427 Free article.

3

The tumor suppressor hamartin enhances Dbl protein transforming activity through interaction with ezrin.

Ognibene M, Vanni C, Segalerba D, Mancini P, Merello E, Torrisi MR, Bosco MC, Varesio L, Eva A. Ognibene M, et al. Among authors: merello e. J Biol Chem. 2011 Aug 26;286(34):29973-83. doi: 10.1074/jbc.M111.270785. Epub 2011 Jun 28. J Biol Chem. 2011. PMID: 21712385 Free PMC article.

4

Galpha13 regulation of proto-Dbl signaling.

Vanni C, Mancini P, Ottaviano C, Ognibene M, Parodi A, Merello E, Russo C, Varesio L, Zheng Y, Torrisi MR, Eva A. Vanni C, et al. Among authors: merello e. Cell Cycle. 2007 Aug 15;6(16):2058-70. doi: 10.4161/cc.6.16.4574. Epub 2007 Jun 8. Cell Cycle. 2007. PMID: 17721084

5

Rare deleterious variants in GRHL3 are associated with human spina bifida.

Lemay P, De Marco P, Emond A, Spiegelman D, Dionne-Laporte A, Laurent S, Merello E, Accogli A, Rouleau GA, Capra V, Kibar Z. Lemay P, et al. Among authors: merello e. Hum Mutat. 2017 Jun;38(6):716-724. doi: 10.1002/humu.23214. Epub 2017 Mar 24. Hum Mutat. 2017. PMID: 28276201

6

Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population.

De Marco P, Calevo MG, Moroni A, Arata L, Merello E, Finnell RH, Zhu H, Andreussi L, Cama A, Capra V. De Marco P, et al. Among authors: merello e. J Hum Genet. 2002;47(6):319-24. doi: 10.1007/s100380200043. J Hum Genet. 2002. PMID: 12111380

7

Mutational screening of the CYP26A1 gene in patients with caudal regression syndrome.

De Marco P, Merello E, Mascelli S, Raso A, Santamaria A, Ottaviano C, Calevo MG, Cama A, Capra V. De Marco P, et al. Among authors: merello e. Birth Defects Res A Clin Mol Teratol. 2006 Feb;76(2):86-95. doi: 10.1002/bdra.20225. Birth Defects Res A Clin Mol Teratol. 2006. PMID: 16463413

8

Brainstem anomalies in two patients affected by congenital central hypoventilation syndrome.

Bachetti T, Robbiano A, Parodi S, Matera I, Merello E, Capra V, Baglietto MP, Rossi A, Ceccherini I, Ottonello G. Bachetti T, et al. Among authors: merello e. Am J Respir Crit Care Med. 2006 Sep 15;174(6):706-9. doi: 10.1164/rccm.200602-266CR. Epub 2006 Jun 8. Am J Respir Crit Care Med. 2006. PMID: 16763219

9

No major role for the EMX2 gene in schizencephaly.

Merello E, Swanson E, De Marco P, Akhter M, Striano P, Rossi A, Cama A, Leventer RJ, Guerrini R, Capra V, Dobyns WB. Merello E, et al. Am J Med Genet A. 2008 May 1;146A(9):1142-50. doi: 10.1002/ajmg.a.32264. Am J Med Genet A. 2008. PMID: 18409201

10

Evaluation of a methylenetetrahydrofolate-dehydrogenase 1958G>A polymorphism for neural tube defect risk.

De Marco P, Merello E, Calevo MG, Mascelli S, Raso A, Cama A, Capra V. De Marco P, et al. Among authors: merello e. J Hum Genet. 2006;51(2):98-103. doi: 10.1007/s10038-005-0329-6. Epub 2005 Nov 29. J Hum Genet. 2006. PMID: 16315005

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