Iolascon A - Search Results

1

Fine mapping of 2q35 high-risk neuroblastoma locus reveals independent functional risk variants and suggests full-length BARD1 as tumor-suppressor.

Cimmino F, Avitabile M, Diskin SJ, Vaksman Z, Pignataro P, Formicola D, Cardinale A, Testori A, Koster J, de Torres C, Devoto M, Maris JM, Iolascon A, Capasso M. Cimmino F, et al. Among authors: iolascon a. Int J Cancer. 2018 Dec 1;143(11):2828-2837. doi: 10.1002/ijc.31822. Epub 2018 Oct 4. Int J Cancer. 2018. PMID: 30132831 Free PMC article.

2

Peculiar allelotype associated with susceptibility to neuroblastoma.

Perri P, Pession A, Mazzocco K, Strigini P, Iolascon A, Basso G, Tonini GP. Perri P, et al. Among authors: iolascon a. Genes Chromosomes Cancer. 1996 Sep;17(1):60-3. doi: 10.1002/(SICI)1098-2264(199609)17:1<60::AID-GCC9>3.0.CO;2-0. Genes Chromosomes Cancer. 1996. PMID: 8889508

3

Restriction fragment length polymorphism analysis reveals different allele frequency and a linkage disequilibrium at locus D1S94 in neuroblastoma patients.

Perri P, Pession A, Mazzocco K, Scaruffi P, Strigini P, Iolascon A, Albergoni MP, Basso G, Tonini GP. Perri P, et al. Among authors: iolascon a. Eur J Cancer. 1997 Oct;33(12):1949-52. doi: 10.1016/s0959-8049(97)00286-4. Eur J Cancer. 1997. PMID: 9516830

4

Neuroblastoma in two siblings supports the role of 1p36 deletion in tumor development.

Lo Cunsolo C, Iolascon A, Cavazzana A, Cusano R, Strigini P, Mazzocco K, Giordani L, Massimo L, De Bernardi B, Conte M, Tonini GP. Lo Cunsolo C, et al. Among authors: iolascon a. Cancer Genet Cytogenet. 1999 Mar;109(2):126-30. doi: 10.1016/s0165-4608(98)00154-x. Cancer Genet Cytogenet. 1999. PMID: 10087945

5

The role of molecular genetics in the pathogenesis and diagnosis of neonatal sepsis.

Del Vecchio A, Laforgia N, Capasso M, Iolascon A, Latini G. Del Vecchio A, et al. Among authors: iolascon a. Clin Perinatol. 2004 Mar;31(1):53-67. doi: 10.1016/j.clp.2004.03.012. Clin Perinatol. 2004. PMID: 15183656 Review.

6

The polymorphisms -318C>T in the promoter and 49A>G in exon 1 of CTLA4 and the risk of aplastic anemia in a Caucasian population.

Svahn J, Capasso M, Lanciotti M, Marrone A, Haupt R, Bacigalupo A, Pongiglione C, Boschetto L, Longoni D, Pillon M, Pistorio A, Di Michele P, Iori AP, Calvillo M, Locasciulli A, Menna G, Riccardi R, Ramenghi U, Dufour C, Iolascon A. Svahn J, et al. Among authors: iolascon a. Bone Marrow Transplant. 2005 Mar;35 Suppl 1:S89-92. doi: 10.1038/sj.bmt.1704855. Bone Marrow Transplant. 2005. PMID: 15812539

7

Microcytic anemia and hepatic iron overload in a child with compound heterozygous mutations in DMT1 (SCL11A2).

Iolascon A, d'Apolito M, Servedio V, Cimmino F, Piga A, Camaschella C. Iolascon A, et al. Blood. 2006 Jan 1;107(1):349-54. doi: 10.1182/blood-2005-06-2477. Epub 2005 Sep 13. Blood. 2006. PMID: 16160008 Free article.

8

Interleukin-10 - 1082 GG polymorphism influences the occurrence and the clinical characteristics of hepatitis C virus infection.

Persico M, Capasso M, Persico E, Masarone M, Renzo Ad, Spano D, Bruno S, Iolascon A. Persico M, et al. Among authors: iolascon a. J Hepatol. 2006 Dec;45(6):779-85. doi: 10.1016/j.jhep.2006.07.026. Epub 2006 Sep 22. J Hepatol. 2006. PMID: 17049666

9

Cytokine gene polymorphisms in Italian preterm infants: association between interleukin-10 -1082 G/A polymorphism and respiratory distress syndrome.

Capasso M, Avvisati RA, Piscopo C, Laforgia N, Raimondi F, de Angelis F, Iolascon A. Capasso M, et al. Among authors: iolascon a. Pediatr Res. 2007 Mar;61(3):313-7. doi: 10.1203/pdr.0b013e318030d108. Pediatr Res. 2007. PMID: 17314689

10

Comparative proteomic expression profile in all-trans retinoic acid differentiated neuroblastoma cell line.

Cimmino F, Spano D, Capasso M, Zambrano N, Russo R, Zollo M, Iolascon A. Cimmino F, et al. Among authors: iolascon a. J Proteome Res. 2007 Jul;6(7):2550-64. doi: 10.1021/pr060701g. Epub 2007 Jun 9. J Proteome Res. 2007. PMID: 17559250 Free article.

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