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Page 1
Inherited rare variants in homologous recombination and neurodevelopmental genes are associated with increased risk of neuroblastoma.
Bonfiglio F, Lasorsa VA, Cantalupo S, D'Alterio G, Aievola V, Boccia A, Ardito M, Furini S, Renieri A, Morini M, Stainczyk S, Westermann F, Paolella G, Eva A, Iolascon A, Capasso M. Bonfiglio F, et al. Among authors: cantalupo s. EBioMedicine. 2023 Jan;87:104395. doi: 10.1016/j.ebiom.2022.104395. Epub 2022 Dec 6. EBioMedicine. 2023. PMID: 36493725 Free PMC article.
HIF-1 transcription activity: HIF1A driven response in normoxia and in hypoxia.
Cimmino F, Avitabile M, Lasorsa VA, Montella A, Pezone L, Cantalupo S, Visconte F, Corrias MV, Iolascon A, Capasso M. Cimmino F, et al. Among authors: cantalupo s. BMC Med Genet. 2019 Feb 26;20(1):37. doi: 10.1186/s12881-019-0767-1. BMC Med Genet. 2019. PMID: 30808328 Free PMC article.
Exploring Shared Susceptibility between Two Neural Crest Cells Originating Conditions: Neuroblastoma and Congenital Heart Disease.
Testori A, Lasorsa VA, Cimmino F, Cantalupo S, Cardinale A, Avitabile M, Limongelli G, Russo MG, Diskin S, Maris J, Devoto M, Keavney B, Cordell HJ, Iolascon A, Capasso M. Testori A, et al. Among authors: cantalupo s. Genes (Basel). 2019 Aug 30;10(9):663. doi: 10.3390/genes10090663. Genes (Basel). 2019. PMID: 31480262 Free PMC article.
Neural crest-derived tumor neuroblastoma and melanoma share 1p13.2 as susceptibility locus that shows a long-range interaction with the SLC16A1 gene.
Avitabile M, Succoio M, Testori A, Cardinale A, Vaksman Z, Lasorsa VA, Cantalupo S, Esposito M, Cimmino F, Montella A, Formicola D, Koster J, Andreotti V, Ghiorzo P, Romano MF, Staibano S, Scalvenzi M, Ayala F, Hakonarson H, Corrias MV, Devoto M, Law MH, Iles MM, Brown K, Diskin S, Zambrano N, Iolascon A, Capasso M. Avitabile M, et al. Among authors: cantalupo s. Carcinogenesis. 2020 May 14;41(3):284-295. doi: 10.1093/carcin/bgz153. Carcinogenesis. 2020. PMID: 31605138 Free PMC article.
Association of PARP1 polymorphisms with response to chemotherapy in patients with high-risk neuroblastoma.
Avitabile M, Lasorsa VA, Cantalupo S, Cardinale A, Cimmino F, Montella A, Capasso D, Haupt R, Amoroso L, Garaventa A, Quattrone A, Corrias MV, Iolascon A, Capasso M. Avitabile M, et al. Among authors: cantalupo s. J Cell Mol Med. 2020 Apr;24(7):4072-4081. doi: 10.1111/jcmm.15058. Epub 2020 Feb 27. J Cell Mol Med. 2020. PMID: 32103589 Free PMC article.
Genetic Predisposition to Solid Pediatric Cancers.
Capasso M, Montella A, Tirelli M, Maiorino T, Cantalupo S, Iolascon A. Capasso M, et al. Among authors: cantalupo s. Front Oncol. 2020 Oct 28;10:590033. doi: 10.3389/fonc.2020.590033. eCollection 2020. Front Oncol. 2020. PMID: 33194750 Free PMC article. Review.
Common variants at 21q22.3 locus influence MX1 and TMPRSS2 gene expression and susceptibility to severe COVID-19.
Andolfo I, Russo R, Lasorsa VA, Cantalupo S, Rosato BE, Bonfiglio F, Frisso G, Abete P, Cassese GM, Servillo G, Esposito G, Gentile I, Piscopo C, Villani R, Fiorentino G, Cerino P, Buonerba C, Pierri B, Zollo M, Iolascon A, Capasso M. Andolfo I, et al. Among authors: cantalupo s. iScience. 2021 Apr 23;24(4):102322. doi: 10.1016/j.isci.2021.102322. Epub 2021 Mar 17. iScience. 2021. PMID: 33748697 Free PMC article.
Regulatory Noncoding and Predicted Pathogenic Coding Variants of CCR5 Predispose to Severe COVID-19.
Cantalupo S, Lasorsa VA, Russo R, Andolfo I, D'Alterio G, Rosato BE, Frisso G, Abete P, Cassese GM, Servillo G, Gentile I, Piscopo C, Della Monica M, Fiorentino G, Russo G, Cerino P, Buonerba C, Pierri B, Zollo M, Iolascon A, Capasso M. Cantalupo S, et al. Int J Mol Sci. 2021 May 20;22(10):5372. doi: 10.3390/ijms22105372. Int J Mol Sci. 2021. PMID: 34065289 Free PMC article.
38 results