Russo R - Search Results

1

Mitapivat reprograms the RBC metabolome and improves anemia in a mouse model of hereditary spherocytosis.

Matte A, Wilson AB, Gevi F, Federti E, Recchiuti A, Ferri G, Brunati AM, Pagano MA, Russo R, Leboeuf C, Janin A, Timperio AM, Iolascon A, Gremese E, Dang L, Mohandas N, Brugnara C, De Franceschi L. Matte A, et al. Among authors: russo r. JCI Insight. 2023 Oct 23;8(20):e172656. doi: 10.1172/jci.insight.172656. JCI Insight. 2023. PMID: 37676741 Free PMC article.

2

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: russo r. 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.

3

A predicted functional single-nucleotide polymorphism of bone morphogenetic protein-4 gene affects mRNA expression and shows a significant association with cutaneous melanoma in Southern Italian population.

Capasso M, Ayala F, Russo R, Avvisati RA, Asci R, Iolascon A. Capasso M, et al. Among authors: russo r. J Cancer Res Clin Oncol. 2009 Dec;135(12):1799-807. doi: 10.1007/s00432-009-0628-y. Epub 2009 Jun 26. J Cancer Res Clin Oncol. 2009. PMID: 19557432

4

[Pharmacogenomics and pharmacogenetics: individual genetic profile and pharmacological response].

Iolascon A, Russo R, Capasso M. Iolascon A, et al. Among authors: russo r. Minerva Pediatr. 2009 Dec;61(6):615-7. Minerva Pediatr. 2009. PMID: 19935509 Italian. No abstract available.

5

Regulation of divalent metal transporter 1 (DMT1) non-IRE isoform by the microRNA Let-7d in erythroid cells.

Andolfo I, De Falco L, Asci R, Russo R, Colucci S, Gorrese M, Zollo M, Iolascon A. Andolfo I, et al. Among authors: russo r. Haematologica. 2010 Aug;95(8):1244-52. doi: 10.3324/haematol.2009.020685. Epub 2010 Apr 21. Haematologica. 2010. PMID: 20410187 Free PMC article.

6

MDM2 SNP309 and p53 Arg72Pro in cutaneous melanoma: association between SNP309 GG genotype and tumor Breslow thickness.

Capasso M, Ayala F, Avvisati RA, Russo R, Gambale A, Mozzillo N, Ascierto PA, Iolascon A. Capasso M, et al. Among authors: russo r. J Hum Genet. 2010 Aug;55(8):518-24. doi: 10.1038/jhg.2010.62. Epub 2010 Jun 10. J Hum Genet. 2010. PMID: 20535124

7

Mutational spectrum in congenital dyserythropoietic anemia type II: identification of 19 novel variants in SEC23B gene.

Russo R, Esposito MR, Asci R, Gambale A, Perrotta S, Ramenghi U, Forni GL, Uygun V, Delaunay J, Iolascon A. Russo R, et al. Am J Hematol. 2010 Dec;85(12):915-20. doi: 10.1002/ajh.21866. Am J Hematol. 2010. PMID: 20941788 Free PMC article.

8

Pediatric pharmacogenetic and pharmacogenomic studies: the current state and future perspectives.

Russo R, Capasso M, Paolucci P, Iolascon A; TEDDY European Network of Excellence. Russo R, et al. Eur J Clin Pharmacol. 2011 May;67 Suppl 1:17-27. doi: 10.1007/s00228-010-0931-1. Epub 2010 Nov 11. Eur J Clin Pharmacol. 2011. PMID: 21069522 Review.

9

A dyserythropoietic anemia associated with homozygous Hb Plasencia [α125(H8)Leu→Arg (α2)] (HBA2:c.377T>G), a variant with an unstable α chain.

Garçon L, Iolascon A, Pissard S, Esposito MR, Russo R, Fenneteau O, Fénéant-Thibault M, Heimpel H, Delaunay J. Garçon L, et al. Among authors: russo r. Hemoglobin. 2010;34(6):576-81. doi: 10.3109/03630269.2010.526922. Hemoglobin. 2010. PMID: 21077766

10

Congenital dyserythropoietic anemias.

Iolascon A, Russo R, Delaunay J. Iolascon A, et al. Among authors: russo r. Curr Opin Hematol. 2011 May;18(3):146-51. doi: 10.1097/MOH.0b013e32834521b0. Curr Opin Hematol. 2011. PMID: 21378561 Review.

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