Andolfo I - Search Results

1

Proteome alterations in erythrocytes with PIEZO1 gain-of-function mutations.

Andolfo I, Monaco V, Cozzolino F, Rosato BE, Marra R, Cerbone V, Pinto VM, Forni GL, Unal S, Iolascon A, Monti M, Russo R. Andolfo I, et al. Blood Adv. 2023 Jun 27;7(12):2681-2693. doi: 10.1182/bloodadvances.2022008673. Blood Adv. 2023. PMID: 36595486 Free PMC article.

2

Identification of ALK germline mutation (3605delG) in pediatric anaplastic medulloblastoma.

Coco S, De Mariano M, Valdora F, Servidei T, Ridola V, Andolfo I, Oberthuer A, Tonini GP, Longo L. Coco S, et al. Among authors: andolfo i. J Hum Genet. 2012 Oct;57(10):682-4. doi: 10.1038/jhg.2012.87. Epub 2012 Jul 19. J Hum Genet. 2012. PMID: 22810114

3

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. Haematologica. 2010 Aug;95(8):1244-52. doi: 10.3324/haematol.2009.020685. Epub 2010 Apr 21. Haematologica. 2010. PMID: 20410187 Free PMC article.

4

Detection of erbB2 copy number variations in plasma of patients with esophageal carcinoma.

Andolfo I, Petrosino G, Vecchione L, De Antonellis P, Capasso M, Montanaro D, Gemei M, Troncone G, Iolascon A, Orditura M, Ciardiello F, De Vita F, Zollo M. Andolfo I, et al. BMC Cancer. 2011 Apr 11;11:126. doi: 10.1186/1471-2407-11-126. BMC Cancer. 2011. PMID: 21481261 Free PMC article.

5

The metallophosphodiesterase Mpped2 impairs tumorigenesis in neuroblastoma.

Liguori L, Andolfo I, de Antonellis P, Aglio V, di Dato V, Marino N, Orlotti NI, De Martino D, Capasso M, Petrosino G, Schramm A, Navas L, Tonini GP, Eggert A, Iolascon A, Zollo M. Liguori L, et al. Among authors: andolfo i. Cell Cycle. 2012 Feb 1;11(3):569-81. doi: 10.4161/cc.11.3.19063. Epub 2012 Feb 1. Cell Cycle. 2012. PMID: 22262177

6

The micro-RNA 199b-5p regulatory circuit involves Hes1, CD15, and epigenetic modifications in medulloblastoma.

Andolfo I, Liguori L, De Antonellis P, Cusanelli E, Marinaro F, Pistollato F, Garzia L, De Vita G, Petrosino G, Accordi B, Migliorati R, Basso G, Iolascon A, Cinalli G, Zollo M. Andolfo I, et al. Neuro Oncol. 2012 May;14(5):596-612. doi: 10.1093/neuonc/nos002. Epub 2012 Mar 12. Neuro Oncol. 2012. PMID: 22411914 Free PMC article.

7

Missense mutations in the ABCB6 transporter cause dominant familial pseudohyperkalemia.

Andolfo I, Alper SL, Delaunay J, Auriemma C, Russo R, Asci R, Esposito MR, Sharma AK, Shmukler BE, Brugnara C, De Franceschi L, Iolascon A. Andolfo I, et al. Am J Hematol. 2013 Jan;88(1):66-72. doi: 10.1002/ajh.23357. Epub 2012 Nov 24. Am J Hematol. 2013. PMID: 23180570 Free article.

8

Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1.

Andolfo I, Alper SL, De Franceschi L, Auriemma C, Russo R, De Falco L, Vallefuoco F, Esposito MR, Vandorpe DH, Shmukler BE, Narayan R, Montanaro D, D'Armiento M, Vetro A, Limongelli I, Zuffardi O, Glader BE, Schrier SL, Brugnara C, Stewart GW, Delaunay J, Iolascon A. Andolfo I, et al. Blood. 2013 May 9;121(19):3925-35, S1-12. doi: 10.1182/blood-2013-02-482489. Epub 2013 Mar 11. Blood. 2013. PMID: 23479567 Free article.

9

Trasferrin receptor 2 gene regulation by microRNA 221 in SH-SY5Y cells treated with MPP⁺ as Parkinson's disease cellular model.

Asci R, Vallefuoco F, Andolfo I, Bruno M, De Falco L, Iolascon A. Asci R, et al. Among authors: andolfo i. Neurosci Res. 2013 Nov;77(3):121-7. doi: 10.1016/j.neures.2013.09.003. Epub 2013 Sep 17. Neurosci Res. 2013. PMID: 24055409

10

Retrospective cohort study of 205 cases with congenital dyserythropoietic anemia type II: definition of clinical and molecular spectrum and identification of new diagnostic scores.

Russo R, Gambale A, Langella C, Andolfo I, Unal S, Iolascon A. Russo R, et al. Among authors: andolfo i. Am J Hematol. 2014 Oct;89(10):E169-75. doi: 10.1002/ajh.23800. Epub 2014 Jul 22. Am J Hematol. 2014. PMID: 25044164 Free article.

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