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Items: 36

1.

Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases.

Grassi L, Alfonsi R, Francescangeli F, Signore M, De Angelis ML, Addario A, Costantini M, Flex E, Ciolfi A, Pizzi S, Bruselles A, Pallocca M, Simone G, Haoui M, Falchi M, Milella M, Sentinelli S, Di Matteo P, Stellacci E, Gallucci M, Muto G, Tartaglia M, De Maria R, Bonci D.

Cell Death Dis. 2019 Feb 27;10(3):201. doi: 10.1038/s41419-019-1453-0.

2.

Clinical and functional characterization of two novel ZBTB20 mutations causing Primrose syndrome.

Stellacci E, Steindl K, Joset P, Mercurio L, Anselmi M, Cecchetti S, Gogoll L, Zweier M, Hackenberg A, Bocchinfuso G, Stella L, Tartaglia M, Rauch A.

Hum Mutat. 2018 Jul;39(7):959-964. doi: 10.1002/humu.23546. Epub 2018 May 17.

PMID:
29737001
3.

Aberrant HRAS transcript processing underlies a distinctive phenotype within the RASopathy clinical spectrum.

Pantaleoni F, Lev D, Cirstea IC, Motta M, Lepri FR, Bottero L, Cecchetti S, Linger I, Paolacci S, Flex E, Novelli A, Carè A, Ahmadian MR, Stellacci E, Tartaglia M.

Hum Mutat. 2017 Jul;38(7):798-804. doi: 10.1002/humu.23224. Epub 2017 May 3.

PMID:
28390077
4.

Congenital immunodeficiency in an individual with Wiedemann-Steiner syndrome due to a novel missense mutation in KMT2A.

Stellacci E, Onesimo R, Bruselles A, Pizzi S, Battaglia D, Leoni C, Zampino G, Tartaglia M.

Am J Med Genet A. 2016 Sep;170(9):2389-93. doi: 10.1002/ajmg.a.37681. Epub 2016 Jun 20. Review.

PMID:
27320412
5.

Molecular Diversity and Associated Phenotypic Spectrum of Germline CBL Mutations.

Martinelli S, Stellacci E, Pannone L, D'Agostino D, Consoli F, Lissewski C, Silvano M, Cencelli G, Lepri F, Maitz S, Pauli S, Rauch A, Zampino G, Selicorni A, Melançon S, Digilio MC, Gelb BD, De Luca A, Dallapiccola B, Zenker M, Tartaglia M.

Hum Mutat. 2015 Aug;36(8):787-96. doi: 10.1002/humu.22809. Epub 2015 Jun 1.

6.

Mutations Impairing GSK3-Mediated MAF Phosphorylation Cause Cataract, Deafness, Intellectual Disability, Seizures, and a Down Syndrome-like Facies.

Niceta M, Stellacci E, Gripp KW, Zampino G, Kousi M, Anselmi M, Traversa A, Ciolfi A, Stabley D, Bruselles A, Caputo V, Cecchetti S, Prudente S, Fiorenza MT, Boitani C, Philip N, Niyazov D, Leoni C, Nakane T, Keppler-Noreuil K, Braddock SR, Gillessen-Kaesbach G, Palleschi A, Campeau PM, Lee BH, Pouponnot C, Stella L, Bocchinfuso G, Katsanis N, Sol-Church K, Tartaglia M.

Am J Hum Genet. 2015 May 7;96(5):816-25. doi: 10.1016/j.ajhg.2015.03.001. Epub 2015 Apr 9.

7.

Mutations in ZBTB20 cause Primrose syndrome.

Cordeddu V, Redeker B, Stellacci E, Jongejan A, Fragale A, Bradley TE, Anselmi M, Ciolfi A, Cecchetti S, Muto V, Bernardini L, Azage M, Carvalho DR, Espay AJ, Male A, Molin AM, Posmyk R, Battisti C, Casertano A, Melis D, van Kampen A, Baas F, Mannens MM, Bocchinfuso G, Stella L, Tartaglia M, Hennekam RC.

Nat Genet. 2014 Aug;46(8):815-7. doi: 10.1038/ng.3035. Epub 2014 Jul 13.

PMID:
25017102
8.

Activating mutations in RRAS underlie a phenotype within the RASopathy spectrum and contribute to leukaemogenesis.

Flex E, Jaiswal M, Pantaleoni F, Martinelli S, Strullu M, Fansa EK, Caye A, De Luca A, Lepri F, Dvorsky R, Pannone L, Paolacci S, Zhang SC, Fodale V, Bocchinfuso G, Rossi C, Burkitt-Wright EM, Farrotti A, Stellacci E, Cecchetti S, Ferese R, Bottero L, Castro S, Fenneteau O, Brethon B, Sanchez M, Roberts AE, Yntema HG, Van Der Burgt I, Cianci P, Bondeson ML, Cristina Digilio M, Zampino G, Kerr B, Aoki Y, Loh ML, Palleschi A, Di Schiavi E, Carè A, Selicorni A, Dallapiccola B, Cirstea IC, Stella L, Zenker M, Gelb BD, Cavé H, Ahmadian MR, Tartaglia M.

Hum Mol Genet. 2014 Aug 15;23(16):4315-27. doi: 10.1093/hmg/ddu148. Epub 2014 Apr 4.

9.

Mutations in PAX2 associate with adult-onset FSGS.

Barua M, Stellacci E, Stella L, Weins A, Genovese G, Muto V, Caputo V, Toka HR, Charoonratana VT, Tartaglia M, Pollak MR.

J Am Soc Nephrol. 2014 Sep;25(9):1942-53. doi: 10.1681/ASN.2013070686. Epub 2014 Mar 27.

10.

A mutation in PAK3 with a dual molecular effect deregulates the RAS/MAPK pathway and drives an X-linked syndromic phenotype.

Magini P, Pippucci T, Tsai IC, Coppola S, Stellacci E, Bartoletti-Stella A, Turchetti D, Graziano C, Cenacchi G, Neri I, Cordelli DM, Marchiani V, Bergamaschi R, Gasparre G, Neri G, Mazzanti L, Patrizi A, Franzoni E, Romeo G, Bordo D, Tartaglia M, Katsanis N, Seri M.

Hum Mol Genet. 2014 Jul 1;23(13):3607-17. doi: 10.1093/hmg/ddu070. Epub 2014 Feb 19.

PMID:
24556213
11.

IκB kinase ε targets interferon regulatory factor 1 in activated T lymphocytes.

Sgarbanti M, Marsili G, Remoli AL, Stellacci E, Mai A, Rotili D, Perrotti E, Acchioni C, Orsatti R, Iraci N, Ferrari M, Borsetti A, Hiscott J, Battistini A.

Mol Cell Biol. 2014 Mar;34(6):1054-65. doi: 10.1128/MCB.01161-13. Epub 2014 Jan 6.

12.

Loss of CBL E3-ligase activity in B-lineage childhood acute lymphoblastic leukaemia.

Martinelli S, Checquolo S, Consoli F, Stellacci E, Rossi C, Silvano M, Franciosa G, Flex E, Cossu C, De Luca A, Foà R, Cazzaniga G, Biondi A, Screpanti I, Tartaglia M.

Br J Haematol. 2012 Oct;159(1):115-9. doi: 10.1111/j.1365-2141.2012.09245.x. Epub 2012 Jul 27. No abstract available.

PMID:
22834886
13.

An integrated approach identifies IFN-regulated microRNAs and targeted mRNAs modulated by different HCV replicon clones.

Bruni R, Marcantonio C, Tritarelli E, Tataseo P, Stellacci E, Costantino A, Villano U, Battistini A, Ciccaglione AR.

BMC Genomics. 2011 Oct 4;12:485. doi: 10.1186/1471-2164-12-485.

14.

Human papillomavirus type 16 E5 protein induces expression of beta interferon through interferon regulatory factor 1 in human keratinocytes.

Muto V, Stellacci E, Lamberti AG, Perrotti E, Carrabba A, Matera G, Sgarbanti M, Battistini A, Liberto MC, Focà A.

J Virol. 2011 May;85(10):5070-80. doi: 10.1128/JVI.02114-10. Epub 2011 Mar 9.

15.

Critical role of IRF-8 in negative regulation of TLR3 expression by Src homology 2 domain-containing protein tyrosine phosphatase-2 activity in human myeloid dendritic cells.

Fragale A, Stellacci E, Ilari R, Remoli AL, Lanciotti A, Perrotti E, Shytaj I, Orsatti R, Lawrence HR, Lawrence NJ, Wu J, Rehli M, Ozato K, Battistini A.

J Immunol. 2011 Feb 15;186(4):1951-62. doi: 10.4049/jimmunol.1000918. Epub 2011 Jan 10.

16.

Heterozygous germline mutations in the CBL tumor-suppressor gene cause a Noonan syndrome-like phenotype.

Martinelli S, De Luca A, Stellacci E, Rossi C, Checquolo S, Lepri F, Caputo V, Silvano M, Buscherini F, Consoli F, Ferrara G, Digilio MC, Cavaliere ML, van Hagen JM, Zampino G, van der Burgt I, Ferrero GB, Mazzanti L, Screpanti I, Yntema HG, Nillesen WM, Savarirayan R, Zenker M, Dallapiccola B, Gelb BD, Tartaglia M.

Am J Hum Genet. 2010 Aug 13;87(2):250-7. doi: 10.1016/j.ajhg.2010.06.015. Epub 2010 Jul 8.

17.

Interaction between the glucocorticoid and erythropoietin receptors in human erythroid cells.

Stellacci E, Di Noia A, Di Baldassarre A, Migliaccio G, Battistini A, Migliaccio AR.

Exp Hematol. 2009 May;37(5):559-72. doi: 10.1016/j.exphem.2009.02.005.

18.

IFN regulatory factor-1 negatively regulates CD4+ CD25+ regulatory T cell differentiation by repressing Foxp3 expression.

Fragale A, Gabriele L, Stellacci E, Borghi P, Perrotti E, Ilari R, Lanciotti A, Remoli AL, Venditti M, Belardelli F, Battistini A.

J Immunol. 2008 Aug 1;181(3):1673-82.

19.

IRF-1 is required for full NF-kappaB transcriptional activity at the human immunodeficiency virus type 1 long terminal repeat enhancer.

Sgarbanti M, Remoli AL, Marsili G, Ridolfi B, Borsetti A, Perrotti E, Orsatti R, Ilari R, Sernicola L, Stellacci E, Ensoli B, Battistini A.

J Virol. 2008 Apr;82(7):3632-41. doi: 10.1128/JVI.00599-07. Epub 2008 Jan 23.

20.

Repression of interferon regulatory factor 1 by hepatitis C virus core protein results in inhibition of antiviral and immunomodulatory genes.

Ciccaglione AR, Stellacci E, Marcantonio C, Muto V, Equestre M, Marsili G, Rapicetta M, Battistini A.

J Virol. 2007 Jan;81(1):202-14. Epub 2006 Oct 18.

21.

IRF-1 deficiency skews the differentiation of dendritic cells toward plasmacytoid and tolerogenic features.

Gabriele L, Fragale A, Borghi P, Sestili P, Stellacci E, Venditti M, Schiavoni G, Sanchez M, Belardelli F, Battistini A.

J Leukoc Biol. 2006 Dec;80(6):1500-11. Epub 2006 Sep 11.

PMID:
16966383
22.

Analysis of the signal transduction pathway leading to human immunodeficiency virus-1-induced interferon regulatory factor-1 upregulation.

Sgarbanti M, Marsili G, Remoli AL, Ridolfi B, Stellacci E, Borsetti A, Ensoli B, Battistini A.

Ann N Y Acad Sci. 2004 Dec;1030:187-95.

PMID:
15659797
23.

Expression of signal transduction proteins during the differentiation of primary human erythroblasts.

di Giacomo V, Matteucci A, Stellacci E, Battistini A, Di Baldassarre A, Capitani S, Alfani E, Migliaccio AR, Cocco L, Migliaccio G.

J Cell Physiol. 2005 Mar;202(3):831-8.

PMID:
15389562
24.

Impaired myelopoiesis in mice devoid of interferon regulatory factor 1.

Testa U, Stellacci E, Pelosi E, Sestili P, Venditti M, Orsatti R, Fragale A, Petrucci E, Pasquini L, Belardelli F, Gabriele L, Battistini A.

Leukemia. 2004 Nov;18(11):1864-71.

PMID:
15385939
25.

On the role of interferon regulatory factors in HIV-1 replication.

Marsili G, Borsetti A, Sgarbanti M, Remoli AL, Ridolfi B, Stellacci E, Ensoli B, Battistini A.

Ann N Y Acad Sci. 2003 Dec;1010:29-42. Review.

PMID:
15033691
26.

Interferon regulatory factor-2 drives megakaryocytic differentiation.

Stellacci E, Testa U, Petrucci E, Benedetti E, Orsatti R, Feccia T, Stafsnes M, Coccia EM, Marziali G, Battistini A.

Biochem J. 2004 Jan 15;377(Pt 2):367-78.

27.

Elevated expression of IL-3Ralpha in acute myelogenous leukemia is associated with enhanced blast proliferation, increased cellularity, and poor prognosis.

Testa U, Riccioni R, Militi S, Coccia E, Stellacci E, Samoggia P, Latagliata R, Mariani G, Rossini A, Battistini A, Lo-Coco F, Peschle C.

Blood. 2002 Oct 15;100(8):2980-8.

28.

Protein inhibitor of activated signal transducer and activator of transcription (STAT)-1 (PIAS-1) regulates the IFN-gamma response in macrophage cell lines.

Coccia EM, Stellacci E, Orsatti R, Benedetti E, Giacomini E, Marziali G, Valdez BC, Battistini A.

Cell Signal. 2002 Jun;14(6):537-45.

PMID:
11897494
29.

Ectopic expression of interferon regulatory factor-1 potentiates granulocytic differentiation.

Coccia EM, Stellacci E, Valtieri M, Masella B, Feccia T, Marziali G, Hiscott J, Testa U, Peschle C, Battistini A.

Biochem J. 2001 Dec 1;360(Pt 2):285-94.

30.

IFN-gamma and IL-4 differently regulate inducible NO synthase gene expression through IRF-1 modulation.

Coccia EM, Stellacci E, Marziali G, Weiss G, Battistini A.

Int Immunol. 2000 Jul;12(7):977-85.

PMID:
10882409
31.

STAT1 activation during monocyte to macrophage maturation: role of adhesion molecules.

Coccia EM, Del Russo N, Stellacci E, Testa U, Marziali G, Battistini A.

Int Immunol. 1999 Jul;11(7):1075-83.

PMID:
10383940
32.

Activation and repression of the 2-5A synthetase and p21 gene promoters by IRF-1 and IRF-2.

Coccia EM, Del Russo N, Stellacci E, Orsatti R, Benedetti E, Marziali G, Hiscott J, Battistini A.

Oncogene. 1999 Mar 25;18(12):2129-37.

33.

Regulation of expression of ferritin H-chain and transferrin receptor by protoporphyrin IX.

Coccia EM, Perrotti E, Stellacci E, Orsatti R, Del Russo N, Marziali G, Testa U, Battistini A.

Eur J Biochem. 1997 Dec 15;250(3):764-72.

34.

Regulation of ferritin H-chain expression in differentiating Friend leukemia cells.

Coccia EM, Stellacci E, Orsatti R, Testa U, Battistini A.

Blood. 1995 Aug 15;86(4):1570-9.

35.

Cells resistant to interferon-beta respond to interferon-gamma via the Stat1-IRF-1 pathway.

Coccia EM, Marziali G, Stellacci E, Perrotti E, Ilari R, Orsatti R, Battistini A.

Virology. 1995 Aug 1;211(1):113-22.

36.

Differential regulation of ferritin expression in Friend leukemia cells by iron compounds.

Coccia EM, Stellacci E, Perrotti E, Marziali G, Battistini A.

J Biol Regul Homeost Agents. 1994 Jul-Sep;8(3):81-7.

PMID:
7754793

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