Cenci T - Search Results

1

Epigenetic alteration of SOCS family members is a possible pathogenetic mechanism in JAK2 wild type myeloproliferative diseases.

Teofili L, Martini M, Cenci T, Guidi F, Torti L, Giona F, Foà R, Leone G, Larocca LM. Teofili L, et al. Among authors: cenci t. Int J Cancer. 2008 Oct 1;123(7):1586-92. doi: 10.1002/ijc.23694. Int J Cancer. 2008. PMID: 18623127

2

Characterization of variants in the promoter of EBV gene BZLF1 in normal donors, HIV-positive patients and in AIDS-related lymphomas.

Martini M, Capello D, Serraino D, Navarra A, Pierconti F, Cenci T, Gaidano G, Larocca LM. Martini M, et al. Among authors: cenci t. J Infect. 2007 Mar;54(3):298-306. doi: 10.1016/j.jinf.2006.04.015. Epub 2006 Jun 19. J Infect. 2007. PMID: 16784778

3

Markers of myeloproliferative diseases in childhood polycythemia vera and essential thrombocythemia.

Teofili L, Giona F, Martini M, Cenci T, Guidi F, Torti L, Palumbo G, Amendola A, Foà R, Larocca LM. Teofili L, et al. Among authors: cenci t. J Clin Oncol. 2007 Mar 20;25(9):1048-53. doi: 10.1200/JCO.2006.08.6884. J Clin Oncol. 2007. PMID: 17369568

4

Different STAT-3 and STAT-5 phosphorylation discriminates among Ph-negative chronic myeloproliferative diseases and is independent of the V617F JAK-2 mutation.

Teofili L, Martini M, Cenci T, Petrucci G, Torti L, Storti S, Guidi F, Leone G, Larocca LM. Teofili L, et al. Among authors: cenci t. Blood. 2007 Jul 1;110(1):354-9. doi: 10.1182/blood-2007-01-069237. Epub 2007 Mar 21. Blood. 2007. PMID: 17376889 Free article.

5

The revised WHO diagnostic criteria for Ph-negative myeloproliferative diseases are not appropriate for the diagnostic screening of childhood polycythemia vera and essential thrombocythemia.

Teofili L, Giona F, Martini M, Cenci T, Guidi F, Torti L, Palumbo G, Amendola A, Leone G, Foà R, Larocca LM. Teofili L, et al. Among authors: cenci t. Blood. 2007 Nov 1;110(9):3384-6. doi: 10.1182/blood-2007-06-094276. Epub 2007 Jul 20. Blood. 2007. PMID: 17644735 Free article.

6

Phosphorylated STAT5 represents a new possible prognostic marker in Hodgkin lymphoma.

Martini M, Hohaus S, Petrucci G, Cenci T, Pierconti F, Massini G, Teofili L, Leone G, Larocca LM. Martini M, et al. Among authors: cenci t. Am J Clin Pathol. 2008 Mar;129(3):472-7. doi: 10.1309/63H1A83HRTBQ07DB. Am J Clin Pathol. 2008. PMID: 18285272

7

A novel heterozygous HIF2AM535I mutation reinforces the role of oxygen sensing pathway disturbances in the pathogenesis of familial erythrocytosis.

Martini M, Teofili L, Cenci T, Giona F, Torti L, Rea M, Foà R, Leone G, Larocca LM. Martini M, et al. Among authors: cenci t. Haematologica. 2008 Jul;93(7):1068-71. doi: 10.3324/haematol.13210. Epub 2008 May 27. Haematologica. 2008. PMID: 18508787 Free article.

8

Prognostic relevance of SOCS3 hypermethylation in patients with glioblastoma multiforme.

Martini M, Pallini R, Luongo G, Cenci T, Lucantoni C, Larocca LM. Martini M, et al. Among authors: cenci t. Int J Cancer. 2008 Dec 15;123(12):2955-60. doi: 10.1002/ijc.23805. Int J Cancer. 2008. PMID: 18770864

9

The mutant JAK2 allele burden in children with essential thrombocythemia.

Teofili L, Cenci T, Martini M, Capodimonti S, Torti L, Giona F, Amendola A, Randi ML, Putti MC, Scapin M, Leone G, Larocca LM. Teofili L, et al. Among authors: cenci t. Br J Haematol. 2009 May;145(3):430-2. doi: 10.1111/j.1365-2141.2009.07591.x. Epub 2009 Feb 4. Br J Haematol. 2009. PMID: 19208099 Free article. No abstract available.

10

Hereditary thrombocytosis caused by MPLSer505Asn is associated with a high thrombotic risk, splenomegaly and progression to bone marrow fibrosis.

Teofili L, Giona F, Torti L, Cenci T, Ricerca BM, Rumi C, Nunes V, Foà R, Leone G, Martini M, Larocca LM. Teofili L, et al. Among authors: cenci t. Haematologica. 2010 Jan;95(1):65-70. doi: 10.3324/haematol.2009.007542. Epub 2009 Aug 27. Haematologica. 2010. PMID: 19713221 Free PMC article.

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