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Lingue
Sezione
Attivitą
Didattica
Utilitą
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31-Dic-2009
Elenco Pubblicazioni
- Luconi M, Mangoni M, Gelmini S, Poli G, Nesi G, Francalanci M, Pratesi N, Cantini G, Lombardi A, Pepi M, Ercolino T, Serio M, Orlando C, Mannelli M. Rosiglitazone impairs proliferation of human adrenocortical cancer: preclinical study in a xenograft mouse model.
Endocr Relat Cancer. 2009 Dec 2. [Epub ahead of print] - Goffrini P, Ercolino T, Panizza E, Giachè V, Cavone L, Chiarugi A, Dima V, Ferrero I, Mannelli M. Functional study in a yeast model of a novel succinate dehydrogenase subunit B gene germline missense mutation (C191Y) diagnosed in a patient affected by a glomus tumor.
Hum Mol Genet. 2009 May 15;18(10):1860-8. - Mannelli M, Castellano M, Schiavi F, Filetti S, Giacchè M, Mori L, Pignataro V, Bernini G, Giachè V, Bacca A, Biondi B, Corona G, Di Trapani G, Grossrubatscher E, Reimondo G, Arnaldi G, Giacchetti G, Veglio F, Loli P, Colao A, Ambrosio MR, Terzolo M, Letizia C, Ercolino T, Opocher G; Italian Pheochromocytoma/Paraganglioma Network.Clinically guided genetic screening in a large cohort of italian patients with pheochromocytomas and/or functional or nonfunctional paragangliomas.
J Clin Endocrinol Metab. 2009 May;94(5):1541-7. - Cantini G, Lombardi A, Piscitelli E, Poli G, Ceni E, Marchiani S, Ercolino T, Galli A, Serio M, Mannelli M, Luconi M. Rosiglitazone Inhibits Adrenocortical Cancer Cell Proliferation by Interfering with the IGF- IR Intracellular Signaling.
PPAR Res. 2008;2008:904041. - Rotondi M, Ercolino T, Fonte R, Lagonigro MS, Leporati P, Villani L, La Manna L, Mannelli M and Chiovato L. Occorrence of medullary thyroid carcinoma, bronchial carcinoid tumor and papillary thyroid carcinoma in a family bearing the G691S polymorphism.
J Endocrinol Invest. 2009 Feb;32(2):115-8. - Ercolino T, Taurino C, Sestini R, Bacca AV, Genuardi M, Mannelli M, and Bernini GP Malignant extra-adrenal pheochromocytoma caused by an SDHB intronic variation leading to a 54-bp deletion in exon 4.
J Endocrinol Invest. Feb;32(2):111-4. - Ercolino T, Lombardi A, Becherini L, Piscitelli E, Cantini G, Gaglianò M.S., Serio M, Luconi M, Mannelli M (2008) The Y606C RET mutation causes a receptor gain of function.
Clin Endocrinol (Oxf). 2008 Jan 29. - Ercolino T, Becherini L, Valeri A, Maiello M, Gaglianò MS, Parenti G, Ramazzotti M, Piscitelli E, Simi L, Pinzani P, Nesi G, Degl'innocenti D, Console N, Bergamini C, Mannelli M. Uncommon clinical presentations of pheochromocytoma and paraganglioma in two different patients affected by two distinct novel VHL germline mutations.
Clin Endocrinol (Oxf). 2008 May;68(5):762-8. - Mannelli M, Ercolino T, Giachè V, Simi L, Cirami C, Parenti G.
Genetic screening for pheochromocytoma: should SDHC gene analysis be included?
J Med Genet. 2007 Sep;44(9):586-7. Epub 2007 Jun 8. - Mannelli M, Simi L, Gaglianò MS, Opocher G, Ercolino T, Becherini L, Parenti G.
Genetics and biology of pheochromocytoma.
Exp Clin Endocrinol Diabetes. 2007 Mar;115(3):160-5. Review. - Mannelli M, Simi L, Ercolino T, Gaglianò MS, Becherini L, Vinci S, Sestini R, Gensini F, Pinzani P, Mascalchi M, Guerrini L, Pratesi C, Nesi G, Torti F, Cipollini F, Bernini GP, Genuardi M. SDH mutations in patients affected by paraganglioma syndromes: a personal experience.
Ann N Y Acad Sci. 2006 Aug;1073:183-9. - Bernini GP, Moretti A, Mannelli M, Ercolino T, Bardini M, Caramella D, Taurino C, Salvetti A. Unique association of non-functioning pheochromocytoma, ganglioneuroma, adrenal cortical adenoma, hepatic and vertebral hemangiomas in a patient with a new intronic variant in the VHL gene.
J Endocrinol Invest. 2005 Dec;28(11):1032-7. - Simi L, Sestini R, Ferruzzi P, Gaglianò MS, Gensini F, Mascalchi M, Guerrini L, Pratesi C, Pinzani P, Nesi G, Ercolino T, Genuardi M, Mannelli M. Phenotype variability of neural crest derived tumours in six Italian families segregating the same founder SDHD mutation Q109X.
J Med Genet. 2005 Aug;42(8):e52. - Menzaghi C, Ercolino T, Salvemini L, Coco A, Fini G, Di Paola R, Doria A, Trischitta V. Lack of evidence for interaction between APM1 and PPARgamma2 genes in modulating insulin sensitivity in nondiabetic Caucasians from Italy.
J Intern Med. 2005 Mar;257(3):315-7. No abstract available. - Bacci S, Menzaghi C, Ercolino T, Ma X, Rauseo A, Salvemini L, Vigna C, Fanelli R, Di Mario U, Doria A, Trischitta V. The +276 G/T single nucleotide polymorphism of the adiponectin gene is associated with coronary artery disease in type 2 diabetic patients.
Diabetes Care. 2004 Aug;27(8):2015-20. - Menzaghi C, Ercolino T, Salvemini L, Coco A, Kim SH, Fini G, Doria A, Trischitta V. Multigenic control of serum adiponectin levels: evidence for a role of the APM1 gene and a locus on 14q13.
Physiol Genomics. 2004 Oct 4;19(2):170-4. Epub 2004 Jul 13. - Kim SH, Ma X, Weremowicz S, Ercolino T, Powers C, Mlynarski W, Bashan KA, Warram JH, Mychaleckyj J, Rich SS, Krolewski AS, Doria A. Identification of a locus for maturity-onset diabetes of the young on chromosome 8p23.
Diabetes. 2004 May;53(5):1375-84. - Menzaghi C, Di Paola R, Baj G, Funaro A, Arnulfo A, Ercolino T, Surico N, Malavasi F, Trischitta V. Insulin modulates PC-1 processing and recruitment in cultured human cells.
Am J Physiol Endocrinol Metab. 2003 Mar;284(3):E514-20. Epub 2002 Nov 19. - Menzaghi C, Ercolino T, Di Paola R, Berg AH, Warram JH, Scherer PE, Trischitta V, Doria A. A haplotype at the adiponectin locus is associated with obesity and other features of the insulin resistance syndrome.
Diabetes. 2002 Jul;51(7):2306-12. - Di Paola R, Frittitta L, Miscio G, Bozzali M, Baratta R, Centra M, Spampinato D, Santagati MG, Ercolino T, Cisternino C, Soccio T, Mastroianno S, Tassi V, Almgren P, Pizzuti A, Vigneri R, Trischitta V. A variation in 3' UTR of hPTP1B increases specific gene expression and associates with insulin resistance.
Am J Hum Genet. 2002 Mar;70(3):806-12. Epub 2002 Feb 6. Erratum in: Am J Hum Genet 2002 May;70(5):1388. - Frittitta L, Ercolino T, Bozzali M, Argiolas A, Graci S, Santagati MG, Spampinato D, Di Paola R, Cisternino C, Tassi V, Vigneri R, Pizzuti A, Trischitta V. A cluster of three single nucleotide polymorphisms in the 3'-untranslated region of human glycoprotein PC-1 gene stabilizes PC-1 mRNA and is associated with increased PC-1 protein content and insulin resistance-related abnormalities.
Diabetes. 2001 Aug;50(8):1952-5. - Frittitta L, Sbraccia P, Costanzo BV, Tassi V, D'Adamo M, Spampinato D, Ercolino T, Purrello F, Tamburrano G, Vigneri R, Trischitta V. High insulin levels do not influence PC-1 gene expression and protein content in human muscle tissue and hepatoma cells.
Diabetes Metab Res Rev. 2000 Jan-Feb;16(1):26-32. - Pizzuti A, Frittitta L, Argiolas A, Baratta R, Goldfine ID, Bozzali M, Ercolino T, Scarlato G, Iacoviello L, Vigneri R, Tassi V, Trischitta V. A polymorphism (K121Q) of the human glycoprotein PC-1 gene coding region is strongly associated with insulin resistance.
Diabetes. 1999 Sep;48(9):1881-4.
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