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Items: 1 to 50 of 147

1.

Dietary Micronutrient and Mineral Intake in the Mediterranean Healthy Eating, Ageing, and Lifestyle (MEAL) Study.

Castiglione D, Platania A, Conti A, Falla M, D'Urso M, Marranzano M.

Antioxidants (Basel). 2018 Jun 23;7(7). pii: E79. doi: 10.3390/antiox7070079.

2.

Macronutrient and Major Food Group Intake in a Cohort of Southern Italian Adults.

Mulè S, Falla M, Conti A, Castiglione D, Blanco I, Platania A, D'Urso M, Marranzano M.

Antioxidants (Basel). 2018 Apr 15;7(4). pii: E58. doi: 10.3390/antiox7040058.

3.

Engineered exosomes emerging from muscle cells break immune tolerance to HER2 in transgenic mice and induce antigen-specific CTLs upon challenge by human dendritic cells.

Anticoli S, Aricò E, Arenaccio C, Manfredi F, Chiozzini C, Olivetta E, Ferrantelli F, Lattanzi L, D'Urso MT, Proietti E, Federico M.

J Mol Med (Berl). 2018 Feb;96(2):211-221. doi: 10.1007/s00109-017-1617-2. Epub 2017 Dec 27.

PMID:
29282521
4.

High adherence to Mediterranean diet, but not individual foods or nutrients, is associated with lower likelihood of being obese in a Mediterranean cohort.

Zappalà G, Buscemi S, Mulè S, La Verde M, D'Urso M, Corleo D, Marranzano M.

Eat Weight Disord. 2018 Oct;23(5):605-614. doi: 10.1007/s40519-017-0454-1. Epub 2017 Nov 9.

PMID:
29124678
5.

IL-33 restricts tumor growth and inhibits pulmonary metastasis in melanoma-bearing mice through eosinophils.

Lucarini V, Ziccheddu G, Macchia I, La Sorsa V, Peschiaroli F, Buccione C, Sistigu A, Sanchez M, Andreone S, D'Urso MT, Spada M, Macchia D, Afferni C, Mattei F, Schiavoni G.

Oncoimmunology. 2017 Apr 20;6(6):e1317420. doi: 10.1080/2162402X.2017.1317420. eCollection 2017.

6.

[Prevalence of thyroid dysfunction in patients with type 2 diabetes mellitus].

Centeno Maxzud M, Gómez Rasjido L, Fregenal M, Arias Calafiore F, Córdoba Lanus M, D'Urso M, Luciardi H.

Medicina (B Aires). 2016;76(6):355-358. Spanish.

7.

The Mediterranean healthy eating, ageing, and lifestyle (MEAL) study: rationale and study design.

Grosso G, Marventano S, D'Urso M, Mistretta A, Galvano F.

Int J Food Sci Nutr. 2017 Aug;68(5):577-586. doi: 10.1080/09637486.2016.1262335. Epub 2016 Dec 5.

PMID:
27919168
8.

Combining Type I Interferons and 5-Aza-2'-Deoxycitidine to Improve Anti-Tumor Response against Melanoma.

Lucarini V, Buccione C, Ziccheddu G, Peschiaroli F, Sestili P, Puglisi R, Mattia G, Zanetti C, Parolini I, Bracci L, Macchia I, Rossi A, D'Urso MT, Macchia D, Spada M, De Ninno A, Gerardino A, Mozetic P, Trombetta M, Rainer A, Businaro L, Schiavoni G, Mattei F.

J Invest Dermatol. 2017 Jan;137(1):159-169. doi: 10.1016/j.jid.2016.08.024. Epub 2016 Sep 10.

9.

The Management of Patients With Diverticulosis and Diverticular Disease in Primary Care: An Online Survey Among Italian General Pratictioners.

De Bastiani R, Sanna G, Fracasso P, D'Urso M, Benedetto E, Tursi A.

J Clin Gastroenterol. 2016 Oct;50 Suppl 1:S89-92. doi: 10.1097/MCG.0000000000000580.

PMID:
27622377
10.

Chemo-immunotherapy induces tumor regression in a mouse model of spontaneous mammary carcinogenesis.

Aricò E, Sestili P, Carpinelli G, Canese R, Cecchetti S, Schiavoni G, D'Urso MT, Belardelli F, Proietti E.

Oncotarget. 2016 Sep 13;7(37):59754-59765. doi: 10.18632/oncotarget.10880.

11.

Variations in stable isotope ratios in lamb blood fractions following dietary changes: a preliminary study.

Bontempo L, Camin F, Ziller L, Biondi L, D'Urso MG, Vasta V, Luciano G.

Rapid Commun Mass Spectrom. 2016 Jan 15;30(1):170-4. doi: 10.1002/rcm.7428.

PMID:
26661984
12.

Glycogen synthase kinase 3 is part of the molecular machinery regulating the adaptive response to LPS stimulation in microglial cells.

Ajmone-Cat MA, D'Urso MC, di Blasio G, Brignone MS, De Simone R, Minghetti L.

Brain Behav Immun. 2016 Jul;55:225-235. doi: 10.1016/j.bbi.2015.11.012. Epub 2015 Nov 22.

PMID:
26593276
13.

A Quick Test of Cognitive Speed: norm-referenced criteria for 121 Italian adults aged 45 to 90 years.

Petrazzuoli F, Palmqvist S, Thulesius H, Buono N, Pirrotta E, Cuffari A, Cambielli M, D'Urso M, Farinaro C, Chiumeo F, Marsala V, Wiig EH.

Int Psychogeriatr. 2014 May 9:1-8. [Epub ahead of print]

PMID:
24810919
14.

Stable isotope ratios of blood components and muscle to trace dietary changes in lambs.

Biondi L, D'Urso MG, Vasta V, Luciano G, Scerra M, Priolo A, Ziller L, Bontempo L, Caparra P, Camin F.

Animal. 2013 Sep;7(9):1559-66. doi: 10.1017/S1751731113000645. Epub 2013 Apr 19.

PMID:
23597321
15.

Unraveling cancer chemoimmunotherapy mechanisms by gene and protein expression profiling of responses to cyclophosphamide.

Moschella F, Valentini M, Aricò E, Macchia I, Sestili P, D'Urso MT, Alessandri C, Belardelli F, Proietti E.

Cancer Res. 2011 May 15;71(10):3528-39. doi: 10.1158/0008-5472.CAN-10-4523. Epub 2011 Mar 28.

16.

Cyclophosphamide synergizes with type I interferons through systemic dendritic cell reactivation and induction of immunogenic tumor apoptosis.

Schiavoni G, Sistigu A, Valentini M, Mattei F, Sestili P, Spadaro F, Sanchez M, Lorenzi S, D'Urso MT, Belardelli F, Gabriele L, Proietti E, Bracci L.

Cancer Res. 2011 Feb 1;71(3):768-78. doi: 10.1158/0008-5472.CAN-10-2788. Epub 2010 Dec 13.

17.

The LCR at the IKBKG locus is prone to recombine.

Fusco F, D'Urso M, Miano MG, Ursini MV.

Am J Hum Genet. 2010 Apr 9;86(4):650-2; author reply 652-3. doi: 10.1016/j.ajhg.2009.12.019. No abstract available.

18.
19.

Exposure to pesticides residues from consumption of Italian blood oranges.

Fallico B, D'Urso MG, Chiappara E.

Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2009 Jul;26(7):1024-32. doi: 10.1080/02652030902839731.

PMID:
19680977
20.

Microdeletion/duplication at the Xq28 IP locus causes a de novo IKBKG/NEMO/IKKgamma exon4_10 deletion in families with Incontinentia Pigmenti.

Fusco F, Paciolla M, Pescatore A, Lioi MB, Ayuso C, Faravelli F, Gentile M, Zollino M, D'Urso M, Miano MG, Ursini MV.

Hum Mutat. 2009 Sep;30(9):1284-91. doi: 10.1002/humu.21069.

PMID:
19603533
21.

DDX11L: a novel transcript family emerging from human subtelomeric regions.

Costa V, Casamassimi A, Roberto R, Gianfrancesco F, Matarazzo MR, D'Urso M, D'Esposito M, Rocchi M, Ciccodicola A.

BMC Genomics. 2009 May 28;10:250. doi: 10.1186/1471-2164-10-250.

22.

Alterations of the IKBKG locus and diseases: an update and a report of 13 novel mutations.

Fusco F, Pescatore A, Bal E, Ghoul A, Paciolla M, Lioi MB, D'Urso M, Rabia SH, Bodemer C, Bonnefont JP, Munnich A, Miano MG, Smahi A, Ursini MV.

Hum Mutat. 2008 May;29(5):595-604. doi: 10.1002/humu.20739.

PMID:
18350553
23.

Phaseless imaging with experimental data: facts and challenges.

D'Urso M, Belkebir K, Crocco L, Isernia T, Litman A.

J Opt Soc Am A Opt Image Sci Vis. 2008 Jan;25(1):271-81.

PMID:
18157235
24.

MRX87 family with Aristaless X dup24bp mutation and implication for polyAlanine expansions.

Laperuta C, Spizzichino L, D'Adamo P, Monfregola J, Maiorino A, D'Eustacchio A, Ventruto V, Neri G, D'Urso M, Chiurazzi P, Ursini MV, Miano MG.

BMC Med Genet. 2007 May 4;8:25.

25.

Ovarian dysfunction and FMR1 alleles in a large Italian family with POF and FRAXA disorders: case report.

Miano MG, Laperuta C, Chiurazzi P, D'Urso M, Ursini MV.

BMC Med Genet. 2007 Apr 11;8:18.

26.

Functional characterization of the TMLH gene: promoter analysis, in situ hybridization, identification and mapping of alternative splicing variants.

Monfregola J, Napolitano G, Conte I, Cevenini A, Migliaccio C, D'Urso M, Ursini MV.

Gene. 2007 Jun 15;395(1-2):86-97. Epub 2007 Feb 28.

PMID:
17408883
27.

Faithful non-linear imaging from only-amplitude measurements of incident and total fields.

Crocco L, D'Urso M, Isernia T.

Opt Express. 2007 Apr 2;15(7):3804-15.

PMID:
19532625
28.

Inverse scattering from phaseless measurements of the total field on open lines.

Bucci OM, Crocco L, D'Urso M, Isernia T.

J Opt Soc Am A Opt Image Sci Vis. 2006 Oct;23(10):2566-77.

PMID:
16985541
29.

Heterozygosity mapping by quantitative fluorescent PCR reveals an interstitial deletion in Xq26.2-q28 associated with ovarian dysfunction.

Fimiani G, Laperuta C, Falco G, Ventruto V, D'Urso M, Ursini MV, Miano MG.

Hum Reprod. 2006 Feb;21(2):529-35. Epub 2005 Oct 20.

PMID:
16239311
30.

The DNA sequence of the human X chromosome.

Ross MT, Grafham DV, Coffey AJ, Scherer S, McLay K, Muzny D, Platzer M, Howell GR, Burrows C, Bird CP, Frankish A, Lovell FL, Howe KL, Ashurst JL, Fulton RS, Sudbrak R, Wen G, Jones MC, Hurles ME, Andrews TD, Scott CE, Searle S, Ramser J, Whittaker A, Deadman R, Carter NP, Hunt SE, Chen R, Cree A, Gunaratne P, Havlak P, Hodgson A, Metzker ML, Richards S, Scott G, Steffen D, Sodergren E, Wheeler DA, Worley KC, Ainscough R, Ambrose KD, Ansari-Lari MA, Aradhya S, Ashwell RI, Babbage AK, Bagguley CL, Ballabio A, Banerjee R, Barker GE, Barlow KF, Barrett IP, Bates KN, Beare DM, Beasley H, Beasley O, Beck A, Bethel G, Blechschmidt K, Brady N, Bray-Allen S, Bridgeman AM, Brown AJ, Brown MJ, Bonnin D, Bruford EA, Buhay C, Burch P, Burford D, Burgess J, Burrill W, Burton J, Bye JM, Carder C, Carrel L, Chako J, Chapman JC, Chavez D, Chen E, Chen G, Chen Y, Chen Z, Chinault C, Ciccodicola A, Clark SY, Clarke G, Clee CM, Clegg S, Clerc-Blankenburg K, Clifford K, Cobley V, Cole CG, Conquer JS, Corby N, Connor RE, David R, Davies J, Davis C, Davis J, Delgado O, Deshazo D, Dhami P, Ding Y, Dinh H, Dodsworth S, Draper H, Dugan-Rocha S, Dunham A, Dunn M, Durbin KJ, Dutta I, Eades T, Ellwood M, Emery-Cohen A, Errington H, Evans KL, Faulkner L, Francis F, Frankland J, Fraser AE, Galgoczy P, Gilbert J, Gill R, Glöckner G, Gregory SG, Gribble S, Griffiths C, Grocock R, Gu Y, Gwilliam R, Hamilton C, Hart EA, Hawes A, Heath PD, Heitmann K, Hennig S, Hernandez J, Hinzmann B, Ho S, Hoffs M, Howden PJ, Huckle EJ, Hume J, Hunt PJ, Hunt AR, Isherwood J, Jacob L, Johnson D, Jones S, de Jong PJ, Joseph SS, Keenan S, Kelly S, Kershaw JK, Khan Z, Kioschis P, Klages S, Knights AJ, Kosiura A, Kovar-Smith C, Laird GK, Langford C, Lawlor S, Leversha M, Lewis L, Liu W, Lloyd C, Lloyd DM, Loulseged H, Loveland JE, Lovell JD, Lozado R, Lu J, Lyne R, Ma J, Maheshwari M, Matthews LH, McDowall J, McLaren S, McMurray A, Meidl P, Meitinger T, Milne S, Miner G, Mistry SL, Morgan M, Morris S, Müller I, Mullikin JC, Nguyen N, Nordsiek G, Nyakatura G, O'Dell CN, Okwuonu G, Palmer S, Pandian R, Parker D, Parrish J, Pasternak S, Patel D, Pearce AV, Pearson DM, Pelan SE, Perez L, Porter KM, Ramsey Y, Reichwald K, Rhodes S, Ridler KA, Schlessinger D, Schueler MG, Sehra HK, Shaw-Smith C, Shen H, Sheridan EM, Shownkeen R, Skuce CD, Smith ML, Sotheran EC, Steingruber HE, Steward CA, Storey R, Swann RM, Swarbreck D, Tabor PE, Taudien S, Taylor T, Teague B, Thomas K, Thorpe A, Timms K, Tracey A, Trevanion S, Tromans AC, d'Urso M, Verduzco D, Villasana D, Waldron L, Wall M, Wang Q, Warren J, Warry GL, Wei X, West A, Whitehead SL, Whiteley MN, Wilkinson JE, Willey DL, Williams G, Williams L, Williamson A, Williamson H, Wilming L, Woodmansey RL, Wray PW, Yen J, Zhang J, Zhou J, Zoghbi H, Zorilla S, Buck D, Reinhardt R, Poustka A, Rosenthal A, Lehrach H, Meindl A, Minx PJ, Hillier LW, Willard HF, Wilson RK, Waterston RH, Rice CM, Vaudin M, Coulson A, Nelson DL, Weinstock G, Sulston JE, Durbin R, Hubbard T, Gibbs RA, Beck S, Rogers J, Bentley DR.

Nature. 2005 Mar 17;434(7031):325-37.

31.

Functional analysis of TMLH variants and definition of domains required for catalytic activity and mitochondrial targeting.

Monfregola J, Cevenini A, Terracciano A, van Vlies N, Arbucci S, Wanders RJ, D'Urso M, Vaz FM, Ursini MV.

J Cell Physiol. 2005 Sep;204(3):839-47.

PMID:
15754339
32.

Incontinentia pigmenti with NEMO mutation in a Turkish family.

Silan F, Aydogan I, Kavak A, Bardaro T, D'Urso M.

Int J Dermatol. 2004 Jul;43(7):527-9. No abstract available.

PMID:
15230896
33.

Molecular analysis of the genetic defect in a large cohort of IP patients and identification of novel NEMO mutations interfering with NF-kappaB activation.

Fusco F, Bardaro T, Fimiani G, Mercadante V, Miano MG, Falco G, Israël A, Courtois G, D'Urso M, Ursini MV.

Hum Mol Genet. 2004 Aug 15;13(16):1763-73. Epub 2004 Jun 30.

PMID:
15229184
34.

VAMP subfamilies identified by specific R-SNARE motifs.

Rossi V, Picco R, Vacca M, D'Esposito M, D'Urso M, Galli T, Filippini F.

Biol Cell. 2004 May;96(4):251-6. Review.

PMID:
15145528
35.

Inverse scattering from phaseless measurements of the total field on a closed curve.

Crocco L, D'Urso M, Isernia T.

J Opt Soc Am A Opt Image Sci Vis. 2004 Apr;21(4):622-31.

PMID:
15078033
36.

Characterization of the human STAT5A and STAT5B promoters: evidence of a positive and negative mechanism of transcriptional regulation.

Crispi S, Sanzari E, Monfregola J, De Felice N, Fimiani G, Ambrosio R, D'Urso M, Ursini MV.

FEBS Lett. 2004 Mar 26;562(1-3):27-34.

37.

Transcriptome analysis of mouse stem cells and early embryos.

Sharov AA, Piao Y, Matoba R, Dudekula DB, Qian Y, VanBuren V, Falco G, Martin PR, Stagg CA, Bassey UC, Wang Y, Carter MG, Hamatani T, Aiba K, Akutsu H, Sharova L, Tanaka TS, Kimber WL, Yoshikawa T, Jaradat SA, Pantano S, Nagaraja R, Boheler KR, Taub D, Hodes RJ, Longo DL, Schlessinger D, Keller J, Klotz E, Kelsoe G, Umezawa A, Vescovi AL, Rossant J, Kunath T, Hogan BL, Curci A, D'Urso M, Kelso J, Hide W, Ko MS.

PLoS Biol. 2003 Dec;1(3):E74. Epub 2003 Dec 22.

38.

Human synaptobrevin-like 1 gene basal transcription is regulated through the interaction of selenocysteine tRNA gene transcription activating factor-zinc finger 143 factors with evolutionary conserved cis-elements.

Di Leva F, Ferrante MI, Demarchi F, Caravelli A, Matarazzo MR, Giacca M, D'Urso M, D'Esposito M, Franzé A.

J Biol Chem. 2004 Feb 27;279(9):7734-9. Epub 2003 Dec 12.

39.

Otosclerosis: exclusion of linkage to the OTSC1 and OTSC2 loci in four Italian families.

Di Leva F, D'Adamo AP, Strollo L, Auletta G, Caravelli A, Carella M, Mari F, Livi W, Renieri A, Gasparini P, D'Urso M, Marciano E, Franzé A.

Int J Audiol. 2003 Dec;42(8):475-80.

PMID:
14658855
40.

High-resolution methylation analysis of the hMLH1 promoter in sporadic endometrial and colorectal carcinomas.

Strazzullo M, Cossu A, Baldinu P, Colombino M, Satta MP, Tanda F, De Bonis ML, Cerase A, D'Urso M, D'Esposito M, Palmieri G.

Cancer. 2003 Oct 1;98(7):1540-6.

41.

Folate treatment and unbalanced methylation and changes of allelic expression induced by hyperhomocysteinaemia in patients with uraemia.

Ingrosso D, Cimmino A, Perna AF, Masella L, De Santo NG, De Bonis ML, Vacca M, D'Esposito M, D'Urso M, Galletti P, Zappia V.

Lancet. 2003 May 17;361(9370):1693-9.

PMID:
12767735
42.

Mapping of MRX81 in Xp11.2-Xq12 suggests the presence of a new gene involved in nonspecific X-linked mental retardation.

Annunziata I, Lanzara C, Conte I, Zullo A, Ventruto V, Rinaldi MM, D'Urso M, Casari G, Ciccodicola A, Miano MG.

Am J Med Genet A. 2003 Apr 30;118A(3):217-22.

PMID:
12673650
43.

Two cases of misinterpretation of molecular results in incontinentia pigmenti, and a PCR-based method to discriminate NEMO/IKKgamma dene deletion.

Bardaro T, Falco G, Sparago A, Mercadante V, Gean Molins E, Tarantino E, Ursini MV, D'Urso M.

Hum Mutat. 2003 Jan;21(1):8-11.

PMID:
12497627
44.

Allelic inactivation of the pseudoautosomal gene SYBL1 is controlled by epigenetic mechanisms common to the X and Y chromosomes.

Matarazzo MR, De Bonis ML, Gregory RI, Vacca M, Hansen RS, Mercadante G, D'Urso M, Feil R, D'Esposito M.

Hum Mol Genet. 2002 Dec 1;11(25):3191-8.

PMID:
12444103
45.

The structure of human STAT5A and B genes reveals two regions of nearly identical sequence and an alternative tissue specific STAT5B promoter.

Ambrosio R, Fimiani G, Monfregola J, Sanzari E, De Felice N, Salerno MC, Pignata C, D'Urso M, Ursini MV.

Gene. 2002 Feb 20;285(1-2):311-8.

PMID:
12039059
46.

The ABCA4 2588G>C Stargardt mutation: single origin and increasing frequency from South-West to North-East Europe.

Maugeri A, Flothmann K, Hemmrich N, Ingvast S, Jorge P, Paloma E, Patel R, Rozet JM, Tammur J, Testa F, Balcells S, Bird AC, Brunner HG, Hoyng CB, Metspalu A, Simonelli F, Allikmets R, Bhattacharya SS, D'Urso M, Gonzàlez-Duarte R, Kaplan J, te Meerman GJ, Santos R, Schwartz M, Van Camp G, Wadelius C, Weber BH, Cremers FP.

Eur J Hum Genet. 2002 Mar;10(3):197-203.

47.

Characterization of 2 novel and 2 recurring BRCA1 germline mutations in breast and/or ovarian carcinoma patients from the area of Naples.

Curci A, Capasso I, Romano A, Bruni P, Motti ML, Pignata S, D'Aiuto G, Casamassimi A, D'Urso M, Fusco A, Viglietto G.

Int J Oncol. 2002 May;20(5):963-70.

PMID:
11956590
48.

Physical and genetic characterization reveals a pseudogene, an evolutionary junction, and unstable loci in distal Xq28.

Aradhya S, Woffendin H, Bonnen P, Heiss NS, Yamagata T, Esposito T, Bardaro T, Poustka A, D'Urso M, Kenwrick S, Nelson DL.

Genomics. 2002 Jan;79(1):31-40.

PMID:
11827455
49.

Functional analysis of MLH1 mutations linked to hereditary nonpolyposis colon cancer.

Nyström-Lahti M, Perrera C, Räschle M, Panyushkina-Seiler E, Marra G, Curci A, Quaresima B, Costanzo F, D'Urso M, Venuta S, Jiricny J.

Genes Chromosomes Cancer. 2002 Feb;33(2):160-7.

PMID:
11793442
50.

MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region.

Vacca M, Filippini F, Budillon A, Rossi V, Della Ragione F, De Bonis ML, Mercadante G, Manzati E, Gualandi F, Bigoni S, Trabanelli C, Pini G, Calzolari E, Ferlini A, Meloni I, Hayek G, Zappella M, Renieri A, D'Urso M, D'Esposito M, Macdonald F, Kerr A, Dhanjal S, Hulten M.

Brain Dev. 2001 Dec;23 Suppl 1:S246-50. Erratum in: Brain Dev. 2012 Nov;34(10):891.

PMID:
11738884

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