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Items: 1 to 20 of 45

1.

Identification of a novel antiviral micro-RNA targeting the NS1 protein of the H1N1 pandemic human influenza virus and a corresponding viral escape mutation.

Bavagnoli L, Campanini G, Forte M, Ceccotti G, Percivalle E, Bione S, Lisa A, Baldanti F, Maga G.

Antiviral Res. 2019 Nov;171:104593. doi: 10.1016/j.antiviral.2019.104593. Epub 2019 Aug 27.

2.

Bi-allelic TARS Mutations Are Associated with Brittle Hair Phenotype.

Theil AF, Botta E, Raams A, Smith DEC, Mendes MI, Caligiuri G, Giachetti S, Bione S, Carriero R, Liberi G, Zardoni L, Swagemakers SMA, Salomons GS, Sarasin A, Lehmann A, van der Spek PJ, Ogi T, Hoeijmakers JHJ, Vermeulen W, Orioli D.

Am J Hum Genet. 2019 Aug 1;105(2):434-440. doi: 10.1016/j.ajhg.2019.06.017.

PMID:
31374204
3.

Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting.

Chauhan G, Adams HHH, Satizabal CL, Bis JC, Teumer A, Sargurupremraj M, Hofer E, Trompet S, Hilal S, Smith AV, Jian X, Malik R, Traylor M, Pulit SL, Amouyel P, Mazoyer B, Zhu YC, Kaffashian S, Schilling S, Beecham GW, Montine TJ, Schellenberg GD, Kjartansson O, Guðnason V, Knopman DS, Griswold ME, Windham BG, Gottesman RF, Mosley TH, Schmidt R, Saba Y, Schmidt H, Takeuchi F, Yamaguchi S, Nabika T, Kato N, Rajan KB, Aggarwal NT, De Jager PL, Evans DA, Psaty BM, Rotter JI, Rice K, Lopez OL, Liao J, Chen C, Cheng CY, Wong TY, Ikram MK, van der Lee SJ, Amin N, Chouraki V, DeStefano AL, Aparicio HJ, Romero JR, Maillard P, DeCarli C, Wardlaw JM, Hernández MDCV, Luciano M, Liewald D, Deary IJ, Starr JM, Bastin ME, Muñoz Maniega S, Slagboom PE, Beekman M, Deelen J, Uh HW, Lemmens R, Brodaty H, Wright MJ, Ames D, Boncoraglio GB, Hopewell JC, Beecham AH, Blanton SH, Wright CB, Sacco RL, Wen W, Thalamuthu A, Armstrong NJ, Chong E, Schofield PR, Kwok JB, van der Grond J, Stott DJ, Ford I, Jukema JW, Vernooij MW, Hofman A, Uitterlinden AG, van der Lugt A, Wittfeld K, Grabe HJ, Hosten N, von Sarnowski B, Völker U, Levi C, Jimenez-Conde J, Sharma P, Sudlow CLM, Rosand J, Woo D, Cole JW, Meschia JF, Slowik A, Thijs V, Lindgren A, Melander O, Grewal RP, Rundek T, Rexrode K, Rothwell PM, Arnett DK, Jern C, Johnson JA, Benavente OR, Wasssertheil-Smoller S, Lee JM, Wong Q, Mitchell BD, Rich SS, McArdle PF, Geerlings MI, van der Graaf Y, de Bakker PIW, Asselbergs FW, Srikanth V, Thomson R, McWhirter R, Moran C, Callisaya M, Phan T, Rutten-Jacobs LCA, Bevan S, Tzourio C, Mather KA, Sachdev PS, van Duijn CM, Worrall BB, Dichgans M, Kittner SJ, Markus HS, Ikram MA, Fornage M, Launer LJ, Seshadri S, Longstreth WT Jr, Debette S; Stroke Genetics Network (SiGN), the International Stroke Genetics Consortium (ISGC), METASTROKE, Alzheimer's Disease Genetics Consortium (ADGC), and the Neurology Working Group of the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium.

Neurology. 2019 Jan 16. pii: 10.1212/WNL.0000000000006851. doi: 10.1212/WNL.0000000000006851. [Epub ahead of print]

4.

Characterization of the biological processes shaping the genetic structure of the Italian population.

Parolo S, Lisa A, Gentilini D, Di Blasio AM, Barlera S, Nicolis EB, Boncoraglio GB, Parati EA, Bione S.

BMC Genet. 2015 Nov 9;16:132. doi: 10.1186/s12863-015-0293-x.

5.

Heritability of young- and old-onset ischaemic stroke.

Bluher A, Devan WJ, Holliday EG, Nalls M, Parolo S, Bione S, Giese AK, Boncoraglio GB, Maguire JM, Müller-Nurasyid M, Gieger C, Meschia JF, Rosand J, Rolfs A, Kittner SJ, Mitchell BD, O'Connell JR, Cheng YC.

Eur J Neurol. 2015 Nov;22(11):1488-91. doi: 10.1111/ene.12827. Epub 2015 Sep 2.

6.

An Association Rule Mining Approach to Discover lncRNAs Expression Patterns in Cancer Datasets.

Cremaschi P, Carriero R, Astrologo S, Colì C, Lisa A, Parolo S, Bione S.

Biomed Res Int. 2015;2015:146250. doi: 10.1155/2015/146250. Epub 2015 Jul 27.

7.

Chronic Replication Problems Impact Cell Morphology and Adhesion of DNA Ligase I Defective Cells.

Cremaschi P, Oliverio M, Leva V, Bione S, Carriero R, Mazzucco G, Palamidessi A, Scita G, Biamonti G, Montecucco A.

PLoS One. 2015 Jul 7;10(7):e0130561. doi: 10.1371/journal.pone.0130561. eCollection 2015.

8.

CorrelaGenes: a new tool for the interpretation of the human transcriptome.

Cremaschi P, Rovida S, Sacchi L, Lisa A, Calvi F, Montecucco A, Biamonti G, Bione S, Sacchi G.

BMC Bioinformatics. 2014;15 Suppl 1:S6. doi: 10.1186/1471-2105-15-S1-S6. Epub 2014 Jan 10.

9.

Blood cell mitochondrial DNA content and premature ovarian aging.

Bonomi M, Somigliana E, Cacciatore C, Busnelli M, Rossetti R, Bonetti S, Paffoni A, Mari D, Ragni G, Persani L; Italian Network for the study of Ovarian Dysfunctions.

PLoS One. 2012;7(8):e42423. Epub 2012 Aug 3.

10.

Are myocardial infarction--associated single-nucleotide polymorphisms associated with ischemic stroke?

Cheng YC, Anderson CD, Bione S, Keene K, Maguire JM, Nalls M, Rasheed A, Zeginigg M, Attia J, Baker R, Barlera S, Biffi A, Bookman E, Brott TG, Brown RD Jr, Chen F, Chen WM, Ciusani E, Cole JW, Cortellini L, Danesh J, Doheny K, Ferrucci L, Grazia Franzosi M, Frossard P, Furie KL, Golledge J, Hankey GJ, Hernandez D, Holliday EG, Hsu FC, Jannes J, Kamal A, Khan MS, Kittner SJ, Koblar SA, Lewis M, Lincz L, Lisa A, Matarin M, Moscato P, Mychaleckyj JC, Parati EA, Parolo S, Pugh E, Rost NS, Schallert M, Schmidt H, Scott RJ, Sturm JW, Yadav S, Zaidi M, Boncoraglio GB, Levi CR, Meschia JF, Rosand J, Sale M, Saleheen D, Schmidt R, Sharma P, Worrall B, Mitchell BD; GARNET Collaborative Research Group; GENEVA Consortium; International Stroke Genetics Consortium.

Stroke. 2012 Apr;43(4):980-6. doi: 10.1161/STROKEAHA.111.632075. Epub 2012 Feb 23. Erratum in: Stroke. 2015 Aug;46(8):e204.

11.

Cross-analysis of gene and miRNA genome-wide expression profiles in human fibroblasts at different stages of transformation.

Ostano P, Bione S, Belgiovine C, Chiodi I, Ghimenti C, Scovassi AI, Chiorino G, Mondello C.

OMICS. 2012 Jan-Feb;16(1-2):24-36. doi: 10.1089/omi.2011.0049.

12.

Association of a variant in the CHRNA5-A3-B4 gene cluster region to heavy smoking in the Italian population.

Sorice R, Bione S, Sansanelli S, Ulivi S, Athanasakis E, Lanzara C, Nutile T, Sala C, Camaschella C, D'Adamo P, Gasparini P, Ciullo M, Toniolo D.

Eur J Hum Genet. 2011 May;19(5):593-6. doi: 10.1038/ejhg.2010.240. Epub 2011 Jan 19.

13.

Heritability and demographic analyses in the large isolated population of Val Borbera suggest advantages in mapping complex traits genes.

Traglia M, Sala C, Masciullo C, Cverhova V, Lori F, Pistis G, Bione S, Gasparini P, Ulivi S, Ciullo M, Nutile T, Bosi E, Sirtori M, Mignogna G, Rubinacci A, Buetti I, Camaschella C, Petretto E, Toniolo D.

PLoS One. 2009 Oct 22;4(10):e7554. doi: 10.1371/journal.pone.0007554.

14.

A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure.

Corre T, Schuettler J, Bione S, Marozzi A, Persani L, Rossetti R, Torricelli F, Giotti I, Vogt P, Toniolo D; Italian Network for the study of Ovarian Dysfunctions.

Hum Reprod. 2009 Aug;24(8):2023-8. doi: 10.1093/humrep/dep090. Epub 2009 Apr 10.

PMID:
19363042
15.

BMP15 mutations associated with primary ovarian insufficiency cause a defective production of bioactive protein.

Rossetti R, Di Pasquale E, Marozzi A, Bione S, Toniolo D, Grammatico P, Nelson LM, Beck-Peccoz P, Persani L.

Hum Mutat. 2009 May;30(5):804-10. doi: 10.1002/humu.20961.

16.

Alterations in the expression, structure and function of progesterone receptor membrane component-1 (PGRMC1) in premature ovarian failure.

Mansouri MR, Schuster J, Badhai J, Stattin EL, Lösel R, Wehling M, Carlsson B, Hovatta O, Karlström PO, Golovleva I, Toniolo D, Bione S, Peluso J, Dahl N.

Hum Mol Genet. 2008 Dec 1;17(23):3776-83. doi: 10.1093/hmg/ddn274. Epub 2008 Sep 9.

17.

Variation of hemoglobin levels in normal Italian populations from genetic isolates.

Sala C, Ciullo M, Lanzara C, Nutile T, Bione S, Massacane R, d'Adamo P, Gasparini P, Toniolo D, Camaschella C.

Haematologica. 2008 Sep;93(9):1372-5. doi: 10.3324/haematol.12915. Epub 2008 Jul 4.

18.

Highly conserved non-coding sequences and the 18q critical region for short stature: a common mechanism of disease?

Rizzolio F, Bione S, Sala C, Tribioli C, Ciccone R, Zuffardi O, di Iorgi N, Maghnie M, Toniolo D.

PLoS One. 2008 Jan 23;3(1):e1460. doi: 10.1371/journal.pone.0001460.

19.

Heterogeneous molecular mechanisms underlie attenuated familial adenomatous polyposis.

Cattaneo F, Molatore S, Mihalatos M, Apessos A, Venesio T, Bione S, Grignani P, Nasioulas G, Ranzani GN.

Genet Med. 2007 Dec;9(12):836-41.

PMID:
18091433
20.

Sequence variation at the human FOXO3 locus: a study of premature ovarian failure and primary amenorrhea.

Gallardo TD, John GB, Bradshaw K, Welt C, Reijo-Pera R, Vogt PH, Touraine P, Bione S, Toniolo D, Nelson LM, Zinn AR, Castrillon DH.

Hum Reprod. 2008 Jan;23(1):216-21. Epub 2007 Oct 23.

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