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Items: 44

1.

Enigmatic Ladies of the Rings: How Cohesin Dysfunction Affects Myeloid Neoplasms Insurgence.

Pezzotta A, Mazzola M, Spreafico M, Marozzi A, Pistocchi A.

Front Cell Dev Biol. 2019 Feb 27;7:21. doi: 10.3389/fcell.2019.00021. eCollection 2019.

2.

High-resolution array-CGH analysis on 46,XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian function.

Bestetti I, Castronovo C, Sironi A, Caslini C, Sala C, Rossetti R, Crippa M, Ferrari I, Pistocchi A, Toniolo D, Persani L, Marozzi A, Finelli P.

Hum Reprod. 2019 Mar 1;34(3):574-583. doi: 10.1093/humrep/dey389.

3.

NIPBL: a new player in myeloid cell differentiation.

Mazzola M, Deflorian G, Pezzotta A, Ferrari L, Fazio G, Bresciani E, Saitta C, Ferrari L, Fumagalli M, Parma M, Marasca F, Bodega B, Riva P, Cotelli F, Biondi A, Marozzi A, Cazzaniga G, Pistocchi A.

Haematologica. 2019 Jul;104(7):1332-1341. doi: 10.3324/haematol.2018.200899. Epub 2019 Jan 10.

4.

HDAC8 regulates canonical Wnt pathway to promote differentiation in skeletal muscles.

Ferrari L, Bragato C, Brioschi L, Spreafico M, Esposito S, Pezzotta A, Pizzetti F, Moreno-Fortuny A, Bellipanni G, Giordano A, Riva P, Frabetti F, Viani P, Cossu G, Mora M, Marozzi A, Pistocchi A.

J Cell Physiol. 2019 May;234(5):6067-6076. doi: 10.1002/jcp.27341. Epub 2018 Sep 24.

5.

Effects of Short-Distance Recreational Mushing on Oxytocin, Gastrin, and Creatinine Kinase in Sled Dogs.

Leggieri LR, Marozzi A, Panebianco A, Gregorio P, Carmanchahi P.

J Appl Anim Welf Sci. 2018 Jul 30:1-9. doi: 10.1080/10888705.2018.1500287. [Epub ahead of print]

PMID:
30058379
6.

Investigating the role of X chromosome breakpoints in premature ovarian failure.

Baronchelli S, Villa N, Redaelli S, Lissoni S, Saccheri F, Panzeri E, Conconi D, Bentivegna A, Crosti F, Sala E, Bertola F, Marozzi A, Pedicini A, Ventruto M, Police MA, Dalprà L.

Mol Cytogenet. 2012 Jul 16;5(1):32. doi: 10.1186/1755-8166-5-32.

7.

Cytogenetics of premature ovarian failure: an investigation on 269 affected women.

Baronchelli S, Conconi D, Panzeri E, Bentivegna A, Redaelli S, Lissoni S, Saccheri F, Villa N, Crosti F, Sala E, Martinoli E, Volontè M, Marozzi A, Dalprà L.

J Biomed Biotechnol. 2011;2011:370195. doi: 10.1155/2011/370195. Epub 2011 Jan 17.

8.

Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiation.

Bodega B, Ramirez GD, Grasser F, Cheli S, Brunelli S, Mora M, Meneveri R, Marozzi A, Mueller S, Battaglioli E, Ginelli E.

BMC Biol. 2009 Jul 16;7:41. doi: 10.1186/1741-7007-7-41.

9.

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
10.

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.

11.

Evolutionary genomic remodelling of the human 4q subtelomere (4q35.2).

Bodega B, Cardone MF, Müller S, Neusser M, Orzan F, Rossi E, Battaglioli E, Marozzi A, Riva P, Rocchi M, Meneveri R, Ginelli E.

BMC Evol Biol. 2007 Mar 14;7:39.

12.

Forced expression of RDH10 gene retards growth of HepG2 cells.

Rossi E, Picozzi P, Bodega B, Lavazza C, Carlo-Stella C, Marozzi A, Ginelli E.

Cancer Biol Ther. 2007 Feb;6(2):238-44. Epub 2007 Feb 25.

PMID:
17218779
13.

The boundary of macaque rDNA is constituted by low-copy sequences conserved during evolution.

Bodega B, Cardone MF, Rocchi M, Meneveri R, Marozzi A, Ginelli E.

Genomics. 2006 Nov;88(5):564-71. Epub 2006 Jun 9.

14.

Skewed X-chromosome inactivation is not associated with premature ovarian failure in a large cohort of Italian patients.

Bione S, Benedetti S, Goegan M, Menditto I, Marozzi A, Ferrari M, Toniolo D.

Am J Med Genet A. 2006 Jun 15;140(12):1349-51. No abstract available.

PMID:
16691602
15.

Identification of new variants of human BMP15 gene in a large cohort of women with premature ovarian failure.

Di Pasquale E, Rossetti R, Marozzi A, Bodega B, Borgato S, Cavallo L, Einaudi S, Radetti G, Russo G, Sacco M, Wasniewska M, Cole T, Beck-Peccoz P, Nelson LM, Persani L.

J Clin Endocrinol Metab. 2006 May;91(5):1976-9. Epub 2006 Feb 7.

PMID:
16464940
16.

Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestation.

Bodega B, Bione S, Dalprà L, Toniolo D, Ornaghi F, Vegetti W, Ginelli E, Marozzi A.

Hum Reprod. 2006 Apr;21(4):952-7. Epub 2005 Dec 16.

PMID:
16361284
17.

Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1B.

Bione S, Rizzolio F, Sala C, Ricotti R, Goegan M, Manzini MC, Battaglia R, Marozzi A, Vegetti W, Dalprà L, Crosignani PG, Ginelli E, Nappi R, Bernabini S, Bruni V, Torricelli F, Zuffardi O, Toniolo D.

Hum Reprod. 2004 Dec;19(12):2759-66. Epub 2004 Sep 30.

PMID:
15459172
18.

Evolution of beta satellite DNA sequences: evidence for duplication-mediated repeat amplification and spreading.

Cardone MF, Ballarati L, Ventura M, Rocchi M, Marozzi A, Ginelli E, Meneveri R.

Mol Biol Evol. 2004 Sep;21(9):1792-9. Epub 2004 Jun 16.

PMID:
15201396
19.

Mutations in the coding region of the FOXL2 gene are not a major cause of idiopathic premature ovarian failure.

Bodega B, Porta C, Crosignani PG, Ginelli E, Marozzi A.

Mol Hum Reprod. 2004 Aug;10(8):555-7. Epub 2004 Jun 4.

PMID:
15181179
20.

Genomic organization and transcription of the human retinol dehydrogenase 10 (RDH10) gene.

Picozzi P, Marozzi A, Fornasari D, Benfante R, Barisani D, Meneveri R, Ginelli E.

FEBS Lett. 2003 Nov 6;554(1-2):59-66.

21.

Gene expression analysis in interstitial lung edema induced by saline infusion.

Sabbadini M, Barisani D, Conforti E, Marozzi A, Ginelli E, Miserocchi G, Meneveri R.

Biochim Biophys Acta. 2003 Jul 14;1638(2):149-56.

22.

Human genome dispersal and evolution of 4q35 duplications and interspersed LSau repeats.

Ballarati L, Piccini I, Carbone L, Archidiacono N, Rollier A, Marozzi A, Meneveri R, Ginelli E.

Gene. 2002 Aug 21;296(1-2):21-7.

PMID:
12383499
23.

Mutation analysis of the inhibin alpha gene in a cohort of Italian women affected by ovarian failure.

Marozzi A, Porta C, Vegetti W, Crosignani PG, Tibiletti MG, Dalprà L, Ginelli E.

Hum Reprod. 2002 Jul;17(7):1741-5.

PMID:
12093833
24.

The structure of duplications on human acrocentric chromosome short arms derived by the analysis of 15p.

Piccini I, Ballarati L, Bassi C, Rocchi M, Marozzi A, Ginelli E, Meneveri R.

Hum Genet. 2001 Jun;108(6):467-77.

PMID:
11499671
25.

Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure.

Marozzi A, Manfredini E, Tibiletti MG, Furlan D, Villa N, Vegetti W, Crosignani PG, Ginelli E, Meneveri R, Dalprà L.

Hum Genet. 2000 Oct;107(4):304-11.

PMID:
11129329
26.

Molecular structure and evolution of DNA sequences located at the alpha satellite boundary of chromosome 20.

Bassi C, Magnani I, Sacchi N, Saccone S, Ventura A, Rocchi M, Marozzi A, Ginelli E, Meneveri R.

Gene. 2000 Oct 3;256(1-2):43-50.

PMID:
11054534
27.

Premature ovarian failure.

Vegetti W, Marozzi A, Manfredini E, Testa G, Alagna F, Nicolosi A, Caliari I, Taborelli M, Tibiletti MG, Dalprà L, Crosignani PG.

Mol Cell Endocrinol. 2000 Mar 30;161(1-2):53-7.

PMID:
10773392
28.

Association between idiopathic premature ovarian failure and fragile X premutation.

Marozzi A, Vegetti W, Manfredini E, Tibiletti MG, Testa G, Crosignani PG, Ginelli E, Meneveri R, Dalprà L.

Hum Reprod. 2000 Jan;15(1):197-202.

PMID:
10611212
29.

FRAXA premutations are not a cause of familial premature ovarian failure.

Marozzi A, Dalprà L, Ginelli E, Tibiletti MG, Crosignani PG.

Hum Reprod. 1999 Feb;14(2):573-5. No abstract available.

PMID:
10100016
30.

Nitric oxide reduces nontransferrin-bound iron transport in HepG2 cells.

Barisani D, Cairo G, Ginelli E, Marozzi A, Conte D.

Hepatology. 1999 Feb;29(2):464-70.

PMID:
9918923
31.

In vitro selection of HIV-1 TAR variants by the Tat protein.

Marozzi A, Meneveri R, Giacca M, Gutierrez MI, Siccardi AG, Ginelli E.

J Biotechnol. 1998 Apr 15;61(2):117-28.

PMID:
9654745
32.

Functional marker chromosomes lacking detectable alpha satellite DNA: a tool for centromere study.

Magnani I, Meneveri R, Marozzi A, Ginelli E, Fuhrman-Conti AM, Darfler M, Monard SP, Sacchi N.

Chromosome Res. 1998 Jan;6(1):69-71. No abstract available.

PMID:
9510515
33.

Molecular characterization of a variant of proviral bovine leukaemia virus (BLV).

Molteni E, Agresti A, Meneveri R, Marozzi A, Malcovati M, Bonizzi L, Poli G, Ginelli E.

Zentralbl Veterinarmed B. 1996 Jun;43(4):201-11.

PMID:
8767766
34.

Expression of distinct conformations of free HLA-Cw4 heavy chains in transfected neuroblastoma cells.

Marozzi A, Meneveri R, De Santis C, Robbioni P, Molteni E, Beretta A, Siccardi AG, Ginelli E.

Immunogenetics. 1996;43(5):289-95.

PMID:
9110932
35.

Analysis of GC-rich repetitive nucleotide sequences in great apes.

Meneveri R, Agresti A, Rocchi M, Marozzi A, Ginelli E.

J Mol Evol. 1995 Apr;40(4):405-12.

PMID:
7769618
36.

Expression of beta 2m-free HLA class I heavy chains in neuroblastoma cell lines.

Marozzi A, Meneveri R, Bunone G, De Santis C, Lopalco L, Beretta A, Agresti A, Siccardi AG, Della Valle G, Ginelli E.

Scand J Immunol. 1993 Jun;37(6):661-7.

PMID:
8316764
37.

Use of polymerase chain reaction to diagnose bovine leukemia virus infection in calves at birth.

Agresti A, Ponti W, Rocchi M, Meneveri R, Marozzi A, Cavalleri D, Peri E, Poli G, Ginelli E.

Am J Vet Res. 1993 Mar;54(3):373-8.

PMID:
8388673
38.

Molecular organization and chromosomal location of human GC-rich heterochromatic blocks.

Meneveri R, Agresti A, Marozzi A, Saccone S, Rocchi M, Archidiacono N, Corneo G, Della Valle G, Ginelli E.

Gene. 1993 Jan 30;123(2):227-34.

PMID:
8428662
39.

Expression of a transfected H-2Kb gene in B16 cells correlates with suppression of liver metastases in triple immunodeficient mice.

Calorini L, Marozzi A, Byers HR, Waneck GL, Lee KW, Isselbacher KJ, Gattoni-Celli S.

Cancer Res. 1992 Jul 15;52(14):4036-41.

40.

High dose intravenous immunoglobulin (IVIgG) in Evans' syndrome.

Bolis S, Marozzi A, Rossini F, Casaroli I, Pogliani EM, Corneo G.

Allergol Immunopathol (Madr). 1991 Sep-Oct;19(5):186. No abstract available.

PMID:
1811414
41.

Partial suppression of metastatic potential of malignant cells in immunodeficient mice caused by transfection of H-2Kb gene.

Gattoni-Celli S, Marozzi A, Timpane R, Kirsch K, Isselbacher KJ.

J Natl Cancer Inst. 1990 Jun 6;82(11):960-3. No abstract available.

PMID:
2342131
42.

Linkage in human heterochromatin between highly divergent Sau3A repeats and a new family of repeated DNA sequences (HaeIII family).

Agresti A, Meneveri R, Siccardi AG, Marozzi A, Corneo G, Gaudi S, Ginelli E.

J Mol Biol. 1989 Feb 20;205(4):625-31.

PMID:
2538633
43.

CNS metastasis in ovarian cancer with microangiopathic hemolytic anemia associated with diffuse intravascular coagulation.

Pogliani EM, Fowst C, Maffé P, Marozzi A, Stefani M, Polli E.

Tumori. 1988 Dec 31;74(6):731-6.

PMID:
3232217
44.

Cerebral parenchymal involvement in acute promyelocytic leukemia. A case report.

Pogliani EM, Fowst C, Marozzi A, Salvatore M, Polli EE.

Haematologica. 1988 Jan-Feb;73(1):71-3. No abstract available.

PMID:
3131209

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