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Corrigendum: 'Building a perfect body': control of vertebrate organogenesis by PBX-dependent regulatory networks.

Selleri L, Zappavigna V, Ferretti E.

Genes Dev. 2019 May 1;33(9-10):590. doi: 10.1101/gad.326298.119. No abstract available.


'Building a perfect body': control of vertebrate organogenesis by PBX-dependent regulatory networks.

Selleri L, Zappavigna V, Ferretti E.

Genes Dev. 2019 Mar 1;33(5-6):258-275. doi: 10.1101/gad.318774.118. Review. Erratum in: Genes Dev. 2019 May 1;33(9-10):590.


Special Issue on HOX Genes in Development.

Zappavigna V.

J Dev Biol. 2017 May 10;5(2). pii: E5. doi: 10.3390/jdb5020005.


HOX cluster-embedded micro-RNAs and cancer.

Fantini S, Salsi V, Zappavigna V.

Biochim Biophys Acta Rev Cancer. 2018 Apr;1869(2):230-247. doi: 10.1016/j.bbcan.2018.03.002. Epub 2018 Mar 11. Review. No abstract available.


The miR-196b miRNA inhibits the GATA6 intestinal transcription factor and is upregulated in colon cancer patients.

Fantini S, Salsi V, Reggiani L, Maiorana A, Zappavigna V.

Oncotarget. 2017 Jan 17;8(3):4747-4759. doi: 10.18632/oncotarget.13580.


NUP98-fusion transcripts characterize different biological entities within acute myeloid leukemia: a report from the AIEOP-AML group.

Bisio V, Zampini M, Tregnago C, Manara E, Salsi V, Di Meglio A, Masetti R, Togni M, Di Giacomo D, Minuzzo S, Leszl A, Zappavigna V, Rondelli R, Mecucci C, Pession A, Locatelli F, Basso G, Pigazzi M.

Leukemia. 2017 Apr;31(4):974-977. doi: 10.1038/leu.2016.361. Epub 2016 Nov 28. No abstract available.


NUP98 fusion oncoproteins interact with the APC/C(Cdc20) as a pseudosubstrate and prevent mitotic checkpoint complex binding.

Salsi V, Fantini S, Zappavigna V.

Cell Cycle. 2016 Sep;15(17):2275-87. doi: 10.1080/15384101.2016.1172156. Epub 2016 Apr 20.


MicroRNA-196b is transcribed from an autonomous promoter and is directly regulated by Cdx2 and by posterior Hox proteins during embryogenesis.

Fantini S, Salsi V, Vitobello A, Rijli FM, Zappavigna V.

Biochim Biophys Acta. 2015 Aug;1849(8):1066-80. doi: 10.1016/j.bbagrm.2015.06.014. Epub 2015 Jul 2.


MafB is a downstream target of the IL-10/STAT3 signaling pathway, involved in the regulation of macrophage de-activation.

Gemelli C, Zanocco Marani T, Bicciato S, Mazza EM, Boraschi D, Salsi V, Zappavigna V, Parenti S, Selmi T, Tagliafico E, Ferrari S, Grande A.

Biochim Biophys Acta. 2014 May;1843(5):955-64. doi: 10.1016/j.bbamcr.2014.01.021. Epub 2014 Jan 25.


NUP98 fusion oncoproteins promote aneuploidy by attenuating the mitotic spindle checkpoint.

Salsi V, Ferrari S, Gorello P, Fantini S, Chiavolelli F, Mecucci C, Zappavigna V.

Cancer Res. 2014 Feb 15;74(4):1079-90. doi: 10.1158/0008-5472.CAN-13-0912. Epub 2013 Dec 26.


The Orosomucoid 1 protein is involved in the vitamin D - mediated macrophage de-activation process.

Gemelli C, Martello A, Montanari M, Zanocco Marani T, Salsi V, Zappavigna V, Parenti S, Vignudelli T, Selmi T, Ferrari S, Grande A.

Exp Cell Res. 2013 Dec 10;319(20):3201-13. doi: 10.1016/j.yexcr.2013.08.017. Epub 2013 Aug 22.


Emx2 is a dose-dependent negative regulator of Sox2 telencephalic enhancers.

Mariani J, Favaro R, Lancini C, Vaccari G, Ferri AL, Bertolini J, Tonoli D, Latorre E, Caccia R, Ronchi A, Ottolenghi S, Miyagi S, Okuda A, Zappavigna V, Nicolis SK.

Nucleic Acids Res. 2012 Aug;40(14):6461-76. doi: 10.1093/nar/gks295. Epub 2012 Apr 11.


An N-terminal G11A mutation in HOXD13 causes synpolydactyly and interferes with Gli3R function during limb pre-patterning.

Brison N, Debeer P, Fantini S, Oley C, Zappavigna V, Luyten FP, Tylzanowski P.

Hum Mol Genet. 2012 Jun 1;21(11):2464-75. doi: 10.1093/hmg/dds060. Epub 2012 Feb 27.


Control of pelvic girdle development by genes of the Pbx family and Emx2.

Capellini TD, Handschuh K, Quintana L, Ferretti E, Di Giacomo G, Fantini S, Vaccari G, Clarke SL, Wenger AM, Bejerano G, Sharpe J, Zappavigna V, Selleri L.

Dev Dyn. 2011 May;240(5):1173-89. doi: 10.1002/dvdy.22617. Epub 2011 Mar 31.


Pbx homeodomain proteins: TALEnted regulators of limb patterning and outgrowth.

Capellini TD, Zappavigna V, Selleri L.

Dev Dyn. 2011 May;240(5):1063-86. doi: 10.1002/dvdy.22605. Epub 2011 Mar 17. Review.


Scapula development is governed by genetic interactions of Pbx1 with its family members and with Emx2 via their cooperative control of Alx1.

Capellini TD, Vaccari G, Ferretti E, Fantini S, He M, Pellegrini M, Quintana L, Di Giacomo G, Sharpe J, Selleri L, Zappavigna V.

Development. 2010 Aug 1;137(15):2559-69. doi: 10.1242/dev.048819.


HOXD13 binds DNA replication origins to promote origin licensing and is inhibited by geminin.

Salsi V, Ferrari S, Ferraresi R, Cossarizza A, Grande A, Zappavigna V.

Mol Cell Biol. 2009 Nov;29(21):5775-88. doi: 10.1128/MCB.00509-09. Epub 2009 Aug 24.


A G220V substitution within the N-terminal transcription regulating domain of HOXD13 causes a variant synpolydactyly phenotype.

Fantini S, Vaccari G, Brison N, Debeer P, Tylzanowski P, Zappavigna V.

Hum Mol Genet. 2009 Mar 1;18(5):847-60. doi: 10.1093/hmg/ddn410. Epub 2008 Dec 5.


Hoxd13 binds in vivo and regulates the expression of genes acting in key pathways for early limb and skeletal patterning.

Salsi V, Vigano MA, Cocchiarella F, Mantovani R, Zappavigna V.

Dev Biol. 2008 May 15;317(2):497-507. doi: 10.1016/j.ydbio.2008.02.048. Epub 2008 Mar 8.


A cup full of functions.

Piccioni F, Zappavigna V, Verrotti AC.

RNA Biol. 2005 Oct-Dec;2(4):125-8. Epub 2005 Dec 14. Review.


Pbx1/Pbx2 requirement for distal limb patterning is mediated by the hierarchical control of Hox gene spatial distribution and Shh expression.

Capellini TD, Di Giacomo G, Salsi V, Brendolan A, Ferretti E, Srivastava D, Zappavigna V, Selleri L.

Development. 2006 Jun;133(11):2263-73. Epub 2006 May 3.


Translational regulation during oogenesis and early development: the cap-poly(A) tail relationship.

Piccioni F, Zappavigna V, Verrotti AC.

C R Biol. 2005 Oct-Nov;328(10-11):863-81. Epub 2005 Jun 8. Review.


Identification of a conserved 125 base-pair Hb9 enhancer that specifies gene expression to spinal motor neurons.

Nakano T, Windrem M, Zappavigna V, Goldman SA.

Dev Biol. 2005 Jul 15;283(2):474-85.


MAB21L2, a vertebrate member of the Male-abnormal 21 family, modulates BMP signaling and interacts with SMAD1.

Baldessari D, Badaloni A, Longhi R, Zappavigna V, Consalez GG.

BMC Cell Biol. 2004 Dec 21;5(1):48.


Cup is a nucleocytoplasmic shuttling protein that interacts with the eukaryotic translation initiation factor 4E to modulate Drosophila ovary development.

Zappavigna V, Piccioni F, Villaescusa JC, Verrotti AC.

Proc Natl Acad Sci U S A. 2004 Oct 12;101(41):14800-5. Epub 2004 Oct 1.


Integration of anteroposterior and dorsoventral regulation of Phox2b transcription in cranial motoneuron progenitors by homeodomain proteins.

Samad OA, Geisen MJ, Caronia G, Varlet I, Zappavigna V, Ericson J, Goridis C, Rijli FM.

Development. 2004 Aug;131(16):4071-83.


An I47L substitution in the HOXD13 homeodomain causes a novel human limb malformation by producing a selective loss of function.

Caronia G, Goodman FR, McKeown CM, Scambler PJ, Zappavigna V.

Development. 2003 Apr;130(8):1701-12. Erratum in: Development. 2003 May;130(10):2289.


Characterization of PREP2, a paralog of PREP1, which defines a novel sub-family of the MEINOX TALE homeodomain transcription factors.

Fognani C, Kilstrup-Nielsen C, Berthelsen J, Ferretti E, Zappavigna V, Blasi F.

Nucleic Acids Res. 2002 May 1;30(9):2043-51.


The recruitment of SOX/OCT complexes and the differential activity of HOXA1 and HOXB1 modulate the Hoxb1 auto-regulatory enhancer function.

Di Rocco G, Gavalas A, Popperl H, Krumlauf R, Mavilio F, Zappavigna V.

J Biol Chem. 2001 Jun 8;276(23):20506-15. Epub 2001 Mar 1.


Control of vertebrate limb outgrowth by the proximal factor Meis2 and distal antagonism of BMPs by Gremlin.

Capdevila J, Tsukui T, Rodríquez Esteban C, Zappavigna V, Izpisúa Belmonte JC.

Mol Cell. 1999 Nov;4(5):839-49.


Two murine and human homologs of mab-21, a cell fate determination gene involved in Caenorhabditis elegans neural development.

Mariani M, Baldessari D, Francisconi S, Viggiano L, Rocchi M, Zappavigna V, Malgaretti N, Consalez GG.

Hum Mol Genet. 1999 Dec;8(13):2397-406.


Definition of the transcriptional activation domains of three human HOX proteins depends on the DNA-binding context.

Viganò MA, Di Rocco G, Zappavigna V, Mavilio F.

Mol Cell Biol. 1998 Nov;18(11):6201-12.


The novel homeoprotein Prep1 modulates Pbx-Hox protein cooperativity.

Berthelsen J, Zappavigna V, Ferretti E, Mavilio F, Blasi F.

EMBO J. 1998 Mar 2;17(5):1434-45.


Prep1, a novel functional partner of Pbx proteins.

Berthelsen J, Zappavigna V, Mavilio F, Blasi F.

EMBO J. 1998 Mar 2;17(5):1423-33.


Functional dissection of a transcriptionally active, target-specific Hox-Pbx complex.

Di Rocco G, Mavilio F, Zappavigna V.

EMBO J. 1997 Jun 16;16(12):3644-54.


HMG1 interacts with HOX proteins and enhances their DNA binding and transcriptional activation.

Zappavigna V, Falciola L, Helmer-Citterich M, Mavilio F, Bianchi ME.

EMBO J. 1996 Sep 16;15(18):4981-91.


Inhibition of proliferation and induction of differentiation of pluripotent human embryonal carcinoma cells by osteogenic protein-1 (or bone morphogenetic protein-7).

Andrews PW, Damjanov I, Berends J, Kumpf S, Zappavigna V, Mavilio F, Sampath K.

Lab Invest. 1994 Aug;71(2):243-51.


Comparison of mouse and human HOX-4 complexes defines conserved sequences involved in the regulation of Hox-4.4.

Renucci A, Zappavigna V, Zàkàny J, Izpisúa-Belmonte JC, Bürki K, Duboule D.

EMBO J. 1992 Apr;11(4):1459-68.


The upstream region of the human homeobox gene HOX3D is a target for regulation by retinoic acid and HOX homeoproteins.

Arcioni L, Simeone A, Guazzi S, Zappavigna V, Boncinelli E, Mavilio F.

EMBO J. 1992 Jan;11(1):265-77.


HOX4 genes encode transcription factors with potential auto- and cross-regulatory capacities.

Zappavigna V, Renucci A, Izpisúa-Belmonte JC, Urier G, Peschle C, Duboule D.

EMBO J. 1991 Dec;10(13):4177-87.


Primary structure and embryonic expression pattern of the mouse Hox-4.3 homeobox gene.

Izpisùa-Belmonte JC, Dollé P, Renucci A, Zappavigna V, Falkenstein H, Duboule D.

Development. 1990 Nov;110(3):733-45.


Molecular mechanisms underlying the expression of the human HOX-5.1 gene.

Cianetti L, Di Cristofaro A, Zappavigna V, Bottero L, Boccoli G, Testa U, Russo G, Boncinelli E, Peschle C.

Nucleic Acids Res. 1990 Aug 11;18(15):4361-8.


Differential expression of human HOX-2 genes along the anterior-posterior axis in embryonic central nervous system.

Giampaolo A, Acampora D, Zappavigna V, Pannese M, D'Esposito M, Carè A, Faiella A, Stornaiuolo A, Russo G, Simeone A, et al.

Differentiation. 1989 Jun;40(3):191-7.


Human acute myelogenous and lymphoid leukemias: pattern of expression of cellular oncogenes.

Sposi NM, Mavilio F, Petrini M, Bottero L, Zappavigna V, Mastroberardino G, De Rossi G, Amadori S, Mandelli F, Peschle C.

Haematologica. 1987 Nov-Dec;72(6 Suppl):23-6. No abstract available.


Two human homeobox genes, c1 and c8: structure analysis and expression in embryonic development.

Simeone A, Mavilio F, Acampora D, Giampaolo A, Faiella A, Zappavigna V, D'Esposito M, Pannese M, Russo G, Boncinelli E, et al.

Proc Natl Acad Sci U S A. 1987 Jul;84(14):4914-8.

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