Vincenzo Zappavigna
Overview
Explore the profile of Vincenzo Zappavigna including associated specialties, affiliations and a list of published articles.
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30
Citations
584
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Recent Articles
11.
Gemelli C, Zanocco Marani T, Bicciato S, Mazza E, Boraschi D, Salsi V, et al.
Biochim Biophys Acta
. 2014 Jan;
1843(5):955-64.
PMID: 24472656
In spite of the numerous reports implicating MafB transcription factor in the molecular control of monocyte-macrophage differentiation, the precise genetic program underlying this activity has been, to date, poorly understood....
12.
Salsi V, Ferrari S, Gorello P, Fantini S, Chiavolelli F, Mecucci C, et al.
Cancer Res
. 2013 Dec;
74(4):1079-90.
PMID: 24371226
NUP98 is a recurrent fusion partner in chromosome translocations that cause acute myelogenous leukemia. NUP98, a nucleoporin, and its interaction partner Rae1, have been implicated in the control of chromosome...
13.
Gemelli C, Martello A, Montanari M, Zanocco Marani T, Salsi V, Zappavigna V, et al.
Exp Cell Res
. 2013 Aug;
319(20):3201-13.
PMID: 23973664
Orosomucoid 1 (ORM1), also named Alpha 1 acid glycoprotein A (AGP-A), is an abundant plasma protein characterized by anti-inflammatory and immune-modulating properties. The present study was designed to identify a...
14.
Brison N, Debeer P, Fantini S, Oley C, Zappavigna V, Luyten F, et al.
Hum Mol Genet
. 2012 Mar;
21(11):2464-75.
PMID: 22373878
Synpolydactyly (SPD) is a distal limb anomaly characterized by incomplete digit separation and the presence of supernumerary digits in the syndactylous web. This phenotype has been associated with mutations in...
15.
Capellini T, Handschuh K, Quintana L, Ferretti E, Di Giacomo G, Fantini S, et al.
Dev Dyn
. 2011 Apr;
240(5):1173-89.
PMID: 21455939
Genes expressed in the somatopleuric mesoderm, the embryonic domain giving rise to the vertebrate pelvis, appear important for pelvic girdle formation. Among such genes, Pbx family members and Emx2 were...
16.
Capellini T, Zappavigna V, Selleri L
Dev Dyn
. 2011 Mar;
240(5):1063-86.
PMID: 21416555
Limb development has long provided an excellent model for understanding the genetic principles driving embryogenesis. Studies utilizing chick and mouse have led to new insights into limb patterning and morphogenesis....
17.
Capellini T, Vaccari G, Ferretti E, Fantini S, He M, Pellegrini M, et al.
Development
. 2010 Jul;
137(15):2559-69.
PMID: 20627960
The genetic pathways underlying shoulder blade development are largely unknown, as gene networks controlling limb morphogenesis have limited influence on scapula formation. Analysis of mouse mutants for Pbx and Emx2...
18.
Salsi V, Ferrari S, Ferraresi R, Cossarizza A, Grande A, Zappavigna V
Mol Cell Biol
. 2009 Aug;
29(21):5775-88.
PMID: 19703996
HOX DNA-binding proteins control patterning during development by regulating processes such as cell aggregation and proliferation. Recently, a possible involvement of HOX proteins in replication origin activity was suggested by...
19.
Fantini S, Vaccari G, Brison N, Debeer P, Tylzanowski P, Zappavigna V
Hum Mol Genet
. 2008 Dec;
18(5):847-60.
PMID: 19060004
The 5' members of the HoxD gene cluster (paralogous groups 9-13) are crucial for correct vertebrate limb patterning. Mutations in the HOXD13 gene have been found to cause synpolydactyly (SPD)...
20.
Salsi V, Vigano M, Cocchiarella F, Mantovani R, Zappavigna V
Dev Biol
. 2008 Apr;
317(2):497-507.
PMID: 18407260
5' HoxD genes are required for the correct formation of limb skeletal elements. Hoxd13, the most 5'-located HoxD gene, is important for patterning the most distal limb region, and its...