Genetic and epigenetic mutations affect the DNA binding capability of human ZFP57 in transient neonatal diabetes type 1

Autor: Baglivo I, Esposito S, De Cesare L, Sparago A, Anvar Z, Riso V, Cammisa M, Fattorusso R, Grimaldi G, Riccio A, Pedone PV.

Publikováno v: FEBS letters
(2013). doi:10.1016/j.febslet.2013.02.045.
info:cnr-pdr/source/autori:Baglivo I, Esposito S, De Cesare L, Sparago A, Anvar Z, Riso V, Cammisa M, Fattorusso R, Grimaldi G, Riccio A, Pedone PV./titolo:Genetic and epigenetic mutations affect the DNA binding capability of human ZFP57 in transient neonatal diabetes type 1./doi:10.1016%2Fj.febslet.2013.02.045./rivista:FEBS letters (Print)/anno:2013/pagina_da:/pagina_a:/intervallo_pagine:/volume

In the mouse, ZFP57 contains three classical Cys2His2 zinc finger domains (ZF) and recognizes the methylated TGCmetCGC target sequence using the first and the second ZFs. In this study, we demonstrate that the human ZFP57 (hZFP57) containing six Cys2

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::743350adf35d6923d3435d9b09ba585d
https://publications.cnr.it/doc/208303

Relaxation of Insulin-like growth factor-2 imprinting and discordant methylation at KvDMR1 in two first-cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes

Autor: SPERANDEO MP, UNGARO P, VERNUCCI M, PEDONE PV, CERRATO F, PERONE L, CASOLA S, CUBELLIS, MARIA VITTORIA, SEBASTIO G, RICCIO A., BRUNI, CARMELO BRUNO, ANDRIA, GENEROSO

Beckwith-Wiedeman syndrome (BWS) and Klippel-Trenaunay-Weber syndrome (KTWS) are different human disorders characterized, among other features, by tissue overgrowth. Deregulation of one or more imprinted genes located at chromosome 11p15.5, of which

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3730::08541dfff4a3959b1c4fbcd6ab375189
http://hdl.handle.net/11588/131549

Deregulation of Insulin Like Growth Factor-2(IGF-2) activity as possible common mechanism in the pathogenesis of different overgrwth disorders: molecular studies on Beckwith-Wiedemann syndrome, Klippel-Trenaunay-Weber syndrome and isolated Hemihypertrophy

Autor: Riccio A, Pedone PV, Ungaro P, Casola S, Vernucci M, Besnard N

Publikováno v: 6th Convention Telethon, 1997
info:cnr-pdr/source/autori:Riccio A, Pedone PV, Ungaro P, Casola S, Vernucci M, Besnard N/congresso_nome:6th Convention Telethon/congresso_luogo:/congresso_data:1997/anno:1997/pagina_da:/pagina_a:/intervallo_pagine

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::066dc040626944851c9fafe4bd933a4a
http://www.cnr.it/prodotto/i/213797

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