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Andrea Riccio
Andrea Riccio
Università della Campania "Luigi Vanvitelli"
Dirección de correo verificada de unicampania.it
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In embryonic stem cells, ZFP57/KAP1 recognize a methylated hexanucleotide to affect chromatin and DNA methylation of imprinting control regions
S Quenneville, G Verde, A Corsinotti, A Kapopoulou, J Jakobsson, ...
Molecular cell 44 (3), 361-372, 2011
6362011
Plasminogen activator inhibitors: hormonally regulated serpins
PA Andreasen, B Georg, LR Lund, A Riccio, SN Stacey
Molecular and cellular endocrinology 68 (1), 1-19, 1990
5751990
Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement.
F Brioude, JM Kalish, A Mussa, AC Foster, J Bliek, GB Ferrero, ...
Nat Rev Endocrinol 14 (4), 229-249, 2018
465*2018
The H19 locus acts in vivo as a tumor suppressor
T Yoshimizu, A Miroglio, MA Ripoche, A Gabory, M Vernucci, A Riccio, ...
Proceedings of the National Academy of Sciences 105 (34), 12417-12422, 2008
4032008
Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndrome
WN Cooper, A Luharia, GA Evans, H Raza, AC Haire, R Grundy, ...
European journal of human genetics 13 (9), 1025-1032, 2005
3402005
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome
A Sparago, F Cerrato, M Vernucci, GB Ferrero, MC Silengo, A Riccio
Nature genetics 36 (9), 958-960, 2004
3392004
Genomic imprinting disorders: lessons on how genome, epigenome and environment interact
D Monk, DJG Mackay, T Eggermann, ER Maher, A Riccio
Nature Reviews Genetics 20 (4), 235-248, 2019
3342019
Transforming growth factor‐beta is a strong and fast acting positive regulator of the level of type‐1 plasminogen activator inhibitor mRNA in WI‐38 human lung fibroblasts.
LR Lund, A Riccio, PA Andreasen, LS Nielsen, P Kristensen, M Laiho, ...
The EMBO journal 6 (5), 1281-1286, 1987
3051987
The human urokinase-plasminogen activator gene and its promoter
A Riccio, G Grimaldi, P Verde, G Sebastio, S Boast, F Blasi
Nucleic acids research 13 (8), 2759-2771, 1985
2921985
The control region of mitochondrial DNA shows an unusual CpG and non-CpG methylation pattern
D Bellizzi, P D'Aquila, T Scafone, M Giordano, V Riso, A Riccio, ...
DNA research 20 (6), 537-547, 2013
2742013
Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith–Wiedemann syndrome
J Bliek, G Verde, J Callaway, SM Maas, A De Crescenzo, A Sparago, ...
European Journal of Human Genetics 17 (5), 611-619, 2009
2662009
Plasminogen activator inhibitor type‐1: reactive center and amino‐terminal heterogeneity determined by protein and cDNA sequencing
PA Andreasen, A Riccio, KG Welinder, R Douglas, R Sartorio, LS Nielsen, ...
FEBS letters 209 (2), 213-218, 1986
2581986
Plasminogen activator inhibitor type 1 gene is located at region q21. 3-q22 of chromosome 7 and genetically linked with cystic fibrosis.
KW Klinger, R Winqvist, A Riccio, PA Andreasen, R Sartorio, LS Nielsen, ...
Proceedings of the National Academy of Sciences 84 (23), 8548-8552, 1987
2061987
Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci
T Eggermann, G Perez de Nanclares, ER Maher, IK Temple, Z Tümer, ...
Clinical epigenetics 7, 1-18, 2015
1872015
Cancer risk in Beckwith-Wiedemann syndrome: a systematic review and meta-analysis outlining a novel (Epi) genotype specific histotype targeted screening protocol
A Mussa, C Molinatto, G Baldassarre, E Riberi, S Russo, L Larizza, ...
The Journal of pediatrics 176, 142-149. e1, 2016
1542016
Transforming Growth Factor βl-Responsive Element: Closely Associated Binding Sites for USF and CCAAT-Binding Transcription Factor-Nuclear Factor I in the Type 1 Plasminogen …
A Riccio, PV Pedone, LR Lund, T Olesen, H Steen Olsen, PA Andreasen
Molecular and Cellular Biology 12 (4), 1846-1855, 1992
1461992
The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith–Wiedemann syndrome and Silver–Russell …
N Chiesa, A De Crescenzo, K Mishra, L Perone, M Carella, O Palumbo, ...
Human molecular genetics 21 (1), 10-25, 2012
1432012
Mechanisms causing imprinting defects in familial Beckwith–Wiedemann syndrome with Wilms' tumour
A Sparago, S Russo, F Cerrato, S Ferraiuolo, P Castorina, A Selicorni, ...
Human molecular genetics 16 (3), 254-264, 2007
1412007
Prevalence of Beckwith–Wiedemann syndrome in north west of Italy
A Mussa, S Russo, A De Crescenzo, N Chiesa, C Molinatto, A Selicorni, ...
American journal of medical genetics Part A 161 (10), 2481-2486, 2013
1402013
(Epi) genotype–phenotype correlations in Beckwith–Wiedemann syndrome
A Mussa, S Russo, A De Crescenzo, A Freschi, L Calzari, S Maitz, ...
European journal of human genetics 24 (2), 183-190, 2016
1392016
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