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- Table of Contents
Journal of Biomedicine and Biotechnology
Volume 2011 (2011), Article ID 864904, 13 pages
A Symphony of Regulations Centered on p63 to Control Development of Ectoderm-Derived Structures
1Department of Biomolecular Science and Biotechnology, University of Milan, 20133 Milano, Italy
2Department of Dermatology, University of Rome “Tor Vergata”, 00133 Rome, Italy
3Rome Oncogenomic Centre, Via Elio Chianesi 53, 00144 Rome, Italy
4Molecular Biotechnology Center, Dulbecco Telethon Institute, University of Torino, 10126 Torino, Italy
Received 5 October 2010; Revised 25 January 2011; Accepted 16 March 2011
Academic Editor: Thomas Lufkin
Copyright © 2011 Luisa Guerrini et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Citations to this Article [13 citations]
The following is the list of published articles that have cited the current article.
- Heather J. Ray, and Lee Niswander, “Mechanisms of tissue fusion during development,” Development, vol. 139, no. 10, pp. 1701–1711, 2012.
- Schindler, Guazzarotti, Mameli, Urbani, Mozzanica, Guerrini, and Zuccotti, “Vomer aplasia in a patient carrying a de novo mutation of the TP63 gene (3q27),” International Journal of Pediatric Otorhinolaryngology, vol. 77, no. 9, pp. 1606–1608, 2013.
- Louise N. Reynard, and John Loughlin, “Insights from human genetic studies into the pathways involved in osteoarthritis,” Nature Reviews Rheumatology, 2013.
- Istiak Mahfuz, Tom Darling, Simon Wilkins, Stefan White, and Wei Cheng, “New insights into the pathogenesis of bladder exstrophy–epispadias complex,” Journal of Pediatric Urology, 2013.
- Maxence Vieux-Rochas, Luisa Guerrini, Yvan Lallemand, Benoît Robert, Giovanni Levi, Giorgio R. Merlo, Kamal Bouhali, Stefano Mantero, Giulia Garaffo, Paolo Provero, Simonetta Astigiano, Ottavia Barbieri, Mariano F. Caratozzolo, and Apollonia Tullo, “BMP-Mediated Functional Cooperation between Dlx5;Dlx6 and Msx1;Msx2 during Mammalian Limb Development,” PLoS ONE, vol. 8, no. 1, 2013.
- Endika Haro, Irene Delgado, Marisa Junco, Yoshihiko Yamada, Ahmed Mansouri, Kerby C. Oberg, and Marian A. Ros, “Sp6 and Sp8 Transcription Factors Control AER Formation and Dorsal-Ventral Patterning in Limb Development,” Plos Genetics, vol. 10, no. 8, 2014.
- Antonio Costanzo, Natalia Pediconi, Alessandra Narcisi, Francesca Guerrieri, Laura Belloni, Francesca Fausti, Elisabetta Botti, and Massimo Levrero, “TP63 and TP73 in cancer, an unresolved “family” puzzle of complexity, redundancy and hierarchy,” FEBS Letters, 2014.
- Joseph N. Nissimov, and Asit Baran Das Chaudhuri, “Hair curvature: a natural dialectic and review,” Biological Reviews, 2014.
- M. Restelli, T. Lopardo, N. Lo Iacono, G. Garaffo, D. Conte, A. Rustighi, M. Napoli, G. Del Sal, D. Perez-Morga, A. Costanzo, G. R. Merlo, and L. Guerrini, “DLX5, FGF8 and the Pin1 isomerase control Np63 protein stability during limb development: a regulatory loop at the basis of the SHFM and EEC congenital malformations,” Human Molecular Genetics, 2014.
- Michela Restelli, Elisa Molinari, Barbara Marinari, Daniele Conte, Nerina Gnesutta, Antonio Costanzo, Giorgio Roberto Merlo, and Luisa Guerrini, “ FGF8, c-Abl and p300 participate in a pathway that controls stability and function of the ΔNp63 α protein ,” Human Molecular Genetics, vol. 24, no. 15, pp. 4185–4197, 2015.
- Evelyn N. Kouwenhoven, Hans van Bokhoven, and Huiqing Zhou, “Gene regulatory mechanisms orchestrated by p63 in epithelial development and related disorders,” Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms, 2015.
- Daniele Conte, Giulia Garaffo, Nadia Lo Iacono, Stefano Mantero, Stefano Piccolo, Michelangelo Cordenonsi, David Perez-Morga, Valeria Orecchia, Valeria Poli, and Giorgio R. Merlo, “ The apical ectodermal ridge of the mouse model of ectrodactyly Dlx5;Dlx6 −/− shows altered stratification and cell polarity, which are restored by exogenous Wnt5a ligand ,” Human Molecular Genetics, vol. 25, no. 4, pp. 740–754, 2015.
- Leandro Ucela Alves, Eliete Pardono, Paulo A. Otto, and Regina Celia Mingroni Netto, “A novel c. 1037C > G (p.Ala346Gly) mutation in TP63 as cause of the ectrodactyly-ectodermal dysplasia and cleft lip/palate (EEC) syndrome,” Genetics And Molecular Biology, vol. 38, no. 1, pp. 37–41, 2015.