Below you can find a list of publications released by or relating to the EuroGrow project.
L. Bonafé, J. Hastbacka, A. de la Chapelle, A.B. Campos-Xavier, C. Chiesa, A. Forlino, A. Superti-Furga and A. Rossi. A novel mutation in the sulphate transporter gene SLC26A2 (DTDST) specific to the Finnish population causes de la Chapelle dysplasia. Journal of Medical Genetics. 2008 Aug 15. [Epub ahead of print]
P. Hermanns, S. Unger, A. Rossi, A. Perez-Aytes, H. Cortina, L. Bonafé, L. Boccone, V. Setzu, M. Dutoit, L. Sangiorgi, F. Pecora, K. Reicherter, G. Nishimura, J. Spranger, B. Zabel and A. Superti-Furga. Congenital Joint Dislocations Caused by Carbohydrate Sulfotransferase 3 Deficiency in Recessive Larsen Syndrome and Humero-Spinal Dysostosis. The American Journal of Human Genetics, 2008 Jun;82(6):1368-74. Erratum in: The American Journal of Human Genetics. 2008 Aug;83(2):293.
D. Belluoccio, B.C. Bernardo, L. Rowley and J.F. Bateman. A microarray approach for comparative expression profiling of the discrete maturation zones of mouse growth plate cartilage. Biochimica et Biophysica Acta 1779 Gene Regulatory Mechanisms, 2008, 330-340.
R. Wilson, D. Belluoccio and J.F. Bateman. Proteomic analysis of cartilage proteins. Methods, 2008, 45(1), 22-31.
R. Wilson and J.F. Bateman. Cartilage proteomics: Challenges, solutions and recent advances. Proteomics: Clinical Applications, 2008, 2(2), 251-263.
S.A. Temtamy, M.S. Aglan, M. Valencia, G. Cocchi, M. Pacheco, A.M. Ashour, K.S. Amr, S.M.H. Helmy, M.A. El-Gammal, M. Wright, P. Lapunzina, J.A. Goodship and V.L. Ruiz-Perez. Long Interspersed Nuclear Element-1 (LINE1) Mediated Deletion of EVC, EVC2, C4orf6 and STK32B in Ellis-van Creveld Syndrome With Borderline Intelligence. Human Mutation, 2008, 29(7), 931-938.
F. Pecora, A. Forlino, B. Gualeni, A. Lupi, S. Giorgetti, L. Marchese, M. Stoppini, R. Tenni, G. Cetta and A. Rossi. A quantitative and qualitative method for direct 2-DE analysis of murine cartilage. Proteomics, 2007, 7, 4003-4007.
