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VACTERL/caudal regression/Currarino syndrome-like malformations in mice with mutation in the proprotein convertase Pcsk5.
Szumska D, Pieles G, Essalmani R, Bilski M, Mesnard D, Kaur K, Franklyn A, El Omari K, Jefferis J, Bentham J, Taylor JM, Schneider JE, Arnold SJ, Johnson P, Tymowska-Lalanne Z, Stammers D, Clarke K, Neubauer S, Morris A, Brown SD, Shaw-Smith C, Cama A, Capra V, Ragoussis J, Constam D, Seidah NG, Prat A, Bhattacharya S. Szumska D, et al. Among authors: capra v. Genes Dev. 2008 Jun 1;22(11):1465-77. doi: 10.1101/gad.479408. Genes Dev. 2008. PMID: 18519639 Free PMC article.
HLXB9 homeobox gene and caudal regression syndrome.
Merello E, De Marco P, Mascelli S, Raso A, Calevo MG, Torre M, Cama A, Lerone M, Martucciello G, Capra V. Merello E, et al. Among authors: capra v. Birth Defects Res A Clin Mol Teratol. 2006 Mar;76(3):205-9. doi: 10.1002/bdra.20234. Birth Defects Res A Clin Mol Teratol. 2006. PMID: 16498628
Urological outcome in patients with Currarino syndrome.
Pio L, Piatelli G, Rossi A, Scarsi P, Merello E, Capra V, Cama A, Buffa P, Torre M. Pio L, et al. Among authors: capra v. J Pediatr Surg. 2014 Nov;49(11):1643-6. doi: 10.1016/j.jpedsurg.2014.05.038. Epub 2014 Oct 31. J Pediatr Surg. 2014. PMID: 25475810
Human neural tube defects: genetic causes and prevention.
De Marco P, Merello E, Cama A, Kibar Z, Capra V. De Marco P, et al. Among authors: capra v. Biofactors. 2011 Jul-Aug;37(4):261-8. doi: 10.1002/biof.170. Epub 2011 Jun 14. Biofactors. 2011. PMID: 21674647 Review.
259 results