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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 29, 2000
The lack of Emx2 causes impairment of Reelin signaling and defects of neuronal migration in the developing cerebral cortexA Mallamaci, S Mercurio, L Muzio, et al.Mechanisms of Development|November 1, 1993
Prox 1, a prospero-related homeobox gene expressed during mouse developmentG Oliver, B Sosa-Pineda, S Geisendorf, et al.Oncogene|February 1, 1990
Tumorigenesis and eye abnormalities in transgenic mice expressing MSV-SV40 large T-antigenF Theuring, W Götz, R Balling, et al.Development (Cambridge, England)|November 1, 1992
PAX8, a human paired box gene: isolation and expression in developing thyroid, kidney and Wilms' tumorsA Poleev, H Fickenscher, S Mundlos, et al.BMC Infectious Diseases|August 20, 2021
A case report of Nocardia spp. infective endocarditis in an injection drug userChukwunyelu Enwezor, Courtney L Russ-Friedman, Zachary P Gruss, et al.Development (Cambridge, England)|February 1, 1988
Coding sequence and expression of the homeobox gene Hox 1.3M Fibi, B Zink, M Kessel, et al.Genes & Development|December 1, 1988
A mouse gene homologous to the Drosophila gene caudal is expressed in epithelial cells from the embryonic intestineP Duprey, K Chowdhury, G R Dressler, et al.Development (Cambridge, England)|June 24, 1998
Vax1 is a novel homeobox-containing gene expressed in the developing anterior ventral forebrainM Hallonet, T Hollemann, R Wehr, et al.Nature|February 13, 1992
Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box geneM Tassabehji, A P Read, V E Newton, et al.Nature Genetics|January 1, 1993
Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2M Tassabehji, A P Read, V E Newton, et al.Pageof 28