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Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|November 19, 2002
The role of reelin in the development and evolution of the cerebral cortexF Tissir, C Lambert de Rouvroit, A M GoffinetMammalian Genome : Official Journal of the International Mammalian Genome Society|June 1, 1994
Assignment of rat Jun family genes to chromosome 19 (Junb), chromosome 5q31-33 (Jun), and chromosome 16 (Jund)C Szpirer, F Tissir, M Rivière, et al.Developmental Dynamics : an Official Publication of the American Association of Anatomists|August 31, 2002
Expression of the ankyrin repeat domain 6 gene (Ankrd6) during mouse brain developmentF Tissir, I Bar, A M Goffinet, et al.The European Journal of Neuroscience|November 19, 2004
Reelin receptors in developing laminated brain structures of mouse and humanC G Perez-Garcia, F Tissir, A M Goffinet, et al.Mechanisms of Development|February 19, 2002
Developmental expression profiles of Celsr (Flamingo) genes in the mouseF Tissir, O De-Backer, A M Goffinet, et al.Cytogenetics and Cell Genetics|January 1, 1996
The rat genes encoding the pancreatitis-associated proteins I, II and III (Pap1, Pap2, Pap3), and the lithostathin/pancreatic stone protein/regeneration protein (Reg) colocalize at 4q33-->q34E Stephanova, F Tissir, N Dusetti, et al.The Journal of Comparative Neurology|January 24, 2003
Reelin expression during embryonic brain development in Crocodylus niloticusF Tissir, C Lambert De Rouvroit, J-Y Sire, et al.Cytogenetics and Cell Genetics|January 1, 1995
Localization of the genes encoding the three rat angiotensin II receptors, Agtr1a, Agtr1b, Agtr2, and the human AGTR2 receptor respectively to rat chromosomes 17q12, 2q24 and Xq34, and the human Xq22F Tissir, M Rivière, D F Guo, et al.Molecular Psychiatry|December 20, 2017
Neural progenitor fate decision defects, cortical hypoplasia and behavioral impairment in Celsr1-deficient miceC Boucherie, C Boutin, Y Jossin, et al.Genomics|April 25, 2000
A clone contig of 12q24.3 encompassing the distal hereditary motor neuropathy type II geneJ Irobi, F Tissir, P De Jonghe, et al.Pageof 2