Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
Contraception, Fertilite, Sexualite (1992)|August 4, 1999
[Sex determination in mammals: state of the art]P Berta, P de Santa Barbara, B Boizet, et al.
Human Molecular Genetics|May 16, 1998
Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoformsB Klamt, A Koziell, F Poulat, et al.
Molecular Pharmacology|July 1, 1990
(trans)-1-amino-cyclopentyl-1,3-dicarboxylate stimulates quisqualate phosphoinositide-coupled receptors but not ionotropic glutamate receptors in striatal neurons and Xenopus oocytesO Manzoni, L Fagni, J P Pin, et al.
Hormone Research|January 1, 1992
Molecular analysis of the sex-determining region from the Y chromosome in two patients with Frasier syndromeP Berta, D Morin, F Poulat, et al.
Nucleic Acids Research|November 3, 2001
SOX7 transcription factor: sequence, chromosomal localisation, expression, transactivation and interference with Wnt signallingW Takash, J Cañizares, N Bonneaud, et al.
Biochimie|January 1, 1994
The human testis determining factor SRY: a new member of the HMG box protein familyS Soullier, F Poulat, B Boizet-Bonhoure, et al.
European Journal of Pharmacology|July 12, 1991
Pharmacological characterization of the quisqualate receptor coupled to phospholipase C (Qp) in striatal neuronsO J Manzoni, F Poulat, E Do, et al.
The Biochemical Journal|January 1, 1996
PEST motifs are not required for rapid calpain-mediated proteolysis of c-fos proteinS Carillo, M Pariat, A m Steff, et al.
Human Molecular Genetics|July 1, 1997
SOX22 is a new member of the SOX gene family, mainly expressed in human nervous tissueP Jay, I Sahly, C Gozé, et al.
Oncogene|September 17, 2008
CEACAM1, a SOX9 direct transcriptional target identified in the colon epitheliumH Zalzali, C Naudin, P Bastide, et al.
Pageof 3