Zobrazeno 1 - 10
of 104
pro vyhledávání: '"Andrée Dierich"'
Autor:
Stéphanie Migrenne, Evelyne Moreau, Pirjo Pakarinen, Andrée Dierich, Jorge Merlet, René Habert, Chrystèle Racine
Publikováno v:
PLoS ONE, Vol 7, Iss 12, p e53257 (2012)
It is currently admitted that Follicle-Stimulating Hormone (FSH) is physiologically involved in the development and function of fetal/neonatal Sertoli cells in the rat but not the mouse. However, FSH is produced by both species from late fetal life o
Externí odkaz:
https://doaj.org/article/ad20107a1fcf45a89e911906bbfa1028
Publikováno v:
Clinical and Developmental Immunology, Vol 3, Iss 4, Pp 239-246 (1994)
Externí odkaz:
https://doaj.org/article/72344f9ed5504f9a872f446f30fa74ea
Publikováno v:
genesis; Vol 50
genesis
genesis
To facilitate the use of the new mutant resource developed in the mouse, we have generated Cre and FlpO deleter mice on a pure inbred C57BL/6N background. The new transgenic constructs were designed to drive either the Cre or FlpO recombinase, fused
Autor:
Jeremie Vitte, Anne Tarrade, Sabrina Courageot, Judith Melki, Etienne Mouisel, Delphine Charvin, Alain Thorel, Andrée Dierich, Nuria Fonknechten, Danielle Seilhean, Coralie Fassier, Natacha Roblot, Leticia Peris, Jean Jacques Hauw
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2006, 15 (24), pp.3544-58. ⟨10.1093/hmg/ddl431⟩
Human Molecular Genetics, 2006, 15 (24), pp.3544-58. ⟨10.1093/hmg/ddl431⟩
Human Molecular Genetics, Oxford University Press (OUP), 2006, 15 (24), pp.3544-58. ⟨10.1093/hmg/ddl431⟩
Human Molecular Genetics, 2006, 15 (24), pp.3544-58. ⟨10.1093/hmg/ddl431⟩
International audience; Mutations of the spastin gene (Sp) are responsible for the most frequent autosomal dominant form of spastic paraplegia, a disease characterized by the degeneration of corticospinal tracts. We show that a deletion in the mouse
Publikováno v:
Blood. 103:3615-3623
PU.1 is a hematopoietic-specific transcriptional activator that is absolutely required for the differentiation of B lymphocytes and myeloid-lineage cells. Although PU.1 is also expressed by early erythroid progenitor cells, its role in erythropoiesis
Publikováno v:
genesis. 39:167-172
To generate temporally controlled targeted somatic mutations selectively and efficiently in hepatocytes, we established SA+/CreERT2 mice in which the tamoxifen-dependent Cre-ERT2 recombinase coding sequence preceded by an internal ribosomal entry sit
Publikováno v:
Journal of Bioenergetics and Biomembranes. 35:19-30
Mice carrying a homozygous germ-line mutation in the nm23-M1 gene that eliminates its protein expression and drives expression of β-galactosidase by nm23-M1 promoter have been generated. nm23-M1 gene inactivation is not teratogenic and the pups can
Autor:
Catherine Tomasetto, Régis Masson, Andrée Dierich, Isabelle Stoll, Catherine H. Régnier, Valérie Kedinger, Marie-Christine Rio, Marie-Pierre Chenard, Julien Textoris
Publikováno v:
Proceedings of the National Academy of Sciences. 99:5585-5590
TRAF4 belongs to the tumor necrosis factor receptor-associated factor (TRAF) family of proteins but, unlike other family members, has not yet been clearly associated to any specific receptor or signaling pathway. To investigate the biological functio
Publikováno v:
genesis. 32:105-108
Autor:
Aleksandr Piskunov, Irwin Davidson, Bernard Jost, Sylvia Urban, Tao Ye, Cécile Rochette-Egly, Samia Gaouar, Ziad Al Tanoury, Andrée Dierich, Céline Keime
Publikováno v:
Journal of cell science. 127(Pt 9)
Retinoic acid (RA) plays key roles in cell differentiation and growth arrest by activating nuclear receptors, RARs (α, β and γ), which are ligand dependent transcriptional factors. RARs are also phosphorylated in response to RA. Here we investigat