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Michel Cohen-Tannoudji
Michel Cohen-Tannoudji
CNRS Institut Pasteur
Adresse e-mail validée de pasteur.fr - Page d'accueil
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The SUMO pathway is essential for nuclear integrity and chromosome segregation in mice
K Nacerddine, F Lehembre, M Bhaumik, J Artus, M Cohen-Tannoudji, ...
Developmental cell 9 (6), 769-779, 2005
6082005
A comparison of the properties of Sox-3 with Sry and two related genes, Sox-1 and Sox-2
J Collignon, S Sockanathan, A Hacker, M Cohen-Tannoudji, D Norris, ...
Development 122 (2), 509-520, 1996
5781996
Disruption of Krox-20 results in alteration of rhombomeres 3 and 5 in the developing hindbrain
S Schneider-Maunoury, P Topilko, T Seitanidou, G Levi, ...
Cell 75 (6), 1199-1214, 1993
5381993
Early determination of a mouse somatosensory cortex marker
M Cohen-Tannoudji, C Babinet, M Wassef
Nature 368 (6470), 460-463, 1994
2111994
I-SceI-Induced Gene Replacement at a Natural Locus in Embryonic Stem Cells
M Cohen-Tannoudji, S Robine, A Choulika, D Pinto, F El Marjou, ...
Molecular and cellular biology 18 (3), 1444-1448, 1998
1811998
In Vivo, Villin Is Required for Ca2+-Dependent F-Actin Disruption in Intestinal Brush Borders
E Ferrary, M Cohen-Tannoudji, G Pehau-Arnaudet, A Lapillonne, ...
The Journal of cell biology 146 (4), 819-830, 1999
1701999
Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domain
M Monet-Leprêtre, B Bardot, B Lemaire, V Domenga, O Godin, ...
Brain 132 (6), 1601-1612, 2009
1452009
Mitotic binding of Esrrb marks key regulatory regions of the pluripotency network
N Festuccia, A Dubois, S Vandormael-Pournin, E Gallego Tejeda, ...
Nature cell biology 18 (11), 1139-1148, 2016
1422016
The archetypal R90C CADASIL–NOTCH3 mutation retains NOTCH3 function in vivo
M Monet, V Domenga, B Lemaire, C Souilhol, F Langa, C Babinet, ...
Human molecular genetics 16 (8), 982-992, 2007
1282007
Naive and primed murine pluripotent stem cells have distinct miRNA expression profiles
A Jouneau, C Ciaudo, O Sismeiro, V Brochard, L Jouneau, ...
Rna 18 (2), 253-264, 2012
1122012
Genome engineering via homologous recombination in mouse embryonic stem (ES) cells: an amazingly versatile tool for the study of mammalian biology
C Babinet, M Cohen-Tannoudji
Anais da Academia Brasileira de Ciências 73, 365-383, 2001
982001
CD4 T cell tolerance to nuclear proteins induced by medullary thymic epithelium
M Oukka, E Colucci-Guyon, PL Tran, M Cohen-Tannoudji, C Babinet, ...
Immunity 4 (6), 545-553, 1996
941996
Transcription factor activity and nucleosome organization in mitosis
N Festuccia, N Owens, T Papadopoulou, I Gonzalez, A Tachtsidi, ...
Genome research 29 (2), 250-260, 2019
832019
Beyond'knock-out'mice: new perspectives for the programmed modification of the mammalian genome.
M Cohen-Tannoudji, C Babinet
Molecular human reproduction 4 (10), 929-938, 1998
801998
Nonpermissiveness for mouse embryonic stem (ES) cell derivation circumvented by a single backcross to 129/Sv strain: establishment of ES cell lines bearing the Om d conditional …
C Kress, S Vandormael-Pournin, P Baldacci, M Cohen-Tannoudji, ...
Mammalian genome 9, 998-1001, 1998
781998
Developmental expression of the Notch signaling pathway genes during mouse preimplantation development
S Cormier, S Vandormael-Pournin, C Babinet, M Cohen-Tannoudji
Gene Expression Patterns 4 (6), 713-717, 2004
772004
Specification of somatosensory area identity in cortical explants
Y Gitton, M Cohen-Tannoudji, M Wassef
Journal of Neuroscience 19 (12), 4889-4898, 1999
751999
Role of thalamic axons in the expression of H-2Z1, a mouse somatosensory cortex specific marker
Y Gitton, M Cohen-Tannoudji, M Wassef
Cerebral Cortex 9 (6), 611-620, 1999
731999
Molecular heterogeneity of progenitors and radial migration in the developing cerebral cortex revealed by transgene expression.
E Soriano, N Dumesnil, C Auladell, M Cohen-Tannoudji, C Sotelo
Proceedings of the National Academy of Sciences 92 (25), 11676-11680, 1995
731995
Disruption of murine Hexa gene leads to enzymatic deficiency and to neuronal lysosomal storage, similar to that observed in Tay-Sachs disease
M Cohen-Tannoudji, P Marchand, S Akli, SA Sheardown, JP Puech, ...
Mammalian Genome 6, 844-849, 1995
731995
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