Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Danièle Depétris"'
Autor:
Danièle Depétris, Frédéric Charlotte, David Klatzmann, Olivier Boyer, Sylvie Bruel, Laurence Lejeune, Benoit Salamon, R. Onclercq, Marie-Geneviève Mattei, Vanessa Dubus-Bonnet, José L. Cohen
Publikováno v:
Transgenic Research. 7:321-330
Dividing cells expressing the Herpes simplex type 1 thymidine kinase (TK) can be killed upon ganciclovir treatment. Likewise, conditional cell knock-out can be obtained in transgenic mice expressing a TK gene placed under the control of tissue-specif
Autor:
Danièle Depétris, Chantal Ripoll, Christian P. Hamel, Marc Lenoir, Fabien Crozet, Rémy Pujol, Dominique Weil, Fabienne Levi-Acobas, Stéphane Blanchard, P. Vago, Christine Petit, Cécile Fizames, Marie-Geneviève Mattei, Aziz El Amraoui
Publikováno v:
Genomics
Genomics, 1997, 40 (2), pp.332-341. ⟨10.1006/geno.1996.4526⟩
Genomics, 1997, 40 (2), pp.332-341. ⟨10.1006/geno.1996.4526⟩
Several lines of evidence indicate a crucial role for unconventional myosins in the function of the sensory hair cells of the inner ear. We report here the characterization of the cDNAs encoding two unconventional type I myosins from a mouse cochlear
Autor:
Claude Kedinger, Danièle Depétris, Marie-Geneviève Mattei, Marc Vigneron, M. Wintzerith, Joël Acker, Nathalie Roeckel
Publikováno v:
Genomics. 20:496-499
The eukaryotic DNA-dependent RNA polymerase II (or B) is composed of 10 to 14 polypeptides ranging from 220 to 10 kDa. To gain further insight into the molecular structure and function of these subunits, we have undertaken the molecular cloning of nu
Autor:
L. Foresti do Almeida-Toledo, Beverly S. Emanuel, James T. Mascarello, R. Prohaska, Peter B. Jacky, John Wiley, B. Wullich, Danièle Depétris, Stuart Schwartz, Robert L. Nussbaum, P. Le Bouteiller, Susanne M. Gollin, H Sprenger, Andrew R. Lloyd, S. Cevario, J.P. Schröder, Pierre Pontarotti, D.W. Hale, Marc Lipinski, Thierry Guillaudeux, Linda A. Cannizzaro, J.A. Westberg, Marie Geneviève Mattei, Eileen Bryant, Jørn Koch, Debra Saxe, William S. Modi, Carla Oliveira, Christian Overton, Linda L. Washburn, S. de Almeida Toledo Filho, J. Hindkjær, S. Lampel, H. Steilen, Kenneth H. Buetow, David J. Kelvin, B. Entler, Patricia Howard-Peebles, Lars Bolund, Peter J. Scambler, C. Terkelsen, Eva M. Eicher, Steen Kølvraa, A.A. Andreata, Klaus-Dieter Zang, Wendy Golden, S. Pedersen, Joost J. Oppenheim, Urvashi Surti
Publikováno v:
Cytogenetic and Genome Research. 63:I-IV
Autor:
Marc Delepine, Samuel F. Berkovic, Caroline Seegmuller, Pierre Cau, Nicolas Lévy, Danièle Depétris, Anne de Saint Martin, Marie-Genevieve Mattei, Nadine Bruneau, Ingrid E. Scheffer, Christian Marescaux, Bernd A. Neubauer, Andrée Robaglia-Schlupp, Annick Massacrier, Edouard Hirsch, Christophe Caloustian, Mark Lathrop, Rivka Ravid, Patrice Roll, Pierre Szepetowski, Elisabeth Flori, Marie-Noëlle Metz-Lutz, Maria-Paola Valenti, Sandrine Pereira, Gabrielle Rudolf, Christophe Beclin, Sarah Jamali, Arnaud Lemainque, Nathalie Roeckel-Trevisiol, Barbara Royer
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2006, 15(7), pp.1195-207
Human Molecular Genetics, 2006, 15(7), pp.1195-207
Human Molecular Genetics, Oxford University Press (OUP), 2006, 15(7), pp.1195-207
Human Molecular Genetics, 2006, 15(7), pp.1195-207
The rolandic and sylvian fissures divide the human cerebral hemispheres and the adjacent areas participate in speech processing. The relationship of rolandic (sylvian) seizure disorders with speech and cognitive impairments is well known, albeit poor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15f85126b537563dd3f0051e8ba377d8
https://hal.archives-ouvertes.fr/hal-00089725
https://hal.archives-ouvertes.fr/hal-00089725
Autor:
Marie-Geneviève Mattei, Danièle Depétris, Alain Aurias, Annie Levy, Nicole Philip, S. Demczuk
Publikováno v:
Human Molecular Genetics. 4:2417-2419
Autor:
Danièle Depétris, Pierre Pontarotti, Marie Geneviève Mattei, P. Le Bouteiller, Thierry Guillaudeux
Publikováno v:
Europe PubMed Central
Otf-3 (Octamer-binding transcription factor 3) is an octamer binding protein encoded by the murine gene Otf-3. Otf-3 belongs to a multigenic family and maps to the mouse Chromosome 17 between the Q and T regions within the major histocompatibility co
Autor:
D. Metras, Danièle Depétris, B. Kreitman, F. Rouault, A. Levy-Mozziconacci, Nicole Philip, Peter J. Scambler, F. Wernert, Marie Geneviève Mattei
Publikováno v:
European journal of pediatrics. 153(11)
DiGeorge sequence (DGS) is a developmental field defect of the third and fourth pharyngeal pouches. The cardinal features of the syndrome are hypo- or aplasia of the thymus and parathyroids, congenital heart defect of the conotruncal type and charact
Autor:
Thierry Guillaudeux, L. Foresti do Almeida-Toledo, Beverly S. Emanuel, J.P. Schröder, Klaus-Dieter Zang, R. Prohaska, H Sprenger, Wendy Golden, C. Terkelsen, Peter B. Jacky, Susanne M. Gollin, S. Cevario, Marc Lipinski, James T. Mascarello, Eileen Bryant, J.A. Westberg, J. Hindkjær, Danièle Depétris, Andrew R. Lloyd, William S. Modi, P. Le Bouteiller, Joost J. Oppenheim, S. de Almeida Toledo Filho, John Wiley, Urvashi Surti, Robert L. Nussbaum, Linda L. Washburn, B. Wullich, B. Entler, Lars Bolund, H. Steilen, Kenneth H. Buetow, Carla Oliveira, A.A. Andreata, S. Pedersen, David J. Kelvin, S. Lampel, Stuart Schwartz, Christian Overton, Peter J. Scambler, Patricia Howard-Peebles, D.W. Hale, Linda A. Cannizzaro, Jørn Koch, Debra Saxe, Marie Geneviève Mattei, Eva M. Eicher, Steen Kølvraa, Pierre Pontarotti
Publikováno v:
Cytogenetic and Genome Research. 63:260-260
Publikováno v:
JNCI: Journal of the National Cancer Institute.
Tumor-specific transplantation antigen (TSTA) activity was investigated (with the use of inbred BALB/c and C3H mice and inbred Fisher and Wistar rats) in various early polyomavirus (Py)-coded proteins by three methodologies: 1) immunoprecipitation by