Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Agnès Robert"'
Autor:
Ágnes Roberts
Publikováno v:
Particles, Vol 7, Iss 3, Pp 717-746 (2024)
A review of the landscape of CPT symmetry tests is presented, centered around the Standard-Model Extension and focusing on tests in the neutral meson system. A discussion of the relevant theories summarizes original ideas. It is followed by a short t
Externí odkaz:
https://doaj.org/article/f73eae6bc3a547a19a7557f0a969b311
Autor:
Eric Assenat, Francis Navarro, Jean Paul Brizard, Pierre Sarda, Dalila Laoudj-Chenivesse, Nicole Bigi, Patrick Maurel, Daniel Lafitte, Jeanne Ramos, Pierre Blanc, Jean-Marc Pascussi, Agnès Robert, Marie-José Vilarem
Publikováno v:
Journal of Hepatology
Journal of Hepatology, Elsevier, 2009, 51 (1), pp.114-26. ⟨10.1016/j.jhep.2009.02.029⟩
Journal of Hepatology, 2009, 51 (1), pp.114-26. ⟨10.1016/j.jhep.2009.02.029⟩
Journal of Hepatology, Elsevier, 2009, 51 (1), pp.114-26. ⟨10.1016/j.jhep.2009.02.029⟩
Journal of Hepatology, 2009, 51 (1), pp.114-26. ⟨10.1016/j.jhep.2009.02.029⟩
International audience; BACKGROUND/AIMS: The aim of this study was to identify human liver proteins that are associated with different stages of liver development. METHODS: We collected liver samples from 14 fetuses between 14 and 41 weeks of develop
Autor:
Thierry Pineau, Agnès Robert, Michèle Garabédian, Jean Saric, Odile Walrant-Debray, Patrick Maurel, Pascal G.P. Martin, Minh Nguyen, Marie José Vilarem, Jean-Marc Pascussi, Fréderic Navarro
Publikováno v:
Journal of Clinical Investigation. 115:177-186
Vitamin D controls calcium homeostasis and the development and maintenance of bones through vitamin D receptor activation. Prolonged therapy with rifampicin or phenobarbital has been shown to cause vitamin D deficiency or osteomalacia, particularly i
Autor:
Agnès Robert, Marie Bernadette Delisle, François Rivier, Yves Chaix, Bernard Echenne, Dominique Mornet, Patrick Calvas
Publikováno v:
Brain and Development. 22:65-68
We report on a boy with a BMD phenotype presenting with a deletion of exons 45-49 in the DMD gene. Immunofluorescence and Western blot analysis of a skeletal muscle sample revealed, as expected, truncated dystrophin with loss in the central rod domai
Autor:
Agnès Robert, Gérald Hugon, Mar Royuela, Armelle Bonet-Kerrache, François Rivier, Dominique Mornet
Publikováno v:
Journal of Muscle Research and Cell Motility. 20:305-314
In this study, various members of the dystrophin family (dystrophin, the short dystrophin product Dp 71, utrophin and DRP2), and different members of the dystrophin-associated glycoprotein (DAG) complex (beta-dystroglycan, alpha-, beta-, gamma- and d
Publikováno v:
Histochemical Journal. 31:603-608
Dystrophin is a 427-kDa cytoskeletal protein, which occurs in scant amounts in vertebrate muscle and nerve cells. No previous references to dystrophin or associated proteins in invertebrates at the protein level have been found, while two recent stud
Autor:
Vincenzo Nigro, François Rivier, Jean Martinez, Gérald Hugon, Agnès Robert, Armelle Bonet-Kerrache, Jean-Alain Fehrentz, Dominique Mornet
Publikováno v:
Histochemical Journal. 31:425-432
Abnormal dystrophin expression is directly responsible for Duchenne and Becker muscular dystrophies. In skeletal muscle, dystrophin provides a link between the actin network and the extracellular matrix via the dystrophin-associated protein complex.
Publikováno v:
FEBS Letters. 408:94-98
Monoclonal antibodies used to distinguish between dystrophin and utrophin were systematically applied to skeletal muscles containing arteries and veins. Small arteries were found to contain long forms of both utrophin and dystrophin, while small vein
Publikováno v:
Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology. 116:19-26
By comparison with localizations of dystrophin family products in rabbit peripheral nerves, we investigated the potential existence and distribution of similar products in peripheral nerves from Torpedo marmorata . In immunofluorescence studies, a sp
Autor:
J. Martinez, Gérald Hugon, E Fabbrizio, Agnès Robert, J. A. Fehrentz, Dominique Mornet, J C Califano, Françoise Pons
Publikováno v:
Circulation. 90:369-374
BACKGROUND The localization of dystrophin at the sarcolemma of cardiac skeletal fibers and cardiac Purkinje fibers has been described. Dystrophin deficiency produces clinical manifestations of disease in skeletal muscles and hearts of patients with D