Zobrazeno 1 - 7 of 7 pro vyhledávání: '"Marc Fraterno"'
1
Erratum to: 'CMTX1 patients' cells present genomic instability corrected by CamKII inhibitors'
Autor: Marc Fraterno, Burkhard Gess, Alexandre Altié, Michel Fontes, Saleh Mones, Peter Young, Franck Peiretti, Benoit Bordignon, Frédéric Bihel
Publikováno v: Orphanet Journal of Rare Diseases (11), . (2016)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, BioMed Central, 2016, 11, ⟨10.1186/s13023-015-0354-2⟩
Orphanet Journal of Rare Diseases, 2016, 11, ⟨10.1186/s13023-015-0354-2⟩
Orphanet journal of rare diseases : OJRD 11, 6 (2015). doi:10.1186/s13023-015-0354-2
Author details NORT. UMR INSERM 1062, INRA 1260, Aix Marseille Universite, Campus Sante La Timone, 27 boulevard Jean Moulin, Marseille 13385 Cedex 53, France. Department of Sleep Medicine and Neuromuscular Disorders, University Hospital Muenster, Mue
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a69318d7cd727546b1af54cf008452b7
http://prodinra.inra.fr/record/349630
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2
CMTX1 patients' cells present genomic instability corrected by CamKII inhibitors
Autor: Saleh, Mones, Burkhardt, Gess, Benoit, Bordignon, Alexandre, Altié, Peter, Young, Frederic, Bihel, Marc, Fraterno, Franck, Peiretti, Michel, Fontes, Mones, Saleh, Gess, Burkhardt, Bordignon, Benoit, Altié, Alexandre, Young, Peter, Bihel, Frederic, Fraterno, Marc, Peiretti, Franck, Fontes, Michel
Publikováno v: Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, BioMed Central, 2015, 10, ⟨10.1186/s13023-015-0270-5⟩
Orphanet Journal of Rare Diseases, 2015, 10, ⟨10.1186/s13023-015-0270-5⟩
Orphanet journal of rare diseases : OJRD 10, 56 (2015). doi:10.1186/s13023-015-0270-5
International audience; Background: We previously described that fibroblasts from animal models of CMTX1 present genomic instability and poor connexon activity. In vivo, these transgenic mice present motor deficits. This phenotype could be significan
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::62bb63140e44c604e9072548779f554b
https://hal.inrae.fr/hal-02634560
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3
Ascorbic acid is a dose-dependent inhibitor of adipocyte differentiation, probably by reducing cAMP pool
Autor: Fadi Al Frouh, Marc Fraterno, Fryad Rahman, Jean-François Landrier, Michel Fontes, Franck Peiretti, Benoit Bordignon
Publikováno v: Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology, Frontiers media, 2014, 2, ⟨10.3389/fcell.2014.00029⟩
Frontiers in Cell and Developmental Biology, 2014, 2, ⟨10.3389/fcell.2014.00029⟩
Frontiers in Cell and Developmental Biology (2), . (2014)
Frontiers in Cell and Developmental Biology, Vol 2 (2014)
Ascorbic acid (AA) is the active component of vitamin C and antioxidant activity was long considered to be the primary molecular mechanism underlying the physiological actions of AA. We recently demonstrated that AA is a competitive inhibitor of aden
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36326efdadc5e57dcfe7da1410f05090
https://hal.archives-ouvertes.fr/hal-01594290/document
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4
Adhesion-related glycocalyx study: quantitative approach with imaging-spectrum in the energy filtering transmission electron microscope (EFTEM)
Autor: Marc Fraterno, Sophie Desplat-Jego, Pierre Bongrand, Colette Foa, L. Ponsonnet, Jean Michel Martin, Béatrice Vacher, M. Soler
Publikováno v: FEBS Letters. (1):89-94
Large polysaccharide molecules composing the glycocalyx have been shown to prevent cell adhesion. However, this process was not observed microscopically. Terbium labeling, combined with a new quantitative imaging method based on electron energy loss
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10ead1ac6d0d727ed467e7a62b9573e1
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7
Akademický článek
CMTX1 patients' cells present genomic instability corrected by CamKII inhibitors.
Autor: Mones S; NORT. UMR INSERM 1062, INRA 1260, Aix Marseille Université, Campus Santé La Timone, 27 boulevard Jean Moulin, Marseille, 13385 Cedex 53, France. saleh.mones@univ-amu.fr., Gess B; Department of Sleep Medicine and Neuromuscular Disorders, University Hospital Muenster, Muenster, Germany. burkhard.gess@gmail.com., Bordignon B; NORT. UMR INSERM 1062, INRA 1260, Aix Marseille Université, Campus Santé La Timone, 27 boulevard Jean Moulin, Marseille, 13385 Cedex 53, France. benoit.bordignon@inserm.fr., Altié A; Service de Microscopie Electronique, Faculté de Médecine de la Timone, 27 boulevard Jean Moulin, Marseille, 13385 Cedex 53, France. alexandre.altie@univ-amu.fr., Young P; Department of Sleep Medicine and Neuromuscular Disorders, University Hospital Muenster, Muenster, Germany. Peter.Young@ukmuenster.de., Bihel F; Laboratoire d'Innovation thérapeutique, UMR7200, CNRS, Université de Strasbourg, Faculté de Pharmacie, 74, route du rhin, Illkirch Graffenstaden, 67400, France. Frederic.bihel@unistra.fr., Fraterno M; Department of Sleep Medicine and Neuromuscular Disorders, University Hospital Muenster, Muenster, Germany. marc.fraterno@univ-amu.fr., Peiretti F; NORT. UMR INSERM 1062, INRA 1260, Aix Marseille Université, Campus Santé La Timone, 27 boulevard Jean Moulin, Marseille, 13385 Cedex 53, France. franck.peiretti@univ-amu.fr., Fontes M; NORT. UMR INSERM 1062, INRA 1260, Aix Marseille Université, Campus Santé La Timone, 27 boulevard Jean Moulin, Marseille, 13385 Cedex 53, France. michel.fontes@univ-amu.fr.
Publikováno v: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2015 May 07; Vol. 10, pp. 56. Date of Electronic Publication: 2015 May 07.
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