Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Antoine Marteyn"'
Autor:
Arthur Bassot, Helena Dragic, Sarah Al Haddad, Laurine Moindrot, Soline Odouard, Francesca Corlazzoli, Eliana Marinari, Alexandra Bomane, Augustin Brassens, Antoine Marteyn, Youssef Hibaoui, Tom J. Petty, Mounira Chalabi-Dchar, Louis Larrouquere, Evgeny M. Zdobnov, Noémie Legrand, Jérôme Tamburini, Hubert Lincet, Marie Castets, Mayra Yebra, Denis Migliorini, Valérie Dutoit, Paul R. Walker, Olivier Preynat-Seauve, Pierre-Yves Dietrich, Érika Cosset
Publikováno v:
Cell Death and Disease, Vol 14, Iss 9, Pp 1-16 (2023)
Abstract Glioblastoma (GBM) is a deadly and the most common primary brain tumor in adults. Due to their regulation of a high number of mRNA transcripts, microRNAs (miRNAs) are key molecules in the control of biological processes and are thereby promi
Externí odkaz:
https://doaj.org/article/97ccca6fa79d4593ba87ea60e407d403
Autor:
German Nacher-Soler, Antoine Marteyn, Natasha Barenzung, Stéphanie Sgroi, Karl-Heinz Krause, Pascal Senn, Francis Rousset
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
The reactive oxygen species (ROS)-generating enzyme NOX3 has recently been implicated in the pathophysiology of several acquired forms of sensorineural hearing loss, including cisplatin-, noise- and age-related hearing loss. NOX3 is highly and specif
Externí odkaz:
https://doaj.org/article/a0b63fc415a141ed9b378c83e6b2103b
Autor:
Francis Rousset, Vivianne B. C. Kokje, Rebecca Sipione, Dominik Schmidbauer, German Nacher-Soler, Sten Ilmjärv, Marta Coelho, Stefan Fink, François Voruz, Antoun El Chemaly, Antoine Marteyn, Hubert Löwenheim, Karl-Heinz Krause, Marcus Müller, Rudolf Glückert, Pascal Senn
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 14 (2020)
Nearly 460 million individuals are affected by sensorineural hearing loss (SNHL), one of the most common human sensory disorders. In mammals, hearing loss is permanent due to the lack of efficient regenerative capacity of the sensory epithelia and sp
Externí odkaz:
https://doaj.org/article/c641ab44f8a34edeafa6d15a020cc3ac
Autor:
Erika Cosset, Tieng Vannary, Frédérique Sloan-Béna, Stefania Gimelli, Eric Gerstel, Karl-Heinz Krause, Antoine Marteyn
Publikováno v:
Stem Cell Research, Vol 48, Iss , Pp 101928- (2020)
Dermal fibroblasts isolated from an apparently healthy 50-year-old man were successfully transformed into induced pluripotent stem cells (iPSCs) by using the integration-free CytoTune-iPS Sendai Reprogramming method. The generated iPSC line has been
Externí odkaz:
https://doaj.org/article/f8fe42d72cf549e99771534875e6b55b
Redox activation of excitatory pathways in auditory neurons as mechanism of age-related hearing loss
Autor:
Francis Rousset, German Nacher-Soler, Marta Coelho, Sten Ilmjarv, Vivianne Beatrix Christina Kokje, Antoine Marteyn, Yves Cambet, Michael Perny, Marta Roccio, Vincent Jaquet, Pascal Senn, Karl Heinz Krause
Publikováno v:
Redox Biology, Vol 30, Iss , Pp - (2020)
Age-related hearing (ARHL) loss affects a large part of the human population with a major impact on our aging societies. Yet, underlying mechanisms are not understood, and no validated therapy or prevention exists. NADPH oxidases (NOX), are important
Externí odkaz:
https://doaj.org/article/7acaa3de12cc454c88aa37a7e2e37b3e
Autor:
Silvin Lito, Patricie Burda, Matthias Baumgartner, Frédérique Sloan-Béna, Zsuzsanna Táncos, Julianna Kobolák, András Dinnyés, Karl-Heinz Krause, Antoine Marteyn
Publikováno v:
Stem Cell Research, Vol 41, Iss , Pp - (2019)
Mucopolysaccharidosis type I-Hurler (MPS1-H) is the most severe form of inherited metabolic diseases caused by mutations in the IDUA gene. The resulting deficiency of alpha L-iduronidase enzyme leads to a progressive accumulation of glycosaminoglycan
Externí odkaz:
https://doaj.org/article/ab0ce14b1bdb4b87825c91680080d914
Autor:
Silvin Lito, Adama Sidibe, Sten Ilmjarv, Patricie Burda, Matthias Baumgartner, Bernhard Wehrle-Haller, Karl-Heinz Krause, Antoine Marteyn
Publikováno v:
Cells, Vol 9, Iss 12, p 2593 (2020)
Background: Mucopolysaccharidosis type I-Hurler (MPS1-H) is a severe genetic lysosomal storage disorder due to loss-of-function mutations in the IDUA gene. The subsequent complete deficiency of alpha l-iduronidase enzyme is directly responsible of a
Externí odkaz:
https://doaj.org/article/c4dd60e3edf341ae89089a985542b793
Autor:
Benjamin B. Tournier, Silvia Sorce, Antoine Marteyn, Roberta Ghidoni, Luisa Benussi, Giuliano Binetti, François R Herrmann, Karl-Heinz Krause, Dina Zekry
IntroductionAs the chemokine receptor5 (CCR5) may play a role in ischemia, we studied the links between CCR5 deficiency, the sensitivity of neurons to oxidative stress, and the development of dementia.MethodsLogistic regression models with CCR5 and A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b491c5edf812d83a421e36d14dec4b0a
https://doi.org/10.1101/2023.02.15.23285967
https://doi.org/10.1101/2023.02.15.23285967
Autor:
German, Nacher-Soler, Antoine, Marteyn, Natasha, Barenzung, Stéphanie, Sgroi, Karl-Heinz, Krause, Pascal, Senn, Francis, Rousset
Publikováno v:
Frontiers in neurology. 13
The reactive oxygen species (ROS)-generating enzyme NOX3 has recently been implicated in the pathophysiology of several acquired forms of sensorineural hearing loss, including cisplatin-, noise- and age-related hearing loss. NOX3 is highly and specif
Autor:
Antoine Marteyn, Adama Sidibé, Matthias R. Baumgartner, Karl-Heinz Krause, Sten Ilmjärv, Patricie Burda, Bernhard Wehrle-Haller, Silvin Lito
Publikováno v:
Cells
Volume 9
Issue 12
Cells, Vol. 9, No 12 (2020) P. 2593
Cells, Vol 9, Iss 2593, p 2593 (2020)
Volume 9
Issue 12
Cells, Vol. 9, No 12 (2020) P. 2593
Cells, Vol 9, Iss 2593, p 2593 (2020)
Background: Mucopolysaccharidosis type I-Hurler (MPS1-H) is a severe genetic lysosomal storage disorder due to loss-of-function mutations in the IDUA gene. The subsequent complete deficiency of alpha l-iduronidase enzyme is directly responsible of a