Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Dorothée, Buttigieg"'
Autor:
Diana Toli, Dorothée Buttigieg, Stéphane Blanchard, Thomas Lemonnier, Boris Lamotte d’Incamps, Sarah Bellouze, Gilbert Baillat, Delphine Bohl, Georg Haase
Publikováno v:
Neurobiology of Disease, Vol 82, Iss , Pp 269-280 (2015)
Amyotrophic lateral sclerosis (ALS) is a severe and incurable neurodegenerative disease. Human motor neurons generated from induced pluripotent stem cells (iPSc) offer new perspectives for disease modeling and drug testing in ALS. In standard iPSc-de
Externí odkaz:
https://doaj.org/article/127b0c1de7534dae9c254c3dc12a0a5d
Publikováno v:
CNS & Neurological Disorders - Drug Targets. 19:227-240
Aim: The aim of this study is to examine the effect of etifoxine on β-amyloid-induced toxicity models. Background: Etifoxine is an anxiolytic compound with a dual mechanism of action; it is a positive allosteric modulator of GABAergic receptors as w
Publikováno v:
ACS chemical neuroscience. 12(12)
Neurodegeneration and impaired neural development are a common feature of many neuropsychiatric disorders. Second-generation antipsychotics (SGAs) and certain atypical antidepressants display neuroprotective effects. Though these drugs interact with
Publikováno v:
Journal of Neuroscience Research. 94:179-189
A growing body of data has shown that recurrent epileptic seizures may be caused by an excessive release of the excitatory neurotransmitter glutamate in the brain. Glutamatergic overstimulation results in massive neuronal influxes of calcium and sodi
Autor:
Dorothée Buttigieg, Stéphane Blanchard, Diana Toli, Delphine Bohl, Georg Haase, Gilbert Baillat, Sarah Bellouze, Thomas Lemonnier, Boris Lamotte d'Incamps
Publikováno v:
Neurobiology of Disease, Vol 82, Iss, Pp 269-280 (2015)
Neurobiology of Disease
Neurobiology of Disease, Elsevier, 2015, 82, pp.269-280. ⟨10.1016/j.nbd.2015.06.011⟩
Neurobiology of Disease, 2015, 82, pp.269-280. ⟨10.1016/j.nbd.2015.06.011⟩
Neurobiology of Disease
Neurobiology of Disease, Elsevier, 2015, 82, pp.269-280. ⟨10.1016/j.nbd.2015.06.011⟩
Neurobiology of Disease, 2015, 82, pp.269-280. ⟨10.1016/j.nbd.2015.06.011⟩
International audience; Amyotrophic lateral sclerosis (ALS) is a severe and incurable neurodegenerative disease. Human motor neurons generated from induced pluripotent stem cells (iPSc) offer new perspectives for disease modeling and drug testing in
Novel combinatorial screening identifies neurotrophic factors for selective classes of motor neurons
Autor:
Sébastien Schaller, Alysson Alory, Georg Haase, Marc Barad, Arnaud Jacquier, Mark Merchant, Pierre de la Grange, David Gentien, Dorothée Buttigieg
Publikováno v:
Proceedings of the National Academy of Sciences. 114
Numerous neurotrophic factors promote the survival of developing motor neurons but their combinatorial actions remain poorly understood; to address this, we here screened 66 combinations of 12 neurotrophic factors on pure, highly viable, and standard
Autor:
Dorothée Buttigieg, Gilbert Baillat, Catherine Rabouille, Georg Haase, Michael K. E. Schäfer, Sarah Bellouze
Publikováno v:
Human Molecular Genetics, 23(22), 5961-75. Oxford University Press
Golgi fragmentation is an early hallmark of many neurodegenerative diseases but its pathophysiological relevance and molecular mechanisms are unclear. We here demonstrate severe and progressive Golgi fragmentation in motor neurons of progressive moto
Autor:
Georg Haase, Catherine Rabouille, Dorothée Buttigieg, Gilbert Baillat, Pierre de la Grange, Sarah Bellouze
Publikováno v:
Molecular Neurodegeneration
Molecular Neurodegeneration, BioMed Central, 2016, 11, pp.43. ⟨10.1186/s13024-016-0111-6⟩
Molecular Neurodegeneration, 2016, 11, pp.43. ⟨10.1186/s13024-016-0111-6⟩
Molecular Neurodegeneration, 11(1). BioMed Central
Molecular Neurodegeneration [E], 11(1). BioMed Central
Molecular Neurodegeneration, BioMed Central, 2016, 11, pp.43. ⟨10.1186/s13024-016-0111-6⟩
Molecular Neurodegeneration, 2016, 11, pp.43. ⟨10.1186/s13024-016-0111-6⟩
Molecular Neurodegeneration, 11(1). BioMed Central
Molecular Neurodegeneration [E], 11(1). BioMed Central
Background Pathological Golgi fragmentation represents a constant pre-clinical feature of many neurodegenerative diseases including amyotrophic lateral sclerosis (ALS) but its molecular mechanisms remain hitherto unclear. Results Here, we show that t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c22dc7d9000feb9f1f2d15617ffabf7e
https://hal-amu.archives-ouvertes.fr/hal-01463801
https://hal-amu.archives-ouvertes.fr/hal-01463801
Autor:
Sandra Marlin, Rémy Steinschneider, Elsa Raban, Johannes Krupp, Dorothée Buttigieg, Camille Nicoleau, Jacquie Maignel, Keith Foster, Sullivan Henriques
Publikováno v:
Toxicon. 156:S84
Publikováno v:
Journal of neuroscience research. 94(2)
A growing body of data has shown that recurrent epileptic seizures may be caused by an excessive release of the excitatory neurotransmitter glutamate in the brain. Glutamatergic overstimulation results in massive neuronal influxes of calcium and sodi