Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Catherine, Gondcaille"'
Autor:
Ali Tawbeh, Quentin Raas, Mounia Tahri-Joutey, Céline Keime, Romain Kaiser, Doriane Trompier, Boubker Nasser, Emma Bellanger, Marie Dessard, Yannick Hamon, Alexandre Benani, Francesca Di Cara, Tânia Cunha Alves, Johannes Berger, Isabelle Weinhofer, Stéphane Mandard, Mustapha Cherkaoui-Malki, Pierre Andreoletti, Catherine Gondcaille, Stéphane Savary
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 16 (2023)
Microglia are crucial for brain homeostasis, and dysfunction of these cells is a key driver in most neurodegenerative diseases, including peroxisomal leukodystrophies. In X-linked adrenoleukodystrophy (X-ALD), a neuroinflammatory disorder, very long-
Externí odkaz:
https://doaj.org/article/911be27ef95548c485aa7100b731715f
Autor:
Quentin Raas, Ali Tawbeh, Mounia Tahri-Joutey, Catherine Gondcaille, Céline Keime, Romain Kaiser, Doriane Trompier, Boubker Nasser, Valerio Leoni, Emma Bellanger, Maud Boussand, Yannick Hamon, Alexandre Benani, Francesca Di Cara, Caroline Truntzer, Mustapha Cherkaoui-Malki, Pierre Andreoletti, Stéphane Savary
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 16 (2023)
Microglial cells ensure essential roles in brain homeostasis. In pathological condition, microglia adopt a common signature, called disease-associated microglial (DAM) signature, characterized by the loss of homeostatic genes and the induction of dis
Externí odkaz:
https://doaj.org/article/e61fd3afe1cd4f0d9a7144d4fea8bc3c
Autor:
Soukaina Essadek, Catherine Gondcaille, Stéphane Savary, Mohammad Samadi, Joseph Vamecq, Gérard Lizard, Riad El Kebbaj, Norbert Latruffe, Alexandre Benani, Boubker Nasser, Mustapha Cherkaoui-Malki, Pierre Andreoletti
Publikováno v:
Antioxidants, Vol 12, Iss 1, p 168 (2023)
Oxidative stress and inflammation are the key players in neuroinflammation, in which microglia dysfunction plays a central role. Previous studies suggest that argan oil attenuates oxidative stress, inflammation, and peroxisome dysfunction in mouse br
Externí odkaz:
https://doaj.org/article/86aa25f10d78404b8c831e4bbfcb5f05
Autor:
Soukaina Essadek, Habiba Bouchab, Riad El Kebbaj, Catherine Gondcaille, Soufiane El Kamouni, Stéphane Savary, Joseph Vamecq, Abdelkhalid Essamadi, Mustapha Cherkaoui-Malki, Boubker Nasser, Pierre Andreoletti
Publikováno v:
Pharmaceuticals, Vol 15, Iss 4, p 465 (2022)
During sepsis, the imbalance between oxidative insult and body antioxidant response causes the dysfunction of organs, including the brain and liver. Exposing mice to bacterial lipopolysaccharides (LPS) results in a similar pathophysiological outcome.
Externí odkaz:
https://doaj.org/article/1779c4e53f084d1caafb16a3c04b9d45
Autor:
Mounia, Tahri-Joutey, Fatima-Ezzahra, Saih, Riad, El Kebbaj, Catherine, Gondcaille, Joseph, Vamecq, Norbert, Latruffe, Gérard, Lizard, Stéphane, Savary, Boubker, Nasser, Mustapha, Cherkaoui-Malki, Pierre, Andreoletti
Publikováno v:
International journal of molecular sciences. 23(19)
Exposure to endotoxins (lipopolysaccharides, LPS) may lead to a potent inflammatory cytokine response and a severe impairment of metabolism, causing tissue injury. The protective effect provided by cactus seed oil (CSO), from
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 6093, p 6093 (2021)
International Journal of Molecular Sciences, Vol 22, Iss 6093, p 6093 (2021)
ATP-binding cassette (ABC) transporters constitute one of the largest superfamilies of conserved proteins from bacteria to mammals. In humans, three members of this family are expressed in the peroxisomal membrane and belong to the subfamily D: ABCD1
Autor:
Amira, Zarrouk, Thomas, Nury, Hammam I, El Hajj, Catherine, Gondcaille, Pierre, Andreoletti, Thibault, Moreau, Mustapha, Cherkaoui-Malki, Johannes, Berger, Mohamed, Hammami, Gérard, Lizard, Anne, Vejux
Publikováno v:
Advances in experimental medicine and biology. 1299
Peroxisomopathies are rare diseases due to dysfunctions of the peroxisome in which this organelle is either absent or with impaired activities. These diseases, at the exception of type I hyperoxaluria and acatalasaemia, affect the central and periphe
Autor:
Catherine Gondcaille, Gérard Lizard, Mohamed Hammami, Anne Vejux, Johannes Berger, Amira Zarrouk, Hammam I El Hajj, Thomas Nury, Thibault Moreau, Mustapha Cherkaoui-Malki, Pierre Andreoletti
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9783030602031
Peroxisomopathies are rare diseases due to dysfunctions of the peroxisome in which this organelle is either absent or with impaired activities. These diseases, at the exception of type I hyperoxaluria and acatalasaemia, affect the central and periphe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9fddb986fa09d28597d1d6bc0f163787
https://doi.org/10.1007/978-3-030-60204-8_8
https://doi.org/10.1007/978-3-030-60204-8_8
Autor:
Quentin Raas, Alexandre M.M. Dias, Catherine Gondcaille, Géraldine Lucchi, Flore Geillon, Caroline Truntzer, Doriane Trompier, Stéphane Savary, Pierre Falson, Patrick Ducoroy, Delphine Pecqueur
Publikováno v:
Journal of Biological Chemistry
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2017, 292 (17), pp.6965-6977. ⟨10.1074/jbc.M116.772806⟩
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2017, 292 (17), pp.6965-6977. ⟨10.1074/jbc.M116.772806⟩
International audience; ABCD1 and its homolog ABCD2 are peroxisomal ATP-binding cassette (ABC) half-transporters of fatty acyl-CoAs with both distinct and overlapping substrate specificities. Although it is established that ABC half-transporters have
Autor:
Gérard Lizard, Claudio Caccia, Valerio Leoni, Doriane Trompier, Yannick Hamon, Franck Ménétrier, Stéphane Savary, Quentin Raas, Catherine Gondcaille
Publikováno v:
Biochimica et Biophysica Acta Molecular and Cell Biology of Lipids
Biochimica et Biophysica Acta Molecular and Cell Biology of Lipids, 2019, 1864 (5), pp.704-714. ⟨10.1016/j.bbalip.2019.02.006⟩
Biochimica et Biophysica Acta Molecular and Cell Biology of Lipids, Elsevier, 2019, 1864 (5), pp.704-714. ⟨10.1016/j.bbalip.2019.02.006⟩
Biochimica Et Biophysica Acta-Molecular and Cell Biology of Lipids
Biochimica Et Biophysica Acta-Molecular and Cell Biology of Lipids, 2019, 1864 (5), pp.704-714. ⟨10.1016/j.bbalip.2019.02.006⟩
Biochimica et Biophysica Acta Molecular and Cell Biology of Lipids, 2019, 1864 (5), pp.704-714. ⟨10.1016/j.bbalip.2019.02.006⟩
Biochimica et Biophysica Acta Molecular and Cell Biology of Lipids, Elsevier, 2019, 1864 (5), pp.704-714. ⟨10.1016/j.bbalip.2019.02.006⟩
Biochimica Et Biophysica Acta-Molecular and Cell Biology of Lipids
Biochimica Et Biophysica Acta-Molecular and Cell Biology of Lipids, 2019, 1864 (5), pp.704-714. ⟨10.1016/j.bbalip.2019.02.006⟩
X-linked adrenoleukodystrophy (X-ALD), the most frequent peroxisomal disorder, is associated with mutation in the ABCD1 gene which encodes a peroxisomal ATP-binding cassette transporter for very long-chain fatty acids (VLCFA). The biochemical hallmar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d40106d37c4c04f02795fae79d1e33fa
https://hal.science/hal-02359446
https://hal.science/hal-02359446