Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mounia Tahri-Joutey"'
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:
Riad El Kebbaj, Habiba Bouchab, Mounia Tahri-Joutey, Soufiane Rabbaa, Youness Limami, Boubker Nasser, Melford C. Egbujor, Paolo Tucci, Pierre Andreoletti, Luciano Saso, Mustapha Cherkaoui-Malki
Publikováno v:
Antioxidants, Vol 13, Iss 3, p 344 (2024)
In recent years, research on the discovery of natural compounds with potent antioxidant properties has resulted in growing interest in these compounds due to their potential therapeutic applications in oxidative-stress-related diseases. Argan oil, de
Externí odkaz:
https://doaj.org/article/04afcec45d9a4e198d9572a62efd946b
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:
Mustapha Cherkaoui-Malki, Saad Shaaban, Mounia Tahri-Joutey, Ahmed Elshobaky, Fatima-Ezzahra Saih, Dominique Vervandier-Fasseur, Claus Jacob, Boubker Nasser, Norbert Latruffe, Pierre Andreoletti
Publikováno v:
Proceedings, Vol 11, Iss 1, p 33 (2019)
Several of the peroxisomal neurodegenerative disorders are the consequence of a specific deficiency of an enzyme or a transporter involved in peroxisomal beta-oxidation of very long chain fatty acids [1,2]. One of the hallmarks in these peroxisomal r
Externí odkaz:
https://doaj.org/article/bde9011027b443fca655154d567b83cd
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::22673f514e2978015ec4a8c4111e7fa3
https://pubmed.ncbi.nlm.nih.gov/36233157
https://pubmed.ncbi.nlm.nih.gov/36233157
Autor:
Imen Ghzaiel, Khouloud Sassi, Amira Zarrouk, Shubhrima Ghosh, Irundika H K Dias, Thomas Nury, Mohamed Ksila, Soukaina Essadek, Mounia Tahri Joutey, Fatiha Brahmi, Wafa Mihoubi, Sandrine Rup-Jacques, Mohammad Samadi, Leila Rezig, Smail Meziane, Taoufik Ghrairi, Olfa Masmoudi-Kouki, Sonia Hammami, Boubker Nasser, Mohamed Hammami, Yuqin Wang, William J Griffiths, Anne Vejux, Gérard Lizard
Publikováno v:
Redox Experimental Medicine
Graphical abstract Abstract 7-Ketocholesterol (or 7-oxocholesterol) is an oxysterol essentially formed by cholesterol autoxidation. It is often found at enhanced levels in the body fluids and/or target tissues of patients with age-related diseases (c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49f0553cd1f9fd482860bb6ca9fec338
https://publications.aston.ac.uk/id/eprint/44060/1/_2755158X_Redox_Experimental_Medicine_Sources_of_7_ketocholesterol_metabolism_and_inactivation_strategies_food_and_biomedical_applications.pdf
https://publications.aston.ac.uk/id/eprint/44060/1/_2755158X_Redox_Experimental_Medicine_Sources_of_7_ketocholesterol_metabolism_and_inactivation_strategies_food_and_biomedical_applications.pdf
Autor:
Imen Ghzaiel, Amira Zarrouk, Soukaina Essadek, Lucy Martine, Souha Hammouda, Aline Yammine, Mohamed Ksila, Thomas Nury, Wiem Meddeb, Mounia Tahri Joutey, Wafa Mihoubi, Claudio Caccia, Valerio Leoni, Mohammad Samadi, Niyazi Acar, Pierre Andreoletti, Sonia Hammami, Taoufik Ghrairi, Anne Vejux, Mohamed Hammami, Gérard Lizard
Peroxisomes play an important role in regulating cell metabolism and RedOx homeostasis. Peroxisomal dysfunctions favor oxidative stress and cell death. The ability of 7β-hydroxycholesterol (7β-OHC; 50 μM, 24 h), known to be increased in patients w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1347a2d5f7cb9025098c10e41afc201
http://hdl.handle.net/10281/369422
http://hdl.handle.net/10281/369422
Autor:
Boubker Nasser, Mustapha Cherkaoui-Malki, Sailesh Surapureddi, Mounia Tahri-Joutey, Norbert Latruffe, Pierre Andreoletti
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 8969, p 8969 (2021)
International Journal of Molecular Sciences, Vol 22, Iss 8969, p 8969 (2021)
In mammalian cells, two cellular organelles, mitochondria and peroxisomes, share the ability to degrade fatty acid chains. Although each organelle harbors its own fatty acid β-oxidation pathway, a distinct mitochondrial system feeds the oxidative ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61b5240a1d02f246b89ee8cce4e2d0fb
https://pubmed.ncbi.nlm.nih.gov/34445672
https://pubmed.ncbi.nlm.nih.gov/34445672
Autor:
Dominique Vervandier-Fasseur, Claus Jacob, Boubker Nasser, Mustapha Cherkaoui-Malki, Norbert Latruffe, Fatima-Ezzahra Saih, Ahmed Elshobaky, Pierre Andreoletti, Saad Shaaban, Mounia Tahri-Joutey
Publikováno v:
Proceedings, Vol 11, Iss 1, p 33 (2019)
Several of the peroxisomal neurodegenerative disorders are the consequence of a specific deficiency of an enzyme or a transporter involved in peroxisomal beta-oxidation of very long chain fatty acids [1,2]. One of the hallmarks in these peroxisomal r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36adb80d561b3f68ebe34e91fc818204
https://doi.org/10.3390/proceedings2019011033
https://doi.org/10.3390/proceedings2019011033