Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Hammam I El-Hajj"'
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:
Gérard Lizard, Pierre Andreoletti, Joseph Vamecq, Soufiane El Kamouni, Riad El Kebbaj, Joseph Gresti, Hammam I. El Hajj, Norbert Latruffe, Boubker Nasser, M'Hammed Saïd El Kebbaj, Mustapha Cherkaoui-Malki
Publikováno v:
Health. :62-69
Pseudo-neonatal adrenoleukodystrophy (P-NALD) is a neurodegenerative disorder caused by acyl-CoA oxidase 1 (ACOX1) deficiency with subsequent impairment of peroxisomal fatty acid β-oxidation, accumulation of very long chain fatty acids (VLCFAs) and
Autor:
Mustapha Cherkaoui-Malki, Amira Zarrouk, Anne Vejux, Jean-Marc Riedinger, Thomas Nury, Hammam I. El Hajj, Madouda Haddad, Gérard Lizard, Mohamed Hammami
Publikováno v:
Oxidative Medicine and Cellular Longevity, Vol 2012 (2012)
Oxidative Medicine and Cellular Longevity
Oxidative Medicine and Cellular Longevity
In Alzheimer's disease, lipid alterations point towards peroxisomal dysfunctions. Indeed, a cortical accumulation of saturated very long chain fatty acids (VLCFAs: C22:0, C24:0, C26:0), substrates for peroxisomalβ-oxidation, has been found in Alzhei
Autor:
Gérard Lizard, Hammam I. El Hajj, Norbert Latruffe, Pierre Andreoletti, Mustapha Cherkaoui-Malki, Fatima-Ezzahra Saih, Joseph Vamecq, Riad El Kebbaj, Boubker Nasser, Youssef El Kharrassi, M'Hammed Saïd El Kebbaj, Stéphane Mandard
Publikováno v:
Biochimie Open
Biochimie Open, Elsevier, 2015, 1, pp.51-59. ⟨10.1016/j.biopen.2015.10.002⟩
Biochimie Open, 2015, 1, pp.51-59. ⟨10.1016/j.biopen.2015.10.002⟩
Biochimie Open, Vol 1, Iss C, Pp 51-59 (2015)
Biochimie Open, [Amsterdam] : Published by Elsevier B.V. on behalf of Société Française de Biochimie et Biologie Moléculaire (SFBBM), [2015]-, 2015, 1, pp.51-59. 〈10.1016/j.biopen.2015.10.002〉
Biochimie Open, Elsevier, 2015, 1, pp.51-59. ⟨10.1016/j.biopen.2015.10.002⟩
Biochimie Open, 2015, 1, pp.51-59. ⟨10.1016/j.biopen.2015.10.002⟩
Biochimie Open, Vol 1, Iss C, Pp 51-59 (2015)
Biochimie Open, [Amsterdam] : Published by Elsevier B.V. on behalf of Société Française de Biochimie et Biologie Moléculaire (SFBBM), [2015]-, 2015, 1, pp.51-59. 〈10.1016/j.biopen.2015.10.002〉
In patients with sepsis, liver metabolism and its capacity to provide other organs with energetic substrates are impaired. This and many other pathophysiological changes seen in human patients are reproduced in mice injected with purified endotoxin (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df3b3dce7a010d7619ed5b7b1e2f9f7e
https://www.hal.inserm.fr/inserm-01534672/file/BiochimieOpen2015ElKebbaj.pdf
https://www.hal.inserm.fr/inserm-01534672/file/BiochimieOpen2015ElKebbaj.pdf
Autor:
Mustapha Cherkaoui-Malki, Gérard Lizard, David Masson, Boubker Nasser, Thomas Nury, Khadija Moustaid, Joseph Vamecq, Mohammad Samadi, Norbert Latruffe, Youssef El Kharrassi, Riad El Kebbaj, Tatiana Lopez, Hammam I. El Hajj, Pierre Andreoletti, M'Hammed Saïd El Kebbaj
Publikováno v:
Biochemical and Biophysical Research Communications
Biochemical and Biophysical Research Communications, Elsevier, 2014, 446 (3, SI), pp.798-804. ⟨10.1016/j.bbrc.2014.02.074⟩
Biochemical and Biophysical Research Communications, Elsevier, 2014, 446 (3, SI), pp.798-804. 〈10.1016/j.bbrc.2014.02.074〉
Biochemical and Biophysical Research Communications, Elsevier, 2014, 446 (3, SI), pp.798-804. ⟨10.1016/j.bbrc.2014.02.074⟩
Biochemical and Biophysical Research Communications, Elsevier, 2014, 446 (3, SI), pp.798-804. 〈10.1016/j.bbrc.2014.02.074〉
International audience; The objective of this study was to evaluate the biological activities of the major phytosterols present in argan oil (AO) and in cactus seed oil (CSO) in BV2 microglial cells. Accordingly, we first determined the sterol compos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d84c2c86e33997f6deaf1855ae84dd1
https://hal.univ-lorraine.fr/hal-01518331
https://hal.univ-lorraine.fr/hal-01518331
Autor:
Sailesh Surapureddi, Mustapha Cherkaoui-Malki, Joseph Vamecq, Hammam I El-Hajj, Pierre Andreoletti
Publikováno v:
Current drug metabolism. 13(10)
Three subhepatocellular compartments concur for fatty acids degradation including ω-oxidation in endoplasmic reticulum and β-oxidation in both mitochondria and peroxisomes. Deficits affecting the peroxisomal physiology may be associated with multip
Autor:
Franck Ménétrier, Mauhamad Baarine, Pierre Andreoletti, Emmanuelle C. Genin, Mustapha Cherkaoui-Malki, Doriane Trompier, M. Said Ghandour, Gérard Lizard, Kévin Ragot, Stéphane Savary, Hammam I. El Hajj
Publikováno v:
Journal of Neurochemistry
Journal of Neurochemistry, Wiley, 2009, 111 (1), pp.119-31. 〈10.1111/j.1471-4159.2009.06311.x〉
Journal of Neurochemistry, Wiley, 2009, 111 (1), pp.119-31. 〈10.1111/j.1471-4159.2009.06311.x〉
International audience; In some neurodegenerative disorders (leukodystrophies) characterized by myelin alterations, the defect of peroxisomal functions on myelin-producing cells (oligodendrocytes) are poorly understood. The development of in vitro mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f5757adeecf69e96086df40e3f8cced
https://hal.archives-ouvertes.fr/hal-00514890/document
https://hal.archives-ouvertes.fr/hal-00514890/document