Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Jonathan Evraerts"'
Autor:
Giulia Jannone, Catherine de Magnée, Roberto Tambucci, Jonathan Evraerts, Joachim Ravau, Mustapha Najimi, Etienne Marc Sokal
Publikováno v:
PLoS ONE, Vol 18, Iss 4, p e0285019 (2023)
IntroductionAlagille syndrome (ALGS) is an autosomal dominant disease characterized by a multisystem involvement including bile duct paucity and cholestasis, caused by JAG1 or NOTCH2 mutations in most of the cases. Jagged1-Notch2 interactions are kno
Externí odkaz:
https://doaj.org/article/505a31a98014439c86c07b0a161bd253
Autor:
Pierre Edouard Dollet, Mei Ju Hsu, Jérôme Ambroise, Milena Rozzi, Joachim Ravau, Floriane André, Jonathan Evraerts, Mustapha Najimi, Etienne Sokal, Catherine Lombard
Publikováno v:
Cell Transplantation, Vol 29 (2020)
Adult-derived human liver stem/progenitor cells (ADHLSCs) are a promising alternative to orthotopic liver transplantation in the treatment of inborn errors of metabolism. However, as is the case with many mesenchymal stromal cells, ADHLSCs have shown
Externí odkaz:
https://doaj.org/article/7703f1701c5a4b08a57a8edf139b91e1
Autor:
Mustapha Najimi, Silvia Berardis, Hoda El-Kehdy, Valérie Rosseels, Jonathan Evraerts, Catherine Lombard, Adil El Taghdouini, Patrick Henriet, Leo van Grunsven, Etienne Marc Sokal
Publikováno v:
Stem Cell Research & Therapy, Vol 8, Iss 1, Pp 1-11 (2017)
Abstract Background Progressive liver fibrosis leads to cirrhosis and end-stage liver disease. This disease is a consequence of strong interactions between matrix-producing hepatic stellate cells (HSCs) and resident and infiltrating immune cell popul
Externí odkaz:
https://doaj.org/article/2fbd8e2e98154697a864a3306c4110af
Autor:
Tanguy Demaret, Jonathan Evraerts, Joachim Ravau, Martin Roumain, Giulio G. Muccioli, Mustapha Najimi, Etienne M. Sokal
Publikováno v:
Cells, Vol 10, Iss 1, p 40 (2020)
Genetic alterations in PEX genes lead to peroxisome biogenesis disorder. In humans, they are associated with Zellweger spectrum disorders (ZSD). No validated treatment has been shown to modify the dismal natural history of ZSD. Liver transplantation
Externí odkaz:
https://doaj.org/article/7e5ace1490694c9a82bf06b5a5c975d6
Autor:
Silvia Berardis, Catherine Lombard, Jonathan Evraerts, Adil El Taghdouini, Valérie Rosseels, Pau Sancho-Bru, Juan Jose Lozano, Leo van Grunsven, Etienne Sokal, Mustapha Najimi
Publikováno v:
PLoS ONE, Vol 9, Iss 1, p e86137 (2014)
Adult-derived human liver stem/progenitor cells (ADHLSC) are obtained after primary culture of the liver parenchymal fraction. The cells are of fibroblastic morphology and exhibit a hepato-mesenchymal phenotype. Hepatic stellate cells (HSC) derived f
Externí odkaz:
https://doaj.org/article/073f7dde1b56455abe511c955f5065ed
Autor:
Brice Sid, Mustapha Najimi, Sivanesan Karthikeyan, Jonathan Evraerts, Pedro Buc Calderon, Devaraj Ezhilarasan, Etienne Sokal
Publikováno v:
Hepatobiliary & Pancreatic Diseases International. 16:80-87
Background Proliferation of hepatic stellate cells (HSCs) plays a pivotal role in the progression of liver fibrosis consequent to chronic liver injury. Silibinin, a flavonoid compound, has been shown to possess anti-fibrogenic effects in animal model
Autor:
Mustapha Najimi, Etienne Sokal, Martin Roumain, Tanguy Demaret, Joachim Ravau, Giulio G. Muccioli, Jonathan Evraerts
Publikováno v:
Cells
Volume 10
Issue 1
Cells, Vol 10, Iss 40, p 40 (2021)
Volume 10
Issue 1
Cells, Vol 10, Iss 40, p 40 (2021)
Genetic alterations in PEX genes lead to peroxisome biogenesis disorder. In humans, they are associated with Zellweger spectrum disorders (ZSD). No validated treatment has been shown to modify the dismal natural history of ZSD. Liver transplantation
Autor:
Catherine Lombard, Mei Ju Hsu, Jonathan Evraerts, Etienne Sokal, Jérôme Ambroise, Floriane André, Joachim Ravau, Pierre Edouard Dollet, Milena Rozzi, Mustapha Najimi
Publikováno v:
Cell Transplantation
Cell Transplantation, Vol. 29, p. 096368972091270 (2020)
Cell Transplantation, Vol 29 (2020)
Cell Transplantation, Vol. 29, p. 096368972091270 [1-14] (2020)
Cell Transplantation, Vol. 29, p. 096368972091270 (2020)
Cell Transplantation, Vol 29 (2020)
Cell Transplantation, Vol. 29, p. 096368972091270 [1-14] (2020)
Adult-derived human liver stem/progenitor cells (ADHLSCs) are a promising alternative to orthotopic liver transplantation in the treatment of inborn errors of metabolism. However, as is the case with many mesenchymal stromal cells, ADHLSCs have shown
Autor:
Mehdi Najar, Patricia Renard, Marino Caruso, Etienne Sokal, Nicki Tiffin, Jean-Baka Domelevo Entfellner, Hoda El-Kehdy, Jonathan Evraerts, Guillaume Pourcher, Thierry Arnould, Catherine Demazy, Antoine Fattaccioli, Anaïs Wanet, Mustapha Najimi
Publikováno v:
Wanet, A, Caruso, M, Domelevo Entfellner, J B, Najar, M, Fattaccioli, A, Demazy, C, Evraerts, J, El-Kehdy, H, Pourcher, G, Sokal, E, Arnould, T, Tiffin, N, Najimi, M & Renard, P 2017, ' The Transcription Factor 7-Like 2-Peroxisome Proliferator-Activated Receptor Gamma Coactivator-1 Alpha Axis Connects Mitochondrial Biogenesis and Metabolic Shift with Stem Cell Commitment to Hepatic Differentiation ', Stem Cells, vol. 35, no. 10, 35(10), pp. 2184-2197 . https://doi.org/10.1002/stem.2688
Increasing evidence supports that modifications in the mitochondrial content, oxidative phosphorylation (OXPHOS) activity, and cell metabolism influence the fate of stem cells. However, the regulators involved in the crosstalk between mitochondria an
Autor:
Jonathan Evraerts, Valérie Rosseels, Mustapha Najimi, Leo A. van Grunsven, Adil El Taghdouini, Silvia Berardis, Hoda El-Kehdy, Catherine Lombard, Etienne Sokal, Patrick Henriet
Publikováno v:
Stem Cell Research & Therapy
Stem Cell Research & Therapy, Vol. 8, no. 1, p. 131 [1-11] (2017)
Stem Cell Research & Therapy, Vol 8, Iss 1, Pp 1-11 (2017)
Stem Cell Research & Therapy, Vol. 8, no.1 (2017)
Stem Cell Research & Therapy, Vol. 8, no. 1, p. 131 [1-11] (2017)
Stem Cell Research & Therapy, Vol 8, Iss 1, Pp 1-11 (2017)
Stem Cell Research & Therapy, Vol. 8, no.1 (2017)
Background Progressive liver fibrosis leads to cirrhosis and end-stage liver disease. This disease is a consequence of strong interactions between matrix-producing hepatic stellate cells (HSCs) and resident and infiltrating immune cell populations. A