Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Farès Namour"'
Autor:
Maurane Theron, Elise Jeannesson, Marie Canton, Farès Namour, Abderrahim Oussalah, François Feillet, Arnaud Wiedemann
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-8 (2023)
Abstract The prognosis of phenylketonuria (PKU) is related to the quality of metabolic control all life-long. PKU treatment is based on a low-Phe diet, 6R-tetrahydrobiopterin (BH4) treatment for the BH4-responsive PKU patients or enzyme replacement t
Externí odkaz:
https://doaj.org/article/82326cd754784914ab622216e2bd3ab9
Autor:
Tom Alix, Céline Chéry, Thomas Josse, Jean-Pierre Bronowicki, François Feillet, Rosa-Maria Guéant-Rodriguez, Farès Namour, Jean-Louis Guéant, Abderrahim Oussalah
Publikováno v:
Human Genomics, Vol 17, Iss 1, Pp 1-15 (2023)
Abstract Background Clinical exome sequencing (CES) provides a comprehensive and effective analysis of relevant disease-associated genes in a cost-effective manner compared to whole exome sequencing. Although several studies have focused on the diagn
Externí odkaz:
https://doaj.org/article/5bd28e834db54a03b60eb70cb3374f2d
Publikováno v:
Cells, Vol 11, Iss 22, p 3607 (2022)
Stem cells are a population of undifferentiated cells with self-renewal and differentiation capacities. Normal and cancer stem cells share similar characteristics in relation to their stemness properties. One-carbon metabolism (OCM), a network of int
Externí odkaz:
https://doaj.org/article/9863754e16884bcab553965e0c9cb783
Autor:
Maëlle Quéré, Jean-Marc Alberto, Franck Broly, Sébastien Hergalant, Christo Christov, Guillaume Gauchotte, Jean-Louis Guéant, Farès Namour, Shyue-Fang Battaglia-Hsu
Publikováno v:
Nutrients, Vol 14, Iss 9, p 1887 (2022)
Previously, the in vitro growth of cancer stem cells in the form of tumor spheres from five different brain cancer cell lines was found to be methionine-dependent. As this earlier work indicated that ALDH1L2, a folate-dependent mitochondria aldehyde
Externí odkaz:
https://doaj.org/article/bd9bb1e0877e4de1949a11eccc1781d7
Autor:
Abderrahim Oussalah, Stanislas Gleye, Isabelle Clerc Urmes, Elodie Laugel, Françoise Barbé, Sophie Orlowski, Catherine Malaplate, Isabelle Aimone-Gastin, Beatrice Maatem Caillierez, Marc Merten, Elise Jeannesson, Raphaël Kormann, Jean-Luc Olivier, Rosa-Maria Rodriguez-Guéant, Farès Namour, Sybille Bevilacqua, Nathalie Thilly, Marie-Reine Losser, Antoine Kimmoun, Luc Frimat, Bruno Levy, Sébastien Gibot, Evelyne Schvoerer, Jean-Louis Guéant
Publikováno v:
EClinicalMedicine, Vol 27, Iss , Pp 100554- (2020)
Background: In patients with severe COVID-19, no data are available on the longitudinal evolution of biochemical abnormalities and their ability to predict disease outcomes. Methods: Using a retrospective, longitudinal cohort study design on consecut
Externí odkaz:
https://doaj.org/article/e2149a7db628491d977b018dd8df1f08
Autor:
Yaohua Zhang, V. Reid Sutton, Youqiong Ye, Chunru Lin, Lan Liao, Zhao Zhang, Yajuan Li, Shuxing Zhang, Nenad Blau, Cristian Coarfa, Manuel Schiff, Ke Liang, Sergey D. Egranov, Zhi Tan, Preethi H. Gunaratne, Qingsong Hu, Kuang-Lei Tsai, Yi Chuan Li, Yao Jun, Jean-Louis Guéant, François Feillet, Mien Chie Hung, Chunlai Li, Nagireddy Putluri, Tina K. Nguyen, David H. Hawke, Heidi Hsiao, George A. Calin, Ania C. Muntau, Zhen Xing, Sujash S. Chatterjee, Liuqing Yang, Farès Namour, Leng Han, Yinghong Pan, Jianming Xu
Publikováno v:
Science
The functional role of long noncoding RNAs (lncRNAs) in inherited metabolic disorders, including phenylketonuria (PKU), is unknown. We demonstrated that the mouse lncRNA Pair and human HULC associate with phenylalanine hydroxylase (PAH). Pair-knockou
Autor:
Roeland A F Evers, Mariusz Ołtarzewski, Georg F. Hoffmann, Vincenzo Leuzzi, Emil Polak, Youngguo Yu, Maria Gizewska, Belén Pérez, Ana Chiesa, Marianne Rohrbach, Alexander V. Polyakov, Lena Fajkusova, Maja Stojiljkovic, Carla Carducci, Beat Thöny, Farès Namour, Jerry Vockley, Andrea Paras, Francjan J. van Spronsen, François Feillet, Sabine Scholl-Bürgi, Francesco Porta, Amaya Belanger-Quintana, Anastasia Skouma, Barbara K. Burton, Pedro E. Bonfim-Freitas, Sergey I. Kutsev, Johannes Zschocke, Uta Lichter-Konecki, Luiz Carlos Santana da Silva, Katya Kneller, Lourdes R. Desviat, Sven F. Garbade, Aviva Eliyahu, Alicia Hillert, Vera Stoppioni, Nenad Blau, Polina Gundorova, Norma Specola, Yair Anikster, John Christodoulou, Alberto Burlina, Maja Đorđević, Daniela Karall, Harvey L. Levy, Nan Shen, Friedrich K. Trefz, Ania C. Muntau
Publikováno v:
Am J Hum Genet
American Journal of Human Genetics, 107(2), 234-250. CELL PRESS
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
American Journal of Human Genetics, 107(2), 234-250. CELL PRESS
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Phenylketonuria (PKU), caused by variants in the phenylalanine hydroxylase (PAH) gene, is the most common autosomal-recessive Mendelian phenotype of amino acid metabolism. We estimated that globally 0.45 million individuals have PKU, with global prev
Autor:
Beatrice Maatem Caillierez, Elodie Laugel, Isabelle Aimone-Gastin, Sophie Orlowski, Nathalie Thilly, Bruno Levy, F Barbé, Evelyne Schvoerer, Sébastien Gibot, Luc Frimat, Sybille Bevilacqua, Abderrahim Oussalah, Marie Reine Losser, Antoine Kimmoun, Stanislas Gleye, Jean-Louis Guéant, Marc Merten, Rosa Maria Rodriguez-Gueant, Farès Namour, Isabelle Clerc Urmes, Raphaël Kormann, Elise Jeannesson, Jean Luc Olivier, Catherine Malaplate
Publikováno v:
EClinicalMedicine
EClinicalMedicine, Elsevier, 2020, 27, pp.100554. ⟨10.1016/j.eclinm.2020.100554⟩
EClinicalMedicine, 2020, 27, pp.100554. ⟨10.1016/j.eclinm.2020.100554⟩
EClinicalMedicine, Vol 27, Iss, Pp 100554-(2020)
EClinicalMedicine, Elsevier, 2020, 27, pp.100554. ⟨10.1016/j.eclinm.2020.100554⟩
EClinicalMedicine, 2020, 27, pp.100554. ⟨10.1016/j.eclinm.2020.100554⟩
EClinicalMedicine, Vol 27, Iss, Pp 100554-(2020)
International audience; Background: In patients with severe COVID-19, no data are available on the longitudinal evolution of biochemical abnormalities and their ability to predict disease outcomes.Methods: Using a retrospective, longitudinal cohort s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5a5f155c11fe258187a3630661e04bc
https://hal.univ-lorraine.fr/hal-03065397
https://hal.univ-lorraine.fr/hal-03065397
Autor:
Elodie Laugel, Isabelle Aimone-Gastin, Isabelle Clerc Urmes, Antoine Kimmoun, Jean-Louis Guéant, Abderrahim Oussalah, Rosa-Maria Rodriguez-Guéant, F Barbé, Sophie Orlowski, Marc Merten, Nathalie Thilly, Sébastien Gibot, Stanislas Gleye, Catherine Malaplate, Beatrice Maatem Caillierez, Jean-Luc Olivier, Raphaël Kormann, Luc Frimat, Farès Namour, Sybille Bevilacqua, Jonas Callet, Bruno Levy, Evelyne Schvoerer, Elise Jeannesson, Marie-Reine Losser
Publikováno v:
Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America
Clinical Infectious Diseases
Clinical Infectious Diseases, Oxford University Press (OUP), 2020, 71 (9), pp.2447-2456. ⟨10.1093/cid/ciaa677⟩
Clinical Infectious Diseases
Clinical Infectious Diseases, Oxford University Press (OUP), 2020, 71 (9), pp.2447-2456. ⟨10.1093/cid/ciaa677⟩
Background In patients with severe coronavirus disease 2019 (COVID-19), data are scarce and conflicting regarding whether chronic use of angiotensin-converting enzyme inhibitor (ACEI) or angiotensin receptor blocker (ARB) influences disease outcomes.
Autor:
Matthieu Garcia Parrilla, Matthieu Koszutski, Paul Voirin, Jean-Louis Guéant, Luc Frimat, Sybille Bevilacqua, Alice Corbel, Asma Alla, Audrey Jacquot, Abderrahim Oussalah, Raphaël Kormann, Bruno Levy, Evelyne Schvoerer, Farès Namour
Publikováno v:
Clinical Kidney Journal
Clinical Kidney Journal, Oxford University Press, 2020, 13 (3), pp.362-370. ⟨10.1093/ckj/sfaa109⟩
Clinical Kidney Journal, Oxford University Press, 2020, 13 (3), pp.362-370. ⟨10.1093/ckj/sfaa109⟩
Background Recent data have shown that severe acute respiratory syndrome coronavirus 2 can infect renal proximal tubular cells via Angiotensin Converting Enzyme 2 (ACE2) . Our objective was to determine whether Fanconi syndrome is a frequent clinical