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TET-Mediated Hypermethylation Primes SDH-Deficient Cells for HIF2α-Driven Mesenchymal Transition.
Cell Rep. 2020 Mar 31;30(13):4551-4566.e7. doi: 10.1016/j.celrep.2020.03.022.
Cell Rep. 2020.
PMID: 32234487
Free article.
Lactate Dehydrogenase B Controls Lysosome Activity and Autophagy in Cancer.
Brisson L, Bański P, Sboarina M, Dethier C, Danhier P, Fontenille MJ, Van Hée VF, Vazeille T, Tardy M, Falces J, Bouzin C, Porporato PE, Frédérick R, Michiels C, Copetti T, Sonveaux P.
Brisson L, et al. Among authors: fontenille mj.
Cancer Cell. 2016 Sep 12;30(3):418-431. doi: 10.1016/j.ccell.2016.08.005.
Cancer Cell. 2016.
PMID: 27622334
Free article.
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Lactate promotes glutamine uptake and metabolism in oxidative cancer cells.
Pérez-Escuredo J, Dadhich RK, Dhup S, Cacace A, Van Hée VF, De Saedeleer CJ, Sboarina M, Rodriguez F, Fontenille MJ, Brisson L, Porporato PE, Sonveaux P.
Pérez-Escuredo J, et al. Among authors: fontenille mj.
Cell Cycle. 2016;15(1):72-83. doi: 10.1080/15384101.2015.1120930.
Cell Cycle. 2016.
PMID: 26636483
Free PMC article.
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Mutations in GFPT1-related congenital myasthenic syndromes are associated with synaptic morphological defects and underlie a tubular aggregate myopathy with synaptopathy.
Bauché S, Vellieux G, Sternberg D, Fontenille MJ, De Bruyckere E, Davoine CS, Brochier G, Messéant J, Wolf L, Fardeau M, Lacène E, Romero N, Koenig J, Fournier E, Hantaï D, Streichenberger N, Manel V, Lacour A, Nadaj-Pakleza A, Sukno S, Bouhour F, Laforêt P, Fontaine B, Strochlic L, Eymard B, Chevessier F, Stojkovic T, Nicole S.
Bauché S, et al. Among authors: fontenille mj.
J Neurol. 2017 Aug;264(8):1791-1803. doi: 10.1007/s00415-017-8569-x. Epub 2017 Jul 15.
J Neurol. 2017.
PMID: 28712002
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Agrin mutations lead to a congenital myasthenic syndrome with distal muscle weakness and atrophy.
Nicole S, Chaouch A, Torbergsen T, Bauché S, de Bruyckere E, Fontenille MJ, Horn MA, van Ghelue M, Løseth S, Issop Y, Cox D, Müller JS, Evangelista T, Stålberg E, Ioos C, Barois A, Brochier G, Sternberg D, Fournier E, Hantaï D, Abicht A, Dusl M, Laval SH, Griffin H, Eymard B, Lochmüller H.
Nicole S, et al. Among authors: fontenille mj.
Brain. 2014 Sep;137(Pt 9):2429-43. doi: 10.1093/brain/awu160. Epub 2014 Jun 20.
Brain. 2014.
PMID: 24951643
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The multiple faces of the ATP1A3-related dystonic movement disorder.
Roubergue A, Roze E, Vuillaumier-Barrot S, Fontenille MJ, Méneret A, Vidailhet M, Fontaine B, Doummar D, Philibert B, Riant F, Nicole S.
Roubergue A, et al. Among authors: fontenille mj.
Mov Disord. 2013 Sep;28(10):1457-9. doi: 10.1002/mds.25396. Epub 2013 Mar 8.
Mov Disord. 2013.
PMID: 23483595
No abstract available.
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