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Items: 9


Molecular Alterations and Buparlisib Efficacy in Patients with Squamous Cell Carcinoma of the Head and Neck: Biomarker Analysis from BERIL-1.

Soulières D, Licitra L, Mesía R, Remenár É, Li SH, Karpenko A, Chol M, Wang YA, Solovieff N, Bourdeau L, Sellami D, Faivre S.

Clin Cancer Res. 2018 Jun 1;24(11):2505-2516. doi: 10.1158/1078-0432.CCR-17-2644. Epub 2018 Feb 28.


Buparlisib and paclitaxel in patients with platinum-pretreated recurrent or metastatic squamous cell carcinoma of the head and neck (BERIL-1): a randomised, double-blind, placebo-controlled phase 2 trial.

Soulières D, Faivre S, Mesía R, Remenár É, Li SH, Karpenko A, Dechaphunkul A, Ochsenreither S, Kiss LA, Lin JC, Nagarkar R, Tamás L, Kim SB, Erfán J, Alyasova A, Kasper S, Barone C, Turri S, Chakravartty A, Chol M, Aimone P, Hirawat S, Licitra L.

Lancet Oncol. 2017 Mar;18(3):323-335. doi: 10.1016/S1470-2045(17)30064-5. Epub 2017 Jan 26.


Cystinosin is a Component of the Vacuolar H+-ATPase-Ragulator-Rag Complex Controlling Mammalian Target of Rapamycin Complex 1 Signaling.

Andrzejewska Z, Nevo N, Thomas L, Chhuon C, Bailleux A, Chauvet V, Courtoy PJ, Chol M, Guerrera IC, Antignac C.

J Am Soc Nephrol. 2016 Jun;27(6):1678-88. doi: 10.1681/ASN.2014090937. Epub 2015 Oct 8.


Inhibition of the diclofenac-induced cyclooxygenase-2 activity by paracetamol in cultured macrophages is not related to the intracellular lipid hydroperoxide tone.

Ayoub SS, Joshi A, Chol M, Gilroy DW, Seed MP.

Fundam Clin Pharmacol. 2011 Apr;25(2):186-90. doi: 10.1111/j.1472-8206.2010.00842.x.


Renal phenotype of the cystinosis mouse model is dependent upon genetic background.

Nevo N, Chol M, Bailleux A, Kalatzis V, Morisset L, Devuyst O, Gubler MC, Antignac C.

Nephrol Dial Transplant. 2010 Apr;25(4):1059-66. doi: 10.1093/ndt/gfp553. Epub 2009 Oct 21.


Glutathione precursors replenish decreased glutathione pool in cystinotic cell lines.

Chol M, Nevo N, Cherqui S, Antignac C, Rustin P.

Biochem Biophys Res Commun. 2004 Nov 5;324(1):231-5.


Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency.

Lebon S, Chol M, Benit P, Mugnier C, Chretien D, Giurgea I, Kern I, Girardin E, Hertz-Pannier L, de Lonlay P, Rötig A, Rustin P, Munnich A.

J Med Genet. 2003 Dec;40(12):896-9.


The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency.

Chol M, Lebon S, Bénit P, Chretien D, de Lonlay P, Goldenberg A, Odent S, Hertz-Pannier L, Vincent-Delorme C, Cormier-Daire V, Rustin P, Rötig A, Munnich A.

J Med Genet. 2003 Mar;40(3):188-91.


Assay of mitochondrial respiratory chain complex I in human lymphocytes and cultured skin fibroblasts.

Chretien D, Bénit P, Chol M, Lebon S, Rötig A, Munnich A, Rustin P.

Biochem Biophys Res Commun. 2003 Jan 31;301(1):222-4.


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