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146 results

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Page 1
TERT promoter status and gene copy number gains: effect on TERT expression and association with prognosis in breast cancer.
Gay-Bellile M, Véronèse L, Combes P, Eymard-Pierre E, Kwiatkowski F, Dauplat MM, Cayre A, Privat M, Abrial C, Bignon YJ, Mouret-Reynier MA, Vago P, Penault-Llorca F, Tchirkov A. Gay-Bellile M, et al. Among authors: combes p. Oncotarget. 2017 Aug 24;8(44):77540-77551. doi: 10.18632/oncotarget.20560. eCollection 2017 Sep 29. Oncotarget. 2017. PMID: 29100407 Free PMC article.
Telomere status in chronic lymphocytic leukemia with TP53 disruption.
Guièze R, Pages M, Véronèse L, Combes P, Lemal R, Gay-Bellile M, Chauvet M, Callanan M, Kwiatkowski F, Pereira B, Vago P, Bay JO, Tournilhac O, Tchirkov A. Guièze R, et al. Among authors: combes p. Oncotarget. 2016 Aug 30;7(35):56976-56985. doi: 10.18632/oncotarget.10927. Oncotarget. 2016. PMID: 27486974 Free PMC article.
ERCC1 and telomere status in breast tumours treated with neoadjuvant chemotherapy and their association with patient prognosis.
Gay-Bellile M, Romero P, Cayre A, Véronèse L, Privat M, Singh S, Combes P, Kwiatkowski F, Abrial C, Bignon YJ, Vago P, Penault-Llorca F, Tchirkov A. Gay-Bellile M, et al. Among authors: combes p. J Pathol Clin Res. 2016 Jul 13;2(4):234-246. doi: 10.1002/cjp2.52. eCollection 2016 Oct. J Pathol Clin Res. 2016. PMID: 27785368 Free PMC article.
Prenatal diagnosis of a rare de novo centromeric chromosome 6 variant.
Goumy C, Kemeny S, Eymard-Pierre E, Richard C, Gouas L, Combes P, Gay-Bellile M, Gallot D, Tchirkov A, Vago P. Goumy C, et al. Among authors: combes p. Gene. 2011 Dec 15;490(1-2):15-7. doi: 10.1016/j.gene.2011.09.008. Epub 2011 Oct 1. Gene. 2011. PMID: 21989483
Sjögren-Larsson syndrome: novel mutations in the ALDH3A2 gene in a French cohort.
Sarret C, Rigal M, Vaurs-Barrière C, Dorboz I, Eymard-Pierre E, Combes P, Giraud G, Wanders RJ, Afenjar A, Francannet C, Boespflug-Tanguy O. Sarret C, et al. Among authors: combes p. J Neurol Sci. 2012 Jan 15;312(1-2):123-6. doi: 10.1016/j.jns.2011.08.006. Epub 2011 Aug 26. J Neurol Sci. 2012. PMID: 21872273
Golli-MBP copy number analysis by FISH, QMPSF and MAPH in 195 patients with hypomyelinating leukodystrophies.
Vaurs-Barriere C, Bonnet-Dupeyron MN, Combes P, Gauthier-Barichard F, Reveles XT, Schiffmann R, Bertini E, Rodriguez D, Vago P, Armour JA, Saugier-Veber P, Frebourg T, Leach RJ, Boespflug-Tanguy O. Vaurs-Barriere C, et al. Among authors: combes p. Ann Hum Genet. 2006 Jan;70(Pt 1):66-77. doi: 10.1111/j.1529-8817.2005.00208.x. Ann Hum Genet. 2006. PMID: 16441258
Presence of multiple recurrent mutations confers poor trial outcome of relapsed/refractory CLL.
Guièze R, Robbe P, Clifford R, de Guibert S, Pereira B, Timbs A, Dilhuydy MS, Cabes M, Ysebaert L, Burns A, Nguyen-Khac F, Davi F, Véronèse L, Combes P, Le Garff-Tavernier M, Leblond V, Merle-Béral H, Alsolami R, Hamblin A, Mason J, Pettitt A, Hillmen P, Taylor J, Knight SJ, Tournilhac O, Schuh A. Guièze R, et al. Among authors: combes p. Blood. 2015 Oct 29;126(18):2110-7. doi: 10.1182/blood-2015-05-647578. Epub 2015 Aug 27. Blood. 2015. PMID: 26316624 Free article. Clinical Trial.
146 results