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DCLRE1B/Apollo germline mutations associated with renal cell carcinoma impair telomere protection.
Bories C, Lejour T, Adolphe F, Kermasson L, Couvé S, Tanguy L, Luszczewska G, Watzky M, Poillerat V, Garnier P, Groisman R, Ferlicot S, Richard S, Saparbaev M, Revy P, Gad S, Renaud F. Bories C, et al. Among authors: richard s. Biochim Biophys Acta Mol Basis Dis. 2024 Apr;1870(4):167107. doi: 10.1016/j.bbadis.2024.167107. Epub 2024 Feb 29. Biochim Biophys Acta Mol Basis Dis. 2024. PMID: 38430974 Free article.
Mutations in BHD and TP53 genes, but not in HNF1beta gene, in a large series of sporadic chromophobe renal cell carcinoma.
Gad S, Lefèvre SH, Khoo SK, Giraud S, Vieillefond A, Vasiliu V, Ferlicot S, Molinié V, Denoux Y, Thiounn N, Chrétien Y, Méjean A, Zerbib M, Benoît G, Hervé JM, Allègre G, Bressac-de Paillerets B, Teh BT, Richard S. Gad S, et al. Among authors: richard s. Br J Cancer. 2007 Jan 29;96(2):336-40. doi: 10.1038/sj.bjc.6603492. Epub 2006 Nov 28. Br J Cancer. 2007. PMID: 17133269 Free PMC article.
[Genetics and angiogenesis: the example of von Hippel-Lindau disease].
Richard S, Ladroue C, Gad S, Giraud S, Gardie B; Réseau national maladie de VHL et prédispositions héréditaires au cancer du rein de l'Institut national du cancer (INCa). Richard S, et al. Bull Cancer. 2007 Jul;94 Spec No:S170-9. Bull Cancer. 2007. PMID: 17846002 Review. French.
PHD2 mutation and congenital erythrocytosis with paraganglioma.
Ladroue C, Carcenac R, Leporrier M, Gad S, Le Hello C, Galateau-Salle F, Feunteun J, Pouysségur J, Richard S, Gardie B. Ladroue C, et al. Among authors: richard s. N Engl J Med. 2008 Dec 18;359(25):2685-92. doi: 10.1056/NEJMoa0806277. N Engl J Med. 2008. PMID: 19092153 Free article.
[Renal oncocytosis: case report].
Ploussard G, Droupy S, Ferlicot S, Ples R, Rocher L, Richard S, Benoit G. Ploussard G, et al. Among authors: richard s. Prog Urol. 2009 Feb;19(2):142-4. doi: 10.1016/j.purol.2008.10.001. Epub 2008 Nov 20. Prog Urol. 2009. PMID: 19168021 French.
Distinct deregulation of the hypoxia inducible factor by PHD2 mutants identified in germline DNA of patients with polycythemia.
Ladroue C, Hoogewijs D, Gad S, Carcenac R, Storti F, Barrois M, Gimenez-Roqueplo AP, Leporrier M, Casadevall N, Hermine O, Kiladjian JJ, Baruchel A, Fakhoury F, Bressac-de Paillerets B, Feunteun J, Mazure N, Pouysségur J, Wenger RH, Richard S, Gardie B. Ladroue C, et al. Among authors: richard s. Haematologica. 2012 Jan;97(1):9-14. doi: 10.3324/haematol.2011.044644. Epub 2011 Sep 20. Haematologica. 2012. PMID: 21933857 Free PMC article.
1,457 results