Pierron G - Search Results

1

DNA methylation heterogeneity defines a disease spectrum in Ewing sarcoma.

Sheffield NC, Pierron G, Klughammer J, Datlinger P, Schönegger A, Schuster M, Hadler J, Surdez D, Guillemot D, Lapouble E, Freneaux P, Champigneulle J, Bouvier R, Walder D, Ambros IM, Hutter C, Sorz E, Amaral AT, de Álava E, Schallmoser K, Strunk D, Rinner B, Liegl-Atzwanger B, Huppertz B, Leithner A, de Pinieux G, Terrier P, Laurence V, Michon J, Ladenstein R, Holter W, Windhager R, Dirksen U, Ambros PF, Delattre O, Kovar H, Bock C, Tomazou EM. Sheffield NC, et al. Among authors: pierron g. Nat Med. 2017 Mar;23(3):386-395. doi: 10.1038/nm.4273. Epub 2017 Jan 30. Nat Med. 2017. PMID: 28134926 Free PMC article.

2

High-resolution mapping of amplicons of the short arm of chromosome 1 in two neuroblastoma tumors by microarray-based comparative genomic hybridization.

Fix A, Peter M, Pierron G, Aurias A, Delattre O, Janoueix-Lerosey I. Fix A, et al. Among authors: pierron g. Genes Chromosomes Cancer. 2004 Jul;40(3):266-70. doi: 10.1002/gcc.20041. Genes Chromosomes Cancer. 2004. PMID: 15139005

3

Incidence and prognostic value of tumour cells detected by RT-PCR in peripheral blood stem cell collections from patients with Ewing tumour.

Vermeulen J, Ballet S, Oberlin O, Peter M, Pierron G, Longavenne E, Laurence V, Kanold J, Chastagner P, Lejars O, Blay JY, Marec-Berard P, Michon J, Delattre O, Schleiermacher G. Vermeulen J, et al. Among authors: pierron g. Br J Cancer. 2006 Nov 20;95(10):1326-33. doi: 10.1038/sj.bjc.6603438. Epub 2006 Oct 31. Br J Cancer. 2006. PMID: 17088915 Free PMC article.

4

hSNF5/INI1-deficient tumours and rhabdoid tumours are convergent but not fully overlapping entities.

Bourdeaut F, Fréneaux P, Thuille B, Lellouch-Tubiana A, Nicolas A, Couturier J, Pierron G, Sainte-Rose C, Bergeron C, Bouvier R, Rialland X, Laurence V, Michon J, Sastre-Garau X, Delattre O. Bourdeaut F, et al. Among authors: pierron g. J Pathol. 2007 Feb;211(3):323-30. doi: 10.1002/path.2103. J Pathol. 2007. PMID: 17152049

5

In neuroblastic tumours, Schwann cells do not harbour the genetic alterations of neuroblasts but may nevertheless share the same clonal origin.

Bourdeaut F, Ribeiro A, Paris R, Pierron G, Couturier J, Peuchmaur M, Delattre O. Bourdeaut F, et al. Among authors: pierron g. Oncogene. 2008 May 8;27(21):3066-71. doi: 10.1038/sj.onc.1210965. Epub 2007 Dec 10. Oncogene. 2008. PMID: 18071318

6

Characterization of amplicons in neuroblastoma: high-resolution mapping using DNA microarrays, relationship with outcome, and identification of overexpressed genes.

Fix A, Lucchesi C, Ribeiro A, Lequin D, Pierron G, Schleiermacher G, Delattre O, Janoueix-Lerosey I. Fix A, et al. Among authors: pierron g. Genes Chromosomes Cancer. 2008 Oct;47(10):819-34. doi: 10.1002/gcc.20583. Genes Chromosomes Cancer. 2008. PMID: 18553563

7

Characterization of the recurrent 8p11-12 amplicon identifies PPAPDC1B, a phosphatase protein, as a new therapeutic target in breast cancer.

Bernard-Pierrot I, Gruel N, Stransky N, Vincent-Salomon A, Reyal F, Raynal V, Vallot C, Pierron G, Radvanyi F, Delattre O. Bernard-Pierrot I, et al. Among authors: pierron g. Cancer Res. 2008 Sep 1;68(17):7165-75. doi: 10.1158/0008-5472.CAN-08-1360. Cancer Res. 2008. PMID: 18757432

8

Somatic and germline activating mutations of the ALK kinase receptor in neuroblastoma.

Janoueix-Lerosey I, Lequin D, Brugières L, Ribeiro A, de Pontual L, Combaret V, Raynal V, Puisieux A, Schleiermacher G, Pierron G, Valteau-Couanet D, Frebourg T, Michon J, Lyonnet S, Amiel J, Delattre O. Janoueix-Lerosey I, et al. Among authors: pierron g. Nature. 2008 Oct 16;455(7215):967-70. doi: 10.1038/nature07398. Nature. 2008. PMID: 18923523

9

Cholinergic switch associated with morphological differentiation in neuroblastoma.

Bourdeaut F, Janoueix-Lerosey I, Lucchesi C, Paris R, Ribeiro A, de Pontual L, Amiel J, Lyonnet S, Pierron G, Michon J, Peuchmaur M, Delattre O. Bourdeaut F, et al. Among authors: pierron g. J Pathol. 2009 Dec;219(4):463-72. doi: 10.1002/path.2614. J Pathol. 2009. PMID: 19768740

10

Incomplete penetrance of the predisposition to medulloblastoma associated with germ-line SUFU mutations.

Brugières L, Pierron G, Chompret A, Paillerets BB, Di Rocco F, Varlet P, Pierre-Kahn A, Caron O, Grill J, Delattre O. Brugières L, et al. Among authors: pierron g. J Med Genet. 2010 Feb;47(2):142-4. doi: 10.1136/jmg.2009.067751. Epub 2009 Oct 14. J Med Genet. 2010. PMID: 19833601

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