Rogers H - Search Results

1

Comparative expression analysis reveals lineage relationships between human and murine gliomas and a dominance of glial signatures during tumor propagation in vitro.

Henriquez NV, Forshew T, Tatevossian R, Ellis M, Richard-Loendt A, Rogers H, Jacques TS, Reitboeck PG, Pearce K, Sheer D, Grundy RG, Brandner S. Henriquez NV, et al. Among authors: rogers h. Cancer Res. 2013 Sep 15;73(18):5834-44. doi: 10.1158/0008-5472.CAN-13-1299. Epub 2013 Jul 25. Cancer Res. 2013. PMID: 23887970

2

Supratentorial and spinal pediatric ependymomas display a hypermethylated phenotype which includes the loss of tumor suppressor genes involved in the control of cell growth and death.

Rogers HA, Kilday JP, Mayne C, Ward J, Adamowicz-Brice M, Schwalbe EC, Clifford SC, Coyle B, Grundy RG. Rogers HA, et al. Acta Neuropathol. 2012 May;123(5):711-25. doi: 10.1007/s00401-011-0904-1. Epub 2011 Nov 23. Acta Neuropathol. 2012. PMID: 22109108 Free PMC article.

3

Loss of INI1 protein expression defines a subgroup of aggressive central nervous system primitive neuroectodermal tumors.

Miller S, Ward JH, Rogers HA, Lowe J, Grundy RG. Miller S, et al. Among authors: rogers ha. Brain Pathol. 2013 Jan;23(1):19-27. doi: 10.1111/j.1750-3639.2012.00610.x. Epub 2012 Jun 25. Brain Pathol. 2013. PMID: 22672440 Free PMC article.

4

PI3K pathway activation provides a novel therapeutic target for pediatric ependymoma and is an independent marker of progression-free survival.

Rogers HA, Mayne C, Chapman RJ, Kilday JP, Coyle B, Grundy RG. Rogers HA, et al. Clin Cancer Res. 2013 Dec 1;19(23):6450-60. doi: 10.1158/1078-0432.CCR-13-0222. Epub 2013 Sep 27. Clin Cancer Res. 2013. PMID: 24077346

5

A retrospective analysis of recurrent pediatric ependymoma reveals extremely poor survival and ineffectiveness of current treatments across central nervous system locations and molecular subgroups.

Ritzmann TA, Rogers HA, Paine SML, Storer LCD, Jacques TS, Chapman RJ, Ellison D, Donson AM, Foreman NK, Grundy RG. Ritzmann TA, et al. Pediatr Blood Cancer. 2020 Sep;67(9):e28426. doi: 10.1002/pbc.28426. Epub 2020 Jul 2. Pediatr Blood Cancer. 2020. PMID: 32614133 Clinical Trial.

6

An investigation of WNT pathway activation and association with survival in central nervous system primitive neuroectodermal tumours (CNS PNET).

Rogers HA, Miller S, Lowe J, Brundler MA, Coyle B, Grundy RG. Rogers HA, et al. Br J Cancer. 2009 Apr 21;100(8):1292-302. doi: 10.1038/sj.bjc.6604979. Epub 2009 Mar 17. Br J Cancer. 2009. PMID: 19293793 Free PMC article.

7

WNT/β-catenin pathway activation in Myc immortalised cerebellar progenitor cells inhibits neuronal differentiation and generates tumours resembling medulloblastoma.

Rogers HA, Sousa S, Salto C, Arenas E, Coyle B, Grundy RG. Rogers HA, et al. Br J Cancer. 2012 Sep 25;107(7):1144-52. doi: 10.1038/bjc.2012.377. Epub 2012 Aug 28. Br J Cancer. 2012. PMID: 22929883 Free PMC article.

8

The role of the WNT/β-catenin pathway in central nervous system primitive neuroectodermal tumours (CNS PNETs).

Rogers HA, Ward JH, Miller S, Lowe J, Coyle B, Grundy RG. Rogers HA, et al. Br J Cancer. 2013 May 28;108(10):2130-41. doi: 10.1038/bjc.2013.170. Epub 2013 Apr 16. Br J Cancer. 2013. PMID: 23591193 Free PMC article.

9

The therapeutic potential of targeting the PI3K pathway in pediatric brain tumors.

Rogers HA, Estranero J, Gudka K, Grundy RG. Rogers HA, et al. Oncotarget. 2017 Jan 10;8(2):2083-2095. doi: 10.18632/oncotarget.13781. Oncotarget. 2017. PMID: 27926496 Free PMC article. Review.

10

Genome-wide molecular characterization of central nervous system primitive neuroectodermal tumor and pineoblastoma.

Miller S, Rogers HA, Lyon P, Rand V, Adamowicz-Brice M, Clifford SC, Hayden JT, Dyer S, Pfister S, Korshunov A, Brundler MA, Lowe J, Coyle B, Grundy RG. Miller S, et al. Neuro Oncol. 2011 Aug;13(8):866-79. doi: 10.1093/neuonc/nor070. Neuro Oncol. 2011. PMID: 21798848 Free PMC article.

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