Fike FM - Search Results

1

Reciprocal regulation of SOCS 1 and SOCS3 enhances resistance to ionizing radiation in glioblastoma multiforme.

Zhou H, Miki R, Eeva M, Fike FM, Seligson D, Yang L, Yoshimura A, Teitell MA, Jamieson CA, Cacalano NA. Zhou H, et al. Among authors: fike fm. Clin Cancer Res. 2007 Apr 15;13(8):2344-53. doi: 10.1158/1078-0432.CCR-06-2303. Clin Cancer Res. 2007. PMID: 17438093

2

Patterned CpG methylation of silenced B cell gene promoters in classical Hodgkin lymphoma-derived and primary effusion lymphoma cell lines.

Doerr JR, Malone CS, Fike FM, Gordon MS, Soghomonian SV, Thomas RK, Tao Q, Murray PG, Diehl V, Teitell MA, Wall R. Doerr JR, et al. Among authors: fike fm. J Mol Biol. 2005 Jul 22;350(4):631-40. doi: 10.1016/j.jmb.2005.05.032. J Mol Biol. 2005. PMID: 15967459

3

B29 gene silencing in pituitary cells is regulated by its 3' enhancer.

Malone CS, Kuraishy AI, Fike FM, Loya RG, Mikkili MR, Teitell MA, Wall R. Malone CS, et al. Among authors: fike fm. J Mol Biol. 2006 Sep 15;362(2):173-83. doi: 10.1016/j.jmb.2006.07.046. Epub 2006 Jul 28. J Mol Biol. 2006. PMID: 16920149 Free PMC article.

4

Assessing 'radiosensitivity' with kinetic profiles of γ-H2AX, 53BP1 and BRCA1 foci.

Martin NT, Nahas SA, Tunuguntla R, Fike F, Gatti RA. Martin NT, et al. Radiother Oncol. 2011 Oct;101(1):35-8. doi: 10.1016/j.radonc.2011.05.065. Epub 2011 Jun 30. Radiother Oncol. 2011. PMID: 21722985 Free PMC article.

5

Comprehensive profiling of radiosensitive human cell lines with DNA damage response assays identifies the neutral comet assay as a potential surrogate for clonogenic survival.

Nahas SA, Davies R, Fike F, Nakamura K, Du L, Kayali R, Martin NT, Concannon P, Gatti RA. Nahas SA, et al. Radiat Res. 2012 Feb;177(2):176-86. doi: 10.1667/rr2580.1. Epub 2011 Sep 30. Radiat Res. 2012. PMID: 21962002 Free PMC article.

6

Mutation of senataxin alters disease-specific transcriptional networks in patients with ataxia with oculomotor apraxia type 2.

Fogel BL, Cho E, Wahnich A, Gao F, Becherel OJ, Wang X, Fike F, Chen L, Criscuolo C, De Michele G, Filla A, Collins A, Hahn AF, Gatti RA, Konopka G, Perlman S, Lavin MF, Geschwind DH, Coppola G. Fogel BL, et al. Hum Mol Genet. 2014 Sep 15;23(18):4758-69. doi: 10.1093/hmg/ddu190. Epub 2014 Apr 23. Hum Mol Genet. 2014. PMID: 24760770 Free PMC article.

7

Arginine-rich cell-penetrating peptide dramatically enhances AMO-mediated ATM aberrant splicing correction and enables delivery to brain and cerebellum.

Du L, Kayali R, Bertoni C, Fike F, Hu H, Iversen PL, Gatti RA. Du L, et al. Hum Mol Genet. 2011 Aug 15;20(16):3151-60. doi: 10.1093/hmg/ddr217. Epub 2011 May 16. Hum Mol Genet. 2011. PMID: 21576124 Free PMC article.

8

Defective DNA double-strand break repair in pediatric systemic lupus erythematosus.

Davies RC, Pettijohn K, Fike F, Wang J, Nahas SA, Tunuguntla R, Hu H, Gatti RA, McCurdy D. Davies RC, et al. Arthritis Rheum. 2012 Feb;64(2):568-78. doi: 10.1002/art.33334. Arthritis Rheum. 2012. PMID: 21905016 Free article.

9

Functional characterization and targeted correction of ATM mutations identified in Japanese patients with ataxia-telangiectasia.

Nakamura K, Du L, Tunuguntla R, Fike F, Cavalieri S, Morio T, Mizutani S, Brusco A, Gatti RA. Nakamura K, et al. Hum Mutat. 2012 Jan;33(1):198-208. doi: 10.1002/humu.21632. Epub 2011 Nov 9. Hum Mutat. 2012. PMID: 22006793 Free PMC article.

10

A-TWinnipeg: Pathogenesis of rare ATM missense mutation c.6200C>A with decreased protein expression and downstream signaling, early-onset dystonia, cancer, and life-threatening radiotoxicity.

Nakamura K, Fike F, Haghayegh S, Saunders-Pullman R, Dawson AJ, Dörk T, Gatti RA. Nakamura K, et al. Mol Genet Genomic Med. 2014 Jul;2(4):332-40. doi: 10.1002/mgg3.72. Epub 2014 Mar 13. Mol Genet Genomic Med. 2014. PMID: 25077176 Free PMC article.

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