Brian L Pike
Affiliations: | University of Southern California, Los Angeles, CA, United States |
Area:
Cancer Genetics, Molecular Genetics, Molecular EpidemiologyGoogle:
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Publications
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| Wang XM, Greiner TC, Bibikova M, et al. (2010) Identification and functional relevance of de novo DNA methylation in cancerous B-cell populations. Journal of Cellular Biochemistry. 109: 818-27 |
| Pike BL, Greiner TC, Wang X, et al. (2008) DNA methylation profiles in diffuse large B-cell lymphoma and their relationship to gene expression status. Leukemia. 22: 1035-43 |
| Wang Z, Lecane PS, Thiemann P, et al. (2007) Synthesis and biologic properties of hydrophilic sapphyrins, a new class of tumor-selective inhibitors of gene expression. Molecular Cancer. 6: 9 |
| Pike BL, Groshen S, Hsu YH, et al. (2006) Comparisons of PCR-based genome amplification systems using CpG island microarrays. Human Mutation. 27: 589-96 |
| Greiner TC, Dasgupta C, Ho VV, et al. (2006) Mutation and genomic deletion status of ataxia telangiectasia mutated (ATM) and p53 confer specific gene expression profiles in mantle cell lymphoma. Proceedings of the National Academy of Sciences of the United States of America. 103: 2352-7 |
| Karaman MW, Groshen S, Lee CC, et al. (2005) Comparisons of substitution, insertion and deletion probes for resequencing and mutational analysis using oligonucleotide microarrays. Nucleic Acids Research. 33: e33 |
| Nagpal S, Karaman MW, Timmerman MM, et al. (2004) Improving the sensitivity and specificity of gene expression analysis in highly related organisms through the use of electronic masks. Nucleic Acids Research. 32: e51 |
| Karaman MW, Houck ML, Chemnick LG, et al. (2003) Comparative analysis of gene-expression patterns in human and African great ape cultured fibroblasts. Genome Research. 13: 1619-30 |
| Fang NY, Greiner TC, Weisenburger DD, et al. (2003) Oligonucleotide microarrays demonstrate the highest frequency of ATM mutations in the mantle cell subtype of lymphoma. Proceedings of the National Academy of Sciences of the United States of America. 100: 5372-7 |
| Oda T, Elkahloun AG, Pike BL, et al. (1997) Mutations in the human Jagged1 gene are responsible for Alagille syndrome. Nature Genetics. 16: 235-42 |