| Year |
Citation |
Score |
| 2014 |
Yoo S, Bieda MC. Differences among brain tumor stem cell types and fetal neural stem cells in focal regions of histone modifications and DNA methylation, broad regions of modifications, and bivalent promoters. Bmc Genomics. 15: 724. PMID 25163646 DOI: 10.1186/1471-2164-15-724 |
1 |
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| 2013 |
Padmanabhan N, Jia D, Geary-Joo C, Wu X, Ferguson-Smith AC, Fung E, Bieda MC, Snyder FF, Gravel RA, Cross JC, Watson ED. Mutation in folate metabolism causes epigenetic instability and transgenerational effects on development. Cell. 155: 81-93. PMID 24074862 DOI: 10.1016/j.cell.2013.09.002 |
1 |
|
| 2012 |
Stropp T, McPhillips T, Ludäscher B, Bieda M. Workflows for microarray data processing in the Kepler environment. Bmc Bioinformatics. 13: 102. PMID 22594911 DOI: 10.1186/1471-2105-13-102 |
1 |
|
| 2012 |
Bieda M. Kepler for 'omics bioinformatics Procedia Computer Science. 9: 1635-1638. DOI: 10.1016/j.procs.2012.04.180 |
1 |
|
| 2009 |
Bieda MC, Su H, Maciver MB. Anesthetics discriminate between tonic and phasic gamma-aminobutyric acid receptors on hippocampal CA1 neurons. Anesthesia and Analgesia. 108: 484-90. PMID 19151276 DOI: 10.1213/ane.0b013e3181904571 |
1 |
|
| 2008 |
Acevedo LG, Bieda M, Green R, Farnham PJ. Analysis of the mechanisms mediating tumor-specific changes in gene expression in human liver tumors. Cancer Research. 68: 2641-51. PMID 18413731 DOI: 10.1158/0008-5472.CAN-07-5590 |
1 |
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| 2008 |
Johnson DS, Li W, Gordon DB, Bhattacharjee A, Curry B, Ghosh J, Brizuela L, Carroll JS, Brown M, Flicek P, Koch CM, Dunham I, Bieda M, Xu X, Farnham PJ, et al. Systematic evaluation of variability in ChIP-chip experiments using predefined DNA targets. Genome Research. 18: 393-403. PMID 18258921 DOI: 10.1101/gr.7080508 |
1 |
|
| 2007 |
Yasui DH, Peddada S, Bieda MC, Vallero RO, Hogart A, Nagarajan RP, Thatcher KN, Farnham PJ, Lasalle JM. Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes. Proceedings of the National Academy of Sciences of the United States of America. 104: 19416-21. PMID 18042715 DOI: 10.1073/pnas.0707442104 |
1 |
|
| 2007 |
Xu X, Bieda M, Jin VX, Rabinovich A, Oberley MJ, Green R, Farnham PJ. A comprehensive ChIP-chip analysis of E2F1, E2F4, and E2F6 in normal and tumor cells reveals interchangeable roles of E2F family members. Genome Research. 17: 1550-61. PMID 17908821 DOI: 10.1101/gr.6783507 |
1 |
|
| 2007 |
Krig SR, Jin VX, Bieda MC, O'Geen H, Yaswen P, Green R, Farnham PJ. Identification of genes directly regulated by the oncogene ZNF217 using chromatin immunoprecipitation (ChIP)-chip assays. The Journal of Biological Chemistry. 282: 9703-12. PMID 17259635 DOI: 10.1074/jbc.M611752200 |
1 |
|
| 2006 |
Bieda M, Xu X, Singer MA, Green R, Farnham PJ. Unbiased location analysis of E2F1-binding sites suggests a widespread role for E2F1 in the human genome. Genome Research. 16: 595-605. PMID 16606705 DOI: 10.1101/gr.4887606 |
1 |
|
| 2004 |
Bieda MC, Copenhagen DR. N-type and L-type calcium channels mediate glycinergic synaptic inputs to retinal ganglion cells of tiger salamanders. Visual Neuroscience. 21: 545-50. PMID 15579220 DOI: 10.1017/S0952523804214055 |
1 |
|
| 2004 |
Bieda MC, MacIver MB. Major role for tonic GABAA conductances in anesthetic suppression of intrinsic neuronal excitability. Journal of Neurophysiology. 92: 1658-67. PMID 15140905 DOI: 10.1152/jn.00223.2004 |
1 |
|
| 2000 |
Bieda MC, Copenhagen DR. Inhibition is not required for the production of transient spiking responses from retinal ganglion cells. Visual Neuroscience. 17: 243-54. PMID 10824678 DOI: 10.1017/S0952523800172062 |
1 |
|
| 1999 |
Bieda MC, Copenhagen DR. Sodium action potentials are not required for light-evoked release of GABA or glycine from retinal amacrine cells. Journal of Neurophysiology. 81: 3092-5. PMID 10368424 |
1 |
|
| 1996 |
Dixon DB, Takahashi K, Bieda M, Copenhagen DR. Quinine, intracellular pH and modulation of hemi-gap junctions in catfish horizontal cells. Vision Research. 36: 3925-31. PMID 9068845 DOI: 10.1016/S0042-6989(96)00129-0 |
1 |
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