Johns Hopkins University, Department of Neuroscience

Seth Blackshaw - Recent Papers

 

  • Rapicavoli, N. A. and Blackshaw, S. (2009) New meaning in the message:  noncoding RNAs and their role in retinal development.  Dev. Dynamics, 238:2103-14.  [PDF]

  • Hu S, Xie Z, Onishi A, Jiang L, Wang H, He X, Rho H-S, Woodard C, Yu X, Lin J, Long S, Blackshaw S*, Qian J, and  Zhu H.  Profiling the Human Protein-DNA Interactome Reveals ERK2 as a Transcriptional Repressor of Interferon Signaling.  Cell, 139:610-22.  [PDF] (* indicates corresponding author)

  • Onishi, A., Peng, G.H., Du, C.H., Alexis, U., Chen, S., and Blackshaw, S. (2009) Pias3 directs rod photoreceptor development via SUMOylation of Nr2e3.  Neuron, 61:234-46.  [PDF]
  • Huang, A.S., Lee, D.A. and Blackshaw, S.  (2008)  D-Aspartate and D-aspartate oxidase show selective and developmentally dynamic localization in mouse retina.  Exper. Eye Res. 86:704-709.  [PDF]
  • Blackshaw, S., Harpavat, S., Trimarchi, J., Cai, L., Huang, H., Kuo, W. P., Fraioli, R. E., Cho, S.-H., Yung, R., Asch, E., Wong, W. H., and Cepko, C. L. (2004) Genomic analysis of mouse retinal development. PLoS Biology,Jun 29;2(9):E247. [PDF]

  • Cai, L., Huang, H., Blackshaw, S., Liu, J. S., Cepko, C. L., and Wong, W. H. (2004) Cluster Analysis of SAGE data: A Poisson Approach. Genome Biology, 5(7):R51. Epub 2004 Jun 29. [PDF]

  • Blackshaw, S., Kuo, W. P., Park, P. J., Tsujikawa, M., Gunnersen, J. M., Scott, H. S., Wee- Boon, M., Tan, S. S., and Cepko, C. L. (2003) MicroSAGE is highly representative and reproducible, but reveals major differences in gene expression between samples obtained from identical tissues. Genome Biology, 4:R17. [PDF]

  • Blackshaw, S. and Livesey, F. J. (2002). Applying genomic technologies to neural development. Current Opinion in Neurobiology, 6:110-14. [PDF]

  • Browne, S. J., Sullivan, L. S., Blanton, S. H., Cepko, C. L., Blackshaw, S., Birch, D. G., Hughbanks-Wheaton, D., Heckenlively, J. R., and Daiger, S. P. (2002). Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa. Hum. Mol. Genet., 11(5):559-568. [PDF]

  • Sharon, D*., Blackshaw, S*. Cepko, C. L., and Dryja, T. P. (2002). Profile of the genes expressed in the human peripheral retina, macula, and retinal pigment epithelium determined through serial analysis of gene expression (SAGE). Proc. Natl. Acad. Sci. USA 99:315-20 (* indicates equal contribution by both authors). [PDF]

  • Blackshaw, S., Fraioli, R. E., Furukawa, T., and Cepko, C. L. (2001). Comprehensive analysis of photoreceptor gene expression and the identification of candidate retinal disease genes. Cell, 107: 579-89. [PDF]

 

 

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