TFII-I, a transcription factor deleted in Williams Syndrome, localizes to areas in mouse brain affected in humans
Danoff SK, Taylor H, Blackshaw S, Desiderio SV. Neuroscience 2004123:931-8.
Danoff SK, Taylor H, Blackshaw S, Desiderio SV. Neuroscience 2004123:931-8.
Blackshaw S, Sawa A, Eliasson M, Krug D, Watkins C, Gupta A, Ferante RJ, Snyder SH. Neuroscience 2003 119:979-90.
Blackshaw S, Kuo WP, Park PJ, Tsujikawa M, Gunnersen JM, Scott HS, Wee- Boon M, Tan SS, Cepko CL. Genome Biol 2003 4:R17.
Sezen SF, Blackshaw S, Steiner JP, Burnett AL. Int J Impot Res 2002 14:506-12.
Akey DT, Zhu X, Dyer M, Li A, Sorensen A, Blackshaw S, Fukuda-Kamitani T, Daiger SP, Craft C, Kamitani T, Sohocki MM. Hum Mol Genet 2002 11:2723-33.
Sharon D*, Blackshaw S*, Cepko CL, Dryja TP. Proc Natl Acad Sci USA 2002 99:315-20 (* indicates equal contribution by both authors).
Browne SJ, Sullivan LS, Blanton SH, Cepko CL, Blackshaw S, Birch DG, Hughbanks-Wheaton D, Heckenlively JR, Daiger SP. Hum Mol Genet 2002 11:559-568.
Blackshaw S, Kim, JB, St. Croix B, Polyak K. Current Protocols in Molecular Biology, Unit 25B.6 2002.
Blackshaw S, Cepko C L. Nature Neuroscience. 2002 5:1251-2.
Blackshaw S, Livesey FJ. Current Opinion in Neurobiology. 2002 6:110-14.