Visualizing neurons one-by-one in vivo: Optical dissection and reconstruction of neural networks with reversible fluorescent proteins
Article first published online: 10 APR 2006
Copyright © 2006 Wiley-Liss, Inc.
Volume 235, Issue 8, pages 2192–2199, August 2006
How to Cite
Aramaki, S. and Hatta, K. (2006), Visualizing neurons one-by-one in vivo: Optical dissection and reconstruction of neural networks with reversible fluorescent proteins. Dev. Dyn., 235: 2192–2199. doi: 10.1002/dvdy.20826
- Issue published online: 17 JUL 2006
- Article first published online: 10 APR 2006
- Manuscript Accepted: 15 MAR 2006
- Ministry of Education, Culture, Sports, Science, and Technology of Japan. Grant Numbers: 15029263, 15300117, 15657054, 17023052
- 2002. An optical marker based on the UV-induced green-to-red photoconversion of a fluorescent protein. Proc Natl Acad Sci U S A 99: 12651–12656. , , , , .
- 2004. Regulated fast nucleocytoplasmic shuttling observed by reversible protein highlighting. Science 306: 1370–1373. , , .
- 2000. Identification of a functional transposase of the Tol2 element, an Ac-like element from the Japanese medaka fish, and its transposition in the zebrafish germ lineage. Proc Natl Acad Sci U S A 97: 11403–11408. , , .
- 2004. A transposon-mediated gene trap approach identifies developmentally regulated genes in zebrafish. Dev Cell 7: 133–144. , , , , , .
- 1995. Stages of embryonic development of the zebrafish. Dev Dyn 203: 253–310. , , , , .
- 2001. Tracing transgene expression in living zebrafish embryos. Dev Biol 233: 329–346. , .
- 2001. An instructive function for Notch in promoting gliogenesis in the zebrafish retina. Development 128: 1099–1107. , , , .