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Cited by 377

The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.

Structure-Guided Transformation of Channelrhodopsin into a Light-Activated Chloride Channel

Open access
Berndt, Andre, Lee, Soo Yeun, Ramakrishnan, Charu, Deisseroth, Karl·2014·Science

Abstract

Optogenetic Insights: Mapping functional neural circuits for many behaviors has been almost impossible, so Vogelstein et al. (p. 386 , published online 27 March; see the Perspective by O'Leary and Marder ) developed a broadly applicable optogenetic method for neuron-behavior mapping and used it to phenotype larval Drosophila and thus developed a reference atlas. As optogenetic experiments become routine in certain fields of neuroscience research, creating even more specialized tools is imperative (see the Perspective by Hayashi ). By engineering channelrhodopsin, Wietek et al. (p. 409 , published online 27 March) and Berndt et al. (p. 420 ) created two different light-gated anion channels to block action potential generation during synaptic stimulation or depolarizing current injections. These new tools not only improve understanding of channelrhodopsins but also provide a way to silence cells.

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Crossref · 10.1126/science.1252367

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Metadata

Authors
Berndt, A., Lee, S. Y., Ramakrishnan, C., & Deisseroth, K.
Venue
Science
Published
2014-04-25
Volume
344
Issue
6182
Pages
420-424
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W1993257206
Cited by
377
References
5
FWCI
24.15
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Structure-Guided Transformation of Channelrhodopsin into a Light-Activated Chloride Channel. https://app.cochat.ai/papers/10.1126/science.1252367
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Berndt, A., Lee, S. Y., Ramakrishnan, C., & Deisseroth, K. (2014). Structure-Guided Transformation of Channelrhodopsin into a Light-Activated Chloride Channel. Science. https://doi.org/10.1126/science.1252367

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Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.