Identification of retinal ganglion cell types and brain nuclei expressing the transcription factor Brn3c/Pou4f3 using a Cre recombinase knock‐in allele-Reference-Cited by-同舟云学术

Identification of retinal ganglion cell types and brain nuclei expressing the transcription factor Brn3c/Pou4f3 using a Cre recombinase knock‐in allele

Published:2020-11-10 Issue:8 Volume:529 Page:1926-1953
ISSN:0021-9967
Container-title:Journal of Comparative Neurology
language:en
Short-container-title:J Comp Neurol

Author:

Parmhans Nadia¹,Fuller Anne Drury¹,Nguyen Eileen¹,Chuang Katherine¹,Swygart David²,Wienbar Sophia Rose²,Lin Tyger¹,Kozmik Zbynek³,Dong Lijin⁴,Schwartz Gregory William²,Badea Tudor Constantin¹^ORCID

Affiliation:

1. Retinal Circuit Development and Genetics Unit, Neurobiology‐Neurodegeneration and Repair Laboratory National Eye Institute, NIH Bethesda Maryland USA

2. Departments of Ophthalmology and Physiology Northwestern University Feinberg School of Medicine Chicago Illinois USA

3. Institute of Molecular Genetics of the Czech Academy of Sciences Prague Czech Republic

4. Genetic Engineering Facility National Eye Institute, NIH Bethesda Maryland USA

Funder

Akademie Věd České Republiky

National Eye Institute

Publisher

Wiley

Subject

General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cne.25065

Reference125 articles.

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2. Morphologies of rabbit retinal ganglion cells with complex receptive fields

3. Morphologies of rabbit retinal ganglion cells with concentric receptive fields

4. Dre recombinase, like Cre, is a highly efficient site-specific recombinase in E. coli, mammalian cells and mice

5. Distinct Roles of Transcription Factors Brn3a and Brn3b in Controlling the Development, Morphology, and Function of Retinal Ganglion Cells

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