Clyde E. Keeler: The Rodless Mouse and the Early Days of Retinal Genetic Research

Daniel M. Albert

doi:10.1016/j.oret.2019.04.019

Clyde E. Keeler: The Rodless Mouse and the Early Days of Retinal Genetic Research

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Abstract

Purpose: To report the lifetime activities and accomplishments of Clyde E. Keeler (1900–1994), a pioneer in the study of retinal genetics. Design: Retrospective review. Methods: Assessment of published and unpublished biographical material. Results: Nearly a century ago, Keeler discovered an inherited abnormality in the mouse that causes the absence of rod photoreceptors and is the mouse counterpart of 1 type of human retinitis pigmentosa. Conclusions: In 1923, Keeler serendipitously discovered the so-called rodless mouse, which is now known to be the result of a mutation in the PDEGB gene. The historical name for the mouse strain is rd. This same defect was reported in human patients with retinitis pigmentosa in 1993. Keeler's mouse model is still used in gene therapy studies seeking to cure retinitis pigmentosa.

Original language	English (US)
Pages (from-to)	716-723
Number of pages	8
Journal	Ophthalmology Retina
Volume	3
Issue number	9
DOIs	https://doi.org/10.1016/j.oret.2019.04.019
State	Published - Sep 2019
Externally published	Yes

ASJC Scopus subject areas

Ophthalmology

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title = "Clyde E. Keeler: The Rodless Mouse and the Early Days of Retinal Genetic Research",

abstract = "Purpose: To report the lifetime activities and accomplishments of Clyde E. Keeler (1900–1994), a pioneer in the study of retinal genetics. Design: Retrospective review. Methods: Assessment of published and unpublished biographical material. Results: Nearly a century ago, Keeler discovered an inherited abnormality in the mouse that causes the absence of rod photoreceptors and is the mouse counterpart of 1 type of human retinitis pigmentosa. Conclusions: In 1923, Keeler serendipitously discovered the so-called rodless mouse, which is now known to be the result of a mutation in the PDEGB gene. The historical name for the mouse strain is rd. This same defect was reported in human patients with retinitis pigmentosa in 1993. Keeler's mouse model is still used in gene therapy studies seeking to cure retinitis pigmentosa.",

author = "Albert, {Daniel M.}",

note = "Funding Information: Supported by the National Institutes of Health, Bethesda, Maryland (grant no.: P30 EY010572); and Research to Prevent Blindness, Inc, New York, New York (unrestricted grant). Publisher Copyright: {\textcopyright} 2019 American Academy of Ophthalmology Copyright: Copyright 2019 Elsevier B.V., All rights reserved.",

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doi = "10.1016/j.oret.2019.04.019",

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AU - Albert, Daniel M.

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PY - 2019/9

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N2 - Purpose: To report the lifetime activities and accomplishments of Clyde E. Keeler (1900–1994), a pioneer in the study of retinal genetics. Design: Retrospective review. Methods: Assessment of published and unpublished biographical material. Results: Nearly a century ago, Keeler discovered an inherited abnormality in the mouse that causes the absence of rod photoreceptors and is the mouse counterpart of 1 type of human retinitis pigmentosa. Conclusions: In 1923, Keeler serendipitously discovered the so-called rodless mouse, which is now known to be the result of a mutation in the PDEGB gene. The historical name for the mouse strain is rd. This same defect was reported in human patients with retinitis pigmentosa in 1993. Keeler's mouse model is still used in gene therapy studies seeking to cure retinitis pigmentosa.

AB - Purpose: To report the lifetime activities and accomplishments of Clyde E. Keeler (1900–1994), a pioneer in the study of retinal genetics. Design: Retrospective review. Methods: Assessment of published and unpublished biographical material. Results: Nearly a century ago, Keeler discovered an inherited abnormality in the mouse that causes the absence of rod photoreceptors and is the mouse counterpart of 1 type of human retinitis pigmentosa. Conclusions: In 1923, Keeler serendipitously discovered the so-called rodless mouse, which is now known to be the result of a mutation in the PDEGB gene. The historical name for the mouse strain is rd. This same defect was reported in human patients with retinitis pigmentosa in 1993. Keeler's mouse model is still used in gene therapy studies seeking to cure retinitis pigmentosa.

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Clyde E. Keeler: The Rodless Mouse and the Early Days of Retinal Genetic Research

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