Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Taylor R. Murphy"'
Autor:
Jennifer L. Thomas, Ryan Thummel, Xixia Luo, Ronald G. Gregg, Aaron D. denDekker, Thomas S. Vihtelic, David R. Hyde, Taylor R. Murphy, Gregory B. Willer
Oculocutaneous albinism (OCA) is a group of genetically inherited conditions that result in pigmentation defects in the eyes, skin, and hair.1 The types of albinism have been divided into tryosinase-negative (no pigmentation) and those that produce v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::729d221f64a9bfa94daf787edbfc5e04
https://europepmc.org/articles/PMC3109019/
https://europepmc.org/articles/PMC3109019/
Autor:
Ronald G. Gregg, Taylor R. Murphy, Vytas A. Bankaitis, David R. Hyde, Kristina E. Ile, Thomas S. Vihtelic, Corey T. Watson, Gregory B. Willer
The zebrafish lens opaque (lop) mutant was previously isolated in a genetic screen and shown to lack rod and cone photoreceptors and exhibit lens opacity, or cataract, at 7 days post-fertilization (dpf). In this manuscript, we provide four different
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60c7ea83f21e1540a4fa3d183731c430
Autor:
Graeme Wistow, Sinéad Howley, David R. Hyde, Taylor R. Murphy, William E. Archer, Rachel L. Harding, Thomas S. Vihtelic, Lee J. Baker
Publikováno v:
Experimental eye research. 86(5)
A zebrafish ortholog of human lengsin was identified by EST analysis of an adult lens cDNA library. During zebrafish development, lengsin transcription is first detected at 24 h post-fertilization (hpf). Immunolocalization, using polyclonal antiserum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28b40cb47638f4a5218d7861df31b027
https://pubmed.ncbi.nlm.nih.gov/18406404
https://pubmed.ncbi.nlm.nih.gov/18406404
