Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Russell W. Mellen"'
Autor:
Russell W. Mellen, Kaitlyn R. Calabro, K. Tyler McCullough, Sean M. Crosson, Alejandro de la Cova, Diego Fajardo, Emily Xu, Sanford L. Boye, Shannon E. Boye
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 30, Iss , Pp 48-64 (2023)
Cone-rod dystrophy 6 (CORD6) is caused by gain-of-function mutations in the GUCY2D gene, which encodes retinal guanylate cyclase-1 (RetGC1). There are currently no treatments available for this autosomal dominant disease, which is characterized by se
Externí odkaz:
https://doaj.org/article/e73f2be0ddd74708a9903c786112e07c
Autor:
Jim Peterson, Giovanni Di Pasquale, Victoria Makal, Diego Fajardo, Shannon E. Boye, Ryan F. Boyd, Hangning Zhang, Matthew T. Leahy, Shreyasi Choudhury, Kaitlyn R. Calabro, Sandra Afione, Sean Crosson, Russell W. Mellen, Sanford L. Boye, John A. Chiorini, Colin K. Jennings
Publikováno v:
Mol Ther
The majority of inherited retinal diseases (IRDs) are caused by mutations in genes expressed in photoreceptors (PRs). The ideal vector to address these conditions is one that transduces PRs in large areas of retina with the smallest volume/lowest tit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25c94893c98264b61bcdf4ed9a5e3cb9
https://doi.org/10.1016/j.ymthe.2020.04.002
https://doi.org/10.1016/j.ymthe.2020.04.002
Autor:
Aishwarya Gurumurthy, Jörg Bungert, Masatoshi Ikeda, Alex Perez, Yong Shen, Cameron R. Guy, Suming Huang, Russell W. Mellen, Rukiye Nar, Isaac J. Knudson, MacLean A. Bassett, Kazuhiko Igarashi, Mir A. Hossain
Publikováno v:
Molecular and Cellular Biology. 38
The organization of the five β-type globin genes on chromosome 11 reflects the timing of expression during erythroid cell development, with the embryonic e-globin gene being located at the 5' end, followed by the two fetal γ-globin genes, and with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ef9ba116e370a8ffd9f42d363ad5231
https://doi.org/10.1128/mcb.00197-18
https://doi.org/10.1128/mcb.00197-18