Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Kaitlyn R. Calabro"'
Autor:
Samantha C. Lau, Mhamed Grati, Kevin Isgrig, Moaz Sinan, Kaitlyn R. Calabro, Jianliang Zhu, Yasuko Ishibashi, Zeynep Ozgur, Talah Wafa, Inna A. Belyantseva, Tracy Fitzgerald, Thomas B. Friedman, Sanford L. Boye, Shannon E. Boye, Wade W. Chien
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 30, Iss , Pp 534-545 (2023)
Usher syndrome is the most common cause of deafness-blindness in the world. Usher syndrome type 1B (USH1B) is associated with mutations in MYO7A. Patients with USH1B experience deafness, blindness, and vestibular dysfunction. In this study, we applie
Externí odkaz:
https://doaj.org/article/ea475ade936f41d5b9fc0d539fc7be4e
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:
Kaitlyn R. Calabro, Sanford L. Boye, Shreyasi Choudhury, Diego Fajardo, James J. Peterson, Wei Li, Sean M. Crosson, Mi-Jung Kim, Dalian Ding, Richard Salvi, Shinichi Someya, Shannon E. Boye
Publikováno v:
Frontiers in Neuroscience, Vol 13 (2019)
Usher’s syndrome is the most common combined blindness–deafness disorder with USH1B, caused by mutations in MYO7A, resulting in the most severe phenotype. The existence of numerous, naturally occurring shaker1 mice harboring variable MYO7A mutati
Externí odkaz:
https://doaj.org/article/8c3c907278374492bd371de6e22e0688
Publikováno v:
Viruses, Vol 9, Iss 8, p 226 (2017)
High-throughput sequencing (HTS) has resulted in data for a number of herpes simplex virus (HSV) laboratory strains and clinical isolates. The knowledge of these sequences has been critical for investigating viral pathogenicity. However, the assembly
Externí odkaz:
https://doaj.org/article/34ad127e3925464295267613b3c03cfd
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:
Christianne E. Strang, Dibyendu Chakraborty, Jim Peterson, Diego Fajardo, Paul D. Gamlin, C. Douglas Witherspoon, Haiyan Jiang, Steven J. Samuelsson, Morgan L. Maeder, Kaitlyn R. Calabro, Shannon E. Boye, Scott Haskett, Sebastian Gloskowski, K. Tyler McCullough, Sanford L. Boye
Publikováno v:
Human Gene Therapy. 30:571-589
Mutations in GUCY2D, the gene encoding retinal guanylate cyclase-1 (retGC1), are the leading cause of autosomal dominant cone-rod dystrophy (CORD6). Significant progress toward clinical application of gene replacement therapy for Leber congenital ama
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::392cdcba89da3c2d5c90495d4de8bcec
https://doi.org/10.1089/hum.2018.193
https://doi.org/10.1089/hum.2018.193
Autor:
Shinichi Someya, Sanford L. Boye, Kaitlyn R. Calabro, Dalian Ding, Mi-Jung Kim, Richard Salvi, Sean Crosson, Diego Fajardo, Shannon E. Boye, Shreyasi Choudhury, Jim Peterson, Wei Li
Publikováno v:
Frontiers in Neuroscience
Frontiers in Neuroscience, Vol 13 (2019)
Frontiers in Neuroscience, Vol 13 (2019)
Usher's syndrome is the most common combined blindness-deafness disorder with USH1B, caused by mutations in MYO7A, resulting in the most severe phenotype. The existence of numerous, naturally occurring shaker1 mice harboring variable MYO7A mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a5b2ff4c3b3c0d05820f6cf90274679
http://europepmc.org/articles/PMC6883748
http://europepmc.org/articles/PMC6883748
Publikováno v:
Viruses; Volume 9; Issue 8; Pages: 226
Viruses
Viruses, Vol 9, Iss 8, p 226 (2017)
Viruses
Viruses, Vol 9, Iss 8, p 226 (2017)
High-throughput sequencing (HTS) has resulted in data for a number of herpes simplex virus (HSV) laboratory strains and clinical isolates. The knowledge of these sequences has been critical for investigating viral pathogenicity. However, the assembly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::118bd57c25f2130ba9542e3b3ef42107
https://doi.org/10.3390/v9080226
https://doi.org/10.3390/v9080226