Gene Therapy to the Retina and the Cochlea

por Crane, Ryan, Conley, Shannon M., Al-Ubaidi, Muayyad R., Naash, Muna I.
Publicado 2021

Expression of the human usherin c.2299delG mutation leads to early-onset auditory loss and stereocilia disorganization

por Crane, Ryan, Tebbe, Lars, Mwoyosvi, Maggie L., Al-Ubaidi, Muayyad R., Naash, Muna I.
Publicado 2023

Riboflavin deficiency leads to irreversible cellular changes in the RPE and disrupts retinal function through alterations in cellular metabolic homeostasis

por Sinha, Tirthankar, Ikelle, Larissa, Makia, Mustafa S., Crane, Ryan, Zhao, Xue, Kakakhel, Mashal, Al-Ubaidi, Muayyad R., Naash, Muna I.
Publicado 2022

The usherin mutation c.2299delG leads to its mislocalization and disrupts interactions with whirlin and VLGR1

por Tebbe, Lars, Mwoyosvi, Maggie L., Crane, Ryan, Makia, Mustafa S., Kakakhel, Mashal, Cosgrove, Dominic, Al-Ubaidi, Muayyad R., Naash, Muna I.
Publicado 2023

Co-Injection of Sulfotyrosine Facilitates Retinal Uptake of Hyaluronic Acid Nanospheres Following Intravitreal Injection

por Eblimit, Aiden, Makia, Mustafa S., Strayve, Daniel, Crane, Ryan, Conley, Shannon M., Sinha, Tirthankar, Acharya, Ghanashyam, Al-Ubaidi, Muayyad R., Naash, Muna I.
Publicado 2021

Comparative study of PRPH2 D2 loop mutants reveals divergent disease mechanism in rods and cones

por Ikelle, Larissa, Makia, Mustafa, Lewis, Tylor, Crane, Ryan, Kakakhel, Mashal, Conley, Shannon M., Birtley, James R., Arshavsky, Vadim Y., Al-Ubaidi, Muayyad R., Naash, Muna I.
Publicado 2023

Correction: Comparative study of PRPH2 D2 loop mutants reveals divergent disease mechanism in rods and cones

por Ikelle, Larissa, Makia, Mustafa, Lewis, Tylor, Crane, Ryan, Kakakhel, Mashal, Conley, Shannon M., Birtley, James R., Arshavsky, Vadim Y., Al-Ubaidi, Muayyad R., Naash, Muna I.
Publicado 2023