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Genes|June 2, 2021
Generation and Genetic Correction of USH2A c.2299delG Mutation in Patient-Derived Induced Pluripotent Stem CellsXuezhong Liu, Justin Lillywhite, Wenliang Zhu, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 27, 2023
Rescue of auditory function by a single administration of AAV-TMPRSS3 gene therapy in aged mice of human recessive deafness DFNB8Wan Du, Volkan Ergin, Corena Loeb, et al.
Biorxiv : the Preprint Server for Biology|March 3, 2023
Rescue of Auditory Function by a Single Administration of AAV- TMPRSS3 Gene Therapy in Aged Mice of Human Recessive Deafness DFNB8Wan Du, Volkan Ergin, Corena Loeb, et al.
Biochemistry|February 12, 2016
Structural Insights into the Activation of Human Relaxin Family Peptide Receptor 1 by Small-Molecule AgonistsXin Hu, Courtney Myhr, Zaohua Huang, et al.
Nature Communications|June 15, 2013
Identification and optimization of small-molecule agonists of the human relaxin hormone receptor RXFP1Jingbo Xiao, Zaohua Huang, Catherine Z Chen, et al.
Scientific Reports|May 5, 2016
Magnetically guided central nervous system delivery and toxicity evaluation of magneto-electric nanocarriersAjeet Kaushik, Rahul D Jayant, Roozbeh Nikkhah-Moshaie, et al.
Frontiers in Endocrinology|September 9, 2015
Activation of Relaxin Family Receptor 1 from Different Mammalian Species by Relaxin Peptide and Small-Molecule Agonist ML290Zaohua Huang, Courtney Myhr, Ross A D Bathgate, et al.
Frontiers in Bioengineering and Biotechnology|May 20, 2020
Development of Multifunctional Biopolymeric Auto-Fluorescent Micro- and Nanogels as a Platform for Biomedical ApplicationsArti Vashist, Venkata Atluri, Andrea Raymond, et al.
European Journal of Medicinal Chemistry|July 15, 2018
Optimization of the first small-molecule relaxin/insulin-like family peptide receptor (RXFP1) agonists: Activation results in an antifibrotic gene expression profileKenneth J Wilson, Jingbo Xiao, Catherine Z Chen, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 29, 2021
A nonsense TMEM43 variant leads to disruption of connexin-linked function and autosomal dominant auditory neuropathy spectrum disorderMinwoo Wendy Jang, Doo-Yi Oh, Eunyoung Yi, et al.
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