 |
|
Genetic Hearing Loss and Gene Therapy
Nathanial T Carpena, Min Young Lee
Genomics Inform. 2018;16(4):e20 Published online 2018 Dec 28 DOI: https://doi.org/10.5808/GI.2018.16.4.e20
|
|
Citations to this article as recorded by
 Natural History of KCNQ4p.G285S Related Hearing Loss, Construction of iPSC and Mouse Model
Xiaolong Zhang, Tao Shi, Jin Li, Xiaonan Wu, Kaili Wu, Danyang Li, Dayong Wang, Jing Guan, Hongyang Wang
The Laryngoscope.2024; 134(5): 2356. CrossRef Adeno‐Associated Virus‐Encapsulated Alginate Microspheres Loaded in Collagen Gel Carriers for Localized Gene Transfer
Yuta Kurashina, Sho Kurihara, Takeshi Kubota, Shuhei Takatsuka, Motoki Hirabayashi, Hajime Shimmura, Hideo Miyahara, Aiki Hioki, Yutaka Matsushita, Jumpei Muramatsu, Yuki Ogawa, Masato Fujioka, Hirotaka J. Okano, Hiroaki Onoe
Advanced Healthcare Materials.2024;[Epub] CrossRef The genetic basis and the diagnostic yield of genetic testing related to nonsyndromic hearing loss in Qatar
Shaza Alkhidir, Karen El-Akouri, Nader Al-Dewik, Houssein Khodjet-El-khil, Sarah Okashah, Nazmul Islam, Tawfeg Ben-Omran, Mashael Al-Shafai
Scientific Reports.2024;[Epub] CrossRef Expression profiling of cochlear genes uncovers sex-based cellular function in mouse cochleae
Mengxiao Ye, Brandon Marzullo, Henry J. Adler, Bo Hua Hu
Hearing Research.2024; 448: 109030. CrossRef CRISPR/Cas9-mediated exon skipping to restore premature translation termination in a DFNB4 mouse model
Chun-Ying Huang, Yi-Hsiu Tsai, Yi-Fen Cheng, Peng-Yu Wu, Yu-Chi Chuang, Po-Yuan Huang, Jai-Shin Liu, Chen-Chi Wu, Yen-Fu Cheng
Gene Therapy.2024; 31(11-12): 531. CrossRef An optimistic review of modernization versus noise-induced hearing loss with the scope of Ayurveda management: a hope or a hype
Satyavati, Shamsa Fiaz, Nasreen Hanifa, Navneet Sharma
Journal of Indian System of Medicine.2024; 12(3): 135. CrossRef TMEM30A is essential for hair cell polarity maintenance in postnatal mouse cochlea
Yazhi Xing, Kun Peng, Qian Yi, Dongzhen Yu, Haibo Shi, Guang Yang, Shankai Yin
Cellular & Molecular Biology Letters.2023;[Epub] CrossRef Postnatal genetic umbilical cord analysis for earliest possible detection of inherited hearing impairment
Manuel Christoph Ketterer, Ralf Birkenhäger, Rainer Beck, Susan Arndt, Antje Aschendorff, Mirjam Kunze
European Archives of Oto-Rhino-Laryngology.2023; 280(11): 4811. CrossRef A review of the auditory-gut-brain axis
Amy S. Graham, Benneth Ben-Azu, Marie-Ève Tremblay, Peter Torre, Marjanne Senekal, Barbara Laughton, Andre van der Kouwe, Marcin Jankiewicz, Mamadou Kaba, Martha J. Holmes
Frontiers in Neuroscience.2023;[Epub] CrossRef Parental knowledge and attitudes towards hereditary hearing loss and genetic technology
Safa Alqudah, Alia Alqudah, Maha Zaitoun, Hussein Alqassem
Electronic Journal of General Medicine.2023; 20(6): em548. CrossRef Gene Therapy for Inherited Hearing Loss: Updates and Remaining Challenges
Roni Hahn, Karen B. Avraham
Audiology Research.2023; 13(6): 952. CrossRef Newborn Hearing Screening Benefits Children, but Global Disparities Persist
Katrin Neumann, Philipp Mathmann, Shelly Chadha, Harald A. Euler, Karl R. White
Journal of Clinical Medicine.2022; 11(1): 271. CrossRef Treatment of autosomal recessive hearing loss via in vivo CRISPR/Cas9-mediated optimized homology-directed repair in mice
Xi Gu, Xinde Hu, Daqi Wang, Zhijiao Xu, Fang Wang, Di Li, Geng-lin Li, Hui Yang, Huawei Li, Erwei Zuo, Yilai Shu
Cell Research.2022; 32(7): 699. CrossRef Preventing autosomal-dominant hearing loss in Bth mice with CRISPR/CasRx-based RNA editing
Ziwen Zheng, Guo Li, Chong Cui, Fang Wang, Xiaohan Wang, Zhijiao Xu, Huiping Guo, Yuxin Chen, Honghai Tang, Daqi Wang, Mingqian Huang, Zheng-Yi Chen, Xingxu Huang, Huawei Li, Geng-Lin Li, Xiaoxiang Hu, Yilai Shu
Signal Transduction and Targeted Therapy.2022;[Epub] CrossRef Assessment and Treatment of a Deaf Patient with Alcohol Use Disorder—Limitations and Special Considerations
Ann Felhofer, Teresa Crowe, Christopher G. AhnAllen, Lisa A. Mistler, Joji Suzuki
Harvard Review of Psychiatry.2022; 30(3): 198. CrossRef Identification of homozygous missense variant in SIX5 gene underlying recessive nonsyndromic hearing impairment
Mohib Ullah Kakar, Muhammad Akram, Muhammad Zubair Mehboob, Muhammad Younus, Muhammad Bilal, Ahmed Waqas, Amina Nazir, Muhammad Shafi, Muhammad Umair, Sajjad Ahmad, Misbahuddin M. Rafeeq, Tao Cai
PLOS ONE.2022; 17(6): e0268078. CrossRef Advancements in prevention and intervention of sensorineural hearing loss
Hongmiao Ren, Bing Hu, Guangli Jiang
Therapeutic Advances in Chronic Disease.2022;[Epub] CrossRef Clinical Impact of Genetic Diagnosis of Sensorineural Hearing Loss in Adults
Patricia Corriols-Noval, Eugenia Carmela López Simón, Juan Cadiñanos, Marta Diñeiro, Raquel Capín, Rocío González Aguado, María Costales Marcos, Carmelo Morales Angulo, Rubén Cabanillas Farpón
Otology & Neurotology.2022; 43(10): 1125. CrossRef Advances in genome editing for genetic hearing loss
Ning Ding, Sangsin Lee, Matan Lieber-Kotz, Jie Yang, Xue Gao
Advanced Drug Delivery Reviews.2021; 168: 118. CrossRef Whole-Exome Sequencing in Idiopathic Short Stature: Rare Mutations Affecting Growth
Shahab Noorian, Nami Mohammadian Khonsari, Shahram Savad, Benyamin Hakak-Zargar, Tessa Voth, Koroush Kabir
Journal of Pediatric Genetics.2021; 10(04): 284. CrossRef Usher Syndrome in the Inner Ear: Etiologies and Advances in Gene Therapy
Evan M. de Joya, Brett M. Colbert, Pei-Ciao Tang, Byron L. Lam, Jun Yang, Susan H. Blanton, Derek M. Dykxhoorn, Xuezhong Liu
International Journal of Molecular Sciences.2021; 22(8): 3910. CrossRef Evaluation of DNA damages in congenital hearing loss patients
Özge Çağlar, Hayal Çobanoğlu, Atilla Uslu, Akın Çayır
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis.2021; 822: 111744. CrossRef
Progression of
KCNQ4
related genetic hearing loss: a narrative review
Xiaolong Zhang, Hongyang Wang, Qiuju Wang
Journal of Bio-X Research.2021; 04(04): 151. CrossRef Genetics of pediatric hearing loss: A functional perspective
Harmon Khela, Margaret A. Kenna
Laryngoscope Investigative Otolaryngology.2020; 5(3): 511. CrossRef In vivo base editing restores sensory transduction and transiently improves auditory function in a mouse model of recessive deafness
Wei-Hsi Yeh, Olga Shubina-Oleinik, Jonathan M. Levy, Bifeng Pan, Gregory A. Newby, Michael Wornow, Rachel Burt, Jonathan C. Chen, Jeffrey R. Holt, David R. Liu
Science Translational Medicine.2020;[Epub] CrossRef Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss
Safoura Zardadi, Ehsan Razmara, Golareh Asgaritarghi, Ehsan Jafarinia, Fatemeh Bitarafan, Sima Rayat, Navid Almadani, Saeid Morovvati, Masoud Garshasbi
Molecular Genetics & Genomic Medicine.2020;[Epub] CrossRef
|