Publications by authors named "Andrew J Griffith"

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SLC26A4-AP-2 mu2 interaction regulates SLC26A4 plasma membrane abundance in the endolymphatic sac.
Hyun Jae Lee, Cristina Fenollar-Ferrer, Kevin Isgrig, Ya-Xian Wang, Kerstin Valente, Andrew J Griffith

Sci Adv· October 2024

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Small Molecule MIF Modulation Enhances Ferroptosis by Impairing DNA Repair Mechanisms.
Deng Chen, Chunlong Zhao, Jianqiu Zhang, Catharina W J Knol, Angelina Osipyan, Andrew J Griffith

Adv Sci (Weinh)· August 2024

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Transgenic Tg(Kcnj10-ZsGreen) fluorescent reporter mice allow visualization of intermediate cells in the stria vascularis.
Dillon Strepay, Rafal T Olszewski, Sydney Nixon, Soumya Korrapati, Samuel Adadey, Andrew J Griffith

Sci Rep· February 2024

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CHD7 variants associated with hearing loss and enlargement of the vestibular aqueduct.
Isabelle Roux, Cristina Fenollar-Ferrer, Hyun Jae Lee, Parna Chattaraj, Ivan A Lopez, Andrew J Griffith

Hum Genet· October 2023

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Transgenic Tg(Kcnj10-ZsGreen) Fluorescent Reporter Mice Allow Visualization of Intermediate Cells in the Stria Vascularis.
Dillon Strepay, Rafal T Olszewski, Sydney Nixon, Soumya Korrapati, Samuel Adadey, Andrew J Griffith

Res Sq· October 2023

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Variants of LRP2, encoding a multifunctional cell-surface endocytic receptor, associated with hearing loss and retinal dystrophy.
Rabia Faridi, Rizwan Yousaf, Shoujun Gu, Sayaka Inagaki, Amy E Turriff, Andrew J Griffith

Clin Genet· June 2023

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Vaccination with human alphapapillomavirus-derived L2 multimer protects against human betapapillomavirus challenge, including in epidermodysplasia verruciformis model mice.
Pola Olczak, Margaret Wong, Hua-Ling Tsai, Hao Wang, Reinhard Kirnbauer, Andrew J Griffith

Virology· October 2022

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AAV8BP2 and AAV8 transduce the mammalian cochlear lateral wall and endolymphatic sac with high efficiency.
Kevin Isgrig, Yasuko Ishibashi, Hyun Jae Lee, Jianliang Zhu, Mhamed Grati, Andrew J Griffith

Mol Ther Methods Clin Dev· September 2022

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Genetic architecture and phenotypic landscape of SLC26A4-related hearing loss.
Keiji Honda, Andrew J Griffith

Hum Genet· April 2022

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Gene Therapy Restores Balance and Auditory Functions in a Mouse Model of Usher Syndrome.
Kevin Isgrig, Jack W Shteamer, Inna A Belyantseva, Meghan C Drummond, Tracy S Fitzgerald, Andrew J Griffith

Mol Ther· February 2022

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Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria.
Adebolajo Adeyemo, Rabia Faridi, Parna Chattaraj, Rizwan Yousaf, Risa Tona, Andrew J Griffith

Eur J Hum Genet· January 2022

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Cochlear Pathomorphogenesis of Incomplete Partition Type II in Slc26a4-Null Mice.
Taku Ito, Taro Fujikawa, Keiji Honda, Ayane Makabe, Hiroki Watanabe, Andrew J Griffith

J Assoc Res Otolaryngol· December 2021

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Disease-specific ACMG/AMP guidelines improve sequence variant interpretation for hearing loss.
Mayher J Patel, Marina T DiStefano, Andrea M Oza, Madeline Y Hughes, Emma H Wilcox, Andrew J Griffith

Genet Med· November 2021

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Proposed therapy, developed in a -deficient mouse, for progressive loss of vision in human Usher syndrome.
Saumil Sethna, Wadih M Zein, Sehar Riaz, Arnaud Pj Giese, Julie M Schultz, Andrew J Griffith

Elife· November 2021

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Dissection of the Endolymphatic Sac from Mice.
Keiji Honda, Hyun Jae Lee, Andrew J Griffith, Isabelle Roux

J Vis Exp· March 2021

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Vestibular phenotype-genotype correlation in a cohort of 90 patients with Usher syndrome.
Talah T Wafa, Rabia Faridi, Kelly A King, Christopher Zalewski, Rizwan Yousaf, Andrew J Griffith

Clin Genet· February 2021

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Expression of a TMC6-TMC8-CIB1 heterotrimeric complex in lymphocytes is regulated by each of the components.
Chuan-Jin Wu, Xing Li, Connie L Sommers, Kiyoto Kurima, Sunmee Huh, Andrew J Griffith

J Biol Chem· November 2020

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Atypical and ultra-rare Usher syndrome: a review.
Rosalie M Nolen, Robert B Hufnagel, Thomas B Friedman, Amy E Turriff, Carmen C Brewer, Andrew J Griffith

Ophthalmic Genet· October 2020

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Systemic Fluorescent Gentamicin Enters Neonatal Mouse Hair Cells Predominantly Through Sensory Mechanoelectrical Transduction Channels.
Ayane Makabe, Yoshiyuki Kawashima, Yuriko Sakamaki, Ayako Maruyama, Taro Fujikawa, Andrew J Griffith

J Assoc Res Otolaryngol· April 2020

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Genetic Hearing Loss Associated With Autoinflammation.
Hiroshi Nakanishi, Pragya Prakash, Taku Ito, H Jeffrey Kim, Carmen C Brewer, Andrew J Griffith

Front Neurol· March 2020

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SLC26A4-linked CEVA haplotype correlates with phenotype in patients with enlargement of the vestibular aqueduct.
Janet R Chao, Parna Chattaraj, Tina Munjal, Keiji Honda, Kelly A King, Andrew J Griffith

BMC Med Genet· July 2019

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Tmc2 expression partially restores auditory function in a mouse model of DFNB7/B11 deafness caused by loss of Tmc1 function.
Hiroshi Nakanishi, Kiyoto Kurima, Bifeng Pan, Philine Wangemann, Tracy S Fitzgerald, Andrew J Griffith

Sci Rep· August 2018

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Gradual Symmetric Progression of DFNA34 Hearing Loss Caused by an NLRP3 Mutation and Cochlear Autoinflammation.
Hiroshi Nakanishi, Yoshiyuki Kawashima, Kiyoto Kurima, Julie A Muskett, H Jeffrey Kim, Andrew J Griffith

Otol Neurotol· March 2018

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Molecular architecture underlying fluid absorption by the developing inner ear.
Keiji Honda, Sung Huhn Kim, Michael C Kelly, Joseph C Burns, Laura Constance, Andrew J Griffith

Elife· October 2017

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mutation and cochlear autoinflammation cause syndromic and nonsyndromic hearing loss DFNA34 responsive to anakinra therapy.
Hiroshi Nakanishi, Yoshiyuki Kawashima, Kiyoto Kurima, Jae Jin Chae, Astin M Ross, Andrew J Griffith

Proc Natl Acad Sci U S A· September 2017

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