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Elife|November 9, 2021
Proposed therapy, developed in a Pcdh15-deficient mouse, for progressive loss of vision in human Usher syndromeSaumil Sethna, Wadih M Zein, Sehar Riaz, et al.ACS Applied Materials & Interfaces|November 22, 2021
Flexible Polymer X-ray Detectors with Non-fullerene Acceptors for Enhanced Stability: Toward Printable Tissue Equivalent Devices for Medical ApplicationsMatthew J Large, Jessie A Posar, Attila J Mozer, et al.Journal of Applied Microbiology|August 8, 2009
Faecal indicator bacteria enumeration in beach sand: a comparison study of extraction methods in medium to coarse sandsA B Boehm, J Griffith, C McGee, et al.European Journal of Human Genetics : EJHG|November 27, 2021
Genomic analysis of childhood hearing loss in the Yoruba population of NigeriaAdebolajo Adeyemo, Rabia Faridi, Parna Chattaraj, et al.Clinical Genetics|October 22, 2020
Vestibular phenotype-genotype correlation in a cohort of 90 patients with Usher syndromeTalah T Wafa, Rabia Faridi, Kelly A King, et al.The Laryngoscope|December 10, 2009
SLC26A4 genotype, but not cochlear radiologic structure, is correlated with hearing loss in ears with an enlarged vestibular aqueductKelly A King, Byung Yoon Choi, Christopher Zalewski, et al.Science Advances|October 9, 2024
SLC26A4-AP-2 mu2 interaction regulates SLC26A4 plasma membrane abundance in the endolymphatic sacHyun Jae Lee, Cristina Fenollar-Ferrer, Kevin Isgrig, et al.Genetics|March 10, 2001
The Neurospora crassa genome: cosmid libraries sorted by chromosomeH S Kelkar, J Griffith, M E Case, et al.Journal of Medical Genetics|August 7, 2017
A common SLC26A4-linked haplotype underlying non-syndromic hearing loss with enlargement of the vestibular aqueductParna Chattaraj, Tina Munjal, Keiji Honda, et al.American Journal of Human Genetics|July 30, 2002
Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locusSadaf Naz, Chantal M Giguere, David C Kohrman, et al.Pageof 68