Showing results (421-430 of 436) with videos related to

Sort By:
Pageof 44
Molecular Therapy. Methods & Clinical Development|October 2, 2025
Functional, sustained recovery of hearing in Otoferlin-deficient mice using DB-OTO, a hair-cell-specific AAV-based gene therapyYoojin Chung, Seth D Koehler, Sarah Cancelarich, et al.
Cell|July 22, 2025
Functional liver genomics identifies hepatokines promoting wasting in cancer cachexiaDoris Kaltenecker, Søren Fisker Schmidt, Peter Weber, et al.
The British Journal of Nutrition|November 10, 2015
Application of dried blood spots to determine vitamin D status in a large nutritional study with unsupervised sampling: the Food4Me projectUlrich Hoeller, Manuela Baur, Franz F Roos, et al.
The New England Journal of Medicine|October 14, 2025
DB-OTO Gene Therapy for Inherited DeafnessVassili Valayannopoulos, Manohar Bance, Daniela S Carvalho, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|September 14, 2020
American Neurotology Society, American Otological Society, and American Academy of Otolaryngology - Head and Neck Foundation Guide to Enhance Otologic and Neurotologic Care During the COVID-19 PandemicElliott D Kozin, Aaron K Remenschneider, Nikolas H Blevins, et al.
Genes & Nutrition|December 23, 2017
Proposed guidelines to evaluate scientific validity and evidence for genotype-based dietary adviceKeith A Grimaldi, Ben van Ommen, Jose M Ordovas, et al.
Human Brain Mapping|May 30, 2020
The ENIGMA-Epilepsy working group: Mapping disease from large data setsSanjay M Sisodiya, Christopher D Whelan, Sean N Hatton, et al.
Brain : a Journal of Neurology|August 21, 2020
White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy studySean N Hatton, Khoa H Huynh, Leonardo Bonilha, et al.
Epilepsia|June 3, 2022
Event-based modeling in temporal lobe epilepsy demonstrates progressive atrophy from cross-sectional dataSeymour M Lopez, Leon M Aksman, Neil P Oxtoby, et al.
Human Mutation|December 24, 2008
Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletionPaola S Denora, David Schlesinger, Carlo Casali, et al.
Pageof 44