Showing results (61-70 of 84) with videos related to

Sort By:
Pageof 9
Plos One|February 27, 2024
Comparative exploration of mammalian deafness gene homologues in the Drosophila auditory organ shows genetic correlation between insect and vertebrate hearingDaniel C Sutton, Jonathan C Andrews, Dylan M Dolezal, et al.
Elife|July 13, 2017
Lunatic fringe-mediated Notch signaling regulates adult hippocampal neural stem cell maintenanceFatih Semerci, William Tin-Shing Choi, Aleksandar Bajic, et al.
Frontiers in Cellular Neuroscience|April 16, 2015
Changes in the regulation of the Notch signaling pathway are temporally correlated with regenerative failure in the mouse cochleaJuan C Maass, Rende Gu, Martin L Basch, et al.
Human Molecular Genetics|January 8, 2011
SOX9 controls epithelial branching by activating RET effector genes during kidney developmentAntoine Reginensi, Michael Clarkson, Yasmine Neirijnck, et al.
Development (Cambridge, England)|October 10, 2015
Suppression of epithelial differentiation by Foxi3 is essential for molar crown patterningMaria Jussila, Anne J Aalto, Maria Sanz Navarro, et al.
Scientific Reports|December 9, 2020
Combinatorial Atoh1 and Gfi1 induction enhances hair cell regeneration in the adult cochleaSungsu Lee, Jae-Jun Song, Lisa A Beyer, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 22, 2017
An Atoh1-S193A Phospho-Mutant Allele Causes Hearing Deficits and Motor ImpairmentWei Rose Xie, Hsin-I Jen, Michelle L Seymour, et al.
Developmental Biology|April 20, 2016
Lineage tracing of Sox2-expressing progenitor cells in the mouse inner ear reveals a broad contribution to non-sensory tissues and insights into the origin of the organ of CortiRende Gu, Rogers M Brown, Chih-Wei Hsu, et al.
Plos One|December 31, 2013
Prestin regulation and function in residual outer hair cells after noise-induced hearing lossAnping Xia, Yohan Song, Rosalie Wang, et al.
The Journal of Allergy and Clinical Immunology|October 11, 2019
Recurrent microdeletions at chromosome 2p11.2 are associated with thymic hypoplasia and features resembling DiGeorge syndromeJoshua D Bernstock, Arthur H Totten, Abdel G Elkahloun, et al.
Pageof 9