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The Laryngoscope|April 29, 2009
Gamma knife radiosurgery for vestibular schwannomas: results of hearing preservation in relation to the cochlear radiation doseFerdinand C A Timmer, Patrick E J Hanssens, Anniek E P van Haren, et al.
Genes|February 25, 2023
Genotype and Phenotype Analyses of a Novel WFS1 Variant (c.2512C>T p.(Pro838Ser)) Associated with DFNA6/14/38Hedwig M Velde, Xanne J J Huizenga, Helger G Yntema, et al.
Biomolecules|February 25, 2022
Genotype-Phenotype Correlations of Pathogenic COCH Variants in DFNA9: A HuGE Systematic Review and Audiometric Meta-AnalysisSybren M M Robijn, Jeroen J Smits, Kadriye Sezer, et al.
The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease|September 17, 2010
South Carolina tuberculosis genotype cluster investigation: a tale of substance abuse and recurrent diseaseA M Buff, P K Moonan, M A Desai, et al.
Plos One|June 19, 2019
The heparin-binding proteome in normal pancreas and murine experimental acute pancreatitisQuentin M Nunes, Dunhao Su, Philip J Brownridge, et al.
European Journal of Biochemistry|December 6, 2000
Oxidative degradation of bilirubin produces vasoactive compoundsK R Kranc, G J Pyne, L Tao, et al.
Molecular & Cellular Proteomics : MCP|January 12, 2016
Direct and Absolute Quantification of over 1800 Yeast Proteins via Selected Reaction MonitoringCraig Lawless, Stephen W Holman, Philip Brownridge, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 12, 2021
A Novel COCH Mutation Affects the vWFA2 Domain and Leads to a Relatively Mild DFNA9 PhenotypeJeroen J Smits, Eline van Beelen, Nicole J D Weegerink, et al.
Journal of Proteome Research|June 16, 2020
PEPPI-MS: Polyacrylamide-Gel-Based Prefractionation for Analysis of Intact Proteoforms and Protein Complexes by Mass SpectrometryAyako Takemori, David S Butcher, Victoria M Harman, et al.
Hearing Research|January 24, 2013
Progressive hereditary hearing impairment caused by a MYO6 mutation resembles presbyacusisA M M Oonk, J M Leijendeckers, E M Lammers, et al.
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