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Hearing Research|January 23, 2019
Hereditary hearing loss; about the known and the unknownHannie KremerHuman Genetics|October 2, 2021
Novel gene discovery for hearing loss and other routes to increased diagnostic ratesHannie KremerMethods in Molecular Biology (Clifton, N.J.)|October 8, 2008
Positional cloning of deafness genesHannie Kremer, Frans P M CremersMethods in Molecular Biology (Clifton, N.J.)|September 2, 2018
Antisense Oligonucleotide Design and Evaluation of Splice-Modulating Properties Using Cell-Based AssaysRalph Slijkerman, Hannie Kremer, Erwin van WijkMolecular Diagnosis & Therapy|June 15, 2006
Comparison of 12 reference genes for normalization of gene expression levels in Epstein-Barr virus-transformed lymphoblastoid cell lines and fibroblastsArjan P M de Brouwer, Hans van Bokhoven, Hannie KremerHuman Molecular Genetics|September 22, 2006
Usher syndrome: molecular links of pathogenesis, proteins and pathwaysHannie Kremer, Erwin van Wijk, Tina Märker, et al.Methods in Molecular Biology (Clifton, N.J.)|February 25, 2022
Generation of Humanized Zebrafish Models for the In Vivo Assessment of Antisense Oligonucleotide-Based Splice Modulation TherapiesRenske Schellens, Erik de Vrieze, Ralph Slijkerman, et al.Roux'S Archives of Developmental Biology : the Official Organ of the EDBO|March 18, 2017
Spermatogenesis inDrosophila hydei: A genetic surveyJohannes H P Hackstein, Heinz Beck, Ron Hochstenbach, et al.Hearing Research|April 28, 2005
GJB2 mutations in Turkish patients with ARNSHL: prevalence and two novel mutationsErsan Kalay, Refik Caylan, Hannie Kremer, et al.Pageof 15