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Danielle R Lenz

Showing results (1-10 of 12) with videos related to

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Hearing Research|June 14, 2011
Hereditary hearing loss: from human mutation to mechanismDanielle R Lenz, Karen B Avraham
The Journal of Clinical Investigation|August 28, 2013
A "Tric" to tighten cell-cell junctions in the cochlea for hearingTomohito Higashi, Danielle R Lenz, Mikio Furuse, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|April 25, 2014
Atrophic thyroid follicles and inner ear defects reminiscent of cochlear hypothyroidism in Slc26a4-related deafnessAmiel A Dror, Danielle R Lenz, Shaked Shivatzki, et al.
American Journal of Otolaryngology|March 9, 2016
Hearing loss patterns after cochlear implantation via the round window in an animal modelJoseph Attias, Roy Hod, Eyal Raveh, et al.
Frontiers in Cell and Developmental Biology|March 16, 2019
Applications of Lgr5-Positive Cochlear Progenitors (LCPs) to the Study of Hair Cell DifferentiationDanielle R Lenz, Niliksha Gunewardene, Dunia E Abdul-Aziz, et al.
Development (Cambridge, England)|November 4, 2018
Transcriptional response to Wnt activation regulates the regenerative capacity of the mammalian cochleaAnshula Samarajeewa, Danielle R Lenz, Lihong Xie, et al.
Cell Reports|February 24, 2017
Clonal Expansion of Lgr5-Positive Cells from Mammalian Cochlea and High-Purity Generation of Sensory Hair CellsWill J McLean, Xiaolei Yin, Lin Lu, et al.
Plos One|April 13, 2011
Integration of transcriptomics, proteomics, and microRNA analyses reveals novel microRNA regulation of targets in the mammalian inner earTal Elkan-Miller, Igor Ulitsky, Ronna Hertzano, et al.
The Journal of Biological Chemistry|May 6, 2010
Calcium oxalate stone formation in the inner ear as a result of an Slc26a4 mutationAmiel A Dror, Yael Politi, Hashem Shahin, et al.
Human Mutation|April 23, 2013
Cytoplasmic mislocalization of POU3F4 due to novel mutations leads to deafness in humans and miceThomas Parzefall, Shaked Shivatzki, Danielle R Lenz, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Hearing Research|June 14, 2011
Hereditary hearing loss: from human mutation to mechanismDanielle R Lenz, Karen B Avraham
The Journal of Clinical Investigation|August 28, 2013
A "Tric" to tighten cell-cell junctions in the cochlea for hearingTomohito Higashi, Danielle R Lenz, Mikio Furuse, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|April 25, 2014
Atrophic thyroid follicles and inner ear defects reminiscent of cochlear hypothyroidism in Slc26a4-related deafnessAmiel A Dror, Danielle R Lenz, Shaked Shivatzki, et al.
American Journal of Otolaryngology|March 9, 2016
Hearing loss patterns after cochlear implantation via the round window in an animal modelJoseph Attias, Roy Hod, Eyal Raveh, et al.
Frontiers in Cell and Developmental Biology|March 16, 2019
Applications of Lgr5-Positive Cochlear Progenitors (LCPs) to the Study of Hair Cell DifferentiationDanielle R Lenz, Niliksha Gunewardene, Dunia E Abdul-Aziz, et al.
Development (Cambridge, England)|November 4, 2018
Transcriptional response to Wnt activation regulates the regenerative capacity of the mammalian cochleaAnshula Samarajeewa, Danielle R Lenz, Lihong Xie, et al.
Cell Reports|February 24, 2017
Clonal Expansion of Lgr5-Positive Cells from Mammalian Cochlea and High-Purity Generation of Sensory Hair CellsWill J McLean, Xiaolei Yin, Lin Lu, et al.
Plos One|April 13, 2011
Integration of transcriptomics, proteomics, and microRNA analyses reveals novel microRNA regulation of targets in the mammalian inner earTal Elkan-Miller, Igor Ulitsky, Ronna Hertzano, et al.
The Journal of Biological Chemistry|May 6, 2010
Calcium oxalate stone formation in the inner ear as a result of an Slc26a4 mutationAmiel A Dror, Yael Politi, Hashem Shahin, et al.
Human Mutation|April 23, 2013
Cytoplasmic mislocalization of POU3F4 due to novel mutations leads to deafness in humans and miceThomas Parzefall, Shaked Shivatzki, Danielle R Lenz, et al.
Pageof 2