ExLibris header image
SFX Logo
Title: Effects of genetic correction on the differentiation of hair cell-like cells from iPSCs with MYO15A mutation
Source:

Cell death and Differentiation [1350-9047] Chen, J-R yr:2016


Collapse list of basic services Basic
Full text
Full text available via Nature
GO
Full text available via PubMed Central
GO
Document delivery
Request document via Library/Bibliothek GO
Users interested in this article also expressed an interest in the following:
1. Sommen, M. "DNA Diagnostics of Hereditary Hearing Loss: A Targeted Resequencing Approach Combined With a Mutation Classification System." Human Mutation 37.8 (2016): 812-819. Link to Full Text for this item Link to SFX for this item
2. Lim, R. "Anatomical and physiological development of the human inner ear." Hearing research 338 (2016): 9-21. Link to SFX for this item
3. Beck, C. "Identification and genotype/phenotype correlation of mutations in a large German cohort with hearing loss." European archives of oto-rhino-laryngology 272.10 (2014): 2765-2776. Link to SFX for this item
4. Lundberg, Yunxia W. "Mechanisms of otoconia and otolith development." Developmental dynamics 244.3 (2014): 239-53. Link to Full Text for this item Link to SFX for this item
5. Bademci, G. "Identification of Copy Number Variants Through Whole-Exome Sequencing in Autosomal Recessive Nonsyndromic Hearing Loss." Genetic testing and molecular biomarkers 18.9 (2014): 658-61. Link to SFX for this item
6. Hackney, Carole M. "The composition and role of cross links in mechanoelectrical transduction in vertebrate sensory hair cells." Journal of cell science 126.8 (2013): 1721-1731. Link to SFX for this item
7. Luigetti, M. "Inherited neuropathies and deafness caused by a PMP22 point mutation: a case report and a review of the literature." Neurological sciences 34.9 (2012): 1705-1707. Link to SFX for this item
8. Mercer, S. "Identification of SLC26A4 Mutations in Patients with Hearing Loss and Enlarged Vestibular Aqueduct Using High-Resolution Melting Curve Analysis." Genetic testing and molecular biomarkers 15,.5 (2011): 365-368. Link to SFX for this item
9. Stephens, S D D. "Auditory rehabilitation." British medical bulletin 43.4 (1987): 999-1026. Link to Full Text for this item Link to SFX for this item
10. Kim TB, B J B M. "A gene responsible for autosomal dominant auditory neuropathy (AUNA1) maps to 13q14-21." Journal of medical genetics 41.11 (2004): 872-6. Link to Full Text for this item Link to SFX for this item
11. Wood, W. "Epithelial fusions in the embryo." Current opinion in cell biology 14.5 (2002): 569-74. Link to Full Text for this item Link to SFX for this item
12. Yasuda, C. "Three-dimensional analysis of inner ear development in human embryos." Anatomical science international 82.3 (2007): 156-63. Link to SFX for this item
13. Jacinto, A. "Dynamic Analysis of Dorsal Closure in Drosophila From Genetics to Cell Biology." Developmental cell 3.1 (2002): 9-19. Link to SFX for this item
14. Gess, B. "Charcot-Marie-Tooth disease: Frequency of genetic subtypes in a German neuromuscular center population." Neuromuscular disorders 23.8 (2013): 647-651. Link to SFX for this item
15. "In situ patch-clamp recordings from Merkel cells in rat whisker hair follicles, an experimental protocol for studying tactile transduction in tactile-end organs." Molecular pain. 11: 23-. Link to SFX for this item
16. Blakemore, C. "lip-reading." The Oxford Companion to The Body (2001): 434-435. Link to SFX for this item
17. Zhao, Y. "The first USH2A mutation analysis of Japanese autosomal recessive retinitis pigmentosa patients: a totally different mutation profile with the lack of frequent mutations found in Caucasian patients." Journal of human genetics 59.9 (2014): 521-8. Link to Full Text for this item Link to SFX for this item
18. Loh, Kyle M M. "Ex uno plures: molecular designs for embryonic pluripotency." Physiological reviews 95.1 (2015): 245-95. Link to SFX for this item
19. Soh, Lip M. "Evaluation of genotype-phenotype relationships in patients referred for endocrine assessment in suspected Pendred syndrome." European journal of endocrinology 172.2 (2015): 217-26. Link to SFX for this item
20. Zhu, James i. "Cervical VEMP Threshold Response Curve in the Identification of Ménière's Disease." Journal of the American Academy of Audiology 25.3 (2014): 278-88. Link to SFX for this item
View More...
View Less...
Select All Clear All

Expand list of advanced services Advanced