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Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 24, p. 3921, doi. 10.1093/hmg/ddi416
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- Article
Brain cross‐protection against SARS‐CoV‐2 variants by a lentiviral vaccine in new transgenic mice.
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- EMBO Molecular Medicine, 2021, v. 13, n. 12, p. 1, doi. 10.15252/emmm.202114459
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- Article
DNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34.
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- European Journal of Human Genetics, 2002, v. 10, n. 3, p. 210, doi. 10.1038/sj.ejhg.5200780
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- Article
A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36.
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- European Journal of Human Genetics, 1998, v. 6, n. 3, p. 245, doi. 10.1038/sj.ejhg.5200177
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- Article
Molecular Characterization of the Ankle-Link Complex in Cochlear Hair Cells and Its Role in the Hair Bundle Functioning.
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- Journal of Neuroscience, 2007, v. 27, n. 24, p. 6478, doi. 10.1523/JNEUROSCI.0342-07.2007
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- Article
An α-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21.
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- Human Molecular Genetics, 1999, v. 8, n. 3, p. 409, doi. 10.1093/hmg/8.3.409
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- Article
Mapping of DFNB12, a Gene for a Non-Syndromal Autosomal Recessive Deafness, to Chromosome 10q21–22.
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- Human Molecular Genetics, 1996, v. 5, n. 7, p. 1061, doi. 10.1093/hmg/5.7.1061
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- Article
A Gene Responsible for a Sensorineural Nonsyndromic Recessive Deafness Maps to Chromosome 2p22–23.
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- Human Molecular Genetics, 1996, v. 5, n. 1, p. 155, doi. 10.1093/hmg/5.1.155
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- Article