Found: 7
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Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31.
- Published in:
- Nature Genetics, 2003, v. 34, n. 4, p. 421, doi. 10.1038/ng1208
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- Article
A gene-driven approach to the identification of ENU mutants in the mouse.
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- Nature Genetics, 2002, v. 30, n. 3, p. 255, doi. 10.1038/ng847
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- Article
Progressive neuronal inclusion formation and axonal degeneration in CHMP2B mutant transgenic mice.
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- Brain: A Journal of Neurology, 2012, v. 135, n. 3, p. 819, doi. 10.1093/brain/aws006
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- Article
A gene-driven ENU-based approach to generating an allelic series in any gene.
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- Mammalian Genome, 2004, v. 15, n. 8, p. 585, doi. 10.1007/s00335-004-2379-z
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- Article
Selective vulnerability of motor neurons and dissociation of pre- and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy.
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- Human Molecular Genetics, 2008, v. 17, n. 7, p. 949, doi. 10.1093/hmg/ddm367
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- Article
Comparison of T-cell receptor diversity of people with myalgic encephalomyelitis versus controls.
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- BMC Research Notes, 2024, v. 17, n. 1, p. 1, doi. 10.1186/s13104-023-06616-4
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- Article
Work of Art, Museum Trophy, Memorial Monument: The Ny Carlsberg Glyptotek's Gloria Victis by Antonin Mercié.
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- Nineteenth-Century Art Worldwide, 2022, v. 21, n. 3, p. 55, doi. 10.29411/ncaw.2022.21.3.4
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- Article