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The giant spectrin βV couples the molecular motors to phototransduction and Usher syndrome type I proteins along their trafficking route.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 18, p. 3773, doi. 10.1093/hmg/ddt228
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- Article
Accumulation of calcium in degenerating photoreceptors of several Drosophila mutants.
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- Visual Neuroscience, 1994, v. 11, n. 4, p. 763, doi. 10.1017/S0952523800003060
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- Article
Novel Transgenic Mice for Inducible Gene Overexpression in Pancreatic Cells Define Glucocorticoid Receptor-Mediated Regulations of Beta Cells.
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- PLoS ONE, 2012, v. 7, n. 2, p. 1, doi. 10.1371/journal.pone.0030210
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- Article
Identification of novel PAX6 mutations in two families with bilateral aniridia.
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- Human Mutation, 1998, v. 12, n. 2, p. 138, doi. 10.1002/(SICI)1098-1004(1998)12:2<138::AID-HUMU18>3.0.CO;2-A
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- Article
Identification of a novel PAX6 gene mutation in an Aniridia patient.
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- Human Mutation, 1996, v. 7, n. 4, p. 377, doi. 10.1002/(SICI)1098-1004(1996)7:4<377::AID-HUMU19>3.0.CO;2-#
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- Article
Eya1 expression in the developing ear and kidney: Towards the understanding of the pathogenesis of branchio-oto-renal (BOR) syndrome.
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- Developmental Dynamics, 1998, v. 213, n. 4, p. 486, doi. 10.1002/(SICI)1097-0177(199812)213:4<486::AID-AJA13>3.0.CO;2-L
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- Article
SOX22 is a New Member of the SOX Gene Family, Mainly Expressed in Human Nervous Tissue.
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- Human Molecular Genetics, 1997, v. 6, n. 7, p. 1069, doi. 10.1093/hmg/6.7.1069
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- Article
Human Usher 1B/Mouse shaker-1: The Retinal Phenotype Discrepancy Explained By The Presence/Absence of Myosin VIIA in The Photoreceptor Cells.
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- Human Molecular Genetics, 1996, v. 5, n. 8, p. 1171, doi. 10.1093/hmg/5.8.1171
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- Article
When reverse genetics meets physiology: the use of site-specific recombinases in mice
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- FEBS Letters, 2002, v. 529, n. 1, p. 116, doi. 10.1016/S0014-5793(02)03266-0
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- Article