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Page 1
Gene therapy strategies for Usher syndrome type 1B.
Williams DS, Lopes VS. Williams DS, et al. Adv Exp Med Biol. 2012;723:235-42. doi: 10.1007/978-1-4614-0631-0_31. Adv Exp Med Biol. 2012. PMID: 22183338 Review. No abstract available.
The many different cellular functions of MYO7A in the retina.
Williams DS, Lopes VS. Williams DS, et al. Biochem Soc Trans. 2011 Oct;39(5):1207-10. doi: 10.1042/BST0391207. Biochem Soc Trans. 2011. PMID: 21936790 Free PMC article. Review.
Mutations in MYO7A (myosin VIIa) cause Usher syndrome type 1B, a disorder involving profound congenital deafness and progressive blindness. ...
Mutations in MYO7A (myosin VIIa) cause Usher syndrome type 1B, a disorder involving profound congenital deafness …
Genetic causes of hearing loss.
Cremers FP. Cremers FP. Curr Opin Neurol. 1998 Feb;11(1):11-6. doi: 10.1097/00019052-199802000-00003. Curr Opin Neurol. 1998. PMID: 9484611 Review.
In the past year, genes involved in the branchio-oto-renal and Treacher-Collins syndromes were cloned. Myosin 7A, a gene previously implicated in Usher syndrome type 1B, was also found to be mutated in non-syndromic hearing loss. ...
In the past year, genes involved in the branchio-oto-renal and Treacher-Collins syndromes were cloned. Myosin 7A, a gene previously implicat …
Assessment of different virus-mediated approaches for retinal gene therapy of Usher 1B.
Lopes VS, Diemer T, Williams DS. Lopes VS, et al. Adv Exp Med Biol. 2014;801:725-31. doi: 10.1007/978-1-4614-3209-8_91. Adv Exp Med Biol. 2014. PMID: 24664764 Review.
Usher syndrome type 1B, which is characterized by congenital deafness and progressive retinal degeneration, is caused by the loss of the function of MYO7A. ...
Usher syndrome type 1B, which is characterized by congenital deafness and progressive retinal degeneration, is c …
Unconventional myosins and the genetics of hearing loss.
Friedman TB, Sellers JR, Avraham KB. Friedman TB, et al. Am J Med Genet. 1999 Sep 24;89(3):147-57. doi: 10.1002/(sici)1096-8628(19990924)89:3<147::aid-ajmg5>3.0.co;2-6. Am J Med Genet. 1999. PMID: 10704189 Review.
The discovery that the mouse shaker1 (Myo7(ash1)) locus encodes myosin VIIA led immediately to the identification of mutations in this gene in Usher syndrome type 1B; subsequently, mutations in this gene were also found associated with recessive and do …
The discovery that the mouse shaker1 (Myo7(ash1)) locus encodes myosin VIIA led immediately to the identification of mutations in this gene …