Publications
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“Microvascular remodeling of nasal mucosa in allergic rhinitis induced by an allergen in Sprague-Dawley rats”, vol. 14, pp. 11624-11630, 2015.
, “A novel mutation of the DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria”, vol. 11, pp. 1731-1737, 2012.
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http://dx.doi.org/10.1067/mjd.2000.103994
PMid:10863235
Cho DS, Yang W, Lee JT, Shiekhattar R, et al. (2003). Requirement of dimerization for RNA editing activity of adenosine deaminases acting on RNA. J. Biol. Chem. 278: 17093-17102.
http://dx.doi.org/10.1074/jbc.M213127200
PMid:12618436
Liu Q, Jiang L, Liu WL, Kang XJ, et al. (2006). Two novel mutations and evidence for haploinsufficiency of the ADAR gene in dyschromatosis symmetrica hereditaria. Br. J. Dermatol. 154: 636-642.
http://dx.doi.org/10.1111/j.1365-2133.2006.07133.x
PMid:16536805
Miyamura Y, Suzuki T, Kono M, Inagaki K, et al. (2003). Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria. Am. J. Hum. Genet. 73: 693-699.
http://dx.doi.org/10.1086/378209
PMid:12916015 PMCid:1180697
Murata I, Hayashi M, Hozumi Y, Fujii K, et al. (2010). Mutation analyses of patients with dyschromatosis symmetrica hereditaria: five novel mutations of the ADAR1 gene. J. Dermatol. Sci. 58: 218-220.
http://dx.doi.org/10.1016/j.jdermsci.2010.04.001
PMid:20439151
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PMid:7862132 PMCid:230363
Oiso N, Murata I, Hayashi M, Amatsu A, et al. (2011). Dermoscopic features in a case of dyschromatosis symmetrica hereditaria. J. Dermatol. 38: 91-93.
http://dx.doi.org/10.1111/j.1346-8138.2010.01110.x
PMid:21175763
Ostlere LS, Ratnavel RC, Lawlor F, Black MM, et al. (1995). Reticulate acropigmentation of Dohi. Clin. Exp. Dermatol. 20: 477-479.
http://dx.doi.org/10.1111/j.1365-2230.1995.tb01382.x
PMid:8857341
Oyama M, Shimizu H, Ohata Y, Tajima S, et al. (1999). Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi): report of a Japanese family with the condition and a literature review of 185 cases. Br. J. Dermatol. 140: 491-496.
http://dx.doi.org/10.1046/j.1365-2133.1999.02716.x
PMid:10233273
Rueter SM, Dawson TR and Emeson RB (1999). Regulation of alternative splicing by RNA editing. Nature 399: 75-80.
http://dx.doi.org/10.1038/19992
PMid:10331393
Schade M, Turner CJ, Kuhne R, Schmieder P, et al. (1999). The solution structure of the Zalpha domain of the human RNA editing enzyme ADAR1 reveals a prepositioned binding surface for Z-DNA. Proc. Natl. Acad. Sci. U. S. A. 96: 12465-12470.
http://dx.doi.org/10.1073/pnas.96.22.12465
PMid:10535945 PMCid:22950
Sun XK, Xu AE, Chen JF and Tang X (2005). The double-RNA-specific adenosine deaminase (DSRAD) gene in dyschromatosis symmetrica hereditaria patients: two novel mutations and one previously described. Br. J. Dermatol. 153: 342-345.
http://dx.doi.org/10.1111/j.1365-2133.2005.06572.x
PMid:16086746
Suzuki N, Suzuki T, Inagaki K, Ito S, et al. (2005). Mutation analysis of the ADAR1 gene in dyschromatosis symmetrica hereditaria and genetic differentiation from both dyschromatosis universalis hereditaria and acropigmentatio reticularis. J. Invest. Dermatol. 124: 1186-1192.
http://dx.doi.org/10.1111/j.0022-202X.2005.23732.x
PMid:15955093
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http://dx.doi.org/10.1016/S1085-5629(97)80039-9
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http://dx.doi.org/10.1073/pnas.86.8.2647
PMid:2704740 PMCid:286974
Zhang XJ, Gao M, Li M, Li M, et al. (2003). Identification of a locus for dyschromatosis symmetrica hereditaria at chromosome 1q11-1q21. J. Invest. Dermatol. 120: 776-780.
http://dx.doi.org/10.1046/j.1523-1747.2003.12130.x
PMid:12713580