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Volumn 53, Issue 1, 2009, Pages 76-77

Four novel mutations of the ADAR1 gene in dyschromatosis symmetrica hereditaria

Author keywords

[No Author keywords available]

Indexed keywords

ADAR1 GENE; AUTOSOMAL DOMINANT DISORDER; BLOOD SAMPLING; CASE REPORT; CONTROLLED STUDY; DNA SEQUENCE; DYSCHROMATOSIS SYMMETRICA HEREDITARIA; GENE; GENE MUTATION; HUMAN; HUMAN TISSUE; JAPANESE; LETTER; NUCLEOTIDE SEQUENCE; PEDIGREE; PRIORITY JOURNAL; RNA SPLICING; SKIN DISEASE;

EID: 57549119335     PISSN: 09231811     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jdermsci.2008.07.011     Document Type: Letter
Times cited : (13)

References (10)
  • 2
    • 0042888576 scopus 로고    scopus 로고
    • Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria
    • Miyamura Y., Suzuki T., Kono M., Inagaki K., Ito S., Suzuki N., et al. Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria. Am J Hum Genet 73 (2003) 693-699
    • (2003) Am J Hum Genet , vol.73 , pp. 693-699
    • Miyamura, Y.1    Suzuki, T.2    Kono, M.3    Inagaki, K.4    Ito, S.5    Suzuki, N.6
  • 3
    • 20544455231 scopus 로고    scopus 로고
    • Mutation analysis of the ADAR1 gene in dyschromatosis symmetrica hereditaria and genetic differentiation from both dyschromatosis universalis hereditaria and acropigmentatio reticularis
    • Suzuki N., Suzuki T., Inagaki K., Ito S., Kono M., Fukai K., et al. 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 (2005) 1186-1192
    • (2005) J Invest Dermatol , vol.124 , pp. 1186-1192
    • Suzuki, N.1    Suzuki, T.2    Inagaki, K.3    Ito, S.4    Kono, M.5    Fukai, K.6
  • 4
    • 27544498010 scopus 로고    scopus 로고
    • A novel deletion mutation of the DSRAD gene in a Taiwanese patient with dyschromatosis symmetrica hereditaria
    • Chao S.C., Lee J.Y., Sheu H.M., and Yang M.H. A novel deletion mutation of the DSRAD gene in a Taiwanese patient with dyschromatosis symmetrica hereditaria. Br J Dermatol 153 (2005) 1064-1066
    • (2005) Br J Dermatol , vol.153 , pp. 1064-1066
    • Chao, S.C.1    Lee, J.Y.2    Sheu, H.M.3    Yang, M.H.4
  • 5
    • 33644873012 scopus 로고    scopus 로고
    • Two novel mutations and evidence for haploinsufficiency of the ADAR gene in dyschromatosis symmetrica hereditaria
    • Liu Q., Jiang L., Liu W.L., Kang X.J., Ao Y., Sun M., et al. Two novel mutations and evidence for haploinsufficiency of the ADAR gene in dyschromatosis symmetrica hereditaria. Br J Dermatol 154 (2006) 636-642
    • (2006) Br J Dermatol , vol.154 , pp. 636-642
    • Liu, Q.1    Jiang, L.2    Liu, W.L.3    Kang, X.J.4    Ao, Y.5    Sun, M.6
  • 6
    • 33846226051 scopus 로고    scopus 로고
    • Ten novel mutations of the ADAR1 gene in Japanese patients with dyschromatosis symmetrica hereditaria
    • Suzuki N., Suzuki T., Inagaki K., Ito S., Kono M., Horikawa T., et al. Ten novel mutations of the ADAR1 gene in Japanese patients with dyschromatosis symmetrica hereditaria. J Invest Dermatol 127 (2007) 309-311
    • (2007) J Invest Dermatol , vol.127 , pp. 309-311
    • Suzuki, N.1    Suzuki, T.2    Inagaki, K.3    Ito, S.4    Kono, M.5    Horikawa, T.6
  • 7
    • 41149140214 scopus 로고    scopus 로고
    • Six novel mutations of the ADAR1 gene in Chinese patients with dyschromatosis symmetrica hereditaria
    • Zhang F., Liu H., Jiang D., Tian H., Wang C., and Yu L. Six novel mutations of the ADAR1 gene in Chinese patients with dyschromatosis symmetrica hereditaria. J Dermatol Sci 50 (2008) 109-114
    • (2008) J Dermatol Sci , vol.50 , pp. 109-114
    • Zhang, F.1    Liu, H.2    Jiang, D.3    Tian, H.4    Wang, C.5    Yu, L.6
  • 8
    • 47149112190 scopus 로고    scopus 로고
    • Six novel mutations of the ADAR1 gene in patients with dyschromatosis symmetrica hereditaria: histological observation and comparison of genotypes and clinical phenotypes
    • Kondo T., Suzuki T., Mitsuhashi Y., Ito S., Kono M., Komine M., et al. Six novel mutations of the ADAR1 gene in patients with dyschromatosis symmetrica hereditaria: histological observation and comparison of genotypes and clinical phenotypes. J Dermatol 35 (2008) 395-406
    • (2008) J Dermatol , vol.35 , pp. 395-406
    • Kondo, T.1    Suzuki, T.2    Mitsuhashi, Y.3    Ito, S.4    Kono, M.5    Komine, M.6
  • 9
    • 0024233053 scopus 로고
    • An unwinding activity that covalently modifies its double-stranded RNA substrate
    • Bass B.L., and Weintraub H. An unwinding activity that covalently modifies its double-stranded RNA substrate. Cell 55 (1988) 1089-1098
    • (1988) Cell , vol.55 , pp. 1089-1098
    • Bass, B.L.1    Weintraub, H.2
  • 10
    • 0024990271 scopus 로고
    • Double-stranded RNA unwinding and modifying activity is detected ubiquitously in primary tissues and cell lines
    • Wagner R.W., Yoo C., Wrabetz L., Kamholz J., Buchhalter J., Hassan N.F., et al. Double-stranded RNA unwinding and modifying activity is detected ubiquitously in primary tissues and cell lines. Mol Cell Biol 10 (1990) 5586-5590
    • (1990) Mol Cell Biol , vol.10 , pp. 5586-5590
    • Wagner, R.W.1    Yoo, C.2    Wrabetz, L.3    Kamholz, J.4    Buchhalter, J.5    Hassan, N.F.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.