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Journal Abstract Search

256 related items for PubMed ID: 24781643

  • 1. Splicing mutation in MVK is a cause of porokeratosis of Mibelli.
    Zeng K, Zhang QG, Li L, Duan Y, Liang YH.
    Arch Dermatol Res; 2014 Oct; 306(8):749-55. PubMed ID: 24781643
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  • 2. Detection of a novel missense mutation in the mevalonate kinase gene in one Chinese family with DSAP.
    Lu WS, Zheng XD, Yao XH, Zhang LF, Hu B, Lu YJ.
    Int J Clin Exp Pathol; 2014 Oct; 7(2):728-32. PubMed ID: 24551296
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  • 6. Exome sequencing identifies MVK mutations in disseminated superficial actinic porokeratosis.
    Zhang SQ, Jiang T, Li M, Zhang X, Ren YQ, Wei SC, Sun LD, Cheng H, Li Y, Yin XY, Hu ZM, Wang ZY, Liu Y, Guo BR, Tang HY, Tang XF, Ding YT, Wang JB, Li P, Wu BY, Wang W, Yuan XF, Hou JS, Ha WW, Wang WJ, Zhai YJ, Wang J, Qian FF, Zhou FS, Chen G, Zuo XB, Zheng XD, Sheng YJ, Gao JP, Liang B, Li P, Zhu J, Xiao FL, Wang PG, Cui Y, Li H, Liu SX, Gao M, Fan X, Shen SK, Zeng M, Sun GQ, Xu Y, Hu JC, He TT, Li YR, Yang HM, Wang J, Yu ZY, Zhang HF, Hu X, Yang K, Wang J, Zhao SX, Zhou YW, Liu JJ, Du WD, Zhang L, Xia K, Yang S, Wang J, Zhang XJ.
    Nat Genet; 2012 Oct; 44(10):1156-60. PubMed ID: 22983302
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  • 9. Clonal Expansion of Second-Hit Cells with Somatic Recombinations or C>T Transitions Form Porokeratosis in MVD or MVK Mutant Heterozygotes.
    Kubo A, Sasaki T, Suzuki H, Shiohama A, Aoki S, Sato S, Fujita H, Ono N, Umegaki-Arao N, Kawai T, Nakabayashi K, Hata K, Yamada D, Matsubara Y, Kosaki K, Amagai M.
    J Invest Dermatol; 2019 Dec; 139(12):2458-2466.e9. PubMed ID: 31207227
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  • 14. Mutation Analysis of the MVD Gene in a Chinese Family with Disseminated Superficial Actinic Porokeratosis and a Chinese Literature Review.
    Qian W, Wu J, Tang H, Zhen Q, Ge H, Gao J, Chen J, Chang Y, Wang W, Sun L.
    Indian J Dermatol; 2021 Dec; 66(2):126-131. PubMed ID: 34188266
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  • 16. A novel non-frameshift deletion in MVK gene responsible for disseminated superficial actinic porokeratosis in one Chinese family.
    Li CX, Sun SL, Liang JY, Yuan YQ, Zhang SQ, Chen PJ, Zeng K, Xie XF, Zhang XB.
    J Eur Acad Dermatol Venereol; 2017 Nov; 31(11):e510-e512. PubMed ID: 28543715
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  • 18. Mutations in mevalonate pathway genes in patients with familial or sporadic porokeratosis.
    Leng Y, Yan L, Feng H, Chen C, Wang S, Luo Y, Cao L.
    J Dermatol; 2018 Jul; 45(7):862-866. PubMed ID: 29722423
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