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feng yongjun
(68 results)?
Functional analysis of a SOX10 gene mutation associated with Waardenburg syndrome II.
Biochem Biophys Res Commun. 2017 Nov 4;493(1):258-262. doi: 10.1016/j.bbrc.2017.09.034. Epub 2017 Sep 9.
Biochem Biophys Res Commun. 2017.
PMID: 28893539
ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss.
Li W, Sun J, Ling J, Li J, He C, Liu Y, Chen H, Men M, Niu Z, Deng Y, Li M, Li T, Wen J, Sang S, Li H, Wan Z, Richard EM, Chapagain P, Yan D, Liu XZ, Mei L, Feng Y.
Li W, et al.
Hum Genet. 2018 Apr;137(4):329-342. doi: 10.1007/s00439-018-1885-0. Epub 2018 Apr 30.
Hum Genet. 2018.
PMID: 29713870
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Wnt signaling pathway involvement in genotypic and phenotypic variations in Waardenburg syndrome type 2 with MITF mutations.
Wang XP, Liu YL, Mei LY, He CF, Niu ZJ, Sun J, Zhao YL, Feng Y, Zhang H.
Wang XP, et al.
J Hum Genet. 2018 May;63(5):639-646. doi: 10.1038/s10038-018-0425-z. Epub 2018 Mar 12.
J Hum Genet. 2018.
PMID: 29531335
Free PMC article.
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Safety and efficacy of sorafenib therapy in patients with hepatocellular carcinoma: final outcome from the Chinese patient subset of the GIDEON study.
Ye SL, Chen X, Yang J, Bie P, Zhang S, Liu F, Liu L, Zhou J, Dou K, Hao C, Shao G, Xia Q, Chen Y, Yang J, Deng X, Liu Y, Yuan Y, Fu Z, Nakajima K, Yip CS, Lu Z.
Ye SL, et al.
Oncotarget. 2016 Feb 9;7(6):6639-48. doi: 10.18632/oncotarget.6781.
Oncotarget. 2016.
PMID: 26735891
Free PMC article.
Clinical Trial.
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