中南大学杜娟

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研究员
入职时间：2004-07-08
所在单位：基础医学院
学历：博士研究生毕业
性别：女
学位：博士学位
在职信息：在职

论文成果

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[1]Yang Q, Wu L, Song K, Lin G, Wang X, Zhou Y, Sun C, Zhang F, Du J*, He L, Zhang Z, Zhou D.Conversion of Fibroblasts to Neural Cells by p53 Depletion[J].Cell Rep, 2014, 9 (6) : 2034-2042.
[2]Lu GX, Li SF, Pan Y, Zou X, Du J*.Non-invasive prenatal molecular detection of a fetal point mutation for congenital adrenal hyperplasia using co-amplification at lower denaturation temperature PCR[J].Chin Med J(Engl), 2010, 123 (22) : 3343-3349.
[3]Du J*, Lin G, Lu G, Tan Y, Yuan S, Zhang Q, Li W, Zhao X, Ma N, Chen J.A rare deep intronic mutation of PKHD1 gene, c.8798-459 c>A, causes autosomal recessive polycystic kidney disease by pseudoexon activation[J].J Hum Genet, 2019, 64 (3) : 207-214.
[4]Lin G, Du J*, Lu G, Chen Y, Chen J, Lu C, Dai J, Zhang S, Cai S, Tan Y, Gong F, Hu L, Dai C.ZP2 pathogenic variants cause in vitro fertilization failure and female infertility[J].Genet Med, 2019, 21 (2) : 431-440.
[5]Du J*, Lin G, Lu GX, Hu L, Li XR, Zhong CG, Zhang QJ, Li W, Zhao XM, Tan YQ, Xiao WJ, He WB.Novel mutations of PKD genes in Chinese patients suffering from autosomal dominant polycystic kidney disease and seeking assisted reproduction[J].BMC Med Genet, 2018, 19: 186-198.
[6]Du J, Lin G, Lu GX, Gong F, Luo KL, Xiong B, Li W, Hu X, Tan YQ, He WB.Expanded carrier screening and preimplantation genetic diagnosis in a couple who delivered a baby affected with congenital factor VII deficiency[J].BMC Med Genet, 2018, 19 (1) : 15-21.
[7]Lu GX, Du J, Chen TJ.Cell growth arrest and apoptosis induced by Oct4 or nanog knockdown in mouse embryonic stem cells: a possible role of Trp53.Mol Biol Rep, 2012, 39: 1855-1861.
[8]Lu GX, Xiong B, Zhou X, Chen TJ, Du J*.Dppa2 knockdown-induced differentiation and repressed proliferation of mouse embryonic stem cells[J].J Biochem, 2010, 147 (2) : 265-271.
[9]Du J*, Tan YQ, Lin G, Lu GX, Meng LL, Zhang YX, He WB, Xiao WJ.In-Frame variants in STAG3 gene cause premature ovarian insufficiency[J].Front Genet, 2019

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