中南大学涂超峰

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特聘副教授
所在单位：基础医学院
学历：研究生(博士)毕业
性别：男
学位：博士学位
在职信息：在职
毕业院校：中南大学

论文成果

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[1]He J, Liu Q, Wang W, Su L, Meng L, Tan C, Zhang H, Zhang Q, Lu G, Du J, Lin G, Tu C, Tan YQ. Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype. Clin Genet. 2023 Apr;103(4):495-497.
[2]Li Y, Li Y, Wang Y, Meng L, Tan C, Du J, Tan YQ, Nie H, Zhang Q, Lu G, Lin G, Li H, Zhang H, Tu C. Identification of novel biallelic LRRC6 variants in male Chinese patients with primary ciliary dyskinesia and infertility. J Assist Reprod Genet. 2023 Jan;40(1):41-51.
[3]Liu C, Si W, Tu C, Tian S, He X, Wang S, Yang X, Yao C, Li C, Kherraf ZE, Ye M, Zhou Z, Ma Y, Gao Y, Li Y, Liu Q, Tang S, Wang J, Saiyin H, Zhao L, Yang L, Meng L, Chen B, Tang D, Zhou Y, Wu H, Lv M, Tan C, Lin G, Kong Q, Shi H, Su Z, Li Z, Yao YG, Jin L, Zheng P, Ray PF, Tan YQ, Cao Y, Zhang F. Deficiency of primate-specific SSX1 induced asthenoteratozoospermia in infertile men and cynomolgus monkey and tree shrew models. Am J Hum Genet. 2023 Mar 2;110(3):516-530.
[4]He J, Su L, Wang W, Li Y, Meng L, Tan C, Lin G, Tan YQ, Zhang Q, Tu C. C9orf131 and C10orf120 are not essential for male fertility in humans or mice. Dev Biol. 2023 May;497:11-17.
[5]Wang W, Meng L, He J, Su L, Li Y, Tan C, Xu X, Nie H, Zhang H, Du J, Lu G, Luo M, Lin G, Tu C, Tan YQ. Bi-allelic variants in SHOC1 cause non-obstructive azoospermia with meiosis arrest in humans and mice. Mol Hum Reprod. 2022 May 27;28(6):gaac015.
[6]Tu C, Wen J, Wang W, Zhu Q, Chen Y, Cheng J, Li Z, Meng L, Li Y, He W, Tan C, Xie C, Fu SM, Du J, Lu G, Lin G, Gou LT, Tan YQ. Loss-of-function variants in human C12orf40 cause male infertility by blocking meiotic progression. Cell Discov. 2023 Aug 22;9(1):87.
[7]Wang W, Su L, Meng L, He J, Tan C, Yi D, Cheng D, Zhang H, Lu G, Du J, Lin G, Zhang Q, Tu C, Tan YQ. Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia. Hum Reprod. 2023 Jul 5;38(7):1399-1411.
[8]Wang R, Yang D, Tu C, Lei C, Ding S, Guo T, Wang L, Liu Y, Lu C, Yang B, Ouyang S, Gong K, Tan Z, Deng Y, Tan Y, Qing J, Luo H. Dynein axonemal heavy chain 10 deficiency causes primary ciliary dyskinesia in humans and mice. Front Med. 2023 Jun 13. doi: 10.1007/s11684-023-0988-8.
[9]Liu C, Tu C, Wang L, Wu H, Houston BJ, Mastrorosa FK, Zhang W, Shen Y, Wang J, Tian S, Meng L, Cong J, Yang S, Jiang Y, Tang S, Zeng Y, Lv M, Lin G, Li J, Saiyin H, He X, Jin L, Touré A, Ray PF, Veltman JA, Shi Q, O'Bryan MK, Cao Y, Tan YQ, Zhang F..Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility.Am J Hum Genet, 2021, 108 (2) : 309-323.
[10]Tu C, Cong J, Zhang Q, He X, Zheng R, Yang X, Gao Y, Wu H, Lv M, Gu Y, Lu S, Liu C, Tian S, Meng L, Wang W, Tan C, Nie H, Li D, Zhang H, Gong F, Hu L, Lu G, Xu W, Lin G, Zhang F, Cao Y, Tan YQ.Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice.Am J Hum Genet, 2021, 108 (8) : 1466-1477.
[11]Tu C, Tan YQ, Li H, Liu X, Wang Y, Li W, Meng L, Wang W, Li Y, Li D, Du J, Lu G, Lin G.TDRD7 participates in lens development and spermiogenesis by mediating autophagosome maturation.Autophagy, 2021, 17 (11) : 3848-3864.
[12]Guo T, Tu CF, Yang DH, Ding SZ, Lei C, Wang RC, Liu LV, Kang X, Shen XQ, Yang YF, Tan ZP, Tan YQ, Luo H.Biallelic BRWD1 variants cause male infertility with asthenoteratozoospermia and likely primary ciliary dyskinesia.Hum Genet, 2021, 140 (5) : 761-773.
[13]Tu C, Wang W, Hu T, Lu G, Lin G, Tan YQ.Genetic underpinnings of asthenozoospermia.Best Pract Res Cl En, 2020, 34 (6) : 101472.
[14]Tu C, Wang Y, Nie H, Meng L, Wang W, Li Y, Li D, Zhang H, Lu G, Lin G, Tan YQ, Du J.An M1AP homozygous splice-site mutation associated with severe oligozoospermia in a consanguineous family.Clin Genet, 2020, 97 (5) : 741-746.
[15]Wang Y, Tu C, Nie H, Meng L, Li D, Wang W, Zhang H, Lu G, Lin G, Tan YQ, Du J.Novel DNAAF6 variants identified by whole-exome sequencing cause male infertility and primary ciliary dyskinesia.J Assist Reprod Genet, 2020, 37 (4) : 811-820.
[16]Tu C, Meng L, Nie H, Yuan S, Wang W, Du J, Lu G, Lin G, Tan YQ.A homozygous RPL10L missense mutation associated with male factor infertility and severe oligozoospermia.Fertil Steril, 2020, 113 (3) : 561-568.
[17]Tu C, Nie H, Meng L, Wang W, Li H, Yuan S, Cheng D, He W, Liu G, Du J, Gong F, Lu G, Lin G, Zhang Q, Tan YQ.Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCD.Hum Genet, 2020, 139 (2) : 257-271.
[18]Wang WL, Tu CF, Tan YQ.Insight on multiple morphological abnormalities of sperm ？agella in male infertility: what’s new?.Asian J Androl, 2019, 22 (3) : 236-245.
[19]Tu C, Nie H, Meng L, Yuan S, He W, Luo A, Li H, Li W, Du J, Lu G, Lin G, Tan YQ.Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagella.Sci Rep, 2019, 9 (1) : 15864.
[20]Tu C, Zeng Z, Qi P, Li X, Guo C, Xiong F, Xiang B, Zhou M, Liao Q, Yu J, Li Y, Li X, Li G, Xiong W.Identification of genomic alterations in nasopharyngeal carcinoma and nasopharyngeal carcinoma-derived Epstein-Barr virus by whole genome sequencing.Carcinogenesis, 2018, 39 (12) : 1517-1528.

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