近期论文
查看导师新发文章
（温馨提示：请注意重名现象，建议点开原文通过作者单位确认）
*: corresponding；#: co-first
Wang L#, Li M#, Qu C, Miao W, Yin Q, Liao J, Cao H, Huang M, Wang K, Zuo E, Peng G, Zhang S, Chen G, Li Q, Tang K, Yu Q, Li Z, Wong C, Xu G, Jing N, Yu X*, Li J*. CRISPR-Cas9-mediated genome editing in one blastomere of two-cell embryos reveals a novel Tet3 function in regulating neocortical development. Cell Research, 2017, 27:815-829.
Wang L#, Zhang Y#, Fu X#, Dong S#, Tang S, Zhang N, Song C, Yang N, Zhang L, Wang H, Shi H, Jin L, Zhang F*, Li J*, Hua K*. Joint utilization of genetic analysis and semi-cloning technology reveals a digenic etiology of Müllerian anomalies. Cell Research, 2020, 30:91-94.
Wang Y#, Chen J#, Huang X#, Wu B, Dai P, Zhang F, Li J, Wang L*. Gene-knockout by iSTOP enables rapid reproductive disease modeling and phenotyping in germ cells of the founder generation. SCIENCE CHINA-Life Sciences, 2023, in press, doi:10.1007/s11427-023-2408-2. http://engine.scichina.com/doi/10.1007/s11427-023-2408-2. (*: corresponding author)
Cong J#, Yang Y#, Wang X#, Shen Y#, Qi H#, Liu C, Tang S, Wu S, Tian S, Zhou Y, He X, Wang L*, Liu M*, Zhang F*. Deficiency of X-linked TENT5D causes male infertility by disrupting the mRNA stability during spermatogenesis. Cell Discovery, 2022, 8: 23. (*:corresponding authors)
Wang Y#, Huang X#, Sun G, Chen J, Wu B, Luo J, Tang S, Dai P, Zhang F, Li J, Wang L*. Coiled-coil domain-containing 38 is required for acrosome biogenesis and fibrous sheath assembly in mice. Journal of Genetics and Genomics, 2023, doi: 10.1016/j.jgg.2023.09.002. https://doi.org/10.1016/j.jgg.2023.09.002. (*: corresponding author)
Chen J, Wang Y, Wu B, Shi H*, Wang L*. Experimental and molecular support for Cfap70 as a causative gene of Multiple Morphological Abnormalities of the Flagella with male infertility. Biology of Reproduction, 2023, 109(4):450-460, doi: 10.1093/biolre/ioad076. https://doi.org/10.1093/biolre/ioad076. (*: corresponding author)
Meng G#, Wang Y#, Luo C#, Tan Y, Li Y, Tan C, Tu C, Zhang Q, Hu L, Zhang H, Meng L, Liu C, Deng L, Lu G, Lin G, Du J, Tan Y, Sha Y*, Wang L*, He W*. Bi-allelic variants in DNAH3 cause male infertility with asthenoteratozoospermia in humans and mice. Human Reproduction Open, 2024, doi:10.1093/hropen/hoae003. https://doi.org/10.1093/hropen/hoae003. (*: corresponding authors)
Wang L, Li J. Expansion of the mutant monkey through cloning. SCIENCE CHINA-Life Sciences, 2019, 62, 865-867.
Wang L, Li J. ‘Artificial spermatid’-mediated genome editing. Biology of Reproduction, 2019, 101, 538-548.
Zhou Y#, Wang Y#, Chen J, Wu B, Tang S, Zhang F*, Liu C*, Wang L*. Dnali1 is required for sperm motility and male fertility in mice. Basic and Clinical Andrology, 2023, 33:32, doi:10.1186/s12610-023-00205-y. (*: corresponding author)
Zhang X#, Wang L#, Ma Y#, Wang Y#, Liu H#, Liu M#, Qin L#, Li J, Jiang C, Zhang X, Shan X, Liu Y, Li J, Li Y, Zheng R, Sun Y, Sun J, Leng X, Liang Y, Zhang F*, Jiang X*, Yang Y*, Shen Y*. CEP128 is involved in spermatogenesis in humans and mice. Nature Communications, 2022, 13: 1395. (#: co-first authors)
Liu C#, Tu C#, Wang L#, Wu H#, Houston B, Mastrorosa F, Zhang W, Shen Y, Wang J, Shixiong Tian, 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 P, Veltman J, Shi Q, O’Bryan M, Cao Y, Tan Y*, Zhang F*. Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility. American Journal of Human Genetics, 2021, 108:309-323. (#: co-first authors)
Liu C#, He X#, Liu W#, Yang S#, Wang L#, Li W, Wu H, Tang S, Ni X, Wang J, Gao Y, Tian S, Zhang L, Cong J, Zhang Z, Tan Q, Zhang J, Li H, Zhong Y, Lv M, Li J, Jin L, Cao Y*, Zhang F*. Bi-allelic mutations in TTC29 cause male subfertility with asthenoteratospermia in humans and mice. American Journal of Human Genetics, 2019, 105:1168-1181. (#: co-first authors)
Li G#, Yang X#, Wang L#, Pan Y, Chen S, Shang L, Zhang Y, Wu Y, Zhou Z, Chen Q, Zhang X, Zhang L, Wang Y, Li J, Jin L, Wu Y*, Zhang X*, Zhang F*. Haploinsufficiency in non-homologous end joining factor 1 induces ovarian dysfunction in humans and mice. Journal of Medical Genetics, 2022, 59:579–588. (#: co-first authors)
Cong J#, Wang X#, Amiri-Yekta A#, Wang L#, Kherraf Z, Liu C, Cazin C, Tang S, Hosseini S, Tian S, Daneshipour A, Wang J, Zhou Y, Zeng Y, Yang S, He X, Li J, Cao Y,Jin L, Ray P*, Zhang F*. Homozygous mutations in CCDC34 cause male infertility with oligoasthenoteratozoospermia in humans and mice. Journal of Medical Genetics, 2022, 59:710–718. (#: co-first authors)
Dai P#, Wang X#, Gou L#, Li Z#, Wen Z#, Chen Z#, Hua M, Zhong A, Wang L, Su H, Wan H, Qian K, Liao L, Li J, Tian B, Li D, Fu X, Shi H*, Zhou Y*, Liu M*. A translation-activating function of MIWI/piRNA during mouse spermiogenesis. Cell, 2019, 179:1566-1581 e1516.
Ke H#, Tang S#, Guo T#, Hou D, Jiao X, Li S, Luo W, Xu B, Zhao S, Li G, Zhang X, Xu S, Wang L, Wu Y, Wang J, Zhang F*, Qin Y*, Jin L*, Chen Z*. 2023. Landscape of pathogenic mutations in premature ovarian insufficiency. Nature Medicine, 2023, 29(2): 483-492.
Jiang J#, Lv W#, Ye X, Wang L, Zhang M, Yang H, Okuka M, Zhou C, Zhang X, Liu L*, Li J*. Zscan4 promotes genomic stability during reprogramming and dramatically improves the quality of iPS cells as demonstrated by tetraploid complementation. Cell Research, 2013, 23, 92-106.
Liu P, Dou X, Liu C, Wang L, Xing C, Peng G, Chen J, Yu F, Qiao Y, Song L, Wu Y, Yue C, Li J, Han J, Tang K, Jing N. Histone deacetylation promotes mouse neural induction by restricting Nodal-dependent mesendoderm fate. Nature Communications, 2015, 6:6830.
Wang X#, Qiao Y#, Xiao M#, Wang L, Chen J, Lv W, Xu L, Li Y, Wang Y, Tan M, Huang C, Li J, Zhao T, Hou Z*, Jing N*, Chin Y*. Opposing roles of acetylation and phosphorylation in LIFR-dependent self-renewal growth signaling in mouse embryonic stem cells. Cell Reports, 2017, 18: 933-946.
Chen Q, Ke H, Luo X, Wang L, Wu Y, Tang S, Li J, Jin L, Zhang F*, Qin Y*, Chen X*. Rare deleterious BUB1B variants induce premature ovarian insufficiency and early menopause.Human Molecular Genetics, 2020, 29, 2698-2707.
Qu C#, Yan M#, Yang S, Wang L, Yin Q, Liu Y, Chen Y, Li J. Haploid embryonic stem cells can be enriched and maintained by simple filtration. Journal of Biological Chemistry, 2018, 293:5230-5235.
Yang J, Guo R, Wang H, Ye X, Zhou Z, Dan J, Wang H, Gong P, Deng W, Yin Y, Mao S, Wang L, Ding J, Li J, Keefe D, Dawlaty M, Wang J, Xu G, Liu L. Tet enzymes regulate telomere maintenance and chromosomal stability of mouse ESCs. Cell Reports, 2016, 15, 1809-1821.
京公网安备 11010802027423号