Biblio

Author Title Type [ Year(Asc)]
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2019
Xiao, N., He, K., Gong, F., Xie, Q., Peng, J., Su, X., Lu, Y., Xia, X., Lin, G., and Cheng, L. (2019). Altered subsets and activities of B lymphocytes in polycystic ovary syndrome.J Allergy Clin Immunol.
Wang, H., Meng, L., Li, W., Du, J., Tan, Y., Gong, F., Lu, G., Lin, G., and Zhang, Q. (2019). Combinations of exonic deletions and rare mutations lead to misdiagnosis of propionic acidemia.Clin Chim Acta.
Liu, L., Leng, L., Liu, C., Lu, C., Yuan, Y., Wu, L., Gong, F., Zhang, S., Wei, X., Wang, M., et al. (2019). An integrated chromatin accessibility and transcriptome landscape of human pre-implantation embryos.Nat Commun10, 364.
He, H., Jing, S., Lu, C.Fu, Tan, Y.Qiu, Luo, K.Li, Zhang, S.Ping, Gong, F., Lu, G.Xiu, and Lin, G. (2019). Neonatal outcomes of live births after blastocyst biopsy in preimplantation genetic testing cycles: a follow-up of 1,721 children.Fertil Steril.
Xie, P., Hu, L., Tan, Y., Gong, F., Zhang, S., Xiong, B., Peng, Y., Lu, G.Xiu, and Lin, G. (2019). Retrospective analysis of meiotic segregation pattern and interchromosomal effects in blastocysts from inversion preimplantation genetic testing cycles.Fertil Steril.
Dai, C., Chen, Y., Hu, L., Du, J., Gong, F., Dai, J., Zhang, S., Wang, M., Chen, J., Guo, J., et al. (2019). ZP1 mutations are associated with empty follicle syndrome: evidence for the existence of an intact oocyte and a zona pellucida in follicles up to the early antral stage. A case report.Hum Reprod.
2018
Zhou, Q.-W., Jing, S., Xu, L., Guo, H., Lu, C.-F., Gong, F., Lu, G.-X., Lin, G., and Gu, Y.-F. (2018). Clinical and neonatal outcomes of patients of different ages following transfer of thawed cleavage embryos and blastocysts cultured from thawed cleavage-stage embryos.Plos One13, e0207340.
Li, Y., Huang, C., Zha, L., Kong, M., Yang, Q., Zhu, Y., Peng, Y., Ouyang, Q., Lu, G., Lin, G., et al. (2018). Generation of NERCe003-A-3, a p53 compound heterozygous mutation human embryonic stem cell line, by CRISPR/Cas9 editing.Stem Cell Res34, 101371.
Meng, L., Tu, C., Lu, G., Lin, G., and Tan, Y. (2018). Novel biallelic PCNT deletion causing microcephalic osteodysplastic primordial dwarfism type II with congenital heart defect.Sci China Life Sci.
Zhang, Y.-X., Li, H.-Y., Bin He, W.-, Tu, C., Du, J., Li, W., Lu, G.-X., Lin, G., Yang, Y., and Tan, Y.-Q. (2018). XRCC2 mutation causes premature ovarian insufficiency as well as non-obstructive azoospermia in humans.Clin Genet.
2016
Ouyang, Y., Tan, Y., Yi, Y., Gong, F., Lin, G., Li, X., and Lu, G. (2016). Correlation between chromosomal distribution and embryonic findings on ultrasound in early pregnancy loss after IVF-embryo transfer.Hum Reprod.
Xie, P., Ouyang, Q., Leng, L., Hu, L., Cheng, D., Tan, Y., Lu, G., and Lin, G. (2016). The dynamic changes of X chromosome inactivation during early culture of human embryonic stem cells.Stem Cell Res17, 84-92.
Zhang, S., Luo, K., Cheng, D., Tan, Y., Lu, C., He, H., Gu, Y., Lu, G., Gong, F., and Lin, G. (2016). The number of biopsied trophectoderm cells is likely to affect the implantation potential of blastocysts with poor trophectoderm quality.Fertil Steril.
2015
Leng, L., Tan, Y., Gong, F., Hu, L., Ouyang, Q., Zhao, Y., Lu, G., and Lin, G. (2015). Differentiation of primordial germ cells from induced pluripotent stem cells of primary ovarian insufficiency.Hum Reprod.
To, K.K.W., Poon, D.C., Wei, Y., Wang, F., Lin, G., and Fu, L. (2015). Pelitinib (EKB-569) targets the upregulation of ABCB1 and ABCG2 under hyperthermia to eradicate lung cancer.Br J Pharmacol.
2014
Han, X.-H., Wang, C.-L., Xie, Y., Ma, J., Zhang, X.-H., Hu, Q.-W., Lin, G., Liu, S., and Lu, J.-G. (2014). Anti-metastatic effect and mechanisms of Wenshen Zhuanggu formula in Human breast Cancer cells.J Ethnopharmacol.
Xu, F., Zhang, Y.-N., Cheng, D.-H., Tan, K., Zhong, C.-G., Lu, G.-X., Lin, G., and Tan, Y.-Q. (2014). The first patient with a pure 1p36 microtriplication associated with severe clinical phenotypes.Mol Cytogenet7, 64.