يعرض 1 - 10 نتائج من 71 نتيجة بحث عن '"Yuan, Shimin"', وقت الاستعلام: 1.15s تنقيح النتائج
  1. 1
    مؤتمر
    Model Selection - Knowledge Distillation Framework for Model Compression

    المؤلفون: Chen, Renhai, Yuan, Shimin, Wang, Shaobo, Li, Zhenghan, Xing, Meng, Feng, Zhiyong

    المصدر: 2021 IEEE Symposium Series on Computational Intelligence (SSCI) Computational Intelligence (SSCI), 2021 IEEE Symposium Series on. :01-06 Dec, 2021

    Relation: 2021 IEEE Symposium Series on Computational Intelligence (SSCI)

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  2. 2
    دورية أكاديمية
    DRC3 is an assembly adapter of the nexin-dynein regulatory complex functional components during spermatogenesis in humans and mice

    المؤلفون: Zhou, ShushuAff1, Aff2, Yuan, Shimin, Zhang, Jintao, Meng, LanlanAff3, Aff4, Zhang, Xin, Liu, Siyu, Lu, GuangxiuAff3, Aff4, Aff5, Lin, GeAff3, Aff4, Aff5, Liu, MingxiAff6, IDs41392022012934_cor9, Tan, Yue-QiuAff3, Aff4, Aff5, IDs41392022012934_cor10

    المصدر: Signal Transduction and Targeted Therapy. 8(1)

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  3. 3
    دورية أكاديمية
    The de novo aberration rate of prenatal karyotype was comparable between 1496 fetuses conceived via IVF/ICSI and 1396 fetuses from natural conception

    المؤلفون: Yuan, Shimin, Guo, Liuliang, Cheng, Dehua, Li, Xiurong, Hu, Hao, Hu, LiangAff1, Aff2, Aff3, Aff4, Lu, GuangxiuAff1, Aff2, Aff3, Aff4, Lin, GeAff1, Aff2, Aff3, Aff4, Gong, FeiAff1, Aff2, Aff3, Aff4, IDs10815022025005_cor9, Tan, Yue-QiuAff1, Aff2, Aff3, Aff4, IDs10815022025005_cor10

    المصدر: Journal of Assisted Reproduction and Genetics: An Official Journal of the American Society for Reproductive Medicine. 39(7):1683-1689

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  4. 4
    دورية أكاديمية

    لا يتم عرض هذه النتيجة على الضيوف.

    View this record from ISI Web of Science
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  5. 5
    دورية أكاديمية
    Clinical outcomes following preimplantation genetic testing and microdissecting junction region in couples with balanced chromosome rearrangement

    المؤلفون: Cheng, Dehua, Hu, LiangAff1, Aff2, Aff3, Aff4, Aff5, Gong, FeiAff1, Aff2, Aff3, Aff4, Aff5, Yuan, Shimin, Luo, KeliAff1, Aff2, Wu, Xianhong, Xie, Pingyuan, Lu, ChangfuAff1, Aff2, Aff3, Aff4, Lu, GuangxiuAff1, Aff2, Aff3, Aff4, Aff5, Tan, Yue-QiuAff1, Aff2, Aff4, Aff5, Lin, GeAff1, Aff2, Aff3, Aff4, Aff5

    المصدر: Journal of Assisted Reproduction and Genetics: An Official Journal of the American Society for Reproductive Medicine. 38(3):735-742

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  6. 6
    دورية أكاديمية
    The genetic cause of intellectual deficiency and/or congenital malformations in two parental reciprocal translocation carriers and implications for assisted reproduction

    المؤلفون: Cheng, DehuaAff1, Aff2, Yuan, ShiminAff1, Aff2, Hu, LiangAff1, Aff2, Aff3, Aff4, Aff5, Yi, DuoAff1, Aff2, Luo, KeliAff1, Aff2, Gong, FeiAff1, Aff2, Aff3, Aff4, Aff5, Lu, ChangfuAff1, Aff2, Aff3, Aff4, Aff5, Lu, GuangxiuAff1, Aff2, Aff3, Aff4, Aff5, Lin, GeAff1, Aff2, Aff3, Aff4, Aff5, Tan, Yue-QiuAff1, Aff2, Aff3, Aff4, IDs10815020019861_cor10

    المصدر: Journal of Assisted Reproduction and Genetics: An Official Journal of the American Society for Reproductive Medicine. 38(1):243-250

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  7. 7
    دورية أكاديمية
    A homozygous RPL10L missense mutation associated with male factor infertility and severe oligozoospermia

    المؤلفون: Tu, Chaofeng, Meng, Lanlan, Nie, Hongchuan, Yuan, Shimin, Wang, Weili, Du, Juan, Lu, Guangxiu, Lin, Ge, Tan, Yue-Qiu

    المصدر: In Fertility and Sterility March 2020 113(3):561-568

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  8. 8
    دورية أكاديمية
    Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCD

    المؤلفون: Tu, ChaofengAff1, Aff2, Aff3, Aff4, Nie, HongchuanAff1, Aff2, Aff3, Meng, Lanlan, Wang, Weili, Li, Haiyu, Yuan, Shimin, Cheng, DehuaAff1, Aff2, Aff3, He, WenbinAff1, Aff2, Aff3, Liu, GangAff1, Aff2, Aff3, Du, JuanAff1, Aff2, Aff3, Gong, FeiAff1, Aff2, Aff3, Lu, GuangxiuAff2, Aff3, Aff4, Lin, GeAff1, Aff2, Aff3, Aff4, Zhang, QianjunAff1, Aff2, Aff3, Tan, Yue-QiuAff1, Aff2, Aff3

    المصدر: Human Genetics. 139(2):257-271

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  9. 9
    دورية أكاديمية
    Analysis of molecular cytogenetic features and PGT-SR for two infertile patients with small supernumerary marker chromosomes

    المؤلفون: Cheng, DehuaAff1, Aff2, Aff3, Yuan, Shimin, Yi, Duo, Luo, KeliAff1, Aff2, Aff3, Xu, Fang, Gong, FeiAff1, Aff2, Aff3, Aff4, Lu, ChangfuAff1, Aff2, Aff3, Aff4, Lu, GuangxiuAff1, Aff2, Aff3, Aff4, Lin, GeAff1, Aff2, Aff3, Aff4, Tan, Yue-QiuAff1, Aff2, Aff3, Aff4

    المصدر: Journal of Assisted Reproduction and Genetics: An Official Journal of the American Society for Reproductive Medicine. 36(12):2533-2539

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  10. 10
    دورية أكاديمية
    Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humans

    المؤلفون: Tan, Yue-QiuAff1, Aff2, Aff3, Tu, ChaofengAff1, Aff3, Meng, LanlanAff1, Aff3, Yuan, ShiminAff1, Aff3, Sjaarda, Calvin, Luo, AixiangAff1, Aff3, Du, JuanAff1, Aff2, Aff3, Li, WenAff1, Aff2, Aff3, Gong, FeiAff1, Aff2, Aff3, Zhong, ChanggaoAff1, Aff2, Aff3, Deng, Han-Xiang, Lu, Guangxiu, Liang, PingAff4, Lin, GeAff1, Aff2, Aff3

    المصدر: Genetics in Medicine: Official journal of the American College of Medical Genetics and Genomics. 21(5):1209-1217

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