Hasil Pencarian - Yue‐Qiu Tan

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  1. 1
    Insight on multiple morphological abnormalities of sperm flagella in male infertility: what is new?

    Insight on multiple morphological abnormalities of sperm flagella in male infertility: what is new? oleh Wei-Li Wang, Chao-Feng Tu, Yue-Qiu Tan

    Diterbitkan 2020-01-01
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  2. 2
    Whole-genome mate-pair sequencing of apparently balanced chromosome rearrangements reveals complex structural variations: two case studies

    Whole-genome mate-pair sequencing of apparently balanced chromosome rearrangements reveals complex structural variations: two case studies oleh Ya-Qi Tan, Yue-Qiu Tan, De-Hua Cheng

    Diterbitkan 2020-05-01
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  3. 3
    Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia

    Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia oleh Yurong Wang, Ling Liu, Chen Tan, Guiquan Meng, Lanlan Meng, Lanlan Meng, Lanlan Meng, Lanlan Meng, Hongchuan Nie, Juan Du, Juan Du, Juan Du, Guang-Xiu Lu, Guang-Xiu Lu, Guang-Xiu Lu, Guang-Xiu Lu, Ge Lin, Ge Lin, Ge Lin, Ge Lin, Wen-Bin He, Wen-Bin He, Wen-Bin He, Wen-Bin He, Wen-Bin He, Yue-Qiu Tan, Yue-Qiu Tan, Yue-Qiu Tan, Yue-Qiu Tan, Yue-Qiu Tan

    Diterbitkan 2022-08-01
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  4. 4
    Risk Factors Affecting Alternate Segregation in Blastocysts From Preimplantation Genetic Testing Cycles of Autosomal Reciprocal Translocations

    Risk Factors Affecting Alternate Segregation in Blastocysts From Preimplantation Genetic Testing Cycles of Autosomal Reciprocal Translocations oleh Pingyuan Xie, Pingyuan Xie, Pingyuan Xie, Liang Hu, Liang Hu, Liang Hu, Liang Hu, Yangqin Peng, Yue-qiu Tan, Yue-qiu Tan, Yue-qiu Tan, Yue-qiu Tan, Keli Luo, Keli Luo, Keli Luo, Keli Luo, Fei Gong, Fei Gong, Fei Gong, Fei Gong, Guangxiu Lu, Guangxiu Lu, Guangxiu Lu, Guangxiu Lu, Ge Lin, Ge Lin, Ge Lin, Ge Lin

    Diterbitkan 2022-06-01
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  5. 5
    Effect of thyroid autoimmunity per se on assisted reproduction treatment outcomes: A meta-analysis

    Effect of thyroid autoimmunity per se on assisted reproduction treatment outcomes: A meta-analysis oleh Hui He, Shuang Jing, Fei Gong, Yue Qiu Tan, Guang Xiu Lu, Ge Lin

    Diterbitkan 2016-04-01
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  6. 6
    In-Frame Variants in STAG3 Gene Cause Premature Ovarian Insufficiency

    In-Frame Variants in STAG3 Gene Cause Premature Ovarian Insufficiency oleh Wen-Juan Xiao, Wen-Bin He, Wen-Bin He, Wen-Bin He, Ya-Xin Zhang, Lan-Lan Meng, Lan-Lan Meng, Guang-Xiu Lu, Guang-Xiu Lu, Guang-Xiu Lu, Ge Lin, Ge Lin, Ge Lin, Yue-Qiu Tan, Yue-Qiu Tan, Yue-Qiu Tan, Juan Du, Juan Du, Juan Du

    Diterbitkan 2019-11-01
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  7. 7
    A novel loss-of-function variant in PNLDC1 inducing oligo-astheno-teratozoospermia and male infertility

    A novel loss-of-function variant in PNLDC1 inducing oligo-astheno-teratozoospermia and male infertility oleh Si-Yi Zhao, Lan-Lan Meng, Zhao-Li Du, Yue-Qiu Tan, Wen-Bin He, Xiong Wang

    Diterbitkan 2023-01-01
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  8. 8
    Maternal interchromosomal insertional translocation leading to 1q43-q44 deletion and duplication in two siblings

    Maternal interchromosomal insertional translocation leading to 1q43-q44 deletion and duplication in two siblings oleh Aixiang Luo, Dehua Cheng, Shimin Yuan, Haiyu Li, Juan Du, Yang Zhang, Chuanchun Yang, Ge Lin, Wenyong Zhang, Yue-Qiu Tan

    Diterbitkan 2018-04-01
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  9. 9
    A rare polypyrimidine tract mutation in the androgen receptor gene results in complete androgen insensitivity syndrome

    A rare polypyrimidine tract mutation in the androgen receptor gene results in complete androgen insensitivity syndrome oleh Shi-Min Yuan, Huan Huang, Chao-Feng Tu, Juan Du, Da-Bao Xu, Ge Lin, Guang-Xiu Lu, Yue-Qiu Tan

    Diterbitkan 2018-01-01
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  10. 10
    DRC3 is an assembly adapter of the nexin-dynein regulatory complex functional components during spermatogenesis in humans and mice

    DRC3 is an assembly adapter of the nexin-dynein regulatory complex functional components during spermatogenesis in humans and mice oleh Shushu Zhou, Shimin Yuan, Jintao Zhang, Lanlan Meng, Xin Zhang, Siyu Liu, Guangxiu Lu, Ge Lin, Mingxi Liu, Yue-Qiu Tan

    Diterbitkan 2023-01-01
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  11. 11
    Novel homozygous variants in TTC12 cause male infertility with asthenoteratozoospermia owing to dynein arm complex and mitochondrial sheath defects in flagella

    Novel homozygous variants in TTC12 cause male infertility with asthenoteratozoospermia owing to dynein arm complex and mitochondrial sheath defects in flagella oleh Lanlan Meng, Lanlan Meng, Qiang Liu, Qiang Liu, Chen Tan, Xilin Xu, Xilin Xu, Wenbin He, Wenbin He, Tongyao Hu, Chaofeng Tu, Chaofeng Tu, Yong Li, Juan Du, Juan Du, Qianjun Zhang, Qianjun Zhang, Qianjun Zhang, Guangxiu Lu, Guangxiu Lu, Guangxiu Lu, Li-Qing Fan, Li-Qing Fan, Li-Qing Fan, Ge Lin, Ge Lin, Ge Lin, Hongchuan Nie, Huan Zhang, Huan Zhang, Yue-Qiu Tan, Yue-Qiu Tan, Yue-Qiu Tan

    Diterbitkan 2023-06-01
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  12. 12
    Inner cell mass incarceration in 8-shaped blastocysts does not increase monozygotic twinning in preimplantation genetic diagnosis and screening patients.

    Inner cell mass incarceration in 8-shaped blastocysts does not increase monozygotic twinning in preimplantation genetic diagnosis and screening patients. oleh Yi-Fan Gu, Qin-Wei Zhou, Shuo-Ping Zhang, Chang-Fu Lu, Fei Gong, Yue-Qiu Tan, Guang-Xiu Lu, Ge Lin

    Diterbitkan 2018-01-01
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  13. 13
    Novel loss‐of‐function mutation in MCM8 causes premature ovarian insufficiency

    Novel loss‐of‐function mutation in MCM8 causes premature ovarian insufficiency oleh Ya‐Xin Zhang, Wen‐Bin He, Wen‐Juan Xiao, Lan‐Lan Meng, Chen Tan, Juan Du, Guang‐Xiu Lu, Ge Lin, Yue‐Qiu Tan

    Diterbitkan 2020-04-01
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  14. 14
    A novel homozygous frameshift mutation in MNS1 associated with severe oligoasthenoteratozoospermia in humans

    A novel homozygous frameshift mutation in MNS1 associated with severe oligoasthenoteratozoospermia in humans oleh Yong Li, Wei-Li Wang, Chao-Feng Tu, Lan-Lan Meng, Tong-Yao Hu, Juan Du, Ge Lin, Hong-Chuan Nie, Yue-Qiu Tan

    Diterbitkan 2021-01-01
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  15. 15
    Expanded carrier screening and preimplantation genetic diagnosis in a couple who delivered a baby affected with congenital factor VII deficiency

    Expanded carrier screening and preimplantation genetic diagnosis in a couple who delivered a baby affected with congenital factor VII deficiency oleh Wen-Bin He, Yue-Qiu Tan, Xiao Hu, Wen Li, Bo Xiong, Ke-Li Luo, Fei Gong, Guang-Xiu Lu, Ge Lin, Juan Du

    Diterbitkan 2018-01-01
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  16. 16
    A novel FAM83H variant causes familial amelogenesis imperfecta with incomplete penetrance

    A novel FAM83H variant causes familial amelogenesis imperfecta with incomplete penetrance oleh Rui‐Qi Bai, Wen‐Bin He, Qian Peng, Su‐Hui Shen, Qian‐Qian Yu, Juan Du, Yue‐Qiu Tan, Yue‐Hong Wang, Bin‐Jie Liu

    Diterbitkan 2022-04-01
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  17. 17
    Sperm flagellar 2 (SPEF2) is essential for sperm flagellar assembly in humans

    Sperm flagellar 2 (SPEF2) is essential for sperm flagellar assembly in humans oleh Dong-Yan Li, Xiao-Xuan Yang, Chao-Feng Tu, Wei-Li Wang, Lan-Lan Meng, Guang-Xiu Lu, Yue-Qiu Tan, Qian-Jun Zhang, Juan Du

    Diterbitkan 2022-01-01
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  18. 18
    Loss-of-function CFTR p.G970D missense mutation might cause congenital bilateral absence of the vas deferens and be associated with impaired spermatogenesis

    Loss-of-function CFTR p.G970D missense mutation might cause congenital bilateral absence of the vas deferens and be associated with impaired spermatogenesis oleh Jian-Wen Hou, Xiao-Liang Li, Li Wang, Cong-Ling Dai, Na Li, Xiao-Hui Jiang, Yue-Qiu Tan, Er-Po Tian, Qin-Tong Li, Wen-Ming Xu

    Diterbitkan 2023-01-01
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  19. 19
    Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature

    Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature oleh Haiyu Li, Juan Du, Wen Li, Dehua Cheng, Wenbin He, Duo Yi, Bo Xiong, Shimin Yuan, Chaofeng Tu, Lanlan Meng, Aixiang Luo, Ge Lin, Guangxiu Lu, Yue-Qiu Tan

    Diterbitkan 2018-02-01
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  20. 20
    Novel mutations of PKD genes in Chinese patients suffering from autosomal dominant polycystic kidney disease and seeking assisted reproduction

    Novel mutations of PKD genes in Chinese patients suffering from autosomal dominant polycystic kidney disease and seeking assisted reproduction oleh Wen-Bin He, Wen-Juan Xiao, Yue-Qiu Tan, Xiao-Meng Zhao, Wen Li, Qian-Jun Zhang, Chang-Gao Zhong, Xiu-Rong Li, Liang Hu, Guang-Xiu Lu, Ge Lin, Juan Du

    Diterbitkan 2018-10-01
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