Search Results - "Cui, Yingxia"

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  1. 1

    The susceptibility of FSHB -211G > T and FSHR G-29A, 919A > G, 2039A > G polymorphisms to men infertility: an association study and meta-analysis by Wu, Qiuyue, Zhang, Jing, Zhu, Peiran, Jiang, Weijun, Liu, Shuaimei, Ni, Mengxia, Zhang, Mingchao, Li, Weiwei, Zhou, Qing, Cui, Yingxia, Xia, Xinyi

    Published in BMC medical genetics (01-08-2017)
    “…Male infertility is a complex disorder caused by genetic, developmental, endocrine, or environmental factors as well as unknown etiology. Polymorphisms in the…”
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    Journal Article
  2. 2

    Long-Term Effects of Phytoestrogen Daidzein on Penile Cavernosal Structures in Adult Rats by Huang, Yufeng, Pan, Lianjun, Xia, Xinyi, Feng, Yao, Jiang, Chunxia, Cui, Yingxia

    Published in Urology (Ridgewood, N.J.) (01-07-2008)
    “…Objectives Daidzein is a soy isoflavone with estrogenic activity present in plant-based food items and health foods and used as an alternative therapy for…”
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    Journal Article
  3. 3

    Exposure of Juvenile Rats to the Phytoestrogen Daidzein Impairs Erectile Function in a Dose-Related Manner in Adulthood by Pan, Lianjun, Xia, Xinyi, Feng, Yao, Jiang, Chunxia, Cui, Yingxia, Huang, Yufeng

    Published in Journal of andrology (01-01-2008)
    “…Health benefits of isoflavones such as genistein and daidzein have led to an increasing interest in consuming soybeans or soy‐containing food. However,…”
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    Journal Article
  4. 4

    Identification of novel mutations and risk assessment of Han Chinese patients with autosomal dominant polycystic kidney disease by Zhang, Mingchao, Liu, Shuaimei, Xia, Xinyi, Cui, Yingxia, Li, Xiaojun

    Published in Nephrology (Carlton, Vic.) (01-05-2019)
    “…ABSTRACT Aim Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary renal disease in humans and is caused by mutations in the PKD1…”
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    Journal Article
  5. 5

    Combinatorial test cases with constraints in software systems by Longshu Li, Yingxia Cui, Yun Yang

    “…Combinatorial testing has become an important approach in software testing, and many algorithms have been developed for generating combinatorial test cases…”
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    Conference Proceeding
  6. 6

    The P20R mutation of αB-crystallin diminishes its anti-apoptotic activity in human lens epithelial cells by Zhu, Peiran, Li, Weiwei, Ni, Mengxia, Zhang, Cui, Liu, Shuaimei, Wu, Qiuyue, Jiang, Weijun, Zhang, Jing, Zhang, Mingchao, Li, Xiaojun, Cui, Yingxia, Xue, Chunyan, Xia, Xinyi

    “…αB-crystallin acts as an anti-apoptosis protein in human lens epithelial (HLE) cells. We recently identified a missense mutation in αB-crystallin that changes…”
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    Journal Article
  7. 7

    Polymorphisms of protamine genes contribute to male infertility susceptibility in the Chinese Han population by Jiang, Weijun, Zhu, Peiran, Zhang, Jing, Wu, Qiuyue, Li, Weiwei, Liu, Shuaimei, Ni, Mengxia, Yu, Maomao, Cao, Jin, Li, Yi, Cui, Yingxia, Xia, Xinyi

    Published in Oncotarget (22-09-2017)
    “…Protamine (PRM) plays important roles in the packaging of DNA within the sperm nucleus. To investigate the role of and transition protein 1 ( ) polymorphisms…”
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    Journal Article
  8. 8

    A New Strategy for Pairwise Test Case Generation by Yingxia Cui, Longshu Li, Sheng Yao

    “…Pairwise testing has become an important approach to software testing because it often provides effective error detection at low cost, and a key problem of it…”
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    Conference Proceeding
  9. 9

    The effect of induced anti-follicle-stimulating hormone autoantibody on serum hormone level and apoptosis in rat testis by Yao, Bing, Yi, Nan, Zhou, Shuigen, OuYang, Weiming, Xu, Huiru, Ge, Yifeng, Cui, Yingxia, Xia, Xinyi

    Published in Life sciences (1973) (21-08-2012)
    “…Anti-follicle-stimulating hormone (FSH) autoantibody was found to highly correlate with oligospermia and asthenospermia, but the actual effect of FSH…”
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    Journal Article
  10. 10

    Meiotic Chromosome Behavior in a Human Male t(8;15) Carrier by Jiang, Hanwei, Wang, Liu, Cui, Yingxia, Xu, Zhipeng, Guo, Tonghang, Cheng, Dongkai, Xu, Peng, Yu, Wen, Shi, Qinghua

    Published in Journal of genetics and genomics (20-03-2014)
    “…Reciprocal translocation is one of the most common structural chromosomal rearrangements in human beings; it is widely recognized to be associated with male…”
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    Journal Article
  11. 11

    Inclusion-Based Multi-level Pointer Analysis by Yingxia Cui, Longshu Li, Sheng Yao

    “…A novel approach for points-to information analysis is presented, which can deal with not only the single dereferenced pointers, but also the multiple…”
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    Conference Proceeding
  12. 12

    Prenatal diagnosis and genetic counseling in a fetus associated with risk of Angelman syndrome with a small supernumerary marker chromosome derived from chromosome 22 by Hu, Yu-An, Cui, Yingxia, Fan, Xiaobo, Wu, Qiuyue, Li, Weiwei, Wang, Weiping

    Published in Molecular cytogenetics (03-05-2016)
    “…Angelman syndrome (AS) is a neurodevelopmental disorder. AS patients concomitant with sSMC are rather rare events. It will provide more useful and proper…”
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    Journal Article
  13. 13

    Meiotic prophase I defects in an oligospermic man with Wolf-Hirschhorn syndrome with ring chromosome 4 by Yao, Qi, Wang, Liu, Yao, Bing, Gao, Hongliu, Li, Weiwei, Xia, Xinyi, Shi, Qinghua, Cui, Yingxia

    Published in Molecular cytogenetics (01-07-2014)
    “…Ring chromosomes are often associated with spermatogenetic failure. However, the mechanism is poorly understood. We here reported a single man with severe…”
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    Journal Article
  14. 14
  15. 15

    Meiotic Chromosome Behavior in a Human Male t(8;15) Carrier by Hanwei Jiang Liu Wang Yingxia Cui Zhipeng Xu Tonghang Guo Dongkai Cheng Peng Xu Wen Yu Qinghua Shi

    Published in 遗传学报:英文版 (2014)
    “…Reciprocal translocation is one of the most common structural chromosomal rearrangements in human beings; it is widely recognized to be associated with male…”
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    Journal Article
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    Prenatal diagnosis and genetic counseling in a fetus associated with risk of Angelman syndrome with a small supernumerary marker chromosome derived from chromosome 22 by Hu, Yu-An, Cui, Yingxia, Fan, Xiaobo, Wu, Qiuyue, Li, Weiwei, Wang, Weiping

    Published in Molecular cytogenetics (01-01-2016)
    “…BACKGROUNDAngelman syndrome (AS) is a neurodevelopmental disorder. AS patients concomitant with sSMC are rather rare events. It will provide more useful and…”
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    Report
  19. 19

    Meiotic prophase I defects in an oligospermic man with Wolf-Hirschhorn syndrome with ring chromosome 4 by Yao, Qi, Wang, Liu, Yao, Bing, Gao, Hongliu, Li, Weiwei, Xia, Xinyi, Shi, Qinghua, Cui, Yingxia

    Published in Molecular cytogenetics (01-01-2014)
    “…BACKGROUNDRing chromosomes are often associated with spermatogenetic failure. However, the mechanism is poorly understood. We here reported a single man with…”
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    Report
  20. 20

    Advances in gonadal differentiation regulated by SRY by Cui, Yingxia, Huang, Yufeng

    Published in Zhonghua nan ke xue (01-05-2004)
    “…Gondadal differentiation is genetically determined in humans. Sex is determined when the bipotential embryologic tissues differentiate into testes or ovary…”
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    Journal Article