Search Results - "Cui, Yingxia"
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The susceptibility of FSHB -211G > T and FSHR G-29A, 919A > G, 2039A > G polymorphisms to men infertility: an association study and meta-analysis
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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Long-Term Effects of Phytoestrogen Daidzein on Penile Cavernosal Structures in Adult Rats
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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Exposure of Juvenile Rats to the Phytoestrogen Daidzein Impairs Erectile Function in a Dose-Related Manner in Adulthood
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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Identification of novel mutations and risk assessment of Han Chinese patients with autosomal dominant polycystic kidney disease
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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Combinatorial test cases with constraints in software systems
Published in Proceedings of the 2012 IEEE 16th International Conference on Computer Supported Cooperative Work in Design (CSCWD) (01-05-2012)“…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 -
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The P20R mutation of αB-crystallin diminishes its anti-apoptotic activity in human lens epithelial cells
Published in Biochemical and biophysical research communications (29-01-2017)“…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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Polymorphisms of protamine genes contribute to male infertility susceptibility in the Chinese Han population
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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A New Strategy for Pairwise Test Case Generation
Published in 2009 Third International Symposium on Intelligent Information Technology Application (01-11-2009)“…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 -
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The effect of induced anti-follicle-stimulating hormone autoantibody on serum hormone level and apoptosis in rat testis
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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Meiotic Chromosome Behavior in a Human Male t(8;15) Carrier
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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Inclusion-Based Multi-level Pointer Analysis
Published in 2009 International Conference on Artificial Intelligence and Computational Intelligence (01-11-2009)“…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 -
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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
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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Meiotic prophase I defects in an oligospermic man with Wolf-Hirschhorn syndrome with ring chromosome 4
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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A first familial G504S mutation of COL2A1 gene results in distinctive spondyloepiphyseal dysplasia congenita
Published in Clinica chimica acta (01-07-2007)Get full text
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Meiotic Chromosome Behavior in a Human Male t(8;15) Carrier
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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AB188. Meiotic prophase I defects in an oligospermic man with Wolf-Hirschhorn syndrome with ring chromosome 4
Published in Translational andrology and urology (01-09-2014)Get full text
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AB197. The prevalence of FSH autoantibodies in the aging male
Published in Translational andrology and urology (01-09-2014)Get full text
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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
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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Meiotic prophase I defects in an oligospermic man with Wolf-Hirschhorn syndrome with ring chromosome 4
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
Advances in gonadal differentiation regulated by SRY
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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