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资源简介：
Sequencing of human X chromosome exons to identify contributors to non-obstructive azoospermia
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创建时间：
2020-05-20
相关数据集
Male Infertility: Genetics of Spermatogenic Failure
Spermatogenesis is a complex biological process that requires the coordination of thousands of genes. Perhaps because of the large number of genes involved, spermatogenic failure occurs frequently and
NIAID Data Ecosystem120
Table_1_Genetic Defects in DNAH2 Underlie Male Infertility With Multiple Morphological Abnormalities of the Sperm Flagella in Humans and Mice.XLSX
Asthenozoospermia accounts for over 80% of primary male infertility cases. Reduced sperm motility in asthenozoospermic patients are often accompanied by teratozoospermia, or defective sperm morphology
NIAID Data Ecosystem70
Exome sequencing reveals pathogenic variants in known and novel candidate genes for severe sperm motility disorders
STUDY QUESTION: What are the causative genetic variants in patients with male infertility due to severe sperm motility disorders? SUMMARY ANSWER: We identified high confidence disease-causing variant
NIAID Data Ecosystem60
Genotype and allelic distribution of the CLOCK and ARNTL polymorphisms of the 517 infertile men and 444 fertile controls.
*ARNTL SNP rs12363415 showed a departure from the Hardy-Weinberg equilibrium and was excluded.
Figshare2015-12-02 更新70
Table3_Case report: The CCDC103 variant causes ultrastructural sperm axonemal defects and total sperm immotility in a professional athlete without primary ciliary diskinesia.docx
Primary ciliary dyskinesia (PCD) is an inherited autosomal-recessive disorder characterized by abnormal ciliary motion, due to a defect in ciliary structure and/or function. This genetic condition lea
NIAID Data Ecosystem60
