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You searched for: Author/Creator He, Xiaojin

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1. A homozygous loss‐of‐function mutation in FBXO43 causes human non‐obstructive azoospermia. Issue 1 (11th October 2021)

4. Artificial oocyte activation to improve reproductive outcomes in couples with various causes of infertility: a retrospective cohort study. Issue 4 (April 2020)

6. Biallelic loss‐of‐function mutations in SEPTIN4 (C17ORF47), encoding a conserved annulus protein, cause thin midpiece spermatozoa and male infertility in humans. Issue 12 (2nd October 2022)

7. Biallelic mutations in CFAP65 cause male infertility with multiple morphological abnormalities of the sperm flagella in humans and mice. Issue 2 (9th September 2019)

9. Bi‐allelic mutations in MCIDAS and CCNO cause human infertility associated with abnormal gamete transport. Issue 6 (20th October 2021)

10. Circular RNAs: Novel potential regulators in embryogenesis, female infertility, and pregnancy‐related diseases. Issue 10 (20th April 2021)