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Publications by Fuping Li

Loss-Of-Function Mutations in QRICH2 Cause Male Infertility With Multiple Morphological Abnormalities of the Sperm Flagella

Nature Communications

Molecular Biology

English

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HomozygousDNAH1frameshift Mutation Causes Multiple Morphological Anomalies of the Sperm Flagella in Chinese

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Mutations in DNAH17, Encoding a Sperm-Specific Axonemal Outer Dynein Arm Heavy Chain, Cause Isolated Male Infertility Due to Asthenozoospermia

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Loss-Of-Function Mutations in Sodium Channel Nav1.7 Cause Anosmia

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Loss-Of-Function Mutations in HPSE2 Cause the Autosomal Recessive Urofacial Syndrome

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Homozygous Loss-Of-Function Mutations in SLC26A7 Cause Goitrous Congenital Hypothyroidism

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Loss of the Deglutamylase CCP5 Perturbs Multiple Steps of Spermatogenesis and Leads to Male Infertility

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Male Infertility-Related Molecules Involved in Sperm-Oocyte Fusion

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Sperm Morphological Normality Under High Magnification Is Correlated to Male Infertility and Predicts Embryo Development

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Mutations in the Prostate Specific Antigen (PSA/KLK3) Correlate With Male Infertility

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