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Publications by Kailai Cai

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

Nature Communications

Molecular Biology

English

Assessing Urinary Metabolomics in Giant Pandas Using Chromatography/Mass Spectrometry: Pregnancy-Related Changes in the Metabolome

Frontiers in Endocrinology

English

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

Clinical Genetics

English

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

American Journal of Human Genetics

English

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

Multidisciplinary

English

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

American Journal of Human Genetics

English

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

Yearbook of Paediatric Endocrinology

English

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

Journal of Cell Science

English

Male Infertility-Related Molecules Involved in Sperm-Oocyte Fusion

Journal of Reproduction and Development

English

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

Reproductive Medicine

English

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

Scientific Reports

Multidisciplinary

English