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Deletion of ACTRT1 is associated with male infertility as sperm acrosomal ultrastructural defects and fertilization failure in human.
- Published in:
- Human Reproduction, 2024, v. 39, n. 5, p. 880, doi. 10.1093/humrep/deae031
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- Article
Novel biallelic variants in DNAH1 cause multiple morphological abnormalities of sperm flagella with favorable outcomes of fertility after ICSI in Han Chinese males.
- Published in:
- Andrology, 2024, v. 12, n. 2, p. 349, doi. 10.1111/andr.13476
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- Article
A novel variant in CFAP69 causes asthenoteratozoospermia with treatable ART outcomes and a literature review.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2023, v. 40, n. 9, p. 2175, doi. 10.1007/s10815-023-02873-1
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- Article
FMRP binds Per1 mRNA and downregulates its protein expression in mice.
- Published in:
- Molecular Brain, 2023, v. 16, n. 1, p. 1, doi. 10.1186/s13041-023-01023-z
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- Article
Brain fingerprints along the language hierarchy .
- Published in:
- Frontiers in Human Neuroscience, 2022, v. 16, p. 1, doi. 10.3389/fnhum.2022.982905
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- Article
Circadian Rhythm Sleep Disorders: Genetics, Mechanisms, and Adverse Effects on Health.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.875342
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- Article