Dongyan Li
Changsha, 410078, China
Last Updated: 09/26/2026
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Found 8 publications
Loss-of-function missense variant of AKAP4 induced male infertility through reduced interaction with QRICH2 during sperm flagella development.
Journal: Human molecular genetics
Published: May 03, 2021
CFAP65 is required in the acrosome biogenesis and mitochondrial sheath assembly during spermiogenesis.
Journal: Human molecular genetics
Published: March 23, 2021
Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice.
Journal: American journal of human genetics
Published: March 08, 2021
TDRD7 participates in lens development and spermiogenesis by mediating autophagosome maturation.
Journal: Autophagy
Published: February 23, 2021
Novel variants of the PCCB gene in Chinese patients with propionic acidemia.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: February 22, 2021
Novel DNAAF6 variants identified by whole-exome sequencing cause male infertility and primary ciliary dyskinesia.
Journal: Journal of assisted reproduction and genetics
Published: January 29, 2020
An M1AP homozygous splice-site mutation associated with severe oligozoospermia in a consanguineous family.
Journal: Clinical genetics
Published: December 16, 2019
CytoCluster: A Cytoscape Plugin for Cluster Analysis and Visualization of Biological Networks.
Journal: International journal of molecular sciences
Published: August 07, 2017
Showing 1-8 of 8
Last Updated: 09/26/2026