Biblio
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Loss-of-function variants in human C12orf40 cause male infertility by blocking meiotic progression. Cell Discov. 2023;9(1):87.
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MEK1/2 is a bottleneck that induces cancer stem cells to activate the PI3K/AKT pathway. Biochem Biophys Res Commun. 2021;583:49-55.
Neurodevelopmental Disorder with Progressive Microcephaly, Spasticity, and Brain Anomalies in China Caused by Novel Mutations of PLAA. Clin Genet. 2019.
. Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype. Clin Genet. 2022.
Novel homozygous variants in cause male infertility with asthenoteratozoospermia owing to dynein arm complex and mitochondrial sheath defects in flagella. Front Cell Dev Biol. 2023;11:1184331.
Novel SPEF2 variants cause male infertility and likely primary ciliary dyskinesia. J Assist Reprod Genet. 2024.
Osteogenic microenvironment affects palatal development through glycolysis. Differentiation. 2023;133:1-11.
. [Paramyotonia congenita caused by a novel mutation of SCN4A gene in a Chinese family]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016;33(2):131-134.
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Silver nanoparticles promote osteogenic differentiation of mouse embryonic fibroblasts . Am J Stem Cells. 2023;12(3):51-59.
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Up-regulation of Dsg2 confered stem cells with malignancy through wnt/β-catenin signaling pathway. Exp Cell Res. 2022:113416.
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