SEC24D depletion induces osteogenic differentiation deficiency by inactivating the ATF6/TGF-β/Runx2 regulatory loop.
- Published in:
- Communications Biology, 2025, v. 8, n. 1, p. 1, doi. 10.1038/s42003-025-08175-9
- By:
- Publication type:
- Article
Works by Yan, You-sheng
Results: 7
1
2
Prenatal Cases Reflect the Complexity of the COL1A1/2 Associated Osteogenesis Imperfecta.
- Published in:
- Genes, 2022, v. 13, n. 9, p. 1578, doi. 10.3390/genes13091578
- By:
- Publication type:
- Article
3
Investigation of a Novel NTRK1 Variation Causing Congenital Insensitivity to Pain With Anhidrosis.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.763467
- By:
- Publication type:
- Article
4
Investigation of a Novel LRP6 Variant Causing Autosomal-Dominant Tooth Agenesis.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.688241
- By:
- Publication type:
- Article
5
NTRK1 knockdown induces mouse cognitive impairment and hippocampal neuronal damage through mitophagy suppression via inactivating the AMPK/ULK1/FUNDC1 pathway.
- Published in:
- Cell Death Discovery, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41420-023-01685-7
- By:
- Publication type:
- Article
6
Functional assessment of a novel biallelic MYH3 variation causing CPSKF1B (contractures, pterygia, and spondylocarpotarsal fusion syndrome1B).
- Published in:
- Molecular Genetics & Genomic Medicine, 2024, v. 12, n. 3, p. 1, doi. 10.1002/mgg3.2401
- By:
- Publication type:
- Article
7
Assessment of a novel variation in DHODH gene causing Miller syndrome: The first report in Chinese population.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 7, p. 1, doi. 10.1002/mgg3.2186
- By:
- Publication type:
- Article