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 matching AU Chen, Wen-qi
Results: 17
1
2
First-principles calculations of structural, electronic, magnetic, elastic and optical properties of tetragonal zircon-type CeVO<sub>4</sub>.
- Published in:
- International Journal of Modern Physics B: Condensed Matter Physics; Statistical Physics; Applied Physics, 2018, v. 32, n. 22, p. N.PAG, doi. 10.1142/S0217979218502399
- By:
- Publication type:
- Article
3
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
4
Ac voltammetric and square wave voltammetric study of the self-assembled monolayers of thiol-functionalized viologen derivative.
- Published in:
- Chinese Journal of Chemistry, 1997, v. 15, n. 2, p. 130, doi. 10.1002/cjoc.19970150207
- By:
- Publication type:
- Article
5
Syntheses of (C<sub>5</sub>H<sub>9</sub>C<sub>5</sub>H<sub>4</sub>)<sub>2</sub>LnCl(THF)<sub> n</sub> (Ln = Nd, Sm, Er, Yb) and crystal structure of [(C<sub>5</sub>H<sub>9</sub>C<sub>5</sub>H<sub>4</sub>)<sub>2</sub>-LnCl(THF)<sub> n</sub>]<sub>2</sub>(Ln = Sm, n = 1; Ln = Er, n = 0)
- Published in:
- Chinese Journal of Chemistry, 1992, v. 10, n. 5, p. 405, doi. 10.1002/cjoc.19920100504
- By:
- Publication type:
- Article
6
Syntheses of (C<sub>8</sub>H<sub>8</sub>)Ln(C<sub>9</sub>H<sub>7</sub>) · (THF)<sub>2</sub>(Ln = Pr,Nd) and crystal structure of (C<sub>8</sub>H<sub>8</sub>)Pr(C<sub>9</sub>H<sub>7</sub>) · (THF)<sub>2</sub>.
- Published in:
- Chinese Journal of Chemistry, 1992, v. 10, n. 4, p. 331, doi. 10.1002/cjoc.19920100407
- By:
- Publication type:
- Article
7
Identification of Novel NSD1 variations in four Pediatric cases with sotos Syndrome.
- Published in:
- 2024
- By:
- Publication type:
- Case Study
8
Long non‐coding RNA SNHG16 decreased SMAD4 to induce gemcitabine resistance in pancreatic cancer via EZH2‐mediated epigenetic modification.
- Published in:
- Kaohsiung Journal of Medical Sciences, 2022, v. 38, n. 10, p. 981, doi. 10.1002/kjm2.12574
- By:
- Publication type:
- Article
9
Identification of critically carcinogenesis-related genes in basal cell carcinoma.
- Published in:
- OncoTargets & Therapy, 2018, v. 11, p. 6957, doi. 10.2147/OTT.S170504
- By:
- Publication type:
- Article
10
The value of Tc-99m MIBI SPECT during isosorbide dinitrate infusion in assessment of viable myocardium in patients with myocardial infarction.
- Published in:
- Annals of Nuclear Medicine, 1996, v. 10, n. 1, p. 13, doi. 10.1007/BF03165049
- By:
- Publication type:
- Article
11
Identification of novel variations in three cases with rare inherited neuromuscular disorder.
- Published in:
- Experimental & Therapeutic Medicine, 2024, v. 27, n. 6, p. N.PAG, doi. 10.3892/etm.2024.12558
- By:
- Publication type:
- Article
12
RBM25 induces trophoblast epithelial-mesenchymal transition and preeclampsia disorder by enhancing the positive feedback loop between Grhl2 and RBM25.
- Published in:
- Experimental Biology & Medicine, 2023, v. 248, n. 14, p. 1267, doi. 10.1177/15353702231191199
- By:
- Publication type:
- Article
13
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
14
Analysis of a Series of 26 Cases With Prenatal Skeletal Dysplasia via Multiplatform Genetic Detection.
- Published in:
- Molecular Genetics & Genomic Medicine, 2025, v. 13, n. 1, p. 1, doi. 10.1002/mgg3.70062
- By:
- Publication type:
- Article
15
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
16
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
17
Identification of a novel pathogenic variant in the MYH3 gene in a five‐generation family with CPSFS1A (Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1A).
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 10, p. 1, doi. 10.1002/mgg3.1440
- By:
- Publication type:
- Article