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Fibroblast growth factor 8 (FGF8) up-regulates gelatinase expression in chondrocytes through nuclear factor-κB p65.
- Published in:
- Journal of Bone & Mineral Metabolism, 2023, v. 41, n. 1, p. 17, doi. 10.1007/s00774-022-01388-6
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- Article
The Extragenic Spacer Length Between the 5′ and 3′ Ends of the Transgene Expression Cassette Affects Transgene Silencing From Plasmid-based Vectors.
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- Molecular Therapy, 2012, v. 20, n. 11, p. 2111, doi. 10.1038/mt.2012.65
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- Article
Distinct requirements for somatic and germline expression of a generally expressed...
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- Genetics, 1997, v. 146, n. 1, p. 227, doi. 10.1093/genetics/146.1.227
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- Article
PDGF‐AA guides cell crosstalk between human dental pulp stem cells in vitro via the PDGFR‐α/PI3K/Akt axis.
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- International Endodontic Journal, 2024, v. 57, n. 5, p. 549, doi. 10.1111/iej.14038
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- Article
TGF‐β3 mediates mitochondrial dynamics through the p‐Smad3/AMPK pathway.
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- Cell Proliferation, 2024, v. 57, n. 5, p. 1, doi. 10.1111/cpr.13579
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- Article
Osteoblasts impair cholesterol synthesis in chondrocytes via Notch1 signalling.
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- Cell Proliferation, 2021, v. 54, n. 12, p. 1, doi. 10.1111/cpr.13156
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- Article
Osteoblasts induce glucose-derived ATP perturbations in chondrocytes through noncontact communication.
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- Acta Biochimica et Biophysica Sinica, 2022, v. 54, n. 5, p. 625, doi. 10.3724/abbs.2022042
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- Article
Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans.
- Published in:
- Nature, 1998, v. 391, n. 6669, p. 806, doi. 10.1038/35888
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- Article
Functional analysis of cone–rod homeobox (CRX) mutations associated with retinal dystrophy.
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- Human Molecular Genetics, 2002, v. 11, n. 8, p. 873, doi. 10.1093/hmg/11.8.873
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- Article
Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function.
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- Human Molecular Genetics, 1999, v. 8, n. 2, p. 299, doi. 10.1093/hmg/8.2.299
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- Article