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The Nuclear Orphan Receptor COUP-TFII Plays an Essential Role in Adipogenesis, Glucose Homeostasis, and Energy Metabolism
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RNAscope smFISH validated increased expression of GRAMD1B, VEGFB, and NR2F2 in mutant MAPT R406W HNOs compared to isogenic controls.
“RNAscope smFISH validated the increased expression of GRAMD1B, VEGFB, and NR2F2 in mutant MAPT R406W HNOs compared to isogenic controls.”
From GRAMD1B is a regulator of lipid homeostasis, autophagic flux and phosphorylated tau (2025) · cites this paper as [70]
Using scRNA-seq, genes (e.g., GRAMD1B, VEGFB, MIAT, COMT, NRP1, DSEL, NR2F2, HMGCS1, and LDLR) and biological pathways related to lipid metabolism are increased in excitatory neurons of MAPT R406W mutant HNOs compared to isogenic control HNOs.
“Using scRNA-seq, we found that genes (e.g., GRAMD1B, VEGFB, MIAT, COMT, NRP1, DSEL, NR2F2, HMGCS1, and LDLR)9,58,66,69–71 and biological pathways related to lipid metabolism are increased in excitatory neurons of MAPT R406W mutant HNOs compared to isogenic control HNOs (Fig. 4a, b and Supplementary Fig. 2a–c).”
From GRAMD1B is a regulator of lipid homeostasis, autophagic flux and phosphorylated tau (2025) · cites this paper as [70]
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Research works printed but not linked: 23
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Cited by
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Hromatka, B. S., Tung, J. Y., Kiefer, A. K., Do, C. B., Hinds, D. A., & Eriksson, N. (2015) · Human Molecular Genetics · doi:10.1093/hmg/ddv028 · Cited by 105
GRAMD1B is a regulator of lipid homeostasis, autophagic flux and phosphorylated tau
Acosta Ingram, D., Turkes, E., Kim, T. Y., Vo, S., Sweeney, N., Bonte, M.-A., Rutherford, R., Julian, D. L., Pan, M., Marsh, J., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-58585-w · Cited by 12
Metadata
- Authors
- Li, L., Xie, X., Qin, J., Jeha, G. S., Saha, P. K., Yan, J., Haueter, C. M., Chan, L., Tsai, S. Y., & Tsai, M.-J.
- Venue
- Cell Metabolism
- Publisher
- Elsevier BV
- Published
- 2009-01
- Volume
- 9
- Issue
- 1
- Pages
- 77-87
- ISSN
- 1550-4131
- PMC
- PMC2630393
- Cited by
- 127
- References
- 0
- Language
- en
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