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EPHX1 mutations cause a lipoatrophic diabetes syndrome due to impaired epoxide hydrolysis and increased cellular senescence.
- Published in:
- eLife, 2021, p. 1, doi. 10.7554/eLife.68445
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- Publication type:
- Article
Biallelic CAV1 null variants induce congenital generalized lipodystrophy with achalasia.
- Published in:
- European Journal of Endocrinology, 2021, v. 185, n. 6, p. 841, doi. 10.1530/EJE-21-0915
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- Publication type:
- Article
Loss of thymidine phosphorylase activity disrupts adipocyte differentiation and induces insulin-resistant lipoatrophic diabetes.
- Published in:
- BMC Medicine, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s12916-022-02296-2
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- Publication type:
- Article
Molecular and Cellular Bases of Lipodystrophy Syndromes.
- Published in:
- Frontiers in Endocrinology, 2022, v. 12, p. 1, doi. 10.3389/fendo.2021.803189
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- Publication type:
- Article
Germination responses of Spartidium saharae (Coss. & Dur.) Pomel (Fabaceae) to temperature and salinity.
- Published in:
- African Journal of Ecology, 2010, v. 48, n. 1, p. 37, doi. 10.1111/j.1365-2028.2009.01070.x
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- Publication type:
- Article
Loss of thymidine phosphorylase activity disrupts adipocyte differentiation and induces insulin-resistant lipoatrophic diabetes.
- Published in:
- 2022
- By:
- Publication type:
- journal article