Found: 16
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An alternative splicing program promotes adipose tissue thermogenesis.
- Published in:
- eLife, 2016, p. 1, doi. 10.7554/eLife.17672
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- Article
Excitatory transmission onto AgRP neurons is regulated by cJun NH<sub>2</sub>- terminal kinase 3 in response to metabolic stress.
- Published in:
- eLife, 2016, p. 1, doi. 10.7554/eLife.10031
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- Publication type:
- Article
Detection of senescence using machine learning algorithms based on nuclear features.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-45421-w
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- Article
A PTG Variant Contributes to a Milder Phenotype in Lafora Disease.
- Published in:
- PLoS ONE, 2011, v. 6, n. 6, p. 1, doi. 10.1371/journal.pone.0021294
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- Publication type:
- Article
Increased Endoplasmic Reticulum Stress and Decreased Proteasomal Function in Lafora Disease Models Lacking the Phosphatase Laforin.
- Published in:
- PLoS ONE, 2009, v. 4, n. 6, p. 1, doi. 10.1371/journal.pone.0005907
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- Article
A New PCSK9 Gene Promoter Variant Affects Gene Expression and Causes Autosomal Dominant Hypercholesterolemia.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2008, v. 93, n. 9, p. 3577, doi. 10.1210/jc.2008-0269
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- Article
Lafora progressive myoclonus epilepsy: NHLRC1 mutations affect glycogen metabolism.
- Published in:
- Journal of Molecular Medicine, 2011, v. 89, n. 9, p. 915, doi. 10.1007/s00109-011-0758-y
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- Article
Adipose tissue mTORC2 regulates ChREBP-driven de novo lipogenesis and hepatic glucose metabolism.
- Published in:
- Nature Communications, 2016, v. 7, n. 4, p. 11365, doi. 10.1038/ncomms11365
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- Publication type:
- Article
Inactivation of nuclear GSK3β by Ser<sup>389</sup> phosphorylation promotes lymphocyte fitness during DNA double-strand break response.
- Published in:
- Nature Communications, 2016, v. 7, n. 1, p. 10553, doi. 10.1038/ncomms10553
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- Publication type:
- Article
Lafora bodies and neurological defects in malin-deficient mice correlate with impaired autophagy.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 19, p. 4366, doi. 10.1093/hmg/dds291
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- Article
Lafora bodies and neurological defects in malin-deficient mice correlate with impaired autophagy.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 7, p. 1521, doi. 10.1093/hmg/ddr590
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- Publication type:
- Article
Laforin, a dual specificity phosphatase involved in Lafora disease, regulates insulin response and whole-body energy balance in mice.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 13, p. 2571, doi. 10.1093/hmg/ddr157
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- Article
A Very Rare Variant in SREBF2 , a Possible Cause of Hypercholesterolemia and Increased Glycemic Levels.
- Published in:
- Biomedicines, 2022, v. 10, n. 5, p. 1178, doi. 10.3390/biomedicines10051178
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- Publication type:
- Article
Dysregulated RNA polyadenylation contributes to metabolic impairment in non-alcoholic fatty liver disease.
- Published in:
- Nucleic Acids Research, 2022, v. 50, n. 6, p. 3379, doi. 10.1093/nar/gkac165
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- Article
A rare missense mutation in a type 2 diabetes patient decreases the transcriptional activity of human sterol regulatory element binding protein-1.
- Published in:
- Human Mutation, 2006, v. 27, n. 2, p. 212, doi. 10.1002/humu.9397
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- Publication type:
- Article
Laforin, the most common protein mutated in Lafora disease, regulates autophagy.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 14, p. 2867, doi. 10.1093/hmg/ddq190
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- Article