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Phenotypic severity of homozygous GCK mutations causing neonatal or childhood-onset diabetes is primarily mediated through effects on protein stability.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6432
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- Publication type:
- Article
Systematic Functional Characterization of Candidate Causal Genes for Type 2 Diabetes Risk Variants.
- Published in:
- 2016
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- Publication type:
- journal article
Loss-of-Function Mutations in the Cell-Cycle Control Gene CDKN2A Impact on Glucose Homeostasis in Humans.
- Published in:
- 2016
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- Publication type:
- journal article
Keys to the kingdom.
- Published in:
- Nature Biotechnology, 2015, v. 33, n. 3, p. 232, doi. 10.1038/nbt.3159
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- Publication type:
- Article
The importance of Context: Uncovering Species- and Tissue-Specific Effects of Genetic Risk Variants for Type 2 Diabetes.
- Published in:
- Frontiers in Endocrinology, 2016, v. 7, p. 1, doi. 10.3389/fendo.2016.00112
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- Publication type:
- Article
Prioritising Causal Genes at Type 2 Diabetes Risk Loci.
- Published in:
- 2017
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- Publication type:
- journal article