Found: 10
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Combination of Ginsenosides Rb2 and Rg3 Promotes Angiogenic Phenotype of Human Endothelial Cells via PI3K/Akt and MAPK/ERK Pathways.
- Published in:
- Frontiers in Pharmacology, 2021, v. 11, p. N.PAG, doi. 10.3389/fphar.2021.618773
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- Publication type:
- Article
Where next for GWAS?
- Published in:
- Briefings in Functional Genomics, 2011, v. 10, n. 2, p. 51, doi. 10.1093/bfgp/elr011
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- Publication type:
- Article
Deletion of Codons 88–92 of the Melanocortin-4 Receptor Gene: A Novel Deleterious Mutation in an Obese Female.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 12, p. 5841, doi. 10.1210/jc.2003-030903
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- Article
Studies of the peptide YY and neuropeptide Y2 receptor genes in relation to human obesity and obesity-related traits.
- Published in:
- 2004
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- Publication type:
- journal article
The CART Gene and Human Obesity.
- Published in:
- Diabetes, 2000, v. 49, n. 5, p. 872, doi. 10.2337/diabetes.49.5.872
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- Publication type:
- Article
A de novo mutation affecting human TrkB associated with severe obesity and developmental delay.
- Published in:
- Nature Neuroscience, 2004, v. 7, n. 11, p. 1187, doi. 10.1038/nn1336
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- Publication type:
- Article
A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 17, p. 3257, doi. 10.1093/hmg/ddp263
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- Publication type:
- Article
Mutations in the human melanocortin-4 receptor gene associated with severe familial obesity disrupts receptor function through multiple molecular mechanisms.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 5, p. 561, doi. 10.1093/hmg/ddg057
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- Publication type:
- Article
A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 17, p. 1997, doi. 10.1093/hmg/11.17.1997
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- Publication type:
- Article
A frameshift mutation in MC4R associated with dominantly inherited human obesity.
- Published in:
- Nature Genetics, 1998, v. 20, n. 2, p. 111, doi. 10.1038/2404
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- Publication type:
- Article