LRP6 Mutation in a Family with Early Coronary Disease and Metabolic Risk Factors
By Arya Mani, J. Radhakrishnan, He Wang, A. Mani, M. Mani, C. Nelson-Williams, Khary S. Carew, Shrikant Mane, H. Najmabadi, D. Wu and 1 more. Science, 2007
617 citations recorded by the source corpus.
Subfields: Endocrinology, Diabetes and Metabolism, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/d6c571b2119e4fa635f952493302038580fa85d9
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In Molecular Biology
Citations in the corpus
- Wnt/β-catenin signaling and disease. (2012, positive): “A loss-of-function mutation in LRP6 is linked to a hereditary disorder characterized by osteoporosis, coronary artery disease, and metabolic syndrome (Table 1; Mani et al., 2007).”