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Two mutations in human BICC1 resulting in Wnt pathway hyperactivity associated with cystic renal dysplasia

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Two mutations in human BICC1 resulting in Wnt pathway hyperactivity associated with cystic renal dysplasia

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Role of the RNA-binding protein Bicaudal-C1 and interacting factors in cystic kidney diseases

Direct coupling analysis of epistasis in allosteric materials

Effect of Single-Point Mutations on Nitric Oxide Rebinding and the Thermodynamic Stability of Myoglobin

Early Urinary Biomarkers in Pediatric Autosomal Dominant Polycystic Kidney Disease (ADPKD): No Evidence in the Interest of Urinary Neutrophil Gelatinase-Associated Lipocalin (uNGAL)

The fitness landscape of the codon space across environments

The NAD(+)-dependent deacetylase SIRT2 attenuates oxidative stress and mitochondrial dysfunction and improves insulin sensitivity in hepatocytes

A systems perspective on brown adipogenesis and metabolic activation

Bioengineering strategies for inducing tolerance in autoimmune diabetes

LRSAM1-mediated ubiquitylation is disrupted in axonal Charcot-Marie-Tooth disease 2P

Renal Fanconi Syndrome and Hypophosphatemic Rickets in the Absence of Xenotropic and Polytropic Retroviral Receptor in the Nephron