Activating mutations in the ABCC8 gene in neonatal diabetes mellitus.

By A. P. Babenko, M. Polak, H. Cavé, K. Busiah, P. Czernichow, R. Scharfmann, J. Bryan, L. Aguilar-Bryan, M. Vaxillaire, Philippe Froguel. New England Journal of Medicine, 2006

631 citations recorded by the source corpus.

Subfields: Endocrinology, Diabetes and Metabolism, Pathology and Forensic Medicine, Surgery

View Paper: https://www.semanticscholar.org/paper/fbd88cbee7e25b31d6224e67c3e6636d781e8f6a

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

1. A. Kashiwagi
2. M. Kasuga
3. E. Araki
4. T. Hanafusa
5. K. Ueki
6. Takashi Kadowaki
7. Kazuharu Furutani
8. Y. Iwamoto

Citations in the corpus

• Inwardly rectifying potassium channels: their structure, function, and physiological roles. (2010, background): “Mutations in the SUR1 gene (33, 155) are found in 27% of PNDM patients (16).”
• Report of the Committee on the Classification and Diagnostic Criteria of Diabetes Mellitus (2010, background): “2 and SUR1, which form the KATP channel in pancreatic b-cells, have been identified [31, 32].”