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American Journal of Human Genetics|August 2, 2007
Permanent neonatal diabetes caused by dominant, recessive, or compound heterozygous SUR1 mutations with opposite functional effectsSian Ellard, Sarah E Flanagan, Christophe A Girard, et al.
Diabetes Care|November 13, 2020
Long-term Follow-up of Glycemic and Neurological Outcomes in an International Series of Patients With Sulfonylurea-Treated ABCC8 Permanent Neonatal DiabetesPamela Bowman, Frances Mathews, Fabrizio Barbetti, et al.
Scientific Reports|December 10, 2016
Chiral Sulfoxide-Induced Single Turn Peptide α-HelicityQingzhou Zhang, Fan Jiang, Bingchuan Zhao, et al.
Brain : a Journal of Neurology|December 17, 2021
Cortical and subcortical pathological burden and neuronal loss in an autopsy series of FTLD-TDP-type CAllegra Kawles, Yasushi Nishihira, Alex Feldman, et al.
Diabetes|December 29, 2007
Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthoodEmma L Edghill, Sarah E Flanagan, Ann-Marie Patch, et al.
Angewandte Chemie (International Ed. in English)|February 13, 2020
RASS-Enabled S/P-C and S-N Bond Formation for DEL SynthesisDillon T Flood, Xuejing Zhang, Xiang Fu, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 17, 2023
Octopamine metabolically reprograms astrocytes to confer neuroprotection against α-synucleinAndrew Shum, Sofia Zaichick, Gregory S McElroy, et al.
Nature Communications|October 14, 2017
Heterozygous RFX6 protein truncating variants are associated with MODY with reduced penetranceKashyap A Patel, Jarno Kettunen, Markku Laakso, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 24, 2025
Basic Science and PathogenesisObed Okwoli Apochi, Rebecca Bernal, Yannick Joel Wadop Ngouongo, et al.
Free Radical Biology & Medicine|January 17, 2025
MnSOD non-acetylation mimic knock-in mice exhibit dilated cardiomyopathyJoseph R Schell, Sung-Jen Wei, Jun Zhang, et al.
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