- A Journey to Understand Glucose Homeostasis: Starting from Rat Glucose Transporter Type 2 Promoter Cloning to Hyperglycemia
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Ahn YH
- KMID: 2449622
- Diabetes Metab J.
- 2018 Dec;42(6):465-471.
- doi: 10.4093/dmj.2018.0116
My professional journey to understand the glucose homeostasis began in the 1990s, starting from cloning of the promoter region of glucose transporter type 2 (GLUT2) gene that led us to... -
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- A Case of Fanconi-Bickel Syndrome with Mild Clinical Signs
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Kim SM, Yoo HW, Kim HW
- KMID: 2267816
- Korean J Med.
- 2013 Aug;85(2):210-213.
Fanconi-Bickel syndrome is a rare autosomal recessive disorder caused by a mutation in the facilitative glucose transporter 2 gene (GLUT2 or SLC2A2 gene) that codes for the glucose transporter protein... -
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- Identification and Functional Characterization of P159L Mutation in HNF1B in a Family with Maturity-Onset Diabetes of the Young 5 (MODY5)
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Kim EK, Lee JS, Cheong HI, Chung SS, Kwak SH, Park KS
- KMID: 2391503
- Genomics Inform.
- 2014 Dec;12(4):240-246.
- doi: 10.5808/GI.2014.12.4.240
Mutation in HNF1B, the hepatocyte nuclear factor-1beta (HNF-1beta) gene, results in maturity-onset diabetes of the young (MODY) 5, which is characterized by gradual impairment of insulin secretion. However, the functional... -
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