Associated Papers
A genome-wide association analysis reveals new pathogenic pathways in gout.
Major TJ et al.
Nature Genetics, 2024
Genetic variation in sodium glucose co-transporter 1 and cardiac structure and function at middle age.
Bavishi A et al.
Esc Heart Failure, 2022
NGS Gene Panel Analysis Revealed Novel Mutations in Patients with Rare Congenital Diarrheal Disorders.
Esposito MV et al.
Diagnostics (basel, Switzerland), 2021
Literature review on congenital glucose-galactose malabsorption from 2001 to 2019.
Wang W et al.
Journal of Paediatrics and Child Health, 2020
Relevance of solute carrier family 5 transporter defects to inherited and acquired human disease.
Cannizzaro M et al.
Journal of Applied Genetics, 2019
Genetic Variants in SGLT1, Glucose Tolerance, and Cardiometabolic Risk.
Seidelmann SB et al.
Journal of the American College of Cardiology, 2018
Genetic determinants of circulating GIP and GLP-1 concentrations.
Almgren P et al.
Jci Insight, 2017
Cross-comparison of the genome sequences from human, chimpanzee, Neanderthal and a Denisovan hominin identifies novel potentially compensated mutations.
Zhang G et al.
Human Genomics, 2011
Multiple sequence variations in SLC5A1 gene are associated with glucose-galactose malabsorption in a large cohort of Old Order Amish.
Xin B et al.
Clinical Genetics, 2011
Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption.
Martín MG et al.
Nature Genetics, 1996
Glucose transport families SLC5 and SLC50.
Wright EM
Molecular Aspects of Medicine, 0
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