Associated Papers
Assessment of TP53 and CDKN2A status as predictive markers of malignant transformation of sinonasal inverted papilloma.
Kwon S et al.
Scientific Reports, 2024
38902320 (PubMed )
Supplement: 41598_2024_64901_MOESM1_ESM.xlsx › SCC
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
Bitterness of glucose/galactose: novel mutations in the SLC5A1 gene.
Pode-Shakked B et al.
Journal of Pediatric Gastroenterology and Nutrition, 2014
Structural insights into genetic variants of Na(+)/glucose cotransporter SGLT1 causing glucose-galactose malabsorption: vSGLT as a model structure.
Raja M et al.
Cell Biochemistry and Biophysics, 2012
Molecular basis for glucose-galactose malabsorption.
Wright EM et al.
Cell Biochemistry and Biophysics, 2002
Missense mutations in SGLT1 cause glucose-galactose malabsorption by trafficking defects.
Lam JT et al.
Biochimica Et Biophysica Acta, 1999
Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption.
Martín MG et al.
Nature Genetics, 1996
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