Associated Papers
Systematic analysis of the intersection of disease mutations with protein modifications.
Simpson CM et al.
Bmc Medical Genomics, 2019
31345222 (PubMed )
Supplement: 12920_2019_543_MOESM6_ESM.xlsx › S5C
Functional characterization of 5-oxoproline transport via SLC16A1/MCT1.
Sasaki S et al.
The Journal of Biological Chemistry, 2015
The monocarboxylate transporter family--role and regulation.
Halestrap AP et al.
Iubmb Life, 2012
Mutations in MCT1 cDNA in patients with symptomatic deficiency in lactate transport.
Merezhinskaya N et al.
Muscle & Nerve, 2000
Select a paper to view details