Associated Papers
Novel compound heterozygous variants in lectin mannose-binding 2-like gene identified in a Chinese autosomal recessive mental retardation-52 (MRT52) patient with phenotype expansion.
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Chinese Medical Journal, 2023
37667433 (PubMed )
Supplement: cm9-136-2107-s002.xls › SHEET
Transport function, regulation, and biology of human monocarboxylate transporter 1 (hMCT1) and 4 (hMCT4).
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Pharmacology & Therapeutics, 2021
Relationships between plasma lactate, plasma alanine, genetic variations in lactate transporters and type 2 diabetes in the Japanese population.
Higuchi I et al.
Drug Metabolism and Pharmacokinetics, 2020
Genetic variations in the monocarboxylate transporter genes (SLC16A1, SLC16A3, and SLC16A11) in the Japanese population.
Kimura Y et al.
Drug Metabolism and Pharmacokinetics, 2018
Genetic variations of the MCT4 (SLC16A3) gene in the Chinese and Indian populations of Singapore.
Lean CB et al.
Drug Metabolism and Pharmacokinetics, 2012
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