Associated Papers
Sex- and Exercise-Dependent Modulation of Hypertrophic Remodeling by the MCT1 rs1049434 Polymorphism.
Fernández-Suárez N et al.
Genes, 2026
The association of SLC16A1 (MCT1) gene polymorphism with body composition changes during weight loss interventions: A randomized trial with sex-dependent analysis.
Cupeiro R et al.
Applied Physiology, Nutrition, and Metabolism = Physiologie Appliquee, Nutrition Et Metabolisme, 2025
Meta-analysis of genomic variants in power and endurance sports to decode the impact of genomics on athletic performance and success.
Psatha A et al.
Human Genomics, 2024
Somatic mutations reveal hyperactive Notch signaling and racial disparities in prurigo nodularis.
Rajeh A et al.
Medrxiv : the Preprint Server for Health Sciences, 2023
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.
Young WJ et al.
Nature Communications, 2022
Transport function, regulation, and biology of human monocarboxylate transporter 1 (hMCT1) and 4 (hMCT4).
Kobayashi M et al.
Pharmacology & Therapeutics, 2021
Targeted transcriptome analysis using synthetic long read sequencing uncovers isoform reprograming in the progression of colon cancer.
Liu S et al.
Communications Biology, 2021
Deleterious variants in genes regulating mammalian reproduction in Neanderthals, Denisovans and extant humans.
Greer C et al.
Human Reproduction (oxford, England), 2021
Pharmacogenomics with red cells: a model to study protein variants of drug transporter genes.
Flegel WA et al.
Vox Sanguinis, 2021
Whole exome sequencing reveals novel candidate gene variants for MODY.
Yalçın Çapan Ö et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2020
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
PTMsnp: A Web Server for the Identification of Driver Mutations That Affect Protein Post-translational Modification.
Peng D et al.
Frontiers in Cell and Developmental Biology, 2020
The use of the SLC16A1 gene as a potential marker to predict race performance in Arabian horses.
Ropka-Molik K et al.
Bmc Genetics, 2019
X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family.
Khan MJ et al.
Scientific Reports, 2018
Identification of 26 novel loci that confer susceptibility to early-onset coronary artery disease in a Japanese population.
Yamada Y et al.
Biomedical Reports, 2018
Genetic variations in the monocarboxylate transporter genes (SLC16A1, SLC16A3, and SLC16A11) in the Japanese population.
Kimura Y et al.
Drug Metabolism and Pharmacokinetics, 2018
Glimepiride treatment in a patient with type A insulin resistance syndrome due to a novel heterozygous missense mutation in the insulin receptor gene.
Huang Z et al.
Journal of Diabetes Investigation, 2018
Analysis of sports-relevant polymorphisms in a large Brazilian cohort of top-level athletes.
Guilherme JPLF et al.
Annals of Human Genetics, 2018
Tumor Sequencing and Patient-Derived Xenografts in the Neoadjuvant Treatment of Breast Cancer.
Goetz MP et al.
Journal of the National Cancer Institute, 2017
Three-dimensional modelling identifies novel genetic dependencies associated with breast cancer progression in the isogenic MCF10 model.
Maguire SL et al.
The Journal of Pathology, 2016
Lack of replication of associations between multiple genetic polymorphisms and endurance athlete status in Japanese population.
Yvert T et al.
Physiological Reports, 2016
Variants of the Solute Carrier SLC16A1 Gene (MCT1) Associated With Metabolic Responses During a Long-Graded Test in Road Cyclists.
González-Haro C et al.
Journal of Strength and Conditioning Research, 2015
Polymorphisms of monocarboxylate transporter genes are associated with clinical outcomes in patients with colorectal cancer.
Fei F et al.
Journal of Cancer Research and Clinical Oncology, 2015
Identification of HPV integration and gene mutation in HeLa cell line by integrated analysis of RNA-Seq and MS/MS data.
Sun H et al.
Journal of Proteome Research, 2015
Whole genome sequencing of an ethnic Pathan (Pakhtun) from the north-west of Pakistan.
Ilyas M et al.
Bmc Genomics, 2015
Functional characterization of 5-oxoproline transport via SLC16A1/MCT1.
Sasaki S et al.
The Journal of Biological Chemistry, 2015
Reproducible Analysis of Post-Translational Modifications in Proteomes--Application to Human Mutations.
Holehouse AS et al.
Plos One, 2015
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
Effect of a poly(ADP-ribose) polymerase-1 inhibitor against esophageal squamous cell carcinoma cell lines.
Nasuno T et al.
Cancer Science, 2014
Glucose metabolism transporters and epilepsy: only GLUT1 has an established role.
Hildebrand MS et al.
Epilepsia, 2014
Integrated mRNA and microRNA transcriptome sequencing characterizes sequence variants and mRNA-microRNA regulatory network in nasopharyngeal carcinoma model systems.
Szeto CY et al.
Febs Open Bio, 2014