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SLC6A18
Neutral Amino Acids in the Urine [5-7]
The Genetic Landscape of the Human Solute Carrier (SLC) Transporter Superfamily
SLC6A19), a Potential Target to Induce Protein Restriction and to Treat Type 2 Diabetes
Pflügers Archiv : European Journal of Physiology, 466(1):25-42
The Concise Guide to PHARMACOLOGY 2015/16: Transporters
Detection of H3k4me3 Identifies Neurohiv Signatures, Genomic
Iminoglycinuria and Hyperglycinuria Are Discrete Human Phenotypes Resulting from Complex Mutations in Proline and Glycine Transporters
Supplemental Data
Diseases Associated with General Amino Acid Transporters of the Solute Carrier 6 Family (SLC6)
D-Serine, an Emerging Biomarker of Kidney Diseases, Is a Hidden Substrate of Sodium-Coupled Monocarboxylate Transporters
Amino Acid Transport Defects in Human Inherited Metabolic Disorders
Supplementary File 1 (PDF, 295 Kib)
Supplemental Table S18. Cellular Process Enrichment Analysis Output
Role of Transmembrane Helix 6 in Substrate Recognition of the Amino Acid Transporter Mhst
Supplementary Table S8. Hyper- and Hypomethylated Genes in Human MDS Patients Analyzed by MCAM
Sodium/Amino Acid Cotransporters from the SLC6 Family Localizing to the Luminal Membrane of Kidney and Intestine
Supplementary Materials
Dichloroacetate Prevents Cisplatin-Induced Nephrotoxicity Without Compromising Cisplatin Anticancer Properties
Top View
The Concise Guide to PHARMACOLOGY 2015/16: Transporters
STAT Autism and Intellectual Disability Panel
THE CONCISE GUIDE to PHARMACOLOGY 2017/18: Transporters
Membrane Transporters in a Human Genome-Scale Metabolic Knowledgebase and Their Implications for Disease
Table of Contents List of Investigators
Of Triple Negative Breast Cancer (TNBC)
Human SLC Transporter Expression List
Hartnup Disorder Is Caused by Mutations in the Gene Encoding the Neutral Amino Acid Transporter SLC6A19