Tyrosine Residues Affecting Sodium Stimulation of Carnitine Transport in the OCTN2 Carnitine/Organic Cation Transporter

This publication has 20 references indexed in Scilit:

• Studies on Functional Sites of Organic Cation/Carnitine Transporter OCTN2 (SLC22A5) Using a Ser467Cys Mutant Protein
  The Journal of Pharmacology and Experimental Therapeutics, 2002
• Phenotype and genotype variation in primary carnitine deficiency
  Genetics in Medicine, 2001
• Molecular and Physiological Evidence for Multifunctionality of Carnitine/Organic Cation Transporter OCTN2
  Molecular Pharmacology, 2001
• Functional analysis of mutations in the OCTN2 transporter causing primary carnitine deficiency: Lack of genotype-phenotype correlation
  Human Mutation, 2000
• Abnormal Sodium Stimulation of Carnitine Transport in Primary Carnitine Deficiency
  Journal of Biological Chemistry, 2000
• A missense mutation in the OCTN2 gene associated with residual carnitine transport activity
  Human Mutation, 2000
• Mutations in Novel Organic Cation Transporter (OCTN2), an Organic Cation/Carnitine Transporter, with Differential Effects on the Organic Cation Transport Function and the Carnitine Transport Function
  Journal of Biological Chemistry, 1999
• Primary and secondary alterations of neonatal carnitine metabolism
  Seminars in Perinatology, 1999
• Molecular and Functional Identification of Sodium Ion-dependent, High Affinity Human Carnitine Transporter OCTN2
  Journal of Biological Chemistry, 1998
• cDNA Sequence, Transport Function, and Genomic Organization of Human OCTN2, a New Member of the Organic Cation Transporter Family
  Biochemical and Biophysical Research Communications, 1998