Molecular and Functional Characterization of Organic Cation/Carnitine Transporter Family in Mice

This publication has 44 references indexed in Scilit:

• Carnitine Transporter OCTN2 Mutations in Systemic Primary Carnitine Deficiency: A Novel Arg169Gln Mutation and a Recurrent Arg282ter Mutation Associated with an Unconventional Splicing Abnormality
  Biochemical and Biophysical Research Communications, 1999
• Carnitine Uptake Defect: Frameshift Mutations in the Human Plasmalemmal Carnitine Transporter Gene
  Biochemical and Biophysical Research Communications, 1998
• Molecular Cloning and Characterization of High-Affinity Carnitine Transporter from Rat Intestine
  Biochemical and Biophysical Research Communications, 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
• Molecular Cloning and Characterization of NKT, a Gene Product Related to the Organic Cation Transporter Family That Is Almost Exclusively Expressed in the Kidney
  Published by Elsevier ,1997
• cDNA Cloning and Functional Expression of a Novel Rat Kidney Organic Cation Transporter, OCT2
  Biochemical and Biophysical Research Communications, 1996
• Role of free L-carnitine and acetyl-L-carnitine in post-gonadal maturation of mammalian spermatozoa
  Human Reproduction Update, 1996
• Carnitine deficiency syndromes
  Pediatric Neurology, 1990
• Primary Carnitine Deficiency Due to a Failure of Carnitine Transport in Kidney, Muscle, and Fibroblasts
  New England Journal of Medicine, 1988
• A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
  Analytical Biochemistry, 1976