Slow transport via folate receptor (lower affinity for methotrexate than for folic acid) Increased drug efflux via ATP-binding cassette (ABC) subfamily transporters ABCC1–ABCC5 and ABCG2 ...
ABSTRACT: Rabson-Mendenhall syndrome (RMS) is a rare autosomal recessive inherited disease marked by insulin resistance. Mutations in the insulin receptor gene seem to be the fundamental mechanism ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback