microsomal triglyceride transfer protein造句
例句與造句
- It works as a gut-selective microsomal triglyceride transfer protein ( MTTP or MTP ) inhibitor.
- Its mechanism of action involves inhibition of microsomal triglyceride transfer protein ( MTP ) which is responsible for the absorption of dietary lipids.
- The " MTTP " gene provides instructions for making a protein called microsomal triglyceride transfer protein, which is essential for creating beta-lipoproteins.
- Lomitapide, an inhibitor of the microsomal triglyceride transfer protein, was approved by the US FDA in December 2012 as an orphan drug for the treatment of homozygous familial hypercholesterolemia.
- Most of the mutations in this gene lead to the production of an abnormally short microsomal triglyceride transfer protein, which prevents the normal creation of beta-lipoproteins in the body.
- It's difficult to find microsomal triglyceride transfer protein in a sentence. 用microsomal triglyceride transfer protein造句挺難的
- Mutations in the microsomal triglyceride transfer protein ( MTTP ) gene has been associated with this condition . ( Apolipoprotein B deficiency, a related condition, is associated with deficiencies of apolipoprotein B .)
- It is caused by a mutation in microsomal triglyceride transfer protein resulting in deficiencies in the apolipoproteins B-48 and B-100, which are used in the synthesis and exportation of chylomicrons and VLDL respectively.
- Microsomal triglyceride transfer protein ( MTTP ) is an endoplasmic reticulum lipid transfer protein involved in the biosynthesis and lipid loading of apolipoprotein B . MTTP is also involved in the late stage of CD1d trafficking in the lysosomal compartment, CD1d being the MHC I-like lipid antigen presenting molecule.
- "' Acanthocytosis "'can refer generally to the presence of this type of crenated red blood cell, such as may be found in severe cirrhosis or pancreatitis, This particular cause of acanthocytosis ( also known as abetalipoproteinemia, apolipoprotein B deficiency, and Bassen-Kornzweig syndrome ) is a rare, genetically inherited, autosomal recessive condition due to the inability to fully digest dietary fats in the intestines as a result of various mutations of the microsomal triglyceride transfer protein ( MTTP ) gene.