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2S -"2-(1H-indol-3-yl)pentanoic" acid
Did you mean 2S -"2-(1H-indio-3-yl)pentanoic" acid?
- ... been found to cause hereditary hemorrhagic telangiectasia type 2. Many ACVRL1 gene mutations substitute one protein building block (amino acid) for another amino acid in the ACVRL1 protein, ...
- ... taken one time, about 3 hours (range of 2 to 4 hours) before the beginning of your surgery. Take aminolevulinic acid exactly as directed. Ask your doctor or pharmacist ...
- ... chain 3-hydroxyacyl-CoA dehydrogenase and long-chain 2-enoyl-CoA hydratase. The beta subunits contain the third enzyme. These enzymes are essential for fatty acid oxidation, which is the multistep process that breaks ...
- ... a severe form of X-linked chondrodysplasia punctata 2 has been reported in males. These cases result from changes involving single amino acids in the 3β-hydroxysteroid-Δ8,Δ7-isomerase enzyme. ...
- ... KCNK9 imprinting syndrome. More About This Health Condition acid-sensitive potassium channel protein TASK-3 K2p9.1 KT3.2 potassium channel subfamily K member 9 potassium channel, ...
- ... characterized by neurological problems that begin around age 2. Most of these mutations change single protein building blocks (amino acids) in folate receptor alpha. FOLR1 gene mutations result ...
- ... These mutations change single protein building blocks (amino acids) in the GPI mannosyltransferase 2 enzyme. The altered protein is less able to ...
- ... These mutations change single protein building blocks (amino acids) in the isocitrate dehydrogenase 2 enzyme. Like the genetic changes that cause the ...
- ... replaces the amino acid arginine with the amino acid glycine at protein position 2 (written as Arg2Gly or R2G). The mutations that ...
- Renal tubular acidosis, RTA, kidneys, acid, urine, acidosis, classical ... kidney transplant, aldosterone, immunosuppressive, growth delays, kidney ...