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Results 91 - 100 of 1,813 for 2S -"2-(1H-indol-3-yl)pentanoic" acid
  1. ... 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, ...
  2. ... 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 ...
  3. ... 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 ...
  4. ... 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. ...
  5. ... 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, ...
  6. ... 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 ...
  7. ... These mutations change single protein building blocks (amino acids) in the GPI mannosyltransferase 2 enzyme. The altered protein is less able to ...
  8. ... These mutations change single protein building blocks (amino acids) in the isocitrate dehydrogenase 2 enzyme. Like the genetic changes that cause the ...
  9. ... replaces the amino acid arginine with the amino acid glycine at protein position 2 (written as Arg2Gly or R2G). The mutations that ...
  10. Renal Tubular Acidosis From the National Institutes of Health (National Institute of Diabetes and Digestive and Kidney Diseases)  
    Renal tubular acidosis, RTA, kidneys, acid, urine, acidosis, classical ... kidney transplant, aldosterone, immunosuppressive, growth delays, kidney ...
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