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Results 31 - 40 of 1,813 for 2S -"2-(1H-indol-3-yl)pentanoic" acid
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  1. PTPN11 gene 
    ... protein building blocks (amino acids) in the SHP-2 protein: One mutation replaces the amino acid tyrosine with the amino acid cysteine at position ... replaces the amino acid threonine with the amino acid methionine at position ... to disrupt the SHP-2 protein's normal function. This decrease in protein ...
    https://medlineplus.gov/genetics/gene/ptpn11 - Genetics
  2. Diabetes and Dietary Supplements: What You Need to Know From the National Institutes of Health (National Center for Complementary and Integrative Health)  
    Diabetes Type 2/Treatments and Therapies ... Diabetes Type 2 ... Diabetic Diet/Related Issues ... Diabetic Diet ... National Center for Complementary and Integrative Health
    https://www.nccih.nih.gov/...etary-supplements-what-you-need-to-know - External Health Links
  3. PSEN2 gene 
    ... building blocks (amino acids) used to make presenilin 2. One mutation replaces the amino acid asparagine with the amino acid isoleucine at position ...
    https://medlineplus.gov/genetics/gene/psen2 - Genetics
  4. TK2 gene 
    ... cytosolic thymidine kinase 1 and mitochondrial thymidine kinase 2: a mini review. Nucleosides Nucleotides Nucleic Acids. 2010 Jun;29(4-6):363-9. doi: ...
    https://medlineplus.gov/genetics/gene/tk2 - Genetics
  5. AKR1D1 gene 
    ... gene have been found to cause congenital bile acid synthesis defect type 2. This condition is characterized by cholestasis, a condition ... to the signs and symptoms of congenital bile acid synthesis defect type 2. More About This Health Condition 3-oxo-5- ...
    https://medlineplus.gov/genetics/gene/akr1d1 - Genetics
  6. H2 blockers 
    ... you find yourself taking these most days for 2 weeks or more for acid reflux symptoms, make sure you see your health care provider about your symptoms. If you have a peptic ulcer, your ... H2 blockers along with 2 or 3 other medicines for up to 2 ...
    https://medlineplus.gov/ency/patientinstructions/000382.htm - Medical Encyclopedia
  7. PRKAG2 gene 
    ... condition changes a single protein building block (amino acid) in the gamma-2 subunit of AMP-activated protein kinase. Specifically, this ... and skeletal muscle. These mutations change single amino acids in the gamma-2 subunit of AMP-activated protein kinase. Individuals with ...
    https://medlineplus.gov/genetics/gene/prkag2 - Genetics
  8. Renal hypouricemia 
    ... N. Pathogenic GLUT9 mutations causing renal hypouricemia type 2 (RHUC2). Nucleosides Nucleotides Nucleic Acids. 2011 Dec;30(12):1105-11. doi: 10. ...
    https://medlineplus.gov/genetics/condition/renal-hypouricemia - Genetics
  9. SLC2A9 gene 
    ... N. Pathogenic GLUT9 mutations causing renal hypouricemia type 2 (RHUC2). Nucleosides Nucleotides Nucleic Acids. 2011 Dec;30(12):1105-11. doi: 10. ...
    https://medlineplus.gov/genetics/gene/slc2a9 - Genetics
  10. ATP7B gene 
    ... protein or its stability, preventing copper-transporting ATPase 2 from functioning properly. A common amino acid substitution replaces the amino acid histidine with the ...
    https://medlineplus.gov/genetics/gene/atp7b - Genetics
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