Results 1 - 10 of 1,941 for 2S -"2-[3-(AMINOMETHYL)PHENYL]-3-[(R)-[(1R)-1-{[(BENZYLOXY)CARBONYL]AMINO}-2-METHYLPROPYL](HYDROXY)PHOSPHORYL]PROPANOIC" ACID
Did you mean 2S -"2-[3-(amino methyl)PHENYL]-3-[(R)-[(1R)-1-{[(BENZYLOXY)CARBONYL]AMINO}-2-METHYLPROPYL](HYDROXY)phosphorus]propionic" ACID?
  1. SLC16A2 gene 
    ... transporters), member 2 solute carrier family 16, member 2 (monocarboxylic acid transporter 8) solute carrier family 16, member 2 ( ... of SLC16A2 PubMed SOLUTE CARRIER FAMILY 16 (MONOCARBOXYLIC ACID TRANSPORTER), MEMBER 2 ClinVar NCBI Gene Dumitrescu AM, Liao XH, Weiss ...
    https://medlineplus.gov/genetics/gene/slc16a2 - Genetics
  2. FA2H gene 
    ... point on a fatty acid to create a 2-hydroxylated fatty acid. Certain 2-hydroxylated fatty acids are important in forming normal myelin; myelin is ... reduce or eliminate the function of the fatty acid 2-hydroxylase enzyme. Reduction of this enzyme's function ...
    https://medlineplus.gov/genetics/gene/fa2h - Genetics
  3. AGPAT2 gene 
    ... acyltransferase beta 1-acylglycerol-3-phosphate O-acyltransferase 2 (lysophosphatidic acid acyltransferase, beta) 1-AGP acyltransferase 2 1-AGPAT2 BSCL1 LPAAB LPAAT-beta lysophosphatidic acid acyltransferase-beta PLCB_HUMAN Tests of AGPAT2 PubMed ...
    https://medlineplus.gov/genetics/gene/agpat2 - Genetics
  4. D2HGDH gene 
    ... involve the brain. More About This Health Condition 2-hydroxypentanedioic acid D2HDH_HUMAN D2HGD FLJ42195 MGC25181 Tests of D2HGDH PubMed D-2-HYDROXYGLUTARATE DEHYDROGENASE ClinVar NCBI Gene Kranendijk M, Struys ...
    https://medlineplus.gov/genetics/gene/d2hgdh - Genetics
  5. Congenital bile acid synthesis defect type 2 
    ... Genetic Testing Registry: Congenital bile acid synthesis defect 2 Congenital bile acid synthesis defect, type 2 Disease InfoSearch National Organization ...
    https://medlineplus.gov/...genital-bile-acid-synthesis-defect-type-2 - Genetics
  6. Metabolic Diseases of Muscle (Muscular Dystrophy Association) - PDF  
    Metabolic Disorders/Specifics ... Metabolic Disorders ... Muscle Disorders/Specifics ... Muscle Disorders ... Muscular Dystrophy Association ... PDF ... metabolic diseases; McArdle ...
    https://www.mda.org/.../publications/Facts_Metabolics_P-207.pdf - External Health Links
  7. Fatty acid hydroxylase-associated neurodegeneration 
    ... point on a fatty acid to create a 2-hydroxylated fatty acid. Certain 2-hydroxylated fatty acids are important in forming normal myelin; myelin is ... reduce or eliminate the function of the fatty acid 2-hydroxylase enzyme. Reduction of this enzyme's function ...
    https://medlineplus.gov/...-hydroxylase-associated-neurodegeneration - Genetics
  8. L-Arginine 
    2-Amino-5-(diaminomethylidene amino) pentanoic acid, 2-Amino-5-guanidinopentanoic Acid, (2S)-2-Amino-5-{[amino (imino) methyl]amino}pentanoic Acid, (S)-2-Amino-5- Guanidinopentanoic Acid, Acide 2-Amino- ...
    https://medlineplus.gov/druginfo/natural/875.html - Drugs and Supplements
  9. GNE gene 
    ... muscle weakness in people with inclusion body myopathy 2. Sialic acid is important for the normal function of many ... working to determine how an accumulation of sialic acid in the body interferes with normal ... UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase DMRV GLCNE GLCNE_HUMAN ...
    https://medlineplus.gov/genetics/gene/gne - Genetics
  10. CPT2 gene 
    ... CPT II deficiency.Without enough functioning carnitine palmitoyltransferase 2, long-chain fatty acids are not properly processed after they enter mitochondria ...
    https://medlineplus.gov/genetics/gene/cpt2 - Genetics
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