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Results 1 - 10 of 967 for 2S -"2-[3-(AMINOMETHYL)PHENYL]-3-[(R)-HYDROXY{(1R)-2-METHYL-1-[(PHENYLSULFONYL)AMINO]PROPYL}PHOSPHORYL]PROPANOIC" ACID
Did you mean 2S -"2-[3-(amino methyl)PHENYL]-3-[(R)-HYDROXY{(1R)-2-METHYL-1-[(PHENYLSULFONYL)AMINO]PROPYL}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; SLC16A2 NCBI Gene ClinVar Dumitrescu AM, Liao XH, ...
    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; D2HGDH NCBI Gene ClinVar Kranendijk M, ...
    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 National Organization for Rare ... NORD) ClinicalTrials.gov BILE ACID SYNTHESIS DEFECT, CONGENITAL, 2; CBAS2 ... PubMed Clayton PT. Disorders of bile acid synthesis. J Inherit Metab Dis. 2011 Jun;34( ...
    https://medlineplus.gov/...genital-bile-acid-synthesis-defect-type-2 - Genetics
  6. 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
  7. DOORS syndrome 
    ... higher-than-normal levels of a substance called 2-oxoglutaric acid in their urine; these levels can fluctuate between ...
    https://medlineplus.gov/genetics/condition/doors-syndrome - Genetics
  8. DLD gene 
    ... dihydrolipoamide dehydrogenase (E3 component of pyruvate dehydrogenase complex, 2-oxo-glutarate complex, branched chain keto acid dehydrogenase complex) dihydrolipoyl dehydrogenase DLDH DLDH_HUMAN E3 ...
    https://medlineplus.gov/genetics/gene/dld - Genetics
  9. 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
  10. SLC26A2 gene 
    ... protein.One common mutation that causes atelosteogenesis type 2 replaces the amino acid arginine with the amino acid tryptophan at position ... This mutation can also occur in atelosteogenesis type 2 and diastrophic ... replaces the amino acid cysteine with the amino acid serine at position ...
    https://medlineplus.gov/genetics/gene/slc26a2 - Genetics
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