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1S -"1-{[(4'-methoxy-1,1'-biphenyl-4-yl)sulfonyl]amino}-2-methylpropylphosphonic" acid
- ... Condition acid sphingomyelinase ASM ASM_HUMAN sphingomyelin phosphodiesterase 1, acid lysosomal sphingomyelin phosphodiesterase 1, acid lysosomal (acid sphingomyelinase) ...
- ... flat nasal bridge, and abnormally turned ears. amino acid transporter 1 ATR1 CSNU1 D2H NBAT RBAT SLC31_HUMAN solute ... carrier family 3 (cystine, dibasic and neutral amino acid transporters), member 1 solute carrier family 3 (cystine, dibasic and neutral ...
- ... About This Health Condition EA6 EAA1_HUMAN EAAT-1 EAAT1 Excitatory amino acid transporter 1 FLJ25094 GLAST GLAST1 Glial high affinity glutamate transporter ...
- ... receptor subunit alpha-1 GABA(A) receptor, alpha 1 gamma-aminobutyric acid (GABA) A receptor, alpha 1 gamma-aminobutyric acid receptor subunit alpha-1 gamma-aminobutyric acid receptor ...
- ... for producing a protein called y+L amino acid transporter 1 (y+LAT-1), which is involved in transporting ... All of these variants impair the y+LAT-1 protein's ability to transport amino acids. People with lysinuric protein intolerance who are of ...
- ... a protein called system B(0) neutral amino acid transporter 1 (B0AT1). This protein transports certain protein building blocks (amino acids), namely those with a neutral charge, into cells. ...
- ... K. Functional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis Syndrome. BMC ...
- ... lysophosphatidic acid acyltransferase, beta) 1-AGP acyltransferase 2 1-AGPAT2 BSCL1 LPAAB LPAAT-beta lysophosphatidic acid acyltransferase-beta PLCB_HUMAN Tests of AGPAT2 PubMed ...
- ... cellular nucleic acid binding protein cellular retroviral nucleic acid-binding protein 1 CNBP1 CNBP_HUMAN DM2 ZCCHC22 zinc finger 9 protein zinc finger protein 273 zinc finger protein 9 zinc finger protein 9 (a cellular retroviral nucleic acid binding protein) ZNF9 Tests of CNBP PubMed CCHC- ...
- ... HUMAN FAAH FAH1 fatty acid alpha-hydroxylase fatty acid hydroxylase domain containing 1 FAXDC1 FLJ25287 SCS7 spastic paraplegia 35 (autosomal recessive) ...