Results 1 - 10 of 1,016 for 1S -"1-{[(4'-methoxy-1,1'-biphenyl-4-yl)sulfonyl]amino}-2-methylpropylphosphonic" acid
  1. ... Condition acid sphingomyelinase ASM ASM_HUMAN sphingomyelin phosphodiesterase 1, acid lysosomal sphingomyelin phosphodiesterase 1, acid lysosomal (acid sphingomyelinase) ...
  2. ... Genetic Testing Registry: Congenital bile acid synthesis defect 1 Congenital bile acid synthesis defect, type 1 Disease InfoSearch National Organization ...
  3. ... About This Health Condition EA6 EAA1_HUMAN EAAT-1 EAAT1 Excitatory amino acid transporter 1 FLJ25094 GLAST GLAST1 Glial high affinity glutamate transporter ...
  4. ... 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 ...
  5. ... 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 ...
  6. ... for producing a protein called y+L amino acid transporter 1 (y+LAT-1), which is involved in transporting ... All of these mutations impair the y+LAT-1 protein's ability to transport amino acids. People with lysinuric protein intolerance who are of ...
  7. ... 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. ...
  8. ... K. Functional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis Syndrome. BMC ...
  9. ... ASAH ASAH1_HUMAN FLJ21558 FLJ22079 N-acylsphingosine amidohydrolase (acid ceramidase) 1 PHP PHP32 Tests of ASAH1 PubMed N-ACYLSPHINGOSINE ... article on PubMed Central Park JH, Schuchman EH. Acid ceramidase and human ... 2006 Sep 1. Review. Citation on PubMed Sands MS. Farber disease: ...
  10. ... amino acid transport defect Genetic Testing Registry: Neutral 1 amino acid transport defect Hartnup disease Disease InfoSearch National Organization ... Sep;36(9):1003-7. Epub 2004 Aug 1. Citation on PubMed
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