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"[" 1S -"1-(5-CHLORO-1-benzathine-3-YL)-2-(2-NAPHTHYLAMINO)-2-OXOETHYL]PHOSPHONIC" ACID
- ... Condition acid sphingomyelinase ASM ASM_HUMAN sphingomyelin phosphodiesterase 1, acid lysosomal sphingomyelin phosphodiesterase 1, acid lysosomal (acid sphingomyelinase) ...
- ... Genetic Testing Registry: Congenital bile acid synthesis defect 1 Congenital bile acid synthesis defect type 1 National Organization for Rare ... deficiency. J Pediatr Gastroenterol Nutr. 2010 Jan;50(1):61-6. doi: 10.1097/MPG.0b013e3181b47b34. Citation on PubMed
- ... 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 ...
- Acid Rain (Environmental Protection Agency)Water Pollution/Specifics ... Water Pollution ... Air Pollution/Specifics ... Air Pollution ... Environmental Protection Agency ... The causes of acid rain, how acid rain affects ...
- ... 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 ...
- ... amino acid transport defect Genetic Testing Registry: Neutral 1 amino acid transport defect Hartnup disease National Organization for Rare ... 7. doi: 10.1038/ng1406. Epub 2004 Aug 1. Citation on PubMed