Results 61 -
70
of
9,281
for
3S -"3-Hydroxyadipyl-CoA"
- ... About This Health Condition B-cell stimulating factor 3 B-cell stimulatory factor 3 BSF-3 BSF3 cardiotrophin-like cytokine cardiotrophin-like cytokine factor ...
- ... one piece (subunit) of an enzyme called phosphatidylinositol 3-kinase (PI3K). The version of PI3K that contains ... Health Condition p110D P110DELTA phosphatidylinositol-4,5-bisphosphate 3-kinase 110 kDa catalytic subunit delta phosphatidylinositol-4, ...
- ... for making a protein called fibroblast growth factor 3 (FGF3). This protein is part of a family ... LAMM syndrome. More About This Health Condition FGF-3 FGF3_HUMAN HBGF-3 heparin-binding growth factor ...
- ... gene provides instructions for making an enzyme called 3-hydroxyacyl-CoA dehydrogenase that is important for converting ... and convert them to energy. The role of 3-hydroxyacyl-CoA dehydrogenase is to metabolize groups of ...
- ... D2H NBAT RBAT SLC31_HUMAN solute carrier family 3 (amino acid transporter heavy chain), member 1 solute carrier family 3 (cystine, dibasic and neutral amino acid transporters), member ...
- ... provides instructions for making a protein called myosin-3. This protein belongs to a group of proteins ... in muscle tensing (contraction). Muscle fibers containing myosin-3 are found primarily in the fetus before birth, ...
- ... from the COL6A3 gene is the alpha(α)3(VI) chain of type VI collagen. This chain ... About This Health Condition CO6A3_HUMAN collagen alpha-3(VI) chain collagen type VI alpha 3 collagen ...
- ... It is named for several of its features: 3-methylglutaconic aciduria (MEG), deafness (D), encephalopathy (E), and ... by abnormally high levels of an acid, called 3-methylglutaconic acid, in the urine (3-methylglutaconic aciduria). ...
- ... making a protein called fibroblast growth factor receptor 3. This protein is part of a family of ... syndrome (also known as fibroblast growth factor receptor 3 epidermal nevus syndrome). This condition is characterized by ...
- ... in progressive cone dystrophy. ACHM3 achromatopsia (rod monochromacy) 3 cyclic nucleotide gated channel beta 3 Tests of CNGB3 PubMed CYCLIC NUCLEOTIDE-GATED CHANNEL, ...
