- N-acetylmannosamine
- N-ac·e·tyl·man·no·sa·mine (as″ə-təl-) (as″ə-tēl″mə-nōsґə-mēn) mannosamine acetylated at its amino group, an intermediate in the biosynthesis and degradation of sialic acids and sialoglycoconjugates.
Medical dictionary. 2011.
N-acetylmannosamine
Look at other dictionaries:
N-Acetylmannosamine — IUPAC name 2 (Acetylamino) 2 deoxy β D mannopyranose … Wikipedia
GNE (gene) — Glucosamine (UDP N acetyl) 2 epimerase/N acetylmannosamine kinase, also known as GNE, is a human gene.cite web | title = Entrez Gene: GNE glucosamine (UDP N acetyl) 2 epimerase/N acetylmannosamine kinase| url =… … Wikipedia
N-acylmannosamine kinase — Identifiers EC number 2.7.1.60 CAS number 9027 53 6 … Wikipedia
RENBP — Renin binding protein, also known as RENBP, is a human gene.cite web | title = Entrez Gene: RENBP renin binding protein| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=5973| accessdate = ] PBB Summary… … Wikipedia
NAGK — N acetylglucosamine kinase PDB rendering based on 2ch5 … Wikipedia
Hereditary inclusion body myopathy — Hereditary inclusion body myopathies (HIBM) are a heterogeneous group of genetic disorders which have different symptoms. Generally, they are neuromuscular disorders characterized by muscle weakness developing in young adults. Hereditary… … Wikipedia
CRMP1 — Collapsin response mediator protein 1, also known as CRMP1, is a human gene.cite web | title = Entrez Gene: CRMP1 collapsin response mediator protein 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=1400|… … Wikipedia
NANS — For other uses, see Nans. N acetylneuraminic acid synthase PDB rendering based on 1wvo … Wikipedia
William A. Gahl — William A. Gahl, MD, PhD is the current Clinical Director of the National Human Genome Research Institute at the NIH main campus in Bethesda, MD.Dr. Gahl graduated with a BS from Massachusetts Institute of Technology in 1972. He earned his MD… … Wikipedia
Muskeldystrophie — Muskeldystrophien, auch progressive Muskeldystrophie (Dystrophia musculorum progressiva), sind eine Gruppe von Muskelerkrankungen. Es handelt sich um Erbkrankheiten, die durch Mutationen im Erbgut verursacht werden, welche meist zu Defekten oder… … Deutsch Wikipedia
