MeSH Browser

MeSH Heading: Lipoprotein Lipase
Tree Number(s): D08.811.277.352.100.430
Unique ID: D008071
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D008071
Annotation: /defic: consider also HYPERLIPOPROTEINEMIA TYPE I
Scope Note: An enzyme of the hydrolase class that catalyzes the reaction of triacylglycerol and water to yield diacylglycerol and a fatty acid anion. The enzyme hydrolyzes triacylglycerols in chylomicrons, very-low-density lipoproteins, low-density lipoproteins, and diacylglycerols. It occurs on capillary endothelial surfaces, especially in mammary, muscle, and adipose tissue. Genetic deficiency of the enzyme causes familial hyperlipoproteinemia Type I. (Dorland, 27th ed) EC 3.1.1.34.
Entry Term(s): Diacylglycerol Lipase; Diglyceride Lipase; Heparin-Clearing Factor; Lipemia-Clearing Factor; Post-Heparin Lipase; Postheparin Lipase; Postheparin Lipoprotein Lipase
CAS Type 1 Name: Triacylglycero-protein acylhydrolase
NLM Classification #: QU 136
See Also: Hyperlipoproteinemia Type I
Online Note: use LIPOPROTEIN LIPASE to search HEPARIN-CLEARING FACTOR & LIPEMIA-CLEARING FACTOR 1966-80
History Note: HEPARIN-CLEARING FACTOR & LIPEMIA-CLEARING FACTOR were see under LIPOPROTEIN LIPASE 1963-80
Date Established: 1960/01/01
Date of Entry: 1999/01/01
Revision Date: 2009/07/06

Allowable Qualifiers: administration & dosage (AD)

adverse effects (AE)

analysis (AN)

antagonists & inhibitors (AI)

biosynthesis (BI)

blood (BL)

cerebrospinal fluid (CF)

chemical synthesis (CS)

chemistry (CH)

classification (CL)

deficiency (DF)

drug effects (DE)

economics (EC)

genetics (GE)

history (HI)

immunology (IM)

isolation & purification (IP)

metabolism (ME)

pharmacokinetics (PK)

pharmacology (PD)

physiology (PH)

poisoning (PO)

radiation effects (RE)

standards (ST)

supply & distribution (SD)

therapeutic use (TU)

toxicity (TO)

ultrastructure (UL)

urine (UR)

Concept UI: M0012578
Scope Note: An enzyme of the hydrolase class that catalyzes the reaction of triacylglycerol and water to yield diacylglycerol and a fatty acid anion. The enzyme hydrolyzes triacylglycerols in chylomicrons, very-low-density lipoproteins, low-density lipoproteins, and diacylglycerols. It occurs on capillary endothelial surfaces, especially in mammary, muscle, and adipose tissue. Genetic deficiency of the enzyme causes familial hyperlipoproteinemia Type I. (Dorland, 27th ed) EC 3.1.1.34.
Terms: Lipoprotein Lipase Preferred Term
Term UI T024060
Date01/01/1999
LexicalTag NON
ThesaurusID NLM (1966); Diglyceride Lipase
Term UI T024057
Date08/01/1980
LexicalTag NON
ThesaurusID UNK (19XX); Heparin-Clearing Factor
Term UI T024058
Date05/22/1980
LexicalTag NON
ThesaurusID UNK (19XX); Postheparin Lipase
Term UI T024061
Date05/19/1982
LexicalTag NON
ThesaurusID UNK (19XX); Diacylglycerol Lipase
Term UI T024056
Date12/09/1981
LexicalTag NON
ThesaurusID UNK (19XX); Post-Heparin Lipase
Term UI T024063
Date05/19/1982
LexicalTag NON
ThesaurusID UNK (19XX); Postheparin Lipoprotein Lipase
Term UI T024062
Date05/19/1982
LexicalTag NON
ThesaurusID UNK (19XX); Lipemia-Clearing Factor
Term UI T024059
Date05/22/1980
LexicalTag NON
ThesaurusID UNK (19XX)

Lipoprotein Lipase MeSH Descriptor Data 2025