Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary for 3.4.21.61 extracted from

  • Graham, M.J.; Lemonidis, K.M.; Whipple, C.P.; Subramaniam, A.; Monia, B.P.; Crooke, S.T.; Crooke, R.M.
    Antisense inhibition of proprotein convertase subtilisin/kexin type 9 reduces serum LDL in hyperlipidemic mice (2007), J. Lipid Res., 48, 763-767.
    View publication on PubMed

Application

Application Comment Organism
medicine antisense inhibition of PCSK9 is an attractive and novel therapeutic approach for treating hypercholesterolemia Mus musculus

Inhibitors

Inhibitors Comment Organism Structure
ISIS 394814 most potent antisense oligonucleotide. Administration to high fat-fed mice for 6 weeks reduces hepatic PCSK9 mRNA levels by 92%, total cholesterol and LDL by 53% and 38%, respectively. Inhibition of PCSK9 expression results in a 2fold increase in hepatic LDLR protein levels Mus musculus

Organism

Organism UniProt Comment Textmining
Mus musculus
-
C57BL/6 mice
-
Mus musculus C57BL/6
-
C57BL/6 mice
-

Source Tissue

Source Tissue Comment Organism Textmining
liver
-
Mus musculus
-

Synonyms

Synonyms Comment Organism
PCSK9
-
Mus musculus
proprotein convertase subtilisin/kexin type 9
-
Mus musculus