Development and Characterization of MDR1 (
ATP Binding Cassette Transporter, Subfamily B
/ genetics
Administration, Oral
Animals
Brain
/ metabolism
CRISPR-Cas Systems
/ genetics
Cytochrome P-450 CYP3A
/ analysis
Digoxin
/ administration & dosage
Female
Gene Knockout Techniques
/ methods
Intestine, Small
/ metabolism
Kidney
/ metabolism
Liver
/ metabolism
Male
Models, Animal
RNA, Messenger
/ analysis
Rats
Rats, Sprague-Dawley
Rats, Transgenic
Journal
Drug metabolism and disposition: the biological fate of chemicals
ISSN: 1521-009X
Titre abrégé: Drug Metab Dispos
Pays: United States
ID NLM: 9421550
Informations de publication
Date de publication:
02 2019
02 2019
Historique:
received:
31
08
2018
accepted:
19
11
2018
pubmed:
28
11
2018
medline:
19
7
2019
entrez:
28
11
2018
Statut:
ppublish
Résumé
Clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein-9 nuclease (Cas9) technology is widely used as a tool for gene editing in rat genome site-specific engineering. Multidrug resistance 1 [MDR1 (also known as P-glycoprotein)] is a key efflux transporter that plays an important role not only in the transport of endogenous and exogenous substances, but also in tumor MDR. In this report, a novel MDR1 (
Identifiants
pubmed: 30478157
pii: dmd.118.084277
doi: 10.1124/dmd.118.084277
doi:
Substances chimiques
ATP Binding Cassette Transporter, Subfamily B
0
RNA, Messenger
0
Digoxin
73K4184T59
multidrug resistance protein 3
9EI49ZU76O
Cytochrome P-450 CYP3A
EC 1.14.14.1
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
71-79Informations de copyright
Copyright © 2019 by The American Society for Pharmacology and Experimental Therapeutics.