000 01322 a2200361 4500
005 20250513141034.0
264 0 _c19980416
008 199804s 0 0 eng d
022 _a0270-9139
024 7 _a10.1002/hep.510270422
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSmit, J W
245 0 0 _aContribution of the murine mdr1a P-glycoprotein to hepatobiliary and intestinal elimination of cationic drugs as measured in mice with an mdr1a gene disruption.
_h[electronic resource]
260 _bHepatology (Baltimore, Md.)
_cApr 1998
300 _a1056-63 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aATP Binding Cassette Transporter, Subfamily B, Member 1
_xgenetics
650 0 4 _aAnimals
650 0 4 _aBile
_xmetabolism
650 0 4 _aBiological Availability
650 0 4 _aIntestinal Mucosa
_xmetabolism
650 0 4 _aLiver
_xmetabolism
650 0 4 _aMale
650 0 4 _aMice
650 0 4 _aMice, Knockout
650 0 4 _aVecuronium Bromide
_xpharmacokinetics
700 1 _aSchinkel, A H
700 1 _aMüller, M
700 1 _aWeert, B
700 1 _aMeijer, D K
773 0 _tHepatology (Baltimore, Md.)
_gvol. 27
_gno. 4
_gp. 1056-63
856 4 0 _uhttps://doi.org/10.1002/hep.510270422
_zAvailable from publisher's website
999 _c9505017
_d9505017