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- '''Cytochrome P-450''' is a "superfamily of hundreds of closely related hemeproteins found thro Cytochrome P-450's role in drug metabolism is described by Wolf:<ref name="pmid10723863">{{c22 KB (2,960 words) - 17:35, 10 February 2024
- 12 bytes (1 word) - 01:10, 31 January 2008
- 213 bytes (25 words) - 17:07, 14 May 2010
- In [[biology]], the '''cytochrome P-450 CYP2D6''' is a "[[cytochrome P-450]] enzyme that catalyzes the hydroxylation of many drugs and environmental c ...due to inhibiting metabolism of [[tamoxifen]] to its active metabolite by cytochrome P-450 CYP2D6.<ref>{{Cite journal | doi = 10.1136/bmj.c693 | volume = 340 | issue3 KB (483 words) - 17:34, 10 February 2024
- ...84">{{cite journal |author=Mega JL, Close SL, Wiviott SD, ''et al'' |title=Cytochrome P-450 Polymorphisms and Response to Clopidogrel |journal=N. Engl. J. Med. |volume8 KB (1,130 words) - 17:34, 10 February 2024
- Auto-populated based on [[Special:WhatLinksHere/Cytochrome P-450]]. Needs checking by a human.926 bytes (114 words) - 15:48, 11 January 2010
- 195 bytes (29 words) - 07:21, 30 September 2009
- Isoenzyme of cytochrome P-450.66 bytes (7 words) - 04:02, 16 December 2011
Page text matches
- #REDIRECT [[Cytochrome P-450]]30 bytes (3 words) - 00:31, 24 February 2009
- Isoenzyme of cytochrome P-450.66 bytes (7 words) - 04:02, 16 December 2011
- Citalopram is metabolised by [[cytochrome P-450]] CYP3A4 and [[Cytochrome P-450 CYP2C19|CYP2C19]]. ...ion]] has issued a warning to not use higher doses because of use of the [[cytochrome P-450]] system and also arrhythmias.<ref>{{cite web |url= http://www.fda.gov/Safe1 KB (123 words) - 11:44, 2 February 2023
- * [[Duloxetine]]. A moderate inhibitor of[[cytochrome P-450 CYP2D6]].<ref name="IndianaP450">[http://medicine.iupui.edu/clinpharm/ddis/ * [[Fluoxetine]] (generic). A strong inhibitor of [[cytochrome P-450 CYP2D6]].<ref name="IndianaP450">[http://medicine.iupui.edu/clinpharm/ddis/3 KB (345 words) - 09:46, 13 February 2011
- {{r|Cytochrome P-450}}349 bytes (43 words) - 08:14, 10 September 2008
- * [[Cytochrome P-450]]445 bytes (51 words) - 02:11, 7 October 2013
- In [[biology]], the '''cytochrome P-450 CYP2D6''' is a "[[cytochrome P-450]] enzyme that catalyzes the hydroxylation of many drugs and environmental c ...due to inhibiting metabolism of [[tamoxifen]] to its active metabolite by cytochrome P-450 CYP2D6.<ref>{{Cite journal | doi = 10.1136/bmj.c693 | volume = 340 | issue3 KB (483 words) - 17:34, 10 February 2024
- Tamoxifen is metabolized in the liver by [[cytochrome P-450 CYP2D6]] to active metabolites. ...en due to inhibiting metabolism of tamoxifen to its active metabolite by [[cytochrome P-450 CYP2D6]].<ref>{{Cite journal | doi = 10.1136/bmj.c693 | volume = 340 | issu2 KB (211 words) - 19:00, 2 July 2010
- {{r|Cytochrome P-450}}490 bytes (63 words) - 17:08, 11 January 2010
- {{r|Cytochrome P-450}}541 bytes (70 words) - 19:39, 11 January 2010
- {{r|Cytochrome P-450}}638 bytes (80 words) - 11:56, 11 January 2010
- {{r|Cytochrome P-450}}666 bytes (86 words) - 11:35, 11 January 2010
- {{r|Cytochrome P-450}}616 bytes (75 words) - 16:49, 11 January 2010
- ...] and [[myoglobin]]."<ref>{{MeSH}}</ref> [[Heme]] is also a component of [[cytochrome P-450]].715 bytes (98 words) - 08:18, 10 September 2008
- {{r|Cytochrome P-450}}798 bytes (96 words) - 10:58, 11 January 2010
- {{r|Cytochrome P-450}}751 bytes (96 words) - 11:59, 11 January 2010
- Paroxetine is metabolized in the liver by [[cytochrome P-450 CYP2D6]]. ...ue to inhibiting metabolism of [[tamoxifen]] to its active metabolite by [[cytochrome P-450 CYP2D6]].<ref>{{Cite journal | doi = 10.1136/bmj.c693 | volume = 340 | issu2 KB (279 words) - 11:00, 10 February 2010
- Auto-populated based on [[Special:WhatLinksHere/Cytochrome P-450]]. Needs checking by a human.926 bytes (114 words) - 15:48, 11 January 2010
- {{r|Cytochrome P-450}}898 bytes (111 words) - 19:11, 11 January 2010
- {{r|Cytochrome P-450}}850 bytes (136 words) - 17:21, 19 June 2008