戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 hway and is inhibited by statins, a class of cholesterol-lowering drugs.
2 effects of rechallenge with statins or other cholesterol-lowering drugs.
3  and cardiac events compared with usual-care cholesterol-lowering drugs.
4 rial interventions including another type of cholesterol-lowering drug and (2) inclusion of data on d
5                          For rosuvastatin, a cholesterol-lowering drug and OATP1A/1B substrate, the l
6 disease; and 44% and 50% taking statin-class cholesterol-lowering drugs and aspirin, respectively.
7 nd the development of the newly approved LDL-cholesterol-lowering drugs and critically review their e
8  coronary events in comparison to usual-care cholesterol-lowering drugs and whether perfusion changes
9 iation between statin use (vs. no use of any cholesterol-lowering drug) and the risk of having abnorm
10 cholesterol diet, with or without ezetimibe (cholesterol-lowering drug), and high-fat/high-cholestero
11 between high circulating cholesterol levels, cholesterol-lowering drugs, and breast cancer are confli
12 etitively, reduce LDL levels more than other cholesterol-lowering drugs, and lower triglyceride level
13  of renal patients of interventions (such as cholesterol-lowering drugs, antihypertensives, aspirin,
14 t studies have indicated statins, a class of cholesterol-lowering drugs, as a potential therapy for A
15 ssociated with increased AD risk, and use of cholesterol-lowering drugs associated with decreased ris
16 e KRAS(G12D)-induced LCH-like mouse with the cholesterol-lowering drug atorvastatin ameliorated the p
17 lytic process involved in the synthesis of a cholesterol-lowering drug, atorvastatin (Lipitor), and w
18  (HMG-CoA) reductase inhibitors are powerful cholesterol-lowering drugs, but their broad use in trans
19   An important example of such drugs are the cholesterol-lowering drugs called 'statins', including Z
20 eral decades are needed to determine whether cholesterol-lowering drugs cause cancer in humans.
21 tin, a Food and Drug Administration-approved cholesterol-lowering drug, could protect against nigrost
22 lutaryl-CoA reductase inhibitors, a class of cholesterol-lowering drugs, could interrupt Ang II signa
23 n of Atorvastatin (AT) versus the non-statin cholesterol-lowering drug, Ezetimibe (EZT) on severity o
24 holesterol homeostasis and its response to a cholesterol-lowering drug, ezetimibe.
25          The medications were pravastatin, a cholesterol-lowering drug for the prevention of cardiova
26                               Current use of cholesterol-lowering drugs for five or more years was no
27                     Statins were designed as cholesterol-lowering drugs for the prevention of coronar
28  metabolites in fungi, such as lovastatin, a cholesterol-lowering drug from Aspergillus terreus.
29                                Lovastatin, a cholesterol-lowering drug, has antiproliferative propert
30 itors, which are the most commonly used oral cholesterol-lowering drugs, have immunomodulatory proper
31 d not forget that niacin is an effective LDL-cholesterol-lowering drug in patients with high LDL leve
32  antihyperglycaemic drugs and non-statin LDL-cholesterol-lowering drugs in patients with type 2 diabe
33                                     Statins, cholesterol-lowering drugs, inhibit these deleterious pr
34  to oral hypoglycemic, antihypertensive, and cholesterol-lowering drugs into its Medicare Advantage q
35  of nonsteroidal anti-inflammatory drugs and cholesterol-lowering drugs is consistent with a macropha
36 tal structures of hCE1 in complexes with the cholesterol-lowering drug mevastatin, the breast cancer
37 e relative risk for current users of general cholesterol-lowering drugs, mostly statins in this cohor
38 later in life and maternal intervention with cholesterol-lowering drugs or antioxidants reduce postna
39       Here, I propose that rather than being cholesterol-lowering drugs per se, statins act as vitami
40 ned the association between long-term use of cholesterol-lowering drugs, predominantly statins, and t
41 tivating the apoAI gene or administering the cholesterol-lowering drug probucol.
42 late caveolin/caveolae expression, including cholesterol-lowering drugs, reversed the increased CCE a
43                                          The cholesterol-lowering drug simvastatin has been shown to
44                                          The cholesterol-lowering drug simvastatin promotes bone form
45 n of hPXR both alone and in complex with the cholesterol-lowering drug SR12813 at resolutions of 2.5
46 ns with the 231 patients who did not use any cholesterol-lowering drugs, statin use was associated wi
47                              The widely used cholesterol-lowering drugs, statins, were reported to re
48  the common chiral side chain of statin-type cholesterol-lowering drugs such as Lipitor (atorvastatin
49 s that could cause adverse drug reactions to cholesterol-lowering drugs such as statins.
50              Similarly, pravastatin, another cholesterol-lowering drug, suppressed microglial inflamm
51                                  Statins are cholesterol-lowering drugs, targeting HMG-CoA reductase,
52  treatment of macrophages with lovastatin, a cholesterol-lowering drug that blocks farnesylation and
53 when the mice were treated with Ezetimibe, a cholesterol-lowering drug that blocks intestinal dietary
54                Statins are widely prescribed cholesterol-lowering drugs that are a first-line treatme
55                                  Statins are cholesterol-lowering drugs that have been proven in rand
56 e A (HMG-CoA) reductase enzyme (statins) are cholesterol-lowering drugs that have shown promise as th
57                                  Statins are cholesterol-lowering drugs that inhibit 3-hydroxy-3-meth
58                        Statins are effective cholesterol-lowering drugs that reduce the risk of cardi
59                      Statins are widely used cholesterol-lowering drugs that selectively inhibit the
60  a decade after the approval of the last LDL-cholesterol-lowering drug, the cholesterol absorption in
61 cal pathway has given rise to a new class of cholesterol-lowering drugs, the proprotein convertase su
62 ls using non-physiological high fat diets or cholesterol-lowering drugs to modify plasma cholesterol,
63 s statins, account for the great majority of cholesterol-lowering drug use.
64 acy of statins, the most prescribed class of cholesterol-lowering drugs used for the prevention and t
65                   In the analysis of general cholesterol-lowering drugs, we ascertained 3420 cases of
66                             Simvastatin is a cholesterol-lowering drug whose pleiotropic effects may
67 ed in part on the assumption that overuse of cholesterol-lowering drugs will otherwise become a probl

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。