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1 duction of the inhibitor was not affected by tretinoin.
2                    Pretreatment of skin with tretinoin (all-trans-retinoic acid) inhibited the induct
3  one year of maintenance therapy with either tretinoin alone or in combination with methotrexate and
4    Retinoic-acid receptors specifically bind tretinoin and alitretinoin, whereas retinoid-X receptors
5                       The proportions of the tretinoin and control groups who developed a BCC at 5 ye
6 RA apparently results in greater exposure to tretinoin and for a longer time.
7 NFRSF11A, and in the pathways related to the tretinoin and H3K27me3 markers.
8                             In some studies, tretinoin and its vehicle were applied to skin under occ
9 ose of currently marketed topical retinoids: tretinoin and tazarotene.
10 s less pronounced with acitretin compared to tretinoin- and tazarotene-containing formulations, sugge
11             A similar effect was observed in tretinoin- and tazarotene-treated mice.
12 despite maintenance L-ATRA and similarity in tretinoin AUC on days 1 and 85, and the other at 5 month
13 131 veterans in the Veterans Affairs Topical Tretinoin Chemoprevention (VATTC) Trial.
14 cted the randomized Veterans Affairs Topical Tretinoin Chemoprevention Trial of high-dose topical tre
15 cinoma (BCC) in the Veterans Affairs topical tretinoin chemoprevention trial, which included individu
16                In contrast to the decline in tretinoin concentration seen within 3 to 4 days of admin
17 es between the area under the curve (AUC) of tretinoin concentration versus time on day 1 and day 15
18                                Because serum tretinoin concentrations are higher, and maintained long
19 PL to either a standard induction regimen of tretinoin, cytarabine, and daunorubicin, followed by 2 c
20 n Chemoprevention Trial of high-dose topical tretinoin for KC prevention.
21 of life difference was worse symptoms in the tretinoin group at 12 months after randomization.
22                                      Topical tretinoin has been used for KC chemoprevention, although
23                    Topical therapy including tretinoins, hydroxy acids, bleaching agents, and sunscre
24                       Treatment with topical tretinoin inhibits irradiation-induced matrix metallopro
25 patients demonstrates that high-dose topical tretinoin is ineffective at reducing risk of KCs.
26  et al. assessed the effects of 0.1% topical tretinoin on NMSC.
27 We randomized 1,131 patients to topical 0.1% tretinoin or a matching vehicle control for 1.5-5.5 year
28 d by 2 courses of consolidation therapy with tretinoin plus daunorubicin, or to the same induction an

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