ライフサイエンスコーパス: 8-methoxypsoralen

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1 hemotherapy was applied after oral intake of 8-methoxypsoralen (0.6 mg/kg body weight) 5x weekly duri

2 dose (3 joules/cm2) ultraviolet A energy and 8-methoxypsoralen (100 ng per ml).

3 t a single 18O atom is incorporated into the 8-methoxypsoralen (8-MOP) and psoralen (P) dihydrodiol m

4 Among the psoralen derivatives, 8-methoxypsoralen (8-MOP) is conventionally applied for

5 Three psoralens, 8-methoxypsoralen (8-MOP), 4'-aminomethyl 4,5', 8-trimet

6 furanocoumarins [5-methoxypsoralen (5-MOP), 8-methoxypsoralen (8-MOP), 5-hydroxypsoralen (5-OH-P), 8

7 ution technique, for assessing the repair of 8-methoxypsoralen (8-MOP)-induced DNA ICLs, as well as m

8 ponse to 4-nitroquinoline-N-oxide (4NQO) and 8-methoxypsoralen (8MOP), compared with WRN-proficient c

9 n in vitiliginous skin following exposure to 8-methoxypsoralen (8MOP).

10 s a 4-log reduction in PCR sensitivity, with 8-methoxypsoralen activity facilitated by UV there was b

11 variation in bioavailability of Methoxsalen (8-methoxypsoralen) after ingestion of the standard dose

12 Upon UVA photoactivation, 8-methoxypsoralen alkylates both strands of DNA at the 5

13 ovel photocross-linking technique using free 8-methoxypsoralen and DNA furan-side monoadducts plus lo

14 otent photoactivated chemotherapeutic agents 8-methoxypsoralen and hypericin.

15 s cognate sequence (E-box) was unimpaired by 8-methoxypsoralen and that cross-linking occurred in nor

16 ubated with serial dilutions of hypericin or 8-methoxypsoralen and then stimulated with the mitogen C

17 olated white blood cells to photoactivatable 8-methoxypsoralen and ultraviolet A radiation, is used c

18 man skin melanoma cells exposed to 500 ng/mL 8-methoxypsoralen and UVA irradiation.

19 ondrial membranes, X-rays, UVB (290-320 nm), 8-methoxypsoralen and UVA, vitamin K3, anti-Fas antibody

20 ators (alpha-melanocyte-stimulating hormone, 8-methoxypsoralen, and 3,4-dihydroxyphenylalanine).

21 rol inoculum-treated PBMCs to photoactivated 8-methoxypsoralen- and hypericin-induced apoptosis.

22 Median serum 8-methoxypsoralen concentration increased from 96 to 143

23 Two hours after ingestion, serum 8-methoxypsoralen concentration was determined and photo

24 ivalent, psoralen plus ultraviolet A-induced 8-methoxypsoralen-DNA adduct formation and p53 protein a

25 here is limited information on the effect of 8-methoxypsoralen dose alterations on phototoxicity with

26 Thus, 8-methoxypsoralen dose changes within individuals, over

27 ) were significantly reduced with increasing 8-methoxypsoralen dose from conventional dose minus 10 m

28 Change in 8-methoxypsoralen dose had no detectable effect on the m

29 We studied the effect of changes of 8-methoxypsoralen dose over a narrow range in 15 subject

30 Topical application of 0.2 mg 8-methoxypsoralen per cm2 followed by exposure to ultrav

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