2001
DOI: 10.1016/s0378-4274(00)00290-3
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Genotoxic effect of hydroquinone on the cultured mouse spleenocytes

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Cited by 21 publications
(8 citation statements)
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“…The spleens of the animals were removed aseptically and washed twice in the sterile PBS. The splenocytes were extracted as described earlier 27 and cultured in RPMI-1640 medium containing 10% FCS and concanavalin-A as mitogen, at 37°C for 72 hours. Duplicate cultures were set from each animal for the each drug/radiation dose.…”
Section: Splenocyte Culturementioning
confidence: 99%
“…The spleens of the animals were removed aseptically and washed twice in the sterile PBS. The splenocytes were extracted as described earlier 27 and cultured in RPMI-1640 medium containing 10% FCS and concanavalin-A as mitogen, at 37°C for 72 hours. Duplicate cultures were set from each animal for the each drug/radiation dose.…”
Section: Splenocyte Culturementioning
confidence: 99%
“…In anodizing of titanium, The outer anodic layer (partly exposed to the electrolyte) has an excess of hydroxyl ions compared to the inner layer and is considered to be Ti(OH) 4 . The inner layer, where the de-hydroxylation of the film (water releasing) has occurred, is represented as TiO 2 .…”
Section: Anodizing Of Titanium and Preparation Of Titaniummentioning
confidence: 99%
“…Male Swiss albino mice (4/dose) were given a single dose of HQ (0, 0.5, 1, 2, 4, and 8 mg/kg body weight; ip) per day for 6 days and killed 24 hours after the last treatment. 36 Splenocytes were isolated from these animals, cultured for 72 hours and examined for micronuclei formation. No signs of HQinduced toxicity were observed over the treatment period.…”
Section: In Vivomentioning
confidence: 99%