|1.||Arunakaran, J: 6 articles (07/2013 - 12/2003)|
|2.||Di Renzo, Gianfranco: 4 articles (01/2015 - 10/2005)|
|3.||Srinivasan, N: 4 articles (12/2004 - 12/2003)|
|4.||Secondo, Agnese: 3 articles (01/2015 - 08/2006)|
|5.||Scorziello, Antonella: 3 articles (01/2015 - 10/2005)|
|6.||Thomas, Peter: 3 articles (01/2011 - 06/2004)|
|7.||Khan, Izhar A: 3 articles (01/2011 - 06/2004)|
|8.||Aruldhas, M M: 3 articles (02/2005 - 12/2003)|
|9.||Prokop'eva, N V: 3 articles (03/2004 - 05/2000)|
|10.||Zahara, Alexander R D: 2 articles (11/2015 - 05/2015)|
10/01/1994 - "The present study was undertaken to confirm and characterize the effects of Aroclor 1254 on tumor number, latency, size and malignancy. "
05/01/1999 - "It has been previously described that Aroclor 1254 can inhibit GJIC in rodent liver cells where it is known to be a tumor promoter, while the possibility that Aroclor 1254 exerts its inhibitory effects on GJIC in human keratinocytes and acts as a human skin tumor promoter, deserves further attention. "
10/01/1988 - "Aroclor 1254 had no effect on DEN-induced hepatocarcinogenesis (80.0% incidence, 3.03 tumors per tumor-bearing fish). "
07/15/1987 - "Subsequent exposure to PB (0.05% in drinking water for 40 weeks) or Aroclor 1254 (6 X 300 mg/kg per month) promoted nodule and cancer development only in livers of DENA-initiated recipients. "
05/01/1985 - "The appearance of unique, potentially preneoplastic lesions and tumors in the liver and stomach in dosed rats which do not usually occur spontaneously in control rats would support the hypothesis that Aroclor 1254 induced or initiated these unique lesions de novo rather than promoted the growth of any naturally occurring lesions. "
|2.||Hepatocellular Carcinoma (Hepatoma)
01/01/1984 - "Prior studies have shown that Aroclor 1254 (PCB) differentially alters the incidence of aflatoxin B1 (AFB1) induced hepatocellular carcinomas in trout, depending upon the time of PCB administration relative to AFB1 exposure (Shelton et al., 1983). "
10/12/1987 - "Cotreatment of rat hepatoma H-4-II E cells or C57BL/6J mice with a dose of 2,3,7,8-TCDD which submaximally induces AHH and EROD and a dose of Aroclor 1254 which exhibited little or no induction activity resulted in significant antagonism of the induction effects of 2,3,7,8-TCDD. "
11/01/1980 - "Null effect of dietary Aroclor 1254 on hepatocellular carcinoma incidence in rainbow trout (Salmo gairdneri) exposed to aflatoxin B1 as embryos."
08/01/1974 - "Induction of adenofibrosis and hepatomas of the liver in BALB-cJ mice by polychlorinated biphenyls (Aroclor 1254)."
11/01/1977 - "At the end of the year, 26 of 37 (70.3%) trout fed 6 ppb AFB1 had hepatocellular carcinomas, compared to 14 of 46 (30.4%) trout fed 6 ppb AFB1 plus 100 ppm Aroclor 1254, a highly significant reduction in tumor incidence in the trout on the Aroclor 1254-containing diet. "
|3.||Body Weight (Weight, Body)
11/01/2000 - "The objective of the study was to ascertain the toxicological and reproductive effects of Aroclor 1254 ingestion at dose levels of 0, 5, 20, 40 or 80 microg Aroclor 1254/kg body weight per day (Arnold et al., 1993a,b, 1995, 1996, 1997). "
02/01/2000 - "Decreased body weight gain was evident in the male 100 ppm Aroclor 1254 dose group and in all female Aroclor 1254 dose groups late in the study (when a linear relationship was assumed between body weight and time), correlating with decreased feed consumption. "
05/01/1996 - "A total of 80 menstruating rhesus monkeys (Macaca mulatta) were equally and randomly divided among groups receiving 0, 5, 20, 40, or 80 mu g of Aroclor 1254/kg body weight/day during a 6-year toxicological-reproduction study. "
11/01/2015 - "Thirty-six birds, divided equally among 4 treatment groups (control = 0 µg, low = 0.35 µg, intermediate = 0.70 µg, and high = 1.05 µg Aroclor 1254/g body weight), were dosed 1 d through 18 d posthatch, then tested 8 mo to 9 mo later in captivity in an analog to an open radial arm maze. "
05/19/2015 - "Birds were orally administered 0 (control), 0.35 (low), 0.70 (intermediate), or 1.05 (high) μg Aroclor 1254/g-body weight by gavage from 1 through 18 days posthatch and later exposed in captivity to a photoperiod shift simulating an autumn migration. "
01/01/2015 - "Here we evaluated the effect of PCB exposure on mitochondrial function using the PCB mixture Aroclor-1254 (A1254) in SH-SY5Y neuroblastoma cells. "
08/15/2006 - "In the present study, we investigated whether nitric oxide (NO) could be involved in aroclor 1254 (A1254; a PCB mixture)-induced cytotoxicity in SH-SY5Y human neuroblastoma cells. "
10/01/2005 - "In SH-SY5Y, a human neuroblastoma cell line, Aroclor 1254 (A1254), induced a dose-dependent (10-50 microg/ml) intracellular calcium concentration ([Ca2+]i) increase. "
01/10/2009 - "This study investigates the effects of the PCB mixture Aroclor 1254 (A1254) and two PCB congeners (coplanar, non-ortho PCB 126, and non coplanar PCB 99) on the expression of N-methyl-D-aspartate receptors (NMDARs) and the subsequent toxic effects using a human SHS5-SY neuroblastoma cell line. "
09/01/2011 - "The repressor element 1-silencing transcription factor is a novel molecular target for the neurotoxic effect of the polychlorinated biphenyl mixture aroclor 1254 in neuroblastoma SH-SY5Y cells."
|2.||Polychlorinated Biphenyls (PCBs)
|5.||Aryl Hydrocarbon Receptors (Aryl Hydrocarbon Receptor)
|6.||Aflatoxin B1 (Aflatoxin B)
|8.||Serotonin (5 Hydroxytryptamine)
|9.||N-Methyl-D-Aspartate Receptors (NMDA Receptors)
|2.||Homologous Transplantation (Allograft)