Id |
Subject |
Object |
Predicate |
Lexical cue |
T30 |
0-60 |
Sentence |
denotes |
Nrf2 knockout ICR mice were kindly provided by Dr. Thomas W. |
T1226 |
0-116 |
Sentence |
denotes |
Nrf2 knockout ICR mice were kindly provided by Dr. Thomas W. Kensler (Johns Hopkins University, Baltimore, MD, USA). |
T31 |
61-116 |
Sentence |
denotes |
Kensler (Johns Hopkins University, Baltimore, MD, USA). |
T1227 |
117-245 |
Sentence |
denotes |
Primary astrocytes were obtained from postnatal 2-day-old Nrf2 wide type (WT) and knockout (KO) mice (6 mice for each genotype). |
T32 |
117-245 |
Sentence |
denotes |
Primary astrocytes were obtained from postnatal 2-day-old Nrf2 wide type (WT) and knockout (KO) mice (6 mice for each genotype). |
T1228 |
246-362 |
Sentence |
denotes |
Following decapitation, the cortices were dissected out, and the meninges and associated blood vessels were removed. |
T33 |
246-362 |
Sentence |
denotes |
Following decapitation, the cortices were dissected out, and the meninges and associated blood vessels were removed. |
T1229 |
363-497 |
Sentence |
denotes |
The tissue was roughly chopped with a scalpel blade, incubated in 0.5% trypsin for 10 minutes at 37°C, and agitated every few minutes. |
T34 |
363-497 |
Sentence |
denotes |
The tissue was roughly chopped with a scalpel blade, incubated in 0.5% trypsin for 10 minutes at 37°C, and agitated every few minutes. |
T1230 |
498-698 |
Sentence |
denotes |
After digestion, the tissue was rinsed twice in DMEM with 10% FBS, followed by a mechanical dissociation in DMEM with 20% FBS and 5 units/mL penicillin, 5 μg/mL streptomycin (complete culture medium). |
T35 |
498-698 |
Sentence |
denotes |
After digestion, the tissue was rinsed twice in DMEM with 10% FBS, followed by a mechanical dissociation in DMEM with 20% FBS and 5 units/mL penicillin, 5 μg/mL streptomycin (complete culture medium). |
T1231 |
699-838 |
Sentence |
denotes |
After incubation for 1 h, the supernatant was transferred to a new flask or dish (Costar, USA) for depleting the residual epithelial cells. |
T36 |
699-838 |
Sentence |
denotes |
After incubation for 1 h, the supernatant was transferred to a new flask or dish (Costar, USA) for depleting the residual epithelial cells. |
T1232 |
839-890 |
Sentence |
denotes |
Then the cells were cultivated at 37°C with 5% CO2. |
T37 |
839-890 |
Sentence |
denotes |
Then the cells were cultivated at 37°C with 5% CO2. |
T1233 |
891-953 |
Sentence |
denotes |
And the complete culture medium was half-changed twice a week. |
T38 |
891-953 |
Sentence |
denotes |
And the complete culture medium was half-changed twice a week. |
T1234 |
954-1011 |
Sentence |
denotes |
Astrocytes expanded for about 7 days to reach confluence. |
T39 |
954-1011 |
Sentence |
denotes |
Astrocytes expanded for about 7 days to reach confluence. |
T1235 |
1012-1136 |
Sentence |
denotes |
Then the flasks or dishes were shaken at 150 rpm for 4 h to deplete the microglia and less adherent cells from the cultures. |
T40 |
1012-1136 |
Sentence |
denotes |
Then the flasks or dishes were shaken at 150 rpm for 4 h to deplete the microglia and less adherent cells from the cultures. |
T1236 |
1137-1297 |
Sentence |
denotes |
After shaking, the resulting cultures were mainly astrocytes, which were determined by immunoreactivity for GFAP (sc-166481, Santa Cruz Biotechnology, CA, USA). |
T41 |
1137-1297 |
Sentence |
denotes |
After shaking, the resulting cultures were mainly astrocytes, which were determined by immunoreactivity for GFAP (sc-166481, Santa Cruz Biotechnology, CA, USA). |
T1237 |
1298-1368 |
Sentence |
denotes |
Cells passaged for 2-3 generations were used in the following studies. |
T42 |
1298-1368 |
Sentence |
denotes |
Cells passaged for 2-3 generations were used in the following studies. |