| Id |
Subject |
Object |
Predicate |
Lexical cue |
| T1 |
0-111 |
Sentence |
denotes |
The development of macrophages from large mononuclear cells in the blood of patients with inflammatory disease. |
| T1 |
0-111 |
Sentence |
denotes |
The development of macrophages from large mononuclear cells in the blood of patients with inflammatory disease. |
| T2 |
112-262 |
Sentence |
denotes |
The origin and function of the increased of "atypical lymphocytes" which appear in the blood of patients with many inflammatory diseases is not known. |
| T2 |
112-262 |
Sentence |
denotes |
The origin and function of the increased of "atypical lymphocytes" which appear in the blood of patients with many inflammatory diseases is not known. |
| T3 |
263-528 |
Sentence |
denotes |
Leukocyte suspensions from eight patients with systemic lupus erythematosus (SLE), five patients with other rheumatic diseases, and five patients with infectious diseases were pulse-labeled with tritiated thymidine (Tdr-(3)H) and sampled after 5 and 72 hr in vitro. |
| T3 |
263-528 |
Sentence |
denotes |
Leukocyte suspensions from eight patients with systemic lupus erythematosus (SLE), five patients with other rheumatic diseases, and five patients with infectious diseases were pulse-labeled with tritiated thymidine (Tdr-(3)H) and sampled after 5 and 72 hr in vitro. |
| T4 |
529-678 |
Sentence |
denotes |
Radioautographs indicated that 35% of the total large, nonphagocytic mononuclear leukocytes incorporated Tdr-(3)H during the initial 5 hr of culture. |
| T4 |
529-678 |
Sentence |
denotes |
Radioautographs indicated that 35% of the total large, nonphagocytic mononuclear leukocytes incorporated Tdr-(3)H during the initial 5 hr of culture. |
| T5 |
679-769 |
Sentence |
denotes |
Tdr-(3)H-labeled large phagocytic or glass-adherent cells were observed only infrequently. |
| T5 |
679-769 |
Sentence |
denotes |
Tdr-(3)H-labeled large phagocytic or glass-adherent cells were observed only infrequently. |
| T6 |
770-952 |
Sentence |
denotes |
After 72 hr one-third of the original number of Tdr-(3)H-labeled cells from patients with SLE developed the morphology of macrophages and the capacity to phagocytose latex particles. |
| T6 |
770-952 |
Sentence |
denotes |
After 72 hr one-third of the original number of Tdr-(3)H-labeled cells from patients with SLE developed the morphology of macrophages and the capacity to phagocytose latex particles. |
| T7 |
953-1051 |
Sentence |
denotes |
Similar findings were observed in patients with other rheumatic diseases and bacterial infections. |
| T7 |
953-1051 |
Sentence |
denotes |
Similar findings were observed in patients with other rheumatic diseases and bacterial infections. |
| T8 |
1052-1222 |
Sentence |
denotes |
In contrast, the thymidine-labeled cells from patients with infectious hepatitis and infectious mononucleosis were poorly viable in culture and rarely became macrophages. |
| T8 |
1052-1222 |
Sentence |
denotes |
In contrast, the thymidine-labeled cells from patients with infectious hepatitis and infectious mononucleosis were poorly viable in culture and rarely became macrophages. |
| T9 |
1223-1272 |
Sentence |
denotes |
Tdr-(3)H-labeled small lymphocytes were uncommon. |
| T9 |
1223-1272 |
Sentence |
denotes |
Tdr-(3)H-labeled small lymphocytes were uncommon. |
| T10 |
1273-1481 |
Sentence |
denotes |
The present experiments suggest that in patients with certain inflammatory diseases large, proliferating "lymphocytelike" cells are very immature monocyte precursors which appear in response to tissue injury. |
| T10 |
1273-1481 |
Sentence |
denotes |
The present experiments suggest that in patients with certain inflammatory diseases large, proliferating "lymphocytelike" cells are very immature monocyte precursors which appear in response to tissue injury. |
| T11 |
1482-1593 |
Sentence |
denotes |
These DNA-synthesizing cells together with mature monocytes may serve as the circulating source of macrophages. |
| T11 |
1482-1593 |
Sentence |
denotes |
These DNA-synthesizing cells together with mature monocytes may serve as the circulating source of macrophages. |