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Volumn 7, Issue 7, 2001, Pages 368-377
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Intercellular adhesion molecule-I (ICAM-I, CD54) deficiency segregates the unique pathophysiological requirements for generating idiopathic pneumonia syndrome (IPS) versus graft-versus-host disease following allogeneic murine bone marrow transplantation
a a a a a |
Author keywords
Allogeneic BMT; ICAM I; Idiopathic pneumonia syndrome
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Indexed keywords
BUFFER;
CHEMOKINE;
CYCLOPHOSPHAMIDE;
CYTOKINE;
GAMMA INTERFERON;
INTERCELLULAR ADHESION MOLECULE 1;
LYMPHOTACTIN;
MACROPHAGE INFLAMMATORY PROTEIN 1ALPHA;
MACROPHAGE INFLAMMATORY PROTEIN 1BETA;
MONOCYTE CHEMOTACTIC PROTEIN 1;
PHOSPHATE;
SODIUM CHLORIDE;
TUMOR NECROSIS FACTOR ALPHA;
ALLOGENIC BONE MARROW TRANSPLANTATION;
ALLOIMMUNITY;
ANIMAL EXPERIMENT;
ANIMAL MODEL;
ANIMAL TISSUE;
ANTIGEN EXPRESSION;
ARTICLE;
CELL MIGRATION;
COLON;
CONTROLLED STUDY;
CYTOKINE PRODUCTION;
DISEASE SEVERITY;
DONOR;
DOSE RESPONSE;
GRAFT VERSUS HOST REACTION;
HOST;
IDIOPATHIC DISEASE;
LETHALITY;
LIVER;
LUNG FUNCTION;
LUNG WEIGHT;
MACROPHAGE;
MORTALITY;
MOUSE;
NEUTROPHIL;
NONHUMAN;
PATHOPHYSIOLOGY;
PNEUMONIA;
RECIPIENT;
REGULATORY MECHANISM;
SPLEEN CELL;
T LYMPHOCYTE;
TISSUE INJURY;
TREATMENT OUTCOME;
WHOLE BODY RADIATION;
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EID: 0034858367
PISSN: 10838791
EISSN: None
Source Type: Journal
DOI: 10.1053/bbmt.2001.v7.pm11529486 Document Type: Article |
Times cited : (29)
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References (57)
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