Matrix metalloproteinase-2 is required for the switch to the angiogenic phenotype in a tumor model

Proceedings of the National Academy of Sciences of the United States of America

Volumn 97, Issue 8, 2000, Pages 3884-3889

  Fang, Jianmin ^a,b   Shing, Yuen ^a,b   Wiederschain, Dmitri ^a   Yan, Li ^a,b   Butterfield, Catherine ^a   Jackson, Geraldine ^a   Harper, Jay ^a   Tamvakopoulos, George ^a   Moses, Marsha A ^a,b  

^a BOSTON CHILDREN S HOSPITAL   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANTISENSE OLIGONUCLEOTIDE; BLOOD CLOTTING FACTOR 8; GELATINASE A;

ANGIOGENESIS; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CANCER INHIBITION; CAPILLARY ENDOTHELIUM; CONTROLLED STUDY; ENZYME ACTIVITY; GEL ELECTROPHORESIS; IMMUNOHISTOCHEMISTRY; MALE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN DEGRADATION; RAT; TUMOR MODEL; TUMOR VASCULARIZATION;

ANIMALS; BASE SEQUENCE; CELL DIVISION; CHONDROSARCOMA; DISEASE MODELS, ANIMAL; DNA PRIMERS; MALE; MATRIX METALLOPROTEINASE 2; NEOVASCULARIZATION, PATHOLOGIC; OLIGONUCLEOTIDES, ANTISENSE; PHENOTYPE; PROTEASE INHIBITORS; RATS; RATS, SPRAGUE-DAWLEY; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION;

ANIMALIA;

EID: 0034635995     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.97.8.3884     Document Type: Article

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