G-CSF administration after myocardial infarction in mice attenuates late ischemic cardiomyopathy by enhanced arteriogenesis

FASEB Journal

Volumn 20, Issue 7, 2006, Pages

  Deindl, Elisabeth ^a   Zaruba, Marc Michael ^a   Brunner, Stefan ^a   Huber, Bruno ^a   Mehl, Ursula ^a   Assmann, Gerald ^b   Hoefer, Imo E ^c   Mueller Hoecker, Josef ^b   Franz, Wolfgang Michael ^a  

^a LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

^b UNIVERSITY OF MUNICH   (Germany)

^c UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

Author keywords

Bone marrow derived cells; Granulocyte colony stimulating factor; Intercellular adhesion molecule 1

Indexed keywords

GRANULOCYTE COLONY STIMULATING FACTOR; INTERCELLULAR ADHESION MOLECULE 1;

ANGIOGENESIS; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANTIGEN EXPRESSION; ARTICLE; BONE MARROW CELL; CELL PROLIFERATION; CONTROLLED STUDY; DIASTOLE; DRUG MECHANISM; HEART FUNCTION; HEART INFARCTION; HISTOLOGY; IMMUNOHISTOCHEMISTRY; ISCHEMIC HEART DISEASE; MALE; MONONUCLEAR CELL; MOUSE; NONHUMAN; PRIORITY JOURNAL; SMOOTH MUSCLE FIBER; STEM CELL; SYSTOLE; ANIMAL; C57BL MOUSE; CORONARY BLOOD VESSEL; CYTOLOGY; DRUG EFFECT; HEART MUSCLE; HEART MUSCLE ISCHEMIA; METABOLISM; PATHOLOGY; T LYMPHOCYTE SUBPOPULATION;

ANIMALIA; MURINAE;

ANIMALS; CORONARY VESSELS; GRANULOCYTE COLONY-STIMULATING FACTOR; MALE; MICE; MICE, INBRED C57BL; MYOCARDIAL INFARCTION; MYOCARDIAL ISCHEMIA; MYOCARDIUM; NEOVASCULARIZATION, PHYSIOLOGIC; T-LYMPHOCYTE SUBSETS;

EID: 33646538730     PISSN: 08926638     EISSN: None     Source Type: Journal    
DOI: 10.1096/fj.05-4763fje     Document Type: Article

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