Microfluidic source-sink model reveals effects of biophysically distinct CXCL12 isoforms in breast cancer chemotaxis

Integrative Biology (United Kingdom)

Volumn 6, Issue 5, 2014, Pages 564-576

  Cavnar, S P ^a   Ray, P ^b   Moudgil, P ^a   Chang, S L ^a   Luker, K E ^b   Linderman, J J ^a   Takayama, S ^a   Luker, G D ^a,b  

^a UNIVERSITY OF MICHIGAN   (United States)

^b UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMOKINE RECEPTOR CXCR4; CHEMOKINE RECEPTOR CXCR7; ISOPROTEIN; STROMAL CELL DERIVED FACTOR 1; STROMAL CELL DERIVED FACTOR 1BETA; STROMAL CELL DERIVED FACTOR 1GAMMA; UNCLASSIFIED DRUG;

ADVANCED CANCER; ANALYTICAL EQUIPMENT; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BINDING AFFINITY; BREAST CANCER; CANCER CELL; CELL MIGRATION; CHEMOTAXIS; CONTROLLED STUDY; CYTOKINE RELEASE; FIBROBLAST; HUMAN; HUMAN CELL; HUMAN TISSUE; IN VITRO STUDY; MICROFLUIDIC DEVICE; MICROFLUIDICS; MOUSE; NONHUMAN; OPEN READING FRAME; PRIMARY TUMOR; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; TIME-LAPSE VIDEO MICROSCOPY; TUMOR XENOGRAFT;

EID: 84899096894     PISSN: 17579694     EISSN: 17579708     Source Type: Journal    
DOI: 10.1039/c4ib00015c     Document Type: Article

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