Hepatocyte growth factor is sequestered in dentine matrix and promotes regeneration-associated events in dental pulp cells

Cytokine

Volumn 61, Issue 2, 2013, Pages 622-629

  Tomson, Phillip L ^a   Lumley, Philip J ^a   Alexander, M Yvonne ^b   Smith, Anthony J ^a   Cooper, Paul R ^a  

^a UNIVERSITY OF BIRMINGHAM   (United Kingdom)

^b UNIVERSITY OF MANCHESTER   (United Kingdom)

Author keywords

Dentine; Hepatocyte growth factor (HGF); Mineral trioxide aggregate (MTA); Pulp; Regeneration

Indexed keywords

COMPLEMENTARY DNA; OSTEOCALCIN; OSTEOPONTIN; OSTERIX; RECOMBINANT PROTEIN; SCATTER FACTOR; SCATTER FACTOR RECEPTOR; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR RUNX2; UNCLASSIFIED DRUG;

ADENOVIRUS; ANIMAL CELL; ANIMAL CELL CULTURE; ANIMAL TISSUE; ARTICLE; CELL DIFFERENTIATION; CELL ISOLATION; CELL PROLIFERATION; CELLS; CONTROLLED STUDY; DENTAL PULP CELL; DENTIN; DENTINE MATRIX; ENZYME LINKED IMMUNOSORBENT ASSAY; EXPOSURE; EXTRACELLULAR MATRIX; GENE EXPRESSION; HUMAN; HUMAN CELL; HUMAN TISSUE; IN VITRO STUDY; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN EXPRESSION; RAT; RNA ISOLATION; SIGNAL TRANSDUCTION; TISSUE REPAIR; UPREGULATION;

RATTUS;

EID: 84873202524     PISSN: 10434666     EISSN: 10960023     Source Type: Journal    
DOI: 10.1016/j.cyto.2012.11.009     Document Type: Article

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