Embryonic origin and Hox status determine progenitor cell fate during adult bone regeneration

Development

Volumn 135, Issue 17, 2008, Pages 2845-2854

  Leucht, Philipp ^a   Kim, Jae Beom ^a   Amasha, Raimy ^a   James, Aaron W ^a   Girod, Sabine ^a   Helms, Jill A ^a  

^a STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Chondrocyte; Graft; Mesoderm; Mouse; Neural crest; Osteoblast; Periosteum

Indexed keywords

HOX PROTEIN; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR HOXA11; UNCLASSIFIED DRUG;

ADULT STEM CELL; ANIMAL CELL; ANIMAL TISSUE; ARTICLE; BONE DEVELOPMENT; BONE REGENERATION; BONE REMODELING; CELL DIFFERENTIATION; CELL FATE; CELL FUNCTION; CELL LINEAGE; CELL POPULATION; CELL PROLIFERATION; CELL TRANSPLANTATION; CHONDROGENESIS; CONTROLLED STUDY; GENE EXPRESSION; HOST CELL; IN VIVO STUDY; JAW DISEASE; MALE; MESODERM; MOUSE; NEURAL CREST CELL; NONHUMAN; OSTEOBLAST; PRIORITY JOURNAL;

AGING; ANIMALS; BONE AND BONES; BONE REGENERATION; CELL DIFFERENTIATION; CELL LINEAGE; CELL PROLIFERATION; CELL SURVIVAL; CELL TRANSPLANTATION; EMBRYO, MAMMALIAN; HOMEODOMAIN PROTEINS; LUMINESCENCE; MESODERM; MICE; NEURAL CREST; OSTEOGENESIS; PERIOSTEUM; STEM CELLS; WOUND HEALING;

MUS;

EID: 53349096948     PISSN: 09501991     EISSN: None     Source Type: Journal    
DOI: 10.1242/dev.023788     Document Type: Article

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