Diseases of the tooth: The genetic and molecular basis of inherited anomalies affecting the dentition

Wiley Interdisciplinary Reviews: Developmental Biology

Volumn 2, Issue 2, 2013, Pages 183-212

  Cobourne, Martyn T ^a   Sharpe, Paul T ^a  

^a KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVIN; AMELOBLASTIN; AMELOGENIN; APC PROTEIN; BETA CATENIN; BONE MORPHOGENETIC PROTEIN 4; CASEIN KINASE I; CYCLIN DEPENDENT KINASE INHIBITOR 1A; ECTODYSPLASIN A; EDAR ASSOCIATED DEATH DOMAIN PROTEIN; EDAR RECEPTOR; FAS ANTIGEN; FIBROBLAST GROWTH FACTOR; FIBROBLAST GROWTH FACTOR 3; FIBROBLAST GROWTH FACTOR 8; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; LATENT TRANSFORMING GROWTH FACTOR BETA BINDING PROTEIN; LOW DENSITY LIPOPROTEIN RECEPTOR RELATED PROTEIN 5; LOW DENSITY LIPOPROTEIN RECEPTOR RELATED PROTEIN 6; MATRIX METALLOPROTEINASE 20; PERICENTRIN; SONIC HEDGEHOG PROTEIN; TRANSCRIPTION FACTOR MSX1; TRANSCRIPTION FACTOR PAX9; TRANSCRIPTION FACTOR PITX2; TRANSCRIPTION FACTOR RUNX2; TUMOR NECROSIS FACTOR; TUMOR NECROSIS FACTOR RECEPTOR ASSOCIATED FACTOR 6; UNINDEXED DRUG; WNT5A PROTEIN;

ADENOMATOUS POLYP; AMELOGENESIS IMPERFECTA; AUTOSOMAL RECESSIVE DISORDER; CLEIDOCRANIAL DYSPLASIA; DISEASE ASSOCIATION; ECTODERMAL DYSPLASIA; FAMILIAL COLON POLYPOSIS; GENE EXPRESSION; GENE MUTATION; HUMAN; HYPODONTIA; HYPOPHOSPHATASIA; NONHUMAN; OLIGODONTIA; POSTNATAL DEVELOPMENT; REVIEW; RIEGER SYNDROME; SIGNAL TRANSDUCTION; TOOTH DEVELOPMENT; TOOTH DISEASE; TOOTH ERUPTION; TOOTH MALFORMATION; TOOTH SIZE; ANIMAL; DENTITION; GENETICS; GROWTH, DEVELOPMENT AND AGING; METABOLISM; MOUSE; PATHOLOGY; TOOTH;

AMELOGENESIS IMPERFECTA; ANIMALS; DENTINOGENESIS IMPERFECTA; DENTITION; HUMANS; MICE; ODONTOGENESIS; TOOTH; TOOTH ABNORMALITIES; TOOTH ERUPTION;

EID: 84886289321     PISSN: 17597684     EISSN: 17597692     Source Type: Journal    
DOI: 10.1002/wdev.66     Document Type: Review

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