Genetic basis for tooth malformations: From mice to men and back again

Clinical Genetics

Volumn 80, Issue 4, 2011, Pages 319-329

  Mitsiadis, Ta ^a   Luder, Hu ^a  

^a UNIVERSITY OF ZURICH   (Switzerland)

Author keywords

Ameloblasts; Amelogenesis imperfecta; BMP; Dental malformations; Dental pathology; Enamel; FGF; Notch; Odontogenesis; Oligodontia; Tooth agenesis; Tooth development; Transcription factors

Indexed keywords

AMELOBLASTIN; KALLIKREIN; MATRIX METALLOPROTEINASE 20; NOTCH RECEPTOR; PROTEIN P63; TRANSCRIPTION FACTOR RUNX2;

AMELOBLAST; AMELOGENESIS IMPERFECTA; ARTICLE; CELL FATE; GENE DELETION; GENE EXPRESSION; GENETIC ANALYSIS; GENETIC DISORDER; HUMAN; HYPODONTIA; MOUTH MUCOSA; NEURAL CREST CELL; NONHUMAN; PRIORITY JOURNAL; TOOTH DEVELOPMENT; TOOTH MALFORMATION;

AMELOBLASTS; AMELOGENESIS IMPERFECTA; ANIMALS; HUMANS; MANDIBLE; MAXILLA; MICE; MOUTH MUCOSA; NEURAL CREST; ODONTOGENESIS; TOOTH ABNORMALITIES;

DANIO RERIO; MUS;

EID: 80052638026     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2011.01762.x     Document Type: Article

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