Related references
Note: Only part of the references are listed.Ultrastructural Analyses of Deciduous Teeth Affected by Hypocalcified Amelogenesis Imperfecta from a Family with a Novel Y458X FAM83H Nonsense Mutation
W. El-Sayed et al.
CELLS TISSUES ORGANS (2010)
Mutations in the Beta Propeller WDR72 Cause Autosomal-Recessive Hypomaturation Amelogenesis Imperfecta
Walid El-Sayed et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
Expression patterns of the Fam83h gene during murine tooth development
Min-Jung Lee et al.
ARCHIVES OF ORAL BIOLOGY (2009)
Fam83h is Associated with Intracellular Vesicles and ADHCAI
Y. Ding et al.
JOURNAL OF DENTAL RESEARCH (2009)
Molecular Decay of the Tooth Gene Enamelin (ENAM) Mirrors the Loss of Enamel in the Fossil Record of Placental Mammals
Robert W. Meredith et al.
PLOS GENETICS (2009)
FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfecta
Jung-Wook Kim et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Hen's teeth with enamel cap: from dream to impossibility
Jean-Yves Sire et al.
BMC EVOLUTIONARY BIOLOGY (2008)
Mutational spectrum ofFAM83H: the C-terminal portion is required for tooth enamel calcification
Sook-Kyung Lee et al.
HUMAN MUTATION (2008)
Morphological and molecular evidence for a stepwise evolutionary transition from teeth to baleen in mysticete whales
Thomas A. Demere et al.
SYSTEMATIC BIOLOGY (2008)
A new locus for autosomal dominant amelogenesis imperfecta on chromosome 8q24.3
Gustavo Mendoza et al.
HUMAN GENETICS (2007)
Mutational analysis of candidate genes in 24 amelogenesis imperfecta families
Jung-Wook Kim et al.
EUROPEAN JOURNAL OF ORAL SCIENCES (2006)
ENAM mutations in autosomal-dominant amelogenesis imperfecta
JW Kim et al.
JOURNAL OF DENTAL RESEARCH (2005)
MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta
JW Kim et al.
JOURNAL OF MEDICAL GENETICS (2005)
Amelogenin p.M1T and p.W4S mutations underlying hypoplastic X-linked amelogenesis imperfecta
JW Kim et al.
JOURNAL OF DENTAL RESEARCH (2004)
Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta
PS Hart et al.
JOURNAL OF MEDICAL GENETICS (2004)
WD-repeat proteins: structure characteristics, biological function, and their involvement in human diseases
D Li et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2001)
Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta
MH Rajpar et al.
HUMAN MOLECULAR GENETICS (2001)
Homology-based method for identification of protein repeats using statistical significance estimates
MA Andrade et al.
JOURNAL OF MOLECULAR BIOLOGY (2000)
Share Paper
