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Amelogenesis Imperfecta, Type III

Known as: Amelogenesis Imperfecta, Hypomineralization Type, AI3, Amelogenesis Imperfecta, Hypocalcification Type, Autosomal Dominant 
National Institutes of Health

Papers overview

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2019
2019
Purpose: The purpose of this study was to evaluate the effect of different dentin deproteinization treatments on the microtensile… 
2017
2017
Amelogenesis imperfecta is a group of rare inherited disorders that affect tooth enamel formation, quantitatively and/or… 
Review
2016
Review
2016
Statement of problem: Amelogenesis imperfecta (AI) is a genetic disorder that causes defective enamel development in both primary… 
Review
2015
Review
2015
Bovine Amelogenin, a 170-residue, ~19 kDa extracellular, hydrophobic, phosphoprotein with an overall ellipsoidal shape, secreted… 
2007
2007
OBJECTIVE To localize the gene (s) responsible for autosomal dominant hypocalcified amelogenesis imperfecta in a Chinese family… 
2002
2002
In order to analyze a multi-player linear-quadratic alternating-move dynamicgame, this paper develops a solution method by making… 
1999
1999
1 2 0 . 0 Dear Editor: Alzheimer's disease (AD) is a progressive disease of the brain leading to intellectual failure and memory… 
1997
1997
Cardiac muscarinic receptors activate an inwardly rectifying K1 channel, IK1Ach, via pertussis toxin (PT)-sensitive… 
1992
1992
Interactions of the 5' and 3' splice sites with intron internal sequences of the yeast mitochondrial group I intron aI3 were…