Clinical and molecular analysis of the enamelin gene ENAM in Colombian families with autosomal dominant amelogenesis imperfecta.

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Genes expressed in dental enamel development are associated with molar-incisor hypomineralization Amelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stress.

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P2860

Clinical and molecular analysis of the enamelin gene ENAM in Colombian families with autosomal dominant amelogenesis imperfecta.

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2012 nî lūn-bûn

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2012年論文

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2012年論文

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2012年論文

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Clinical and molecular analysi ...... inant amelogenesis imperfecta.

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Clinical and molecular analysi ...... inant amelogenesis imperfecta.

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Clinical and molecular analysi ...... inant amelogenesis imperfecta.

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Clinical and molecular analysi ...... inant amelogenesis imperfecta.

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Clinical and molecular analysi ...... inant amelogenesis imperfecta.

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Clinical and molecular analysi ...... inant amelogenesis imperfecta.

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P1476

Clinical and molecular analysi ...... inant amelogenesis imperfecta.

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Ana Maria Gómez

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Diana Torres

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Eliana Baquero

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Ignacio Briceño

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Sandra Gutiérrez

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P2860

FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfecta

Mutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfecta

Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects

A simple salting out procedure for extracting DNA from human nucleated cells

Enamelin (Enam) is essential for amelogenesis: ENU-induced mouse mutants as models for different clinical subtypes of human amelogenesis imperfecta (AI)

Enamel defects and ameloblast-specific expression in Enam knock-out/lacz knock-in mice

ENAM Mutations in Autosomal-dominant Amelogenesis Imperfecta

Enamelin and autosomal-dominant amelogenesis imperfecta.

Cloning human enamelin cDNA, chromosomal localization, and analysis of expression during tooth development.

Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta.

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scholarly article

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10.1590/S1415-47572012000400003

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Clinical and molecular analysis of the enamelin gene ENAM in Colombian families with autosomal dominant amelogenesis imperfecta.

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P2860

P2860

Clinical and molecular analysis of the enamelin gene ENAM in Colombian families with autosomal dominant amelogenesis imperfecta.

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P1433

P1476

P2093

P2860

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P356

P433

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P577

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P356

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P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P932