Rat wct mutation prevents differentiation of maturation-stage ameloblasts resulting in hypo-mineralization in incisor teeth. (Q53472393)

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2 January 2020

title

Rat wct mutation prevents differentiation of maturation-stage ameloblasts resulting in hypo-mineralization in incisor teeth (English)

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author name string

Masaru Osawa

1

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2 January 2020

Shin Kenmotsu

2

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2 January 2020

Taku Masuyama

3

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2 January 2020

Kazuyuki Taniguchi

4

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2 January 2020

Takashi Uchida

5

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2 January 2020

Chikara Saito

6

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publication date

17 July 2007

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Histochemistry and Cell Biology

2 January 2020

published in

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volume

128

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issue

3

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2 January 2020

page(s)

183-193

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https://scigraph.springernature.com/pub.10.1007/s00418-007-0297-3

2 January 2020

exact match

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Autosomal-dominant hypoplastic form of amelogenesis imperfecta caused by an enamelin gene mutation at the exon-intron boundary

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

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A radioautographic study of the incorporation of iron 55 by the ameloblasts in the zone of maturation of rat incisors

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Mutational analysis of candidate genes in 24 amelogenesis imperfecta families

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Full-length sequence, localization, and chromosomal mapping of ameloblastin. A novel tooth-specific gene

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Synthesis, secretion, degradation, and fate of ameloblastin during the matrix formation stage of the rat incisor as shown by immunocytochemistry and immunochemistry using region-specific antibodies

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Amelogenin p.M1T and p.W4S mutations underlying hypoplastic X-linked amelogenesis imperfecta

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A nomenclature for X-linked amelogenesis imperfecta

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Mutational analysis of X-linked amelogenesis imperfecta in multiple families

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A novel autosomal-recessive mutation, whitish chalk-like teeth, resembling amelogenesis imperfecta, maps to rat chromosome 14 corresponding to human 4q21

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

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Immunochemical and immunohistochemical studies, using antisera against porcine 25 kDa amelogenin, 89 kDa enamelin and the 13-17 kDa nonamelogenins, on immature enamel of the pig and rat.

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A nonsense mutation in the enamelin gene causes local hypoplastic autosomal dominant amelogenesis imperfecta (AIH2).

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12 December 2020

Cytochemical studies on the ferritin-containing vesicles of the rat incisor ameloblasts with special reference to the acid phosphatase activity

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12 December 2020

Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation

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Dental enamel formation and its impact on clinical dentistry

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

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Ameloblastin gene (AMBN) maps within the critical region for autosomal dominant amelogenesis imperfecta at chromosome 4q21.

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12 December 2020

Cloning of rat amelotin and localization of the protein to the basal lamina of maturation stage ameloblasts and junctional epithelium

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12 December 2020

Amelogenin-deficient mice display an amelogenesis imperfecta phenotype

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12 December 2020

Unique enamel phenotype associated with amelogenin gene (AMELX) codon 41 point mutation

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Laminin gamma2 expression is developmentally regulated during murine tooth morphogenesis and is intense in ameloblasts

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10.1007/S00418-007-0297-3

Identifiers

DOI

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2 January 2020

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