A novel missense mutation (p.P52R) in amelogenin gene causing X-linked amelogenesis imperfecta.
about
MMP20 hemopexin domain mutation in amelogenesis imperfectaEnamel ribbons, surface nodules, and octacalcium phosphate in C57BL/6 Amelx(-/-) mice and Amelx(+/-) lyonizationTarget gene analyses of 39 amelogenesis imperfecta kindredsPremature stop codon in MMP20 causing amelogenesis imperfecta.Candidate gene strategy reveals ENAM mutations.Defining a new candidate gene for amelogenesis imperfecta: from molecular genetics to biochemistry.Amelogenin splice isoforms stimulate chondrogenic differentiation of ATDC5 cells.Amelogenin-enamelin association in phosphate-buffered saline.
P2860
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P2860
A novel missense mutation (p.P52R) in amelogenin gene causing X-linked amelogenesis imperfecta.
description
2007 nî lūn-bûn
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2007年の論文
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name
A novel missense mutation (p.P ...... inked amelogenesis imperfecta.
@en
type
label
A novel missense mutation (p.P ...... inked amelogenesis imperfecta.
@en
prefLabel
A novel missense mutation (p.P ...... inked amelogenesis imperfecta.
@en
P2093
P2860
P1476
A novel missense mutation (p.P ...... inked amelogenesis imperfecta.
@en
P2093
H Sekiguchi
S Minamitake
S Takabayashi
Y Sakiyama
P2860
P356
10.1177/154405910708600111
P407
P577
2007-01-01T00:00:00Z