about
Evolutionary and structural relationships among the group-specific component, albumin and alpha-fetoproteinHuman group-specific component (Gc) is a member of the albumin familyLocalization of the genes for histatins to human chromosome 4q13 and tissue distribution of the mRNAsMolecular genetics of human chromosome 4.The impact of molecular genetics on oral health paradigms.Dentin phosphoprotein gene locus is not associated with dentinogenesis imperfecta types II and III.Pairwise linkage analysis of 11 loci on human chromosome 4.Genetic mapping of the dentinogenesis imperfecta type II locus.Hereditary dentin defects.Cloning and expression analysis of the bovine dentin matrix acidic phosphoprotein gene.Understanding enamel formation from mutations causing X-linked amelogenesis imperfecta.Genetic aspects of dental disorders.Genetic influences in caries and periodontal diseases.A comprehensive analysis of normal variation and disease-causing mutations in the human DSPP gene.Dentin matrix protein-1, a candidate gene for dentinogenesis imperfecta.Rough endoplasmic reticulum trafficking errors by different classes of mutant dentin sialophosphoprotein (DSPP) cause dominant negative effects in both dentinogenesis imperfecta and dentin dysplasia by entrapping normal DSPP.The non-collagenous dentin matrix proteins are involved in dentinogenesis imperfecta type II (DGI-II).
P2860
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P2860
description
1982 nî lūn-bûn
@nan
1982年の論文
@ja
1982年論文
@yue
1982年論文
@zh-hant
1982年論文
@zh-hk
1982年論文
@zh-mo
1982年論文
@zh-tw
1982年论文
@wuu
1982年论文
@zh
1982年论文
@zh-cn
name
Linkage between dentinogenesis imperfecta and Gc.
@en
type
label
Linkage between dentinogenesis imperfecta and Gc.
@en
prefLabel
Linkage between dentinogenesis imperfecta and Gc.
@en
P2093
P2860
P1476
Linkage between dentinogenesis imperfecta and Gc.
@en
P2093
P2860
P356
10.1111/J.1469-1809.1982.TB00693.X
P407
P577
1982-01-01T00:00:00Z