| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/S00439-004-1084-Z |
| P698 | PubMed publication ID | 14758537 |
| P2093 | author name string | S Lindskog | |
| A Elgadi | |||
| B Malmgren | |||
| S Norgren | |||
| P2860 | cites work | Dentin phosphoprotein and dentin sialoprotein are cleavage products expressed from a single transcript coded by a gene on human chromosome 4. Dentin phosphoprotein DNA sequence determination | Q24312880 |
| Molecular cloning of a human dentin sialophosphoprotein gene | Q28137931 | ||
| DSPP mutation in dentinogenesis imperfecta Shields type II | Q28200045 | ||
| Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP | Q28200065 | ||
| Dentin matrix proteins | Q28267456 | ||
| Genomic organization, chromosomal mapping, and promoter analysis of the mouse dentin sialophosphoprotein (Dspp) gene, which codes for both dentin sialoprotein and dentin phosphoprotein. | Q32067766 | ||
| Characterization of porcine dentin sialoprotein (DSP) and dentin sialophosphoprotein (DSPP) cDNA clones | Q33185890 | ||
| The HUGO Gene Nomenclature Committee (HGNC). | Q34111138 | ||
| MEPE/OF45, a new dentin/bone matrix protein and candidate gene for dentin diseases mapping to chromosome 4q21. | Q34165637 | ||
| Manifestations of genetic diseases in the human pulp | Q39893923 | ||
| Inherited defects in tooth structure | Q39903479 | ||
| Mutation of the signal peptide region of the bicistronic gene DSPP affects translocation to the endoplasmic reticulum and results in defective dentine biomineralization | Q44159131 | ||
| Dentin sialophosphoprotein knockout mouse teeth display widened predentin zone and develop defective dentin mineralization similar to human dentinogenesis imperfecta type III. | Q46287190 | ||
| A novel rat 523 amino acid phosphophoryn: nucleotide sequence and genomic organization | Q48342157 | ||
| Nomenclature for the description of human sequence variations | Q48738393 | ||
| Rat dentin matrix protein 3 is a compound protein of rat dentin sialoprotein and phosphophoryn | Q48750766 | ||
| Six decades of dentinogenesis research. Historical and prospective views on phosphophoryn and dentin sialoprotein. | Q52189019 | ||
| Six generations of hereditary opalescent dentin: report of case | Q66840498 | ||
| Dentinogenesis imperfecta in a six-generation family. A clinical, radiographic and histologic comparison of two branches through three generations | Q67924038 | ||
| Dentinogenesis imperfecta: genetic variations in a six-generation family | Q70995660 | ||
| Assessment of dysplastic dentin in osteogenesis imperfecta and dentinogenesis imperfecta | Q73488033 | ||
| Refinement of the dentinogenesis imperfecta type II locus to an interval of less than 2 centiMorgans at chromosome 4q21 and the creation of a yeast artificial chromosome contig of the critical region | Q77889388 | ||
| P433 | issue | 5 | |
| P921 | main subject | dentinogenesis imperfecta | Q548984 |
| P1104 | number of pages | 8 | |
| P304 | page(s) | 491-498 | |
| P577 | publication date | 2004-02-03 | |
| P1433 | published in | Human Genetics | Q5937167 |
| P1476 | title | Clinical, histopathologic, and genetic investigation in two large families with dentinogenesis imperfecta type II. | |
| P478 | volume | 114 |
| Q36665293 | A DSPP mutation causing dentinogenesis imperfecta and characterization of the mutational effect. |
| Q41172686 | A comprehensive analysis of normal variation and disease-causing mutations in the human DSPP gene |
| Q37391232 | A dentin sialophosphoprotein mutation that partially disrupts a splice acceptor site causes type II dentin dysplasia |
| Q33530548 | A novel DSPP mutation causes dentinogenesis imperfecta type II in a large Mongolian family |
| Q21261443 | A novel DSPP mutation is associated with type II dentinogenesis imperfecta in a Chinese family |
| Q46170833 | A novel mutation in the DSPP gene associated with dentinogenesis imperfecta type II. |
| Q47228958 | A novel splice acceptor mutation in the DSPP gene causing dentinogenesis imperfecta type II. |
| Q52033211 | A rat 8 kb dentin sialoprotein-phosphophoryn (DSP-PP) promoter directs spatial and temporal LacZ activity in mouse tissues. |
| Q28506931 | Amelogenesis imperfecta in a new animal model--a mutation in chromosome 5 (human 4q21) |
| Q33555689 | Dentin Sialophophoprotein (DSPP) and Dentin |
| Q38330183 | Dentin glycoprotein: the protein in the middle of the dentin sialophosphoprotein chimera |
| Q34104443 | Dentin sialophosphoprotein in biomineralization |
| Q52004411 | Dentin sialophosphoprotein is processed by MMP-2 and MMP-20 in vitro and in vivo. |
| Q37197265 | Dentinogenesis Imperfecta : A Family which was Affected for Over Three Generations |
| Q33649653 | Dentinogenesis and Dentin Sialophosphoprotein (DSPP) |
| Q50578145 | Dentinogenesis imperfecta type II- genotype and phenotype analyses in three Danish families. |
| Q36637825 | Detection of a Novel DSPP Mutation by NGS in a Population Isolate in Madagascar |
| Q36841898 | Developmental biology and genetics of dental malformations |
| Q36197243 | Disorders of human dentin |
| Q36420274 | Dspp mutations disrupt mineralization homeostasis during odontoblast differentiation |
| Q35697998 | Enamel malformations associated with a defined dentin sialophosphoprotein mutation in two families. |
| Q40170261 | Establishment of porcine pulp-derived cell lines and expression of recombinant dentin sialoprotein and recombinant dentin matrix protein-1. |
| Q34503330 | Exclusion of p63 as a candidate gene for autosomal-dominant amelogenesis imperfecta. |
| Q46379662 | Functional splicing assay of DSPP mutations in hereditary dentin defects |
| Q97517299 | Gelatinases Cleave Dentin Sialoprotein Intracellularly |
| Q36798995 | Hereditary dentin defects |
| Q37330583 | Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia |
| Q51896986 | Identification of the DSPP mutation in a new kindred and phenotype-genotype correlation. |
| Q38239448 | Isolated dentinogenesis imperfecta and dentin dysplasia: revision of the classification |
| Q83396525 | Mutation identification of the DSPP in a Chinese family with DGI-II and an up-to-date bioinformatic analysis |
| Q38515714 | Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type II. |
| Q36872617 | N-terminal Dentin Sialoprotein fragment induces type I collagen production and upregulates dentinogenesis marker expression in osteoblasts |
| Q37000972 | Overlapping DSPP mutations cause dentin dysplasia and dentinogenesis imperfecta |
| Q40428302 | Phenotype and genotype analyses in seven families with dentinogenesis imperfecta or dentin dysplasia |
| Q33666435 | Phenotype characterization and DSPP mutational analysis of three Brazilian dentinogenesis imperfecta type II families |
| Q51143019 | Phenotypes and genotypes in 2 DGI families with different DSPP mutations. |
| Q24650972 | Phenotypic variation in dentinogenesis imperfecta/dentin dysplasia linked to 4q21 |
| Q37146131 | Porcine dentin sialophosphoprotein: length polymorphisms, glycosylation, phosphorylation, and stability |
| Q33811338 | Porcine dentin sialoprotein glycosylation and glycosaminoglycan attachments |
| Q38334422 | Porcine dentin sialoprotein is a proteoglycan with glycosaminoglycan chains containing chondroitin 6-sulfate |
| Q28591626 | Proteolytic processing of dentin sialophosphoprotein (DSPP) is essential to dentinogenesis |
| Q42027856 | 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. |
| Q57280181 | Structural features, processing mechanism and gene splice variants of dentin sialophosphoprotein |
| Q36878852 | The molecular control of and clinical variations in root formation |
| Q58769725 | Whole exome sequencing identifies an AMBN missense mutation causing severe autosomal-dominant amelogenesis imperfecta and dentin disorders |
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