Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Hereditary dentine diseases resulting from mutations in DSPP gene.

Journal of dentistry - 1 Jul 2012

Maciejewska Izabela, Chomik Ewa

Abstract excerpt

OBJECTIVES: This review groups the newest results of molecular analyses of DSPP gene for patients diagnosed either with dentinogenesis imperfecta type II/III or dentine dysplasia and tries to link the phenotypes with specific mutations in the DSPP gene. DATA: The review includes biochemical data introducing a specificity of DSPP protein which justifies it as a critical factor for dentine mineralization and...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Codon, Nonsense
Share to Dentinogenesis Imperfecta
Share to Extracellular Matrix Proteins

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Frameshift Mutation

Share to INDEL Mutation

Share to Phosphoproteins

Share to Repetitive Sequences, Nucleic Acid

Share to Sialoglycoproteins

Source

Identifiers

PMID: 22521702
DOI: 10.1016/j.jdent.2012.04.004

Genes

DSPP
DSP

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hereditary dentine diseases resulting from mutations in DSPP gene.PMID 22521702Read ↗

Dentin dysplasia type I—A dental disease with genetic heterogeneitySemantic proximity Read ↗

Hereditary dentin defects.Semantic proximity Read ↗

Dentinogenesis imperfecta type II- genotype and phenotype analyses in three Danish families.Semantic proximity Read ↗

Molecular basis of human dentin diseases.Semantic proximity Read ↗

A DSPP mutation causing dentinogenesis imperfecta and characterization of the mutational effect.Semantic proximity Read ↗

Isolated dentinogenesis imperfecta and dentin dysplasia: revision of the classification.Semantic proximity Read ↗

A comprehensive analysis of normal variation and disease-causing mutations in the human<i>DSPP</i>geneSemantic proximity Read ↗

Identification of DSPP Novel Variants and Phenotype Analysis in dentinogenesis dysplasia shields type II PatientsSemantic proximity Read ↗

A novel DSPP frameshift mutation causing dentin dysplasia type 2 and disease management strategies.Semantic proximity Read ↗

Identification of DSPP novel variants and phenotype analysis in dentinogenesis dysplasia Shields type II patients.Semantic proximity Read ↗

A novel mutation in the DSPP gene associated with dentinogenesis imperfecta type II.Semantic proximity Read ↗

Phenotypes and genotypes in 2 DGI families with different DSPP mutations.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.