Human ameloblastin gene: genomic organization and mutation analysis in amelogenesis imperfecta patients
- 1 February 2001
- journal article
- research article
- Published by Wiley in European Journal of Oral Sciences
- Vol. 109 (1) , 8-13
- https://doi.org/10.1034/j.1600-0722.2001.00979.x
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Cloning, characterization and immunolocalization of human ameloblastinEuropean Journal of Oral Sciences, 2000
- Ameloblastin Gene (AMBN) Maps within the Critical Region for Autosomal Dominant Amelogenesis Imperfecta at Chromosome 4q21Genomics, 1997
- An amelogenin gene defect associated with human X-linked amelogenesis imperfectaArchives of Oral Biology, 1997
- Mapping of the Locus for Autosomal Dominant Amelogenesis Imperfecta (AIH2) to a 4-Mb YAC Contig on Chromosome 4q11–q21Genomics, 1997
- A novel gene expressed in rat ameloblasts codes for proteins with cell binding domainsJournal of Bone and Mineral Research, 1996
- Full-length Sequence, Localization, and Chromosomal Mapping of AmeloblastinJournal of Biological Chemistry, 1996
- Amelogenin signal peptide mutation: correlation between mutations in the amelogenin gene (AMGX) and manifestations of X-linked amelogenesis imperfectaGenomics, 1995
- IMMUNOCHEMICAL AND IMMUNOCYTOCHEMICAL STUDY OF A 15 kDa NON-AMELOGENIN AND RELATED PROTEINS IN THE PORCINE IMMATURE ENAMEL: PROPOSAL OF A NEW GROUP OF ENAMEL PROTEINS ‘SHEATH PROTEINS’ Biomedical Research, 1995
- PCR-SSCP: A method for detection of mutationsGenetic Analysis: Biomolecular Engineering, 1992
- A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1)Genomics, 1991