Unexpected identification of a recurrent mutation in theDLX3gene causing amelogenesis imperfecta
Published 2016 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Unexpected identification of a recurrent mutation in theDLX3gene causing amelogenesis imperfecta
Authors
Keywords
-
Journal
ORAL DISEASES
Volume 22, Issue 4, Pages 297-302
Publisher
Wiley
Online
2016-01-14
DOI
10.1111/odi.12439
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Morphological analyses and a novelde novo DLX3mutation associated with tricho-dento-osseous syndrome in a Chinese family
- (2015) Yue Li et al. EUROPEAN JOURNAL OF ORAL SCIENCES
- DNA-dependent formation of transcription factor pairs alters their binding specificity
- (2015) Arttu Jolma et al. NATURE
- Transcriptional Factor DLX3 Promotes the Gene Expression of Enamel Matrix Proteins during Amelogenesis
- (2015) Zhichun Zhang et al. PLoS One
- A system for exact and approximate genetic linkage analysis of SNP data in large pedigrees
- (2012) M. Silberstein et al. BIOINFORMATICS
- Neural Crest Deletion of Dlx3 Leads to Major Dentin Defects through Down-regulation of Dspp
- (2012) Olivier Duverger et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- In vivoimpact of Dlx3 conditional inactivation in neural crest-derived craniofacial bones
- (2012) Olivier Duverger et al. JOURNAL OF CELLULAR PHYSIOLOGY
- DLX3 Homeodomain Mutations Cause Tricho-Dento-Osseous Syndrome with Novel Phenotypes
- (2011) Pekka Nieminen et al. CELLS TISSUES ORGANS
- The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
- (2010) A. McKenna et al. GENOME RESEARCH
- Unkämmbare Haare und atopische Dermatitis bei tricho-dentoossärem Syndrom
- (2010) Dagmara E. Y. Mayer et al. JOURNAL DER DEUTSCHEN DERMATOLOGISCHEN GESELLSCHAFT
- Thickness and microhardness of deciduous tooth enamel with known DLX3 mutation
- (2009) Hong-Keun Hyun et al. ARCHIVES OF ORAL BIOLOGY
- The Sequence Alignment/Map format and SAMtools
- (2009) H. Li et al. BIOINFORMATICS
- DLX3 Mutation in a New Family and Its Phenotypic Variations
- (2009) S.-K. Lee et al. JOURNAL OF DENTAL RESEARCH
- DLX3 c.561_562delCT mutation causes attenuated phenotype of tricho-dento-osseous syndrome
- (2008) J. Timothy Wright et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Dlx3 is a crucial regulator of hair follicle differentiation and cycling
- (2008) J. Hwang et al. DEVELOPMENT
- Physiological implications of DLX homeoproteins in enamel formation
- (2008) Frédéric Lézot et al. JOURNAL OF CELLULAR PHYSIOLOGY
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now