Associated Papers
Salt Dependence of DNA Binding Activity of Human Transcription Factor Dlx3.
Jin HS et al.
International Journal of Molecular Sciences, 2022
Novel DLX3 variants in amelogenesis imperfecta with attenuated tricho-dento-osseous syndrome.
Whitehouse LLE et al.
Oral Diseases, 2019
Tricho-dento-osseous syndrome and precocious eruption.
Jain P et al.
Journal of Clinical and Experimental Dentistry, 2017
Senescence: novel insight into DLX3 mutations leading to enhanced bone formation in Tricho-Dento-Osseous syndrome.
Zhao N et al.
Scientific Reports, 2016
27924851 (PubMed )
Supplement: srep38680-s1.pdf
Unexpected identification of a recurrent mutation in the DLX3 gene causing amelogenesis imperfecta.
Kim YJ et al.
Oral Diseases, 2016
DLX3 homeodomain mutations cause tricho-dento-osseous syndrome with novel phenotypes.
Nieminen P et al.
Cells, Tissues, Organs, 2011
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