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A novel PITX2 mutation in non‐syndromic orodental anomalies

Oral diseases, 2018-05, Vol.24 (4), p.611-618

2018

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A novel de novo mutation substantiates KDF1 as a gene causing ectodermal dysplasia

British journal of dermatology (1951), 2019-08, Vol.181 (2), p.419-420

2019

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A novel GJA1 mutation in oculodentodigital dysplasia with extensive loss of enamel

Oral diseases, 2017-09, Vol.23 (6), p.795-800

2017

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Novel compound heterozygous mutations in KREMEN1 confirm it as a disease gene for ectodermal dysplasia

British journal of dermatology (1951), 2018-09, Vol.179 (3), p.758-760

2018

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Dental properties, ultrastructure, and pulp cells associated with a novel DSPP mutation

Oral diseases, 2018-05, Vol.24 (4), p.619-627

2018

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Excess NF-κB Induces Ectopic Odontogenesis in Embryonic Incisor Epithelium

Journal of dental research, 2015-01, Vol.94 (1), p.121-128

2015

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Gene expression, micro‐CT and histomorphometrical analysis of sinus floor augmentation with biphasic calcium phosphate and deproteinized bovine bone mineral: A randomized controlled clinical trial

Clinical implant dentistry and related research, 2024-04, Vol.26 (2), p.402-414

2024

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Cole‐Carpenter syndrome in a patient from Thailand

American journal of medical genetics. Part A, 2018-08, Vol.176 (8), p.1706-1710

2018

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A novel de novo mutation substantiates KDF 1 as a gene causing ectodermal dysplasia

British journal of dermatology (1951), 2019-08, Vol.181 (2), p.419-420

2019

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Lrp4 modulates extracellular integration of cell signaling pathways in development

PloS one, 2008-12, Vol.3 (12), p.e4092-e4092

2008

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A novel GJA 1 mutation in oculodentodigital dysplasia with extensive loss of enamel

Oral diseases, 2017-09, Vol.23 (6), p.795-800

2017

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Wnt signaling in the murine diastema

European journal of orthodontics, 2012-08, Vol.34 (4), p.518-524

2012

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A novel de novo mutation substantiates KDF1 as a gene causing ectodermal dysplasia

The British journal of dermatology, 2019, Vol.181 (2), p.419-420

2019

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Novel compound heterozygous mutations in KREMEN1 confirm it as a disease gene for ectodermal dysplasia

The British journal of dermatology, 2018, Vol.179 (3), p.758-760

2018

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Unraveling metagenomics through long-read sequencing: a comprehensive review

Journal of translational medicine, 2024-01, Vol.22 (1), p.111-19, Article 111

2024

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MBTPS2, a membrane bound protease, underlying several distinct skin and bone disorders

Journal of translational medicine, 2021-03, Vol.19 (1), p.114-114, Article 114

2021

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Comparative transcriptome profiles of human dental pulp stem cells from maxillary and mandibular teeth

Scientific reports, 2022-05, Vol.12 (1), p.8860-8860, Article 8860

2022

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Patterns of nonsyndromic tooth agenesis and sexual dimorphism

BMC oral health, 2023-01, Vol.23 (1), p.37-37, Article 37

2023

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Tooth agenesis patterns and variants in PAX9: A systematic review

The Japanese dental science review, 2023-12, Vol.59, p.129-137

2023

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Periodic stripe formation by a Turing mechanism operating at growth zones in the mammalian palate

Nature genetics, 2012-03, Vol.44 (3), p.348-351

2012

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Four novel mutations of FAM20A in amelogenesis imperfecta type IG and review of literature for its genotype and phenotype spectra

Molecular genetics and genomics : MGG, 2020-07, Vol.295 (4), p.923-931

2020

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Functional consequences of C-terminal mutations in RUNX2

Scientific reports, 2023-07, Vol.13 (1), p.12202-12202, Article 12202

2023

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Human dental pulp stem cell responses to different dental pulp capping materials

BMC oral health, 2021-04, Vol.21 (1), p.209-13, Article 209

2021

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Craniosynostosis: orofacial and oral health perspectives with masticatory insights

BMC oral health, 2024-07, Vol.24 (1), p.1-11, Article 767

2024

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Patterns of molar agenesis associated with p.P20L and p.R77Q variants in PAX9

European journal of oral sciences, 2022-04, Vol.130 (2), p.e12855-n/a

2022

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A novel PITX2 mutation in non‐syndromic orodental anomalies

A novel de novo mutation substantiates KDF1 as a gene causing ectodermal dysplasia

A novel GJA1 mutation in oculodentodigital dysplasia with extensive loss of enamel

Novel compound heterozygous mutations in KREMEN1 confirm it as a disease gene for ectodermal dysplasia

Dental properties, ultrastructure, and pulp cells associated with a novel DSPP mutation

Excess NF-κB Induces Ectopic Odontogenesis in Embryonic Incisor Epithelium

Gene expression, micro‐CT and histomorphometrical analysis of sinus floor augmentation with biphasic calcium phosphate and deproteinized bovine bone mineral: A randomized controlled clinical trial

Cole‐Carpenter syndrome in a patient from Thailand

A novel de novo mutation substantiates KDF 1 as a gene causing ectodermal dysplasia

Lrp4 modulates extracellular integration of cell signaling pathways in development

A novel GJA 1 mutation in oculodentodigital dysplasia with extensive loss of enamel

Wnt signaling in the murine diastema

A novel de novo mutation substantiates KDF1 as a gene causing ectodermal dysplasia

Novel compound heterozygous mutations in KREMEN1 confirm it as a disease gene for ectodermal dysplasia

Unraveling metagenomics through long-read sequencing: a comprehensive review

MBTPS2, a membrane bound protease, underlying several distinct skin and bone disorders

Comparative transcriptome profiles of human dental pulp stem cells from maxillary and mandibular teeth

Patterns of nonsyndromic tooth agenesis and sexual dimorphism

Tooth agenesis patterns and variants in PAX9: A systematic review

Periodic stripe formation by a Turing mechanism operating at growth zones in the mammalian palate

Four novel mutations of FAM20A in amelogenesis imperfecta type IG and review of literature for its genotype and phenotype spectra

Functional consequences of C-terminal mutations in RUNX2

Human dental pulp stem cell responses to different dental pulp capping materials

Craniosynostosis: orofacial and oral health perspectives with masticatory insights

Patterns of molar agenesis associated with p.P20L and p.R77Q variants in PAX9

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