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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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Etiologies of non-surgical root canal treatment and its association with risk factors in a selected Thai population

BMC oral health, 2024-08, Vol.24 (1), p.985-16

2024

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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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Salivary proteomic signatures in severe dental fluorosis

Scientific reports, 2024-08, Vol.14 (1), p.18372-12, Article 18372

2024

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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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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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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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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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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

Etiologies of non-surgical root canal treatment and its association with risk factors in a selected Thai population

Patterns of nonsyndromic tooth agenesis and sexual dimorphism

Salivary proteomic signatures in severe dental fluorosis

Tooth agenesis patterns and variants in PAX9: A systematic review

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

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

Functional consequences of C-terminal mutations in RUNX2

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

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