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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.1-16

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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Cathepsin C in health and disease: from structural insights to therapeutic prospects

Journal of translational medicine, 2024-08, Vol.22 (1), p.777-25

2024

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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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A novel BAG5 variant impairs the ER stress response pathway, causing dilated cardiomyopathy and arrhythmia

Scientific reports, 2024-05, Vol.14 (1), p.11980-11980, Article 11980

2024

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Phenotypic and Genotypic Features of Thai Patients With Nonsyndromic Tooth Agenesis and WNT10A Variants

Frontiers in physiology, 2020-11, Vol.11, p.573214-573214

2020

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The association of polymorphisms in BMP2/MYO1H and skeletal Class II div.1 maxillary and mandibular dimensions. A preliminary ‘report

Saudi journal of biological sciences, 2022-10, Vol.29 (10), p.103405-103405, Article 103405

2022

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Genetic Variants in KCTD1 Are Associated with Isolated Dental Anomalies

International journal of molecular sciences, 2024-05, Vol.25 (10), p.5179

2024

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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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Next generation phenotyping for diagnosis and phenotype-genotype correlations in Kabuki syndrome

Scientific reports, 2024-01, Vol.14 (1), p.2330-2330, Article 2330

2024

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Editorial: Contemporary Views on the Genetics of Dental and Craniofacial Anomalies

Frontiers in dental medicine, 2022-06, Vol.3

2022

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Novel ITGB6 variants cause hypoplastic-hypomineralized amelogenesis imperfecta and taurodontism: characterization of tooth phenotype and review of literature

BDJ open, 2023-04, Vol.9 (1), p.15-15, Article 15

2023

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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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Cleidocranial dysplasia and novel RUNX2 variants: dental, craniofacial, and osseous manifestations

Journal of applied oral science, 2022, Vol.30, p.e20220028-e20220028

2022

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A novel mutation in COL1A2 leads to osteogenesis imperfecta/Ehlers-Danlos overlap syndrome with brachydactyly

Genes & diseases, 2019-06, Vol.6 (2), p.138-146

2019

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Expanding the Oro-Dental and Mutational Spectra of Kabuki Syndrome and Expression of KMT2D and KDM6A in Human Tooth Germs

International journal of biological sciences, 2018-01, Vol.14 (4), p.381-389

2018

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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

Cathepsin C in health and disease: from structural insights to therapeutic prospects

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

Craniosynostosis: orofacial and oral health perspectives with masticatory insights

A novel BAG5 variant impairs the ER stress response pathway, causing dilated cardiomyopathy and arrhythmia

Phenotypic and Genotypic Features of Thai Patients With Nonsyndromic Tooth Agenesis and WNT10A Variants

The association of polymorphisms in BMP2/MYO1H and skeletal Class II div.1 maxillary and mandibular dimensions. A preliminary ‘report

Genetic Variants in KCTD1 Are Associated with Isolated Dental Anomalies

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

Next generation phenotyping for diagnosis and phenotype-genotype correlations in Kabuki syndrome

Editorial: Contemporary Views on the Genetics of Dental and Craniofacial Anomalies

Novel ITGB6 variants cause hypoplastic-hypomineralized amelogenesis imperfecta and taurodontism: characterization of tooth phenotype and review of literature

Lrp4 modulates extracellular integration of cell signaling pathways in development

Cleidocranial dysplasia and novel RUNX2 variants: dental, craniofacial, and osseous manifestations

A novel mutation in COL1A2 leads to osteogenesis imperfecta/Ehlers-Danlos overlap syndrome with brachydactyly

Expanding the Oro-Dental and Mutational Spectra of Kabuki Syndrome and Expression of KMT2D and KDM6A in Human Tooth Germs

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