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Fibrin is a critical regulator of neutrophil effector function at the oral mucosal barrier

Science (American Association for the Advancement of Science), 2021-12, Vol.374 (6575), p.eabl5450-3026

2021

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Biglycan in the Skeleton

Journal of Histochemistry & Cytochemistry, 2020-11, Vol.68 (11), p.747-762

2020

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Abrogation of epithelial BMP2 and BMP4 causes Amelogenesis Imperfecta by reducing MMP20 and KLK4 expression

Scientific reports, 2016-05, Vol.6 (1), p.25364-25364, Article 25364

2016

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FAM20C regulates osteoblast behaviors and intracellular signaling pathways in a cell‐autonomous manner

Journal of cellular physiology, 2018-04, Vol.233 (4), p.3476-3486

2018

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Transgenic expression of Dspp partially rescued the long bone defects of Dmp1-null mice

Matrix biology, 2016-05, Vol.52-54, p.95-112

2016

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The Role of Type VI Collagen in Alveolar Bone

International journal of molecular sciences, 2022-11, Vol.23 (22), p.14347

2022

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The peroxisomal disorder spectrum and Heimler syndrome: Deep phenotyping and review of the literature

American journal of medical genetics. Part C, Seminars in medical genetics, 2020-09, Vol.184 (3), p.618-630

2020

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Oral health-related quality of life in Loeys-Dietz syndrome, a rare connective tissue disorder: an observational cohort study

Orphanet journal of rare diseases, 2019-12, Vol.14 (1), p.291-291, Article 291

2019

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Immortalized Mouse Floxed Fam20c Dental Papillar Mesenchymal and Osteoblast Cell Lines Retain Their Primary Characteristics

Journal of cellular physiology, 2015-11, Vol.230 (11), p.2581-2587

2015

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Accelerated enamel mineralization in Dspp mutant mice

Matrix biology, 2016-05, Vol.52-54, p.246-259

2016

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Noggin inhibition of mouse dentinogenesis

Journal of oral biosciences, 2020-03, Vol.62 (1), p.72-79

2020

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Case Report: Rare Presentation of Dentin Abnormalities in Loeys-Dietz Syndrome Type I

Frontiers in dental medicine, 2021-08, Vol.2

2021

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Type VI Collagen Regulates Endochondral Ossification in the Temporomandibular Joint

JBMR plus, 2022-05, Vol.6 (5), p.e10617-n/a

2022

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Role of the NH2-terminal fragment of dentin sialophosphoprotein in dentinogenesis

European journal of oral sciences, 2013-04, Vol.121 (2), p.76-85

2013

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Quantitative Craniofacial Analysis and Generation of Human Induced Pluripotent Stem Cells for Muenke Syndrome: A Case Report

Journal of developmental biology, 2021-09, Vol.9 (4), p.39

2021

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Overexpressing the NH2-terminal fragment of dentin sialophosphoprotein (DSPP) aggravates the periodontal defects in Dspp knockout mice

Journal of oral biosciences, 2014-11, Vol.56 (4), p.143-148

2014

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TMJ Symptoms Resolve With Orthognathic Surgery and Are Associated With Condylar Remodeling

Journal of oral and maxillofacial surgery, 2023-09, Vol.81 (9), p.S4-S5

2023

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Bite Force Control Capacity Differs Between Dentofacial Differences and Improves With Orthognathic Surgery

Journal of oral and maxillofacial surgery, 2023-09, Vol.81 (9), p.S37-S38

2023

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Normative 3D Mandibular and TMJ Kinematics in Orthognathic Asymptomatic and Symptomatic Patients

Journal of oral and maxillofacial surgery, 2023-09, Vol.81 (9), p.S5-S7

2023

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The role of bone morphogenetic proteins 2 and 4 in mouse dentinogenesis

Archives of oral biology, 2018-06, Vol.90, p.33-39

2018

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Loeys-Dietz and Shprintzen-Goldberg syndromes: analysis of TGF-β-opathies with craniofacial manifestations using an innovative multimodality method

Journal of medical genetics, 2022-10, Vol.59 (10), p.938-946

2022

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Inactivation of bone morphogenetic protein 1 (Bmp1) and tolloid-like 1 (Tll1) in cells expressing type I collagen leads to dental and periodontal defects in mice

Journal of molecular histology, 2017-04, Vol.48 (2), p.83-98

2017

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OPG-Fc treatment partially rescues low bone mass phenotype in mature Bgn/Fmod deficient mice but is deleterious to the young mouse skeleton

Journal of structural biology, 2020-12, Vol.212 (3), p.107627-107627, Article 107627

2020

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Severity of oro-dental anomalies in Loeys-Dietz syndrome segregates by gene mutation

Journal of medical genetics, 2020-10, Vol.57 (10), p.699-707

2020

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DDX58(RIG-I)-related disease is associated with tissue-specific interferon pathway activation

Journal of medical genetics, 2022-03, Vol.59 (3), p.294-304

2022

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Fibrin is a critical regulator of neutrophil effector function at the oral mucosal barrier

Biglycan in the Skeleton

Abrogation of epithelial BMP2 and BMP4 causes Amelogenesis Imperfecta by reducing MMP20 and KLK4 expression

FAM20C regulates osteoblast behaviors and intracellular signaling pathways in a cell‐autonomous manner

Transgenic expression of Dspp partially rescued the long bone defects of Dmp1-null mice

The Role of Type VI Collagen in Alveolar Bone

The peroxisomal disorder spectrum and Heimler syndrome: Deep phenotyping and review of the literature

Oral health-related quality of life in Loeys-Dietz syndrome, a rare connective tissue disorder: an observational cohort study

Immortalized Mouse Floxed Fam20c Dental Papillar Mesenchymal and Osteoblast Cell Lines Retain Their Primary Characteristics

Accelerated enamel mineralization in Dspp mutant mice

Noggin inhibition of mouse dentinogenesis

Case Report: Rare Presentation of Dentin Abnormalities in Loeys-Dietz Syndrome Type I

Type VI Collagen Regulates Endochondral Ossification in the Temporomandibular Joint

Role of the NH2-terminal fragment of dentin sialophosphoprotein in dentinogenesis

Quantitative Craniofacial Analysis and Generation of Human Induced Pluripotent Stem Cells for Muenke Syndrome: A Case Report

Overexpressing the NH2-terminal fragment of dentin sialophosphoprotein (DSPP) aggravates the periodontal defects in Dspp knockout mice

TMJ Symptoms Resolve With Orthognathic Surgery and Are Associated With Condylar Remodeling

Bite Force Control Capacity Differs Between Dentofacial Differences and Improves With Orthognathic Surgery

Normative 3D Mandibular and TMJ Kinematics in Orthognathic Asymptomatic and Symptomatic Patients

The role of bone morphogenetic proteins 2 and 4 in mouse dentinogenesis

Loeys-Dietz and Shprintzen-Goldberg syndromes: analysis of TGF-β-opathies with craniofacial manifestations using an innovative multimodality method

Inactivation of bone morphogenetic protein 1 (Bmp1) and tolloid-like 1 (Tll1) in cells expressing type I collagen leads to dental and periodontal defects in mice

OPG-Fc treatment partially rescues low bone mass phenotype in mature Bgn/Fmod deficient mice but is deleterious to the young mouse skeleton

Severity of oro-dental anomalies in Loeys-Dietz syndrome segregates by gene mutation

DDX58(RIG-I)-related disease is associated with tissue-specific interferon pathway activation

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