I-Ping Chen, DDS, PhDProfessor, Endodontics
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Degree | Institution | Major |
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MS | University of Pennsylvania | Master of Science in Oral Biology |
Certificate | University of Pennsylvania | Endodontics |
PhD | University of Connecticut Health | Biomedical Sciences |
Awards
Name of Award/Honor | Awarding Organization |
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Outstanding Researcher Faculty Award | |
P.J. Robinson Award | |
Young Investigator Award | Rare Bone Disease Research Summit |
Harold M. Frost Young Investigator Award | The American Society of Bone and Mineral Research (ASBMR) |
Dentist Scientist Pathway to Independence Award (K99/R00) | NIDCR |
In the Chen laboratory, we mainly focus on the investigation of pathogenic mechanisms of craniometaphyseal dysplasia (CMD) using multiple genetic and molecular biology approaches including a knock-in mouse model for CMD and induced pluripotent stem cells (iPSCs) from CMD patients. We have characterized the CMD mouse model replicating many features of human CMD and identified abnormal properties of osteoclasts and osteoblasts in CMD. Subsequently, I have generated integration-free induced pluripotent stem (iPS) cells from peripheral blood of CMD patients and control subjects. These hiPSCs will be differentiated into osteoclasts to study osteoclast defects in CMD. My long-term goal is to develop therapeutic strategies that can benefit patients with CMD and similar rare bone disorders.
As an endodontist, I am also interested in dental research. In collaboration with Dr. Chon, a biomedical engineer, we aim to develop a quantitative and objective measurement for dental pain. We examine the use of electrodermal activity to assist pulpal diagnosis and assess dental pain. My laboratory has been funded by the American Association of Endodontists to establish a 3D culture modeling system that can be easily analyzed and improve or complement the current assays for testing new dental materials.
Not Accepting Lab Rotation Students at this time
Journal Articles
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ENPP1 enzyme replacement therapy improves ectopic calcification but does not rescue skeletal phenotype in a mouse model for craniometaphyseal dysplasia.
JBMR plus 2024 Sep;8(9):ziae103
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Differentiating between stress- and EPT-induced electrodermal activity during dental examination.
Computers in biology and medicine 2023 Mar;155106695
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The use of electrodermal activity in pulpal diagnosis and dental pain assessment.
International endodontic journal 2023 Mar;56(3):356-368
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Design and Validation of a Multimodal Wearable Device for Simultaneous Collection of Electrocardiogram, Electromyogram, and Electrodermal Activity.
Sensors (Basel, Switzerland) 2022 Nov;22(22):
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Muscle LIM Protein Force-Sensing Mediates Sarcomeric Biomechanical Signaling in Human Familial Hypertrophic Cardiomyopathy.
Circulation 2022 Apr;145(16):1238-1253
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Tlr2/4-Mediated Hyperinflammation Promotes Cherubism-Like Jawbone Expansion in Sh3bp2 (P416R) Knockin Mice.
JBMR plus 2022 Jan;6(1):e10562
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Sensitive Physiological Indices of Pain Based on Differential Characteristics of Electrodermal Activity.
IEEE transactions on bio-medical engineering 2021 Oct;68(10):3122-3130
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Real-Time High-Level Acute Pain Detection Using a Smartphone and a Wrist-Worn Electrodermal Activity Sensor.
Sensors (Basel, Switzerland) 2021 Jun;21(12):
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Generation of Keratinocytes from Human Induced Pluripotent Stem Cells Under Defined Culture Conditions.
Cellular reprogramming 2020 Dec;
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Use of 3D-Printed Guide in Hemisection and Autotransplantation of a Fusion Tooth: a Case Report.
Journal of endodontics 2020 Dec;
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Biodegradable nanofiber-based piezoelectric transducer.
Proceedings of the National Academy of Sciences of the United States of America 2020 Jan;
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Rapid degradation of progressive ankylosis protein (ANKH) in craniometaphyseal dysplasia.
Scientific reports 2018 Oct;8(1):15710
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Rescue of a cherubism bone marrow stromal culture phenotype by reducing TGFβ signaling.
Bone 2018 Mar;11128-35
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Craniometaphyseal Dysplasia Mutations in ANKH Negatively Affect Human Induced Pluripotent Stem Cell Differentiation into Osteoclasts.
Stem cell reports 2017 Oct;91369-1376
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Human Dendritic Cell-Derived Induced Pluripotent Stem Cell Lines Are Not Immunogenic.
Journal of immunology (Baltimore, Md. : 1950) 2017 Jan;1981875-1886
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Dietary phosphate supplement does not rescue skeletal phenotype in a mouse model for craniometaphyseal dysplasia.
Journal of negative results in biomedicine 2016 Oct;15(1):18
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Comparison of the Osteogenic Potential of Mineral Trioxide Aggregate and Endosequence Root Repair Material in a 3-dimensional Culture System.
Journal of endodontics 2016 Mar;42(5):760-765
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Dental Anomalies Associated with Craniometaphyseal Dysplasia.
Journal of dental research 2014 Mar;93(6):553-558
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Induced pluripotent stem cell reprogramming by integration-free Sendai virus vectors from peripheral blood of patients with craniometaphyseal dysplasia.
Cellular reprogramming 2013 Dec;15(6):503-13
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Subtelomeric hotspots of aberrant 5-hydroxymethylcytosine-mediated epigenetic modifications during reprogramming to pluripotency.
Nature cell biology 2013 Jun;15(6):700-11
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Dental abnormalities in a mouse model for craniometaphyseal dysplasia.
Journal of dental research 2013 Feb;92(2):173-9
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A novel autosomal recessive GJA1 missense mutation linked to Craniometaphyseal dysplasia.
PloS one 2013 Jan;8(8):e73576
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Oculofaciocardiodental syndrome: a rare case and review of the literature.
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2012 Sep;49(5):e55-60
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Two novel large ANKH deletion mutations in sporadic cases with craniometaphyseal dysplasia.
Clinical genetics 2012 Jan;81(1):93-5
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A Phe377del mutation in ANK leads to impaired osteoblastogenesis and osteoclastogenesis in a mouse model for craniometaphyseal dysplasia (CMD).
Human molecular genetics 2011 Mar;20(5):948-61
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Inhibitory activities of omega-3 Fatty acids and traditional african remedies on keloid fibroblasts.
Wounds : a compendium of clinical research and practice 2011 Jan;23(4):97-106
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Cherubism gene Sh3bp2 is important for optimal bone formation, osteoblast differentiation, and function.
American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics 2010 Aug;138(2):140.e1-140.e11; discussion 140-1
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Pro416Arg cherubism mutation in Sh3bp2 knock-in mice affects osteoblasts and alters bone mineral and matrix properties.
Bone 2010 May;46(5):1306-1315
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Introduction of a Phe377del mutation in ANK creates a mouse model for craniometaphyseal dysplasia.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2009 Jul;24(7):1206-15
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Conventional and surgical endodontic retreatment of a maxillary first molar: unusual anatomy.
Journal of endodontics 2006 Mar;32(3):228-30
Reviews
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Dental abnormalities in rare genetic bone diseases: Literature review.
Clinical anatomy (New York, N.Y.) 2023 Sep;
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The Use of Patient-Specific Induced Pluripotent Stem Cells (iPSCs) to Identify Osteoclast Defects in Rare Genetic Bone Disorders.
Journal of clinical medicine 2014 Dec;3(4):1490-510
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