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I-Ping Chen, Ph.D. - Publications

Affiliations: 
2009 University of Connecticut, Storrs, CT, United States 
Area:
Molecular Biology
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24 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Fujii Y, Okabe I, Hatori A, Sah SK, Kanaujiya J, Fisher M, Norris R, Terasaki M, Reichenberger EJ, Chen IP. Skeletal abnormalities caused by a Connexin43 mutation in a mouse model for autosomal recessive craniometaphyseal dysplasia. Research Square. PMID 38405920 DOI: 10.21203/rs.3.rs-3906170/v1  0.758
2023 Iwata E, Sah SK, Chen IP, Reichenberger E. Dental abnormalities in rare genetic bone diseases: Literature review. Clinical Anatomy (New York, N.Y.). PMID 37737444 DOI: 10.1002/ca.24117  0.65
2021 Fujii Y, Monteiro N, Sah SK, Javaheri H, Ueki Y, Fan Z, Reichenberger EJ, Chen IP. Tlr2/4-Mediated Hyperinflammation Promotes Cherubism-Like Jawbone Expansion in Sh3bp2 (P416R) Knockin Mice. Jbmr Plus. 6: e10562. PMID 35079675 DOI: 10.1002/jbm4.10562  0.67
2020 Chen IP. Differentiation of Human Induced Pluripotent Stem Cells (hiPSCs) into Osteoclasts. Bio-Protocol. 10: e3854. PMID 33659501 DOI: 10.21769/BioProtoc.3854  0.324
2020 Fujii Y, Kozak E, Dutra E, Varadi A, Reichenberger EJ, Chen IP. Restriction of Dietary Phosphate Ameliorates Skeletal Abnormalities in a Mouse Model for Craniometaphyseal Dysplasia. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 35: 2070-2081. PMID 33463757 DOI: 10.1002/Jbmr.4110  0.729
2020 Sah SK, Kanaujiya JK, Chen IP, Reichenberger EJ. Generation of Keratinocytes from Human Induced Pluripotent Stem Cells Under Defined Culture Conditions. Cellular Reprogramming. PMID 33373529 DOI: 10.1089/cell.2020.0046  0.621
2018 Kanaujiya J, Bastow E, Luxmi R, Hao Z, Zattas D, Hochstrasser M, Reichenberger EJ, Chen IP. Rapid degradation of progressive ankylosis protein (ANKH) in craniometaphyseal dysplasia. Scientific Reports. 8: 15710. PMID 30356088 DOI: 10.1038/S41598-018-34157-5  0.715
2018 Liu Y, Sharma T, Chen IP, Reichenberger E, Ueki Y, Arif Y, Parisi D, Maye P. Rescue of a cherubism bone marrow stromal culture phenotype by reducing TGFβ signaling. Bone. PMID 29530719 DOI: 10.1016/J.Bone.2018.03.009  0.704
2017 Chen IP, Luxmi R, Kanaujiya J, Hao Z, Reichenberger EJ. Craniometaphyseal Dysplasia Mutations in ANKH Negatively Affect Human Induced Pluripotent Stem Cell Differentiation into Osteoclasts. Stem Cell Reports. PMID 29056330 DOI: 10.1016/J.Stemcr.2017.09.016  0.756
2017 Chhabra A, Chen IP, Batra D. Human Dendritic Cell-Derived Induced Pluripotent Stem Cell Lines Are Not Immunogenic. Journal of Immunology (Baltimore, Md. : 1950). PMID 28115528 DOI: 10.4049/Jimmunol.1601676  0.301
2016 Liu Y, Dutra EH, Reichenberger EJ, Chen IP. Dietary phosphate supplement does not rescue skeletal phenotype in a mouse model for craniometaphyseal dysplasia. Journal of Negative Results in Biomedicine. 15: 18. PMID 27784318 DOI: 10.1186/S12952-016-0061-0  0.736
2016 Rifaey HS, Villa M, Zhu Q, Wang YH, Safavi K, Chen IP. Comparison of the Osteogenic Potential of Mineral Trioxide Aggregate and Endosequence Root Repair Material in a 3-dimensional Culture System. Journal of Endodontics. PMID 26994596 DOI: 10.1016/J.Joen.2016.02.001  0.393
2014 Chen IP. The Use of Patient-Specific Induced Pluripotent Stem Cells (iPSCs) to Identify Osteoclast Defects in Rare Genetic Bone Disorders. Journal of Clinical Medicine. 3: 1490-1510. PMID 25621177 DOI: 10.3390/Jcm3041490  0.543
2014 Chen IP, Tadinada A, Dutra EH, Utreja A, Uribe F, Reichenberger EJ. Dental Anomalies Associated with Craniometaphyseal Dysplasia. Journal of Dental Research. 93: 553-8. PMID 24663682 DOI: 10.1177/0022034514529304  0.728
2013 Chen IP, Fukuda K, Fusaki N, Iida A, Hasegawa M, Lichtler A, Reichenberger EJ. Induced pluripotent stem cell reprogramming by integration-free Sendai virus vectors from peripheral blood of patients with craniometaphyseal dysplasia. Cellular Reprogramming. 15: 503-13. PMID 24219578 DOI: 10.1089/Cell.2013.0037  0.726
2013 Hu Y, Chen IP, de Almeida S, Tiziani V, Do Amaral CM, Gowrishankar K, Passos-Bueno MR, Reichenberger EJ. A novel autosomal recessive GJA1 missense mutation linked to Craniometaphyseal dysplasia. Plos One. 8: e73576. PMID 23951358 DOI: 10.1371/Journal.Pone.0073576  0.717
2013 Dutra EH, Chen IP, Reichenberger EJ. Dental abnormalities in a mouse model for craniometaphyseal dysplasia. Journal of Dental Research. 92: 173-9. PMID 23160629 DOI: 10.1177/0022034512468157  0.681
2012 Dutra EH, Chen IP, McGregor TL, Ranells JD, Reichenberger EJ. Two novel large ANKH deletion mutations in sporadic cases with craniometaphyseal dysplasia. Clinical Genetics. 81: 93-5. PMID 22150416 DOI: 10.1111/j.1399-0004.2011.01700.x  0.636
2012 Davoody A, Chen IP, Nanda R, Uribe F, Reichenberger EJ. Oculofaciocardiodental syndrome: a rare case and review of the literature. The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association. 49: e55-60. PMID 21740180 DOI: 10.1597/10-256  0.63
2011 Olaitan PB, Chen IP, Norris JE, Feinn R, Oluwatosin OM, Reichenberger EJ. Inhibitory activities of omega-3 Fatty acids and traditional african remedies on keloid fibroblasts. Wounds : a Compendium of Clinical Research and Practice. 23: 97-106. PMID 24489452  0.566
2011 Chen IP, Wang L, Jiang X, Aguila HL, Reichenberger EJ. A Phe377del mutation in ANK leads to impaired osteoblastogenesis and osteoclastogenesis in a mouse model for craniometaphyseal dysplasia (CMD). Human Molecular Genetics. 20: 948-61. PMID 21149338 DOI: 10.1093/Hmg/Ddq541  0.753
2010 Mukherjee PM, Wang CJ, Chen IP, Jafarov T, Olsen BR, Ueki Y, Reichenberger EJ. 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. 138: 140.e1-140.e11; disc. PMID 20691350 DOI: 10.1016/J.Ajodo.2009.05.021  0.743
2010 Wang CJ, Chen IP, Koczon-Jaremko B, Boskey AL, Ueki Y, Kuhn L, Reichenberger EJ. Pro416Arg cherubism mutation in Sh3bp2 knock-in mice affects osteoblasts and alters bone mineral and matrix properties. Bone. 46: 1306-15. PMID 20117257 DOI: 10.1016/J.Bone.2010.01.380  0.76
2009 Chen IP, Wang CJ, Strecker S, Koczon-Jaremko B, Boskey A, Reichenberger EJ. 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. 24: 1206-15. PMID 19257826 DOI: 10.1359/Jbmr.090218  0.775
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