Ernst Reichenberger - Publications

University of Connecticut, Storrs, CT, United States 
Molecular Biology

46 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
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  0.72
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  0.72
2020 Kittaka M, Yoshimoto T, Schlosser C, Kajiya M, Kurihara H, Reichenberger EJ, Ueki Y. Microbe-Dependent Exacerbated Alveolar Bone Destruction in Heterozygous Cherubism Mice. Jbmr Plus. 4: e10352. PMID 32537546 DOI: 10.1002/jbm4.10352  0.32
2020 Sharma T, Cotney J, Singh V, Sanjay A, Reichenberger EJ, Ueki Y, Maye P. Investigating global gene expression changes in a murine model of cherubism. Bone. 115315. PMID 32165349 DOI: 10.1016/J.Bone.2020.115315  0.32
2019 Kittaka M, Yoshimoto T, Schlosser C, Rottapel R, Kajiya M, Kurihara H, Reichenberger EJ, Ueki Y. Alveolar Bone Protection by Targeting the SH3BP2-SYK Axis in Osteoclasts. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. PMID 31613396 DOI: 10.1002/Jbmr.3882  0.32
2019 Gupta S, Singh K, Garg A, Bhandari PS, Sah SK, Reichenberger E, Kapoor S, Jain S, Trehanpati N. Clinicoradiologic follow up of cherubism with aggressive characteristics: a series of 3 cases. Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology. PMID 30904497 DOI: 10.1016/J.Oooo.2019.01.082  0.36
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  0.72
2018 Yoshimoto T, Hayashi T, Kondo T, Kittaka M, Reichenberger EJ, Ueki Y. Second-generation SYK inhibitor entospletinib ameliorates fully established inflammation and bone destruction in the cherubism mouse model. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. PMID 29669173 DOI: 10.1002/jbmr.3449  0.32
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  0.72
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  0.72
2017 Santos-Cortez RLP, Hu Y, Sun F, Benahmed-Miniuk F, Tao J, Kanaujiya JK, Ademola S, Fadiora S, Odesina V, Nickerson DA, Bamshad MJ, Olaitan PB, Oluwatosin OM, Leal SM, Reichenberger EJ. Identification of ASAH1 as a susceptibility gene for familial keloids. European Journal of Human Genetics : Ejhg. 25: 1155-1161. PMID 28905881 DOI: 10.1038/Ejhg.2017.121  0.36
2017 Jin L, Liu Y, Sun F, Collins MT, Blackwell K, Woo AS, Reichenberger EJ, Hu Y. Three novel ANO5 missense mutations in Caucasian and Chinese families and sporadic cases with gnathodiaphyseal dysplasia. Scientific Reports. 7: 40935. PMID 28176803 DOI: 10.1038/srep40935  0.44
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  0.72
2014 Yoshitaka T, Mukai T, Kittaka M, Alford LM, Masrani S, Ishida S, Yamaguchi K, Yamada M, Mizuno N, Olsen BR, Reichenberger EJ, Ueki Y. Enhanced TLR-MYD88 signaling stimulates autoinflammation in SH3BP2 cherubism mice and defines the etiology of cherubism. Cell Reports. 8: 1752-66. PMID 25220465 DOI: 10.1016/J.Celrep.2014.08.023  0.4
2014 Xin X, Jiang X, Wang L, Stover ML, Zhan S, Huang J, Goldberg AJ, Liu Y, Kuhn L, Reichenberger EJ, Rowe DW, Lichtler AC. A Site-Specific Integrated Col2.3GFP Reporter Identifies Osteoblasts Within Mineralized Tissue Formed In Vivo by Human Embryonic Stem Cells. Stem Cells Translational Medicine. 3: 1125-37. PMID 25122686 DOI: 10.5966/Sctm.2013-0128  0.4
2014 Yoshitaka T, Ishida S, Mukai T, Kittaka M, Reichenberger EJ, Ueki Y. Etanercept administration to neonatal SH3BP2 knock-in cherubism mice prevents TNF-α-induced inflammation and bone loss. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 29: 1170-82. PMID 24978678 DOI: 10.1002/jbmr.2125  0.4
2014 Mukai T, Ishida S, Ishikawa R, Yoshitaka T, Kittaka M, Gallant R, Lin YL, Rottapel R, Brotto M, Reichenberger EJ, Ueki Y. SH3BP2 cherubism mutation potentiates TNF-α-induced osteoclastogenesis via NFATc1 and TNF-α-mediated inflammatory bone loss. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 29: 2618-35. PMID 24916406 DOI: 10.1002/Jbmr.2295  0.4
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  0.72
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  0.72
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  0.72
2013 Marneros AG, Beck AE, Turner EH, McMillin MJ, Edwards MJ, Field M, de Macena Sobreira NL, Perez AB, Fortes JA, Lampe AK, Giovannucci Uzielli ML, Gordon CT, Plessis G, Le Merrer M, Amiel J, ... Reichenberger E, et al. Mutations in KCTD1 cause scalp-ear-nipple syndrome. American Journal of Human Genetics. 92: 621-6. PMID 23541344 DOI: 10.1016/J.Ajhg.2013.03.002  0.4
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  0.72
2012 Reichenberger EJ, Levine MA, Olsen BR, Papadaki ME, Lietman SA. The role of SH3BP2 in the pathophysiology of cherubism. Orphanet Journal of Rare Diseases. 7: S5. PMID 22640988 DOI: 10.1186/1750-1172-7-S1-S5  0.4
2012 Papadaki ME, Lietman SA, Levine MA, Olsen BR, Kaban LB, Reichenberger EJ. Cherubism: best clinical practice. Orphanet Journal of Rare Diseases. 7: S6. PMID 22640403 DOI: 10.1186/1750-1172-7-S1-S6  0.4
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  0.4
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  0.72
2012 Davoody A, Chen IP, Nanda R, Uribe F, Reichenberger EJ. Oculofaciocardiodental syndrome: A rare case and review of the literature Cleft Palate-Craniofacial Journal. 49: e55-e60. DOI: 10.1597/10-256  0.4
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  0.72
2011 Levaot N, Simoncic PD, Dimitriou ID, Scotter A, La Rose J, Ng AH, Willett TL, Wang CJ, Janmohamed S, Grynpas M, Reichenberger E, Rottapel R. 3BP2-deficient mice are osteoporotic with impaired osteoblast and osteoclast functions. The Journal of Clinical Investigation. 121: 3244-57. PMID 21765218 DOI: 10.1016/J.Bone.2011.03.080  0.4
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  0.72
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  0.4
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  0.72
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  0.72
2007 Ueki Y, Lin CY, Senoo M, Ebihara T, Agata N, Onji M, Saheki Y, Kawai T, Mukherjee PM, Reichenberger E, Olsen BR. Increased myeloid cell responses to M-CSF and RANKL cause bone loss and inflammation in SH3BP2 "cherubism" mice. Cell. 128: 71-83. PMID 17218256 DOI: 10.1016/J.Cell.2006.10.047  0.4
2006 Turk BE, Lee DH, Yamakoshi Y, Klingenhoff A, Reichenberger E, Wright JT, Simmer JP, Komisarof JA, Cantley LC, Bartlett JD. MMP-20 is predominately a tooth-specific enzyme with a deep catalytic pocket that hydrolyzes type V collagen Biochemistry. 45: 3863-3874. PMID 16548514 DOI: 10.1021/Bi052252O  0.4
2004 Marneros AG, Norris JE, Watanabe S, Reichenberger E, Olsen BR. Genome scans provide evidence for keloid susceptibility loci on chromosomes 2q23 and 7p11. The Journal of Investigative Dermatology. 122: 1126-32. PMID 15140214 DOI: 10.1111/J.0022-202X.2004.22327.X  0.4
2001 Marneros AG, Norris JEC, Olsen BR, Reichenberger E. Clinical genetics of familial keloids Archives of Dermatology. 137: 1429-1434. PMID 11708945 DOI: 10.1001/Archderm.137.11.1429  0.4
2001 Marneros AG, Mehenni H, Reichenberger E, Antonarakis SE, Krieg T, Olsen BR. Gene for the human transmembrane-type protein tyrosine phosphatase H (PTPRH): Genomic structure, fine-mapping and its exclusion as a candidate for Peutz-Jeghers syndrome Cytogenetics and Cell Genetics. 92: 213-216. PMID 11435690 DOI: 10.1159/000056905  0.4
2001 Ueki Y, Tiziani V, Santanna C, Fukai N, Maulik C, Garfinkle J, Ninomiya C, Doamaral C, Peters H, Habal M, Rhee-Morris L, Doss JB, Kreiborg S, Olsen BR, Reichenberger E. Mutations in the gene encoding c-Abl-binding protein SH3BP2 cause cherubism Nature Genetics. 28: 125-126. PMID 11381256 DOI: 10.1038/88832  0.4
2001 Reichenberger E, Tiziani V, Watanabe S, Park L, Ueki Y, Santanna C, Baur ST, Shiang R, Grange DK, Beighton P, Gardner J, Hamersma H, Sellars S, Ramesar R, Lidral AC, et al. Autosomal dominant craniometaphyseal dysplasia is caused by mutations in the transmembrane protein ANK. American Journal of Human Genetics. 68: 1321-6. PMID 11326338 DOI: 10.1086/320612  0.4
2001 Rieger DK, Reichenberger E, McLean W, Sidow A, Olsen BR. A double-deletion mutation in the Pitx3 gene causes arrested lens development in aphakia mice. Genomics. 72: 61-72. PMID 11247667 DOI: 10.1006/Geno.2000.6464  0.4
2000 Reichenberger E, Baur S, Sukotjo C, Olsen BR, Karimbux NY, Nishimura I. Collagen XII mutation disrupts matrix structure of periodontal ligament and skin. Journal of Dental Research. 79: 1962-8. PMID 11201046 DOI: 10.1177/00220345000790120701  0.4
1999 Kania AM, Reichenberger E, Baur ST, Karimbux NY, Taylor RW, Olsen BR, Nishimura I. Structural variation of type XII collagen at its carboxyl-terminal NC1 domain generated by tissue-specific alternative splicing. The Journal of Biological Chemistry. 274: 22053-9. PMID 10419532 DOI: 10.1074/Jbc.274.31.22053  0.4
1999 Tiziani V, Reichenberger E, Buzzo CL, Niazi S, Fukai N, Stiller M, Peters H, Salzano FM, Raposo Do Amaral CM, Olsen BR. The gene for cherubism maps to chromosome 4p16 American Journal of Human Genetics. 65: 158-166. PMID 10364528 DOI: 10.1086/302456  0.4
1997 Kania AM, Reichenberger E, Baur ST, Karimbux NY, Olsen BR, Nishimura I. Structural variation of type XII collagen at its carboxyl-terminal generated by tissue specific alternative splicing Matrix Biology. 16: 126. DOI: 10.1016/S0945-053X(97)90058-5  0.32
1996 Reichenberger E, Olsen BR. Collagens as organizers of extracellular matrix during morphogenesis Seminars in Cell and Developmental Biology. 7: 631-638. DOI: 10.1006/Scdb.1996.0077  0.4
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