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The bone phenotype associated with cherubism is independent of Caspase-1-dependent inflammasome activation in the mouse
Author / Creator:Rabhi, Badre-Victor ; Thomasseau, Sylvie ; Decrouy, Xavier ; Cohen-Solal, Martine ; Deckert, Marcel ; Coudert, Amélie E ; Brial, François
Publisher:United States: Public Library of Science
Journal title:PloS one, 2025-02, Vol.20 (2), p.e0318826
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Reciprocal stabilization of ABL and TAZ regulates osteoblastogenesis through transcription factor RUNX2
Author / Creator:Matsumoto, Yoshinori ; La Rose, Jose ; Kent, Oliver A ; Wagner, Melany J ; Narimatsu, Masahiro ; Levy, Aaron D ; Omar, Mitchell H ; Tong, Jiefei ; Krieger, Jonathan R ; Riggs, Emily ; Storozhuk, Yaryna ; Pasquale, Julia ; Ventura, Manuela ; Yeganeh, Behzad ; Post, Martin ; Moran, Michael F ; Grynpas, Marc D ; Wrana, Jeffrey L ; Superti-Furga, Giulio ; Koleske, Anthony J ; Pendergast, Ann Marie ; Rottapel, Robert
Publisher:United States: American Society for Clinical Investigation
Journal title:The Journal of clinical investigation, 2016-12, Vol.126 (12), p.4482-4496
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Nonfamilial cherubism in a 6-month-old infant: a case report
Author / Creator:Hamzavi, Seyedeh Sedigheh ; Askari, Alireza ; Bahrololoom, Rosemina ; Mokhtari, Maral ; Sanaei Dashti, Anahita ; Yarmahmoodi, Fatemeh ; Rashidi, Somaye
Publisher:England: BioMed Central Ltd
Journal title:BMC pediatrics, 2024-06, Vol.24 (1), p.402-6, Article 402
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The role of SH3BP2 in the pathophysiology of cherubism
Author / Creator:Reichenberger, Ernst J ; Levine, Michael A ; Olsen, Bjorn R ; Papadaki, Maria E ; Lietman, Steven A
Publisher:England: BioMed Central
Journal title:Orphanet journal of rare diseases, 2012-05, Vol.7 Suppl 1 (Suppl 1), p.S5-S5
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Cherubism as a systemic skeletal disease: evidence from an aggressive case
Author / Creator:Morice, Anne ; Joly, Aline ; Ricquebourg, Manon ; Maruani, Gérard ; Durand, Emmanuel ; Galmiche, Louise ; Amiel, Jeanne ; Vial, Yoann ; Cavé, Hélène ; Belhous, Kahina ; Piketty, Marie ; Cohen-Solal, Martine ; Berdal, Ariane ; Collet, Corinne ; Picard, Arnaud ; Coudert, Amelie E ; Kadlub, Natacha
Publisher:England: BioMed Central Ltd
Journal title:BMC musculoskeletal disorders, 2020-08, Vol.21 (1), p.564-564, Article 564
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Cherubism allele heterozygosity amplifies microbe-induced inflammatory responses in murine macrophages
Author / Creator:Prod'Homme, Virginie ; Boyer, Laurent ; Dubois, Nicholas ; Mallavialle, Aude ; Munro, Patrick ; Mouska, Xavier ; Coste, Isabelle ; Rottapel, Robert ; Tartare-Deckert, Sophie ; Deckert, Marcel
Publisher:United States: American Society for Clinical Investigation
Journal title:The Journal of clinical investigation, 2015-04, Vol.125 (4), p.1396-1400
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Variable expressivity familial cherubism: woman transmitting cherubism without suffering the disease
Author / Creator:Pérez-Sayáns, Mario ; Barros-Angueira, Francisco ; Suárez-Peñaranda, Jos Ém ; García-García, Abel
Publisher:England: BioMed Central Ltd
Journal title:Head & face medicine, 2013-11, Vol.9 (1), p.33-33, Article 33
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Unexpected matrix diseases and novel therapeutic strategies
Author / Creator:Nicolae, Claudia ; Olsen, Bjorn R
Publisher:Berlin/Heidelberg: Berlin/Heidelberg : Springer-Verlag
Journal title:Cell and tissue research, 2010, Vol.339 (1), p.155-165
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NFATc1 in mice represses osteoprotegerin during osteoclastogenesis and dissociates systemic osteopenia from inflammation in cherubism
Author / Creator:Aliprantis, Antonios O ; Ueki, Yasuyoshi ; Sulyanto, Rosalyn ; Park, Arnold ; Sigrist, Kirsten S ; Sharma, Sudarshana M ; Ostrowski, Michael C ; Olsen, Bjorn R ; Glimcher, Laurie H
Publisher:United States: American Society for Clinical Investigation
Journal title:The Journal of clinical investigation, 2008-11, Vol.118 (11), p.3775-3789
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Cherubism: best clinical practice
Author / Creator:Papadaki, Maria E ; Lietman, Steven A ; Levine, Michael A ; Olsen, Bjorn R ; Kaban, Leonard B ; Reichenberger, Ernst J
Publisher:England: BioMed Central
Journal title:Orphanet journal of rare diseases, 2012-05, Vol.7 Suppl 1 (S1), p.S6-S6, Article S6
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Cherubism and anaesthesia
Author / Creator:E Gentili, Marc ; Levreil, Edwige ; Bedhet, Nicolas
Publisher:Poland: Termedia sp. z o.o
Journal title:Anaesthesiology intensive therapy : official publication of the Polish Society of Anaesthesiology and Intensive Therapy, 2021-01, Vol.53 (3), p.286-287
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Mutations in the gene encoding c-Abl-binding protein SH3BP2 cause cherubism
Author / Creator:Ueki, Yasuyoshi ; Tiziani, Valdenize ; Santanna, Carla ; Fukai, Naomi ; Maulik, Chris ; Garfinkle, Judah ; Ninomiya, Chisho ; doAmaral, Cassio ; Peters, Hartmut ; Habal, Mutaz ; Rhee-Morris, Laila ; Doss, Jeffrey B. ; Kreiborg, Sven ; Olsen, Bjorn R. ; Reichenberger, Ernst
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2001-06, Vol.28 (2), p.125-126
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Bilateral Central Giant Cell Granuloma of the mandibular angle in three females from the same family
Author / Creator:Tecco, Simona ; Caruso, Silvia ; Nota, Alessandro ; Leocata, Pietro ; Cipollone, Gianluca ; Gatto, Roberto ; Cutilli, Tommaso
Publisher:England: BioMed Central Ltd
Journal title:Head & face medicine, 2018-09, Vol.14 (1), p.14-14, Article 14
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SOS1 and PTPN11 mutations in five cases of Noonan syndrome with multiple giant cell lesions
Author / Creator:Beneteau, Claire ; Cavé, Hélène ; Moncla, Anne ; Dorison, Nathalie ; Munnich, Arnold ; Verloes, Alain ; Leheup, Bruno
Publisher:Cham: Springer International Publishing
Journal title:European journal of human genetics : EJHG, 2009-10, Vol.17 (10), p.1216-1221
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Cherubism
Author / Creator:Thompson, Lester D
Publisher:United States: Sage Publications, Inc
Journal title:Ear, nose, & throat journal, 2015-01, Vol.94 (1), p.22, 24-E-24
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Frequency of USP6 rearrangements in myositis ossificans, brown tumor, and cherubism: molecular cytogenetic evidence that a subset of “myositis ossificans-like lesions” are the early phases in the form...
Author / Creator:Sukov, William R. ; Franco, Marcello F. ; Erickson-Johnson, Michele ; Chou, Margaret M. ; Unni, K. Krishnan ; Wenger, Doris E. ; Wang, Xiaoke ; Oliveira, Andre M.
Publisher:Berlin/Heidelberg: Springer-Verlag
Journal title:Skeletal radiology, 2008-04, Vol.37 (4), p.321-327
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Identification of a novel mutation of SH3BP2 in cherubism and demonstration that SH3BP2 mutations lead to increased NFAT activation
Author / Creator:Lietman, Steven A. ; Kalinchinko, Natasha ; Deng, Xichao ; Kohanski, Ronald ; Levine, Michael A.
Publisher:Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Journal title:Human mutation, 2006-07, Vol.27 (7), p.717-718
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Diagnostic Potential of 3D-Data–Based Reconstruction Software: An Analysis of the Rare Disease Pattern of Cherubism
Author / Creator:Holst, Alexandra Ioana ; Hirschfelder, Ursula ; Holst, Stefan
Publisher:Los Angeles, CA: SAGE Publications
Journal title:The Cleft palate-craniofacial journal, 2009-03, Vol.46 (2), p.215-219
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Novel treatment of a rare genetic bone disease
Author / Creator:McMahon, Mark S
Publisher:United States: SLACK INCORPORATED
Journal title:Orthopedics (Thorofare, N.J.), 2007-02, Vol.30 (2), p.91-91
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Familial craniofacial fibrous dysplasia: absence of linkage to GNAS1 and the gene for cherubism
Author / Creator:Mangion, J ; Edkins, S ; Goss, A N ; Stratton, M R ; Flanagan, A M
Publisher:England: BMJ Group
Journal title:Journal of medical genetics, 2000-11, Vol.37 (11), p.E37-37
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The bone phenotype associated with cherubism is independent of Caspase-1-dependent inflammasome activation in the mouse

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Reciprocal stabilization of ABL and TAZ regulates osteoblastogenesis through transcription factor RUNX2

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Nonfamilial cherubism in a 6-month-old infant: a case report

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The role of SH3BP2 in the pathophysiology of cherubism

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Cherubism as a systemic skeletal disease: evidence from an aggressive case

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Cherubism allele heterozygosity amplifies microbe-induced inflammatory responses in murine macrophages

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Variable expressivity familial cherubism: woman transmitting cherubism without suffering the disease

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Unexpected matrix diseases and novel therapeutic strategies

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NFATc1 in mice represses osteoprotegerin during osteoclastogenesis and dissociates systemic osteopenia from inflammation in cherubism

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Cherubism: best clinical practice

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Cherubism and anaesthesia

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Mutations in the gene encoding c-Abl-binding protein SH3BP2 cause cherubism

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Bilateral Central Giant Cell Granuloma of the mandibular angle in three females from the same family

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SOS1 and PTPN11 mutations in five cases of Noonan syndrome with multiple giant cell lesions

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Cherubism

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Frequency of USP6 rearrangements in myositis ossificans, brown tumor, and cherubism: molecular cytogenetic evidence that a subset of “myositis ossificans-like lesions” are the early phases in the form...

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Identification of a novel mutation of SH3BP2 in cherubism and demonstration that SH3BP2 mutations lead to increased NFAT activation

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Diagnostic Potential of 3D-Data–Based Reconstruction Software: An Analysis of the Rare Disease Pattern of Cherubism

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Novel treatment of a rare genetic bone disease

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Familial craniofacial fibrous dysplasia: absence of linkage to GNAS1 and the gene for cherubism

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