Cherubism: best clinical practice von Papadaki, Maria E, Lietman, Steven A, Levine, Michael A, Olsen, Bjorn R, Kaban, Leonard B, Reichenberger, Ernst J

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The role of SH3BP2 in the pathophysiology of cherubism von Reichenberger, Ernst J, Levine, Michael A, Olsen, Bjorn R, Papadaki, Maria E, Lietman, Steven A

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Alveolar Bone Protection by Targeting the SH3BP2‐SYK Axis in Osteoclasts von Kittaka, Mizuho, Yoshimoto, Tetsuya, Schlosser, Collin, Rottapel, Robert, Kajiya, Mikihito, Kurihara, Hidemi, Reichenberger, Ernst J, Ueki, Yasuyoshi

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A novel autosomal recessive GJA1 missense mutation linked to Craniometaphyseal dysplasia von Hu, Ying, Chen, I-Ping, de Almeida, Salome, Tiziani, Valdenize, Do Amaral, Cassio M Raposo, Gowrishankar, Kalpana, Passos-Bueno, Maria Rita, Reichenberger, Ernst J

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Second‐Generation SYK Inhibitor Entospletinib Ameliorates Fully Established Inflammation and Bone Destruction in the Cherubism Mouse Model von Yoshimoto, Tetsuya, Hayashi, Tatsuhide, Kondo, Toshio, Kittaka, Mizuho, Reichenberger, Ernst J, Ueki, Yasuyoshi

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Genetic Disruption of Anoctamin 5 in Mice Replicates Human Gnathodiaphyseal Dysplasia (GDD) von Wang, Xiaoyu, Liu, Xiu, Dong, Rui, Liang, Chao, Reichenberger, Ernst J., Hu, Ying

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Investigating global gene expression changes in a murine model of cherubism von Sharma, Tulika, Cotney, Justin, Singh, Vijender, Sanjay, Archana, Reichenberger, Ernst J., Ueki, Yasuyoshi, Maye, Peter

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Enhanced TLR-MYD88 Signaling Stimulates Autoinflammation in SH3BP2 Cherubism Mice and Defines the Etiology of Cherubism von Yoshitaka, Teruhito, Mukai, Tomoyuki, Kittaka, Mizuho, Alford, Lisa M., Masrani, Salome, Ishida, Shu, Yamaguchi, Ken, Yamada, Motohiko, Mizuno, Noriyoshi, Olsen, Bjorn R., Reichenberger, Ernst J., Ueki, Yasuyoshi

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Etanercept Administration to Neonatal SH3BP2 Knock‐In Cherubism Mice Prevents TNF‐α‐Induced Inflammation and Bone Loss von Yoshitaka, Teruhito, Ishida, Shu, Mukai, Tomoyuki, Kittaka, Mizuho, Reichenberger, Ernst J, Ueki, Yasuyoshi

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Restriction of Dietary Phosphate Ameliorates Skeletal Abnormalities in a Mouse Model for Craniometaphyseal Dysplasia von Fujii, Yasuyuki, Kozak, Eszter, Dutra, Eliane, Varadi, Andras, Reichenberger, Ernst J, Chen, I‐Ping

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Generation of Keratinocytes from Human Induced Pluripotent Stem Cells Under Defined Culture Conditions von Sah, Shyam Kishor, Kanaujiya, Jitendra K, Chen, I-Ping, Reichenberger, Ernst J

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SH3BP2 Cherubism Mutation Potentiates TNF‐α–Induced Osteoclastogenesis via NFATc1 and TNF‐α–Mediated Inflammatory Bone Loss von Mukai, Tomoyuki, Ishida, Shu, Ishikawa, Remi, Yoshitaka, Teruhito, Kittaka, Mizuho, Gallant, Richard, Lin, Yi‐Ling, Rottapel, Robert, Brotto, Marco, Reichenberger, Ernst J, Ueki, Yasuyoshi

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Etanercept Administration to Neonatal SH3BP2 Knock-In Cherubism Mice Prevents TNF-[alpha]-Induced Inflammation and Bone Loss von Yoshitaka, Teruhito, Ishida, Shu, Mukai, Tomoyuki, Kittaka, Mizuho, Reichenberger, Ernst J, Ueki, Yasuyoshi

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Three novel ANO5 missense mutations in Caucasian and Chinese families and sporadic cases with gnathodiaphyseal dysplasia von Jin, Lingling, Liu, Yi, Sun, Fanyue, Collins, Michael T., Blackwell, Keith, Woo, Albert S., Reichenberger, Ernst J., Hu, Ying

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Skeletal abnormalities caused by a Connexin43R239Q mutation in a mouse model for autosomal recessive craniometaphyseal dysplasia von Fujii, Yasuyuki, Okabe, Iichiro, Hatori, Ayano, Sah, Shyam Kishor, Kanaujiya, Jitendra, Fisher, Melanie, Norris, Rachael, Terasaki, Mark, Reichenberger, Ernst J, Chen, I-Ping

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Identification of ASAH1 as a susceptibility gene for familial keloids von Santos-Cortez, Regie Lyn P, Hu, Ying, Sun, Fanyue, Benahmed-Miniuk, Fairouz, Tao, Jian, Kanaujiya, Jitendra K, Ademola, Samuel, Fadiora, Solomon, Odesina, Victoria, Nickerson, Deborah A, Bamshad, Michael J, Olaitan, Peter B, Oluwatosin, Odunayo M, Leal, Suzanne M, Reichenberger, Ernst J

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A Phe377del mutation in ANK leads to impaired osteoblastogenesis and osteoclastogenesis in a mouse model for craniometaphyseal dysplasia (CMD) von CHEN, I-Ping, LIPING WANG, XI JIANG, AGUILA, Hector Leonardo, REICHENBERGER, Ernst J

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Rapid degradation of progressive ankylosis protein (ANKH) in craniometaphyseal dysplasia von Kanaujiya, Jitendra, Bastow, Edward, Luxmi, Raj, Hao, Zhifang, Zattas, Dimitrios, Hochstrasser, Mark, Reichenberger, Ernst J., Chen, I-Ping

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Craniometaphyseal Dysplasia Mutations in ANKH Negatively Affect Human Induced Pluripotent Stem Cell Differentiation into Osteoclasts von Chen, I-Ping, Luxmi, Raj, Kanaujiya, Jitendra, Hao, Zhifang, Reichenberger, Ernst J.

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ENPP1 enzyme replacement therapy improves ectopic calcification but does not rescue skeletal phenotype in a mouse model for craniometaphyseal dysplasia von Reichenberger, Ernst J, O'Brien, Kevin, Hatori, Ayano, Carpenter, Thomas O, van de Wetering, Koen, Flaman, Lisa, Howe, Jennifer, Ortiz, Daniel, Sabbagh, Yves, Chen, I-Ping

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