Mutations Impairing GSK3-Mediated MAF Phosphorylation Cause Cataract, Deafness, Intellectual Disability, Seizures, and a Down Syndrome-like Facies von Niceta, Marcello, Stellacci, Emilia, Gripp, Karen W, Zampino, Giuseppe, Kousi, Maria, Anselmi, Massimiliano, Traversa, Alice, Ciolfi, Andrea, Stabley, Deborah, Bruselles, Alessandro, Caputo, Viviana, Cecchetti, Serena, Prudente, Sabrina, Fiorenza, Maria T, Boitani, Carla, Philip, Nicole, Niyazov, Dmitriy, Leoni, Chiara, Nakane, Takaya, Keppler-Noreuil, Kim, Braddock, Stephen R, Gillessen-Kaesbach, Gabriele, Palleschi, Antonio, Campeau, Philippe M, Lee, Brendan H L, Pouponnot, Celio, Stella, Lorenzo, Bocchinfuso, Gianfranco, Katsanis, Nicholas, Sol-Church, Katia, Tartaglia, Marco

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Quantitative imaging of murine osteoarthritic cartilage by phase‐contrast micro–computed tomography von Ruan, Merry Z. C., Dawson, Brian, Jiang, Ming‐Ming, Gannon, Francis, Heggeness, Michael, Lee, Brendan H. L.

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Osteocyte-specific WNT1 regulates osteoblast function during bone homeostasis von Joeng, Kyu Sang, Lee, Yi-Chien, Lim, Joohyun, Chen, Yuqing, Jiang, Ming-Ming, Munivez, Elda, Ambrose, Catherine, Lee, Brendan H

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Gene therapy for repair and regeneration of bone and cartilage von Grol, Matthew W, Lee, Brendan H

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Notch Activation as a Driver of Osteogenic Sarcoma von Tao, Jianning, Jiang, Ming-Ming, Jiang, Lichun, Salvo, Jason S., Zeng, Huan-Chang, Dawson, Brian, Bertin, Terry K., Rao, Pulivarthi H., Chen, Rui, Donehower, Lawrence A., Gannon, Francis, Lee, Brendan H.

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MicroRNA miR-23a cluster promotes osteocyte differentiation by regulating TGF-β signalling in osteoblasts von Zeng, Huan-Chang, Bae, Yangjin, Dawson, Brian C., Chen, Yuqing, Bertin, Terry, Munivez, Elda, Campeau, Philippe M., Tao, Jianning, Chen, Rui, Lee, Brendan H.

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Disease‐Modifying Osteoarthritis Treatment With Interleukin‐1 Receptor Antagonist Gene Therapy in Small and Large Animal Models von Nixon, Alan J., Grol, Matthew W., Lang, Hayley M., Ruan, Merry Z. C., Stone, Adrianne, Begum, Laila, Chen, Yuqing, Dawson, Brian, Gannon, Francis, Plutizki, Stanislav, Lee, Brendan H. L., Guse, Kilian

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Impairment of an Endothelial NAD+-H2S Signaling Network Is a Reversible Cause of Vascular Aging von Das, Abhirup, Huang, George X., Bonkowski, Michael S., Longchamp, Alban, Li, Catherine, Schultz, Michael B., Kim, Lynn-Jee, Osborne, Brenna, Joshi, Sanket, Lu, Yuancheng, Treviño-Villarreal, Jose Humberto, Kang, Myung-Jin, Hung, Tzong-tyng, Lee, Brendan, Williams, Eric O., Igarashi, Masaki, Mitchell, James R., Wu, Lindsay E., Turner, Nigel, Arany, Zolt, Guarente, Leonard, Sinclair, David A.

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A Recurrent PDGFRB Mutation Causes Familial Infantile Myofibromatosis von Cheung, Yee Him, Gayden, Tenzin, Campeau, Philippe M., LeDuc, Charles A., Russo, Donna, Nguyen, Van-Hung, Guo, Jiancheng, Qi, Ming, Guan, Yanfang, Albrecht, Steffen, Moroz, Brenda, Eldin, Karen W., Lu, James T., Schwartzentruber, Jeremy, Malkin, David, Berghuis, Albert M., Emil, Sherif, Gibbs, Richard A., Burk, David L., Vanstone, Megan, Lee, Brendan H., Orchard, David, Boycott, Kym M., Chung, Wendy K., Jabado, Nada

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Differential effects of collagen prolyl 3-hydroxylation on skeletal tissues von Homan, Erica P, Lietman, Caressa, Grafe, Ingo, Lennington, Jennifer, Morello, Roy, Napierala, Dobrawa, Jiang, Ming-Ming, Munivez, Elda M, Dawson, Brian, Bertin, Terry K, Chen, Yuqing, Lua, Rhonald, Lichtarge, Olivier, Hicks, John, Weis, Mary Ann, Eyre, David, Lee, Brendan H L

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Foodborne Disease and the Need for Greater Foodborne Disease Surveillance in the Caribbean von Lee, Brendan

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Genotype–Phenotype Correlation — Promiscuity in the Era of Next-Generation Sequencing von Lu, James T, Campeau, Philippe M, Lee, Brendan H

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Combinatorial Prg4 and Il-1ra Gene Therapy Protects Against Hyperalgesia and Cartilage Degeneration in Post-Traumatic Osteoarthritis von Stone, Adrianne, Grol, Matthew W, Ruan, Merry Z C, Dawson, Brian, Chen, Yuqing, Jiang, Ming-Ming, Song, I-Wen, Jayaram, Prathap, Cela, Racel, Gannon, Francis, Lee, Brendan H L

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Sites of Cre‐recombinase activity in mouse lines targeting skeletal cells von Couasnay, Greig, Madel, Maria‐Bernadette, Lim, Joohyun, Lee, Brendan, Elefteriou, Florent

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Mutations in ANAPC1, Encoding a Scaffold Subunit of the Anaphase-Promoting Complex, Cause Rothmund-Thomson Syndrome Type 1 von Ajeawung, Norbert F., Nguyen, Thi Tuyet Mai, Lu, Linchao, Kucharski, Thomas J., Rousseau, Justine, Molidperee, Sirinart, Atienza, Joshua, Gamache, Isabel, Jin, Weidong, Plon, Sharon E., Lee, Brendan H., Teodoro, Jose G., Wang, Lisa L., Campeau, Philippe M.

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Transcriptome-directed analysis for Mendelian disease diagnosis overcomes limitations of conventional genomic testing von Murdock, David R, Dai, Hongzheng, Burrage, Lindsay C, Rosenfeld, Jill A, Ketkar, Shamika, Müller, Michaela F, Yépez, Vicente A, Gagneur, Julien, Liu, Pengfei, Chen, Shan, Jain, Mahim, Zapata, Gladys, Bacino, Carlos A, Chao, Hsiao-Tuan, Moretti, Paolo, Craigen, William J, Hanchard, Neil A, Lee, Brendan

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Notch Signaling in Skeletal Stem Cells von Chen, Shan, Lee, Brendan H., Bae, Yangjin

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Dimorphic effects of Notch signaling in bone homeostasis von Engin, Feyza, Yao, Zhenqiang, Yang, Tao, Zhou, Guang, Bertin, Terry, Jiang, Ming Ming, Chen, Yuqing, Wang, Lisa, Zheng, Hui, Sutton, Richard E, Boyce, Brendan F, Lee, Brendan

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Yunis-Varón Syndrome Is Caused by Mutations in FIG4, Encoding a Phosphoinositide Phosphatase von Campeau, Philippe M., Lenk, Guy M., Lu, James T., Bae, Yangjin, Burrage, Lindsay, Turnpenny, Peter, Román Corona-Rivera, Jorge, Morandi, Lucia, Mora, Marina, Reutter, Heiko, Vulto-van Silfhout, Anneke T., Faivre, Laurence, Haan, Eric, Gibbs, Richard A., Meisler, Miriam H., Lee, Brendan H.

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Notch Signaling in Skeletal Development, Homeostasis and Pathogenesis von Zieba, Jennifer T, Chen, Yi-Ting, Lee, Brendan H, Bae, Yangjin

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