Notch Activation as a Driver of Osteogenic Sarcoma
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.
Published in Cancer cell (08.09.2014)
Published in Cancer cell (08.09.2014)
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The swaying mouse as a model of osteogenesis imperfecta caused by WNT1 mutations
Joeng, Kyu Sang, Lee, Yi-Chien, Jiang, Ming-Ming, Bertin, Terry K, Chen, Yuqing, Abraham, Annie M, Ding, Hao, Bi, Xiaohong, Ambrose, Catherine G, Lee, Brendan H
Published in Human molecular genetics (01.08.2014)
Published in Human molecular genetics (01.08.2014)
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E-selectin ligand 1 regulates bone remodeling by limiting bioactive TGF-β in the bone microenvironment
Yang, Tao, Grafe, Ingo, Bae, Yangjin, Chen, Shan, Chen, Yuqing, Bertin, Terry K., Jiang, Ming-Ming, Ambrose, Catherine G., Lee, Brendan
Published in Proceedings of the National Academy of Sciences - PNAS (30.04.2013)
Published in Proceedings of the National Academy of Sciences - PNAS (30.04.2013)
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Connective tissue alterations in Fkbp10-/- mice
Lietman, Caressa D, Rajagopal, Abbhirami, Homan, Erica P, Munivez, Elda, Jiang, Ming-Ming, Bertin, Terry K, Chen, Yuqing, Hicks, John, Weis, MaryAnn, Eyre, David, Lee, Brendan, Krakow, Deborah
Published in Human molecular genetics (15.09.2014)
Published in Human molecular genetics (15.09.2014)
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Differential effects of collagen prolyl 3-hydroxylation on skeletal tissues
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
Published in PLoS genetics (01.01.2014)
Published in PLoS genetics (01.01.2014)
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Transcriptional repression of the Dspp gene leads to dentinogenesis imperfecta phenotype in Col1a1-Trps1 transgenic mice
Napierala, Dobrawa, Sun, Yao, Maciejewska, Izabela, Bertin, Terry K, Dawson, Brian, D'Souza, Rena, Qin, Chunlin, Lee, Brendan
Published in Journal of bone and mineral research (01.08.2012)
Published in Journal of bone and mineral research (01.08.2012)
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Requirement of argininosuccinate lyase for systemic nitric oxide production
Erez, Ayelet, Nagamani, Sandesh C S, Shchelochkov, Oleg A, Premkumar, Muralidhar H, Campeau, Philippe M, Chen, Yuqing, Garg, Harsha K, Li, Li, Mian, Asad, Bertin, Terry K, Black, Jennifer O, Zeng, Heng, Tang, Yaoping, Reddy, Anilkumar K, Summar, Marshall, O'Brien, William E, Harrison, David G, Mitch, William E, Marini, Juan C, Aschner, Judy L, Bryan, Nathan S, Lee, Brendan
Published in Nature medicine (01.12.2011)
Published in Nature medicine (01.12.2011)
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CRTAP Is Required for Prolyl 3- Hydroxylation and Mutations Cause Recessive Osteogenesis Imperfecta
Morello, Roy, Bertin, Terry K., Chen, Yuqing, Hicks, John, Tonachini, Laura, Monticone, Massimiliano, Castagnola, Patrizio, Rauch, Frank, Glorieux, Francis H., Vranka, Janice, Bächinger, Hans Peter, Pace, James M., Schwarze, Ulrike, Byers, Peter H., Weis, MaryAnn, Fernandes, Russell J., Eyre, David R., Yao, Zhenqiang, Boyce, Brendan F., Lee, Brendan
Published in Cell (20.10.2006)
Published in Cell (20.10.2006)
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CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta
Baldridge, Dustin, Schwarze, Ulrike, Morello, Roy, Lennington, Jennifer, Bertin, Terry K, Pace, James M, Pepin, Melanie G, Weis, MaryAnn, Eyre, David R, Walsh, Jennifer, Lambert, Deborah, Green, Andrew, Robinson, Haynes, Michelson, Melonie, Houge, Gunnar, Lindman, Carl, Martin, Judith, Ward, Jewell, Lemyre, Emmanuelle, Mitchell, John J, Krakow, Deborah, Rimoin, David L, Cohn, Daniel H, Byers, Peter H, Lee, Brendan
Published in Human mutation (01.12.2008)
Published in Human mutation (01.12.2008)
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A Transgenic Mouse Model of OI Type V Supports a Neomorphic Mechanism of the IFITM5 Mutation
Lietman, Caressa D, Marom, Ronit, Munivez, Elda, Bertin, Terry K, Jiang, Ming‐Ming, Chen, Yuqing, Dawson, Brian, Weis, Mary Ann, Eyre, David, Lee, Brendan
Published in Journal of bone and mineral research (01.03.2015)
Published in Journal of bone and mineral research (01.03.2015)
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Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice
Beck, Tyler F, Veenma, Danielle, Shchelochkov, Oleg A, Yu, Zhiyin, Kim, Bum Jun, Zaveri, Hitisha P, van Bever, Yolande, Choi, Sunju, Douben, Hannie, Bertin, Terry K, Patel, Pragna I, Lee, Brendan, Tibboel, Dick, de Klein, Annelies, Stockton, David W, Justice, Monica J, Scott, Daryl A
Published in Human molecular genetics (15.04.2020)
Published in Human molecular genetics (15.04.2020)
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Toll-like Receptor 9 Triggers an Innate Immune Response to Helper-dependent Adenoviral Vectors
Cerullo, Vincenzo, Seiler, Michael P, Mane, Viraj, Brunetti-Pierri, Nicola, Clarke, Christian, Bertin, Terry K, Rodgers, John R, Lee, Brendan
Published in Molecular therapy (01.02.2007)
Published in Molecular therapy (01.02.2007)
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Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice
Beck, Tyler F, Veenma, Danielle, Shchelochkov, Oleg A, Yu, Zhiyin, Kim, Bum Jun, Zaveri, Hitisha P, van Bever, Yolande, Choi, Sunju, Douben, Hannie, Bertin, Terry K, Patel, Pragna I, Lee, Brendan, Tibboel, Dick, de Klein, Annelies, Stockton, David W, Justice, Monica J, Scott, Daryl A
Published in Human molecular genetics (01.03.2013)
Published in Human molecular genetics (01.03.2013)
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Brachy-syndactyly caused by loss of Sfrp2 function
Morello, Roy, Bertin, Terry K., Schlaubitz, Silke, Shaw, Chad A., Kakuru, Sujatha, Munivez, Elda, Hermanns, Pia, Chen, Yuqing, Zabel, Bernhard, Lee, Brendan
Published in Journal of cellular physiology (01.10.2008)
Published in Journal of cellular physiology (01.10.2008)
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Skeletal defects in paternal uniparental disomy for chromosome 14 are re-capitulated in the mouse model (paternal uniparental disomy 12)
SUTTON, V. Reid, MCALISTER, William H, BERTIN, Terry K, KAFFE, Sara, WANG, Jin-Chen C, YANO, Shoji, SHAFFER, Lisa G, LEE, Brendan, EPSTEIN, Charles J, VILLAR, Angela J
Published in Human genetics (01.10.2003)
Published in Human genetics (01.10.2003)
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Capsid-modified adenoviral vectors for improved muscle-directed gene therapy
Guse, Kilian, Suzuki, Masataka, Sule, Gautam, Bertin, Terry K, Tyynismaa, Henna, Ahola-Erkkilä, Sofia, Palmer, Donna, Suomalainen, Anu, Ng, Philip, Cerullo, Vincenzo, Hemminki, Akseli, Lee, Brendan
Published in Human gene therapy (01.10.2012)
Published in Human gene therapy (01.10.2012)
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NOD2 signaling contributes to the innate immune response against helper-dependent adenovirus vectors independently of MyD88 in vivo
Suzuki, Masataka, Cela, Racel, Bertin, Terry K, Sule, Gautam, Cerullo, Vincenzo, Rodgers, John R, Lee, Brendan
Published in Human gene therapy (01.09.2011)
Published in Human gene therapy (01.09.2011)
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Origins of U.S. Hispanics. Implications for diabetes
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Conference Proceeding
MyD88-dependent silencing of transgene expression during the innate and adaptive immune response to helper-dependent adenovirus
Suzuki, Masataka, Cerullo, Vincenzo, Bertin, Terry K, Cela, Racel, Clarke, Christian, Guenther, Margaretha, Brunetti-Pierri, Nicola, Lee, Brendan
Published in Human gene therapy (01.03.2010)
Published in Human gene therapy (01.03.2010)
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