Telomere dysfunction induces metabolic and mitochondrial compromise von Sahin, Ergün, Colla, Simona, Liesa, Marc, Moslehi, Javid, Müller, Florian L., Guo, Mira, Cooper, Marcus, Kotton, Darrell, Fabian, Attila J., Walkey, Carl, Maser, Richard S., Tonon, Giovanni, Foerster, Friedrich, Xiong, Robert, Wang, Y. Alan, Shukla, Sachet A., Jaskelioff, Mariela, Martin, Eric S., Heffernan, Timothy P., Protopopov, Alexei, Ivanova, Elena, Mahoney, John E., Kost-Alimova, Maria, Perry, Samuel R., Bronson, Roderick, Liao, Ronglih, Mulligan, Richard, Shirihai, Orian S., Chin, Lynda, DePinho, Ronald A.

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SCF(FBW7) regulates cellular apoptosis by targeting MCL1 for ubiquitylation and destruction von Inuzuka, Hiroyuki, Shaik, Shavali, Onoyama, Ichiro, Gao, Daming, Tseng, Alan, Maser, Richard S, Zhai, Bo, Wan, Lixin, Gutierrez, Alejandro, Lau, Alan W, Xiao, Yonghong, Christie, Amanda L, Aster, Jon, Settleman, Jeffrey, Gygi, Steven P, Kung, Andrew L, Look, Thomas, Nakayama, Keiichi I, DePinho, Ronald A, Wei, Wenyi

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Connecting Chromosomes, Crisis, and Cancer von Maser, Richard S., DePinho, Ronald A.

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Telomere Shortening and Mood Disorders: Preliminary Support for a Chronic Stress Model of Accelerated Aging von Simon, Naomi M., Smoller, Jordan W., McNamara, Kate L., Maser, Richard S., Zalta, Alyson K., Pollack, Mark H., Nierenberg, Andrew A., Fava, Maurizio, Wong, Kwok-Kin

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Rhbdf2 mutations increase its protein stability and drive EGFR hyperactivation through enhanced secretion of amphiregulin von Hosur, Vishnu, Johnson, Kenneth R, Burzenski, Lisa M, Stearns, Timothy M, Maser, Richard S, Shultz, Leonard D

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Improved Murine MHC-Deficient HLA Transgenic NOD Mouse Models for Type 1 Diabetes Therapy Development von Racine, Jeremy J, Stewart, Isabel, Ratiu, Jeremy, Christianson, Greg, Lowell, Emily, Helm, Kelsay, Allocco, Jennifer, Maser, Richard S, Chen, Yi-Guang, Lutz, Cathleen M, Roopenian, Derry, Schloss, Jennifer, DiLorenzo, Teresa P, Serreze, David V

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Genetic mapping in Diversity Outbred mice identifies a Trpa1 variant influencing late-phase formalin response von Recla, Jill M., Bubier, Jason A., Gatti, Daniel M., Ryan, Jennifer L., Long, Katie H., Robledo, Raymond F., Glidden, Nicole C., Hou, Guoqiang, Churchill, Gary A., Maser, Richard S., Zhang, Zhong-wei, Young, Erin E., Chesler, Elissa J., Bult, Carol J.

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Genetic mapping in Diversity Outbred mice identifies a Trpa1 variant influencing late-phase formalin response von Recla, Jill M, Bubier, Jason A, Gatti, Daniel M, Ryan, Jennifer L, Long, Katie H, Robledo, Raymond F, Glidden, Nicole C, Hou, Guoqiang, Churchill, Gary A, Maser, Richard S, Zhang, Zhong-Wei, Young, Erin E, Chesler, Elissa J, Bult, Carol J

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Chromosomally unstable mouse tumours have genomic alterations similar to diverse human cancers von MASER, Richard S, CHOUDHURY, Bhudipa, LIN, Eric, MANI, Vidya, SHAN JIANG, MCNAMARA, Kate, ZAGHLUL, Sara, EDKINS, Sarah, STEVENS, Claire, BRENNAN, Cameron, MARTIN, Eric S, WIEDEMEYER, Ruprecht, CAMPBELL, Peter J, KABBARAH, Omar, NOGUEIRA, Cristina, HISTEN, Gavin, ASTER, Jon, MANSOUR, Marc, DUKE, Veronique, FORONI, Letizia, FIELDING, Adele K, GOLDSTONE, Anthony H, ROWE, Jacob M, BIN FENG, WANG, Yaoqi A, LOOK, A. Thomas, STRATTON, Michael R, CHIN, Lynda, FUTREAL, P. Andrew, DEPINHO, Ronald A, WONG, Kwok-Kin, PROTOPOPOV, Alexei, O'NEIL, Jennifer, GUTIERREZ, Alejandro, IVANOVA, Elena, PERNA, Iiana

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ATM phosphorylates p95/nbs1 in an S-phase checkpoint pathway von Kastan, Michael B, Lim, Dae-Sik, Kim, Seong-Tae, Xu, Bo, Maser, Richard S, Lin, Junyu, Petrini, John H.J

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Telomere dysfunction and Atm deficiency compromises organ homeostasis and accelerates ageing von DePinho, Ronald A, Wong, Kwok-Kin, Maser, Richard S, Bachoo, Robert M, Menon, Jayant, Carrasco, Daniel R, Gu, Yansong, Alt, Frederick W

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Telomere-based crisis: functional differences between telomerase activation and ALT in tumor progression von Chang, Sandy, Khoo, Christine M, Naylor, Maria L, Maser, Richard S, DePinho, Ronald A

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The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder von Stewart, G S, Maser, R S, Stankovic, T, Bressan, D A, Kaplan, M I, Jaspers, N G, Raams, A, Byrd, P J, Petrini, J H, Taylor, A M

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An alternative mode of translation permits production of a variant NBS1 protein from the common Nijmegen breakage syndrome allele von Petrini, John H.J, Maser, Richard S, Zinkel, Robert

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In Situ Visualization of DNA Double-Strand Break Repair in Human Fibroblasts von Nelms, Benjamin E., Maser, Richard S., MacKay, James F., Lagally, Max G., John H. J. Petrini

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Generating Mouse Models Using CRISPR‐Cas9‐Mediated Genome Editing von Qin, Wenning, Kutny, Peter M., Maser, Richard S., Dion, Stephanie L., Lamont, Jeffrey D., Zhang, Yingfan, Perry, Greggory A., Wang, Haoyi

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The hMre11/hRad50 Protein Complex and Nijmegen Breakage Syndrome: Linkage of Double-Strand Break Repair to the Cellular DNA Damage Response von Carney, James P, Maser, Richard S, Olivares, Heidi, Davis, Elizabeth M, Le Beau, Michelle, Yates, John R, Hays, Lara, Morgan, William F, Petrini, John H.J

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DNA-Dependent Protein Kinase Catalytic Subunit Is Not Required for Dysfunctional Telomere Fusion and Checkpoint Response in the Telomerase-Deficient Mouse von Maser, Richard S., Wong, Kwok-Kin, Sahin, Erguen, Xia, Huili, Naylor, Maria, Hedberg, H. Mason, Artandi, Steven E., DePinho, Ronald A.

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Alu elements mediate MYB gene tandem duplication in human T-ALL von O'Neil, Jennifer, Tchinda, Joelle, Gutierrez, Alejandro, Moreau, Lisa, Maser, Richard S, Wong, Kwok-Kin, Li, Wei, McKenna, Keith, Liu, X Shirley, Feng, Bin, Neuberg, Donna, Silverman, Lewis, DeAngelo, Daniel J, Kutok, Jeffery L, Rothstein, Rodney, DePinho, Ronald A, Chin, Lynda, Lee, Charles, Look, A Thomas

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Telomeres and the DNA damage response: why the fox is guarding the henhouse von Maser, Richard S., DePinho, Ronald A.

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