Aqp4 stop codon readthrough facilitates amyloid-β clearance from the brain von Sapkota, Darshan, Florian, Colin, Doherty, Brookelyn M, White, Kelli M, Reardon, Kate M, Ge, Xia, Garbow, Joel R, Yuede, Carla M, Cirrito, John R, Dougherty, Joseph D

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Characterization of early markers of disease in the mouse model of mucopolysaccharidosis IIIB von McCullough, Katherine B, Titus, Amanda, Reardon, Kate, Conyers, Sara, Dougherty, Joseph D, Ge, Xia, Garbow, Joel R, Dickson, Patricia, Yuede, Carla M, Maloney, Susan E

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Induction of Thioredoxin-Interacting Protein by a Histone Deacetylase Inhibitor, Entinostat, Is Associated with DNA Damage and Apoptosis in Esophageal Adenocarcinoma von Feingold, Paul L, Surman, Deborah R, Brown, Kate, Xu, Yuan, McDuffie, Lucas A, Shukla, Vivek, Reardon, Emily S, Crooks, Daniel R, Trepel, Jane B, Lee, Sunmin, Lee, Min-Jung, Gao, Shaojian, Xi, Sichuan, McLoughlin, Kaitlin C, Diggs, Laurence P, Beer, David G, Nancarrow, Derek J, Neckers, Leonard M, Davis, Jeremy L, Hoang, Chuong D, Hernandez, Jonathan M, Schrump, David S, Ripley, R Taylor

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Built Environment and Walking to School: Findings from a Student Travel Behavior Survey in Massachusetts von Ito, Kate, Reardon, Timothy G., Arcaya, Mariana C., Shamsuddin, Shomon, Gute, David M., Srinivasan, Sumeeta

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How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum von BANKA, Siddharth, VEERAMACHANENI, Ratna, METCALFE, Kay, CHANDLER, Kate, MAGEE, Alex, STEWART, Fiona, MCCONNELL, Vivienne Pm, DONNELLY, Deirdre E, BERLAND, Siren, HOUGE, Gunnar, MORTON, Jenny E, OLEY, Christine, REARDON, William, REVENCU, Nicole, PARK, Soo-Mi, DAVIES, Sally J, FRY, Andrew E, ANN LYNCH, Sally, GILL, Harinder, SCHWEIGER, Susann, LAM, Wayne Wk, TOLMIE, John, MOHAMMED, Shehla N, HOWARD, Emma, HOBSON, Emma, SMITH, Audrey, BLYTH, Moira, BENNETT, Christopher, VASUDEVAN, Pradeep C, GARCIA-MINAUR, Sixto, HENDERSON, Alex, GOODSHIP, Judith, WRIGHT, Michael J, FISHER, Richard, BUNSTONE, Sancha, GIBBONS, Richard, PRICE, Susan M, DE SILVA, Deepthi C, KAREN TEMPLE, I, COLLINS, Amanda L, LACHLAN, Katherine, ELMSLIE, Frances, MCENTAGART, Meriel, CASTLE, Bruce, CLAYTON-SMITH, Jill, RAGGE, Nicola, BLACK, Graeme C, DONNAI, Dian, PARKER, Michael J, CROW, Yanick J, KERR, Bronwyn, KINGSTON, Helen

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Molecular Analysis of SALL1 Mutations in Townes-Brocks Syndrome von Kohlhase, Jürgen, Taschner, Peter E.M., Burfeind, Peter, Pasche, Bastian, Newman, Bill, Blanck, Christopher, Breuning, Martijn H., ten Kate, Leo P., Maaswinkel-Mooy, Petra, Mitulla, Beate, Seidel, Jörg, Kirkpatrick, Susan J., Pauli, Richard M., Wargowski, David S., Devriendt, Koen, Proesmans, Willem, Gabrielli, Orazio, Coppa, Giovanni V., Wesby–van Swaay, Eveline, Trembath, Richard C., Schinzel, Albert A., Reardon, William, Seemanova, Eva, Engel, Wolfgang

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HBR at 100: The Most Influential and Innovative Articles from Harvard Business Review's First Century von Review, Harvard Business, Porter, Michael E, Christensen, Clayton M, Kim, W. Chan, Mauborgne, Renee A

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Molecular analysis of SALLI mutations in Townes-Brocks syndrome von KOHLHASE, J, TASCHNER, P. E. M, SEIDEL, J, KIRKPATRICK, S. J, PAULI, R. M, WARGOWSKI, D. S, DEVRIENDT, K, PROESMANS, W, GABRIELLI, O, COPPA, G. V, SWAAY, E. W.-V, TREMBATH, R. C, BURFEIND, P, SCHINZEL, A. A, REARDON, W, SEEMANOVA, E, ENGEL, W, PASCHE, B, NEWMAN, B, BLANCK, C, BREUNING, M. H, TEN KATE, L. P, MAASWINKEL-MOOY, P, MITULLA, B

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Molecular analysis of SALL1 mutations in Townes-Brocks syndrome von Kohlhase, Jürgen, Taschner, Peter E M, Burfeind, Peter, Pasche, Bastian, Newman, Bill, Blanck, Christopher, Breuning, Martijn H, ten Kate, Leo P, Maaswinkel-Mooy, Petra, Mitulla, Beate, Seidel, Jörg, Kirkpatrick, Susan J, Pauli, Richard M, Wargowski, David S, Devriendt, Koen, Proesmans, Willem, Gabrielli, Orazio, Coppa, Giovanni V, Wesby-van Swaay, Eveline, Trembath, Richard C, Schinzel, Albert, Reardon, William, Seemanova, Eva, Engelsberger, Wolfgang R

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