Engineering Antibodies with C-Terminal Sortase-Mediated Modification for Targeted Nanomedicine von Hashad, Rania A., Lange, Jaclyn L., Tan, Natasha C. W., Alt, Karen, Hagemeyer, Christoph E.

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A clinical trial of non-invasive imaging with an anti-HIV antibody labelled with copper-64 in people living with HIV and uninfected controls von McMahon, James H., Zerbato, Jennifer M., Lau, Jillian S.Y., Lange, Jaclyn L., Roche, Michael, Tumpach, Carolin, Dantanarayana, Ashanti, Rhodes, Ajantha, Chang, Judy, Rasmussen, Thomas A., Mackenzie, Charlene A., Alt, Karen, Hagenauer, Michelle, Roney, Janine, O'Bryan, Jessica, Carey, Alexandra, McIntyre, Richard, Beech, Paul, O'Keefe, Graeme J., Wichmann, Christian W., Scott, Fiona E., Guo, Nancy, Lee, Sze-Ting, Liu, Zhanqi, Caskey, Marina, Nussenzweig, Michel C., Donnelly, Paul S., Egan, Gary, Hagemeyer, Christoph E., Scott, Andrew M., Lewin, Sharon R.

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An octadentate chelator based on 3,4-hydroxypyridinones for ^sup 89^Zr^sup 4+^ and ^sup 213^Bi^sup 3+^ chelation von Cusnir, Ruslan, Foley, Calum, Lange, Jaclyn, Imberti, Cinzia, Morgenstern, Alfred, Bruchertseifer, Frank, Blower, Philip, Ma, Michelle

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Synthesis and in vivo evaluation of PEG-BP-BaYbF5 nanoparticles for computed tomography imaging and their toxicity von Imberti, Cinzia, Abelha, Thais Fedatto, Yan, Yong, Lange, Jaclyn, Cui, Xianjin, Szanda, Istvan, Goh, Vicky, Dailey, Lea Ann, de Rosales, Rafael T. M.

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Synthesis and evaluation of PEG-BP-BaYbF nanoparticles for computed tomography imaging and their toxicity von Imberti, Cinzia, Fedatto Abelha, Thais, Yan, Yong, Lange, Jaclyn, Cui, Xianjin, Szanda, Istvan, Goh, Vicky, Dailey, Lea Ann, de Rosales, Rafael

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Soluble CD14: Genomewide Association Analysis and Relationship to Cardiovascular Risk and Mortality in Older Adults von Reiner, Alex P, Lange, Ethan M, Jenny, Nancy S, Chaves, Paulo H.M, Ellis, Jaclyn, Li, Jin, Walston, Jeremy, Lange, Leslie A, Cushman, Mary, Tracy, Russell P

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Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction von Do, Ron, Stitziel, Nathan O., Won, Hong-Hee, Jørgensen, Anders Berg, Duga, Stefano, Angelica Merlini, Pier, Kiezun, Adam, Farrall, Martin, Goel, Anuj, Zuk, Or, Guella, Illaria, Asselta, Rosanna, Lange, Leslie A., Peloso, Gina M., Auer, Paul L., Girelli, Domenico, Martinelli, Nicola, Farlow, Deborah N., DePristo, Mark A., Roberts, Robert, Stewart, Alexander F. R., Saleheen, Danish, Danesh, John, Epstein, Stephen E., Sivapalaratnam, Suthesh, Kees Hovingh, G., Kastelein, John J., Samani, Nilesh J., Schunkert, Heribert, Erdmann, Jeanette, Shah, Svati H., Kraus, William E., Davies, Robert, Nikpay, Majid, Johansen, Christopher T., Wang, Jian, Hegele, Robert A., Hechter, Eliana, Marz, Winfried, Kleber, Marcus E., Huang, Jie, Johnson, Andrew D., Li, Mingyao, Burke, Greg L., Gross, Myron, Liu, Yongmei, Assimes, Themistocles L., Heiss, Gerardo, Lange, Ethan M., Folsom, Aaron R., Taylor, Herman A., Olivieri, Oliviero, Hamsten, Anders, Clarke, Robert, Reilly, Dermot F., Yin, Wu, Rivas, Manuel A., Donnelly, Peter, Rossouw, Jacques E., Psaty, Bruce M., Herrington, David M., Wilson, James G., Rich, Stephen S., Bamshad, Michael J., Tracy, Russell P., Adrienne Cupples, L., Rader, Daniel J., Reilly, Muredach P., Spertus, John A., Cresci, Sharon, Hartiala, Jaana, Wilson Tang, W. H., Hazen, Stanley L., Allayee, Hooman, Reiner, Alex P., Carlson, Christopher S., Kooperberg, Charles, Jackson, Rebecca D., Boerwinkle, Eric, Lander, Eric S., Schwartz, Stephen M., Siscovick, David S., McPherson, Ruth, Tybjaerg-Hansen, Anne, Abecasis, Goncalo R., Watkins, Hugh, Nickerson, Deborah A., Ardissino, Diego, Sunyaev, Shamil R., O'Donnell, Christopher J., Altshuler, David, Gabriel, Stacey, Kathiresan, Sekar

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Genetic Modifiers of Liver Disease in Cystic Fibrosis von Bartlett, Jaclyn R, Friedman, Kenneth J, Ling, Simon C, Pace, Rhonda G, Bell, Scott C, Bourke, Billy, Castaldo, Giuseppe, Castellani, Carlo, Cipolli, Marco, Colombo, Carla, Colombo, John L, Debray, Dominique, Fernandez, Adriana, Lacaille, Florence, Macek, Milan, Rowland, Marion, Salvatore, Francesco, Taylor, Christopher J, Wainwright, Claire, Wilschanski, Michael, Zemková, Dana, Hannah, William B, Phillips, M. James, Corey, Mary, Zielenski, Julian, Dorfman, Ruslan, Wang, Yunfei, Zou, Fei, Silverman, Lawrence M, Drumm, Mitchell L, Wright, Fred A, Lange, Ethan M, Durie, Peter R, Knowles, Michael R, Gene Modifier Study Group, for the

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Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants von Fu, Wenqing, O’Connor, Timothy D., Jun, Goo, Kang, Hyun Min, Abecasis, Goncalo, Leal, Suzanne M., Gabriel, Stacey, Rieder, Mark J., Altshuler, David, Shendure, Jay, Nickerson, Deborah A., Bamshad, Michael J., NHLBI Exome Sequencing Project, Akey, Joshua M.

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Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project von Auer, Paul L, Nalls, Mike, Meschia, James F, Worrall, Bradford B, Longstreth, W. T, Seshadri, Sudha, Kooperberg, Charles, Burger, Kathleen M, Carlson, Christopher S, Carty, Cara L, Chen, Wei-Min, Cupples, L. Adrienne, DeStefano, Anita L, Fornage, Myriam, Hardy, John, Hsu, Li, Jackson, Rebecca D, Jarvik, Gail P, Kim, Daniel S, Lakshminarayan, Kamakshi, Lange, Leslie A, Manichaikul, Ani, Quinlan, Aaron R, Singleton, Andrew B, Thornton, Timothy A, Nickerson, Deborah A, Peters, Ulrike, Rich, Stephen S

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Genome-wide association of body fat distribution in African ancestry populations suggests new loci von Liu, Ching-Ti, Monda, Keri L, Taylor, Kira C, Lange, Leslie, Demerath, Ellen W, Palmas, Walter, Wojczynski, Mary K, Ellis, Jaclyn C, Vitolins, Mara Z, Liu, Simin, Papanicolaou, George J, Irvin, Marguerite R, Xue, Luting, Griffin, Paula J, Nalls, Michael A, Adeyemo, Adebowale, Liu, Jiankang, Li, Guo, Ruiz-Narvaez, Edward A, Chen, Wei-Min, Chen, Fang, Henderson, Brian E, Millikan, Robert C, Ambrosone, Christine B, Strom, Sara S, Guo, Xiuqing, Andrews, Jeanette S, Sun, Yan V, Mosley, Thomas H, Yanek, Lisa R, Shriner, Daniel, Haritunians, Talin, Rotter, Jerome I, Speliotes, Elizabeth K, Smith, Megan, Rosenberg, Lynn, Mychaleckyj, Josyf, Nayak, Uma, Spruill, Ida, Garvey, W Timothy, Pettaway, Curtis, Nyante, Sarah, Bandera, Elisa V, Britton, Angela F, Zonderman, Alan B, Rasmussen-Torvik, Laura J, Chen, Yii-Der Ida, Ding, Jingzhong, Lohman, Kurt, Kritchevsky, Stephen B, Zhao, Wei, Peyser, Patricia A, Kardia, Sharon L R, Kabagambe, Edmond, Broeckel, Ulrich, Chen, Guanjie, Zhou, Jie, Wassertheil-Smoller, Sylvia, Neuhouser, Marian L, Rampersaud, Evadnie, Psaty, Bruce, Kooperberg, Charles, Manson, Joann E, Kuller, Lewis H, Ochs-Balcom, Heather M, Johnson, Karen C, Sucheston, Lara, Ordovas, Jose M, Palmer, Julie R, Haiman, Christopher A, McKnight, Barbara, Howard, Barbara V, Becker, Diane M, Bielak, Lawrence F, Liu, Yongmei, Allison, Matthew A, Grant, Struan F A, Burke, Gregory L, Patel, Sanjay R, Schreiner, Pamela J, Borecki, Ingrid B, Evans, Michele K, Taylor, Herman, Sale, Michele M, Howard, Virginia, Carlson, Christopher S, Rotimi, Charles N, Cushman, Mary, Harris, Tamara B, Reiner, Alexander P, Cupples, L Adrienne, North, Kari E, Fox, Caroline S

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Pathogenic Variants for Mendelian and Complex Traits in Exomes of 6,517 European and African Americans: Implications for the Return of Incidental Results von Tabor, Holly K., Auer, Paul L., Jamal, Seema M., Chong, Jessica X., Yu, Joon-Ho, Gordon, Adam S., Graubert, Timothy A., O’Donnell, Christopher J., Rich, Stephen S., Nickerson, Deborah A., Bamshad, Michael J.

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Multi-ethnic fine-mapping of 14 central adiposity loci von Liu, Ching-Ti, Buchkovich, Martin L, Winkler, Thomas W, Heid, Iris M, Borecki, Ingrid B, Fox, Caroline S, Mohlke, Karen L, North, Kari E, Adrienne Cupples, L

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Rare loss of function variants in candidate genes and risk of colorectal cancer von Rosenthal, Elisabeth A., Shirts, Brian H., Amendola, Laura M., Horike-Pyne, Martha, Robertson, Peggy D., Hisama, Fuki M., Bennett, Robin L., Dorschner, Michael O., Nickerson, Deborah A., Stanaway, Ian B., Nassir, Rami, Vickers, Kathy T., Li, Christopher, Grady, William M., Peters, Ulrike, Jarvik, Gail P.

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Joint Linkage and Association Analysis with Exome Sequence Data Implicates SLC25A40 in Hypertriglyceridemia von Rosenthal, Elisabeth A., Ranchalis, Jane, Crosslin, David R., Burt, Amber, Brunzell, John D., Motulsky, Arno G., Nickerson, Deborah A., Wijsman, Ellen M., Jarvik, Gail P.

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Fine-scale patterns of population stratification confound rare variant association tests von O'Connor, Timothy D, Kiezun, Adam, Bamshad, Michael, Rich, Stephen S, Smith, Joshua D, Turner, Emily, Leal, Suzanne M, Akey, Joshua M

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Soluble CD14: genome-wide association analysis and relationship to cardiovascular risk and mortality in the older adults von Reiner, Alex P., Lange, Ethan M., Jenny, Nancy S., Chaves, Paulo H.M., Ellis, Jaclyn, Li, Jin, Walston, Jeremy, Lange, Leslie A., Cushman, Mary, Tracy, Russell P.

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Panhandle and Reverse-Panhandle PCR Enable Cloning of Der(11) and Der(other) Genomic Breakpoint Junctions of MLL Translocations and Identify Complex Translocation of MLL, AF-4, and... von Raffini, Leslie J., Slater, Diana J., Rappaport, Eric F., Lo Nigro, Luca, Cheung, Nai-Kong V., Biegel, Jaclyn A., Nowell, Peter C., Lange, Beverly J., Felix, Carolyn A.

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Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis von Emond, Mary J, Louie, Tin, Emerson, Julia, Zhao, Wei, Mathias, Rasika A, Knowles, Michael R, Wright, Fred A, Rieder, Mark J, Tabor, Holly K, Nickerson, Deborah A, Barnes, Kathleen C, Gibson, Ronald L, Bamshad, Michael J

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Genome-wide linkage scan for prostate cancer susceptibility from the university of michigan prostate cancer genetics project: Suggestive evidence for linkage at 16q23 von Lange, Ethan M., Beebe-Dimmer, Jennifer L., Ray, Anna M., Zuhlke, Kimberly A., Ellis, Jaclyn, Wang, Yunfei, Walters, Sarah, Cooney, Kathleen A.

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