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    Whole genome‐wide sequence analysis of long‐lived families (Long‐Life Family Study) identifies MTUS2 gene associated with late‐onset Alzheimer's disease von Vardarajan, Badri, Andersen, Stacy L., Thyagarajan, Bharat, Yashin, Anatoli, Krinsky‐McHale, Sharon, Handen, Benjamin L., Schupf, Nicole, Lee, Joseph H., Barral, Sandra, Bell, Karen, Bulova, Peter, Cohen, Ann D., Constantino, John N., Handen, Benjamin L., Head, Elizabeth, Honig, Lawrence, Ikonomovic, Milos D., Keator, David, Lao, Patrick, Lott, Ira T., Mapstone, Mark, Parisi, Melissa, Pulsifer, Margaret, Varadarajan, Badri, Zaman, Shahid, Adams, Perrie M., Allen, Mariet, Atwood, Craig S., Ayres, Gayle, Barral, Sandra, Beecham, Gary W., Biber, Sarah A., Boeve, Bradley F., Bush, William S., Byrd, Goldie, Chan, Kwun C., Chen, Yen‐Chi, Chesselet, Marie‐Francoise, Chin, Nathaniel A., Cranney, Marissa, Cruchaga, Carlos, DeToledo, John C., Ertekin‐Taner, Nilufer, Faber, Kelley M., Fallin, Daniele, Farrer, Lindsay A., Galasko, Douglas R., Gefen, Tamar, Goate, Alison M., Grabowski, Thomas, Haines, Jonathan L., Hakonarson, Hakon, Hall, Kathleen, Hall, James R., Harari, Oscar, Honig, Lawrence S., Hyman, Bradley T., Hynan, Linda, Johnson, Kimberly, Jun, Gyungah, Kamboh, M. Ilyas, Khaleeq, Aisha, Kunkle, Brian W., LaFerla, Frank M., Lah, James J., Lieberman, Andrew P., Lipton, Richard B., Lopez, Oscar L., Marquez, David, Marson, Daniel C., Masurkar, Arjun V., Mukherjee, Shubhabrata, Nudelman, Kelley, Parisi, Joseph E., Pavlik, Valory, Perez, Victoria, Petersen, Ronald C., Polk, Marsha, Qu, Liming, Quiceno, Mary, Raj, Ashok, Rajabli, Farid, Roberson, Erik D., Royall, Donald R., Sano, Mary, Song, Yeunjoo, George‐Hyslop, Peter St, Stern, Robert A., Stevens, Alan, Sultzer, David, Valladares, Otto, Van Deerlin, Vivianna M., Vance, Jeffery M., Vassar, Robert, Welsh‐Bohmer, Kathleen A., Wilms, Henrick, Wisniewski, Thomas, Woon, Martin, Younkin, Steven G., Zhu, Congcong

    Veröffentlicht in Alzheimer's & dementia

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    Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy von Schoch, Kelly, Kranz, Peter G., Markert, M. Louise, Arbogast, Thomas, Muraresku, Colleen, Adams, David R., Alvarez, Raquel L., Balasubramanyam, Ashok, Bamshad, Michael, Beck, Anita, Behrens, Edward, Bejerano, Gill, Bellen, Hugo J., Bohnsack, John, Bonner, Devon, Botto, Lorenzo, Brown, Gabrielle, Butte, Manish J., Byrd, William E., Carrasquillo, Olveen, Cassini, Thomas, Chanprasert, Sirisak, Chinn, Ivan, Clark, Gary D., Coggins, Matthew, Cope, Heidi, Craigen, William J., D’Souza, Precilla, Dipple, Katrina, Doherty, Daniel, Fisher, Paul G., Fogel, Brent L., Glass, Ian, Gochuico, Bernadette, Godfrey, Rena A., Hahn, Sihoun, Hamid, Rizwan, Introne, Wendy, Jamal, Fariha, Jean-Marie, Orpa, Kobren, Shilpa N., Krakow, Deborah, Krasnewich, Donna M., Kravets, Elijah, LeBlanc, Kimberly, Lee, Brendan H., Loo, Sandra K., Loscalzo, Joseph, Mahoney, Rachel, Malicdan, May Christine V., Mamounas, Laura A., Marom, Ronit, Martínez-Agosto, Julian A., McConkie-Rosell, Allyn, Merritt, J. Lawrence, Might, Matthew, Mulvihill, John, Newman, John H., Nieves-Rodriguez, Shirley, Orengo, James P., Pace, Laura, Papp, Jeanette C., Parker, Neil H., Pusey Swerdzewski, Barbara N., Quinlan, Aaron, Raper, Anna, Reuter, Chloe M., Rives, Lynette, Robertson, Amy K., Rodan, Lance H., Rossignol, Francis, Sampson, Jacinda B., Saporta, Mario, Schaechter, Judy, Schoch, Kelly, Scott, C. Ron, Seto, Elaine, Sinsheimer, Janet S., Solnica-Krezel, Lilianna, Spillmann, Rebecca C., Stoler, Joan M., Sullivan, Jennifer A., Sun, Angela, Sutton, Shirley, Tabor, Holly K., Tan, Queenie K.-G., Telischi, Fred, Tifft, Cynthia J., Urv, Tiina K., Wahl, Colleen E., Wang, Lee-kai, Wangler, Michael F., Wheeler, Matthew T., Worley, Kim, Xiao, Changrui, Yamamoto, Shinya, Tyndall, Amanda V., Woodward, Kristine E., Wright, Nicola A.M., Davis, Erica E.

    Veröffentlicht in Genetics in medicine

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