Clinical management of patients with ASXL1 mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance von Russell, Bianca, Johnston, Jennifer J., Biesecker, Leslie G., Kramer, Nancy, Pickart, Angela, Rhead, William, Tan, Wen-Hann, Brownstein, Catherine A., Kate Clarkson, L., Dobson, Amy, Rosenberg, Avi Z., Vergano, Samantha A. Schrier, Helm, Benjamin M., Harrison, Rachel E., Graham Jr, John M.

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Unique Cerebrovascular Anomalies in Noonan Syndrome With RAF1 Mutation von Zarate, Yuri A., Lichty, Angie W., Champion, Kristen J., Clarkson, L. Kate, Holden, Kenton R., Matheus, M. Gisele

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Clinical utility of the X-chromosome array von Zarate, Yuri A., Dwivedi, Alka, Bartel, Frank O., Bellomo, M. Allison, Cathey, Sara S., Champaigne, Neena L., Clarkson, L. Kate, DuPont, Barbara R., Everman, David B., Geer, Joseph S., Gordon, Barbara C., Lichty, Angie W., Lyons, Michael J., Rogers, R. Curtis, Saul, Robert A., Schroer, Richard J., Skinner, Steven A., Stevenson, Roger E.

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The GHB analogue HOCPCA improves deficits in cognition and sensorimotor function after MCAO via CaMKIIα von Griem-Krey, Nane, Klein, Anders B, Clausen, Bettina H, Namini, Mathias RJ, Nielsen, Pernille V, Bhuiyan, Mozammel, Nagaraja, Raghavendra Y, De Silva, T Michael, Sobey, Christopher G, Cheng, Heung-Chin, Orset, Cyrille, Vivien, Denis, Lambertsen, Kate L, Clarkson, Andrew N, Wellendorph, Petrine

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IMI 2021 Yearly Digest von Jong, Monica, Jonas, Jost B., Wolffsohn, James S., Berntsen, David A., Cho, Pauline, Clarkson-Townsend, Danielle, Flitcroft, Daniel I., Gifford, Kate L., Haarman, Annechien E. G., Pardue, Machelle T., Richdale, Kathryn, Sankaridurg, Padmaja, Tedja, Milly S., Wildsoet, Christine F., Bailey-Wilson, Joan E., Guggenheim, Jeremy A., Hammond, Christopher J., Kaprio, Jaakko, MacGregor, Stuart, Mackey, David A., Musolf, Anthony M., Klaver, Caroline C. W., Verhoeven, Virginie J. M., Vitart, Veronique, Smith, Earl L.

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Oceanographic and climatic evolution of the southeastern subtropical Atlantic over the last 3.5 Ma von Petrick, Benjamin, McClymont, Erin L., Littler, Kate, Rosell-Melé, Antoni, Clarkson, Matthew O., Maslin, Mark, Röhl, Ursula, Shevenell, Amelia E., Pancost, Richard D.

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Immune Response Characterization after Controlled Infection with Lyophilized Shigella sonnei 53G von Clarkson, Kristen A., Frenck, Robert W., Dickey, Michelle, Suvarnapunya, Akamol E., Chandrasekaran, Lakshmi, Weerts, Hailey P., Heaney, Christopher D., McNeal, Monica, Detizio, Kate, Parker, Susan, Hoeper, Amy, Bourgeois, August L., Porter, Chad K., Venkatesan, Malabi M., Kaminski, Robert W.

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Large-scale evaluation of outcomes after a genetic diagnosis in children with severe developmental disorders von Copeland, Harriet, Low, Karen J., Wynn, Sarah L., Ahmed, Ayesha, Arthur, Victoria, Balasubramanian, Meena, Bennett, Katya, Berg, Jonathan, Bertoli, Marta, Bryson, Lisa, Bucknall, Catrin, Campbell, Jamie, Chandler, Kate, Chauhan, Jaynee, Clarkson, Amy, Coles, Rachel, Conti, Hector, Costello, Philandra, Coupar, Tessa, Craig, Amy, Dean, John, Dillon, Amy, Dixit, Abhijit, Drew, Kathryn, Eason, Jacqueline, Forzano, Francesca, Foulds, Nicola, Gardham, Alice, Ghali, Neeti, Green, Andrew, Hanna, William, Harrison, Rachel, Hegarty, Mairead, Higgs, Jenny, Holder, Muriel, Irving, Rachel, Jain, Vani, Johnson, Katie, Jolley, Rachel, Jones, Wendy D., Jones, Gabriela, Joss, Shelagh, Kalinauskiene, Ruta, Kanani, Farah, Kavanagh, Karl, Khan, Mahmudur, Khan, Naz, Kivuva, Emma, Lahiri, Nayana, Lakhani, Neeta, Lampe, Anne, Lynch, Sally Ann, Mansour, Sahar, Marsden, Alice, Massey, Hannah, McKee, Shane, Mohammed, Shehla, Naik, Swati, Nesarajah, Mithushanaa, Newbury-Ecob, Ruth, Osborne, Fiona, Parker, Michael J., Patterson, Jenny, Pottinger, Caroline, Prapa, Matina, Prescott, Katrina, Quinn, Shauna, Radley, Jessica A., Robart, Sarah, Ross, Alison, Rosti, Giulia, Sansbury, Francis H., Sarkar, Ajoy, Searle, Claire, Shannon, Nora, Shears, Debbie, Smithson, Sarah, Stewart, Helen, Suri, Mohnish, Tadros, Shereen, Theobald, Rachel, Thomas, Rhian, Tsoulaki, Olga, Vasudevan, Pradeep, Rodriguez, Maribel Verdesoto, Vittery, Emma, Whyte, Sinead, Woods, Emily, Wright, Thomas, Zocche, David, Firth, Helen V., Wright, Caroline F.

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A Novel GLRA1 Mutation Associated with An Atypical Hyperekplexia Phenotype von Gregory, Mary L., Guzauskas, Greg F., Edgar, Terence S., Clarkson, Kate B., Srivastava, Anand K., Holden, Kenton R.

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Characterization of a naturally-occurring polymorphism in the UHR-1 gene encoding the putative rat prolactin-releasing peptide receptor von Ellacott, Kate L.J., Donald, Emma L., Clarkson, Paul, Morten, John, Masters, Dave, Brennand, John, Luckman, Simon M.

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Sea surface temperature reconstruction (TEX86) from ODP Site 175-1087 von Petrick, Benjamin F, McClymont, Erin L, Littler, Kate, Rosell-Melé, Antoni, Clarkson, Matthew O, Maslin, Mark, Röhl, Ursula, Shevenell, Amelia E, Pancost, Richard D

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Alkenone accumulation rates (MAR) from ODP Site 175-1087 von Petrick, Benjamin F, McClymont, Erin L, Littler, Kate, Rosell-Melé, Antoni, Clarkson, Matthew O, Maslin, Mark, Röhl, Ursula, Shevenell, Amelia E, Pancost, Richard D

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XRF analysis from ODP Site 175-1087 von Petrick, Benjamin F, McClymont, Erin L, Littler, Kate, Rosell-Melé, Antoni, Clarkson, Matthew O, Maslin, Mark, Röhl, Ursula, Shevenell, Amelia E, Pancost, Richard D

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Chorins accumulation rates (MAR) from ODP Site 175-1087 von Petrick, Benjamin F, McClymont, Erin L, Littler, Kate, Rosell-Melé, Antoni, Clarkson, Matthew O, Maslin, Mark, Röhl, Ursula, Shevenell, Amelia E, Pancost, Richard D

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Sea surface temperature reconstruction (UK'37) from ODP Site 175-1087 von Petrick, Benjamin F, McClymont, Erin L, Littler, Kate, Rosell-Melé, Antoni, Clarkson, Matthew O, Maslin, Mark, Röhl, Ursula, Shevenell, Amelia E, Pancost, Richard D

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Albright hereditary osteodystrophy and del(2)(q37.3) in four unrelated individuals von Phelan Ph.D., Mary C., Rogers, R. Curtis, Clarkson, Kate B., Bowyer, Frank P., Levine, Michael A., Estabrooks, Laurel L., Severson, Michael C., Dobyns, William B.

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