Výsledky vyhledávání - Galea, Charles

Disruption of an intermonomer salt bridge in the p53 tetramerization domain results in an increased propensity to form amyloid fibrils Autor Galea, Charles, Bowman, Prentice, Kriwacki, Richard W.

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Regulation of Cell Division by Intrinsically Unstructured Proteins; Intrinsic Flexibility, Modularity and Signaling Conduits Autor Galea, Charles A., Wang, Yuefeng, Sivakolundu, Sivashankar G., Kriwacki, Richard W.

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Role of Intrinsic Flexibility in Signal Transduction Mediated by the Cell Cycle Regulator, p27(Kip1) Autor Galea, Charles A., Nourse, Amanda, Wang, Yuefeng, Sivakolundu, Sivashankar G., Heller, William T., Kriwacki, Richard W.

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Intracellular Trafficking of the K(V)1.3 Potassium Channel Is Regulated by the Prodomain of a Matrix Metalloprotease Autor Nguyen, Hai M., Galea, Charles A., Schmunk, Galina, Smith, Brian J., Edwards, Robert A., Norton, Raymond S., Chandy, K. George

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Expression and isotopic labelling of the potassium channel blocker ShK toxin as a thioredoxin fusion protein in bacteria Autor Chang, Shih Chieh, Galea, Charles A., Leung, Eleanor W W., Tajhya, Rajeev B., Beeton, Christine, Pennington, Michael W., Norton, Raymond S.

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A Helical Conotoxin from Conus imperialis Has a Novel Cysteine Framework and Defines a New Superfamily Autor Ye, Mingyu, Khoo, Keith K., Xu, Shaoqiong, Zhou, Mi, Boonyalai, Nonlawat, Perugini, Matthew A., Shao, Xiaoxia, Chi, Chengwu, Galea, Charles A., Wang, Chunguang, Norton, Raymond S.

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Large-scale Analysis of Thermo-stable, Mammalian Proteins Provides Insights into the Intrinsically Disordered Proteome Autor Galea, Charles A., High, Anthony, Obenauer, John C., Mishra, Ashutosh, Park, Cheon-Gil, Punta, Marco, Schlessinger, Avner, Ma, Jing, Rost, Burkhard, Slaughter, Clive A., Kriwacki, Richard W.

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DCC mutation update: congenital mirror movements, isolated agenesis of the corpus callosum and developmental split brain syndrome Autor Marsh, Ashley PL, Edwards, Timothy J, Galea, Charles, Cooper, Helen M, Engle, Elizabeth C, Jamuar, Saumya S, Méneret, Aurélie, Moutard, Marie-Laure, Nava, Caroline, Rastetter, Agnès, Robinson, Gail, Rouleau, Guy, Roze, Emmanuel, Spencer-Smith, Megan, Trouillard, Oriane, de Villemeur, Thierry Billette, Walsh, Christopher A, Yu, Timothy W, Heron, Delphine, Sherr, Elliott H, Richards, Linda J, Depienne, Christel, Leventer, Richard J, Lockhart, Paul J

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Mutations in RAB39B Cause X-Linked Intellectual Disability and Early-Onset Parkinson Disease with α-Synuclein Pathology Autor Wilson, Gabrielle R., Sim, Joe C.H., McLean, Catriona, Giannandrea, Maila, Galea, Charles A., Riseley, Jessica R., Stephenson, Sarah E.M., Fitzpatrick, Elizabeth, Haas, Stefan A., Pope, Kate, Hogan, Kirk J., Gregg, Ronald G., Bromhead, Catherine J., Wargowski, David S., Lawrence, Christopher H., James, Paul A., Churchyard, Andrew, Gao, Yujing, Phelan, Dean G., Gillies, Greta, Salce, Nicholas, Stanford, Lynn, Marsh, Ashley P.L., Mignogna, Maria L., Hayflick, Susan J., Leventer, Richard J., Delatycki, Martin B., Mellick, George D., Kalscheuer, Vera M., D’Adamo, Patrizia, Bahlo, Melanie, Amor, David J., Lockhart, Paul J.

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Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance Autor Marsh, Ashley P L, Heron, Delphine, Edwards, Timothy J, Quartier, Angélique, Galea, Charles, Nava, Caroline, Rastetter, Agnès, Moutard, Marie-Laure, Anderson, Vicki, Bitoun, Pierre, Bunt, Jens, Faudet, Anne, Garel, Catherine, Gillies, Greta, Gobius, Ilan, Guegan, Justine, Heide, Solveig, Keren, Boris, Lesne, Fabien, Lukic, Vesna, Mandelstam, Simone A, McGillivray, George, McIlroy, Alissandra, Méneret, Aurélie, Mignot, Cyril, Morcom, Laura R, Odent, Sylvie, Paolino, Annalisa, Pope, Kate, Riant, Florence, Robinson, Gail A, Spencer-Smith, Megan, Srour, Myriam, Stephenson, Sarah E M, Tankard, Rick, Trouillard, Oriane, Welniarz, Quentin, Wood, Amanda, Brice, Alexis, Rouleau, Guy, Attié-Bitach, Tania, Delatycki, Martin B, Mandel, Jean-Louis, Amor, David J, Roze, Emmanuel, Piton, Amélie, Bahlo, Melanie, de Villemeur, Thierry Billette, Sherr, Elliott H, Leventer, Richard J, Richards, Linda J, Lockhart, Paul J, Depienne, Christel

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