检索结果 - Galea, Charles

Disruption of an intermonomer salt bridge in the p53 tetramerization domain results in an increased propensity to form amyloid fibrils 由 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 由 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) 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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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