Resultats de la cerca - Galea, Charles
- Mostrar 1 - 10 resultats de 10
-
1
-
2
-
3
Role of Intrinsic Flexibility in Signal Transduction Mediated by the Cell Cycle Regulator, p27(Kip1) per Galea, Charles A., Nourse, Amanda, Wang, Yuefeng, Sivakolundu, Sivashankar G., Heller, William T., Kriwacki, Richard W.
Publicat 2007Text -
4
Intracellular Trafficking of the K(V)1.3 Potassium Channel Is Regulated by the Prodomain of a Matrix Metalloprotease per Nguyen, Hai M., Galea, Charles A., Schmunk, Galina, Smith, Brian J., Edwards, Robert A., Norton, Raymond S., Chandy, K. George
Publicat 2013Text -
5
Expression and isotopic labelling of the potassium channel blocker ShK toxin as a thioredoxin fusion protein in bacteria per Chang, Shih Chieh, Galea, Charles A., Leung, Eleanor W W., Tajhya, Rajeev B., Beeton, Christine, Pennington, Michael W., Norton, Raymond S.
Publicat 2012Text -
6
A Helical Conotoxin from Conus imperialis Has a Novel Cysteine Framework and Defines a New Superfamily per 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.
Publicat 2012Text -
7
Large-scale Analysis of Thermo-stable, Mammalian Proteins Provides Insights into the Intrinsically Disordered Proteome per 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.
Publicat 2009Text -
8
DCC mutation update: congenital mirror movements, isolated agenesis of the corpus callosum and developmental split brain syndrome per 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
Publicat 2017Text -
9
Mutations in RAB39B Cause X-Linked Intellectual Disability and Early-Onset Parkinson Disease with α-Synuclein Pathology per 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.
Publicat 2014Text -
10
Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance per 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
Publicat 2017Text