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Results: 1-6 |
Results: 6

Authors: Donger, C Georges, JL Nicaud, V Morrison, C Evans, A Kee, F Arveiler, D Tiret, L Cambien, F
Citation: C. Donger et al., New polymorphisms in the interleukin-10 gene - relationships to myocardialinfarction, EUR J CL IN, 31(1), 2001, pp. 9-14

Authors: Verret, C Poussard, S Touyarot, K Donger, C Savart, M Cottin, P Ducastaing, A
Citation: C. Verret et al., Degradation of protein kinase M alpha by mu-calpain in a mu-calpain-protein kinase C alpha complex, BBA-PROT ST, 1430(1), 1999, pp. 141-148

Authors: Neyroud, N Richard, P Vignier, N Donger, C Denjoy, I Demay, L Shkolnikova, M Pesce, R Chevalier, P Hainque, B Coumel, P Schwartz, K Guicheney, P
Citation: N. Neyroud et al., Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome, CIRCUL RES, 84(3), 1999, pp. 290-297

Authors: Berthet, M Denjoy, I Donger, C Demay, L Hammoude, H Klug, D Schulze-Bahr, E Richard, P Funke, H Schwartz, K Coumel, P Hainque, B Guicheney, P
Citation: M. Berthet et al., C-terminal HERG mutations - The role of hypokalemia and a KCNQ1-associatedmutation in cardiac event occurrence, CIRCULATION, 99(11), 1999, pp. 1464-1470

Authors: Murray, A Donger, C Fenske, C Spillman, I Richard, P Dong, YB Neyroud, N Chevalier, P Denjoy, I Carter, N Syrris, P Afzal, AR Patton, MA Guicheney, P Jeffery, S
Citation: A. Murray et al., Splicing mutations in KCNQ1 - A mutation hot spot at codon 344 that produces in frame transcripts, CIRCULATION, 100(10), 1999, pp. 1077-1084

Authors: Denjoy, I Lupoglazoff, JM Donger, C Berthet, M Richard, P Neyroud, N Villain, E Lucet, V Coumel, P Guicheney, P
Citation: I. Denjoy et al., Congenital long QT syndrome: The value of genetics in assessing the prognosis, ARCH MAL C, 92(5), 1999, pp. 557-563
Risultati: 1-6 |