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Results:
1-8
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Results: 8
Authors:
Kumar-Singh, S
De Jonghe, C
Cruts, M
Kleinert, R
Wang, R
Mercken, M
De Strooper, B
Vanderstichele, H
Lofgren, A
Vanderhoeven, I
Backhovens, H
Vanmechelen, E
Kroisel, PM
Van Broeckhoven, C
Citation: S. Kumar-singh et al., Nonfibrillar diffuse amyloid deposition due to a gamma(42)-secretase site mutation points to an essential role for N-truncated A beta(42) in Alzheimer's disease, HUM MOL GEN, 9(18), 2000, pp. 2589-2598
Authors:
Van Gassen, G
De Jonghe, C
Pype, S
Van Criekinge, W
Julliams, A
Vanderhoeven, I
Woodrow, S
Beyaert, R
Huylebroeck, D
Van Broeckhoven, C
Citation: G. Van Gassen et al., Alzheimer's disease associated presenilin 1 interacts with HC5 and ZETA, subunits of the catalytic 20S proteasome, NEUROBIOL D, 6(5), 1999, pp. 376-391
Authors:
De Jonghe, C
Cras, P
Vanderstichele, H
Cruts, M
Vanderhoeven, I
Smouts, I
Vanmechelen, E
Martin, JJ
Hendriks, L
Van Broeckhoven, C
Citation: C. De Jonghe et al., Evidence that A beta 42 plasma levels in presenilin-1 mutation carriers donot allow for prediction of their clinical phenotype, NEUROBIOL D, 6(4), 1999, pp. 280-287
Authors:
De Jonghe, C
Cruts, M
Rogaeva, EA
Tysoe, C
Singleton, A
Vanderstichele, H
Meschino, W
Dermaut, D
Vanderhoeven, I
Backhovens, H
Vanmechelen, E
Morris, CM
Hardy, J
Rubinsztein, DC
St George-Hyslop, PH
Van Broeckhoven, C
Citation: C. De Jonghe et al., Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased A beta 42 secretion, HUM MOL GEN, 8(8), 1999, pp. 1529-1540
Authors:
Vanderhoeven, I
Cras, P
Martin, JJ
Van Broeckhoven, C
De Jonghe, C
Citation: I. Vanderhoeven et al., Proteolytic processing of presenilin-1 in human lymphoblasts is not affected by the presence of the I143Tand G384A mutations, NEUROSCI L, 274(3), 1999, pp. 183-186
Authors:
Julliams, A
Vanderhoeven, I
Kuhn, S
Van Broeckhoven, C
De Jonghe, C
Citation: A. Julliams et al., No influence of presenilin 1 I143Tand G384A mutations on endogenous tau phosphorylation in human and mouse neuroblastoma cells, NEUROSCI L, 269(2), 1999, pp. 83-86
Authors:
van de Craen, M
de Jonghe, C
van den Brande, I
Declercq, W
van Gassen, G
van Criekinge, W
Vanderhoeven, I
Fiers, W
van Broeckhoven, C
Hendriks, L
Vandenabeele, P
Citation: M. Van De Craen et al., Identification of caspases that cleave presenilin-1 and presenilin-2 - Five presenilin-1 (PS1) mutations do not alter the sensitivity of PS1 to caspases, FEBS LETTER, 445(1), 1999, pp. 149-154
Authors:
De Jonghe, C
Tysoe, C
Cruts, M
Vanderhoeven, I
Vanderstichele, H
Vanmechelen, E
Van Broeckhoven, C
Rubinsztein, DC
Hendriks, L
Citation: C. De Jonghe et al., A presenilin-1 truncating mutation causing Alzheimer's disease, ALZHEIMER'S DISEASE AND RELATED DISORDERS, 1999, pp. 81-86
Risultati:
1-8
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