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Results: 1-18 |
Results: 18

Authors: De Jonghe, C Esselens, C Kumar-Singh, S Craessaerts, K Serneels, S Checler, F Annaert, W Van Broeckhoven, C De Strooper, B
Citation: C. De Jonghe et al., Pathogenic APP mutations near the gamma-secretase cleavage site differentially affect A beta secretion and APP C-terminal fragment stability, HUM MOL GEN, 10(16), 2001, pp. 1665-1671

Authors: Roymans, D Vissenberg, K De Jonghe, C Grobben, B Claes, P Verbelen, JP Van Broeckhoven, C Slegers, H
Citation: D. Roymans et al., Phosphatidylinositol 3-kinase activity is required for the expression of glial fibrillary acidic protein upon cAMP-dependent induction of differentiation in rat C6 glioma, J NEUROCHEM, 76(2), 2001, pp. 610-618

Authors: Roymans, D Vissenberg, K De Jonghe, C Willems, R Engler, G Kimura, N Grobben, B Claes, P Verbelen, JP Van Broeckhoven, C Slegers, H
Citation: D. Roymans et al., Identification of the tumor metastasis suppressor Nm23-H1/Nm23-R1 as a constituent of the centrosome, EXP CELL RE, 262(2), 2001, pp. 145-153

Authors: Van Gassen, G De Jonghe, C Kuhn, S Lubke, U Kumar-Singh, S Martin, JJ Van Broeckhoven, C
Citation: G. Van Gassen et al., Effect of presenilin 1 expression on 20S proteasome subcellular localization, ALZHEIM REP, 3(2), 2000, pp. 89-95

Authors: Van Gassen, G De Jonghe, C Nishimura, M Yu, G Kuhn, S St George-Hyslop, PS Van Broeckhoven, C
Citation: G. Van Gassen et al., Evidence that the beta-catenin nuclear translocation assay allows for measuring presenilin 1 dysfunction, MOL MED, 6(7), 2000, pp. 570-580

Authors: Kumar-Singh, S Dewachter, I Moechars, D Lubke, U De Jonghe, C Ceuterick, C Checler, F Naidu, A Cordell, B Cras, P Van Broeckhoven, C Van Leuven, F
Citation: S. Kumar-singh et al., Behavioral disturbances without amyloid deposits in mice overexpressing human amyloid precursor protein with Flemish (A692G) or Dutch (E693Q) mutation, NEUROBIOL D, 7(1), 2000, pp. 9-22

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: Roymans, D Willems, R Vissenberg, K De Jonghe, C Grobben, B Claes, P Lascu, I Van Bockstaele, D Verbelen, JP Van Broeckhoven, C Slegers, H
Citation: D. Roymans et al., Nucleoside diphosphate kinase beta (Nm23-R1/NDPK beta) is associated with intermediate filaments and becomes upregulated upon cAMP-induced differentiation of rat C6 glioma, EXP CELL RE, 261(1), 2000, pp. 127-138

Authors: Singleton, AB Hall, R Ballard, CG Perry, RH Xuereb, JH Rubinsztein, DC Tysoe, C Matthews, P Cordell, B Kumar-Singh, S De Jonghe, C Cruts, M van Broeckhoven, C Morris, CM
Citation: Ab. Singleton et al., Pathology of early-onset Alzheimer's disease cases bearing the Thr113-114ins presenilin-1 mutation, BRAIN, 123, 2000, pp. 2467-2474

Authors: Roks, G Van Harskamp, F De Koning, I Cruts, M De Jonghe, C Kumar-Singh, S Tibben, A Tanghe, H Niermeijer, MF Hofman, A Van Swieten, JC Van Broeckhoven, C Van Duijn, CM
Citation: G. Roks et al., Presentation of amyloidosis in carriers of the codon 692 mutation in the amyloid precursor protein gene (APP692), BRAIN, 123, 2000, pp. 2130-2140

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: Dermaut, B Cruts, M Slooter, AJC Van Gestel, S De Jonghe, C Vanderstichele, H Vanmechelen, E Breteler, MM Hofman, A van Duijn, CM Van Broeckhoven, C
Citation: B. Dermaut et al., The Glu318Gly substitution in presenilin 1 is not causally related to Alzheimer disease, AM J HU GEN, 64(1), 1999, pp. 290-292

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

Authors: Dermaut, B Cruts, M Slooter, AJC Van Gestel, S De Jonghe, C Backhovens, H Vanderstichele, H Vanmechelen, E Breteler, MMB Hofman, A Hendriks, L Van Duijn, CM Van Broeckhoven, C
Citation: B. Dermaut et al., Glu318Gly in presenilin-1 is a neutral mutation in relation to dementia: The Rotterdam study, ALZHEIMER'S DISEASE AND RELATED DISORDERS, 1999, pp. 87-92
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