Ghent University Academic Bibliography

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Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer's disease due to a novel presenilin 1 mutation

Bart Dermaut (UGent) , S Kumar-Singh, C De Jonghe, M Cruts, A Löfgren, U Lübke, P Cras, R Dom, PP De Deyn, JJ Martin, et al.

(2001) BRAIN. 124(12). p.2383-2392
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Alzheimer's disease associated presenilin 1 interacts with HC5 and ZETA, subunits of the catalytic 20S proteasome.

G VAN GASSEN, C DE JONGHE, S PYPE, Wim Van Criekinge (UGent) , A JULLIAMS, I VANDERHOEVEN, S WOODROW, Rudi Beyaert (UGent) , D HUYLEBROECK and C VAN BROECKHOVEN

(1999) NEUROBIOLOGY OF DISEASE. 6(5). p.376-391
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Identification of caspases that cleave presenilin-1 and presenilin-2 - Five presenilin-1 (PS1) mutations do not alter the sensitivity of PS1 to caspases.

Marc Van De Craen, C DE JONGHE, I VAN DEN BRANDE, Wim Declercq (UGent) , G VAN GASSEN, Wim Van Criekinge (UGent) , I VANDERHOEVEN, Walter Fiers, C VAN BROECKHOVEN, L HENDRIKS, et al.

(1999) FEBS LETTERS. 445(1). p.149-154
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- Conference Paper
- P1
Glu318gly in presenilin-1 is a neutral mutation in relation to dementia: the Rotterdam study

Bart Dermaut (UGent) , M Cruts, AJC Slooter, S Van Gestel, C De Jonghe, H Backhovens, H Vanderstichele, E Vanmechelen, MMB Breteler, A Hofman, et al.

(1999) Alzheimer's disease and related disorders : etiology, pathogenesis and therapeutics. p.87-92
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- Conference Paper
- C3
Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimers disease by increased a beta 42 secretion

M Cruts, C De Jonghe, EA Rogaeva, C Tysoe, A Singleton, H Vanderstichele, W Meschino, Bart Dermaut (UGent) , I Vanderhoeven, H Backhovens, et al.

(1999) AMERICAN JOURNAL OF HUMAN GENETICS. 65(4, suppl.). p.A291-A291

Academic Bibliography

Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer's disease due to a novel presenilin 1 mutation

Alzheimer's disease associated presenilin 1 interacts with HC5 and ZETA, subunits of the catalytic 20S proteasome.

Identification of caspases that cleave presenilin-1 and presenilin-2 - Five presenilin-1 (PS1) mutations do not alter the sensitivity of PS1 to caspases.

Glu318gly in presenilin-1 is a neutral mutation in relation to dementia: the Rotterdam study

Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimers disease by increased a beta 42 secretion

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