[HTML][HTML] Mitochondrial rhomboid PARL regulates cytochrome c release during apoptosis via OPA1-dependent cristae remodeling

S Cipolat, T Rudka, D Hartmann, V Costa, L Serneels… - Cell, 2006 - cell.com
Rhomboids, evolutionarily conserved integral membrane proteases, participate in crucial
signaling pathways. Presenilin-associated rhomboid-like (PARL) is an inner mitochondrial …

The disintegrin/metalloprotease ADAM 10 is essential for Notch signalling but not for α-secretase activity in fibroblasts

D Hartmann, B De Strooper, L Serneels… - Human molecular …, 2002 - academic.oup.com
The metalloprotease ADAM 10 is an important APP α-secretase candidate, but in vivo proof
of this is lacking. Furthermore, invertebrate models point towards a key role of the ADAM 10 …

[HTML][HTML] Presenilins form ER Ca2+ leak channels, a function disrupted by familial Alzheimer's disease-linked mutations

…, Z Wang, SF Lee, YH Hao, L Serneels… - Cell, 2006 - cell.com
Alzheimer's disease (AD) is a progressive and irreversible neurodegenerative disorder.
Mutations in presenilins 1 and 2 (PS1 and PS2) account for ∼40% of familial AD (FAD) cases. …

Total inactivation of γ–secretase activity in presenilin-deficient embryonic stem cells

A Herreman, L Serneels, W Annaert, D Collen… - Nature cell …, 2000 - nature.com
* Neuronal Cell Biology Laboratory, CME, KU Leuven and Flanders Interuniversitary Institute
for Biotechnology (VIB4), Herestraat 49, 3000 Leuven, Belgium† Thromb–X, NV, Herestraat …

The mechanism of γ‐secretase dysfunction in familial Alzheimer disease

…, H Esselmann, J Wiltfang, L Serneels… - The EMBO …, 2012 - embopress.org
The mechanisms by which mutations in the presenilins (PSEN) or the amyloid precursor
protein (APP) genes cause familial Alzheimer disease (FAD) are controversial. FAD mutations …

Presenilin 2 deficiency causes a mild pulmonary phenotype and no changes in amyloid precursor protein processing but enhances the embryonic lethal phenotype of …

…, P Saftig, K Craessaerts, L Serneels… - Proceedings of the …, 1999 - National Acad Sciences
Mutations in the homologous presenilin 1 (PS1) and presenilin 2 (PS2) genes cause the most
common and aggressive form of familial Alzheimer’s disease. Although PS1 function and …

[HTML][HTML] Phenotypic and biochemical analyses of BACE1-and BACE2-deficient mice

…, T Huth, K Cryns, S Deforce, L Serneels… - Journal of Biological …, 2005 - ASBMB
β-Secretase (BACE1) is the rate-limiting protease for the generation of the amyloid β-peptide
(Aβ) in Alzheimer disease. Mice in which the bace1 gene is inactivated are reported to be …

The disintegrin/metalloproteinase ADAM10 is essential for the establishment of the brain cortex

…, S Weber, R Schwanbeck, L Serneels… - Journal of …, 2010 - Soc Neuroscience
The metalloproteinase and major amyloid precursor protein (APP) α-secretase candidate
ADAM10 is responsible for the shedding of proteins important for brain development, such as …

γ-Secretase heterogeneity in the Aph1 subunit: relevance for Alzheimer's disease

L Serneels, J Van Biervliet, K Craessaerts, T Dejaegere… - Science, 2009 - science.org
The γ-secretase complex plays a role in Alzheimer’s disease and cancer progression. The
development of clinically useful inhibitors, however, is complicated by the role of the γ-…

Neuronal deficiency of presenilin 1 inhibits amyloid plaque formation and corrects hippocampal long-term potentiation but not a cognitive defect of amyloid precursor …

…, K Spittaels, L Umans, L Serneels… - Journal of …, 2002 - Soc Neuroscience
In the brain of Alzheimer's disease (AD) patients, neurotoxic amyloid peptides accumulate
and are deposited as senile plaques. A major therapeutic strategy aims to decrease …