Accès ouvert
2026
article
OpenAlex
Oliviero Cini, Alan Miranda, Daan Willocx, Angeliki Karakasidi et autres
Abstract Background Cysteine cathepsin L (CatL) is emerging as a key biomarker of cancer progression, making it an attractive candidate for non-invasive molecular imaging. To monitor enzymatic activity directly, rather than merely protein expression, activity-based probes (ABPs) enable selective targeting of enzymes …
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Accès ouvert
2026
article
OpenAlex
Oliviero Cini, Alan Miranda, Daan Willocx, Angeliki Karakasidi et autres
Supplementary Material 1
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Accès ouvert
2026
article
OpenAlex
Oliviero Cini, Alan Miranda, Daan Willocx, Angeliki Karakasidi et autres
Supplementary Material 1
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Accès ouvert
2026
article
OpenAlex
Oliviero Cini, Alan Miranda, Daan Willocx, Angeliki Karakasidi et autres
Supplementary Material 1
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2026
article
OpenAlex
Alan Miranda, Filipe Elvas, Steven G. Staelens
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Accès ouvert
2026
article
OpenAlex
Liesbeth Everix, Alan Miranda, Jordy Akkermans, Vinod K. Khetarpal et autres
Deficits in the synaptic vesicle protein 2A (SV2A) have been reported in various neurodegenerative diseases including Alzheimer’s and Huntington’s disease (HD). SV2A levels can be investigated using positron emission tomography (PET) radioligands such as [ 11 C]UCB-J, [ 18 F]UCB-J, and [ …
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2026
conference-abstract
OpenAlex
Umberto Maria Battisti, Marcel Martin, Vladimir Shalgunov, Filipe Elvas et autres
Abstract The successful use of diagnostic radiotracers targeting the pan-tumor marker fibroblast activation protein (FAP) across numerous cancer types is well established; however, translating these agents into effective therapeutics remains challenging. Compared with monomeric FAP inhibitors (FAPi), FAPi dimers—containing two FAP-targeting vectors—exhibit …
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Accès ouvert
2026
dataset
OpenAlex
Liesbeth Everix, Alan Miranda, Jordy Akkermans, Vinod K. Khetarpal et autres
Accès ouvert
2025
article
OpenAlex
Franziska Zajicek, Liesbeth Everix, Annemie Van Eetveldt, Jeroen A.J. Verhaeghe et autres
Huntington’s disease (HD) is a neurodegenerative disorder caused by an expanded trinucleotide repeat in the huntingtin gene (HTT) that subsequently leads to aggregation of the mutant huntingtin (mHTT) protein. Thus, lowering mHTT is a key therapeutic approach used by several candidate therapeutics …
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Accès ouvert
2025
article
OpenAlex
Franziska Zajicek, Filipe Elvas, Alan Miranda, Jordy Akkermans et autres
Aggregation of mutant huntingtin (mHTT) is a neurologic hallmark of Huntington disease (HD), a neurodegenerative disorder caused by the expansion of a cytosine–adenine–guanine repeat tract in the huntingtin gene (HTT). With a considerable number of candidate therapeutic interventions aimed at lowering mHTT …
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Accès ouvert
2025
article
OpenAlex
Charissa Millevert, Nicholas Vidas-Guscic, Mohit H. Adhikari, Alan Miranda et autres
BACKGROUND: KCNQ2-developmental and epileptic encephalopathy (KCNQ2-DEE) is a severe neurodevelopmental disorder (NDD) characterised by early-life seizures but persistent cognitive impairment. The absence of early, quantifiable preclinical biomarkers for neurodevelopmental dysfunction limits the evaluation of new treatments. We hypothesise that key brain maturation …
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2025
article
OpenAlex
Karuna Adhikari, Sergei Grintsevich, Anke de Groot, Emile Verhulst et autres
Fibroblast activation protein (FAP) is upregulated in cancer and fibrosis, making it an ideal target for imaging and therapy. Most FAP radioligands are large, highly polar, chelator-based molecules that suffer from limited tissue penetration and rapid tumor washout. In this study, we …
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