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1. A single nuclear transcriptomic characterisation of mechanisms responsible for impaired angiogenesis and blood-brain barrier function in Alzheimer’s disease

2. Mass spectrometry imaging highlights dynamic patterns of lipid co‐expression with Aβ plaques in mouse and human brains

3. Glial and neuronal mechanisms contributing to differential risks in TREM2 R47H and R62H variants in Alzheimer’s Disease

4. Single‐nuclei RNA sequencing provides evidence for glial senescence in Alzheimer’s disease

5. Atypical presentations of autosomal dominant familial Alzheimer’s disease: insights into genetic, neuropathological and clinical heterogeneity

6. Signalling pathways associated with impaired angiogenesis in Alzheimer’s Disease

8. The PSEN1 E280G mutation leads to increased amyloid-β43 production in induced pluripotent stem cell neurons and deposition in brain tissue

9. Mechanisms contributing to differential genetic risks for TREM2 R47H and R62H variants in Alzheimer’s Disease

10. Single nuclear transcriptional signatures of dysfunctional brain vascular homeostasis in Alzheimer’s disease

12. Plasma amyloid-β ratios in autosomal dominant Alzheimer’s disease: the influence of genotype

13. Plasma Aβ ratios in autosomal dominant Alzheimer’s disease: the influence of genotype

14. Familial Alzheimer’s Disease Mutations in PSEN1 Lead to Premature Human Stem Cell Neurogenesis

15. Premature neuronal differentiation in familial Alzheimer’s disease human stem cells in vitro and in postmortem brain tissue

18. O1‐03‐04: CORTICAL NEURONS AND CEREBRAL ORGANOIDS FROM APP AND PSEN1 MUTATION CARRIERS REVEAL MUTATION‐SPECIFIC EFFECTS ON Aβ PRODUCTION

19. Familial Alzheimer’s disease patient-derived neurons reveal distinct mutation-specific effects on amyloid beta

20. Association ofMAPThaplotype-tagging polymorphisms with cerebrospinal fluid biomarkers of Alzheimer's disease: A preliminary study in a Croatian cohort

21. P1‐188: MODELLING AMYLOID BETA PROFILES IN IPSC‐DERIVED CORTICAL NEURONS OF MULTIPLE FAMILIAL ALZHEIMER'S DISEASE GENOTYPES, INCLUDING A CASE STUDY OF SAME DONOR CULTURE MEDIA, CSF AND BRAIN TISSUE

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