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3. NACC2, a molecular effector of miR-132 regulation at the interface between adult neurogenesis and Alzheimer’s disease

4. MEG3 activates necroptosis in human neuron xenografts modeling Alzheimer’s disease

9. Presenilin 2 Deficiency Causes a Mild Pulmonary Phenotype and no Changes in Amyloid Precursor Protein Processing but Enhances the Embryonic Lethal Phenotype of Presenilin 1 Deficiency

10. Early alterations in the MCH system link aberrant neuronal activity and sleep disturbances in a mouse model of Alzheimer’s disease

11. MEG3 activates necroptosis in human neuron xenografts modeling Alzheimer's disease

13. Astrocytes mediate neuronal network hyperactivity in early AD

15. Astrocyte calcium dysfunction causes early network hyperactivity in Alzheimer’s disease

16. Deep proteomic analysis of human microglia and model systems reveal fundamental biological differences ofin vitroandex vivocells

18. γ-Secretase Heterogeneity in the Aph1 Subunit: Relevance for Alzheimer's Disease

20. Restoring miR-132 expression rescues adult hippocampal neurogenesis and memory deficits in Alzheimer’s disease

21. Restoring miR-132 expression rescues adult hippocampal neurogenesis and memory deficits in Alzheimer's disease

22. [Gamma]-secretase heterogeneity in the Aph1 subunit: relevance for Alzheimer's disease

23. Melanin Concentrating Hormone- and sleep-dependent synaptic downscaling is impaired in Alzheimer’s Disease

24. Deep proteomic analysis of microglia reveals fundamental biological differences between model systems

26. Spatial Transcriptomics and In Situ Sequencing to Study Alzheimer's Disease

27. Differential contribution of the three Aph1 genes to [gamma]-secretase activity in vivo

29. Spatial Transcriptomics and In Situ Sequencing to Study Alzheimer’s Disease

30. Impaired adult hippocampal neurogenesis in Alzheimer’s disease is mediated by microRNA-132 deficiency and can be restored by microRNA-132 replacement

31. A presenilin-1-dependent gamma-secretase-like protease mediates release of Notch intracellular domain

32. Deficiency of presenilin-1 inhibits the normal cleavage of amyloid precursor protein

40. Spatial and temporal transcriptomics reveal microglia-astroglia crosstalk in the amyloid-β plaque cell niche of Alzheimer’s disease

42. Mitochondrial rhomboid PARL regulates cytochrome c release during apoptosis via OPA1-dependent cristae remodeling

43. Cardiolipin promotes electron transport between ubiquinone and complex I to rescue PINK1 deficiency

44. Transitional B cells commit to marginal zone B cell fate by Taok3-mediated surface expression of ADAM10

45. The discrepancy between presenilin subcellular localization and [Gamma]-secretase processing of amyloid precursor protein

48. Mutations in the Intellectual Disability Gene Ube2a Cause Neuronal Dysfunction and Impair Parkin-Dependent Mitophagy

49. Phenotypic and biochemical analyses of BACE1- and BACE2-deficient mice

50. Analysis of the γ-secretase interactome and validation of its association with tetraspanin-enriched microdomains

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