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1. Genetically Engineered iPSC-Derived FTDP-17 MAPT Neurons Display Mutation-Specific Neurodegenerative and Neurodevelopmental Phenotypes

2. IP-LC-MSMS Enables Identification of Three Tau O-GlcNAcylation Sites as O-GlcNAcase Inhibition Pharmacodynamic Readout in Transgenic Mice Overexpressing Human Tau

4. Systemic immune‐checkpoint blockade with anti‐PD1 antibodies does not alter cerebral amyloid‐β burden in several amyloid transgenic mouse models

6. Tau pathology modulates Pin1 post-translational modifications and may be relevant as biomarker

13. Diazaspirononane Nonsaccharide Inhibitors of O-GlcNAcase (OGA) for the Treatment of Neurodegenerative Disorders

15. Additional file 1: of Tau phosphorylation regulates the interaction between BIN1â s SH3 domain and Tauâ s proline-rich domain

16. Additional file 10: of Tau phosphorylation regulates the interaction between BIN1’s SH3 domain and Tau’s proline-rich domain

17. Additional file 5: of Tau phosphorylation regulates the interaction between BIN1’s SH3 domain and Tau’s proline-rich domain

18. Additional file 8: of Tau phosphorylation regulates the interaction between BIN1’s SH3 domain and Tau’s proline-rich domain

19. Additional file 9: of Tau phosphorylation regulates the interaction between BIN1’s SH3 domain and Tau’s proline-rich domain

20. Additional file 7: of Tau phosphorylation regulates the interaction between BIN1’s SH3 domain and Tau’s proline-rich domain

21. Additional file 4: of Tau phosphorylation regulates the interaction between BIN1’s SH3 domain and Tau’s proline-rich domain

22. of Tau phosphorylation regulates the interaction between BIN1â s SH3 domain and Tauâ s proline-rich domain

23. Additional file 2: of Tau phosphorylation regulates the interaction between BIN1â s SH3 domain and Tauâ s proline-rich domain

24. Additional file 6: of Tau phosphorylation regulates the interaction between BIN1’s SH3 domain and Tau’s proline-rich domain

25. Genetically Engineered iPSC-Derived FTDP-17 MAPT Neurons Display Mutation-Specific Neurodegenerative and Neurodevelopmental Phenotypes

26. Systemic immune-checkpoint blockade with anti-PD1 antibodies does not alter cerebral amyloid-β burden in several amyloid transgenic mouse models

27. Tau phosphorylation regulates the interaction between BIN1’s SH3 domain and Tau’s proline-rich domain

28. P4-032: MOLECULAR CHARACTERISATION OF BRIDGING INTEGRATOR 1 (BIN1) INTERACTION WITH TAU

30. Two-dimensional electrophoresis of tau mutants reveals specific phosphorylation pattern likely linked to early tau conformational changes.

32. Neurogenesis and cell cycle-reactivated neuronal death during pathogenic tau aggregation.

34. Anesthesia-induced hypothermia mediates decreased ARC gene and protein expression through ERK/MAPK inactivation

35. Distinct phosphorylation pattern of Peptidyl prolyl isomerase Pin1 during neurofibrillary degeneration in Alzheimer and Tau transgenic mouse brains.

36. Alzheimer's disease-like tau neuropathology leads to memory deficits and loss of functional synapses in a novel mutated tau transgenic mouse without any motor deficits.

37. p25/Cdk5-mediated retinoblastoma phosphorylation is an early event in neuronal cell death

46. P1-049: Alzheimer-type neurofibrillary lesions and neurofilamentous inclusions are cell-type specific in transgenic mice expressing mutated tau proteins G272V/P301S

47. S3-03-06: Tau phosphorylation, tauopathies, mitosis-related disease

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