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2. Teaching the physiology of the human body in non-formal spaces: pilot experience of a Service-Learning methodology and the interaction between students of different educational levels

4. SERVICE-LEARNING EDUCATIONAL APPROACH FOR UNDERGRADUATE STUDENTS: DEVELOPMENT OF AN OUTREACH WORKSHOP FOR HIGH SCHOOL STUDENTS

9. Ex Vivo Maturation of 3D-Printed, Chondrocyte-Laden, Polycaprolactone-Based Scaffolds Prior to Transplantation Improves Engineered Cartilage Substitute Properties and Integration

11. Delay of EGF-Stimulated EGFR Degradation in Myotonic Dystrophy Type 1 (DM1)

12. Pathogenic LRRK2 regulates centrosome cohesion via Rab10/RILPL1-mediated CDK5RAP2 displacement

13. Striatal synaptic bioenergetic and autophagic decline in premotor experimental parkinsonism

17. The parkinsonian LRRK2 R1441G mutation shows macroautophagy-mitophagy dysregulation concomitant with endoplasmic reticulum stress

18. Patient-specific iPSC-derived cellular models of LGMDR1

20. Metabolic alterations in plasma from patients with familial and idiopathic Parkinson’s disease

21. Toxicity of Necrostatin-1 in Parkinson’s Disease Models

26. RAB8, RAB10 and RILPL1 contribute to both LRRK2 kinase–mediated centrosomal cohesion and ciliogenesis deficits

27. Impaired Mitophagy and Protein Acetylation Levels in Fibroblasts from Parkinson’s Disease Patients

29. Acetylome in Human Fibroblasts From Parkinson's Disease Patients

30. Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation

31. PARKINSON’S DISEASE-ASSOCIATED MUTATIONS IN LRRK2 CAUSE CENTROSOMAL DEFECTS VIA RAB8A PHOSPHORYLATION

33. Identification and Characterization of the Dermal Panniculus Carnosus Muscle Stem Cells

36. G2019S LRRK2 mutant fibroblasts from Parkinson’s disease patients show increased sensitivity to neurotoxin 1-methyl-4-phenylpyridinium dependent of autophagy

37. G.P.199

41. Murine Muscle Engineered from Dermal Precursors: An In Vitro Model for Skeletal Muscle Generation, Degeneration, and Fatty Infiltration

42. In Vitro Correction of a Pseudoexon-Generating Deep Intronic Mutation in LGMD2A by Antisense Oligonucleotides and Modified Small Nuclear RNAs

43. Expanded CTG repeats trigger miRNA alterations in Drosophila that are conserved in myotonic dystrophy type 1 patients

44. The MAPK1/3 pathway is essential for the deregulation of autophagy observed in G2019S LRRK2 mutant fibroblasts

45. The LRRK2 G2019S mutant exacerbates basal autophagy through activation of the MEK/ERK pathway

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