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1. Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia

2. Transcriptomic and proteomic profiling of bi-partite and tri-partite murine iPSC-derived neurospheroids under steady-state and inflammatory condition

5. C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts

6. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

8. Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.

9. Overlapping Neuroimmune Mechanisms and Therapeutic Targets in Neurodegenerative Disorders

10. Overlapping Neuroimmune Mechanisms and Therapeutic Targets in Neurodegenerative Disorders

12. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

13. C9orf72, AAO and ancestry help discriminating behavioural from language variants in FTLD cohorts

14. Overexpression of human wild-type FUS causes progressive motor neuron degeneration in an age- and dose-dependent fashion.

15. Emerging Trends in the Field of Inflammation and Proteinopathy in ALS/FTD Spectrum Disorder

19. Overlapping Neuroimmune Mechanisms and Therapeutic Targets in Neurodegenerative Disorders.

27. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

28. Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6

29. TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis

31. Interactome screening ofC9orf72dipeptide repeats reveals VCP sequestration and functional impairment by polyGA

34. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

41. Common and rare variant association analyses in Amyotrophic Lateral Sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

46. A feedback loop between dipeptide-repeat protein, TDP-43 and karyopherin-α mediates C9orf72-related neurodegeneration

47. The X11 proteins, A[beta] production and Alzheimer's disease

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