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3. Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

9. Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

10. Hippocampal aggregation signatures of pathogenic UBQLN2 in amyotrophic lateral sclerosis and frontotemporal dementia.

14. Distribution of ubiquilin 2 and TDP‐43 aggregates throughout the CNS in UBQLN2 p.T487I‐linked amyotrophic lateral sclerosis and frontotemporal dementia

17. Distribution of ubiquilin 2 and TDP‐43 aggregates throughout the CNS in UBQLN2 p.T487I‐linked amyotrophic lateral sclerosis and frontotemporal dementia.

20. Distribution of ubiquilin 2 and TDP-43 aggregates throughout the CNS inUBQLN2p.T487I-linked amyotrophic lateral sclerosis and frontotemporal dementia

29. Hippocampal protein aggregation signatures fully distinguish pathogenic and wildtypeUBQLN2in amyotrophic lateral sclerosis

30. Single-cell image analysis reveals over-expression of organic anion transporting polypeptides (OATPs) in human glioblastoma tissue

35. Novel mutations support a role for Profilin 1 in the pathogenesis of ALS

36. Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

39. Single-cell image analysis reveals a protective role for microglia in glioblastoma

42. Additional file 1 of Identification of a dysfunctional microglial population in human Alzheimer’s disease cortex using novel single-cell histology image analysis

45. Blood-spinal cord barrier leakage is independent of motor neuron pathology in ALS

47. Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

48. The heat shock response plays an important role in TDP-43 clearance:evidence for dysfunction in amyotrophic lateral sclerosis

50. Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis

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