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1. Generation and characterization of monoclonal antibodies against pathologically phosphorylated TDP-43.

2. TDP-43 and other hnRNPs regulate cryptic exon inclusion of a key ALS/FTD risk gene, UNC13A.

3. Neuronal intermediate filament inclusion disease may be incorrectly classified as a subtype of FTLD-FUS

4. ABI3 and PLCG2 missense variants as risk factors for neurodegenerative diseases in Caucasians and African Americans

5. Depletion of AADC activity in caudate nucleus and putamen of Parkinson's disease patients; implications for ongoing AAV2-AADC gene therapy trial.

6. p62 Pathology Model in the Rat Substantia Nigra with Filamentous Inclusions and Progressive Neurodegeneration.

7. Alterations of PINK1-PRKN signaling in mice during normal aging

8. Exonic Re-Sequencing of the Chromosome 2q24.3 Parkinson's Disease Locus.

9. Apoptosis in oligodendrocytes is associated with axonal degeneration in P301L tau mice

10. Pin1 colocalization with phosphorylated tau in Alzheimer's disease and other tauopathies

11. Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias.

12. Divergent phenotypes in mutant TDP-43 transgenic mice highlight potential confounds in TDP-43 transgenic modeling.

13. Linking protective GAB2 variants, increased cortical GAB2 expression and decreased Alzheimer's disease pathology.

14. Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants.

15. Three repeat isoforms of tau inhibit assembly of four repeat tau filaments.

16. Concordant association of insulin degrading enzyme gene (IDE) variants with IDE mRNA, Abeta, and Alzheimer's disease.

17. Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis.

18. Comparison of Clinical, Genetic, and Pathologic Features of Limbic and Diffuse Transactive Response DNA-Binding Protein 43 Pathology in Alzheimer’s Disease Neuropathologic Spectrum

20. Accumulation of pTau231 at the Postsynaptic Density in Early Alzheimer’s Disease

22. <scp>APOE2</scp> Exacerbates <scp>TDP</scp> ‐43 Related Toxicity in the Absence of Alzheimer Pathology

23. A novel clinicopathologic entity causing rapidly progressive cerebellar ataxia?

24. Elevated granulocyte colony stimulating factor ( <scp>CSF</scp> ) causes cerebellar deficits and anxiety in a model of <scp>CSF</scp> ‐1 receptor related leukodystrophy

25. Two FTD-ALS genes converge on the endosomal pathway to induce TDP-43 pathology and degeneration

26. Differential Vulnerability of Hippocampal Subfields in Primary Age-Related Tauopathy and Chronic Traumatic Encephalopathy

27. Optimum Differentiation of Frontotemporal Lobar Degeneration from Alzheimer Disease Achieved with Cross‐Sectional Tau <scp>Positron Emission Tomography</scp>

28. Tau-PET and multimodal imaging in clinically atypical multiple system atrophy masquerading as progressive supranuclear palsy

29. Lysosomal polygenic risk is associated with the severity of neuropathology in Lewy body disease

30. β-Amyloid Load on PET Along the Continuum of Dementia With Lewy Bodies

32. Creating the Pick’s disease International Consortium: Association study of MAPT H2 haplotype with risk of Pick’s disease

33. Neuropathology and emerging biomarkers in corticobasal syndrome

34. APOE4 exacerbates α-synuclein seeding activity and contributes to neurotoxicity in Alzheimer’s disease with Lewy body pathology

35. New insights into the genetic etiology of Alzheimer's disease and related dementias

37. Clinical and pathological characteristics of later onset multiple system atrophy

38. TDP-43 represses cryptic exon inclusion in the FTD–ALS gene UNC13A

39. Diagnosis of Alzheimer’s disease and tauopathies on whole slide histopathology images using a weakly supervised deep learning algorithm

40. Brain bank questionnaire helps in differential diagnosis of parkinsonian disorders: an autopsy study of 150 patients

41. Genome-wide structural variant analysis identifies risk loci for non-Alzheimer's dementias

43. The temporal onset of the core features in dementia with Lewy bodies

44. Genome-wide association study and functional validation implicates JADE1 in tauopathy

45. Autopsy Validation of Progressive Supranuclear Palsy‐Predominant Speech/Language Disorder Criteria

46. Global neuropathologic severity of Alzheimer’s disease and locus coeruleus vulnerability influences plasma phosphorylated tau levels

47. Nuclear import receptors are recruited by FG-nucleoporins to rescue hallmarks of TDP-43 proteinopathy

48. TDP‐43 pathology effect on volume and flortaucipir uptake in Alzheimer's disease

49. Single Cell Approaches Reveal Perturbed Brain Vascular Molecules in Alzheimer’s Disease

50. TAR DNA‐binding protein 43 (TDP‐43) contributes to the mismatch between medial temporal volumes and flortaucipir uptake in elderly patients with Alzheimer’s disease neuropathologic changes

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