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

2. Elevated methylation levels, reduced expression levels, and frequent contractions in a clinical cohort of C9orf72 expansion carriers

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

4. Prosaposin is a regulator of progranulin levels and oligomerization

5. Long-read targeted sequencing uncovers clinicopathological associations for C9orf72-linked diseases

6. Shared brain transcriptomic signature in TDP-43 type A FTLD patients with or without GRN mutations

7. Replication of progressive supranuclear palsy genome-wide association study identifies SLCO1A2 and DUSP10 as new susceptibility loci

8. Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study

9. Novel GRN mutation presenting as an aphasic dementia and evolving into corticobasal syndrome

10. TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementia

11. Abnormal expression of homeobox genes and transthyretin in

12. Soluble sortilin is present in excess and positively correlates with progranulin in CSF of aging individuals

13. Cytokine and Leukocyte Profiling Reveal Pro-Inflammatory and Autoimmune Features in Frontotemporal Dementia Patients

14. Network-driven plasma proteomics expose molecular changes in the Alzheimer’s brain

15. Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids

16. Identification of common variants influencing risk of the tauopathy Progressive Supranuclear Palsy

17. Characterization of Monocarboxylate Transporter 1 (MCT1) Binding Affinity for Basigin Gene Products and L1cam

18. Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members

19. Novel clinical associations with specific C9ORF72 transcripts in patients with repeat expansions in C9ORF72

20. Genetic Screening and Functional Characterization of PDGFRB Mutations Associated with Basal Ganglia Calcification of Unknown Etiology

21. TMEM106B p.T185S regulates TMEM106B protein levels: implications for frontotemporal dementia

22. Progranulin regulates neuronal outgrowth independent of Sortilin

23. Similar clinical and neuroimaging features in monozygotic twin pair with mutation in progranulin

24. Hippocampal sclerosis in the elderly: genetic and pathologic findings, some mimicking Alzheimer disease clinically

25. TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers

26. Human Genetics as a Tool to Identify Progranulin Regulators

27. Pathogenicity of exonic indels in fused in sarcoma in amyotrophic lateral sclerosis

28. De Novo Truncating FUS Gene Mutation as a Cause of Sporadic Amyotrophic Lateral Sclerosis

29. Hydrophobic interactions stabilize the basigin-MCT1 complex

30. Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia

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

32. Genome-wide Screen Identifies rs646776 near Sortilin as a Regulator of Progranulin Levels in Human Plasma

33. Erratum to: Network-driven plasma proteomics expose molecular changes in the Alzheimer’s brain

34. Extensive transcriptomic study emphasizes importance of vesicular transport in C9orf72 expansion carriers

35. Replication of progressive supranuclear palsy genome-wide association study identifies SLCO1A2 and DUSP10 as new susceptibility loci

36. Loss of Tmem106b is unable to ameliorate frontotemporal dementia-like phenotypes in an AAV mouse model of C9ORF72-repeat induced toxicity

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