Search

Your search keyword '"Mccann, Emily"' showing total 140 results

Search Constraints

Start Over You searched for: Author "Mccann, Emily" Remove constraint Author: "Mccann, Emily"
140 results on '"Mccann, Emily"'

Search Results

1. Letter to the editor on: Hornerin deposits in neuronal intranuclear inclusion disease: direct identification of proteins with compositionally biased regions in inclusions by Park et al. (2022)

6. Short tandem repeat expansions in sporadic amyotrophic lateral sclerosis and frontotemporal dementia

7. Clinical testing panels for ALS : global distribution, consistency, and challenges

11. Citizen Schools' Partner-Dependent Expanded Learning Model

12. Clinical testing panels for ALS: global distribution, consistency, and challenges

16. A comprehensive analysis of known and candidate amyotrophic lateral sclerosis genes

17. Genetic and genomic investigations of Amyotrophic lateral sclerosis

19. Splicing factor proline and glutamine rich intron retention, reduced expression and aggregate formation are pathological features of amyotrophic lateral sclerosis

20. Genetic Analysis of Tryptophan Metabolism Genes in Sporadic Amyotrophic Lateral Sclerosis

21. Genetic analysis of GLT8D1 and ARPP21 in Australian familial and sporadic amyotrophic lateral sclerosis

23. SFPQ intron retention, reduced expression and aggregate formation in central nervous system tissue are pathological features of amyotrophic lateral sclerosis

24. Evidence for polygenic and oligogenic basis of Australian sporadic amyotrophic lateral sclerosis

25. Genetic and immunopathological analysis of CHCHD10 in Australian amyotrophic lateral sclerosis and frontotemporal dementia and transgenic TDP-43 mice

27. IBD analysis of Australian amyotrophic lateral sclerosis SOD1-mutation carriers identifies five founder events and links sporadic cases to existing ALS families

28. Monozygotic twins and triplets discordant for amyotrophic lateral sclerosis display differential methylation and gene expression

30. Evidence for polygenic and oligogenic basis of Australian sporadic amyotrophic lateral sclerosis.

31. Genetic and immunopathological analysis of CHCHD10 in Australian amyotrophic lateral sclerosis and frontotemporal dementia and transgenic TDP-43 mice.

32. Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis

33. Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis

34. Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis

36. Non-nuclear Pool of Splicing Factor SFPQ Regulates Axonal Transcripts Required for Normal Motor Development

38. Theme 4 In vivo experimental models.

39. Theme 3 In vitro experimental models.

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

42. CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia

43. Defects in optineurin- and myosin VI-mediated cellular trafficking in amyotrophic lateral sclerosis

44. Novel TBK1 truncating mutation in a familial amyotrophic lateral sclerosis patient of Chinese origin

47. Genetic and Pathological Assessment of hnRNPA1, hnRNPA2/B1, and hnRNPA3 in Familial and Sporadic Amyotrophic Lateral Sclerosis.

48. A novel amyotrophic lateral sclerosis mutation in OPTN induces ER stress and Golgi fragmentation in vitro.

Catalog

Books, media, physical & digital resources