140 results on '"Mccann, Emily"'
Search Results
2. Wild fish responses to wastewater treatment plant upgrades in the Grand River, Ontario
3. Pareidolias are a function of visuoperceptual impairment
4. Increased Resolution of Structural MRI at 3T Improves Estimation of Regional Cortical Degeneration in Individual Dementia Patients Using Surface Thickness Maps
5. Identity by descent analysis identifies founder events and links SOD1 familial and sporadic ALS cases
6. Short tandem repeat expansions in sporadic amyotrophic lateral sclerosis and frontotemporal dementia
7. Clinical testing panels for ALS : global distribution, consistency, and challenges
8. Characterising the Genetic Landscape of Amyotrophic Lateral Sclerosis: A Catalogue and Assessment of Over 1,000 Published Genetic Variants.
9. Gothic Futures
10. Neurophysiology of the cortical attentional network
11. Citizen Schools' Partner-Dependent Expanded Learning Model
12. Clinical testing panels for ALS: global distribution, consistency, and challenges
13. Genetic determinants of antimicrobial resistance in three multi-drug resistant strains of Cutibacterium acnes isolated from patients with acne: a predictive in silico study
14. Gothic Futures: Edith Sitwell and Women’s Labor in Interwar British Modernism
15. Defects in optineurin- and myosin VI-mediated cellular trafficking in amyotrophic lateral sclerosis
16. A comprehensive analysis of known and candidate amyotrophic lateral sclerosis genes
17. Genetic and genomic investigations of Amyotrophic lateral sclerosis
18. Defects in optineurin- and myosin VI-mediated cellular trafficking in 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
22. Mutation analysis of MATR3 in Australian familial 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
26. TRIBES: A user-friendly pipeline for relatedness detection and disease gene discovery
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
29. Lipase-Catalyzed Regioselective Ester Hydrolysis as a Key Step in an Alternative Synthesis of a Buprenorphine Pro-Drug
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
35. Postnatal Development of Spasticity Following Transgene Insertion in the Mouse βIV Spectrin Gene (SPTBN4)
36. Non-nuclear Pool of Splicing Factor SFPQ Regulates Axonal Transcripts Required for Normal Motor Development
37. Reduction of Intersex in a Wild Fish Population in Response to Major Municipal Wastewater Treatment Plant Upgrades
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
41. A novel amyotrophic lateral sclerosis mutation in OPTN induces ER stress and Golgi fragmentation in vitro
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
45. Young Ireland, Yeats, and Irish Citizenship
46. 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.
49. Towards a better understanding of the lived experience of vulvodynia and its impact upon gender identity
50. Disease gene discovery in amyotrophic lateral sclerosis using innovative next generation sequencing and genetic linkage strategies
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