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2. Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data

5. Genome-wide structural variant analysis identifies risk loci for non-Alzheimer’s dementias

6. What Next After MBSR/MBCT? An Open Trial of an 8-Week Follow-on Program Exploring Mindfulness of Feeling Tone (vedanā)

7. Pharmacometabolomics applied to low‐dose interleukin‐2 treatment in amyotrophic lateral sclerosis

10. Establishing mRNA and microRNA interactions driving disease heterogeneity in amyotrophic lateral sclerosis patient survival

11. TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions.

12. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

13. Genome-wide structural variant analysis identifies risk loci for non-Alzheimer’s dementias

17. A Y374X TDP43 truncation leads to an altered metabolic profile in amyotrophic lateral sclerosis fibroblasts driven by pyruvate and TCA cycle intermediate alterations

18. Genome-wide structural variant analysis identifies risk loci for non-Alzheimer’s dementias

19. Chapter Genetics of Familial Amyotrophic Lateral Sclerosis

23. AtypicalTDP‐43 protein expression in anALSpedigree carrying a p.Y374Xtruncation mutation inTARDBP

24. ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function

25. Dipeptide repeat pathology in C9orf72-ALS is associated with redox, mitochondrial and NRF2 pathway imbalance

29. Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

30. Multicentre appraisal of amyotrophic lateral sclerosis biofluid biomarkers shows primacy of blood neurofilament light chain

34. Atypical TDP‐43 protein expression in an ALS pedigree carrying a p.Y374X truncation mutation in TARDBP.

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

42. Loss of nuclear TDP-43 in amyotrophic lateral sclerosis (ALS) causes altered expression of splicing machinery and widespread dysregulation of RNA splicing in motor neurones

47. Value of systematic genetic screening of patients with amyotrophic lateral sclerosis

48. Rare variant burden analysis within enhancers identifies CAV1 as an ALS risk gene

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

50. Amyotrophic lateral sclerosis transcriptomics reveals immunological effects of low-dose interleukin-2

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