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 Protein Neurodegeneration Spinal cord Gene Central nervous system SOD1 Motor neuron Mutation Frontotemporal dementia Phenotype Amyotrophic lateral sclerosis Messenger RNA Western blot Apoptosis Acid Memory Oxidative stress Magnetic resonance imaging Multiple sclerosis Neuropathic pain DNA Polymerase chain reaction Syndrome Superoxide dismutase Axon Dementia Thiamine pyrophosphate Biomarker
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Publications tagged with this subject: 50

Note: Top 50 publications shown only. Open an item panel to view more info


1. Development of an electrooculogram-based eye-computer interface for communication of individuals with amyotrophic lateral sclerosis

2. Comorbidity of dementia with amyotrophic lateral sclerosis (ALS): insights from a large multicenter Italian cohort

3. Assessing the Combined Toxicity of BMAA and Its Isomers 2,4-DAB and AEG In Vitro Using Human Neuroblastoma Cells

4. Pathogenic mutation in the ALS/FTD gene, CCNF, causes elevated Lys48-linked ubiquitylation and defective autophagy

5. Animal and cellular models of familial dysautonomia

6. Experience matters: neurologists’ perspectives on ALS patients’ well-being

7. Glycoprotein NMB: an Emerging Role in Neurodegenerative Disease

8. CSF concentrations of adipsin and adiponectin in patients with amyotrophic lateral sclerosis

9. Mutant TDP-43 does not impair mitochondrial bioenergetics in vitro and in vivo

10. Evidence for an early innate immune response in the motor cortex of ALS

11. Repetitive nerve stimulation as a diagnostic aid for distinguishing cervical spondylotic amyotrophy from amyotrophic lateral sclerosis

12. Upregulation of Vesicular Glutamate Transporter 2 and STAT3 Activation in the Spinal Cord of Mice Receiving 3,3′-Iminodipropionitrile

13. Present Uses, Future Applications, and Technical Underpinnings of Electrical Impedance Myography

14. A Genome-wide Expression Association Analysis Identifies Genes and Pathways Associated with Amyotrophic Lateral Sclerosis

15. Pesticide exposure assessed through agricultural crop proximity and risk of amyotrophic lateral sclerosis

16. Significance of long chain polyunsaturated fatty acids in human health

17. Immunochemical characterization on pathological oligomers of mutant Cu/Zn-superoxide dismutase in amyotrophic lateral sclerosis

18. Peripheral nerve diffusion tensor imaging as a measure of disease progression in ALS

19. Conjugal amyotrophic lateral sclerosis: a case report from Scotland

20. Bidirectional nucleolar dysfunction in C9orf72 frontotemporal lobar degeneration

21. A data-driven approach links microglia to pathology and prognosis in amyotrophic lateral sclerosis

22. Modelling FUS Mislocalisation in an In Vitro Model of Innervated Human Muscle

23. Genetic mutations in RNA-binding proteins and their roles in ALS

24. Liver X Receptor Genes Variants Modulate ALS Phenotype

25. Spontaneous brain activity in the sensorimotor cortex in amyotrophic lateral sclerosis can be negatively regulated by corticospinal fiber integrity

26. Ultrastructural features of aberrant glial cells isolated from the spinal cord of paralytic rats expressing the amyotrophic lateral sclerosis-linked SOD1G93A mutation

27. Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains

28. Medical history of chemotherapy or immunosuppressive drug treatment and risk of amyotrophic lateral sclerosis (ALS)

29. DNA methylation age-acceleration is associated with disease duration and age at onset in C9orf72 patients

30. Consensus-based feature extraction in rs-fMRI data analysis

31. Maximum inspiratory pressure as a clinically meaningful trial endpoint for neuromuscular diseases: a comprehensive review of the literature

32. The Contribution of Necroptosis in Neurodegenerative Diseases

33. Neurotoxicity of the Cyanotoxin BMAA Through Axonal Degeneration and Intercellular Spreading

34. Assessing Cyanobacterial Harmful Algal Blooms as Risk Factors for Amyotrophic Lateral Sclerosis

35. Downregulated Glia Interplay and Increased miRNA-155 as Promising Markers to Track ALS at an Early Stage

36. Edinburgh Cognitive and Behavioural ALS Screen (ECAS)-Italian version: regression based norms and equivalent scores

37. Maximum Tongue Pressure is Associated with Swallowing Dysfunction in ALS Patients

38. Spinal poly-GA inclusions in a C9orf72 mouse model trigger motor deficits and inflammation without neuron loss

39. ALS/FTLD: experimental models and reality

40. Brugada syndrome in a patient with amyotrophic lateral sclerosis: a case report

41. Quantitative analysis of cryptic splicing associated with TDP-43 depletion

42. Endoplasmic reticulum stress and inflammation in the central nervous system

43. Glycine-alanine dipeptide repeat protein contributes to toxicity in a zebrafish model of C9orf72 associated neurodegeneration

44. Therapeutic Strategies Under Development Targeting Inflammatory Mechanisms in Amyotrophic Lateral Sclerosis

45. Cryptic exon incorporation occurs in Alzheimer’s brain lacking TDP-43 inclusion but exhibiting nuclear clearance of TDP-43

46. Chromosome 21-Encoded microRNAs (mRNAs): Impact on Down’s Syndrome and Trisomy-21 Linked Disease

47. Conserved DNA methylation combined with differential frontal cortex and cerebellar expression distinguishes C9orf72-associated and sporadic ALS, and implicates SERPINA1 in disease

48. Implications of fALS Mutations on Sod1 Function and Oligomerization in Cell Models

49. CRISPR/Cas9-mediated targeted gene correction in amyotrophic lateral sclerosis patient iPSCs

50. The heat shock response in neurons and astroglia and its role in neurodegenerative diseases


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