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9. Low T-cell reactivity to TDP-43 peptides in ALS

16. sj-docx-1-gae-10.1177_25168657231172159 – Supplemental material for DNA Methylation Analysis in Monozygotic Twins Discordant for ALS in Blood Cells

17. SQSTM1/p62 variants in 486 patients with familial ALS from Germany and Sweden

20. Hot-spot KIF5A mutations cause familial ALS

21. Peripheral monocytes are functionally altered and invade the CNS in ALS patients

22. Spreading of alpha-synuclein between different cell types

26. Extracellular vesicle sorting of α-Synuclein is regulated by sumoylation

29. NEK1 mutations in familial amyotrophic lateral sclerosis

32. Mutual exacerbation of peroxisome proliferator-activated receptor γ coactivator 1α deregulation and α-synuclein oligomerization

33. A serum microRNA sequence reveals fragile X protein pathology in amyotrophic lateral sclerosis

34. Increased NF-L levels in the TDP-43G298S ALS mouse model resemble NF-L levels in ALS patients.

37. Protein Binding Partners of Dysregulated miRNAs in Parkinson’s Disease Serum

38. A serum microRNA sequence reveals fragile X protein pathology in amyotrophic lateral sclerosis

41. Hemizygous deletion of Tbk1 worsens neuromuscular junction pathology in TDP-43 transgenic mice

43. SQSTM1/p62 variants in 486 patients with familial ALS from Germany and Sweden

48. Enhanced Hyaluronan Signaling and Autophagy Dysfunction by VPS35 D620N

49. SQSTM1/p62 variants in 486 patients with familial ALS from Germany and Sweden

50. Haploinsufficiency of TANK-binding kinase 1 prepones age-associated neuroinflammatory changes without causing motor neuron degeneration in aged mice

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