Search

Your search keyword '"Drepper, C."' showing total 45 results

Search Constraints

Start Over You searched for: Author "Drepper, C." Remove constraint Author: "Drepper, C."
45 results on '"Drepper, C."'

Search Results

1. Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis

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

7. NEK1 variants confer susceptibility to amyotrophic lateral sclerosis

8. Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis

9. Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis

10. Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

11. Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72

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

13. Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis

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

15. A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

17. Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72

18. Dysregulated IGFBP5 expression causes axon degeneration and motoneuron loss in diabetic neuropathy

22. Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis

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

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

25. Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72

26. Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72.

28. Loss-of-Function Models of the Metabotropic Glutamate Receptor Genes Grm8a and Grm8b Display Distinct Behavioral Phenotypes in Zebrafish Larvae ( Danio rerio ).

29. Loss of full-length hnRNP R isoform impairs DNA damage response in motoneurons by inhibiting Yb1 recruitment to chromatin.

30. Increased locomotor activity via regulation of GABAergic signalling in foxp2 mutant zebrafish-implications for neurodevelopmental disorders.

31. Anxiety risk SNPs on chromosome 2 modulate arousal in children in a fear generalization paradigm.

32. Distribution of transcripts of the GFOD gene family members gfod1 and gfod2 in the zebrafish central nervous system.

33. Transcript Analysis of Zebrafish GLUT3 Genes, slc2a3a and slc2a3b , Define Overlapping as Well as Distinct Expression Domains in the Zebrafish ( Danio rerio ) Central Nervous System.

34. Transcranial sonography in psychiatry as a potential tool in diagnosis and research.

35. C9ORF72 interaction with cofilin modulates actin dynamics in motor neurons.

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

37. Developmental exposure to acetaminophen does not induce hyperactivity in zebrafish larvae.

38. Dysregulated IGFBP5 expression causes axon degeneration and motoneuron loss in diabetic neuropathy.

39. Deep proteomic evaluation of primary and cell line motoneuron disease models delineates major differences in neuronal characteristics.

41. C-terminal FUS/TLS mutations in familial and sporadic ALS in Germany.

42. PTEN depletion rescues axonal growth defect and improves survival in SMN-deficient motor neurons.

43. Isolation and enrichment of embryonic mouse motoneurons from the lumbar spinal cord of individual mouse embryos.

44. A functional screen implicates microRNA-138-dependent regulation of the depalmitoylation enzyme APT1 in dendritic spine morphogenesis.

45. Mutation of Vps54 causes motor neuron disease and defective spermiogenesis in the wobbler mouse.

Catalog

Books, media, physical & digital resources