40 results on '"Xiao, Shangxi"'
Search Results
2. Synaptic localization of C9orf72 regulates post-synaptic glutamate receptor 1 levels
3. Unaffected mosaic C9orf72 case: RNA foci, dipeptide proteins, but upregulated C9orf72 expression
4. A C-Terminally Truncated TDP-43 Splice Isoform Exhibits Neuronal Specific Cytoplasmic Aggregation and Contributes to TDP-43 Pathology in ALS
5. Low molecular weight species of TDP-43 generated by abnormal splicing form inclusions in amyotrophic lateral sclerosis and result in motor neuron death
6. MTHFSD and DDX58 are novel RNA-binding proteins abnormally regulated in amyotrophic lateral sclerosis
7. Isoform-specific antibodies reveal distinct subcellular localizations of C9orf72 in amyotrophic lateral sclerosis
8. A two-hybrid screen identifies an unconventional role for the intermediate filament peripherin in regulating the subcellular distribution of the SNAP25-interacting protein, SIP30
9. TDP-43 stabilizes G3BP1 mRNA: relevance to amyotrophic lateral sclerosis/frontotemporal dementia
10. RNA targets of TDP-43 identified by UV-CLIP are deregulated in ALS
11. TDP-43 stabilizes transcripts encoding stress granule protein G3BP1: potential relevance to ALS/FTD
12. Immunohistochemical detection of C9orf72 protein in frontotemporal lobar degeneration and motor neurone disease: patterns of immunostaining and an evaluation of commercial antibodies
13. A novel peripherin isoform generated by alternative translation is required for normal filament network formation
14. Evidence That TDP-43 is Not the Major Ubiquitinated Target Within the Pathological Inclusions of Amyotrophic Lateral Sclerosis
15. Implementation of an antibody characterization process: Application to the major ALS/FTD disease gene C9ORF72
16. Immunohistochemical detection of C9orf72 protein in Frontotemporal Lobar Degeneration and Motor Neurone Disease: patterns of immunostaining and an evaluation of commercial antibodies
17. Unaffected mosaic C9orf72 case
18. C9orf72 isoforms in Amyotrophic Lateral Sclerosis and Frontotemporal Lobar Degeneration
19. Immunohistochemical detection of C9orf72 protein in frontotemporal lobar degeneration and motor neurone disease: patterns of immunostaining and an evaluation of commercial antibodies.
20. Unaffected mosaic case: RNA foci, dipeptide proteins, but upregulated C9orf72 expression.
21. MTHFSD and DDX58 are novel RNA-binding proteins abnormally regulated in amyotrophic lateral sclerosis
22. Isoform‐specific antibodies reveal distinct subcellular localizations of C 9orf72 in amyotrophic lateral sclerosis
23. Gene Targeting of Mouse Tardbp Negatively Affects Masp2 Expression
24. Genome-wide association analyses in Han Chinese identify two new susceptibility loci for amyotrophic lateral sclerosis
25. Erratum: Genome-wide association analyses in Han Chinese identify two new susceptibility loci for amyotrophic lateral sclerosis
26. Genome-wide association analyses in Han Chinese identify two new susceptibility loci for amyotrophic lateral sclerosis
27. Genetic studies of GRN and IFT74 in amyotrophic lateral sclerosis
28. Understanding the mechanistic basis of TDP-43-induced neurotoxicity in amyotrophic lateral sclerosis’
29. An Aggregate-Inducing Peripherin Isoform Generated through Intron Retention Is Upregulated in Amyotrophic Lateral Sclerosis and Associated with Disease Pathology
30. A novel peripherin isoform generated by alternative translation is required for normal filament network formation
31. Lack of TDP-43 abnormalities in mutant SOD1 transgenic mice shows disparity with ALS
32. Neuronal intermediate filaments and ALS: A new look at an old question
33. The γS-Crystallin Gene Is Mutated in Autosomal Recessive Cataract in Mouse
34. A New Locus for Hereditary Gingival Fibromatosis (GINGF2) Maps to 5q13–q22
35. Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP
36. Refinement of the Locus for Autosomal Dominant Hereditary Gingival Fibromatosis (GINGF) to a 3.8-cM Region on 2p21
37. Gene Targeting of Mouse Tardbp Negatively Affects Masp2 Expression.
38. Single-nucleus multiomic atlas of frontal cortex in amyotrophic lateral sclerosis with a deep learning-based decoding of alternative polyadenylation mechanisms.
39. The gamma S-crystallin gene is mutated in autosomal recessive cataract in mouse.
40. A study of the ultrastructure and gene location of hereditary gingival fibromatosis.
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