Pages that link to "Q44850501"

The following pages link to C-terminal FUS/TLS mutations in familial and sporadic ALS in Germany (Q44850501):

Displaying 27 items.

• ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import (Q24630100) (← links)
• FUS transgenic rats develop the phenotypes of amyotrophic lateral sclerosis and frontotemporal lobar degeneration (Q27342067) (← links)
• The complex molecular biology of amyotrophic lateral sclerosis (ALS) (Q28263899) (← links)
• CRISPR/Cas9-mediated targeted gene correction in amyotrophic lateral sclerosis patient iPSCs. (Q33628110) (← links)
• Mutant human FUS Is ubiquitously mislocalized and generates persistent stress granules in primary cultured transgenic zebrafish cells (Q33727167) (← links)
• De novo truncating FUS gene mutation as a cause of sporadic amyotrophic lateral sclerosis (Q34070072) (← links)
• FUS-immunoreactive inclusions are a common feature in sporadic and non-SOD1 familial amyotrophic lateral sclerosis (Q34118590) (← links)
• The tip of the iceberg: RNA-binding proteins with prion-like domains in neurodegenerative disease. (Q34263380) (← links)
• A de novo missense mutation of the FUS gene in a "true" sporadic ALS case (Q34274164) (← links)
• Residue-by-Residue View of In Vitro FUS Granules that Bind the C-Terminal Domain of RNA Polymerase II (Q36172715) (← links)
• The molecular basis of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum (Q36485513) (← links)
• Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China (Q37239868) (← links)
• FTD and ALS: A Tale of Two Diseases (Q37241079) (← links)
• Clinical neurogenetics: amyotrophic lateral sclerosis (Q37274526) (← links)
• Tar DNA-binding protein-43 (TDP-43) regulates axon growth in vitro and in vivo (Q37706265) (← links)
• RNA processing pathways in amyotrophic lateral sclerosis (Q37720436) (← links)
• TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration (Q37733168) (← links)
• Research Advances in Amyotrophic Lateral Sclerosis, 2009 to 2010 (Q37809803) (← links)
• RNA-binding proteins with prion-like domains in ALS and FTLD-U (Q37918720) (← links)
• Clinical and genetic heterogeneity of amyotrophic lateral sclerosis (Q38078984) (← links)
• TARDBP and FUS mutations associated with amyotrophic lateral sclerosis: summary and update (Q38096349) (← links)
• The role of FUS gene variants in neurodegenerative diseases (Q38212812) (← links)
• Evidence for an oligogenic basis of amyotrophic lateral sclerosis (Q42650955) (← links)
• Sustained expression of TDP-43 and FUS in motor neurons in rodent's lifetime. (Q42736731) (← links)
• Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis. (Q48021519) (← links)
• FUS/TLS-immunoreactive neuronal and glial cell inclusions increase with disease duration in familial amyotrophic lateral sclerosis with an R521C FUS/TLS mutation (Q48414675) (← links)
• The prospects of CRISPR-based genome engineering in the treatment of neurodegenerative disorders (Q49335959) (← links)