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Background. An intronic G4C2 repeat expansion in the C9orf72 gene is the major known cause for Amyotrophic Lateral Sclerosis. There is evidence forthree possible disease mechanisms: a pathological gain of function of nuclear repeat RNA foci, repeat associated noncanonical (RAN) translation into toxi...
ORGANISM(S): Homo sapiens (Human) 
2025-03-07 | PXD034016 | Pride
Pulldown with G4C2 RNA, missing files from submission #586786
ORGANISM(S): Homo sapiens (Human) 
2025-03-07 | PXD034097 | Pride
Background. An intronic G4C2 repeat expansion in the C9orf72 gene is the major known cause for Amyotrophic Lateral Sclerosis. There is evidence forthree possible disease mechanisms: a pathological gain of function of nuclear repeat RNA foci, repeat associated noncanonical (RAN) translation into toxi...
ORGANISM(S): Homo sapiens (Human) 
2025-03-07 | PXD034093 | Pride
Background. An intronic G4C2 repeat expansion in the C9orf72 gene is the major known cause for Amyotrophic Lateral Sclerosis. There is evidence forthree possible disease mechanisms: a pathological gain of function of nuclear repeat RNA foci, repeat associated noncanonical (RAN) translation into toxi...
ORGANISM(S): Homo sapiens (Human) 
2025-03-07 | PXD034092 | Pride
Discovery and characterization of a novel WRN inhibitor
ORGANISM(S): Homo sapiens (Human) 
2024-01-31 | PXD044202 | Pride
BRD9 degraders unleash GBAFCHromatin Remodeling Activity in Synovial Sarcoma
ORGANISM(S): Homo sapiens (Human) 
2026-06-23 | PXD079388 | Pride
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