Proteomics

Dataset Information

RTN4IP1 deficiency causes a severe CI assembly defect


ABSTRACT: Here we used complexome profiling to characterize the functional consequences of RTN4IP1 mutations in RTN4IP1 cells.

INSTRUMENT(S):

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Cell Culture

SUBMITTER: Ilka Wittig  

LAB HEAD: Robert Taylor

PROVIDER: PXD064861 | Pride | 2025-08-08

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
Data_Analysis.xlsx Xlsx
Gel.jpg Other
MQ_txt_Output_Files.zip Other
P21_129_Newcastle_Sample1_01.raw Raw
P21_129_Newcastle_Sample1_02.raw Raw
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