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Unknown
(3)
Proteomics
(1)
Organisms
Escherichia phage MS2
(1)
Escherichia phage phiX174
(1)
Heteractis magnifica
(1)
Leptospira interrogans serovar Icterohaemorrhagiae
(1)
Crotalus durissus ruruima
(1)
Conus frigidus
(1)
Aspergillus terreus NIH2624
(1)
Betula pendula
(1)
Alnus glutinosa
(1)
Argopecten irradians
(1)
Legionella pneumophila subsp. pneumophila
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Bacillota bacterium
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Bacteroidota
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Enterobacteriaceae bacterium S16791
(1)
Streptococcus suis
(1)
uncultured soil bacterium S0164
(1)
Pseudomonas syringae pv. actinidiae str. Shaanxi_M228
(1)
Yersinia pestis YN2179
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Streptococcus parasanguinis
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Veillonella parvula
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Rhodotorula mucilaginosa
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Palleniella intestinalis
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Cupriavidus pauculus
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Plasmodium falciparum SenT032.09
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Thermus brevis
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Lanistes nyassanus
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Pila pesmei
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Klebsiella ornithinolytica
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Asobara japonica
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Candidatus Methanoperedens
(1)
Repository
pride
(1)
Tissue
Skeletal muscle myoblast
(1)
Cell culture
(1)
Technology Type
Data-dependent acquisition
(1)
Bottom-up proteomics
(1)
Mass Spectrometry
(1)
Publication Date
2026
(1)
Release Date
2025
(1)
2023
(1)
2019
(1)
Lab affiliation
Physiology, University of Galway, Ireland
(1)
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Proteomic analysis of C2C12 myoblasts treated with Tunicamycin
Label free proteomic analysis of C2C12 myoblasts treated with either Tunicamycin (0.2ug/ml) alone or with PERK AMG44 (2uM) for 8h and followed by 16h recovery.
ORGANISM(S):
Mus musculus (Mouse)
2026-04-27
|
PXD059735
|
Pride
Tunicamycin
Er stress
Skeletal muscle
Perk amg44
Cite
Molecular modeling provides a structural basis for PERK inhibitor selectivity towards RIPK1.
Not available
S-EPMC9092956
|
biostudies-literature
Cite
ER stress sensor PERK promotes T cell pathogenicity in GVHD by regulating ER-associated degradation.
Not available
S-EPMC12646671
|
biostudies-literature
Cite
Activation of the integrated stress response by inhibitors of its kinases.
Not available
S-EPMC10491595
|
biostudies-literature
Cite
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