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Unknown
(21)
Proteomics
(2)
Organisms
Homo sapiens
(2)
Repository
pride
(2)
Tissue
Cell culture
(1)
Cervical cancer cell line
(1)
Cervical region
(1)
Epithelial cell
(1)
HeLa cell
(1)
Technology Type
Mass Spectrometry
(2)
Bottom-up proteomics
(1)
Data-independent acquisition
(1)
Gel-based experiment
(1)
Publication Date
2026
(1)
2020
(1)
Release Date
2022
(5)
2020
(4)
2023
(3)
2015
(2)
2025
(1)
2021
(1)
2019
(1)
2017
(1)
2014
(1)
2013
(1)
2006
(1)
Lab affiliation
CEA-Marcoule, ProGenoMIX platform, DRF-Li2D, 30207 Bagnols-sur-Ceze, France
(1)
Head of the Curie Institute Mass Spectrometry Platform
(1)
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In Vivo Sustained Release of the Retrograde Transport Inhibitor Retro-2.1 Formulated in a Thermosensitive Hydrogel.
Not available
S-EPMC9735573
|
biostudies-literature
Cite
A New Derivative of Retro-2 Displays Antiviral Activity against Respiratory Syncytial Virus.
Not available
S-EPMC10778932
|
biostudies-literature
Cite
Autophagic Degradation Is Involved in Cell Protection against Ricin Toxin.
Not available
S-EPMC10222476
|
biostudies-literature
Cite
Shiga Toxin Uptake and Sequestration in Extracellular Vesicles Is Mediated by Its B-Subunit.
Not available
S-EPMC7404996
|
biostudies-literature
Cite
LPS2336, a New TREK-1 Channel Activator Identified by High Throughput Screening.
Not available
S-EPMC12109561
|
biostudies-literature
Cite
Retrograde Trafficking Inhibitor of Shiga Toxins Reduces Morbidity and Mortality of Mice Infected with Enterohemorrhagic Escherichia coli.
Not available
S-EPMC4505253
|
biostudies-literature
Cite
DABMA: A Derivative of ABMA with Improved Broad-Spectrum Inhibitory Activity of Toxins and Viruses.
Not available
S-EPMC6691562
|
biostudies-literature
Cite
Ouabain and chloroquine trigger senolysis of BRAF-V600E-induced senescent cells by targeting autophagy.
Not available
S-EPMC8564827
|
biostudies-literature
Cite
(S)-N-Methyldihydroquinazolinones are the Active Enantiomers of Retro-2 Derived Compounds against Toxins.
Not available
S-EPMC4027625
|
biostudies-literature
Cite
Genetic identification of the main opportunistic Mucorales by PCR-restriction fragment length polymorphism.
Not available
S-EPMC1393117
|
biostudies-literature
Cite
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