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ProteomicsATG9A is a component of the ESCRT system and governs plasma membrane repair
ATG9 is often described as the sole transmembrane protein among the core autophagy factors. The mammalian ATG9A is notorious for trafficking through numerous cellular compartments including the plasma membrane. The reasons for ATG9As wide intracellular distribution and its role at the PM are not ful...
ORGANISM(S): Homo 
2019-10-30 | MSV000084519 | MassIVE
GenomicsExcess muscle plasma membrane leak disrupts extracellular matrix content and shifts macrophage-mediated muscle repair
Excess muscle plasma membrane leak disrupts extracellular matrix content and shifts macrophage-mediated muscle repair
PRJNA1455691 | ENA
GenomicsExcess muscle plasma membrane leak disrupts extracellular matrix content and shifts macrophage-mediated muscle repair [scRNA-Seq]
Excess muscle plasma membrane leak disrupts extracellular matrix content and shifts macrophage-mediated muscle repair [scRNA-Seq]
PRJNA1455955 | ENA
TranscriptomicsGlobal Genome-Nucleotide Excision Repair is Organised into Domains Promoting Efficient DNA Repair in Chromatin
The rates at which lesions are removed by DNA repair can vary widely throughout the genome with important implications for genomic stability. We measured the distribution of nucleotide excision repair (NER) rates for UV induced lesions throughout the yeast genome. By plotting these repair rates in r...
ORGANISM(S): Saccharomyces cerevisiae 
2016-07-21 | E-MTAB-4641 | biostudies-arrayexpress
ProteomicsLabel-free quantification of Xkr4 interactors
Membrane fractions of XRCC4 KO PLB cells expressing SPOT-Xkr4-FLAG and XRCC4 (WT or R270A) were solubilized by detergent and immunoprecipitated with anti-SPOT nanobody-conjugated beads to precipitate Xkr4 interactors, followed by mass spectrometry.
ORGANISM(S): Homo Sapiens (human) 
2021-01-12 | PXD023536 | JPOST Repository
GenomicsElevated Labile Iron Contributes to Membrane Repair Deficits in FSHD
Elevated Labile Iron Contributes to Membrane Repair Deficits in FSHD
PRJNA1294895 | ENA
UnknownPhenothiazines alter plasma membrane properties and sensitize cancer cells to injury by inhibiting annexin-mediated repair.
Not available
S-EPMC8363839 | biostudies-literature
TranscriptomicsExcess muscle plasma membrane leak disrupts extracellular matrix content and shifts macrophage-mediated muscle repair
Plasma membrane repair is critical for tissue integrity, especially for elongated contractile muscle cells. Genetically-mediated defects in plasma membrane resealing produce persistent leak, leading to a disordered extracellular matrix. Loss of the membrane repair protein dysferlin slows sarcolemmal...
ORGANISM(S): Mus musculus 
2026-06-15 | GSE328583 | GEO
ProteomicsExcess muscle plasma membrane leak disrupts extracellular matrix content and shifts macrophage-mediated muscle repair
Plasma membrane repair is critical for tissue integrity, especially for elongated contractile muscle cells. Genetically-mediated defects in plasma membrane resealing produce persistent leak, leading to a disordered extracellular matrix. Loss of the membrane repair protein dysferlin slows sarcolemma...
ORGANISM(S): Mus musculus (Mouse) 
2026-06-15 | PXD077779 | Pride
Macrophage Muscle injury Dysferlin Duchenne muscular dystrophy Limb girdle muscular dystrophy Annexin Extracellular matrix 
TranscriptomicsExcess muscle plasma membrane leak disrupts extracellular matrix content and shifts macrophage-mediated muscle repair [scRNA-Seq]
Plasma membrane repair is critical for tissue integrity, especially for elongated contractile muscle cells. Genetically-mediated defects in plasma membrane resealing produce persistent leak, leading to a disordered extracellular matrix. Loss of the membrane repair protein dysferlin slows sarcolemmal...
ORGANISM(S): Mus musculus 
2026-06-15 | GSE328601 | GEO
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