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p32/C1QBP regulates OMA1-dependent proteolytic processing of OPA1 to maintain mitochondrial connectivity related to mitochondrial dysfunction and apoptosis | Scientific Reports
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Identification of new OPA1 cleavage site reveals that short isoforms regulate mitochondrial fusion | Molecular Biology of the Cell
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Western blot analysis and quantitative analysis of OPA1 protein levels... | Download Scientific Diagram
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OPA1‐dependent cristae modulation is essential for cellular adaptation to metabolic demand | The EMBO Journal
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Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophy | Molecular Neurodegeneration | Full Text
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HIGD‑1B inhibits hypoxia‑induced mitochondrial fragmentation by regulating OPA1 cleavage in cardiomyocytes
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Frontiers | OPA1-Exon4b Binds to mtDNA D-Loop for Transcriptional and Metabolic Modulation, Independent of Mitochondrial Fusion
![OPA1 Mouse anti-Human, Mouse, Porcine, Rat, Clone: 1B2D8, Proteintech 150 μL; Unconjugated Products | Fisher Scientific OPA1 Mouse anti-Human, Mouse, Porcine, Rat, Clone: 1B2D8, Proteintech 150 μL; Unconjugated Products | Fisher Scientific](https://assets.fishersci.com/TFS-Assets/LSG/antibodies/66583-1-IG-OPA1-WB-20190227152956.jpg-650.jpg)
OPA1 Mouse anti-Human, Mouse, Porcine, Rat, Clone: 1B2D8, Proteintech 150 μL; Unconjugated Products | Fisher Scientific
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Genes | Free Full-Text | Reduced OPA1, Mitochondrial Fragmentation and Increased Susceptibility to Apoptosis in Granular Corneal Dystrophy Type 2 Corneal Fibroblasts
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Identification of new OPA1 cleavage site reveals that short isoforms regulate mitochondrial fusion | Molecular Biology of the Cell
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OPA1 disease-causing mutants have domain-specific effects on mitochondrial ultrastructure and fusion | PNAS
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OPA1 disease-causing mutants have domain-specific effects on mitochondrial ultrastructure and fusion | PNAS
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