As Kunde Intelligenz opa1 western blot Persönlichkeit Systematisch Suri
Genes | Free Full-Text | Reduced OPA1, Mitochondrial Fragmentation and Increased Susceptibility to Apoptosis in Granular Corneal Dystrophy Type 2 Corneal Fibroblasts
OPA1 Polyclonal Antibody (PA5-57874)
OPA1 processing controls mitochondrial fusion and is regulated by mRNA splicing, membrane potential, and Yme1L
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
OPA1 disease-causing mutants have domain-specific effects on mitochondrial ultrastructure and fusion | PNAS
OPA1 antibody (27733-1-AP) | Proteintech
Western blot analysis and quantification of OPA1 protein expression (A)... | Download Scientific Diagram
Anti-OPA1 antibody (ab42364) | Abcam
OPA1 Antibody (1284B) - Azide and BSA Free (NBP2-80894): Novus Biologicals
OPA1‐dependent cristae modulation is essential for cellular adaptation to metabolic demand | The EMBO Journal
Proteolytic Processing of OPA1 Links Mitochondrial Dysfunction to Alterations in Mitochondrial Morphology - ScienceDirect
Defective mitochondrial fusion, altered respiratory function, and distorted cristae structure in skin fibroblasts with heterozygous OPA1 mutations - ScienceDirect
OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions
Western blot analysis and quantitative analysis of OPA1 protein levels... | Download Scientific Diagram
Western blot analysis of OPA1. (A) Western blot analysis of OPA1... | Download Scientific Diagram
Anti-OPA1 Antibody (A16345) | Antibodies.com
Anti-OPA1 Antibody Picoband™ | Bosterbio
Frontiers | OPA1-Exon4b Binds to mtDNA D-Loop for Transcriptional and Metabolic Modulation, Independent of Mitochondrial Fusion
OPA1 Antibody (D-9) | SCBT - Santa Cruz Biotechnology
p32/C1QBP regulates OMA1-dependent proteolytic processing of OPA1 to maintain mitochondrial connectivity related to mitochondrial dysfunction and apoptosis | Scientific Reports
Human OPA1 Antibody MAB9506-100: R&D Systems
ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy - Caporali - 2020 - Annals of Neurology - Wiley Online Library
Biomedicines | Free Full-Text | PBMC of Multiple Sclerosis Patients Show Deregulation of OPA1 Processing Associated with Increased ROS and PHB2 Protein Levels