As Kunde Intelligenz opa1 western blot Persönlichkeit Systematisch Suri
OPA1 (D6U6N) Rabbit mAb | Cell Signaling Technology
Identification of new OPA1 cleavage site reveals that short isoforms regulate mitochondrial fusion | Molecular Biology of the Cell
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
Anti-OPA1 antibody (ab42364) | Abcam
Identification of new OPA1 cleavage site reveals that short isoforms regulate mitochondrial fusion | Molecular Biology of the Cell
Defective mitochondrial fusion, altered respiratory function, and distorted cristae structure in skin fibroblasts with heterozygous OPA1 mutations - ScienceDirect
OPA1 Antibody - BSA Free (NB110-55290): Novus Biologicals
Human OPA1 Antibody MAB9506-100: R&D Systems
p32/C1QBP regulates OMA1-dependent proteolytic processing of OPA1 to maintain mitochondrial connectivity related to mitochondrial dysfunction and apoptosis | Scientific Reports
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
ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy - Caporali - 2020 - Annals of Neurology - Wiley Online Library