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OPA1 Modulates Mitochondrial Ca2+ Uptake Through ER-Mitochondria Coupling.
Autosomal Dominant Optic Atrophy (ADOA), a disease that causes blindness and other neurological disorders, is linked to OPA1 mutations. OPA1, dependent on its GTPase and GED domains, governs inner mitochondrial membrane (IMM)...
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Phosphoinositide 3-kinase beta controls replication factor C assembly and function.
Genomic integrity is preserved by the action of protein complexes that control DNA homeostasis. These include the sliding clamps, trimeric protein rings that are arranged around DNA by clamp loaders. Replication factor C (RFC)...
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