Mitochondrial targeting sequence

Mitochondrion, Mitochondrial disease, Mitochondrial DNA, Human mitochondrial genetics, Mitochondrial myopathy, Mitochondrial DNA (journal), Mitochondrial Eve, Mitochondrial matrix, Mitochondrial membrane transport protein, Mitochondrial ribosome, Human mitochondrial DNA haplogroup, Mitochondrial carrier, Mitochondrial neurogastrointestinal encephalopathy syndrome, Mitochondrial replacement therapy, Inner mitochondrial membrane, Mitochondrial dynamics protein MID49, Mitochondrial DNA depletion syndrome, Mitochondrial calcium uniporter, Mitochondrial fusion, Invertebrate mitochondrial code, Mitochondrial tRNA pseudouridine27/28 synthase, Mitochondrial complex II deficiency, Vertebrate mitochondrial code, Circulating mitochondrial DNA, Anti-mitochondrial antibody, Mitochondrial intermediate peptidase, Mitochondrial permeability transition pore, Nuclear mitochondrial DNA segment, Pterobranchia mitochondrial code, Mitochondrial fusion promoter M1, Mitochondrial ribosomal protein L13, MRC Mitochondrial Biology Unit, Ascidian mitochondrial code, Mitochondrial processing peptidase, Mitochondrial outer membrane permeabilization, Alternative flatworm mitochondrial code, Echinoderm and flatworm mitochondrial code, Yeast mitochondrial code, MELAS syndrome, Mitochondrial fission, Mitochondrial biogenesis

Mitochondrial encephalomyopathy, Mitochondrial theory of ageing, Mitochondrial fission factor, Mitochondrial apoptosis-induced channel, Mitochondrial ROS, MT-TV (mitochondrial), Paternal mtDNA transmission, Mitochondrial antiviral-signaling protein, Mitochondrial trifunctional protein, Mitochondrial folate transporter, Mitochondrial ferritin, Translocase of the outer membrane, TIM/TOM complex, Mitochondrial toxicity, Mitochondrial ribosomal protein L23, Mitochondrial ribosomal protein L41, Mitochondrial ribosomal protein L12, Mitochondrial trifunctional protein deficiency, Mitochondrial dicarboxylate carrier, TFAM, Mitochondrial ribosomal protein L10, Mitochondrial ribosomal protein L37, Mitochondrial ribosomal protein L3, Respiratory complex I, Human mitochondrial molecular clock, Mitochondrial ribosomal protein L30, Mitochondrial ribosomal protein L22, Cephalodiscidae mitochondrial code, Mitochondrial ribosomal protein L33, Tricarboxylate transport protein, mitochondrial, Mitochondrial ribosomal protein L1, Mitochondrial ribosomal protein L42, Mitochondrial pyruvate carrier 1, Trematode mitochondrial code, Mitochondrial pyruvate carrier, Mitochondrial ribosomal protein L18, Mitochondrial ribosomal protein L4, Mitochondrial ribosomal protein L11, Mitochondrial ribosomal protein L17, Phosphate carrier protein, mitochondrial, Mitochondrial ribosomal protein L32, Mitochondrial ribosomal protein L15, Mitochondrial uncoupling protein 4, Mitochondrial ribosomal protein L39, Mitochondrial ribosomal protein L19, Mitochondrial ribosomal protein L24, Mitochondrial ribosomal protein L20, Mitochondrial optic neuropathies, Mitochondrial ribosomal protein L40, Mitochondrial ribosomal protein L28

Mitochondrion, Mitochondrial disease, Mitochondrial DNA, Human mitochondrial genetics, Mitochondrial myopathy, Mitochondrial DNA (journal), Mitochondrial Eve, Mitochondrial matrix, Mitochondrial membrane transport protein, Mitochondrial ribosome, Human mitochondrial DNA haplogroup, Mitochondrial carrier, Mitochondrial neurogastrointestinal encephalopathy syndrome, Mitochondrial replacement therapy, Inner mitochondrial membrane, Mitochondrial dynamics protein MID49, Mitochondrial DNA depletion syndrome, Mitochondrial calcium uniporter, Mitochondrial fusion, Invertebrate mitochondrial code, Mitochondrial tRNA pseudouridine27/28 synthase, Mitochondrial complex II deficiency, Vertebrate mitochondrial code, Circulating mitochondrial DNA, Anti-mitochondrial antibody, Mitochondrial intermediate peptidase, Mitochondrial permeability transition pore, Nuclear mitochondrial DNA segment, Pterobranchia mitochondrial code, Mitochondrial fusion promoter M1, Mitochondrial ribosomal protein L13, MRC Mitochondrial Biology Unit, Ascidian mitochondrial code, Mitochondrial processing peptidase, Mitochondrial outer membrane permeabilization, Alternative flatworm mitochondrial code, Echinoderm and flatworm mitochondrial code, Yeast mitochondrial code, MELAS syndrome, Mitochondrial fission, Mitochondrial biogenesis, Mitochondrial encephalomyopathy, Mitochondrial theory of ageing, Mitochondrial fission factor, Mitochondrial apoptosis-induced channel, Mitochondrial ROS, MT-TV (mitochondrial), Paternal mtDNA transmission, Mitochondrial antiviral-signaling protein, Mitochondrial trifunctional protein, Mitochondrial folate transporter, Mitochondrial ferritin, Translocase of the outer membrane, TIM/TOM complex, Mitochondrial toxicity, Mitochondrial ribosomal protein L23, Mitochondrial ribosomal protein L41, Mitochondrial ribosomal protein L12, Mitochondrial trifunctional protein deficiency, Mitochondrial dicarboxylate carrier, TFAM, Mitochondrial ribosomal protein L10, Mitochondrial ribosomal protein L37, Mitochondrial ribosomal protein L3, Respiratory complex I, Human mitochondrial molecular clock, Mitochondrial ribosomal protein L30, Mitochondrial ribosomal protein L22, Cephalodiscidae mitochondrial code, Mitochondrial ribosomal protein L33, Tricarboxylate transport protein, mitochondrial, Mitochondrial ribosomal protein L1, Mitochondrial ribosomal protein L42, Mitochondrial pyruvate carrier 1, Trematode mitochondrial code, Mitochondrial pyruvate carrier, Mitochondrial ribosomal protein L18, Mitochondrial ribosomal protein L4, Mitochondrial ribosomal protein L11, Mitochondrial ribosomal protein L17, Phosphate carrier protein, mitochondrial, Mitochondrial ribosomal protein L32, Mitochondrial ribosomal protein L15, Mitochondrial uncoupling protein 4, Mitochondrial ribosomal protein L39, Mitochondrial ribosomal protein L19, Mitochondrial ribosomal protein L24, Mitochondrial ribosomal protein L20, Mitochondrial optic neuropathies, Mitochondrial ribosomal protein L40, Mitochondrial ribosomal protein L28, Thymidine kinase 2, mitochondrial, Brain mitochondrial carrier protein 1, Thraustochytrium mitochondrial code, Mitochondrial pyruvate carrier 2, Mitochondrial amidoxime reducing component 1, Mitochondrial 2-oxodicarboxylate carrier, Haplogroup A (mtDNA), Carbonic anhydrase 5B, mitochondrial, Cytochrome c oxidase subunit I, Crista, Mitochondrial glycine transporter, Mitochondrial thiamine pyrophosphate carrier, Mitochondrial unfolded protein response, Mitochondrial translational release factor 1, Serine protease HTRA2, mitochondrial, Mitochondrial shuttle, DAP3, Carbonic anhydrase 5A, mitochondrial, Calcium-binding mitochondrial carrier protein Aralar1, Haplogroup V (mtDNA), Scenedesmus obliquus mitochondrial code, WARS2, Chlorophycean mitochondrial code, Cytonuclear discordance, Calcium-binding mitochondrial carrier protein SCaMC-1, ATP5F1A, Mitochondrial Eve (novelette), Sengers syndrome, Mitochondrial 2-oxoglutarate/malate carrier protein, Fatty acid synthesis, 21S rRNA (uridine2791-2'-O)-methyltransferase, Electron transport chain, Mitochondrial membrane protein-associated neurodegeneration, Mpv17 mitochondrial inner membrane protein like 2, ATPIF1, ATP synthase, Translocator protein, Intermediate cleaving peptidase 55, Carnitine palmitoyltransferase I, Oxidative phosphorylation, Cytochrome b, Mitochondria associated membranes, Target peptide, Cytochrome c oxidase, HADHA, Uncoupler, Coenzyme Q – cytochrome c reductase, Succinate dehydrogenase, ADCK3, Nonsyndromic deafness, The mold, protozoan, and coelenterate mitochondrial code and the mycoplasma/spiroplasma code, Y-chromosomal Adam, Alpha-aminoadipic semialdehyde synthase, Apoptosis, Hormesis, Aubrey de Grey, Sodium-calcium exchanger, Parasite Eve (video game), Beta-ketothiolase deficiency, Noah23