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Mitochondrial genome

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Mitochondrial DNA

Information related to "Mitochondrial genome" :

Mitochondrial DNA

Mitochondrial disease

Human mitochondrial genetics

Mitochondrial myopathy

Mitochondrial Eve

Mitochondrial DNA (journal)

Mitochondrial matrix

Mitochondrial ribosome

Mitochondrial membrane transport protein

Mitochondrial carrier

Human mitochondrial DNA haplogroup

Mitochondrial neurogastrointestinal encephalopathy syndrome

Mitochondrial replacement therapy

Mitochondrial dynamics protein MID49

Mitochondrial DNA depletion syndrome

Mitochondrial calcium uniporter

Inner mitochondrial membrane

Invertebrate mitochondrial code

Vertebrate mitochondrial code

Mitochondrial tRNA pseudouridine27/28 synthase

Anti-mitochondrial antibody

Mitochondrial fusion

Mitochondrial complex II deficiency

Mitochondrial intermediate peptidase

Pterobranchia mitochondrial code

Circulating mitochondrial DNA

Nuclear mitochondrial DNA segment

Mitochondrial permeability transition pore

Mitochondrial processing peptidase

Ascidian mitochondrial code

Alternative flatworm mitochondrial code

Mitochondrial ribosomal protein L13

Yeast mitochondrial code

MRC Mitochondrial Biology Unit

Echinoderm and flatworm mitochondrial code

Mitochondrial outer membrane permeabilization

Mitochondrial fission

Mitochondrial biogenesis

Mitochondrial ROS

Mitochondrial fission factor

Mitochondrial theory of ageing

Mitochondrial apoptosis-induced channel

Mitochondrial encephalomyopathy

MT-TV (mitochondrial)

Paternal mtDNA transmission

Mitochondrial antiviral-signaling protein

Mitochondrial trifunctional protein

TIM/TOM complex

Mitochondrial ferritin

Mitochondrial folate transporter

Translocase of the outer membrane

Mitochondrial toxicity

Mitochondrial ribosomal protein L33

Mitochondrial ribosomal protein L41

Mitochondrial ribosomal protein L12

Mitochondrial trifunctional protein deficiency

Mitochondrial dicarboxylate carrier

Mitochondrial ribosomal protein L10

Mitochondrial ribosomal protein L23

Mitochondrial ribosomal protein L37

Phosphate carrier protein, mitochondrial

Mitochondrial ribosomal protein L22

Human mitochondrial molecular clock

Mitochondrial pyruvate carrier 1

Cephalodiscidae mitochondrial code

Mitochondrial ribosomal protein L3

Mitochondrial ribosomal protein L28

Mitochondrial ribosomal protein L30

Mitochondrial ribosomal protein L19

Mitochondrial ribosomal protein L24

Mitochondrial ribosomal protein L1

Mitochondrial ribosomal protein L42

Trematode mitochondrial code

Mitochondrial ribosomal protein L11

Tricarboxylate transport protein, mitochondrial

Mitochondrial ribosomal protein L18

Mitochondrial ribosomal protein L32

Mitochondrial ribosomal protein L17

Mitochondrial pyruvate carrier

Mitochondrial ribosomal protein L39

Thymidine kinase 2, mitochondrial

Mitochondrial ribosomal protein L4

Mitochondrial ribosomal protein L15

Mitochondrial ribosomal protein L20

Mitochondrial optic neuropathies

Mitochondrial pyruvate carrier 2

Mitochondrial 2-oxodicarboxylate carrier

Mitochondrial uncoupling protein 4

Mitochondrial ribosomal protein L40

Mitochondrial thiamine pyrophosphate carrier

Brain mitochondrial carrier protein 1

Cytochrome c oxidase subunit I

Mitochondrial unfolded protein response

Mitochondrial glycine transporter

Carbonic anhydrase 5B, mitochondrial

Mitochondrial amidoxime reducing component 1

Thraustochytrium mitochondrial code

Serine protease HTRA2, mitochondrial

Mitochondrial translational release factor 1

Respiratory complex I

Carbonic anhydrase 5A, mitochondrial

Mitochondrial shuttle

Calcium-binding mitochondrial carrier protein Aralar1

Scenedesmus obliquus mitochondrial code

Haplogroup V (mtDNA)

Chlorophycean mitochondrial code

Calcium-binding mitochondrial carrier protein SCaMC-1

Mitochondrial 2-oxoglutarate/malate carrier protein

Sengers syndrome

Electron transport chain

21S rRNA (uridine2791-2'-O)-methyltransferase

Mpv17 mitochondrial inner membrane protein like 2

Mitochondrial membrane protein-associated neurodegeneration

Translocator protein

Intermediate cleaving peptidase 55

Carnitine palmitoyltransferase I

Mitochondria associated membranes

Oxidative phosphorylation

Cytochrome c oxidase

Cytochrome c oxidase subunit III

Cytochrome c oxidase subunit 2

Coenzyme Q – cytochrome c reductase

Pearson syndrome

Sorting and assembly machinery

Diabetes and deafness

Cambridge Reference Sequence

Hypervariable region

Succinate dehydrogenase

Kearns–Sayre syndrome

Neuropathy, ataxia, and retinitis pigmentosa

MtDNA control region

Rebecca L. Cann

Haplogroup P (mtDNA)

Haplogroup Q (mtDNA)

Douglass Turnbull

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