Experimental Factor Ontology
4252 terms(s) returned
| Term Type: | Record: 3251 to 3300 of 4252 Records | Page: 66 of 86, First Previous Next Last | Show Records Per Page |
- mitochondrial import inner membrane translocase subunit TIM50
- mitochondrial import inner membrane translocase subunit TIM50 (human)
- mitochondrial import inner membrane translocase subunit Tim10
- mitochondrial import inner membrane translocase subunit Tim10 (human)
- mitochondrial import inner membrane translocase subunit Tim10 B (human)
- mitochondrial import inner membrane translocase subunit Tim13
- mitochondrial import inner membrane translocase subunit Tim13 (human)
- mitochondrial import inner membrane translocase subunit Tim21
- mitochondrial import inner membrane translocase subunit Tim21 (human)
- mitochondrial import inner membrane translocase subunit Tim23
- mitochondrial import inner membrane translocase subunit Tim23 (human)
- mitochondrial import inner membrane translocase subunit Tim8 A
- mitochondrial import inner membrane translocase subunit Tim8 A (human)
- mitochondrial import inner membrane translocase subunit Tim9 B
- mitochondrial import inner membrane translocase subunit Tim9 B amount in blood
- mitochondrial import receptor subunit TOM20
- mitochondrial import receptor subunit TOM20 homolog (human)
- mitochondrial inner membrane protease ATP23
- mitochondrial inner membrane protease ATP23 amount in blood
- mitochondrial inner membrane protease ATP23 homolog (human)
- mitochondrial inner membrane protease subunit 2
- mitochondrial inner membrane protease subunit 2 (human)
- mitochondrial intermembrane space
- mitochondrial membrane transport disorder
- mitochondrial myopathy with diabetes
- mitochondrial myopathy with reversible cytochrome C oxidase deficiency
- mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome
- mitochondrial myopathy-lactic acidosis-deafness syndrome
- mitochondrial neurogastrointestinal encephalomyopathy
- mitochondrial non-syndromic sensorineural hearing loss
- mitochondrial oxidative phosphorylation disorder
- mitochondrial peptide methionine sulfoxide reductase (human)
- mitochondrial peptide methionine sulfoxide reductase measurement
- mitochondrial potassium channel
- mitochondrial potassium channel (human)
- mitochondrial protein C2orf69
- mitochondrial protein import disorder
- mitochondrial proton-transporting ATP synthase complex deficiency
- mitochondrial proton/calcium exchanger protein
- mitochondrial pyruvate carrier 1 (human)
- mitochondrial pyruvate carrier 1, initiator methionine removed form (human)
- mitochondrial pyruvate carrier deficiency
- mitochondrial respiratory chain complex deficiency
- mitochondrial respiratory-chain inhibitor
- mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency
- mitochondrial sodium/hydrogen exchanger 9B2 measurement
- mitochondrial substrate carrier disorder
- mitochondrial translation release factor in rescue
- mitochondrial translation release factor in rescue (human)
- mitochondrial transmembrane transport
