MIT : KMLE 의학 검색 엔진 - 의학사전, 의학용어, 의학약어, 의학논문, 약품/의약품 검색

MeSH(Medical Subject Headings) 맞춤 검색 (http://www.nlm.nih.gov) 결과 : 5 페이지: 2

Mitochondria, Liver - 새창 Mitochondria in hepatocytes. As in all mitochondria, there are an outer membrane and an inner membrane, together creating two separate mitochondrial compartments: the internal matrix space and a much narrower intermembrane space. In the liver mitochondrion, an estimated 67% of the total mitochondrial proteins is located in the matrix. (From Alberts et al., Molecular Biology of the Cell, 2d ed, p343-4)
Synonyms : Liver Mitochondrion, Mitochondrion, Liver
Mitochondria, Muscle - 새창 Mitochondria of skeletal and smooth muscle. It does not include myocardial mitochondria for which MITOCHONDRIA, HEART is available.
Synonyms : Mitochondrion, Muscle, Muscle Mitochondria, Muscle Mitochondrion, Sarcosome
Mitochondrial ADP, ATP Translocases - 새창 A class of nucleotide translocases found abundantly in mitochondria that function as integral components of the inner mitochondrial membrane. They facilitate the exchange of ADP and ATP between the cytosol and the mitochondria, thereby linking the subcellular compartments of ATP production to those of ATP utilization.
Synonyms : ADP Translocase, ATP Translocase, ATP, ADP-Carrier, ATP-ADP Translocase, Adenine Nucleotide Carrier (Mitochondrial), Mitochondrial ADP-ATP Carriers, ADP-ATP Carriers, Mitochondrial, Mitochondrial ADP ATP Carriers
Mitochondrial Diseases - 새창 Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes.
Synonyms : Mitochondrial Disorders, Mitochondrial Electron Transport Chain Deficiencies, Mitochondrial Respiratory Chain Deficiencies, Deficiencies, Oxidative Phosphorylation, Deficiencies, Respiratory Chain, Deficiency, Oxidative Phosphorylation, Mitochondrial Disease
Mitochondrial Encephalomyopathies - 새창 A heterogenous group of disorders characterized by alterations of mitochondrial metabolism that result in muscle and nervous system dysfunction. These are often multisystemic and vary considerably in age at onset (usually in the first or second decade of life), distribution of affected muscles, severity, and course. (From Adams et al., Principles of Neurology, 6th ed, pp984-5)
Synonyms : Encephalomyopathy, Mitochondrial, Mitochondrial Encephalomyopathy