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Mitochondria, Heart -- metabolism. : Mitochondria and their role in cardiovascular disease / by José Marín-García ; with contributions by Alexander Akhmedov and Vitalyi Rybin, Gordon W. Moe  2013 1
Mitochondria, Liver. : Mitochondria in liver disease / edited by Derick Han, Neil Kaplowitz  2016 1
Mitochondria -- metabolism.   31
Mitochondria, Muscle. : Muscle mitochondrial function and biogenesis with aging / Russell T. Hepple  2007 1
Mitochondria, Muscle -- metabolism.   3
Mitochondria, Muscle -- physiology.   2
 

Mitochondria, Myocardial -- See Mitochondria, Heart


The mitochondria of the myocardium
  1
 

Mitochondria Origin -- See Mitochondria Formation


  1
 

Mitochondria Pathology -- See Mitochondrial pathology


  1
Mitochondria -- pathology.   12
Mitochondria -- Periodicals : Mitochondrion (Online)  2001- 1
Mitochondria -- physiology   13
Mitochondria -- Treatment : Cellular and molecular basis of mitochondrial inheritance : mitochondrial disease and fitness / Peter Sutovsky, editor  2019 1
Mitochondria -- ultrastructure. : Mitochondrial morphology and ultrastructure in skeletal muscle / Martin Picard  2018 1
 

Mitochondrial ADP-ATP Carriers -- See Mitochondrial ADP, ATP Translocases


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
  1
Mitochondrial ADP, ATP Translocases.   2
 

Mitochondrial Biogenesis -- See Organelle Biogenesis


The natural growth and development within living CELLS
  1
 

Mitochondrial Contraction -- See Mitochondria


Semiautonomous, self-reproducing organelles that occur in the cytoplasm of all cells of most, but not all, eukaryotes. Each mitochondrion is surrounded by a double limiting membrane. The inner membrane is highly invaginated, and its projections are called cristae. Mitochondria are the sites of the reactions of oxidative phosphorylation, which result in the formation of ATP. They contain distinctive RIBOSOMES, transfer RNAs (RNA, TRANSFER); AMINO ACYL T RNA SYNTHETASES; and elongation and termination factors. Mitochondria depend upon genes within the nucleus of the cells in which they reside for many essential messenger RNAs (RNA, MESSENGER). Mitochondria are believed to have arisen from aerobic bacteria that established a symbiotic relationship with primitive protoeukaryotes. (King & Stansfield, A Dictionary of Genetics, 4th ed)
  1
 

Mitochondrial Contractions -- See Mitochondria


Semiautonomous, self-reproducing organelles that occur in the cytoplasm of all cells of most, but not all, eukaryotes. Each mitochondrion is surrounded by a double limiting membrane. The inner membrane is highly invaginated, and its projections are called cristae. Mitochondria are the sites of the reactions of oxidative phosphorylation, which result in the formation of ATP. They contain distinctive RIBOSOMES, transfer RNAs (RNA, TRANSFER); AMINO ACYL T RNA SYNTHETASES; and elongation and termination factors. Mitochondria depend upon genes within the nucleus of the cells in which they reside for many essential messenger RNAs (RNA, MESSENGER). Mitochondria are believed to have arisen from aerobic bacteria that established a symbiotic relationship with primitive protoeukaryotes. (King & Stansfield, A Dictionary of Genetics, 4th ed)
  1
Mitochondrial Degradation.   4
 

Mitochondrial Disease -- See Mitochondrial Diseases


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
  1
Mitochondrial Diseases.   12
Mitochondrial Diseases -- diagnosis. : Mitochondrial medicine : Mitochondrial metabolism, diseases, diagnosis and therapy / Anna Gvozdjáková, editor  2008 1
Mitochondrial Diseases -- diet therapy. : Mitochondria in health and disease : personalized nutrition for healthcare practitioners / Ray Griffiths  2018 1
Mitochondrial Diseases -- epidemiology. : Mitochondrial diseases : an update / Ayesha Saleem  2020 1
Mitochondrial Diseases -- etiology.   2
Mitochondrial Diseases -- genetics.   3
Mitochondrial Diseases -- pathology. : Mitochondrial dysfunction in neurodegenerative disorders / Amy Katherine Reeve [and others], editors  2012 1
Mitochondrial Diseases -- Periodicals : Mitochondrion (Online)  2001- 1
Mitochondrial Diseases -- physiopathology.   2
Mitochondrial Diseases -- therapy.   2
 

Mitochondrial Disorder -- See Mitochondrial Diseases


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
  1
  Mitochondrial Disorders -- 2 Related Subjects   2
 

Mitochondrial DNA -- See DNA, Mitochondrial


Double-stranded DNA of MITOCHONDRIA. In eukaryotes, the mitochondrial GENOME is circular and codes for ribosomal RNAs, transfer RNAs, and about 10 proteins
  1
Mitochondrial DNA.   15
Mitochondrial DNA -- Abnormalities   2
Mitochondrial DNA -- Analysis.   3
 

Mitochondrial DNA disorders -- See Mitochondrial DNA Abnormalities


  1
Mitochondrial DNA -- Periodicals   3
 

Mitochondrial Dynamic -- See Mitochondrial Dynamics


The continuous remodeling of MITOCHONDRIA shape by fission and fusion in response to physiological conditions
  1
Mitochondrial Dynamics.   3
 

Mitochondrial Electron Transport Chain Deficiencies -- See Mitochondrial Diseases


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
  1
 

Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes -- See MELAS Syndrome


A mitochondrial disorder characterized by focal or generalized seizures, episodes of transient or persistent neurologic dysfunction resembling strokes, and ragged-red fibers on muscle biopsy. Affected individuals tend to be normal at birth through early childhood, then experience growth failure, episodic vomiting, and recurrent cerebral insults resulting in visual loss and hemiparesis. The cortical lesions tend to occur in the parietal and occipital lobes and are not associated with vascular occlusion. VASCULAR HEADACHE is frequently associated and the disorder tends to be familial. (From Joynt, Clinical Neurology, 1992, Ch56, p117)
  1
 

Mitochondrial Fission -- See Mitochondrial Dynamics


The continuous remodeling of MITOCHONDRIA shape by fission and fusion in response to physiological conditions
  1
 

Mitochondrial Fission and Fusion -- See Mitochondrial Dynamics


The continuous remodeling of MITOCHONDRIA shape by fission and fusion in response to physiological conditions
  1
 

Mitochondrial Fissions -- See Mitochondrial Dynamics


The continuous remodeling of MITOCHONDRIA shape by fission and fusion in response to physiological conditions
  1
 

Mitochondrial Fusion -- See Mitochondrial Dynamics


The continuous remodeling of MITOCHONDRIA shape by fission and fusion in response to physiological conditions
  1
 

Mitochondrial Fusion and Fission -- See Mitochondrial Dynamics


The continuous remodeling of MITOCHONDRIA shape by fission and fusion in response to physiological conditions
  1
 

Mitochondrial Fusions -- See Mitochondrial Dynamics


The continuous remodeling of MITOCHONDRIA shape by fission and fusion in response to physiological conditions
  1
 

Mitochondrial Gene -- See Genes, Mitochondrial


Genes that are located on the MITOCHONDRIAL DNA. Mitochondrial inheritance is often referred to as maternal inheritance but should be differentiated from maternal inheritance that is transmitted chromosomally
  1
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