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Mitochondrial Diseases -- prevention & control : Mitochondrial replacement techniques : ethical, social, and policy considerations / Anne Claiborne, Rebecca English, Jeffrey Kahn, editors ; Committee on the Ethical and Social Policy Considerations of Novel Techniques for Prevention of Maternal Transmission of Mitochondrial DNA Diseases, Board on Health Sciences Policy, Institute of Medicine, National Academies of Sciences, Engineering, and Medicine  2016 1
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.   25
Mitochondrial DNA -- Abnormalities.   5
Mitochondrial DNA -- Abnormalities -- United States : Mitochondrial replacement techniques : ethical, social, and policy considerations / Anne Claiborne, Rebecca English, Jeffrey Kahn, editors ; Committee on the Ethical and Social Policy Considerations of Novel Techniques for Prevention of Maternal Transmission of Mitochondrial DNA Diseases, Board on Health Sciences Policy, Institute of Medicine, National Academies of Sciences, Engineering, and Medicine  2016 1
Mitochondrial DNA -- Analysis.   4
 

Mitochondrial DNA disorders -- See Mitochondrial DNA Abnormalities


  1
Mitochondrial DNA -- Laboratory manuals   4
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   2
 

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
 

Mitochondrial Genes -- 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
Mitochondrial genetics. : Plant diversity and evolution : genotypic and phenotypic variation in higher plants / edited by Robert J. Henry  2005 1
 

Mitochondrial genome -- See Mitochondrial DNA


  1
 

Mitochondrial genomes -- See Mitochondrial DNA


  1
 

Mitochondrial Inheritance -- 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
 

Mitochondrial Membrane -- See Mitochondrial Membranes


The two lipoprotein layers in the MITOCHONDRION. The outer membrane encloses the entire mitochondrion and contains channels with TRANSPORT PROTEINS to move molecules and ions in and out of the organelle. The inner membrane folds into cristae and contains many ENZYMES important to cell METABOLISM and energy production (MITOCHONDRIAL ATP SYNTHASE)
  1
 

Mitochondrial Membrane, Inner -- See Mitochondrial Membranes


The two lipoprotein layers in the MITOCHONDRION. The outer membrane encloses the entire mitochondrion and contains channels with TRANSPORT PROTEINS to move molecules and ions in and out of the organelle. The inner membrane folds into cristae and contains many ENZYMES important to cell METABOLISM and energy production (MITOCHONDRIAL ATP SYNTHASE)
  1
 

Mitochondrial Membrane, Outer -- See Mitochondrial Membranes


The two lipoprotein layers in the MITOCHONDRION. The outer membrane encloses the entire mitochondrion and contains channels with TRANSPORT PROTEINS to move molecules and ions in and out of the organelle. The inner membrane folds into cristae and contains many ENZYMES important to cell METABOLISM and energy production (MITOCHONDRIAL ATP SYNTHASE)
  1
Mitochondrial Membrane Transport Proteins   2
Mitochondrial membranes.   5
 

Mitochondrial Membranes, Inner -- See Mitochondrial Membranes


The two lipoprotein layers in the MITOCHONDRION. The outer membrane encloses the entire mitochondrion and contains channels with TRANSPORT PROTEINS to move molecules and ions in and out of the organelle. The inner membrane folds into cristae and contains many ENZYMES important to cell METABOLISM and energy production (MITOCHONDRIAL ATP SYNTHASE)
  1
 

Mitochondrial Membranes, Outer -- See Mitochondrial Membranes


The two lipoprotein layers in the MITOCHONDRION. The outer membrane encloses the entire mitochondrion and contains channels with TRANSPORT PROTEINS to move molecules and ions in and out of the organelle. The inner membrane folds into cristae and contains many ENZYMES important to cell METABOLISM and energy production (MITOCHONDRIAL ATP SYNTHASE)
  1
 

Mitochondrial Myopathy, Encephalopathy, 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 Myopathy, Lactic Acidosis, Stroke-Like Episode -- 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 pathology -- See Also the narrower term Mitochondrial DNA Abnormalities


  1
Mitochondrial pathology.   55
Mitochondrial pathology -- Case studies : Mitochondrial case studies : underlying mechanisms and diagnosis / edited by Russell P. Saneto, Department of Neurology/Division of Pediatric Neurology, Seattle Children's Hospital/University of Washington, Seattle, WA, USA, Sumit Parikh, Cleveland Clinic Lerner College of Medicine & Case Western Reserve University, Cleveland, OH, USA ; Neurogenetics, Metabolism and Mitochondrial Disease Center, Cleveland Clinic, Cleveland, OH, USA, Bruce H. Cohen, Northeast Ohio Medical University, Rootstown, OH, USA ; the NeuroDevelopmental Science Center and Division of Neurology, Department of Pediatrics, Children's Hospital and Medical Center of Akron, Akron, OH, USA  2016 1
Mitochondrial pathology -- Diagnosis -- Case studies : Mitochondrial case studies : underlying mechanisms and diagnosis / edited by Russell P. Saneto, Department of Neurology/Division of Pediatric Neurology, Seattle Children's Hospital/University of Washington, Seattle, WA, USA, Sumit Parikh, Cleveland Clinic Lerner College of Medicine & Case Western Reserve University, Cleveland, OH, USA ; Neurogenetics, Metabolism and Mitochondrial Disease Center, Cleveland Clinic, Cleveland, OH, USA, Bruce H. Cohen, Northeast Ohio Medical University, Rootstown, OH, USA ; the NeuroDevelopmental Science Center and Division of Neurology, Department of Pediatrics, Children's Hospital and Medical Center of Akron, Akron, OH, USA  2016 1
Mitochondrial pathology -- Diet therapy : Mitochondria in health and disease / Ray Griffiths ; foreword by Lorraine Nicolle  2018 1
Mitochondrial pathology -- Genetic aspects : Sequence-specific DNA binders for the therapy of mitochondrial diseases / Takuya Hidaka  2022 1
Mitochondrial pathology -- Handbooks, manuals, etc : Handbook of mitochondrial dysfunction / edited by Shamim I. Ahmad  2019 1
Mitochondrial pathology -- Laboratory manuals   3
Mitochondrial pathology -- Popular works : Mitochondria and the future of medicine : the key to understanding disease, chronic illness, aging, and life itself / Lee Know, ND  2018 1
Mitochondrial pathology -- United States : Mitochondrial replacement techniques : ethical, social, and policy considerations / Anne Claiborne, Rebecca English, Jeffrey Kahn, editors ; Committee on the Ethical and Social Policy Considerations of Novel Techniques for Prevention of Maternal Transmission of Mitochondrial DNA Diseases, Board on Health Sciences Policy, Institute of Medicine, National Academies of Sciences, Engineering, and Medicine  2016 1
 

Mitochondrial Protein -- See Mitochondrial Proteins


Proteins encoded by the mitochondrial genome or proteins encoded by the nuclear genome that are imported to and resident in the MITOCHONDRIA
  1
Mitochondrial Proteins   4
Mitochondrial Proteins -- metabolism : Principles of bioenergetics / Vladimir P. Skulachev, Alexander V. Bogachev, Felix O. Kasparinsky  2013 1
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