No abstract listed.
Studies on the control of 4-aminobutyrate metabolism in 'synaptosomal' and free rat brain mitochondria
The respiratory chain of Paramecium tetraurelia in wild type and the mutant Cl1. I. Spectral properties and redox potentials
Rapid diagnosis of pyruvate and ketoglutarate dehydrogenase deficiencies in platelet-enriched preparations from blood
Mitochondrial respiratory chain of Tetrahymena pyriformis. The thermodynamic and spectral properties
Cytochrome b of fish mitochondria is strongly resistant to funiculosin, a powerful inhibitor of respiration
Coenzyme Q-pool function in glycerol-3-phosphate oxidation in hamster brown adipose tissue mitochondria
Structural and functional aspects of the respiratory chain of synaptic and nonsynaptic mitochondria derived from selected brain regions
The cytochrome b of the sea urchin Paracentrotus lividus is naturally resistant to myxothiazol and mucidin
Enzyme activities in perikaryal and synaptic mitochondrial fractions from rat hippocampus during development
Malonyl-CoA binding site and the overt carnitine palmitoyltransferase activity reside on the opposite sides of the outer mitochondrial membrane
Studies with ubiquinone-depleted submitochondrial particles. Quantitative incorporation of small amounts of ubiquinone and its effects on the NADH and succinate oxidase activities
Mitochondrial malic enzyme: the source of reduced nicotinamide adenine dinucleotide phosphate for steroid hydroxylation in bovine adrenal cortex mitochondria
The low-temperature spectral properties of mammalian cytochromes oxidase. II. The enzyme isolated from beef-heart mitochondria
Reversible reaction of epsilon-amino groups of cytochrome c with salicylaldehyde to produce cytochrome c polymers
Various conditions for spectrophotometric determination of succinate dehydrogenase and cytochrome oxidase activity in cerebral mitochondria
On the determination of the transmembrane pH difference in bacterial chromatophores using 9-aminoacridine
Molecular proportion of the fixed cytochrome components of the respiratory chain of Keilin-Hartree particles and beef heart mitochondria
Regional studies of catecholamines in the rat brain. 3. Subcellullar distribution of endogenous and exogenous catecholamines in various brain regions
DCCD inhibits proton translocation and electron flow at the second site of the mitochondrial respiratory chain
Kinetics of ubiquinol-1-cytochrome c reductase in bovine heart mitochondria and submitochondrial particles
Coenzyme Q content in synaptic and non-synaptic mitochondria from different brain regions in the ageing rat
Polarographic analyses of subsarcolemmal and intermyofibrillar mitochondria from rat skeletal and cardiac muscle
Functional alterations of the mitochondrially encoded ND4 subunit associated with Leber's hereditary optic neuropathy
Steady-state kinetics of the reduction of coenzyme Q analogs by complex I (NADH:ubiquinone oxidoreductase) in bovine heart mitochondria and submitochondrial particles
Lack of major changes in ATPase activity in mitochondria from liver, heart, and skeletal muscle of rats upon ageing
Protonophoric activity of NADH coenzyme Q reductase and ATP synthase in coupled submitochondrial particles from horse platelets
Decrease of rotenone inhibition is a sensitive parameter of complex I damage in brain non-synaptic mitochondria of aged rats
Steady-state kinetics of reduction of coenzyme Q analogs by glycerol-3-phosphate dehydrogenase in brown adipose tissue mitochondria
Catalytic activities of mitochondrial ATP synthase in patients with mitochondrial DNA T8993G mutation in the ATPase 6 gene encoding subunit a
Detergent-solubilized bovine cytochrome c oxidase: dimerization depends on the amphiphilic environment
Expression of uncoupling protein-3 in subsarcolemmal and intermyofibrillar mitochondria of various mouse muscle types and its modulation by fasting
The respiratory metabolism of insect flight muscle. III. Low-temperature spectra of the cytochromes of flight muscle sarcosomes
ON THE MECHANISM OF OXIDATIVE PHOSPHORYLATION. IX. ENERGY-DEPENDENT REDUCTION OF NICOTINAMIDE ADENINE DINUCLEOTIDE BY ASCORBATE AND UBIQUINONE OR MENADIONE
Mitochondrial complex I mutations in Caenorhabditis elegans produce cytochrome c oxidase deficiency, oxidative stress and vitamin-responsive lactic acidosis
New application of a subcellular fractionation method to kidney and testis for the determination of conjugated linoleic acid in selected cell organelles of healthy and cancerous human tissues
The topology of superoxide production by complex III and glycerol 3-phosphate dehydrogenase in Drosophila mitochondria
Isolation of mitochondria with high respiratory control from primary cultures of neurons and astrocytes using nitrogen cavitation
A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine
Selective inhibition of mitochondrial JNK signaling achieved using peptide mimicry of the Sab kinase interacting motif-1 (KIM1)
Knockdown of DAPIT (diabetes-associated protein in insulin-sensitive tissue) results in loss of ATP synthase in mitochondria.
Mitochondrial c-Jun N-terminal kinase (JNK) signaling initiates physiological changes resulting in amplification of reactive oxygen species generation.
Assessing actual contribution of IF1, inhibitor of mitochondrial FoF1, to ATP homeostasis, cell growth, mitochondrial morphology, and cell viability.
Inhibition of JNK mitochondrial localization and signaling is protective against ischemia/reperfusion injury in rats.
Mitochondrion as a novel site of dichloroacetate biotransformation by glutathione transferase zeta 1
Small peptides against the mutant SOD1/Bcl-2 toxic mitochondrial complex restore mitochondrial function and cell viability in mutant SOD1-mediated ALS
DHA Hydroperoxides as a Potential Inducer of Neuronal Cell Death: a Mitochondrial Dysfunction-Mediated Pathway
Mitochondrial import of PKCepsilon is mediated by HSP90: a role in cardioprotection from ischaemia and reperfusion injury
Comparative analysis of changes of myocardial angiogenesis and energy metabolism in postinfarction and diabetic damage of rat heart
Complete mitochondrial genome sequences of thirteen globally sourced strains of fruit fly (Drosophila melanogaster) form a powerful model for mitochondrial research
Protective effects of edaravone, a free radical scavenger, on lipopolysaccharide-induced acute kidney injury in a rat model of sepsis
Low energy costs of F1Fo ATP synthase reversal in colon carcinoma cells deficient in mitochondrial complex IV
In vitro and in vivo studies of the ALS-FTLD protein CHCHD10 reveal novel mitochondrial topology and protein interactions.
Para-hydroxyphenylpyruvate inhibits the pro-inflammatory stimulation of macrophage preventing LPS-mediated nitro-oxidative unbalance and immunometabolic shift
The legs at odd angles (Loa) mutation in cytoplasmic dynein ameliorates mitochondrial function in SOD1G93A mouse model for motor neuron disease.
Isolation of mitochondrial subpopulations from skeletal muscle: Optimizing recovery and preserving integrity
Ataxia-Telangiectasia Mutated is located in cardiac mitochondria and impacts oxidative phosphorylation
Modulation of the ASK1-MKK3/6-p38/MAPK signalling pathway mediates sildenafil protection against chemical hypoxia caused by malonate
Structural re-arrangement and peroxidase activation of cytochrome c by anionic analogues of vitamin E, tocopherol succinate and tocopherol phosphate.
Subpopulation-specific Differences in Skeletal Muscle Mitochondria in Humans with Obesity Insights from Studies Employing Acute Nutritional and Exercise Stimuli
Protein profiling and functional analysis of liver mitochondria from rats with nonalcoholic steatohepatitis
COMP-prohibitin 2 interaction maintains mitochondrial homeostasis and controls smooth muscle cell identity
Role of mitochondrial complex I and protective effect of CoQ10 supplementation in propofol induced cytotoxicity
Differential apoptosis-related protein expression, mitochondrial properties, proteolytic enzyme activity, and DNA fragmentation between skeletal muscles
G1P3 (IFI6), a mitochondrial localised antiapoptotic protein, promotes metastatic potential of breast cancer cells through mtROS
Dysregulation of Amyloid Precursor Protein Impairs Adipose Tissue Mitochondrial Function and Promotes Obesity
Electrophysiological properties of the mitochondrial permeability transition pores: Channel diversity and disease implication.
Coronaviruses encompass a large family of viruses that cause the common cold as well as more serious diseases, such as the ongoing outbreak of coronavirus disease 2019 (COVID-19; formally known as 2019-nCoV). Coronaviruses can spread from animals to humans; symptoms include fever, cough, shortness of breath, and breathing difficulties; in more severe cases, infection can lead to death. This feed covers recent research on COVID-19.
Alzheimer's Disease: MS4A
Variants within the membrane-spanning 4-domains subfamily A (MS4A) gene cluster have recently been implicated in Alzheimer's disease in genome-wide association studies. Here is the latest research on Alzheimer's disease and MS4A.
Pediculosis pubis is a disease caused by a parasitic insect known as Pthirus pubis, which infests human pubic hair, as well as other areas with hair including eye lashes. Here is the latest research.
Rh isoimmunization is a potentially preventable condition that occasionally is associated with significant perinatal morbidity or mortality. Discover the latest research on Rh Isoimmunization here.
Genetic Screens in iPSC-derived Brain Cells
Genetic screening is a critical tool that can be employed to define and understand gene function and interaction. This feed focuses on genetic screens conducted using induced pluripotent stem cell (iPSC)-derived brain cells. It also follows CRISPR-Cas9 approaches to generating genetic mutants as a means of understanding the effect of genetics on phenotype.
This feed focuses on molecular models of enzyme evolution and new approaches (such as adaptive laboratory evolution) to metabolic engineering of microorganisms. Here is the latest research.
Chronic Fatigue Syndrome
Chronic fatigue syndrome is a disease characterized by unexplained disabling fatigue; the pathology of which is incompletely understood. Discover the latest research on chronic fatigue syndrome here.
Pharmacology of Proteinopathies
This feed focuses on the pharmacology of proteinopathies - diseases in which proteins abnormally aggregate (i.e. Alzheimer’s, Parkinson’s, etc.). Discover the latest research in this field with this feed.
Alignment-free Sequence Analysis Tools
Alignment-free sequence analyses have been applied to problems ranging from whole-genome phylogeny to the classification of protein families, identification of horizontally transferred genes, and detection of recombined sequences. Here is the latest research.