All Stories

  1. Involvement of increased p53 expression in the decrease of mitochondrial DNA copy number and increase of SUVmax of FDG-PET scan in esophageal squamous cell carcinoma
  2. Alterations of oxygen consumption and extracellular acidification rates by glutamine in PBMCs of SLE patients
  3. Low mitochondrial DNA copy number of resected cecum appendix correlates with high severity of acute appendicitis
  4. Assessment of zero-valent iron-based nanotherapeutics for ferroptosis induction and resensitization strategy in cancer cells
  5. Sirt3 is required in adipogenic differentiation of stem cells and plays a role in type 2 diabetes.
  6. Generation of two isogenic human induced pluripotent stem cell lines from a 15 year-old female patient with MERRF syndrome and A8344G mutation of mitochondrial DNA
  7. Essential role of connective tissue growth factor (CTGF) in transforming growth factor-β1 (TGF-β1)-induced myofibroblast transdifferentiation from Graves’ orbital fibroblasts
  8. ATOH1/RFX1/RFX3 transcription factors facilitate the differentiation and characterisation of inner ear hair cell-like cells from patient-specific induced pluripotent stem cells harbouring A8344G mutation of mitochondrial DNA
  9. Sirt3 activates mitochondrial enzymes and antioxidant defense in differentiating stem cells.
  10. Connective tissue growth factor decreases mitochondrial metabolism through ubiquitin-mediated degradation of mitochondrial transcription factor A in oral squamous cell carcinoma
  11. Generation of an induced pluripotent stem cell (iPSC) line from a 40-year-old patient with the A8344G mutation of mitochondrial DNA and MERRF (myoclonic epilepsy with ragged red fibers) syndrome
  12. Promoter analysis and transcriptional regulation of human carbonic anhydrase VIII gene in a MERRF disease cell model
  13. Generation of an induced pluripotent stem cell line from a 39-year-old female patient with severe-to-profound non-syndromic sensorineural hearing loss and a A1555G mutation in the mitochondrial MTRNR1 gene
  14. Role of mitochondrial function in the invasiveness of human colon cancer cells
  15. Significant Association Between Low Mitochondrial DNA Content in Peripheral Blood Leukocytes and Ischemic Stroke
  16. AB001. Low mitochondrial DNA copy number is associated with low mitochondrial DNA integrity and advanced T-status in non-small cell lung cancer
  17. AB002. Relationship between mitochondrial DNA copy number and maximum standard uptake value of 18F-fluorodeoxyglucose positron emission tomography scan in esophageal squamous cell carcinoma
  18. Role of mitochondrial dysfunction and dysregulation of Ca2+ homeostasis in the pathophysiology of insulin resistance and type 2 diabetes
  19. Peptide-mediated delivery of donor mitochondria improves mitochondrial function and cell viability in human cybrid cells with the MELAS A3243G mutation
  20. ROS and Oxidative Stress in Stem Cells
  21. The pathogenesis of systemic lupus erythematosus - From the viewpoint of oxidative stress and mitochondrial dysfunction
  22. Expression and clinical significance of connective tissue growth factor (CTGF) in Graves' ophthalmopathy
  23. Hyaluronan Upregulates Mitochondrial Biogenesis and Reduces Adenoside Triphosphate Production for Efficient Mitochondrial Function in Slow-Proliferating Human Mesenchymal Stem Cells
  24. Role of Mitochondrial DNA Copy Number Alteration in Human Renal Cell Carcinoma
  25. Mitochondria in mesenchymal stem cell biology and cell therapy: From cellular differentiation to mitochondrial transfer
  26. Cigarette Smoke Extract-Induced Oxidative Stress and Fibrosis-Related Genes Expression in Orbital Fibroblasts from Patients with Graves’ Ophthalmopathy
  27. Alteration of Connective Tissue Growth Factor (CTGF) Expression in Orbital Fibroblasts from Patients with Graves’ Ophthalmopathy
  28. 2-Deoxy-d-Glucose Can Complement Doxorubicin and Sorafenib to Suppress the Growth of Papillary Thyroid Carcinoma Cells
  29. The Core Pattern Analysis on Chinese Herbal Medicine for Sjögren's syndrome: A Nationwide Population-Based Study
  30. Correlation of NADH fluorescence lifetime and oxidative phosphorylation metabolism in the osteogenic differentiation of human mesenchymal stem cell
  31. Transient Increase in Circulating Myeloid-Derived Suppressor Cells after Partial Bladder Outlet Obstruction
  32. Special issue on “Oxidative stress and mitochondrial alterations in aging and disease”
  33. Differential patterns of effects of age and sex on metabolic syndrome in Taiwan: Implication for the inadequate internal consistency of the current criteria
  34. Cisd2 mediates lifespan: is there an interconnection among Ca2+homeostasis, autophagy, and lifespan?
  35. Roles of sirtuins in the regulation of antioxidant defense and bioenergetic function of mitochondria under oxidative stress
  36. Cisd2 modulates the differentiation and functioning of adipocytes by regulating intracellular Ca2+ homeostasis
  37. Effects of carbonic anhydrase-related protein VIII on human cells harbouring an A8344G mitochondrial DNA mutation
  38. Role of AMPK-mediated adaptive responses in human cells with mitochondrial dysfunction to oxidative stress
  39. Mitochondrial DNA association study of type 2 diabetes with or without ischemic stroke in Taiwan
  40. Inhibitory Effects of Hypoxia on Metabolic Switch and Osteogenic Differentiation of Human Mesenchymal Stem Cells
  41. Integrated three-dimensional system-on-chip for direct quantitative detection of mitochondrial DNA mutation in affected cells
  42. Isolation and Characterization of a Novel Strain of Mesenchymal Stem Cells from Mouse Umbilical Cord: Potential Application in Cell-Based Therapy
  43. Resveratrol Impedes the Stemness, Epithelial-Mesenchymal Transition, and Metabolic Reprogramming of Cancer Stem Cells in Nasopharyngeal Carcinoma through p53 Activation
  44. Mitochondrial Dysfunction in Insulin Insensitivity and Type 2 Diabetes and New Insights for Their Prevention and Management
  45. Functional Recovery of Human Cells Harbouring the Mitochondrial DNA Mutation MERRF A8344G via Peptide-Mediated Mitochondrial Delivery
  46. High Mitochondrial DNA Copy Number and Bioenergetic Function Are Associated with Tumor Invasion of Esophageal Squamous Cell Carcinoma Cell Lines
  47. Cigarette Smoking and hOGG1 Ser326Cys Polymorphism are Associated with 8-OHdG Accumulation on Mitochondrial DNA in Thoracic Esophageal Squamous Cell Carcinoma
  48. Leukocyte Mitochondrial DNA Alteration in Systemic Lupus Erythematosus and Its Relevance to the Susceptibility to Lupus Nephritis
  49. Mitochondrial bioenergetic function and metabolic plasticity in stem cell differentiation and cellular reprogramming
  50. Associated microsatellite alterations in mitochondrial DNA and in TP53 in thoracic esophageal squamous cell carcinoma
  51. AMPK-mediated increase of glycolysis as an adaptive response to oxidative stress in human cells: Implication of the cell survival in mitochondrial diseases
  52. Mitochondria and Aging
  53. Oxidative Stress and its Biochemical Consequences in Mitochondrial DNA Mutation-Associated Diseases: Implications of Redox Therapy for Mitochondrial Diseases
  54. Induction of primitive pigment cell differentiation by visible light (helium–neon laser): a photoacceptor-specific response not replicable by UVB irradiation
  55. The Cross-Talk Between Mitochondria and the Nucleus in the Response to Oxidative Stress Associated with Mitochondrial Dysfunction in Mitochondrial Encephalomyopathies
  56. The Effect of Photo-oxidative Stress and Inflammatory Cytokine on Complement Factor H Expression in Retinal Pigment Epithelial Cells
  57. Increased penile expression of transforming growth factor and elevated systemic oxidative stress in rabbits with chronic partial bladder outlet obstruction
  58. Aberrant Cell Proliferation by Enhanced Mitochondrial Biogenesis via mtTFA in Arsenical Skin Cancers
  59. Abstract 482: High CD44/CD24 expressive cells presented cancer stem cell characteristics and undergo mitochondrial resetting and metabolic shift in nasopharyngeal carcinoma
  60. Increase of reduced nicotinamide adenine dinucleotide fluorescence lifetime precedes mitochondrial dysfunction in staurosporine-induced apoptosis of HeLa cells
  61. Increase of 8-Hydroxy-2′-Deoxyguanosine in Aqueous Humor of Patients with Exudative Age-Related Macular Degeneration
  62. Oxidative stress biomarkers in urine and plasma of rabbits with partial bladder outlet obstruction
  63. Determination of the minimal melatonin exposure required to induce osteoblast differentiation from human mesenchymal stem cells and these effects on downstream signaling pathways
  64. Mitochondrial dysfunction in insulin insensitivity: implication of mitochondrial role in type 2 diabetes
  65. Mitochondrial respiratory dysfunction-elicited oxidative stress and posttranslational protein modification in mitochondrial diseases
  66. Mitochondrial DNA Mutation-Elicited Oxidative Stress, Oxidative Damage, and Altered Gene Expression in Cultured Cells of Patients with MERRF Syndrome
  67. Somatic mutations of mitochondrial genome in hepatocellular carcinoma
  68. Upregulation of mitochondrial function and antioxidant defense in the differentiation of stem cells
  69. The role of mitochondrial DNA alterations in esophageal squamous cell carcinomas
  70. Mitochondrial Respiratory Function Decline in Aging and Life-Span Extension by Caloric Restriction
  71. Response to the increase of oxidative stress and mutation of mitochondrial DNA in aging
  72. Role of Reactive Oxygen Species-elicited Apoptosis in the Pathophysiology of Mitochondrial and Neurodegenerative Diseases Associated With Mitochondrial DNA Mutations
  73. Activation of PKCδ and ERK1/2 in the sensitivity to UV-induced apoptosis of human cells harboring 4977 bp deletion of mitochondrial DNA
  74. The difference in oxidative stress of the blood between using 5% glucose water and distilled water as the irrigant for BPH patients undergoing transurethral resection of the prostate
  75. Fluorescence Supravital Stain of Human Sperm: Correlation with Sperm Motility Measured by a Transmembrane Migration Method/Supravital-Fluoreszenz-Färbung von menschlichen Spermatozoen: Korrelation zur Spermatozoenmotilität (Messung mittels Transmembran-Mi
  76. Low copy number and high 4977 deletion of mitochondrial DNA in uterosacral ligaments are associated with pelvic organ prolapse progression
  77. Mitochondrial dysfunction-induced amphiregulin upregulation mediates chemo-resistance and cell migration in HepG2 cells
  78. Prognostic Variables in Thoracic Esophageal Squamous Cell Carcinoma
  79. Mitochondrial DNA Instability and Metabolic Shift in Human Cancers
  80. Peripheral blood mitochondrial DNA content and dysregulation of glucose metabolism
  81. GST M1 Polymorphism Associates with DNA Oxidative Damage and Mortality among Hemodialysis Patients
  82. Oxidative stress in patients with Graves' ophthalmopathy: relationship between oxidative DNA damage and clinical evolution
  83. Intravenous Iron Exacerbates Oxidative DNA Damage in Peripheral Blood Lymphocytes in Chronic Hemodialysis Patients
  84. Increase of oxidative stress in human sperm with lower motility
  85. Coordinated Changes of Mitochondrial Biogenesis and Antioxidant Enzymes During Osteogenic Differentiation of Human Mesenchymal Stem Cells
  86. Attenuation of Oxidative Stress After Varicocelectomy in Subfertile Patients With Varicocele
  87. Depletion of mitochondrial DNA in leukocytes of patients with poly-Q diseases
  88. Differentiation of apoptosis from necrosis by dynamic changes of reduced nicotinamide adenine dinucleotide fluorescence lifetime in live cells
  89. Reduced nicotinamide adenine dinucleotide fluorescence lifetime separates human mesenchymal stem cells from differentiated progenies
  90. Mitochondrial DNA alterations in blood of the humans exposed to N,N-dimethylformamide
  91. Quantitative effect of 4977 bp deletion of mitochondrial DNA on the susceptibility of human cells to UV-induced apoptosis
  92. B-group vitamins, MTHFR C677T polymorphism and carotid intima-media thickness in clinically healthy subjects
  93. A Common Mitochondrial DNA Variant and Increased Body Mass Index as Associated Factors for Development of Type 2 Diabetes: Additive Effects of Genetic and Environmental Factors
  94. A Follow-up Study in a Taiwanese Family with Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis and Stroke-like Episodes Syndrome
  95. Association of the Y402H Polymorphism in Complement Factor H Gene and Neovascular Age-Related Macular Degeneration in Chinese Patients
  96. Leber's hereditary optic neuropathy: A multifactorial disease
  97. Involvement of protein kinase C delta in the alteration of mitochondrial mass in human cells under oxidative stress
  98. Oculopharyngeal somatic myopathy in a patient with a novel large-scale 3399bp deletion and a homoplasmic T5814C transition of the mitochondrial DNA
  99. Alteration in the copy number of mitochondrial DNA in leukocytes of patients with mitochondrial encephalomyopathies
  100. Visualizing common deletion of mitochondrial DNA-augmented mitochondrial reactive oxygen species generation and apoptosis upon oxidative stress
  101. Increases of Mitochondrial Mass and Mitochondrial Genome in Association with Enhanced Oxidative Stress in Human Cells Harboring 4,977 BP-Deleted Mitochondrial DNA
  102. Mitochondrial DNA mutations and mitochondrial DNA depletion in breast cancer
  103. INHIBITION OF LUNG CANCER CELL GROWTH BY QUERCETIN GLUCURONIDES VIA G2/M ARREST AND INDUCTION OF APOPTOSIS
  104. Accumulation of mitochondrial DNA with 4977-bp deletion in knee cartilage – an association with idiopathic osteoarthritis
  105. Effects of nitric oxide donors on cybrids harbouring the mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) A3243G mitochondrial DNA mutation
  106. Increased oxidative DNA damage, 8-hydroxydeoxy- guanosine, in human pterygium
  107. Mitochondrial DNA Mutation, Oxidative Stress, and Alteration of Gene Expression in Human Aging
  108. Cadmium Toxicity toward Caspase-Independent Apoptosis through the Mitochondria-Calcium Pathway in mtDNA-Depleted Cells
  109. Repeated Ovarian Stimulations Induce Oxidative Damage and Mitochondrial DNA Mutations in Mouse Ovaries
  110. Alteration of the Copy Number of Mitochondrial DNA in Leukocytes of Patients with Hyperlipidemia
  111. Attenuation of UV-Induced Apoptosis by Coenzyme Q10in Human Cells Harboring Large-Scale Deletion of Mitochondrial DNA
  112. Enhanced Generation of Mitochondrial Reactive Oxygen Species in Cybrids Containing 4977-bp Mitochondrial DNA Deletion
  113. High Prevalence of the COII/tRNALysIntergenic 9-bp Deletion in Mitochondrial DNA of Taiwanese Patients with MELAS or MERRF Syndrome
  114. Increased Oxidative Damage with Altered Antioxidative Status in Type 2 Diabetic Patients Harboring the 16189 T to C Variant of Mitochondrial DNA
  115. Mitochondrial Genome Instability and mtDNA Depletion in Human Cancers
  116. Oxidative Stress-Induced Depolymerization of Microtubules and Alteration of Mitochondrial Mass in Human Cells
  117. Upregulation of Matrix Metalloproteinase 1 and Disruption of Mitochondrial Network in Skin Fibroblasts of Patients with MERRF Syndrome
  118. Differential expression of antioxidant enzymes in various hepatocellular carcinoma cell lines
  119. Effects of glycolic acid on the induction of apoptosis via caspase-3 activation in human leukemia cell line (HL-60)
  120. 8-HYDROXY-2′-DEOXYGUANOSINE IN LEUKOCYTE DNA OF SPERMATIC VEIN AS A BIOMARKER OF OXIDATIVE STRESS IN PATIENTS WITH VARICOCELE
  121. MAGNOLOL ALTERS THE COURSE OF ENDOTOXIN TOLERANCE AND PROVIDES EARLY PROTECTION AGAINST ENDOTOXIN CHALLENGE FOLLOWING SUBLETHAL HEMORRHAGE IN RATS
  122. Depletion of mitochondrial DNA is a factor of poor quality of human spermatozoa.
  123. Pulsatile ocular blood flow in patients with Graves' ophthalmopathy
  124. Quantification of Plasma Epstein–Barr Virus DNA in Patients with Advanced Nasopharyngeal Carcinoma
  125. A prevalent POLG CAG microsatellite length allele in humans and African great apes
  126. Increased 8-Hydroxy-2′-Deoxyguanosine in Leukocyte DNA in Leber’s Hereditary Optic Neuropathy
  127. Alteration of the copy number and deletion of mitochondrial DNA in human hepatocellular carcinoma
  128. Prenatal diagnosis of a fetus harboring an intermediate load of the A3243G mtDNA mutation in a maternal carrier diagnosed with MELAS syndrome
  129. Association of the Mitochondrial DNA 16189 T to C Variant with Lacunar Cerebral Infarction: Evidence from a Hospital-Based Case-Control Study
  130. Mitochondrial DNA 4,977-bp Deletion in Paired Oral Cancer and Precancerous Lesions Revealed by Laser Microdissection and Real-Time Quantitative PCR
  131. Mitochondrial DNA Mutation and Depletion Increase the Susceptibility of Human Cells to Apoptosis
  132. Somatic mutations in the D-loop and decrease in the copy number of mitochondrial DNA in human hepatocellular carcinoma
  133. Genetic polymorphism of hOGG1 and risk of pterygium in Chinese
  134. Mitochondrial DNA mutations can cause many human diseases.
  135. Mediating of caspase-independent apoptosis by cadmium through the mitochondria-ROS pathway in MRC-5 fibroblasts
  136. Mitochondrial DNA Mutation and Depletion Increase the Susceptibility of Human Cells to Apoptosis
  137. Increased expression of manganese-superoxide dismutase in fibroblasts of patients with CPEO syndrome
  138. Oxidative damage to mitochondrial DNA in atrial muscle of patients with atrial fibrillation
  139. Clinical Research. Genetic analysis in Leber's hereditary optic neuropathy using the comparative genomic hybridization technique
  140. Mitochondria-mediated caspase-independent apoptosis induced by cadmium in normal human lung cells
  141. Oxidative-stress-related changes in the livers of bile-duct-ligated rats
  142. Early prediction of response to intravenous iron supplementation by reticulocyte haemoglobin content and high-fluorescence reticulocyte count in haemodialysis patients
  143. Mitochondrial DNA mutations and oxidative stress in mitochondrial diseases
  144. Oxidative Stress, Mitochondrial DNA Mutation, and Impairment of Antioxidant Enzymes in Aging
  145. Increase of mitochondrial DNA in blood cells of patients with Leber's hereditary optic neuropathy with 11778 mutation
  146. Clinical phenotype, prognosis and mitochondrial DNA mutation load in mitochondrial encephalomyopathies
  147. Mitochondrial DNA mutations and oxidative damage in skeletal muscle of patients with chronic uremia
  148. PCR detection of circulating tumor cells in nasopharyngeal carcinoma patients with distant metastasis: Effect of enzyme and sampling
  149. Multiple rearrangements of mitochondrial DNA in unfertilized human oocytes
  150. Increased Oxidative Damage to Peripheral Blood Leukocyte DNA in Chronic Peritoneal Dialysis Patients
  151. Detection of DNA mutations associated with mitochondrial diseases by Agilent 2100 bioanalyzer
  152. Polymorphisms of glutathione S-transferase M1 and male infertility in Taiwanese patients with varicocele
  153. Leber's Hereditary Optic Neuropathy—The Spectrum of Mitochondrial DNA Mutations in Chinese Patients
  154. Evaluation of cytokeratin-19 mRNA as a tumor marker in the peripheral blood of nasopharyngeal carcinoma patients receiving concurrent chemoradiotherapy
  155. Antioxidant and Anticonvulsant Effect of a Modified Formula of Chaihu-Longu-Muli-Tang
  156. Wernicke’s Encephalopathy in a Patient with Multiple Symmetrical Lipomatosis and the A8344G Mutation of Mitochondrial DNA
  157. Enhanced oxidative damage in human cells harboring A3243G mutation of mitochondrial DNA: implication of oxidative stress in the pathogenesis of mitochondrial diabetes
  158. Molecular analysis of diabetes mellitus-associated A3243G mitochondrial DNA mutation in Taiwanese cases
  159. Mutations at the mitochondrial DNA polymerase (POLG) locus associated with male infertility
  160. A novel mutation in the mitochondrial 16S rRNA gene in a patient with MELAS syndrome, diabetes mellitus, hyperthyroidism and cardiomyopathy
  161. Erythropoietin and iron: the role of ascorbic acid
  162. Oxidative damage to proteins and decrease of antioxidant capacity in patients with varicocele
  163. Accumulation of mitochondrial DNA deletions in human oral tissues — effects of betel quid chewing and oral cancer
  164. Detection of Epstein-Barr Virus DNA in the Peripheral-Blood Cells of Patients With Nasopharyngeal Carcinoma: Relationship to Distant Metastasis and Survival
  165. Biomarkers of DNA damage in patients with end‐stage renal disease: mitochondrial DNA mutation in hair follicles
  166. Involvement of nervous system in maternally inherited diabetes and deafness (MIDD) with the A3243G mutation of mitochondrial DNA
  167. 8-Hydroxy-2′-Deoxyguanosine of leukocyte DNA as a marker of oxidative stress in chronic hemodialysis patients
  168. Large-scale mitochondrial DNA deletions in skeletal muscle of patients with end-stage renal disease
  169. Effect of vitamin E-bonded membrane on the 8-hydroxy 2′-deoxyguanosine level in leukocyte DNA of hemodialysis patients
  170. Autoantibody against oxidized low-density lipoproteins may be enhanced by cigarette smoking
  171. Increase of mitochondria and mitochondrial DNA in response to oxidative stress in human cells
  172. Increase of mitochondria and mitochondrial DNA in response to oxidative stress in human cells
  173. Mitochondrial DNA deletion of the human detrusor after partial bladder outlet obstruction—correlation with urodynamic analysis
  174. Lipophilic Antioxidants and Iron Status in ESRD Patients on Hemodialysis
  175. Interferon-α2a effects on complement activation and regulation in MS patients
  176. MORPHOLOGICAL AND MORPHOMETRIC ANALYSIS OF HUMAN DETRUSOR MITOCHONDRIA WITH URODYNAMIC CORRELATION AFTER PARTIAL BLADDER OUTLET OBSTRUCTION
  177. Mitochondrial role in life and death of the cell
  178. Correction of Pancreatic β-Cell Dysfunction with Coenzyme Q10 in a Patient with Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-Like Episodes Syndrome and Diabetes mellitus
  179. Enhanced oxidative stress in haemodialysis patients receiving intravenous iron therapy
  180. Intravenous ascorbic acid as an adjuvant therapy for recombinant erythropoietin in hemodialysis patients with hyperferritinemia
  181. Quantitation and origin of the mitochondrial membrane potential in human cells lacking mitochondrial DNA
  182. Exclusive Homoplasmic 11778 Mutation in Mitochondrial DNA of Chinese Patients With Leber's Hereditary Optic Neuropathy
  183. Tissue mosaicism in the skeletal muscle and sural nerve biopsies in the MELAS syndrome
  184. Concurrent Increase of Oxidative DNA Damage and Lipid Peroxidation Together with Mitochondrial DNA Mutation in Human Lung Tissues During Aging—Smoking Enhances Oxidative Stress on the Aged Tissues
  185. Decreased ATP synthesis is phenotypically expressed during increased energy demand in fibroblasts containing mitochondrial tRNA mutations
  186. Age-Associated Alteration of Blood Thiol-Group-Related Antioxidants in Smokers
  187. Oxidative damage elicited by imbalance of free radical scavenging enzymes is associated with large-scale mtDNA deletions in aging human skin
  188. Human lung accumulates mitochondrial DNA mutations in aging and in smokers.
  189. The paper contends that mtDNA mutations accumulate in aging human tissues.
  190. Smoking-Associated Mitochondrial DNA Mutations and Lipid Peroxidation in Human Lung Tissues
  191. Alterations of small-molecular-weight antioxidants in the blood of smokers
  192. Oxidative Damage and Mutation to Mitochondrial DNA and Age-dependent Decline of Mitochondrial Respiratory Functiona
  193. Bioenergetic consequences of accumulating the common 4977-bp mitochondrial DNA deletion
  194. Multiple deletions of mitochondrial DNA are associated with the decline of motility and fertility of human spermatozoa
  195. AT-rich sequences flanking the 5′-end breakpoint of the 4977-bp deletion of human mitochondrial DNA are located between two bent-inducing DNA sequences that assume distorted structure in organello
  196. Independent occurrence of somatic mutations in mitochondrial DNA of human skin from subjects of various ages
  197. Oxidative Stress and Mitochondrial DNA Mutations in Human Aging
  198. Role of mitochondria in human aging
  199. In vitro and in vivo protective effect of honokiol on rat liver from peroxidative injury
  200. Prevalence of apolipoprotein E genotypes in ischaemic cerebrovascular disease in end-stage renal disease patients
  201. Phenytoin-mediated oxidative stress in serum of female epileptics: A possible pathogenesis in the fetal hydantoin syndrome
  202. Smoking-associated mitochondrial DNA mutations in human hair follicles
  203. Peripheral Neuropathy in Mitochondrial Encephalomyopathies
  204. Leigh syndrome associated with mitochondrial DNA 8993 T → G mutation and ragged-red fibers
  205. Simultaneous Increase of Mitochondrial DNA Deletions and Lipid Peroxidation in Human Aging
  206. Tissue distribution of mutant mitochondrial DNA in a patient with MERRF syndrome
  207. Compensatory elevation of complex II activity in Leber's hereditary optic neuropathy.
  208. Defective mitochondrial oxidative phosphorylation in varicocele-bearinc testicles
  209. The 4977 bp deletion of mitochondrial DNA may contribute to diminished human sperm fertility.
  210. Human Skin Mitochondrial DNA Deletions Associated with Light Exposure
  211. A specific 4977-bp deletion of mitochondrial DNA in human ageing skin
  212. MELAS syndrome with mitochondrial tRNA(Leu(UUR)) gene mutation in a Chinese family.
  213. Differential accumulations of 4,977 bp deletion in mitochondrial DNA of various tissues in human ageing
  214. Age-dependent increase of mitochondrial DNA deletions together with lipid peroxides and superoxide dismutase in human liver mitochondria
  215. Astragalus Membranaceus and Polygonum Multijlorum Protect Rat Heart Mitochondria Against Lipid Peroxidation
  216. Ophthalmologic Manifestations in MELAS Syndrome
  217. Our team discovered that mitochondrial DNA mutations accumulate in human aging tissues.
  218. Production of cellulolytic enzymes from theXylaria andHypoxylon species of xylariaceae
  219. Ageing-associated 5 kb deletion in human liver mitochondrial DNA
  220. Human Follicular Fluid Stimulates the Motility of Washed Human Sperm
  221. Effect of Emitted Bioenergy on Biochemical Functions of Cells
  222. Immobilized enzyme system for determination of sialic acid in serum or urine
  223. Liver mitochondrial respiratory functions decline with age
  224. Comparative Study on Biochemical Effects of Alcohols on Rat Liver Mitochondrial Respiration and Oxidative Phosphorylation
  225. Stabilized ubisemiquinone in reconstituted succinate ubiquinone reductase
  226. Biochemical Characterization of Boar Sperm Cytochrome Oxidase
  227. Isolation, purification, and properties of boar sperm cytochrome oxidase
  228. The inhibitory effect of some ionophores on human sperm motility
  229. Inhibitory effect in vitro of PR toxin, a mycotoxin from Penicillium roqueforti, on the mitochondrial HCO3−-ATPase of the rat brain, heart and kidney
  230. Effect of ochratoxin A on rat liver mitochondrial respiration and oxidative phosphorylation
  231. Involvement of calcium in the caffeine stimulation of human sperm motility.
  232. Inhibition of the mitochondrial Mg2+-ATPase by propranolol
  233. Activities of Transport Adenosine Triphosphatases in Erythrocyte Membranes of Healthy and Hypertensive Subjects
  234. Calcium antagonists stimulate sperm motility in ejaculated human semen.
  235. CALCIUM CHELATORS STIMULATE SPERM MOTILITY IN EJACULATED HUMAN SEMEN
  236. Electron paramagnetic resonance- (EPR-) resolved kinetics of cryogenic nitric oxide recombination to cytochrome c oxidase and myoglobin
  237. Mitochondrial respiration inhibitors and human sperm motility: implication in the development of spermicides.
  238. ChemInform Abstract: RESONANCE RAMAN AND ELECTRONIC SPECTRA OF HEME A COMPLEXES AND CYTOCHROME OXIDASE
  239. Amino acid sequence of bovine heart cytochrome oxidase subunit IV (Albany)
  240. Effect of Phospholipid on EPR Visible Copper Signal of Cytochrome Oxidase
  241. Epr and Endor of NO-Ligated Cytochrome c Oxidase
  242. The effect of phospholipid depletion on the EPR behavior of cytochrome oxidase
  243. Ubisemiquinone radicals from the cytochrome b−c1 complex of the mitochondrial electron transport chain—Demonstration of QP-S radical formation
  244. Electron nuclear double resonance of cytochrome oxidase: Nitrogen and proton endor from the ‘copper’ EPR signal
  245. ELECTRON NUCLEAR DOUBLE RESONANCE OF CYTOCHROME OXIDASE
  246. Amino acid sequence of the heme a subunit of bovine heart cytochrome oxidase and sequence homology with hemoglobin