| P2093 | author name string | Salvatore Alesci | |
| | Yan A Su | |
| | Daniel S Johnston | |
| P2860 | cites work | Normal oxidative damage to mitochondrial and nuclear DNA is extensive | Q24649831 |
| | Frequency and phenotypic implications of mitochondrial DNA mutations in human squamous cell cancers of the head and neck | Q24674610 |
| | INTRAMITOCHONDRIAL FIBERS WITH DNA CHARACTERISTICS. I. FIXATION AND ELECTRON STAINING REACTIONS | Q24683004 |
| | Sequence and organization of the human mitochondrial genome | Q27860659 |
| | Sequence analysis of cDNAs for the human and bovine ATP synthase beta subunit: mitochondrial DNA genes sustain seventeen times more mutations | Q28283523 |
| | Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy | Q28292821 |
| | A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine | Q29547303 |
| | Dysfunction of mitochondria in human skeletal muscle in type 2 diabetes | Q29616567 |
| | Genome-wide expression profiling of mid-gestation placenta and embryo using a 15,000 mouse developmental cDNA microarray | Q30892639 |
| | Development of mitochondria-specific mouse oligonucleotide microarray and validation of data by real-time PCR. | Q31113739 |
| | Workgroup report: Review of genomics data based on experience with mock submissions--view of the CDER Pharmacology Toxicology Nonclinical Pharmacogenomics Subcommittee | Q33238356 |
| | Development of a human mitochondrial oligonucleotide microarray (h-MitoArray) and gene expression analysis of fibroblast cell lines from 13 patients with isolated F1Fo ATP synthase deficiency. | Q33316556 |
| | Facile whole mitochondrial genome resequencing from nipple aspirate fluid using MitoChip v2.0. | Q33327587 |
| | Mitochondrial medicine--recent advances | Q33711128 |
| | Glucocorticoids and muscle catabolism | Q33716942 |
| | Mitochondrial myopathies and encephalomyopathies | Q33785697 |
| | Mitochondrial DNA haplogroups influence the therapeutic response to riboflavin in migraineurs. | Q34017384 |
| | Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions | Q34082583 |
| | The contribution of mitochondria to common disorders | Q34271106 |
| | Mitochondria as a pharmacological target | Q34547399 |
| | Mitochondrial functions and aging | Q34594198 |
| | Comparison of the cytotoxicity of the nitroaromatic drug flutamide to its cyano analogue in the hepatocyte cell line TAMH: evidence for complex I inhibition and mitochondrial dysfunction using toxicogenomic screening | Q34663837 |
| | Mitochondrial abnormalities in muscle and other aging cells: classification, causes, and effects | Q34981294 |
| | Searching for nuclear-mitochondrial genes | Q35053411 |
| | Mitochondrial DNA mutations in preneoplastic lesions of the gastrointestinal tract: a biomarker for the early detection of cancer | Q35574219 |
| | DNA microarrays as a tool in toxicogenomics | Q35768455 |
| | An oligonucleotide microarray for high-throughput sequencing of the mitochondrial genome | Q35790280 |
| | Toxicogenomics in drug discovery: from preclinical studies to clinical trials | Q35937248 |
| | A focused microarray to study human mitochondrial and nuclear gene expression. | Q36683816 |
| | Stage-specific gene expression is a fundamental characteristic of rat spermatogenic cells and Sertoli cells | Q36751491 |
| | Dysregulated mitochondrial genes and networks with drug targets in postmortem brain of patients with posttraumatic stress disorder (PTSD) revealed by human mitochondria-focused cDNA microarrays. | Q36817945 |
| | Replication and Transcription of Vertebrate Mitochondrial DNA | Q37037905 |
| | Mitochondrial genome analysis in biofluids for early cancer detection and monitoring | Q38089732 |
| | MITOCHIP assessment of differential gene expression in the skeletal muscle of Ant1 knockout mice: coordinate regulation of OXPHOS, antioxidant, and apoptotic genes | Q39444118 |
| | Third-generation human mitochondria-focused cDNA microarray and its bioinformatic tools for analysis of gene expression. | Q40153318 |
| | The rat epididymal transcriptome: comparison of segmental gene expression in the rat and mouse epididymides | Q40260520 |
| | A DNA microarray system for forensic SNP analysis | Q40386241 |
| | Metabolic coupling factors in pancreatic beta-cell signal transduction | Q40422075 |
| | The Human MitoChip: a high-throughput sequencing microarray for mitochondrial mutation detection. | Q40559987 |
| | Human mitochondrial complex I deficiency: investigating transcriptional responses by microarray. | Q40656228 |
| | Mitochondrial dysfunction in neurodegenerative disorders | Q40845642 |
| | Nucleoside reverse transcriptase inhibitors (NRTIs)-induced expression profile of mitochondria-related genes in the mouse liver | Q44005668 |
| | Chronic corticosteroid administration causes mitochondrial dysfunction in skeletal muscle | Q44114055 |
| | Identifying toxic mechanisms using DNA microarrays: evidence that an experimental inhibitor of cell adhesion molecule expression signals through the aryl hydrocarbon nuclear receptor | Q44264860 |
| | Possible relationship between mitochondrial DNA polymorphisms and lithium response in bipolar disorder | Q44646535 |
| | Gene expression profiles of transcripts in amyloid precursor protein transgenic mice: up-regulation of mitochondrial metabolism and apoptotic genes is an early cellular change in Alzheimer's disease. | Q44872334 |
| | A century of mitochondrial research: achievements and perspectives | Q46535835 |
| | Development of a toxicogenomics in vitro assay for the efficient characterization of compounds | Q46974118 |
| | Transcriptome analysis reveals link between proteasomal and mitochondrial pathways in Parkinson's disease. | Q48540299 |
| | Mitochondrial resequencing arrays detect tumor-specific mutations in salivary rinses of patients with head and neck cancer. | Q51898098 |
| | Accessing genetic information with high-density DNA arrays. | Q52293633 |
| | Mitochondrial DNA control region sequence variation in migraine headache and cyclic vomiting syndrome. | Q52967316 |
| | Transcriptional profiling for understanding the basis of mitochondrial involvement in disease and toxicity using the mitochondria-specific MitoChip. | Q53582315 |
| | Mitochondrial DNA haplogroups: role in the prevalence and severity of knee osteoarthritis. | Q54522179 |
| | A microarray system for genotyping 150 single nucleotide polymorphisms in the coding region of human mitochondrial DNA. | Q54623162 |
| | Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies | Q59055292 |
| P433 | issue | 10 | |
| P921 | main subject | mitochondrion | Q39572 |
| P304 | page(s) | 1645-1655 | |
| P577 | publication date | 2009-10-01 | |
| P1433 | published in | Pharmacogenomics | Q15724625 |
| P1476 | title | Mitochondrial gene profiling: translational perspectives | |
| P478 | volume | 10 | |