| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0091-679X(06)80024-5 |
| P698 | PubMed publication ID | 17445710 |
| P2093 | author name string | Carlos T Moraes | |
| Sion L Williams | |||
| P2860 | cites work | Principle and applications of digital PCR | Q28237698 |
| Quantitative amplification of genomic DNA from histological tissue sections after staining with nuclear dyes and laser capture microdissection | Q28354335 | ||
| High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease | Q29619113 | ||
| Mitochondrial DNA deletion mutations colocalize with segmental electron transport system abnormalities, muscle fiber atrophy, fiber splitting, and oxidative damage in sarcopenia | Q30649164 | ||
| Mitochondrial DNA deletion mutations are concomitant with ragged red regions of individual, aged muscle fibers: analysis by laser-capture microdissection | Q30760899 | ||
| Microdissection of histologic sections: past, present, and future | Q30844836 | ||
| Frequent mutations in the mitochondrial control region DNA in breast tissue | Q31112986 | ||
| A simple combined microdissection and aspiration device for the rapid procurement of single cells from clinical peripheral blood smears | Q31931772 | ||
| The laser in the Lowry technique for microdissection of freeze-dried tissue slices | Q32066517 | ||
| Detection of deleted mitochondrial DNA in Kearns-Sayre syndrome using laser capture microdissection. | Q33194853 | ||
| The increase of mitochondrial DNA content in endometrial adenocarcinoma cells: a quantitative study using laser-captured microdissected tissues | Q33215975 | ||
| Mitochondrial neurogastrointestinal encephalomyopathy: evidence of mitochondrial DNA depletion in the small intestine | Q33236131 | ||
| Loss of heterozygosity in lobular carcinoma in situ of the breast | Q33836982 | ||
| Double-strand breaks of mouse muscle mtDNA promote large deletions similar to multiple mtDNA deletions in humans | Q34062921 | ||
| Rapid directional shift of mitochondrial DNA heteroplasmy in animal tissues by a mitochondrially targeted restriction endonuclease | Q34063452 | ||
| Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation | Q34152888 | ||
| Mutant mitochondrial helicase Twinkle causes multiple mtDNA deletions and a late-onset mitochondrial disease in mice | Q34201844 | ||
| Single-sperm typing: determination of genetic distance between the G gamma-globin and parathyroid hormone loci by using the polymerase chain reaction and allele-specific oligomers | Q34323318 | ||
| Somatic mutations of the mitochondrial genome in human colorectal tumours | Q34478926 | ||
| Somatic mitochondrial DNA mutations in prostate cancer and normal appearing adjacent glands in comparison to age-matched prostate samples without malignant histology | Q35790237 | ||
| Two direct repeats cause most human mtDNA deletions | Q35864144 | ||
| Single-molecule PCR: an artifact-free PCR approach for the analysis of somatic mutations | Q36252221 | ||
| Mitochondrial DNA mutations in human colonic crypt stem cells | Q36524727 | ||
| Atypical ductal hyperplasia of the breast: clonal proliferation with loss of heterozygosity on chromosomes 16q and 17p. | Q37263268 | ||
| The determination of complete human mitochondrial DNA sequences in single cells: implications for the study of somatic mitochondrial DNA point mutations | Q39096996 | ||
| Detection and quantification of mitochondrial DNA deletions in individual cells by real-time PCR. | Q39681978 | ||
| Cell-by-cell scanning of whole mitochondrial genomes in aged human heart reveals a significant fraction of myocytes with clonally expanded deletions | Q39730030 | ||
| Recombination of mitochondrial DNA in skeletal muscle of individuals with multiple mitochondrial DNA heteroplasmy | Q41809981 | ||
| A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA. | Q41951578 | ||
| Myoclonic epilepsy and ragged red fibers (MERRF) syndrome: selective vulnerability of CNS neurons does not correlate with the level of mitochondrial tRNAlys mutation in individual neuronal isolates. | Q46607163 | ||
| Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons | Q48588748 | ||
| Somatic mitochondrial DNA mutations in single neurons and glia | Q48719653 | ||
| Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial disease | Q48933491 | ||
| Monoclonal Origin of Multicentric Kaposi's Sarcoma Lesions | Q58366797 | ||
| Repeat unit sequence variation in minisatellites: a novel source of DNA polymorphism for studying variation and mutation by single molecule analysis | Q68929075 | ||
| Phenotype-genotype correlations in skeletal muscle of patients with mtDNA deletions | Q71852983 | ||
| Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathy | Q72372563 | ||
| Quantification and sequencing of somatic deleted mtDNA in single cells: evidence for partially duplicated mtDNA in aged human tissues | Q73341946 | ||
| The dangers of extended PCR in the clinic | Q78199393 | ||
| MtDNA point mutations are associated with deletion mutations in aged rat | Q81513728 | ||
| P921 | main subject | microdissection | Q4293202 |
| P304 | page(s) | 481-501 | |
| P577 | publication date | 2007-01-01 | |
| P1433 | published in | Methods in Cell Biology | Q2638096 |
| P1476 | title | Microdissection and analytical PCR for the investigation of mtDNA lesions | |
| P478 | volume | 80 |
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