scholarly article | Q13442814 |
P356 | DOI | 10.1007/BF01560726 |
P698 | PubMed publication ID | 3003930 |
P2093 | author name string | Wallace DC | |
P2860 | cites work | Assignment of the chloramphenicol resistance gene to mitochondrial deoxyribonucleic acid and analysis of its expression in cultured human cells | Q36956970 |
Assignment of two mitochondrially synthesized polypeptides to human mitochondrial DNA and their use in the study of intracellular mitochondrial interaction | Q36970433 | ||
P433 | issue | 1 | |
P921 | main subject | chloramphenicol | Q274515 |
P304 | page(s) | 41-49 | |
P577 | publication date | 1986-01-01 | |
P1433 | published in | Somatic Cell and Molecular Genetics | Q7559232 |
P1476 | title | Mitotic segregation of mitochondrial DNAs in human cell hybrids and expression of chloramphenicol resistance. | |
P478 | volume | 12 |
Q35188343 | A review of primary hereditary optic neuropathies |
Q24677055 | Amerindian mitochondrial DNAs have rare Asian mutations at high frequencies, suggesting they derived from four primary maternal lineages |
Q36416150 | Deletion-mutant mtDNA increases in somatic tissues but decreases in female germ cells with age. |
Q35196308 | Distribution and threshold expression of the tRNA(Lys) mutation in skeletal muscle of patients with myoclonic epilepsy and ragged-red fibers (MERRF) |
Q36234091 | Human mitochondria and mitochondrial genome function as a single dynamic cellular unit |
Q34264417 | Human mitochondrial DNA diseases |
Q36689236 | In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria |
Q38642980 | In vivo mammalian mutagenesis: in transition to DNA molecules |
Q39991458 | Influence of mitochondrial DNA level on cellular energy metabolism: implications for mitochondrial diseases |
Q37258708 | Mitochondrial DNA genetics and the heteroplasmy conundrum in evolution and disease. |
Q37904334 | Mitochondrial DNA in sickness and in health |
Q43714643 | Mitochondrial DNA mutation in an Italian family with Leber hereditary optic neuropathy |
Q35744723 | Mitochondrial DNA sequence variation in human evolution and disease. |
Q28138400 | Mitochondrial DNA variation in human evolution and disease |
Q69487919 | Mitochondrial diseases |
Q41378809 | Mitochondrial diseases and aging. |
Q43146278 | Mitochondrial genetics: principles and practice |
Q35017647 | Mitochondrial threshold effects. |
Q67468907 | Molecular analysis of the muscle pathology associated with mitochondrial DNA deletions |
Q35944038 | Molecular genetic basis of primary inherited optic neuropathies. |
Q33659290 | ND4L gene concurrent 10609T>C and 10663T>C mutations are associated with Leber's hereditary optic neuropathy in a large pedigree from Kuwait |
Q37408409 | Neurometabolic disorders and dysfunction in autism spectrum disorders |
Q40560640 | Rapid detection of the A----G(8344) mutation of mtDNA in Italian families with myoclonus epilepsy and ragged-red fibers (MERRF). |
Q61797390 | Sequence analysis of a deleted mitochondrial DNA molecule in heteroplasmic mice |
Q42558990 | Single-cell analysis of intercellular heteroplasmy of mtDNA in Leber hereditary optic neuropathy. |
Q40953874 | Strategies and applications of DNA level diagnosis in genetic diseases: past experiences and future directions. |
Q46160032 | Targeted delivery of DNA to the mitochondrial compartment via import sequence-conjugated peptide nucleic acid |
Q52454076 | The generation of transplasmic Drosophila simulans by cytoplasmic injection: effects of segregation and selection on the perpetuation of mitochondrial DNA heteroplasmy. |
Q40405120 | The genetic basis of paediatric heart disease |
Q73084810 | The interorganellar interaction between distinct human mitochondria with deletion mutant mtDNA from a patient with mitochondrial disease and with HeLa mtDNA |
Q41717827 | Towards gene therapy of mitochondrial disorders |
Q41730723 | Variable genotype of Leber's hereditary optic neuropathy patients. |
Q32139005 | What do mitochondrial diseases teach us about normal mitochondrial functions...that we already knew: threshold expression of mitochondrial defects. |
Search more.