Pages that link to "Q34044264"
Jump to navigation
Jump to search
The following pages link to Random genetic drift determines the level of mutant mtDNA in human primary oocytes (Q34044264):
Displaying 50 items.
- Preimplantation genetic diagnosis for mitochondrial DNA disorders: ethical guidance for clinical practice (Q24599498) (← links)
- Mitochondrial DNA mutations in human disease (Q24676881) (← links)
- Germline energetics, aging, and female infertility (Q26861413) (← links)
- Evolutionary defined role of the mitochondrial DNA in fertility, disease and ageing (Q27024089) (← links)
- Strong purifying selection in transmission of mammalian mitochondrial DNA (Q27333828) (← links)
- Mitochondrial DNA disease and developmental implications for reproductive strategies (Q28649392) (← links)
- External contamination in single cell mtDNA analysis (Q33292683) (← links)
- Fluorescent duplex allele-specific PCR and amplicon melting for rapid homogeneous mtDNA haplogroup H screening and sensitive mixture detection (Q33519569) (← links)
- A wide range of 3243A>G/tRNALeu(UUR) (MELAS) mutation loads may segregate in offspring through the female germline bottleneck (Q33578068) (← links)
- Transmission of mitochondrial DNA diseases and ways to prevent them. (Q33658696) (← links)
- Previous estimates of mitochondrial DNA mutation level variance did not account for sampling error: comparing the mtDNA genetic bottleneck in mice and humans (Q33772977) (← links)
- Evolutionary toxicology: contaminant-induced genetic mutations in mosquitofish from Sumgayit, Azerbaijan (Q33818295) (← links)
- The strength and timing of the mitochondrial bottleneck in salmon suggests a conserved mechanism in vertebrates (Q33927048) (← links)
- PGD and heteroplasmic mitochondrial DNA point mutations: a systematic review estimating the chance of healthy offspring (Q34264208) (← links)
- Mitochondrial disorders: genetics, counseling, prenatal diagnosis and reproductive options. (Q34386775) (← links)
- Three-parent in vitro fertilization: gene replacement for the prevention of inherited mitochondrial diseases (Q34395166) (← links)
- Gene therapy for the treatment of mitochondrial DNA disorders (Q34401459) (← links)
- Mitochondrial replacement: from basic research to assisted reproductive technology portfolio tool-technicalities and possible risks. (Q34449553) (← links)
- The transmission of mitochondrial DNA following assisted reproductive techniques (Q34484088) (← links)
- Segregation of mtDNA throughout human embryofetal development: m.3243A>G as a model system (Q34677878) (← links)
- Neutral mitochondrial heteroplasmy and the influence of aging (Q34718136) (← links)
- A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes (Q34742495) (← links)
- Poor correlations in the levels of pathogenic mitochondrial DNA mutations in polar bodies versus oocytes and blastomeres in humans. (Q34768360) (← links)
- Mitochondrial nucleoids maintain genetic autonomy but allow for functional complementation (Q34788426) (← links)
- Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotype (Q35606234) (← links)
- Mitochondrial disease: clinical aspects, molecular mechanisms, translational science, and clinical frontiers. (Q35997215) (← links)
- Variation in germline mtDNA heteroplasmy is determined prenatally but modified during subsequent transmission (Q36382138) (← links)
- Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneck (Q36581411) (← links)
- Mitochondrial DNA and the mammalian oocyte. (Q36707790) (← links)
- Selection against pathogenic mtDNA mutations in a stem cell population leads to the loss of the 3243A-->G mutation in blood (Q36719116) (← links)
- Transmission of human mtDNA heteroplasmy in the Genome of the Netherlands families: support for a variable-size bottleneck (Q36756740) (← links)
- Attitudes toward prevention of mtDNA-related diseases through oocyte mitochondrial replacement therapy (Q36823140) (← links)
- Modifying the Mitochondrial Genome (Q36894373) (← links)
- The distribution of mitochondrial DNA heteroplasmy due to random genetic drift (Q37156189) (← links)
- Protein kinase Cδ upregulation in microglia drives neuroinflammatory responses and dopaminergic neurodegeneration in experimental models of Parkinson's disease. (Q37198050) (← links)
- Mitochondrial DNA genetics and the heteroplasmy conundrum in evolution and disease. (Q37258708) (← links)
- The inheritance of pathogenic mitochondrial DNA mutations (Q37419954) (← links)
- mtDNA mutations variously impact mtDNA maintenance throughout the human embryofetal development (Q38293604) (← links)
- Preventing the transmission of mitochondrial DNA disorders using prenatal or preimplantation genetic diagnosis (Q38574817) (← links)
- Concise Review: Heteroplasmic Mitochondrial DNA Mutations and Mitochondrial Diseases: Toward iPSC-Based Disease Modeling, Drug Discovery, and Regenerative Therapeutics (Q38724510) (← links)
- Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutations. (Q38727568) (← links)
- Genetic Counselling for Maternally Inherited Mitochondrial Disorders. (Q39325696) (← links)
- Inheritance of mitochondrial disorders (Q40394628) (← links)
- Mitochondrial DNA mutation load: chance or destiny? (Q42409243) (← links)
- Analysis of mtDNA variant segregation during early human embryonic development: a tool for successful NARP preimplantation diagnosis (Q43146786) (← links)
- Tissue specific distribution of the 3243A->G mtDNA mutation. (Q43169874) (← links)
- Stability of the m.8993T->G mtDNA mutation load during human embryofetal development has implications for the feasibility of prenatal diagnosis in NARP syndrome (Q43232425) (← links)
- A novel mitochondrial tRNA(Leu(UUR)) mutation in a patient with features of MERRF and Kearns-Sayre syndrome (Q44516814) (← links)
- Mitochondrial DNA, nuclear context, and the risk for carcinogenesis (Q48247976) (← links)
- A systematic analysis of the suitability of preimplantation genetic diagnosis for mitochondrial diseases in a heteroplasmic mitochondrial mouse model. (Q48608470) (← links)