Sentence examples for mitochondrial genetics and from inspiring English sources

To examine linkages between mitochondrial genetics and preterm birth by assessing the risk for preterm birth associated with the inheritance of nuclear haplotypes that are ancestrally distinct from mitochondrial haplogroup.

Mitochondrial genetics and nuclear genetics differ in several key ways.

The complex relationship between mitochondrial genetics and longevity has been further puzzled when somatic mtDNA variability is considered.

17 The identification of pathological mutations in the mtDNA can be unclear due to mitochondrial genetics and physiology.

Given the complexity of mitochondrial genetics and biochemistry, mitochondrial inherited diseases may present with a vast range of symptoms, organ involvement, severity, age of onset, and outcome.

Mitochondrial genetics and the degree of ATP production and oxidative reactive species as well as other undefined etiologies likely differentiate between onset and type of disorder.

We don't know the rules," says Douglas Wallace, a geneticist at the University of Pennsylvania, who has studied mitochondrial genetics for decades and was not involved in the new study.

In the past decade, there has been an explosion of scientific inquiry in the areas of mitochondrial genetics, cell biology and biochemistry [ 82].

Early investigations of single, large scale mitochondrial DNA deletion disease found little connection between mitochondrial genetics, biochemical defects and clinical phenotype (Zeviani et al., 1988; Holt et al., 1989; Moraes et al., 1989; Rotig et al., 1995).

Gene structure and function; the impact of mutation and polymorphism as they relate to developmental pathways and human disease; mitochondrial genetics; approaches to the study of complex genetic conditions; GWAS and genome sequencing technologies; variant interpretation; gene therapy, stem cell biology, and pharmacogenetics.

This diversity reaffirms the heterogeneity seen in the phenotype genotype relationship of mt-tRNA mutations, which arises due to the complex interactions between nuclear and mitochondrial genetics, the dramatic variations in tissue segregation of heteroplasmic mt-tRNA point mutations, and the threshold effect for pathogenicity.