What is he best known for?
The fields of study he is best known for:
His primary areas of study are Mitochondrion, Mitochondrial biogenesis, Biochemistry, Endocrinology and Mitochondrial DNA.
His Mitochondrion research incorporates themes from Biogenesis, Gene family, mitochondrial fusion, Skeletal muscle and Metabolism.
His Mitochondrial biogenesis research is multidisciplinary, incorporating perspectives in Coactivator, PPARGC1A, Myogenesis, Muscle contraction and Citrate synthase.
His Citrate synthase research focuses on Sperm motility and how it connects with Ecology.
His study connects Energy metabolism and Biochemistry.
His studies deal with areas such as Receptor and Transfection as well as Endocrinology.
His most cited work include:
- Mitochondrial biogenesis during cellular differentiation (180 citations)
- Sperm swimming speed and energetics vary with sperm competition risk in bluegill (Lepomis macrochirus) (172 citations)
- Predicting Postrelease Survival in Large Pelagic Fish (142 citations)
What are the main themes of his work throughout his whole career to date?
Christopher D. Moyes spends much of his time researching Biochemistry, Mitochondrion, Citrate synthase, Cytochrome c oxidase and Endocrinology.
His Biochemistry study typically links adjacent topics like Osmoregulation.
Christopher D. Moyes studies Mitochondrion, namely Mitochondrial biogenesis.
His Citrate synthase study also includes fields such as
- Messenger RNA that connect with fields like Gene expression,
- Pyruvate kinase that intertwine with fields like Lepomis.
His study in Cytochrome c oxidase is interdisciplinary in nature, drawing from both Ecology, Molecular biology, Protein subunit and Mitochondrial DNA.
His Endocrinology research is multidisciplinary, relying on both Cell culture and Intracellular pH.
He most often published in these fields:
- Biochemistry (42.37%)
- Mitochondrion (26.27%)
- Citrate synthase (19.49%)
What were the highlights of his more recent work (between 2012-2021)?
- Comparative Biochemistry (5.08%)
- Cytochrome c oxidase (16.95%)
- Ecology (11.86%)
In recent papers he was focusing on the following fields of study:
His scientific interests lie mostly in Comparative Biochemistry, Cytochrome c oxidase, Ecology, Cold acclimation and Protein subunit.
The Cytochrome c oxidase study combines topics in areas such as Molecular genetics, Protein Biochemistry, Adaptation and Evolutionary biology.
His research integrates issues of Peptide sequence, Billfish, Fishery and Adenosine triphosphate in his study of Ecology.
In his study, which falls under the umbrella issue of Protein subunit, Gene and Mitochondrion is strongly linked to Energy metabolism.
Christopher D. Moyes has researched Mitochondrion in several fields, including Zoology and Endocrinology.
As part of his studies on Biochemistry, Christopher D. Moyes frequently links adjacent subjects like Function.
Between 2012 and 2021, his most popular works were:
- Sensing and responding to energetic stress: The role of the AMPK-PGC1α-NRF1 axis in control of mitochondrial biogenesis in fish ☆ (22 citations)
- Sensing and responding to energetic stress: Evolution of the AMPK network. (21 citations)
- Evolution of the oxygen sensitivity of cytochrome c oxidase subunit 4. (19 citations)
In his most recent research, the most cited papers focused on:
The scientist’s investigation covers issues in Ecology, Cytochrome c oxidase, Enzyme, AMPK and Biochemistry.
His Ecology research integrates issues from Isozyme, Billfish, Fishery and Binding site.
His studies in Cytochrome c oxidase integrate themes in fields like Evolutionary biology, Protein Biochemistry, Adaptation and Comparative Biochemistry.
His Enzyme research is multidisciplinary, incorporating elements of Molecular genetics, Computational biology, Phosphorylation and Effector.
The various areas that Christopher D. Moyes examines in his AMPK study include Zebrafish, Cold acclimation and NRF1, Mitochondrial biogenesis.
His Biochemistry study focuses mostly on Coactivator, AMP-activated protein kinase, Electron Transport Complex IV, Cysteine and Peptide sequence.
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