Miki Nakajima

What is she best known for?

The fields of study she is best known for:

• Enzyme
• Gene
• DNA

Molecular biology, Biochemistry, Cytochrome P450, Pharmacology and CYP2A6 are her primary areas of study. Her Molecular biology study combines topics from a wide range of disciplines, such as Luciferase, Three prime untranslated region, Messenger RNA, microRNA and Regulation of gene expression. Her Cytochrome P450 research includes elements of Metabolite, Isozyme and In vivo.

Her work is dedicated to discovering how Pharmacology, CYP2B6 are connected with Enzyme inhibitor and Drug interaction and other disciplines. Her CYP2A6 research is multidisciplinary, relying on both Estrogen-related receptor alpha and Nicotine. Her Nicotine study integrates concerns from other disciplines, such as Pharmacogenetics and Allele, Allele frequency.

Her most cited work include:

• Cytochrome P450-mediated metabolism of estrogens and its regulation in human (407 citations)
• MicroRNA Regulates the Expression of Human Cytochrome P450 1B1 (335 citations)
• Genetic polymorphisms of human organic anion transporters OATP-C (SLC21A6) and OATP-B (SLC21A9): allele frequencies in the Japanese population and functional analysis. (288 citations)

What are the main themes of her work throughout her whole career to date?

Miki Nakajima mainly investigates Pharmacology, Biochemistry, Molecular biology, Microsome and Cytochrome P450. Her Pharmacology research incorporates elements of Hydrolase and Nicotine. Her works in Enzyme, Metabolite, Drug metabolism, Metabolism and Isozyme are all subjects of inquiry into Biochemistry.

The study incorporates disciplines such as Luciferase and Regulation of gene expression, Messenger RNA, Gene, microRNA in addition to Molecular biology. She has researched Microsome in several fields, including Endocrinology, Carboxylesterase and Internal medicine. Her Cytochrome P450 study frequently involves adjacent topics like In vivo.

She most often published in these fields:

• Pharmacology (33.60%)
• Biochemistry (28.34%)
• Molecular biology (25.10%)

What were the highlights of her more recent work (between 2014-2020)?

• microRNA (12.55%)
• Pharmacology (33.60%)
• Biochemistry (28.34%)

In recent papers she was focusing on the following fields of study:

Her primary areas of study are microRNA, Pharmacology, Biochemistry, Molecular biology and RNA editing. The microRNA study combines topics in areas such as Post-transcriptional regulation, Luciferase, HEK 293 cells, Toxicity and Single-nucleotide polymorphism. Her biological study spans a wide range of topics, including Microsome, Cytochrome P450 and Enzyme.

Hydrolase is closely connected to Carboxylesterase in her research, which is encompassed under the umbrella topic of Microsome. Her research is interdisciplinary, bridging the disciplines of Function and Biochemistry. Her Xenobiotic research focuses on Gene and how it relates to CYP2A6.

Between 2014 and 2020, her most popular works were:

• A-to-I RNA Editing Up-regulates Human Dihydrofolate Reductase in Breast Cancer (38 citations)
• RNA Editing Modulates Human Hepatic Aryl Hydrocarbon Receptor Expression by Creating MicroRNA Recognition Sequence (31 citations)
• CYP2A7 pseudogene transcript affects CYP2A6 expression in human liver by acting as a decoy for miR-126. (27 citations)

In her most recent research, the most cited papers focused on:

• Enzyme
• Gene
• DNA

Her primary scientific interests are in microRNA, Molecular biology, Biochemistry, Enzyme and Microsome. Her microRNA research integrates issues from ADAR, Bioinformatics, Post-transcriptional regulation, Luciferase and Untranslated region. Her research integrates issues of Gene knockdown, RNA, RNA editing, Messenger RNA and HEK 293 cells in her study of Molecular biology.

Her biological study deals with issues like CYP2A6, which deal with fields such as Gene. Her study in Biochemistry is interdisciplinary in nature, drawing from both Adduct and Drug development. Her studies in Microsome integrate themes in fields like Hydrolase, Carboxylesterase and Pharmacology.

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