Manabu T. Nakamura

Molecular Biology · 2004–2014

A researcher in the Science corpus: 2 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.

Subfields

Whom Manabu T. Nakamura trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

  1. C. Funk
  2. Jiandie D. Lin
  3. Toshimasa Yamauchi
  4. Matthew J. Potthoff
  5. Jay D. Horton
  6. J. Repa
  7. Christoph Handschin
  8. E. Olson
  9. E. Rosen
  10. R. Bassel-Duby

Papers from Manabu T. Nakamura's perspective

Ordered by how strongly the researchers Manabu T. Nakamura trusts endorse each paper. Same corpus, a different order for every researcher.

  1. Restoration of insulin-sensitive glucose transporter (GLUT4) gene expression in muscle cells by the transcriptional coactivator PGC-1 (Proceedings of the National Academy of Sciences of the United States of America)
  2. Proteolytic cleavage product of 30-kDa adipocyte complement-related protein increases fatty acid oxidation in muscle and causes weight loss in mice. (Proceedings of the National Academy of Sciences of the United States of America)
  3. Transcriptional co-activator PGC-1 alpha drives the formation of slow-twitch muscle fibres. (Nature)
  4. Disruption of Adiponectin Causes Insulin Resistance and Neointimal Formation* (Journal of Biological Chemistry)
  5. The estrogen-related receptor alpha (ERRalpha) functions in PPARgamma coactivator 1alpha (PGC-1alpha)-induced mitochondrial biogenesis. (Proceedings of the National Academy of Sciences of the United States of America)
  6. Cloning of adiponectin receptors that mediate antidiabetic metabolic effects (Nature)
  7. Diet-induced insulin resistance in mice lacking adiponectin/ACRP30 (Nature Medicine)
  8. Adiponectin stimulates glucose utilization and fatty-acid oxidation by activating AMP-activated protein kinase (Nature Medicine)
  9. Targeted disruption of AdipoR1 and AdipoR2 causes abrogation of adiponectin binding and metabolic actions (Nature Medicine)
  10. Insulin-regulated hepatic gluconeogenesis through FOXO1-PGC-1alpha interaction. (Nature)

Their papers