scispace - formally typeset
J

James Scott

Researcher at Hammersmith Hospital

Publications -  69
Citations -  5931

James Scott is an academic researcher from Hammersmith Hospital. The author has contributed to research in topics: Apolipoprotein B & RNA editing. The author has an hindex of 33, co-authored 67 publications receiving 5780 citations. Previous affiliations of James Scott include Medical Research Council.

Papers
More filters
Journal ArticleDOI

An anthropoid-specific locus of orphan C to U RNA-editing enzymes on chromosome 22.

TL;DR: Tissue-specific expression of these genes in a variety of cell lines, along with other evidence, suggests a role for these enzymes in growth or cell cycle control, and similarity in amino acid sequence with APOBEC1, conserved intron/exon organization, tissue- specific expression, homodimerization, and zinc and RNA binding similar to APOB EC1 is concluded.
Journal ArticleDOI

The apolipoprotein B gene is constitutively expressed in HepG2 cells: regulation of secretion by oleic acid, albumin, and insulin, and measurement of the mRNA half-life.

TL;DR: It is concluded that the apoB gene is constitutively expressed in HepG2 cells and that the mechanism of acute regulation of apiB production by these cells must involve co- or post-translational processes.
Journal ArticleDOI

Yeast SNF1 is functionally related to mammalian AMP-activated protein kinase and regulates acetyl-CoA carboxylase in vivo

TL;DR: SNF1 undergoes a time-dependent increase in activity during growth in glucose-derepressing conditions, providing the first evidence that SNF1 activity is regulated by the level of available glucose.
Journal ArticleDOI

The p27 catalytic subunit of the apolipoprotein B mRNA editing enzyme is a cytidine deaminase.

TL;DR: It is concluded that p27 is the catalytic subunit of the apolipoprotein B mRNA editing enzyme and is a zinc-containing cytidine deaminase.
Journal ArticleDOI

The α1 and α2 isoforms of the AMP-activated protein kinase have similar activities in rat liver but exhibit differences in substrate specificity in vitro

TL;DR: It is shown that the αl‐ and α2‐containing complexes contribute approximately equally to total AMPK activity in rat liver, and that both complexes have equal specific activity measured with the SAMS peptide.