K. Nakamura

Publications88
h-index34
Citations5,421
Highly Influential Citations159
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The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans.
The metabolism of the anticonvulsant drug mephenytoin exhibits a genetic polymorphism in humans, with the poor metabolizer trait being inherited in an autosomal recessive fashion. There are large… Expand
Identification of a new genetic defect responsible for the polymorphism of (S)-mephenytoin metabolism in Japanese.
A genetic polymorphism in the metabolism of the anticonvulsant drug (S)-mephenytoin has been well documented in humans. There are marked interracial differences in the frequency of the poor… Expand
Propeptide of a precursor to a plant vacuolar protein required for vacuolar targeting.
Sporamin is a protein without glycans that accumulates in large quantities in the vacuoles of the tuberous root of the sweet potato. It is synthesized as a prepro precursor with an N-terminal… Expand
L-152,804: orally active and selective neuropeptide Y Y5 receptor antagonist.
Neuropeptide Y (NPY) elicits food intake through the action of hypothalamic G-protein-coupled receptors. Previous publications indicate that the Y5 receptor may represent one of these postulated… Expand
Proteome analysis of Bacillus subtilis extracellular proteins: a two-dimensional protein electrophoretic study.
To analyse the proteome of Bacillus subtilis extracellular proteins, extracellular protein samples were prepared from culture media (minimal medium containing 0.4% glucose) of parental B. subtilis… Expand
Cloning and sequencing of human LH/hCG receptor cDNA.
We have isolated and sequenced a cDNA encoding the human luteinizing hormone--choriogonadotropin (LH/hCG) receptor. The deduced amino acid sequence (699 residues) containing seven putative… Expand
Targeted disruption of exon 52 in the mouse dystrophin gene induced muscle degeneration similar to that observed in Duchenne muscular dystrophy.
Duchenne muscular dystrophy (DMD) is a degenerative disorder of the skeletal muscle in human and is caused by mutations in the dystrophin gene. The mdx mouse is a spontaneous mutant and an animal… Expand
The effect of Srb, a homologue of the mammalian SRP receptor alpha-subunit, on Bacillus subtilis growth and protein translocation.
To determine the signal recognition particle (SRP)-SRP receptor (Srb) system in Bacillus subtilis (Bs), we cloned the Bs srb gene, which encodes a homologue of the mammalian SRP receptor… Expand
The outer membrane proteins of Gram-negative bacteria: biosynthesis, assembly, and functions.
Cloning and characterization of a Bacillus subtilis gene homologous to E. coli secY.
A 3.5-kb HindIII DNA fragment containing the secY gene of Bacillus subtilis has been cloned into plasmid pUC13 using the Escherichia coli secY gene as a probe. The complete nucleotide sequence of the… Expand
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