K. Metoki

The pH of mitochondria of fibroblasts from a hyperornithinaemia, hyperammonaemia, homocitrullinuria-syndrome patient

K. Metoki, F. Hommes, 1984, Journal of Inherited Metabolic Disease.

A possible rate limiting factor in urea synthesis by isolated hepatocytes: the transport of ornithine into hepatocytes and mitochondria.

K. Metoki, F. Hommes, 1984, The International journal of biochemistry.

Ultrastructural changes in fibroblast mitochondria of a patient with HHH-syndrome

P. Dyken, J. Trefz, K. Metoki, 1984, Journal of Inherited Metabolic Disease.

Impact of fasting time on hepatic lipid metabolism in nutritional animal studies

T. Yanagita, H. Shirakawa, M. Komai, 2014, Bioscience, biotechnology, and biochemistry.

316 DEVELOPMENTAL COMPETENCE OF OOCYTES SELECTED BY THE BRILLIANT CRESYL BLUE STAINING IN PREPUBERTAL AND ADULT CATTLE

K. Imai, S. Matoba, K. Metoki, 2007 .

Studies on a case of HHH-syndrome (hyperammonemia, hyperornithinemia, homocitrullinuria).

P. Hartlage, P. Dyken, K. Metoki, 1986, Neuropediatrics.

The uptake of ornithine and lysine by isolated hepatocytes and fibroblasts.

K. Metoki, F. Hommes, 1984, The International journal of biochemistry.

Further evidence for a separate enzymic entity for the synthesis of homocitrulline, distinct from the regular ornithine transcarbamylase.

A. Eller, K. Metoki, F. Hommes, 1984, Enzyme.