Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

K Metoki

Showing results (1-10 of 12) with videos related to

Pageof 2
Sort By:
The International Journal of Biochemistry|January 1, 1984
A possible rate limiting factor in urea synthesis by isolated hepatocytes: the transport of ornithine into hepatocytes and mitochondriaK Metoki, F A Hommes
Journal of Inherited Metabolic Disease|January 1, 1984
The pH of mitochondria of fibroblasts from a hyperornithinaemia, hyperammonaemia, homocitrullinuria-syndrome patientK Metoki, F A Hommes
The International Journal of Biochemistry|January 1, 1984
The uptake of ornithine and lysine by isolated hepatocytes and fibroblastsK Metoki, F A Hommes
Advances in Experimental Medicine and Biology|January 1, 1982
A new method for screening of hyperammonemiaK Tada, H Tateda, K Metoki
Journal of Inherited Metabolic Disease|January 1, 1984
Ultrastructural changes in fibroblast mitochondria of a patient with HHH-syndromeK Metoki, F A Hommes, P Dyken, et al.
No to Shinkei = Brain and Nerve|August 1, 1982
[Familial nonprogressive chorea: report of four cases in a family]T Ito, H Suzuki, M Yamada, et al.
Enzyme|January 1, 1984
Further evidence for a separate enzymic entity for the synthesis of homocitrulline, distinct from the regular ornithine transcarbamylaseA L Carter, A G Eller, S Rufo, et al.
Neuropediatrics|February 1, 1986
Studies on a case of HHH-syndrome (hyperammonemia, hyperornithinemia, homocitrullinuria)F A Hommes, R A Roesel, K Metoki, et al.
The Tohoku Journal of Experimental Medicine|July 1, 1982
Comparison of cytosolic and mitochondrial enzyme alterations in the livers of propionic or methylmalonic acidemia: a reduction of cytochrome oxidase activityK Hayasaka, K Metoki, T Satoh, et al.
European Journal of Pediatrics|July 1, 1987
Partial ornithine transcarbamylase deficiency in females: diagnosis by an immunohistochemical methodK Hayasaka, K Metoki, S Ishiguro, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
The International Journal of Biochemistry|January 1, 1984
A possible rate limiting factor in urea synthesis by isolated hepatocytes: the transport of ornithine into hepatocytes and mitochondriaK Metoki, F A Hommes
Journal of Inherited Metabolic Disease|January 1, 1984
The pH of mitochondria of fibroblasts from a hyperornithinaemia, hyperammonaemia, homocitrullinuria-syndrome patientK Metoki, F A Hommes
The International Journal of Biochemistry|January 1, 1984
The uptake of ornithine and lysine by isolated hepatocytes and fibroblastsK Metoki, F A Hommes
Advances in Experimental Medicine and Biology|January 1, 1982
A new method for screening of hyperammonemiaK Tada, H Tateda, K Metoki
Journal of Inherited Metabolic Disease|January 1, 1984
Ultrastructural changes in fibroblast mitochondria of a patient with HHH-syndromeK Metoki, F A Hommes, P Dyken, et al.
No to Shinkei = Brain and Nerve|August 1, 1982
[Familial nonprogressive chorea: report of four cases in a family]T Ito, H Suzuki, M Yamada, et al.
Enzyme|January 1, 1984
Further evidence for a separate enzymic entity for the synthesis of homocitrulline, distinct from the regular ornithine transcarbamylaseA L Carter, A G Eller, S Rufo, et al.
Neuropediatrics|February 1, 1986
Studies on a case of HHH-syndrome (hyperammonemia, hyperornithinemia, homocitrullinuria)F A Hommes, R A Roesel, K Metoki, et al.
The Tohoku Journal of Experimental Medicine|July 1, 1982
Comparison of cytosolic and mitochondrial enzyme alterations in the livers of propionic or methylmalonic acidemia: a reduction of cytochrome oxidase activityK Hayasaka, K Metoki, T Satoh, et al.
European Journal of Pediatrics|July 1, 1987
Partial ornithine transcarbamylase deficiency in females: diagnosis by an immunohistochemical methodK Hayasaka, K Metoki, S Ishiguro, et al.
Pageof 2