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

I Nonaka

Showing results (251-260 of 503) with videos related to

Pageof 51
Sort By:
Biological & Pharmaceutical Bulletin|January 5, 2002
Antiproliferative constituents in the plant 8. Seeds of Rhynchosia volubilisJ Kinjo, S Nagao, T Tanaka, et al.
Muscle & Nerve|November 1, 1992
An experimental model of mitochondrial myopathy: germanium-induced myopathy and coenzyme Q10 administrationC M Wu, T Matsuoka, M Takemitsu, et al.
Muscle & Nerve|November 1, 1991
Muscle histology in Becker muscular dystrophyM Kaido, K Arahata, E P Hoffman, et al.
Molecular Biology and Evolution|May 27, 2011
Retained orthologous relationships of the MHC Class I genes during euteleost evolutionMayumi I Nonaka, Kouichi Aizawa, Hiroshi Mitani, et al.
No to Hattatsu = Brain and Development|March 21, 2000
[A case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II)]M Tojo, T Gunji, S Yamaguchi, et al.
Journal of Biochemistry|July 1, 1983
Immunocytochemical localization of cathepsin B in degenerating rat skeletal muscle induced by a local anesthetic, bupivacaineS Ishiura, I Nonaka, H Nakase, et al.
Muscle & Nerve. Supplement|January 1, 1995
Mitochondrial DNA mutation and muscle pathology in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodesS Mita, M Tokunaga, T Kumamoto, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 30, 1995
Genetic analysis of Japanese patients with myophosphorylase deficiency (McArdle's disease): single-codon deletion in exon 17 is the predominant mutationH Sugie, Y Sugie, M Ito, et al.
Brain & Development|January 1, 1996
Long-term therapy with cytochrome c, flavin mononucleotide and thiamine diphosphate for a patient with Kearns-Sayre syndromeE Nakagawa, S Osari, H Yamanouchi, et al.
Rinsho Shinkeigaku = Clinical Neurology|February 1, 1994
[Dystrophin-related protein in diaphragm, limb and myoblast transferred muscles of mdx mouse]M Takemitsu, R Koga, S Ishiura, et al.
Pageof 51

Showing results (251-260 of 503) with videos related to

Sort By:
Pageof 51
Biological & Pharmaceutical Bulletin|January 5, 2002
Antiproliferative constituents in the plant 8. Seeds of Rhynchosia volubilisJ Kinjo, S Nagao, T Tanaka, et al.
Muscle & Nerve|November 1, 1992
An experimental model of mitochondrial myopathy: germanium-induced myopathy and coenzyme Q10 administrationC M Wu, T Matsuoka, M Takemitsu, et al.
Muscle & Nerve|November 1, 1991
Muscle histology in Becker muscular dystrophyM Kaido, K Arahata, E P Hoffman, et al.
Molecular Biology and Evolution|May 27, 2011
Retained orthologous relationships of the MHC Class I genes during euteleost evolutionMayumi I Nonaka, Kouichi Aizawa, Hiroshi Mitani, et al.
No to Hattatsu = Brain and Development|March 21, 2000
[A case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II)]M Tojo, T Gunji, S Yamaguchi, et al.
Journal of Biochemistry|July 1, 1983
Immunocytochemical localization of cathepsin B in degenerating rat skeletal muscle induced by a local anesthetic, bupivacaineS Ishiura, I Nonaka, H Nakase, et al.
Muscle & Nerve. Supplement|January 1, 1995
Mitochondrial DNA mutation and muscle pathology in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodesS Mita, M Tokunaga, T Kumamoto, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 30, 1995
Genetic analysis of Japanese patients with myophosphorylase deficiency (McArdle's disease): single-codon deletion in exon 17 is the predominant mutationH Sugie, Y Sugie, M Ito, et al.
Brain & Development|January 1, 1996
Long-term therapy with cytochrome c, flavin mononucleotide and thiamine diphosphate for a patient with Kearns-Sayre syndromeE Nakagawa, S Osari, H Yamanouchi, et al.
Rinsho Shinkeigaku = Clinical Neurology|February 1, 1994
[Dystrophin-related protein in diaphragm, limb and myoblast transferred muscles of mdx mouse]M Takemitsu, R Koga, S Ishiura, et al.
Pageof 51