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 Matsuda

Showing results (161-170 of 603) with videos related to

Pageof 61
Sort By:
Journal of Pediatric Gastroenterology and Nutrition|January 1, 1987
Acarboxy prothrombin (PIVKA-II) as a marker of hepatoblastoma in infantsK Motohara, F Endo, I Matsuda, et al.
Journal of Inherited Metabolic Disease|January 1, 1986
Restriction fragment length polymorphisms in the 5' end region of the human argininosuccinate synthetase geneY Jinno, N Niikawa, K Shimada, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|September 1, 1988
Sequence heterogeneity of human liver arginase cDNAs and restriction fragment length polymorphism of the gene locusY Haraguchi, M Takiguchi, I Matsuda, et al.
Pediatric Research|December 1, 1987
Immunochemical studies of human prolidase with monoclonal and polyclonal antibodies: absence of the subunit of prolidase in erythrocytes from a patient with prolidase deficiencyF Endo, K Motohara, Y Indo, et al.
The Journal of Pediatrics|February 1, 1988
Zinc balance in premature infants given the minimal dietary zinc requirementA Higashi, T Ikeda, K Iribe, et al.
Nihon Funin Gakkai Zasshi|October 1, 1974
[208 case studies on Dalkon shield (author's transl)]T Kobayashi, H Tadano, I Matsuda, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 28, 1973
Alpha-L-fucosidase and alpha-D-mannosidase activity in the white blood cells in the disease and carrier state of fucosidosisI Matsuda, S Arashima, M Anakura, et al.
European Journal of Pediatrics|September 1, 1979
Response to transfer factor to immunodeficiency in handicaps treated with phenytoinT Ikeda, A Higashi, I Matsuda, et al.
Endocrinologia Japonica|February 1, 1985
The negative correlation between prolactin and ionic calcium in cord blood of full term infantsS Nishiyama, S Fujimoto, M Kodama, et al.
Genomics|January 1, 1995
A nonsense mutation in the 4-hydroxyphenylpyruvic acid dioxygenase gene (Hpd) causes skipping of the constitutive exon and hypertyrosinemia in mouse strain IIIF Endo, H Awata, H Katoh, et al.
Pageof 61

Showing results (161-170 of 603) with videos related to

Sort By:
Pageof 61
Journal of Pediatric Gastroenterology and Nutrition|January 1, 1987
Acarboxy prothrombin (PIVKA-II) as a marker of hepatoblastoma in infantsK Motohara, F Endo, I Matsuda, et al.
Journal of Inherited Metabolic Disease|January 1, 1986
Restriction fragment length polymorphisms in the 5' end region of the human argininosuccinate synthetase geneY Jinno, N Niikawa, K Shimada, et al.
Jinrui Idengaku Zasshi. the Japanese Journal of Human Genetics|September 1, 1988
Sequence heterogeneity of human liver arginase cDNAs and restriction fragment length polymorphism of the gene locusY Haraguchi, M Takiguchi, I Matsuda, et al.
Pediatric Research|December 1, 1987
Immunochemical studies of human prolidase with monoclonal and polyclonal antibodies: absence of the subunit of prolidase in erythrocytes from a patient with prolidase deficiencyF Endo, K Motohara, Y Indo, et al.
The Journal of Pediatrics|February 1, 1988
Zinc balance in premature infants given the minimal dietary zinc requirementA Higashi, T Ikeda, K Iribe, et al.
Nihon Funin Gakkai Zasshi|October 1, 1974
[208 case studies on Dalkon shield (author's transl)]T Kobayashi, H Tadano, I Matsuda, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 28, 1973
Alpha-L-fucosidase and alpha-D-mannosidase activity in the white blood cells in the disease and carrier state of fucosidosisI Matsuda, S Arashima, M Anakura, et al.
European Journal of Pediatrics|September 1, 1979
Response to transfer factor to immunodeficiency in handicaps treated with phenytoinT Ikeda, A Higashi, I Matsuda, et al.
Endocrinologia Japonica|February 1, 1985
The negative correlation between prolactin and ionic calcium in cord blood of full term infantsS Nishiyama, S Fujimoto, M Kodama, et al.
Genomics|January 1, 1995
A nonsense mutation in the 4-hydroxyphenylpyruvic acid dioxygenase gene (Hpd) causes skipping of the constitutive exon and hypertyrosinemia in mouse strain IIIF Endo, H Awata, H Katoh, et al.
Pageof 61