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

Yoichi Matsubara

Showing results (91-100 of 165) with videos related to

Pageof 17
Sort By:
Stroke|May 19, 2007
Direct correlation between ischemic injury and extracellular glycine concentration in mice with genetically altered activities of the glycine cleavage multienzyme systemMasaya Oda, Shigeo Kure, Taku Sugawara, et al.
Pediatric Research|December 19, 2003
Long-term treatment and diagnosis of tetrahydrobiopterin-responsive hyperphenylalaninemia with a mutant phenylalanine hydroxylase geneHaruo Shintaku, Shigeo Kure, Toshihiro Ohura, et al.
Leukemia Research|May 18, 2012
Casitas B-cell lymphoma mutation in childhood T-cell acute lymphoblastic leukemiaYuka Saito, Yoko Aoki, Hideki Muramatsu, et al.
Annals of Neurology|April 25, 2006
Rapid diagnosis of glycine encephalopathy by 13C-glycine breath testShigeo Kure, Stanley H Korman, Junko Kanno, et al.
American Journal of Medical Genetics. Part A|February 24, 2015
Mutations in PIGL in a patient with Mabry syndromeIkuma Fujiwara, Yoshiko Murakami, Tetsuya Niihori, et al.
Journal of Human Genetics|March 1, 2013
Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failureRumiko Izumi, Tetsuya Niihori, Yoko Aoki, et al.
Journal of Human Genetics|July 18, 2019
Entire FGF12 duplication by complex chromosomal rearrangements associated with West syndromeYoichiro Oda, Yuri Uchiyama, Ai Motomura, et al.
The Journal of Clinical Endocrinology and Metabolism|June 3, 2016
Complex Genomic Rearrangement Within the GNAS Region Associated With Familial Pseudohypoparathyroidism Type 1bAkie Nakamura, Erika Hamaguchi, Reiko Horikawa, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|November 26, 2013
Hepatocyte transplantation using a living donor reduced graft in a baby with ornithine transcarbamylase deficiency: a novel source of hepatocytesShin Enosawa, Reiko Horikawa, Akiko Yamamoto, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|January 10, 2021
Guide for diagnosis and treatment of hyperphenylalaninemiaHaruo Shintaku, Toshihiro Ohura, Masaki Takayanagi, et al.
Pageof 17

Showing results (91-100 of 165) with videos related to

Sort By:
Pageof 17
Stroke|May 19, 2007
Direct correlation between ischemic injury and extracellular glycine concentration in mice with genetically altered activities of the glycine cleavage multienzyme systemMasaya Oda, Shigeo Kure, Taku Sugawara, et al.
Pediatric Research|December 19, 2003
Long-term treatment and diagnosis of tetrahydrobiopterin-responsive hyperphenylalaninemia with a mutant phenylalanine hydroxylase geneHaruo Shintaku, Shigeo Kure, Toshihiro Ohura, et al.
Leukemia Research|May 18, 2012
Casitas B-cell lymphoma mutation in childhood T-cell acute lymphoblastic leukemiaYuka Saito, Yoko Aoki, Hideki Muramatsu, et al.
Annals of Neurology|April 25, 2006
Rapid diagnosis of glycine encephalopathy by 13C-glycine breath testShigeo Kure, Stanley H Korman, Junko Kanno, et al.
American Journal of Medical Genetics. Part A|February 24, 2015
Mutations in PIGL in a patient with Mabry syndromeIkuma Fujiwara, Yoshiko Murakami, Tetsuya Niihori, et al.
Journal of Human Genetics|March 1, 2013
Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failureRumiko Izumi, Tetsuya Niihori, Yoko Aoki, et al.
Journal of Human Genetics|July 18, 2019
Entire FGF12 duplication by complex chromosomal rearrangements associated with West syndromeYoichiro Oda, Yuri Uchiyama, Ai Motomura, et al.
The Journal of Clinical Endocrinology and Metabolism|June 3, 2016
Complex Genomic Rearrangement Within the GNAS Region Associated With Familial Pseudohypoparathyroidism Type 1bAkie Nakamura, Erika Hamaguchi, Reiko Horikawa, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|November 26, 2013
Hepatocyte transplantation using a living donor reduced graft in a baby with ornithine transcarbamylase deficiency: a novel source of hepatocytesShin Enosawa, Reiko Horikawa, Akiko Yamamoto, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|January 10, 2021
Guide for diagnosis and treatment of hyperphenylalaninemiaHaruo Shintaku, Toshihiro Ohura, Masaki Takayanagi, et al.
Pageof 17