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

T Orii

Showing results (231-240 of 276) with videos related to

Pageof 28
Sort By:
Clinical Genetics|June 1, 1991
Gene deletions in Japanese patients with Duchenne and Becker muscular dystrophies: deletion study and carrier detectionJ Asano, S Tomatsu, K Sukegawa, et al.
Pediatric Research|May 1, 1996
Correction by gene expression of biochemical abnormalities in fibroblasts from Zellweger patientsN Shimozawa, Y Suzuki, S Tomatsu, et al.
Scandinavian Journal of Immunology|October 1, 1993
Expression of secreted immunoglobulin heavy chain genes and immunoglobulin-secreting cells in human lymphocytesN Kondo, R Inoue, H Agata, et al.
Human Molecular Genetics|November 18, 1998
Temperature-sensitive mutation in PEX1 moderates the phenotypes of peroxisome deficiency disordersA Imamura, S Tamura, N Shimozawa, et al.
International Journal of Clinical Pharmacology and Therapeutics|November 1, 1994
The design of oral sustained-release theophylline dosing after conversion from intravenous to oral therapyM Yamazaki, O Fukutomi, N Kondo, et al.
Molecular Genetics and Metabolism|May 14, 2013
Review of clinical presentation and diagnosis of mucopolysaccharidosis IVAC J Hendriksz, P Harmatz, M Beck, et al.
Asian Pacific Journal of Allergy and Immunology|December 1, 1994
Sensitization to sugar cane pollen in Okinawan allergic childrenH Agata, N Kondo, A Yomo, et al.
Experimental and Clinical Immunogenetics|January 1, 1993
Defective calcium-dependent signal transduction in B lymphocytes of a certain common variable immunodeficiencyN Kondo, R Inoue, M Yano, et al.
Human Genetics|February 1, 1995
Polymerase chain reaction detection of two novel human N-acetylgalactosamine-6-sulfate sulfatase gene polymorphisms by single-strand conformation polymorphism analysis or by StyI and StuI cleavagesS Tomatsu, S Fukuda, A Uchiyama, et al.
Human Mutation|January 1, 1995
Molecular, biochemical, and clinical characterization of mitochondrial acetoacetyl-coenzyme A thiolase deficiency in two further patientsA Wakazono, T Fukao, S Yamaguchi, et al.
Pageof 28

Showing results (231-240 of 276) with videos related to

Sort By:
Pageof 28
Clinical Genetics|June 1, 1991
Gene deletions in Japanese patients with Duchenne and Becker muscular dystrophies: deletion study and carrier detectionJ Asano, S Tomatsu, K Sukegawa, et al.
Pediatric Research|May 1, 1996
Correction by gene expression of biochemical abnormalities in fibroblasts from Zellweger patientsN Shimozawa, Y Suzuki, S Tomatsu, et al.
Scandinavian Journal of Immunology|October 1, 1993
Expression of secreted immunoglobulin heavy chain genes and immunoglobulin-secreting cells in human lymphocytesN Kondo, R Inoue, H Agata, et al.
Human Molecular Genetics|November 18, 1998
Temperature-sensitive mutation in PEX1 moderates the phenotypes of peroxisome deficiency disordersA Imamura, S Tamura, N Shimozawa, et al.
International Journal of Clinical Pharmacology and Therapeutics|November 1, 1994
The design of oral sustained-release theophylline dosing after conversion from intravenous to oral therapyM Yamazaki, O Fukutomi, N Kondo, et al.
Molecular Genetics and Metabolism|May 14, 2013
Review of clinical presentation and diagnosis of mucopolysaccharidosis IVAC J Hendriksz, P Harmatz, M Beck, et al.
Asian Pacific Journal of Allergy and Immunology|December 1, 1994
Sensitization to sugar cane pollen in Okinawan allergic childrenH Agata, N Kondo, A Yomo, et al.
Experimental and Clinical Immunogenetics|January 1, 1993
Defective calcium-dependent signal transduction in B lymphocytes of a certain common variable immunodeficiencyN Kondo, R Inoue, M Yano, et al.
Human Genetics|February 1, 1995
Polymerase chain reaction detection of two novel human N-acetylgalactosamine-6-sulfate sulfatase gene polymorphisms by single-strand conformation polymorphism analysis or by StyI and StuI cleavagesS Tomatsu, S Fukuda, A Uchiyama, et al.
Human Mutation|January 1, 1995
Molecular, biochemical, and clinical characterization of mitochondrial acetoacetyl-coenzyme A thiolase deficiency in two further patientsA Wakazono, T Fukao, S Yamaguchi, et al.
Pageof 28