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

S Tomatsu

Showing results (1-10 of 108) with videos related to

Pageof 11
Sort By:
Surgical Endoscopy|January 1, 1987
The response to medical litholytic treatment of gallstones according to their specific gravityS Tomatsu
Ryoikibetsu Shokogun Shirizu|June 30, 1998
[Mucopolysaccharidosis type IV (Morquio syndrome, beta-galactosidase deficiency)]K Sukegawa, S Tomatsu, N Kondo, et al.
Ryoikibetsu Shokogun Shirizu|June 30, 1998
[Mucopolysaccharidosis type VII (Sly disease)]K Sukegawa, S Tomatsu, N Kondo, et al.
Ryoikibetsu Shokogun Shirizu|June 30, 1998
[Mucopolysaccharidosis type I (Hurler syndrome, Scheie syndrome)]K Sukegawa, S Tomatsu, N Kondo, et al.
Ryoikibetsu Shokogun Shirizu|June 30, 1998
[Mucopolysaccharidosis type III (Sanfilippo syndrome)]K Sukegawa, S Tomatsu, N Kondo, et al.
Ryoikibetsu Shokogun Shirizu|June 30, 1998
[Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome)]K Sukegawa, S Tomatsu, N Kondo, et al.
Ryoikibetsu Shokogun Shirizu|June 30, 1998
[Mucopolysaccharidosis type II (Hunter syndrome)]K Sukegawa, S Tomatsu, N Kondo, et al.
Human Genetics|January 1, 1990
Non-existence of a tight association between a 444leucine to proline mutation and phenotypes of Gaucher disease: high frequency of a NciI polymorphism in the non-neuronopathic formM Masuno, S Tomatsu, K Sukegawa, et al.
Nihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1995
[Mucopolysaccharidoses]S Fukuda, K Sukegawa, S Tomatsu, et al.
Cell Structure and Function|April 1, 1992
Optimization of electroporation for transfection of human fibroblast cell lines with origin-defective SV40 DNA: development of human transformed fibroblast cell lines with mucopolysaccharidoses (I-VII)H Okamoto, K Sukegawa, S Tomatsu, et al.
Pageof 11

Showing results (1-10 of 108) with videos related to

Sort By:
Pageof 11
Surgical Endoscopy|January 1, 1987
The response to medical litholytic treatment of gallstones according to their specific gravityS Tomatsu
Ryoikibetsu Shokogun Shirizu|June 30, 1998
[Mucopolysaccharidosis type IV (Morquio syndrome, beta-galactosidase deficiency)]K Sukegawa, S Tomatsu, N Kondo, et al.
Ryoikibetsu Shokogun Shirizu|June 30, 1998
[Mucopolysaccharidosis type VII (Sly disease)]K Sukegawa, S Tomatsu, N Kondo, et al.
Ryoikibetsu Shokogun Shirizu|June 30, 1998
[Mucopolysaccharidosis type I (Hurler syndrome, Scheie syndrome)]K Sukegawa, S Tomatsu, N Kondo, et al.
Ryoikibetsu Shokogun Shirizu|June 30, 1998
[Mucopolysaccharidosis type III (Sanfilippo syndrome)]K Sukegawa, S Tomatsu, N Kondo, et al.
Ryoikibetsu Shokogun Shirizu|June 30, 1998
[Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome)]K Sukegawa, S Tomatsu, N Kondo, et al.
Ryoikibetsu Shokogun Shirizu|June 30, 1998
[Mucopolysaccharidosis type II (Hunter syndrome)]K Sukegawa, S Tomatsu, N Kondo, et al.
Human Genetics|January 1, 1990
Non-existence of a tight association between a 444leucine to proline mutation and phenotypes of Gaucher disease: high frequency of a NciI polymorphism in the non-neuronopathic formM Masuno, S Tomatsu, K Sukegawa, et al.
Nihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1995
[Mucopolysaccharidoses]S Fukuda, K Sukegawa, S Tomatsu, et al.
Cell Structure and Function|April 1, 1992
Optimization of electroporation for transfection of human fibroblast cell lines with origin-defective SV40 DNA: development of human transformed fibroblast cell lines with mucopolysaccharidoses (I-VII)H Okamoto, K Sukegawa, S Tomatsu, et al.
Pageof 11