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

M Shimadzu

Showing results (1-10 of 24) with videos related to

Pageof 3
Sort By:
Zeitschrift Fur Allgemeine Mikrobiologie|January 1, 1981
Characterization of a radiation-resistant AcinetobacterY Nishimura, E Kairiyama, M Shimadzu, et al.
Kansenshogaku Zasshi. the Journal of the Japanese Association for Infectious Diseases|February 1, 1996
[Development of multi-drug resistant mutants of clinical isolates of Pseudomonas aeruginosa after exposure to fluoroquinolone]M Hasegawa, I Kobayashi, T Saika, et al.
Biofactors (Oxford, England)|July 29, 2006
Estimation of plasma and saliva levels of coenzyme Q10 and influence of oral supplementationK Sekine, N Ota, M Nishii, et al.
American Journal of Medical Genetics|June 19, 1998
Oculocerebrorenal syndrome of Lowe: three mutations in the OCRL1 gene derived from three patients with different phenotypesT Kawano, Y Indo, H Nakazato, et al.
Neurology|February 13, 2001
Dopa-responsive dystonia simulating spastic paraplegia due to tyrosine hydroxylase (TH) gene mutationsY Furukawa, W D Graf, H Wong, et al.
The Journal of Antimicrobial Chemotherapy|June 6, 2000
Comparison of gyrA and parC mutations and resistance levels among fluoroquinolone-resistant isolates and laboratory-derived mutants of oral streptococciA Kaneko, J Sasaki, M Shimadzu, et al.
Kidney International|August 1, 2000
Clinical and genetic studies of CLCN5 mutations in Japanese families with Dent's diseaseT Igarashi, J Inatomi, T Ohara, et al.
American Journal of Medical Genetics|August 23, 1996
Prenatal monitoring in a family at high risk for ornithine transcarbamylase (OTC) deficiency: a new mutation of an A-to-C transversion in position +4 of intron 1 of the OTC gene that is likely to abolish enzyme activityR Hoshide, T Matsuura, Y Sagara, et al.
Biochimica Et Biophysica Acta|January 2, 1995
Structural organization of the gene for CD40 ligand: molecular analysis for diagnosis of X-linked hyper-IgM syndromeM Shimadzu, H Nunoi, H Terasaki, et al.
International Journal of Hematology|May 22, 1998
Recombinant adeno-associated virus-mediated gene transfer into human leukemia cell linesT Itou, K Miyamura, A Abe, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Zeitschrift Fur Allgemeine Mikrobiologie|January 1, 1981
Characterization of a radiation-resistant AcinetobacterY Nishimura, E Kairiyama, M Shimadzu, et al.
Kansenshogaku Zasshi. the Journal of the Japanese Association for Infectious Diseases|February 1, 1996
[Development of multi-drug resistant mutants of clinical isolates of Pseudomonas aeruginosa after exposure to fluoroquinolone]M Hasegawa, I Kobayashi, T Saika, et al.
Biofactors (Oxford, England)|July 29, 2006
Estimation of plasma and saliva levels of coenzyme Q10 and influence of oral supplementationK Sekine, N Ota, M Nishii, et al.
American Journal of Medical Genetics|June 19, 1998
Oculocerebrorenal syndrome of Lowe: three mutations in the OCRL1 gene derived from three patients with different phenotypesT Kawano, Y Indo, H Nakazato, et al.
Neurology|February 13, 2001
Dopa-responsive dystonia simulating spastic paraplegia due to tyrosine hydroxylase (TH) gene mutationsY Furukawa, W D Graf, H Wong, et al.
The Journal of Antimicrobial Chemotherapy|June 6, 2000
Comparison of gyrA and parC mutations and resistance levels among fluoroquinolone-resistant isolates and laboratory-derived mutants of oral streptococciA Kaneko, J Sasaki, M Shimadzu, et al.
Kidney International|August 1, 2000
Clinical and genetic studies of CLCN5 mutations in Japanese families with Dent's diseaseT Igarashi, J Inatomi, T Ohara, et al.
American Journal of Medical Genetics|August 23, 1996
Prenatal monitoring in a family at high risk for ornithine transcarbamylase (OTC) deficiency: a new mutation of an A-to-C transversion in position +4 of intron 1 of the OTC gene that is likely to abolish enzyme activityR Hoshide, T Matsuura, Y Sagara, et al.
Biochimica Et Biophysica Acta|January 2, 1995
Structural organization of the gene for CD40 ligand: molecular analysis for diagnosis of X-linked hyper-IgM syndromeM Shimadzu, H Nunoi, H Terasaki, et al.
International Journal of Hematology|May 22, 1998
Recombinant adeno-associated virus-mediated gene transfer into human leukemia cell linesT Itou, K Miyamura, A Abe, et al.
Pageof 3