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 Miyatake

Showing results (121-130 of 130) with videos related to

Pageof 13
Sort By:
You have reached the last page of results.This site can display upto 130 results.
Clinical Genetics|May 26, 2018
PRUNE1-related disorder: Expanding the clinical spectrumE Imagawa, Y Yamamoto, S Mitsuhashi, et al.
Sports Biomechanics|August 30, 2019
Different volumes and intensities of static stretching affect the range of motion and muscle force output in well-trained subjectsPaulo H Marchetti, Marcelo M S Miyatake, Roberto A Magalhaes, et al.
Cancer Gene Therapy|April 9, 1999
Experimental gene therapy against subcutaneously implanted glioma with a herpes simplex virus-defective vector expressing interferon-gammaH Kanno, S Hattori, H Sato, et al.
Clinical Genetics|February 27, 2016
Different X-linked KDM5C mutations in affected male siblings: is maternal reversion error involved?A Fujita, C Waga, Y Hachiya, et al.
Applied Radiation and Isotopes : Including Data, Instrumentation and Methods for Use in Agriculture, Industry and Medicine|March 4, 2011
Boron neutron capture therapy for clear cell sarcoma (CCS): biodistribution study of p-borono-L-phenylalanine in CCS-bearing animal modelsT Andoh, T Fujimoto, T Sudo, et al.
Clinical Genetics|May 22, 2018
Confirmation of SLC5A7-related distal hereditary motor neuropathy 7 in a family outside WalesK Hamanaka, K Takahashi, S Miyatake, et al.
Clinical Genetics|May 31, 2017
Novel biallelic SZT2 mutations in 3 cases of early-onset epileptic encephalopathyN Tsuchida, M Nakashima, A Miyauchi, et al.
Neurology|March 2, 2012
Homozygous c.14576G>A variant of RNF213 predicts early-onset and severe form of moyamoya diseaseS Miyatake, N Miyake, H Touho, et al.
Clinical Genetics|April 28, 2018
Genetic analysis of adult leukoencephalopathy patients using a custom-designed gene panelM Kunii, H Doi, Y Ishii, et al.
Clinical Genetics|September 24, 2017
Detection of copy number variations in epilepsy using exome dataN Tsuchida, M Nakashima, M Kato, et al.
Pageof 13

Showing results (121-130 of 130) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 130 results.
Clinical Genetics|May 26, 2018
PRUNE1-related disorder: Expanding the clinical spectrumE Imagawa, Y Yamamoto, S Mitsuhashi, et al.
Sports Biomechanics|August 30, 2019
Different volumes and intensities of static stretching affect the range of motion and muscle force output in well-trained subjectsPaulo H Marchetti, Marcelo M S Miyatake, Roberto A Magalhaes, et al.
Cancer Gene Therapy|April 9, 1999
Experimental gene therapy against subcutaneously implanted glioma with a herpes simplex virus-defective vector expressing interferon-gammaH Kanno, S Hattori, H Sato, et al.
Clinical Genetics|February 27, 2016
Different X-linked KDM5C mutations in affected male siblings: is maternal reversion error involved?A Fujita, C Waga, Y Hachiya, et al.
Applied Radiation and Isotopes : Including Data, Instrumentation and Methods for Use in Agriculture, Industry and Medicine|March 4, 2011
Boron neutron capture therapy for clear cell sarcoma (CCS): biodistribution study of p-borono-L-phenylalanine in CCS-bearing animal modelsT Andoh, T Fujimoto, T Sudo, et al.
Clinical Genetics|May 22, 2018
Confirmation of SLC5A7-related distal hereditary motor neuropathy 7 in a family outside WalesK Hamanaka, K Takahashi, S Miyatake, et al.
Clinical Genetics|May 31, 2017
Novel biallelic SZT2 mutations in 3 cases of early-onset epileptic encephalopathyN Tsuchida, M Nakashima, A Miyauchi, et al.
Neurology|March 2, 2012
Homozygous c.14576G>A variant of RNF213 predicts early-onset and severe form of moyamoya diseaseS Miyatake, N Miyake, H Touho, et al.
Clinical Genetics|April 28, 2018
Genetic analysis of adult leukoencephalopathy patients using a custom-designed gene panelM Kunii, H Doi, Y Ishii, et al.
Clinical Genetics|September 24, 2017
Detection of copy number variations in epilepsy using exome dataN Tsuchida, M Nakashima, M Kato, et al.
Pageof 13