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 Tsuji

Showing results (951-960 of 990) with videos related to

Pageof 99
Sort By:
International Immunopharmacology|August 23, 2001
Interferon gamma-producing ability in blood lymphocytes of patients with lung cancer through activation of the innate immune system by BCG cell wall skeletonM Matsumoto, T Seya, S Kikkawa, et al.
International Journal for Equity in Health|January 23, 2025
We cannot repeat history again: a call to action to centre indigenous leadership as we prepare for the next pandemicKristy Crooks, Fatima Ahmed, Eric N Liberda, et al.
Genomics|May 23, 1998
A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17qT Ikeuchi, K Sanpei, H Takano, et al.
Brain : a Journal of Neurology|December 1, 1996
Clinical and molecular analysis of a large family with three distinct phenotypes of progressive muscular dystrophyS N Illarioshkin, I A Ivanova-Smolenskaya, H Tanaka, et al.
Environmental Science & Technology|December 24, 2009
Importance of considering the framework principles in risk assessment for metalsCharles A Menzie, Linda M Ziccardi, Yvette W Lowney, et al.
Human Molecular Genetics|July 7, 2001
Localization of a novel susceptibility gene for familial ovarian cancer to chromosome 3p22-p25M Sekine, H Nagata, S Tsuji, et al.
American Journal of Human Genetics|August 1, 1997
Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1K Ishikawa, H Tanaka, M Saito, et al.
Archives of Neurology|May 18, 2001
Spinocerebellar ataxia type 1 in China: molecular analysis and genotype-phenotype correlation in 5 familiesY X Zhou, W H Qiao, W H Gu, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 12, 2001
Mutational analysis of BRCA1 and BRCA2 and clinicopathologic analysis of ovarian cancer in 82 ovarian cancer families: two common founder mutations of BRCA1 in Japanese populationM Sekine, H Nagata, S Tsuji, et al.
Japanese Journal of Cancer Research : Gann|April 1, 1997
Mutational analysis of BRCA1 gene in ovarian and breast-ovarian cancer families in JapanM Takano, H Aida, I Tsuneki, et al.
Pageof 99

Showing results (951-960 of 990) with videos related to

Sort By:
Pageof 99
International Immunopharmacology|August 23, 2001
Interferon gamma-producing ability in blood lymphocytes of patients with lung cancer through activation of the innate immune system by BCG cell wall skeletonM Matsumoto, T Seya, S Kikkawa, et al.
International Journal for Equity in Health|January 23, 2025
We cannot repeat history again: a call to action to centre indigenous leadership as we prepare for the next pandemicKristy Crooks, Fatima Ahmed, Eric N Liberda, et al.
Genomics|May 23, 1998
A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17qT Ikeuchi, K Sanpei, H Takano, et al.
Brain : a Journal of Neurology|December 1, 1996
Clinical and molecular analysis of a large family with three distinct phenotypes of progressive muscular dystrophyS N Illarioshkin, I A Ivanova-Smolenskaya, H Tanaka, et al.
Environmental Science & Technology|December 24, 2009
Importance of considering the framework principles in risk assessment for metalsCharles A Menzie, Linda M Ziccardi, Yvette W Lowney, et al.
Human Molecular Genetics|July 7, 2001
Localization of a novel susceptibility gene for familial ovarian cancer to chromosome 3p22-p25M Sekine, H Nagata, S Tsuji, et al.
American Journal of Human Genetics|August 1, 1997
Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1K Ishikawa, H Tanaka, M Saito, et al.
Archives of Neurology|May 18, 2001
Spinocerebellar ataxia type 1 in China: molecular analysis and genotype-phenotype correlation in 5 familiesY X Zhou, W H Qiao, W H Gu, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 12, 2001
Mutational analysis of BRCA1 and BRCA2 and clinicopathologic analysis of ovarian cancer in 82 ovarian cancer families: two common founder mutations of BRCA1 in Japanese populationM Sekine, H Nagata, S Tsuji, et al.
Japanese Journal of Cancer Research : Gann|April 1, 1997
Mutational analysis of BRCA1 gene in ovarian and breast-ovarian cancer families in JapanM Takano, H Aida, I Tsuneki, et al.
Pageof 99