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

I Ohtsuki

Showing results (51-60 of 56) with videos related to

Pageof 6
Sort By:
You have reached the last page of results.This site can display upto 56 results.
Journal of Biochemistry|May 1, 1984
A 26K fragment of troponin T from rabbit skeletal muscleI Ohtsuki, F Shiraishi, N Suenaga, et al.
Journal of Biochemistry|March 25, 2000
Functional consequences of the deletion mutation deltaGlu160 in human cardiac troponin TK Harada, F Takahashi-Yanaga, R Minakami, et al.
Cancer|November 1, 1983
Infantile digital fibromatosis. Identification of actin filaments in cytoplasmic inclusions by heavy meromyosin bindingH Iwasaki, M Kikuchi, I Ohtsuki, et al.
The American Journal of Physiology|August 13, 1999
Functional changes in troponin T by a splice donor site mutation that causes hypertrophic cardiomyopathyH Nakaura, S Morimoto, F Yanaga, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 5, 2002
Ca(2+)-desensitizing effect of a deletion mutation Delta K210 in cardiac troponin T that causes familial dilated cardiomyopathyS Morimoto, Q-W Lu, K Harada, et al.
Journal of Molecular and Cellular Cardiology|December 12, 2001
Functional consequences of the mutations in human cardiac troponin I gene found in familial hypertrophic cardiomyopathyF Takahashi-Yanaga, S Morimoto, K Harada, et al.
Pageof 6

Showing results (51-60 of 56) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 56 results.
Journal of Biochemistry|May 1, 1984
A 26K fragment of troponin T from rabbit skeletal muscleI Ohtsuki, F Shiraishi, N Suenaga, et al.
Journal of Biochemistry|March 25, 2000
Functional consequences of the deletion mutation deltaGlu160 in human cardiac troponin TK Harada, F Takahashi-Yanaga, R Minakami, et al.
Cancer|November 1, 1983
Infantile digital fibromatosis. Identification of actin filaments in cytoplasmic inclusions by heavy meromyosin bindingH Iwasaki, M Kikuchi, I Ohtsuki, et al.
The American Journal of Physiology|August 13, 1999
Functional changes in troponin T by a splice donor site mutation that causes hypertrophic cardiomyopathyH Nakaura, S Morimoto, F Yanaga, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 5, 2002
Ca(2+)-desensitizing effect of a deletion mutation Delta K210 in cardiac troponin T that causes familial dilated cardiomyopathyS Morimoto, Q-W Lu, K Harada, et al.
Journal of Molecular and Cellular Cardiology|December 12, 2001
Functional consequences of the mutations in human cardiac troponin I gene found in familial hypertrophic cardiomyopathyF Takahashi-Yanaga, S Morimoto, K Harada, et al.
Pageof 6