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C REDWOOD

Showing results (11-20 of 15) with videos related to

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The Journal of Physiology|February 19, 2005
Effects of the mutation R145G in human cardiac troponin I on the kinetics of the contraction-relaxation cycle in isolated cardiac myofibrilsM Kruger, S Zittrich, C Redwood, et al.
Biochimica Et Biophysica Acta|September 28, 1998
Physiological regulation of eukaryotic topoisomerase IIR J Isaacs, S L Davies, M I Sandri, et al.
Acta Crystallographica. Section D, Biological Crystallography|June 19, 2008
An investigation into the protonation states of the C1 domain of cardiac myosin-binding protein CS J Fisher, J R Helliwell, S Khurshid, et al.
Human Molecular Genetics|May 24, 2001
Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesisE Blair, C Redwood, H Ashrafian, et al.
Circulation Research|June 13, 2000
Investigation of a truncated cardiac troponin T that causes familial hypertrophic cardiomyopathy: Ca(2+) regulatory properties of reconstituted thin filaments depend on the ratio of mutant to wild-type proteinC Redwood, K Lohmann, W Bing, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
The Journal of Physiology|February 19, 2005
Effects of the mutation R145G in human cardiac troponin I on the kinetics of the contraction-relaxation cycle in isolated cardiac myofibrilsM Kruger, S Zittrich, C Redwood, et al.
Biochimica Et Biophysica Acta|September 28, 1998
Physiological regulation of eukaryotic topoisomerase IIR J Isaacs, S L Davies, M I Sandri, et al.
Acta Crystallographica. Section D, Biological Crystallography|June 19, 2008
An investigation into the protonation states of the C1 domain of cardiac myosin-binding protein CS J Fisher, J R Helliwell, S Khurshid, et al.
Human Molecular Genetics|May 24, 2001
Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesisE Blair, C Redwood, H Ashrafian, et al.
Circulation Research|June 13, 2000
Investigation of a truncated cardiac troponin T that causes familial hypertrophic cardiomyopathy: Ca(2+) regulatory properties of reconstituted thin filaments depend on the ratio of mutant to wild-type proteinC Redwood, K Lohmann, W Bing, et al.
Pageof 2