Search research articles
Contact Us
Filters
Showing results (41-50 of 52) with videos related to
Page
of 6
Sort By:
Journal of Molecular and Cellular Cardiology
|
July 27, 2018
Temperature-sensitive sarcomeric protein post-translational modifications revealed by top-down proteomics
Wenxuan Cai, Zachary L Hite, Beini Lyu, et al.
The Journal of Surgical Research
|
January 16, 2022
Hotter Than It Looks: A Retrospective Review of Patients With Cholecystitis and With Negative Imaging
Kathrine A Kelly-Schuette, Alistair J Chapman, Lauren E Messer, et al.
Cardiovascular Research
|
March 30, 2013
Familial dilated cardiomyopathy mutations uncouple troponin I phosphorylation from changes in myofibrillar Ca²⁺ sensitivity
Massimiliano Memo, Man-Ching Leung, Douglas G Ward, et al.
Circulation. Heart Failure
|
October 8, 2009
Functional analysis of a unique troponin c mutation, GLY159ASP, that causes familial dilated cardiomyopathy, studied in explanted heart muscle
Emma C Dyer, Adam M Jacques, Anita C Hoskins, et al.
Journal of Health Care Chaplaincy
|
May 9, 2009
A tribute to Andrew J. Weaver
Kevin J Flannelly, Harold G Koenig, John Preston, et al.
Cardiovascular Research
|
October 26, 2012
Myofibrillar Ca(2+) sensitivity is uncoupled from troponin I phosphorylation in hypertrophic obstructive cardiomyopathy due to abnormal troponin T
Christopher R Bayliss, Adam M Jacques, Man-Ching Leung, et al.
Cardiovascular Research
|
April 16, 2008
The molecular phenotype of human cardiac myosin associated with hypertrophic obstructive cardiomyopathy
Adam M Jacques, Natalia Briceno, Andrew E Messer, et al.
Scientific Reports
|
November 3, 2017
Abnormal contractility in human heart myofibrils from patients with dilated cardiomyopathy due to mutations in TTN and contractile protein genes
Petr G Vikhorev, Natalia Smoktunowicz, Alex B Munster, et al.
Scientific Reports
|
September 26, 2018
Author Correction: Abnormal contractility in human heart myofibrils from patients with dilated cardiomyopathy due to mutations in TTN and contractile protein genes
Petr G Vikhorev, Natalia Smoktunowicz, Alex B Munster, et al.
Journal of Muscle Research and Cell Motility
|
January 14, 2009
Myofilament dysfunction in cardiac disease from mice to men
Nazha Hamdani, Monique de Waard, Andrew E Messer, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 52) with videos related to
Sort By:
Page
of 6
Journal of Molecular and Cellular Cardiology
|
July 27, 2018
Temperature-sensitive sarcomeric protein post-translational modifications revealed by top-down proteomics
Wenxuan Cai, Zachary L Hite, Beini Lyu, et al.
The Journal of Surgical Research
|
January 16, 2022
Hotter Than It Looks: A Retrospective Review of Patients With Cholecystitis and With Negative Imaging
Kathrine A Kelly-Schuette, Alistair J Chapman, Lauren E Messer, et al.
Cardiovascular Research
|
March 30, 2013
Familial dilated cardiomyopathy mutations uncouple troponin I phosphorylation from changes in myofibrillar Ca²⁺ sensitivity
Massimiliano Memo, Man-Ching Leung, Douglas G Ward, et al.
Circulation. Heart Failure
|
October 8, 2009
Functional analysis of a unique troponin c mutation, GLY159ASP, that causes familial dilated cardiomyopathy, studied in explanted heart muscle
Emma C Dyer, Adam M Jacques, Anita C Hoskins, et al.
Journal of Health Care Chaplaincy
|
May 9, 2009
A tribute to Andrew J. Weaver
Kevin J Flannelly, Harold G Koenig, John Preston, et al.
Cardiovascular Research
|
October 26, 2012
Myofibrillar Ca(2+) sensitivity is uncoupled from troponin I phosphorylation in hypertrophic obstructive cardiomyopathy due to abnormal troponin T
Christopher R Bayliss, Adam M Jacques, Man-Ching Leung, et al.
Cardiovascular Research
|
April 16, 2008
The molecular phenotype of human cardiac myosin associated with hypertrophic obstructive cardiomyopathy
Adam M Jacques, Natalia Briceno, Andrew E Messer, et al.
Scientific Reports
|
November 3, 2017
Abnormal contractility in human heart myofibrils from patients with dilated cardiomyopathy due to mutations in TTN and contractile protein genes
Petr G Vikhorev, Natalia Smoktunowicz, Alex B Munster, et al.
Scientific Reports
|
September 26, 2018
Author Correction: Abnormal contractility in human heart myofibrils from patients with dilated cardiomyopathy due to mutations in TTN and contractile protein genes
Petr G Vikhorev, Natalia Smoktunowicz, Alex B Munster, et al.
Journal of Muscle Research and Cell Motility
|
January 14, 2009
Myofilament dysfunction in cardiac disease from mice to men
Nazha Hamdani, Monique de Waard, Andrew E Messer, et al.
Page
of 6